Abstract
Echinostoma flukes armed with 37 collar spines on their head collar are called as 37-collar-spined Echinostoma spp. (group) or ‘Echinostoma revolutum group’. At least 56 nominal species have been described in this group. However, many of them were morphologically close to and difficult to distinguish from the other, thus synonymized with the others. However, some of the synonymies were disagreed by other researchers, and taxonomic debates have been continued. Fortunately, recent development of molecular techniques, in particular, sequencing of the mitochondrial (nad1 and cox1) and nuclear genes (ITS region; ITS1-5.8S-ITS2), has enabled us to obtain highly useful data on phylogenetic relationships of these 37-collar-spined Echinostoma spp. Thus, 16 different species are currently acknowledged to be valid worldwide, which include E. revolutum, E. bolschewense, E. caproni, E. cinetorchis, E. deserticum, E. lindoense, E. luisreyi, E. mekongi, E. miyagawai, E. nasincovae, E. novaezealandense, E. paraensei, E. paraulum, E. robustum, E. trivolvis, and Echinostoma sp. IG of Georgieva et al., 2013. The validity of the other 10 species is retained until further evaluation, including molecular analyses; E. acuticauda, E. barbosai, E. chloephagae, E. echinatum, E. jurini, E. nudicaudatum, E. parvocirrus, E. pinnicaudatum, E. ralli, and E. rodriguesi. In this review, the history of discovery and taxonomic debates on these 26 valid or validity-retained species are briefly reviewed.
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Key words: Echinostoma, Echinostoma revolutum, ‘revolutum’ group, 37-collar-spined echinostome, historical review
INTRODUCTION
Echinostomes, including families Echinostomatidae, Himasthlidae, and Echinochasmidae, are a large group of trematodes parasitizing the small intestines of fish, reptiles, birds, and mammals [
1]. Among the Echinostomatidae,
Echinostoma is the most important genus in public health as well as veterinary medical aspects. The type species of the genus
Echinostoma is
E. revolutum (Froelich, 1802) Dietz, 1909, and within this genus numerous species have been described from birds and mammals [
2,
3]. At least 120 species were listed by Yamaguti [
1] until the 1960s which included 101 species infecting birds and 22 species infecting mammals; among them 3 species were reported from both mammals and birds [
1]. Later, a lot of new species have been described from various parts of the world. However, host specificity of many species was further studied and redefined, and many of them were synonymized with the others [
4–
6].
E. revolutum and other 37-collar-spined
Echinostoma spp. are a large group of echinostomes representing the Echinostomatidae in various aspects. They are also called as 37-collar-spined
Echinostoma spp. (group), ‘
E. revolutum group’ [
4,
7], or simply ‘
revolutum’ group [
8–
11]. Kanev [
4] proposed that “worms with 37 collar spines belonging to the genus
Echinostoma and occurring in naturally infected birds in Europe and Asia be referred to as ‘
E. revolutum group’. However, in the present review, for comprehensiveness and convenience, all 37-collar-spined
Echinostoma spp. ever reported from naturally infected birds and/or mammals around the world have been assigned as ‘37-collar-spined
Echinostoma spp.’ or ‘
E. revolutum group’.
More than 56 nominal species have been described in this group (
Tables 1,
2). However, there have long been debates on the taxonomy and classification of these species. More than a half of them have been synonymized with the others (
Table 2). At present, 16 species (14 of them have molecular data) (
Figs. 1,
2) are regarded as valid species, and 10 should be further evaluated for their validity (
Table 1). Among them, zoonotic species infecting humans are at least 8, including
E. revolutum,
E. cinetorchis,
E. echinatum (needs confirmation),
E. lindoense, E. mekongi, E. miyagawai (experimental),
E. paraensei (from the coprolite of a human mummy), and
E. paraulum [
2,
3,
5,
12–
15]. In this review, the historical aspects and current status of 26 valid or validity-retained species of 37-collar-spined
Echinostoma group are briefly reviewed.
BRIEF HISTORY
After revision and set-up new systematics of echinostomes in the early 1900s by Dietz [
16,
17], hundreds of articles have dealt with taxonomy and biology of echinostomes [
18]. Among the workers, Beaver [
19] was the one who extensively studied and reviewed the taxonomy of 37-collar-spined echinostomes. He obtained adult flukes from experimentally infected birds and mammals originating from the freshwater snail
Helisoma trivolvis and described the worm as
E. revolutum in USA (later turned out to be
Echinostoma trivolvis by Kanev et al. [
6]) and morphologically compared this species with previously reported species from the world. He synonymized 9 species with
E. revolutum, including
Echinostoma armigerum Barker & Irvine, 1915,
Echinostoma cinetorchis Ando & Ozaki, 1923,
Echinostoma coalitum Barker & Beaver, 1915,
Echinostoma columbae Zunker, 1925,
Echinostoma echinatum (Zeder, 1803) de Blainville, 1828,
Echinostoma limicoli Johnson, 1920,
Echinostoma miyagawai Ishii, 1932,
Echinostoma mendax Dietz, 1909, and
Echinostoma paraulum Dietz, 1909. In addition, he treated 11 species as synonyms inquirenda, which included
Echinostoma acuticauda Nicoll, 1914,
Echinostomas armatum (Molin, 1850) Yamaguti, 1971,
Echinostoma callawayensis Barker & Noll, 1915,
Echinostoma dilatatum (Miram, 1840) Cobbold, 1960,
Echinostoma echinocephalum (Rudolphi, 1819) Cobbold, 1860,
Echinostoma erraticum Lutz, 1924,
Echinostoma microrchis Lutz, 1924,
Echinostoma neglectum Lutz, 1924,
Echinostoma nephrocystis Lutz, 1924,
Echinostoma oxycephalum (Rudolphi, 1819) Railliet, 1896, and
Echinostoma sudanense Odhner, 1911. Later, however, some of these species, including
E. revolutum of Beaver [
19],
E. armigerum,
E. coalitum, and
E. callawayensis, were synonymized with
Echinostoma trivolvis (Cort, 1914) Kanev, 1985 [
6,
20]. Kanev et al. [
6] also synonymized
Echinostoma multispinosum Pérez Vigueras, 1944,
E. paraulum of Miller, 1937, and
Echinoparyphium contiguum Barker & Bastron, 1915 with
E. trivolvis. However, the validity of
E. miyagawai,
E. cinetorchis, and
E. paraulum were re-evaluated and acknowledged by Kostadinova et al. [
21], Chai [
3,
22], and Georgieva et al. [
10], respectively. The morphologies of
E. miyagawai and
E. paraulum were redescribed [
11,
21]. The name
E. acuticauda is still used by other researchers [
23,
24], although this species needs re-evaluation. The 4 species of 37-collar-spined
Echinostoma from Brazil, including
E. erraticum,
E. microrchis,
E. neglectum, and
E. nephrocystis, and 2 non-37-collar-spined species,
Echinostoma exile (43–45 collar spines) and
Echinostoma parsespinosum (29–33 collar spines), were re-examined and redescribed by Kohn and Fernandes [
25]. Kostadinova and Gibson [
26] stated that the 4 species of 37-collar-spined species redescribed by them [
25] exhibited significant morphological differences suggesting their taxonomic significance. In addition, a checklist of cercariae in molluscs from Brazil listed the names of
E. erraticum (infecting
Spirulina and
Drepanotrema snails) and
E. nephrocystis (infecting
Physa sp. snails) [
27]. However, in the present review, these 4 species were tentatively regarded as synonyms of
E. revolutum, as suggested by Beaver [
19].
Echinostoma equinatus gigas Marco del Pont, 1926 [
28] was reported from Argentina, but the worms were later assigned to
Echinoparyphium recurvatum by Lunaschi et al. [
29].
Echinostoma chloephagae Sutton and Lunaschi, 1980 also reported from Argentina attracted no much taxonomic attention but listed in a checklist of parasites of birds from Argentina [
29].
Echinostoma ralli Yamaguti, 1934 was reported in Japan and this name was used by Yoshino et al. [
30]. The taxonomic validity of
Echinostoma robustum Yamaguti, 1935 which was originally reported from Taiwan was supported by Detwiler et al. [
31] through molecular analyses of specimens from USA and Brazil. However, the specific diagnosis of these worms as
E. robustum needs reconfirmation.
Echinostoma goldi Oschmarin, 1956 was reported from the intestine of the bird
Pernis apivorus in Russian Far East [
32]; this species was mentioned to have 37 collar spines by Yamaguti [
1] but the figure presented by Skrjabin and Bashikirova [
32] shows that it has 35 collar spines. Therefore, this species (species inquirenda) is excluded from the 37-collar-spined
Echinostoma group until further studies are performed to confirm that it evidently has 37 collar spines.
Echinostoma revolutum var.
japonicum Kurisu, 1932 and
Echinostoma stromi Bashikirova, 1946 have been synonymized with
E. revolutum by Yamaguti [
1].
Echinostoma revolutum tenuicolle Bashikirova, 1941 seems to be a synonym of
E. revolutum. Among the 3 species reported from UK, including
Echinostoma nudicaudatum Nasir, 1960,
Echinostoma pinnicaudatum Nasir, 1961, and
Echinostoma londonensis Khan, 1961, the former 2 have seldom attracted taxonomic attention, whereas
E. londonensis was suggested to be identical with
E. echinatum by Kanev [
4].
Kanev [
4,
20] studied on the life cycle of
E. revolutum in Europe (from Germany) using the freshwater snail
Lymnaea stagnalis as the starting point and redescribed the morphology of larval and adult
E. revolutum. Kanev [
4] and Kanev et al. [
5,
6] synonymized
Echinostoma audyi Lie & Umathevy, 1965,
Echinostoma ivaniosi Mahandas, 1973, and
E. paraulum Dietz, 1909 with
E. revolutum. Also, Kanev [
4,
20], Huffman and Fried [
7], and Kanev et al. [
5,
6,
33] synonymized
Echinostoma lindoense Sandground & Bonne, 1940,
Echinostoma barbosai Lie & Basch, 1966,
E. miyagawai Ishii, 1932, and
E. revolutum of Nasincova, 1986 with
E. echinatum. Kanev et al. [
5] also synonymized
Echinostoma sisjakowi (Skvortsov, 1935) Yamaguti, 1971,
Echinostoma orlovi Romashov, 1966, and
Echinostoma bolschewense (Kotova, 1939) Nasincova, 1991 with
E. jurini (Skvortsov, 1924) Kanev, 1985. Meanwhile,
Echinostoma liei Jeyarasasingam et al., 1972,
Echinostoma togoensis Jourdan & Kulo, 1981, and
Echinostoma paraensei Lie & Basch, 1967 were synonymized with
Echinostoma caproni Richard, 1964 by Huffman and Fried [
7]. Thus, Kanev [
4] listed only 5 species in the 37-collar-spined
Echinostoma group, which included
E. revolutum (sensu stricto),
E. trivolvis,
E. caproni,
E. jurini, and
E. echinatum. Later, however,
E. paraensei was acknowledged as a distinct species because of its unique isoenzymatic patterns [
34] and unique DNA sequences [
35]. In addition, Kostadinova and Gibson [
26] and Kostadinova et al. [
21,
36] reconsidered
E. miyagawai as a distinct species, and rather questioned about the taxonomic status of
E. echinatum.
In the meantime,
Echinostoma rodriguesi Hsu et al., 1968 was reported as a new 37-collar-spined group from Brazil [
37], and
Echinostoma parvocirrus Nassi and Dupouy [
38], 1988 from Guadeloupe, French West Indies.
Echinostoma friedi Toledo et al. [
39], 2000 was described as a new species in Spain. Thereby, Kostadinova et al. [
26] listed 8 species in the ‘
revolutum’ group, which included
E. revolutum (sensu stricto),
E. jurini,
E. trivolvis,
E. paraensei,
E. caproni,
E. miyagawai,
E. parvocirrus, and
E. friedi but did not include
E. rodriguesi. According to Kostadinova et al. [
40], a voucher specimen of
E. revolutum designated by Morgan and Blair [
41] from Australia was found to be affiliated to
E. robustum (?) although they did not favor this specific diagnosis; later Georgieva et al. [
10] assigned this isolate to
E. miyagawai. However, the validity of
E. robustum was supported by Detwiler et al. [
31,
42] based on materials from North America and Brazil. After then,
Echinostoma deserticum Kechemir et al., 2002 was reported as a new 37-collar-spined species from Africa [
43], and
Echinostoma luisreyi Maldonado et al., 2003 as a new member from Brazil [
44]. Fried and Graczyk [
8] listed 10 species in the 37-collar-spined
Echinostoma spp., including
E. revolutum,
E. caproni,
E. echinatum,
E. friedi,
E. jurini,
E. luisreyi,
E. miyagawai,
E. paraensei,
E. parvocirrus, and
E. trivolvis; however, they did not mention about
E. deserticum,
E. rodriguesi, and
E. robustum. Toledo et al. [
9] listed 10 species, including
E. revolutum,
E. caproni,
E. deserticum,
E. friedi,
E. jurini,
E. luisreyi,
E. miyagawai,
E. paraensei,
E. parvocirrus, and
E. trivolvis, but did not mention on
E. echinatum,
E. rodriguesi, and
E. robustum.
Based on molecular, morphological, and ecological data, the classification of 37-collar-spined
Echinostoma species became more diverse and have been continuously changing [
10,
11,
24,
31,
42,
45,
46]. Faltýnková et al. [
11] synonymized
E. friedi with
E. miyagawai based on morphological data. Mohanta et al. [
46] suggested synonymy of
E. robustum,
E. miyagawai, and
E. friedi, but the synonymy between
E. miyagawai (
E. friedi) and
E. robustum is disagreed by other workers [
47]. It is also noteworthy that several new cryptic 37-collar-spined
Echinostoma spp. have been discovered in different parts of the world, which included
Echinostoma sp. IG by Georgieva et al., 2013 [
45],
Echinostoma spp. clade 3 by
nad1 and ITS2 analyses by Noikong et al. [
48],
Echinostoma nasincovae Georgieva et al., 2014 [
10,
11],
Echinostoma novaezealandense Georgieva et al., 2017 [
24], and
Echinostoma mekongi Cho et al., 2020 [
49]. Synonymies previously based only on morphological characters should be reconsidered until the results are firmly supported by molecular evidences.
SPECIES REPORTED IN EACH CONTINENT
Asia
At least 11 species, including
E. revolutum [
50–
57],
E. audyi [
58],
E. cinetorchis [
59–
61],
E. ivaniosi [
62],
E. lindoense [
63],
E. mekongi [
49],
E. miyagawai [
64,
65],
E. paraulum [
14,
66,
67],
E. ralli [
68],
E. revolutum var.
japonicum [
69], and
E. robustum [
70] were reported to have 37 collar spines.
E. audyi and
E. ivaniosi were synonymized with
E. revolutum by Kanev [
4], and
E. revolutum var.
japonicum with
E. revolutum by Yamaguti [
1]. Beaver [
19] synonymized
E. cinetorchis with
E. revolutum; however,
E. cinetorchis is characteristic in having testes which are mobile to other locations within the body; one or both testes even disappear from the body while they grow to be adults [
2,
3,
13,
22,
71].
E. lindoense was synonymized with
E. echinatum by Kanev et al. [
33]; however, the status of
E. echinatum is questioned by many workers [
10,
11,
26]. In addition,
E. lindoense has unique larval and adult morphology discriminating from
E. revolutum (see
E. lindoense section), and thus the name
E. lindoense is retained in this review.
E. mekongi was reported as a new species from human infections in 2 provinces of Cambodia along the Mekong River, which is morphologically close to
E. revolutum and
E. miyagawai but molecularly distinct from them and also 12 other 37-collar-spined
Echinostoma spp. available in GenBank [
49]. A recent mitochondrial DNA study reported that 2 distinct species, including
E. revolutum and
E. miyagawai, exist in Thailand and Lao PDR [
72]. In China, complete mitochondrial genome of
E. miyagawai has been obtained and characterized [
73,
74]. A synonymy between
E. miyagawai and
E. robustum was suggested based on molecular analysis in Bangladesh [
46]; however, this synonymy is disagreed by Heneberg [
47].
Cytochrome B gene was found to be useful to differentiate Asian
E. revolutum from African
E. caproni and South American
E. paraensei [
75]. Thus, at least 8 species, including
E. revolutum,
E. cinetorchis,
E. lindoense,
E. mekongi,
E. miyagawai,
E. paraulum,
E. ralli, and
E. robustum, are recognized to be existing in Asia (
Table 3).
More than 18 species of 37-collar-spined
Echinostoma spp. were reported from European countries, including Germany, Bulgaria, UK, Austria, Czech Republic, Spain, and Russia;
E. revolutum,
E. bolschewense,
E. columbae,
E. dilatatum,
E. echinatum,
E. friedi,
E. goldi,
E. jurini,
E. londonensis,
E. miyagawai,
E. nasincovae,
E. nudicaudatum,
E. orlovi,
E. oxycephalum,
E. paraulum,
E. pinnicaudatum,
E. sisjakowi, and
Echinostoma sp. IG of Georgieva et al., 2013 [
45]. Among them,
E. columbae,
E. dilatatum, and
E. oxycephalum were synonymized with
E. revolutum or put as species inquirenda by Beaver [
19].
E. orlovi and
E. sisjakowi were synonymized with
E. jurini by Kanev et al. [
5].
E. goldi had 35 collar spines in the figure of Skrjabin and Bashikirova [
32] thus considered not a member of 37-collar-spined group.
E. bolschewense and
E. londonensis were synonymized with
E. jurini and
E. echinatum, respectively, and
E. paraulum was synonymized with
E. revolutum by Kanev [
4] and Kanev et al. [
5]. However, the synonymy of
E. bolschewense with
E. jurini was denied because of morphological differences in their cercariae [
11]. Thus,
E. bolschewense was regarded as a distinct species, and the the status of
E. jurini was retained [
11]. In addition,
E. paraulum was revalidated as distinct species [
10,
11]. On the other hand,
E. friedi reported by Toledo et al. [
39] was synonymized with
E. miyagawai by Faltýnková et al. [
11].
E. robustum Yamaguti, 1935 has been acknowledged as a distinct species based on specimens harvested from a duck in UK [
76]; this species was also recorded from birds in Poland [
77] and Russia [
78,
79].
E. miyagawai originally reported from Japan was later reported also in Bulgaria and Czech Republic [
21,
36]. Put together, in Europe, at least 11 species of 37-collar-spined echinostomes can be currently acknowledged to be valid or validity-retained;
E. revolutum (sensu stricto),
E. bolschewense,
E. echinatum,
E. jurini,
E. miyagawai,
E. nasincovae,
E. nudicaudatum,
E. paraulum,
E. pinnicaudatum,
E. robustum, and
Echinostoma sp. IG [
11,
76] (
Table 3).
More than 5 species of 37-collar-spined
Echinostoma spp. were nominally described, including
E. caproni [
80,
81],
E. deserticum [
43],
E. revolutum [
82],
E. liei [
83], and
E. togoensis [
84]. However, Kanev [
4] suggested that
E. revolutum described by Bisseru [
82] was actually
E. caproni. Fried and Huffman [
85] also suggested that the studies performed under the name
E. revolutum,
E. liei, and
E. togoensis using materials from Africa actually dealt with
E. caproni. Thereby, only 2 species,
E. caproni and
E. deserticum can be currently recognizable as the 37-collar-spined
Echinostoma spp. existing in Africa (
Table 3).
The taxonomy of 37-collar-spined
Echinostoma spp. in North and Central America has not yet been properly revised or settled [
10]. In North America, 5 species were reported at an earlier time, including
E. trivolvis,
E. armigerum,
E. coalitum,
E. collawayensis, and
Echinoparyphium contiguum [
6,
10]. Beaver [
19] treated 4 of the above (
E. armigerum,
E. coalitum,
E. collawayensis, and
E. contiguum) as synonyms of
E. revolutum or synonyms inquirenda. However, Kanev [
20] pointed out that the
E. revolutum of Beaver [
19] and many articles published from North America under the name
E. revolutum during 1968–1988 should be reconsidered to have been actually
E. trivolvis. The true existence of
E. revolutum in North America was later confirmed in 1997–1998 by Sorensen et al. [
86,
87] through morphological as well as molecular studies. Later, based on
nad1 gene sequences, the American
E. revolutum was shown to be genetically distinct from European populations, and further studies seemed necessary on the taxonomy of North American 37-collar-spined
Echinostoma spp. [
10,
31]. In addition, Detwiler et al. [
31] detected the presence of
E. robustum from Indiana and Minnesota, USA, and also from Brazil. From Guadeloupe (French West Indies),
E. parvocirrus was reported [
38]. Thus, in North and Central America, at least 4 species can be listed as the ‘
revolutum’ group;
E. revolutum,
E. parvocirrus,
E. robustum, and
E. trivolvis [
38,
42] (
Table 3).
More than 14 species, namely,
E. revolutum,
E. armatum,
E. barbosai,
E. chloephagae,
E. equinatus gigas,
E. erraticum,
E. luisreyi,
E. mendax,
E. microrchis,
E. neglectum,
E. nephrocystis,
E. paraensei,
E. robustum, and
E. rodriguesi, have been described in South America [
19,
31,
42,
44,
88–
90]. The presence of
E. revolutum in Brazil has been reported by various workers, including Brasil and Amato [
91], as reviewed by Maldonado and Lanfredi [
92].
E. barbosai was synonymized with
E. echinatum by Kanev et al. [
33]; however, the status of
E. echinatum is not recognized by other workers [
10,
11]. Therefore, the name
E. barbosai is retained until further confirmatory studies are performed. Beaver [
19] treated the 4 species reported from Brazil by Lutz [
88], i.e.,
E. erraticum,
E. neglectum,
E. microrchis, and
E. nephrocystis, as synonym inquirenda. These might be identical with
E. revolutum or
E. trivolvis. However, Kanev et al. [
6] did not recognize the presence of
E. trivolvis in South America; although, the possible existence of
E. trivolvis in South America remains to be confirmed. In the present review, the 4 species reported by Lutz [
88] were tentatively synonymized with
E. revolutum.
E. equinatus gigas reported by Marco del Pont [
28] was later assigned to
Echinoparyphium recurvatum [
29]. Kanev [
20] considered
E. paraensei a synonym of
E. caproni, and Huffman and Fried [
7] accepted this synonymy. However,
E. paraensei was acknowledged as a distinct species because of its unique isoenzymatic patterns [
34] and DNA sequences [
35]. The presence of
E. robustum in South America was first suggested by molecular analysis of materials obtained from Brazil [
31]. Therefore, the existence of at least 7 species of 37-collar-spined echinostomes, including
E. revolutum,
E. barbosai,
E. chloephagae,
E. luisreyi,
E. paraensei,
E. robustum, and
E. rodriguesi, is currently recognized to be valid or validity-retained in South America (
Table 3). It is of considerable interest that in a mummified human body in Brazil, eggs presumed to be of
E. paraensei (or
E. luisreyi) were detected by a molecular technique [
15].
A total of 5 species of 37-collar-spined echinostomes have been reported;
E. acuticauda,
E. miyagawai,
E. novaezealandense,
E. paraensei, and
E. revolutum (
Table 1).
E. acuticauda was reported in 1914 in Australia [
93], and soon synonymized (synonym inquirenda) with
E. revolutum by Beaver [
19]. However, this synonymy is not agreed by other workers, and the name
E. acuticauda has been used by Jones and Anderson [
23] and Georgieva et al. [
24]. Morgan and Blair [
41] reported that 3 metacercarial isolates (LMeta-1, PMeta-1, and PMeta-2) from Townsville showed greater than 98% sequence similarity with
E. revolutum from Europe. Later, Kostadinova et al. [
40] suggested all these isolates to be
E. robustum (?). However, Georgieva et al. [
10] placed all these isolates among the clusters of
E. miyagawai. Thus, the presence of
E. robustum in Australia needs reconfirmation. Morgan and Blair [
41] also isolated
E. paraensei (PCerc-1) cercariae from
Glyptophysa sp. snails in Townsville, Australia by molecular analysis [
41]. In New Zealand, a species closely allied to
E. revolutum was found by molecular studies [
41], and 2 more species,
E. novaezealandense and
E. miyagawai, were discovered [
24]. Thus, at least 5 species are existing in Oceania, including
E. revolutum,
E. acuticauda,
E. miyagawai,
E. novaezealandense, and
E. paraensei (
Table 3).
SPECIES OF 37-COLLAR-SPINED ECHINOSTOMA GROUP
Echinostoma revolutum (Froelich, 1802) Dietz, 1909
[syn. Echinostoma armatum Barker & Irvine, 1915; Echinostoma audyi Lie & Umathevy, 1965; Echinostoma columbae Zunker, 1925; Echinostoma dilatatum (Miram, 1940) Cobbold, 1860; Echinostoma echinocephalum (Rudolphi, 1819) Cobbold, 1860; Echinostoma erraticum Lutz, 1924; Echinostoma ivaniosi Mahandas, 1973; Echinostoma limicoli Johnson, 1920; Echinostoma mendax Dietz, 1909; Echinostoma microrchis Lutz, 1924; Echinostoma neglectum Lutz, 1924; Echinostoma nephrocystis Lutz, 1924; Echinostoma oxycephalum (Rudolphi, 1819) Railliet, 1896; Echinostoma revolutum tenuicollis Bashikirova, 1941; Echinostoma revolutum var. japonicum Kurisu, 1932; Echinostoma stromi Bashikirova, 1946; Echinostoma sudanense Odhner, 1910]
This species (
Fig. 3) was originally described under the name
Fasciola revoluta based on adult flukes found in the large intestine of wild ducks
Anas boschas fereae dissected on July 20, 1798 in Germany [
4]. It was about 11 mm long and had 37 collar spines, and these morphological features have served as the main basis for further definitions of
E. revolutum [
4]. A year later,
E. echinatum (under the name
Distoma echinatum) was described by Zeder in Germany, and this name (
D. echinatum or
E. echinatum) had been used for about a hundred years until Dietz [
16,
17] renamed
F. revoluta as
Echinostoma revolutum in his systematic reorganization of the Echinostomatidae and synonymized
E. echinatum with
E. revolutum. Dietz [
16,
17] also synonymized
Echinostoma dilatatum (under the name
Distoma dilatatum Miram, 1940) and
Echinostoma armatum (under the name
Distoma armatum Molin, 1858) with
E. revolutum. This was a big milestone for the taxonomy of
E. revolutum and 37-collar-spined
Echinostoma group. After Dietz [
16,
17], adult worms and larval stages found in Europe, Asia, Africa, Australia, and North and South America have been described as
E. revolutum for at least 70–80 years [
1,
4,
19,
20,
32,
88,
94–
98] (
Table 4). On the other hand, Kanev [
20] and Kanev et al. [
33] suggested the taxonomic validity of
E. echinatum, and Schuster [
99], Christensen et al. [
100], and Huffman and Fried [
7] supported it (see
E. echinatum section). However, the validity of
E. echinatum was recently put to a question by Kostadinova and Gibson [
26], Georgieva et al. [
10], and Faltýnková et al. [
11].
Human infection with
E. revolutum was first described in Taiwan in 1929 [
101]. Later, in 1982, the prevalence of
E. revolutum among Taiwan population was reported to be 0.11–0.65% [
102]. Further human infections were reported in mainland China [
12], Indonesia [
103], Thailand [
104], Cambodia [
51], and Lao PDR [
56]. However, all of these reports are not based on molecular confirmation and need further verification regarding the species identification.
Kanev [
4] studied on almost all previous records on
E. revolutum and other 37-collar-spined group and delimited the definition of
E. revolutum. He stated that 37-collar-spined echinostomes cannot be morphologically identified only by adult flukes but they can be more clearly discriminated by the morphology of larval stages, in particular, the cercariae, and host-parasite relationships. Thus,
E. revolutum was delimited as those flukes having (1) lymnaeid snails as the 1st intermediate host, (2) various pulmonate and prosobranch snails, mussels, frogs, and freshwater turtles as the second intermediate host, (3) only birds as the definitive host, (4) cercariae and adults armed with 37 collar spines, (5) geographical distribution only in Europe and Asia, (6)
Cercaria echinata Siebold, 1937,
E. echinatum, and
E. jurini as closely related species in Europe, and (7) specific characteristics only in larvae and host-parasite relationships [
4]. However, some of these delimitations had to be revised because of various new findings. Using molecular data, Detwiler et al. [
31] confirmed that both lymnaeid and planorbid snails can serve as the 1st intermediate host of
E. revolutum. Detwiler et al. [
42] also confirmed that
E. revolutum can infect a mammalian host, the muskrat
Ondatra zibethicus, in USA. The geographical distribution of
E. revolutum was extended to North and South America, and Oceania [
31,
41,
42,
91] (
Tables 3,
4). Faltýnková et al. [
11] redescribed the morphology of rediae, cercariae, and adults of
E. revolutum based on European samples (from Germany, Finland, Czech Republic, Poland, Bulgaria, and Iceland). In comparison with the report of Kanev [
4], they found in the cercariae 6 outlets of penetration gland-cells (4 outlets in Kanev [
4]) and total 12 outlets of paraesophageal gland-cells (16–20 outlets in Kanev [
4]) [
11] (
Table 5).
Molecular analysis of
E. revolutum was started by Morgan and Blair [
35]. They compared the nucleotide sequences of ITS region (ITS1-5.8S-ITS2) of
E. revolutum (originated from Germany) with those of
E. trivolvis,
E. paraensei,
E. caproni (including
E. liei and
Echinostoma sp. II from Africa), and
Echinostoma sp. I from Africa (
E. deserticum). They concluded that
E. revolutum was phylogenetically close to
E. trivolvis and
E. paraensei but distinct from one another, and far from
E. caproni and
E. deserticum. Morgan and Blair [
41,
105] further compared the usefulness of ITS region and 2 mitochondrial loci (
cox1 and
nad1) to discriminate the species and found that
nad1 appeared to be the most informative locus for investigating phylogenetic relationships within the 37-collar-spined
Echinostoma group. The molecularly distinct status of
E. revolutum in relation to other species and other genera has been supported by Kostadinova et al. [
40].
The existence of
E. revolutum in North America (under the name
E. echinatum, actually
E. trivolvis) was first documented in 1888 [
106] followed by others in 1895 [
107] and 1896 [
108]. In the first document, the specimen was found in muskrats from Pennsylvania [
19,
42], and the next documents were about findings from rabbits and chickens, respectively [
107,
108]. In 1937, Beaver [
19] reported
E. revolutum from experimentally infected birds and mammals, and Fried and coworkers performed extensive works thereafter (more than 70 studies during 1968–1988) under the name
E. revolutum [
7]. However, Kanev [
4,
20] mentioned that
E. revolutum of Beaver [
19] and all other North American literature dealing with
E. revolutum until 1988 were supposed to have been
E. trivolvis.
The true existence of
E. revolutum in North America was first confirmed by Sorensen et al. [
86] who found naturally infected freshwater snails
Lymnaea elodes shedding 37-collar-spined cercariae in Indiana, USA. They experimentally infected various snail species to obtain the metacercariae, which were given to chicken and geese to obtain the adult flukes. Sorensen et al. [
87] notified intraspecific variation in ITS loci sequences among isolates of
E. revolutum (North American and European) and also
E. trivolvis (different localities in Indiana). The existence of
E. revolutum in North America was again confirmed by Detwiler et al. [
31,
42] through molecular analysis of ITS region,
cox1, and
nad1 loci. In addition, Detwiler et al. [
31] reported that both lymnaeid and planorbid snails can serve as the first intermediate host of
E. revolutum and
E. trivolvis in USA. Detwiler et al. [
42] also confirmed that
E. revolutum can infect a mammalian host, the muskrat in USA. Phylogenetic trees based on mitochondrial
cox1 (
Fig. 1) and
nad1 (
Fig. 2) sequences of 7 and 14
Echinostoma species, respectively, show their phylogenetic relationships.
The
nad1 sequence variation among the “
E. revolutum group” indicated that
E. revolutum haplotypes from Europe formed a monophyletic group which clustered closely with a monophyletic group of isolates from North America [
45]. In Asia, molecular genetic studies were conducted on
E. revolutum in comparison with
Hypoderaeum conoideum,
Echinoparyphium recurvatum, and
Artyfechinostomum malayanum (under the name
Echinostoma malayanum) using multilocus enzyme electrophoresis and sequencing of ITS1 and
cox1 [
52,
53,
109,
110]. However, isolates from Southeast Asia were not included in the study of Georgieva et al. [
45] due to the lack of
nad1 data [
72]. Subsequently, it was found that
E. revolutum from Southeast Asia (Thailand and Lao PDR) clustered as a monophyletic clade with the European isolates, named as “Eurasian lineage”, and this was distinct from the American isolates, which was named as “American lineage” [
72]. This
nad1-based genetic variation of
E. revolutum according to geographical locations has been supported by an analysis of
cytochrome B (
CYTB) gene [
75]. Mohanta et al. [
46] accepted the 2 genetic lineages of
E. revolutum using ITS2 and
nad1 sequences. However, Buddhachat and Chontananarth [
111] used DNA barcoding of
cox1 and
nad1 in combination with high-resolution melting analysis to identify
E. revolutum and found that the
E. revolutum clade of
nad1 phylogeny obtained from the Thai isolate formed a different lineage from the Eurasian lineage. Thus, the
nad1 phylogenetic tree revealed 3 lineages of
E. revolutum; Asian, Eurasian, and American lineages [
111]. The complete mitochondrial genome (17,030 bp) of
E. revolutum was obtained and characterized by Le et al. [
112] in comparison with 9 echinostome species, including
E. caproni,
E. miyagawai, and
E. paraensei. They concluded that
E. revolutum grouped in a monophyletic subclade as a sister taxon to
E. miyagawai and paraphyletic to other echinostomatids in the Echinostomatidae [
112]. A multiplex PCR technique targeting the
nad1 gene has been developed for differential detection of 4 medically important echinostome species, including
E. revolutum [
113].
After
E. miyagawai was first described from domestic fowls and domestic and wild ducks in 1932 in Japan [
114], Beaver [
19] raised synonymy of
E. miyagawai with
E. revolutum. Yamaguti [
1,
97] accepted this synonymy but Russian researchers, including Bashikirova [
96] and Skrjabin and Bashikirova [
32], denied the synonymy. Kosupko [
115,
116] was the first who applied complex morphological and ecological approaches to distinguish
E. revolutum and
E. miyagawai and validated the 2 species as separate taxa on the basis of their morphological differences in cercariae and adults, ontogenic development, first intermediate and final host preferences, and their distribution in the host intestine. Nevertheless, Kanev [
4] denied the validity of
E. miyagawai and synonymized it with
E. echinatum. Kostadinova et al. [
21] re-validated
E. miyagawai to be distinct from
E. revolutum and
E. echinatum of Kanev [
1,
20] on the basis of experimental completion of its life cycle. According to them, the adult worms of
E. miyagawai were characterized by having a very elongate body with a constriction at the posterior border of the ventral sucker (no constriction in
E. revolutum), a large head collar with relatively small collar spines (larger collar spines in
E. revolutum), a spherical ventral sucker which is only about half the maximum body width (larger ventral sucker in
E. revolutum), a long cirrus-sac reaching posteriorly to the middle of the ventral sucker (to the anterior border of ventral sucker in
E. revolutum), indented subglobular testes (globular or slightly lobed in
E. revolutum), and vitellaria forming 2 lateral fields of follicles which are almost confluent in the post-testicular space (not confluent in
E. revolutum) [
21] (
Table 5). In addition, they [
36] suggested 5 morphometric variables to distinguish
E. miyagawai from
E. revolutum, which included body width at posterior border of the ventral sucker, head collar width, length of the esophagus, width of the ventral sucker, and length of the pre-ovarian region.
This species was originally described from a bird (straw-necked ibis
Carphibis spinicollis) in North Queensland, Australia [
93]. It was put to a synonymy with
E. revolutum as a synonym inquirenda by Beaver [
19]; however, this synonymy has not been followed by succeeding authors, for example, Mendheim [
95], Jones and Anderson [
23], Georgieva et al. [
24], and Memon et al. [
67]. This species is morphologically close to
E. novaezealandense described from New Zealand but has a shorter forebody, more anteriorly located ovary and testes, and much larger eggs [
24]. However, the taxonomic status of
E. acuticauda should be re-evaluated by detailed morphological as well as molecular studies in the near future.
E. barbosai was originally described from pigeons, chicks, and ducklings experimentally infected with the metacercariae from
Biomphalaria glabrata snails in Brazil [
117]. This species resembled
E. audyi (a synonym of
E. revolutum) but was smaller in size of adults and different in cercarial characteristics and the first intermediate host [
117].
E. barbosai was also found in Bulgaria by Kanev group [
118]. However, Mutafova and Kanev [
119] synonymized this species with
E. echinatum, because the karyotype of
E. barbosai was completely corresponded to that of
E. echinatum. This synonymy was agreed by Huffman and Fried [
7] and Fried and Graczyk [
8]. However, Kostadinova and Gibson [
26] doubted the status of both species,
E. echinatum and
E. barbosai. Meanwhile, Latin American authors continue to use the name
E. barbosai [
27,
30,
120,
121]. Under this situation, the name
E. barbosai should be retained until further confirmatory studies with molecular data are provided.
Echinostoma bolschewense (Kotova, 1939) Nasincova, 1991
This species originates from
Cercaria bolschewensis Kotova, 1939 shed from prosobranch snails in the European part of Russia [
122]. Later, the adult fluke, named as
E. bolschewense, was collected from the small intestine of experimentally infected hamsters through a life cycle study in South Bohemia, Czech Republic [
122]. Kanev [
4] and Kanev et al. [
5] regarded this species a synonym of
E. jurini. However, Georgieva et al. [
10] studied on
nad1 and 28S rDNA sequences of
E. bolschewense in the cercarial stage from Slovak Republic and found that
E. bolschewense is genetically distinct from
E. revolutum,
E. trivolvis,
E. caproni,
E. paraulum, and
E. miyagawai (but molecular data of
E. jurini are yet unavailable). In addition, Faltýnková et al. [
11] analyzed the differential morphological features of larval and adult stages of
E. bolschewense in comparison with those of
E. juri reported by Kanev et al. [
5] and acknowledged the validity of
E. bolschewense. However, they did not place
E. jurini in synonymy with
E. bolschewense. To re-validate the 2 closely related species,
E. bolschewense and
E. jurini, comparative molecular studies are required.
[syn. Echinostoma liei Jeyarasasingam et al., 1972; Echinostoma togoensis Jourdan & Kulo, 1981]
This echinostome was originally reported from the small intestine of naturally infected birds (kestrels;
Falco newtoni) and a domestic fowl experimentally infected with the metacercariae in a freshwater snail
Bulinus liratus in Madagascar [
80]. The cercariae (under the name
E. liei) were also found in
Biomphalaria alexandrina snails collected in Egypt which were experimentally infected to
B. glabrata and other snail species to obtain the metacercariae and then to chicks and hamsters to obtain the adult flukes [
83]. This echinostome was also reported in Togo (under the name
E. togoensis) which developed into rediae in
Biomphalaria pfeifferi, metacercariae in aquatic pulmonate snails, and adults in laboratory mice [
84]. The synonymy of
E. liei and
E. togoensis with
E. caproni was proposed by Huffman and Fried [
7] and Fried and Huffman [
85] which was followed by other workers [
3,
26]. In addition, Kanev [
20], Huffman and Fried [
7], and Christensen et al. [
100] synonymized
E. paraensei with
E. caproni. However, Sloss et al. [
34] and Morgan and Blair [
35] suggested that
E. paraensei is distinct from
E. caproni based on different isoenzyme electrophoretic patterns and DNA sequences of ITS region.
E. caproni was studied also under the name of
E. revolutum by many workers, including Barus et al. [
123], Christensen [
124], Christensen et al. [
125–
128], Bindseil and Christensen [
129], and Simonsen and Andersen [
130] as mentioned by Fried and Huffman [
85].
The molecular data (
cox1 and
nad1) of
E. caproni have been available by Morgan and Blair [
35,
41,
105] and Macilla [
72].
E. caproni was phylogenetically close to
E. trivolvis as shown by
cox1 sequences [
72].
Cytochrome B gene was also found to be useful to differentiate African
E. caproni from South American
E. paraensei and Asian
E. revolutum [
75].
E. chloephagae was first discovered from the rectum of a bird
Chloephaga picta melanoptera in Argentina [
131]. This species continued to be recorded from naturally infected birds, including
C. picta leucoptera, in Argentina [
29]. Metacercariae of seemingly
E. chloephagae were detected in a bivalve species
Diplodon chilensis in Argentina, and adult flukes were obtained from experimentally infected chickens with the metacercariae [
30]. The taxonomic validity of this species in comparison with other 37-collar-spined
Echinostoma spp. should be evaluated in the near future, through morphological as well as molecular studies.
Echinostoma cinetorchis Ando & Ozaki, 1923
This echinostome (
Fig. 3) was originally described based on specimens recovered from the small intestine of wild rats in Japan by Ando and Ozaki [
59], and redescribed by Dollfus [
132] in French. Kurisu [
69] and Sugimoto [
133] found this echinostome in the intestine of domestic fowls in Japan and a dog in Taiwan, respectively. Tanabe and Takeishi [
134] reported a low prevalence (1.65%) of
E. cinetorchis in rats
Rattus norvegicus captured around Tokyo, Japan. In South Korea, this echinostome was reported from wild rats [
135,
136] and dogs [
137]. Its life cycle was successfully completed in the laboratory using
Hippeutis cantori snails as the source for cercariae and metacercariae [
61]. Human infection with
E. cinetorchis was first reported in Japan [
138–
140], and then in Korea [
60,
141–
144]. Now, it is well known as a zoonotic echinostome infecting humans, rodents, and poultries in Asian countries, including Japan, South Korea, China, Taiwan, Indonesia, and Vietnam [
3,
92,
145–
148].
Beaver [
19] synonymized
E. cinetorchis with
E. revolutum based on their morphologic similarities, including the number of collar spines (n=37) and dimensions of internal organs and eggs. However, this synonymy was not justified by other workers due to various reasons, including, in particular, the unique feature of
E. cinetorchis having testes that move to abnormal locations and even disappear from the body during the worms grow up to be adults (
Table 5) as well as differences in selecting the snail host [
1,
3]. This species is thought to reproduce parthenogenetically without testes and sperms. Now
E. cinetorchis is acknowledged as a distinct species [
2,
3,
92,
149].
In 2016, nad1 sequences of E. cinetorchis were deposited based on materials (adult flukes) obtained from South Korea by Lee et al. (to be published) in GenBank; the sequences are unique and clearly separated from those of E. revolutum Eurasian and American lineages.
Echinostoma deserticum Kechemir, Jourdane & Mas-Coma, 2002
E. deserticum was described as a new species from the small intestine of the African grass rat
Arvicanthis niloticus from Niger [
43]. The majority of adult flukes do not have testes; some have only 1 testis and very rarely 2 testes [
43] which is highly similar to
E. cinetorchis. This species is thought to reproduce parthenogenetically without testes and sperms [
43]. Sporocysts and rediae were isolated from
Bulinus truncatus and
B. globosus snails from south of Algeria and Niger [
43].
Molecular studies on this species were done under the name of
Echinostoma sp. I from Niger by Morgan and Blair [
35,
41,
105] in 1995 before it was formally described as a new species in 2002. The sequences of ITS region and mitochondrial
cox1 and
nad1 loci indicated that
E. deserticum is the most distinct in comparison with other 37-collar-spined echinostomes, including
E. revolutum,
E. trivolvis,
E. paraensei, and
E. caproni (also
E. liei and
Echinostoma sp. II) [
35,
41,
87,
105]. In addition, the
nad1 sequence of
E. deserticum appears to be markedly different from that of the morphologically similar species,
E. cinetorchis, deposited in GanBank, with sequence homology of only 84.7%.
[syn. Echinostoma londonensis Khan, 1961]
E. echinatum was described in 1803 under the name
Distoma echinatum from birds and mammals (?) in Germany, with detailed descriptions of collar spines [
4,
150]. A year before (1802),
Fasciola revoluta (=
E. revolutum) was described by Froelich from birds in Germany [
4]. In 1809, Rudolphi erected a subgeneric group
Echinis (
Echinostoma) within the genus
Distoma and placed
F. revoluta as the type species [
4]. After Rudolphi, however,
F. revoluta was out of use, and its function as the type species was replaced by
Distoma echinatum Zeder, 1803 [
4]. Practically almost all 37-collar-spined echinostomes found in Europe from Rudolphi in 1809 until Dietz in 1909 were diagnosed as
D. echinatum [
4]. However, Dietz [
16,
17] restored the validity of
F. revoluta renaming it as
E. revolutum in his systematic reorganization of the echinostomatid flukes and synonymized
D. echinatum with
E. revolutum. A list of adult and larval worms described under the name
D. echinatum was transferred to
E. revolutum by Dietz [
4]. Thereafter, over 500 articles dealing with this echinostome have described the species name as
E. revolutum [
4]. Beaver [
19], Mendheim [
95], Bashikirova [
96], Skrjabin and Bashikirova [
32], and Yamaguti [
1,
97] followed this synonymy, and the name
E. echinatum disappeared for some time.
Later, however,
E. echinatum was revived by Kanev [
4,
20] and Kanev et al. [
5,
33] based on various differential characters from
E. revolutum and
E. jurini; for example,
E. echinatum took both lymnaeid and planorbid snails as the first intermediate host, whereas
E. revolutum and
E. jurini took only lymnaeid and viviparid snails, respectively. The definitive host of
E. echinatum was birds and mammals, including humans, whereas
E. revolutum infected only avian hosts, and
E. jurini infected only mammalian animals [
5]. The 3 species also differed in the cercarial chaetotaxy and developmental period of eggs and cercariae [
5,
33]. The validity of
E. echinatum was supported by other workers, including Schuster [
99], Christensen et al. [
100], Huffman and Fried [
7], and Fried and Graczyk [
8].
However, some of the differential characters suggested above were denied by succeeding authors; for example, it turned out that
E. revolutum can infect mammalian hosts too, i.e., muskrats in USA, based on molecular analysis of
nad1 sequences [
42]. In addition,
E. revolutum can take both lymnaeid and planorbid snails as the first intermediate host in USA [
31,
42]. Moreover, Kostadinova [
151] criticized Kanev and coworkers’ report of
E. echinatum (sensu Kanev [
4,
20] and Kanev et al. [
33]) stating that re-examination of the voucher specimens identified by Kanev et al. [
33] as
E. echinatum showed 2 other distinct species;
Echinostoma sarcinum Dietz, 1909 possessing 47 collar spines and
Echinostoma sp. (
E. echinatum?) with 37 collar spines.
Regarding
E. lindoense, its geographical distribution was reported to extend from the original Asian countries (Indonesia and Malaysia) to Brazil [
152], Poland, Czechoslovakia (now Czech Republic and Slovak Republic) [
153], and Spain [
154]. Based on this, Kanev [
4] described that
E. echinatum is distributed in different geographical regions of Asia, South America, and Europe, including Germany, where
E. echinatum was originally described. However, Kostadinova and Gibson [
26] doubted the synonymy of
E. lindoense with
E. echinatum because of the remarkable differences in the cercarial morphology. Moreover, the validity of
E. echinatum remains to be re-validated because
E. echinatum has not been formally described in a taxonomic publication [
10,
11,
45]. In GenBank, molecular data under the name
E. echinatum is so far unavailable and should be provided in order to re-validate its taxonomic status. Because of the unique cercarial and adult worm morphology (see
E. lindoense section), the name
E. lindoense should be retained until molecular data in comparison with
E. echinatum (currently unavailable) become available.
[syn. Echinostoma orlovi Romashov, 1966; Echinostoma sisjakowi (Skvortsov, 1935) Yamaguti, 1971]
E. jurini was originally described under the name
Cercaria jurini based on cercariae shed from viviparid snails collected along the Volga River in Russia [
5]. Nasinkova [
122] stated that the description of
C. jurini Skvortsov, 1924 was so inaccurate and incomplete that it cannot be considered a description of a species. Later, this species was redescribed by Kanev [
20] and Kanev et al. [
5] based on larvae and adults obtained experimentally starting from naturally infected
Viviparus contectus and
V. viviparus snails collected along the Danube River in Bulgaria. The metacercariae were obtained from the renopericardial sac of laboratory-raised snails,
Physa acuta and
P. fontinalis after exposure to the cercariae, and adults were recovered from experimental hamsters, rats, and mice [
5]. The morphology of adult flukes closely resembled that of
E. revolutum; however, Kanev [
4] and Kanev et al. [
5] validated this species because of differences in selecting intermediate and definitive hosts and differences in the morphology of cercariae. They stated that
E. jurini infects viviparid snails and mammals, whereas
E. revolutum infects lymnaeid snails and avian hosts. They put a variety of echinostome species in possible synonymy with
E. jurini, which included
E. orlovi Romashov, 1966,
Echinostoma sisjakowi (Skvortsov, 1934) Yamaguti, 1971, and
Echinoparyphium sisjakowi (Skvortsov, 1934).
The validity of
E. jurini was acknowledged by Kostadinova and Gibson [
26], Fried and Graczyk [
8], and Toledo et al. [
9]. However, Kostadinova and Gibson [
26] criticized that the conclusions made by Kanev et al. [
5] that “Practically, all 37-collar-spined adults of
Echinostoma spp. in mammals in Europe (including
E. bolschewense) might be identical with
E. jurini.” appeared to be an overestimate of the degree of morphological variability in the absence of an experimental support. Moreover, Georgieva et al. [
10] obtained
nad1 and 28S rDNA sequences of
E. bolschewense adults originating from
Viviparus acerosus snails in the river Danube, Slovak Republic and found that
E. bolschewense is genetically distinct from
E. revolutum,
E. trivolvis,
E. caproni,
E. paraulum, and
E. miyagawai. However, molecular data of
E. jurini have not yet been reported [
72]. Faltýnková et al. [
11] analyzed differential morphological features of larval and adult stages of
E. bolschewense in comparison with those of
E. juri reported by Kanev et al. [
5]. The cercariae of
E. jurini had 6 outlets for the penetration gland-cells and 8–10 outlets for the paraesophageal gland-cells on the dorsal lip of the oral sucker [
5]; however, the cercariae of
E. bolschewense possessed 10 outlets for the penetration gland-cells (6 median and 4 medio-lateral) and lacks paraesophageal gland-cells [
11]. Furthermore, the adults of
E. bolschewense had much larger eggs (138–162×75–85 μm) than those of
E. jurini (96–132×72–88 μm) [
11]. Based on these characters, they denied the synonymy raised by Kanev et al. [
5] giving remarks on the validity of
E. bolschewense. They neither placed
E. jurini in synonymy with
E. bolschewense. To re-validate these 2 closely related species comparative molecular studies seem to be urgently needed.
This species was first described from human patients in the Lake Lindoe region of Central Celebes, Indonesia [
63]. This echinostome was also discovered from humans in Jakarta, Indonesia and then animals, including rats in Malaysia, Thailand, and the Philippines [
155–
157]. An echinostome species similar in their morphology and biology to
E. lindoense was also found in Brazil [
152] and European countries, including Bulgaria, Poland, Czech Republic, Slovak Republic, Germany, Austria, UK, and Russia [
153,
158]. However, the
E. lindoense reported from Europe and South America needs reconfirmation through molecular analysis with Asian (Indonesian) species.
The major differential points of
E. lindoense from
E. revolutum included morphology of larval stages (particularly the cercariae) and adults; in cercariae
E. lindoense had 2 dorsal, 2 ventral, and 2 small ventrolateral tail fin-folds, whereas
E. revolutum had only 1 small dorsal fin-fold near the tip of the tail [
158]. In addition, the testes of
E. lindoense in adults were deeply indented (Asian strain) or superficially lobed (Brazilian strain; this needs re-evaluation), but those of
E. revolutum are smooth or only slightly lobated [
4,
152] (
Table 5).
E. lindoense has shorter and wider collar spines than
E. revolutum which has longer and slender collar spines with more or less pointed ends [
103].
The larval and adult stages of
E. lindoense were morphologically and biologically similar to those of
E. echinatum originating from Germany, and thus
E. lindoense was synonymized with
E. echinatum by Kanev and coworkers [
4–
6,
20,
33]. This synonymy was accepted by Huffman and Fried [
7], Fried and Graczyk [
8], Toledo et al. [
149], and Toledo and Esteban [
148]. However, Kostadinova and Gibson [
26] and Kostadinova et al. [
21,
36] questioned about the taxonomic validity of
E. echinatum, because of its many uncertain points, for example, a wide range (more than 20) of the number of paraesophageal gland-cell outlets in cercariae, and
E. echinatum has not been properly reported as a taxonomic publication. The questionable status of
E. echinatum was agreed in subsequent publications, including Georgieva et al. [
10,
45] and Fáltynková et al. [
11]. Unfortunately,
E. lindoense has not yet been molecularly analyzed. Chai [
3] tentatively acknowledged the validity of
E. lindoense.
E. luisreyi Maldonado et al., 2003 was originally described from mice and hamsters experimentally infected with metacercariae from
Physa marmorata and
B. glabrata snails in Brazil [
44]. The most important morphological character of this species was the oral corner spines that increase in size from the latero-oral to the ventro-oral regions [
44]. Later, a rodent species,
Akodon montensis, was found to be a natural definitive host [
159]. Fried and Graczyk [
8], Toledo et al. [
9], and Georgieva et al. [
10] recognized this species to be distinct among the 37-collar-spined
E. revolutum group, and Pinto and Melo [
27] mentioned about the cercariae of this species that emerged from
P. marmorata snails in Brazil. This echinostome might have been zoonotic 600–1,200 years ago in Brazil, since eggs morphologically suggestive of
E. luisreyi were found from the coprolites of human mummies [
160]. Another report suggesting
E. luisreyi or
E. paraensei infection in a mummified body (520–600 years before present) of a human in Brazil mentioned that the eggs in coprolites were morphologically similar to
E. luisreyi but molecularly (
cox1 gene; 83 bp) closer to
E. paraensei [
15]. Molecular data of
E. luisreyi are not yet available in GenBank.
Echinostoma mekongi Cho, Jung, Chang, Sohn, Sinuon & Chai, 2020
E. mekongi (
Fig. 3) was reported based on adult flukes recovered from human infections after praziquantel treatment and purging in Kratie and Takeo Province, Cambodia along the Mekong River, which is molecularly distinct from
E. revolutum and 13 other 37-collar-spined
Echinostoma spp. deposited in GenBank [
49]. Adults of this species were 9.0–13.1 in length and 1.3–2.5 mm in maximum width and the eggs in feces and worm uterus were 98–132 μm long and 62–90 μm wide [
49]. The adult worms closely resembled those of
E. revolutum,
E. miyagawai, and several other 37-collar-spined
Echinostoma species [
49]. However, this species revealed remarkable variation in body shape and morphology of the testes (globular, slightly or deeply lobed), and smaller head collar, collar spines, oral and ventral suckers, and cirrus sac compared to
E. revolutum and
E. miyagawai [
49] (
Table 5). Sequencing of 2 mitochondrial genes (
nad1 and
cox1) and a nuclear ITS region (ITS1-5.8S rRNA-ITS2) revealed unique features distinct from
E. revolutum (Southeast Asian, Eurasian, European, and American lineages) and other 37-collar-spined
Echinostoma group available in GenBank (
E. bolschewense,
E. caproni,
E. cinetorchis,
E. miyagawai,
E. nasincovae,
E. novaezealandense,
E. paraensei,
E. paraulum,
E. robustum,
E. trivolvis, and
Echinostoma sp. IG) [
49]. Studies on biological and epidemiological characteristics, including the life cycle, geographical distribution, and source of human infections, are urgently needed [
49].
Echinostoma miyagawai Ishii, 1932
[syn. Echinostoma friedi Toledo, Muñoz-Antolí & Esteben, 2000]
This species was first described from domestic fowls, domestic ducks, and wild ducks in Japan [
114]. Later, an experimental human infection was found successful in China [
12]. Beaver [
19] synonymized
E. miyagawai with
E. revolutum because of their morphological similarities, including the size and arrangement of collar spines, morphology of 2 testes, and size of the oral and ventral suckers, pharynx, and other internal organs. Yamaguti [
1,
97] accepted this synonymy. However, Russian researchers, including Bashikirova [
96] and Skrjabin and Bashikirova [
32], denied this synonymy. In particular, Kosupko [
115–
116] applied complex morphological and ecological approaches to distinguish
E. revolutum and
E. miyagawai and validated the 2 species on the basis of their morphological differences in the cercariae and adults, ontogenic development, first intermediate and final host preferences, and their distribution in the host intestine. Opposed to this, Cooper [
161] and Kanev [
4] denied the validity of
E. miyagawai and synonymized it with
E. revolutum or
E. echinatum, respectively. Later, however, Kostadinova [
162] and Kostadinova et al. [
21,
36] re-validated
E. miyagawai on the basis of unique cercarial chaetotaxy and morphometric data of
E. miyagawai in comparison with
E. revolutum through experimental completion of its life cycle. The adult worms of
E. miyagawai were characterized by a considerably elongate body with a constriction at the posterior border of the ventral sucker, a large head collar with relatively small collar spines, a spherical ventral sucker which is only about half the maximum body width, a long cirrus-sac reaching posteriorly to the middle of the ventral sucker, indented subglobular testes, and vitellaria forming 2 lateral fields of follicles which are almost confluent in the post-testicular space [
21] (
Table 5). In addition, Kostadinova et al. [
36] suggested 5 morphometric variables to distinguish
E. miyagawai from
E. revolutum, which included body width at the posterior border of ventral sucker, head collar width, length of esophagus, width of ventral sucker, and length of the pre-ovarian region. Fried and Graczyk [
8] and Toledo et al. [
9] acknowledged the taxonomic validity of this species.
E. friedi reported as a new species by Toledo et al. [
39] in 2000 was synonymized with
E. miyagawai based on morphological data by Faltýnková et al. [
11].
Molecular data (
nad1 and 28S rRNA) of
E. miyagawai have been available since Georgieva et al. [
10]. The
nad1 analysis showed that
E. miyagawai is in a distinct clade clearly separated from
E. revolutum (sensu stricto; European),
E. revolutum (American lineages),
E. paraulum, and
E. caproni [
10]. This
E. miyagawai clade incorporates
E. friedi reported in GenBank by Marcilla et al. (AJ564379, Valencia, Spain) [
10] and
E. revolutum German strain (AF065832) by Morgan and Blair [
41,
105]. Nagataki et al. [
72] found that
E. miyagawai from Southeast Asia was monophyletic with European isolates, named as “Eurasian lineage”, which was slightly different from “Australian lineage” with no significant genetic differentiation being observed between these lineages. Fu et al. [
73] and Li et al. [
74] obtained the complete mitochondrial genome of
E. miyagawai (Hunan isolate or Heilongjiang isolate, China) which was 14,416 or 14,468 bp in size and consisted of 12 protein-coding genes, 22 transfer RNA genes, 2 ribosomal RNA genes, and 1 non-coding region. Mohanta et al. [
46] suggested a synonymy of
E. robustum,
E. miyagawai, and
E. friedi based on
nad1 sequence analysis. However, Heneberg [
47] did not agree to this synonymy but suggested that G1-G11 isolates from Bangladesh designated as
E. robustum were in fact
E. miyagawai. The taxonomic validities of both
E. miyagawai and
E. robustum have been acknowledged by various workers [
21,
31,
36,
42].
The geographical distribution of
E. miyagawai has been extended from Japan [
163] to South Korea [
64,
65], Russia [
164], China [
12,
73,
74], Vietnam [
165], Thailand, Lao PDR [
72], Bulgaria [
21,
36,
162], Austria and Hungary [
166], Poland [
167], Spain (under the name of
E. friedi) [
39], Czech Republic [
11], and New Zealand [
24] (
Table 4).
[syn. Echinostoma spiniferum (La Valette, 1855) sensu Nasincova, 1992; Echinostoma revolutum of Nasincova, 1986]
Našincová [
168] described the life cycle of an echinostome species she believed to be
E. revolutum in Central Europe, which she had completed in the laboratory based on cercariae from
Planorbarius corneus snails [
11]. Later, she recognized that the cercariae described from
P. corneus differs from the cercariae of
E. revolutum in the pattern of paraesophageal gland-cells and used the name
Echinostoma spiniferum in her Ph.D. thesis in 1992 [
11]. Later, Georgieva et al. [
10] described a new species of
Echinostoma (named as
Echinostoma n. sp.) based on molecular dataset of
nad1 and 28S rDNA sequences during the analyses of 37-collar-spined
Echinostoma spp. in Europe. This
Echinostoma n. sp. formed a unique genetic clade neighbored with
E. paraensei and 3 lineages (A-C) of
E. trivolvis [
31,
42] and remotely joined by 3 isolates of
E. caproni [
10]. Faltýnková et al. [
11] described this as a new species,
E. nasincovae, synonymizing
E. revolutum of Našincová [
168] and
E. spiniferum (La Valette, 1855) sensu Našincová, 1992 with
E. nasincovae. They [
11] described that its snail intermediate host is
P. corneus, the definitive host is experimental hamsters, and the geographical localities included Czech Republic and Slovak Republic. In 2008, Faltýnková et al. [
166] found
Gyraulus albus,
P. corneus,
Planorbis planorbis, and
Bathyomphalus contortus from Czech Republic, Slovak Republic, Germany, and Poland acting as the snail hosts for
E. spiniferum (synonym of
E. nasincovae). Schwelm et al. [
169] also listed
G. albus as a snail host for
E. nasincovae.
The cercariae of
E. nasincovae differed from the cercariae of other species of
Echinostoma within the ‘
revolutum’ group in small body size, 6 ducts of penetration gland-cells opening on the dorsal lip of the oral sucker, and 30–39 outlets of paraesophageal gland-cells, of which 8 are located in the region of the oral sucker and 22–31 are confined to the area between esophagus and the dilated portion of the main collecting excretory ducts [
11]. The adult of
E. nasincovae was most similar to
E. revolutum and
E. bolschewense. However, compared with
E. revolutum,
E. nasincovae had smaller body and organs, smaller angle, lateral, and dorsal collar spines, and smaller eggs [
11]. Compared with
E. bolschewense,
E. nasincovae had smaller body length and width, smaller egg length, smaller lateral and dorsal spine length, and smaller ovary and testes [
11].
In 1998, Morgan and Blair [
41] discovered an unidentified 37-collar-spined
Echinostoma sp. adults (NZ-Ad) from the gut of a wild Canada goose (
Branta canadensis) in New Zealand. This isolate (AF026289) was molecularly distinct from
E. revolutum and
E. paraensei based on the sequence of
nad1 gene [
41]. Later, the same flukes were recovered from the small intestine and rectum of 2 avian species, a wild duck (
Anas platyrhynchos) and a black swan (
Cygnus atratus), in Central Otago District, New Zealand, and morphological and molecular studies (
nad1 and 28S rDNA) were performed [
24]. The
nad1 sequences of 2 isolates from the ducks (KY436398 and KY436399) and 1 isolate from the swan (KY436397) revealed strong association with that of NZ-Ad (AF026289) of Morgan and Blair showing a unique position in the phylogenetic tree neighboring with
E. miyagawai,
E. paraulum, and
E. robustum/
friedi lineages [
24]. The 28S rDNA sequence of 1 isolate from the swan (KY436407) also revealed a unique position neighboring with
E. miyagawai,
E. paraulum,
E. revolutum,
Echinostoma sp. IG,
E. trivolvis,
E. paraensei, and
E. nasincovae [
24]. Thus, the adult specimens were described as a new species,
E. novaezealandense [
24]. This species was morphologically close to
E. acuticauda described in Australia but differed in having a longer forebody, more posteriorly located ovary and testes, and much smaller eggs [
24]. This species is now listed among the helminth fauna of birds in New Zealand [
170].
This species was first described from the intestine of experimental pigeons infected with the metacercariae from
L. stagnalis snails in Birmingham, UK [
171]. The species name came from the fact that the cercariae had no fin-folds on the tail [
171]. The cercariae of
E. revolutum have a fin-fold on the tail, rod-like cystogenous gland-cells, and 36 (possibly more) flame cells, but those of
E. nudicaudatum were in the complete lack of a fin-fold on the tail, granular gland-cells in the cercarial body, and at least 94 flame cells [
171]. The adults of
E. nudicaudatum differed from those of
E. revolutum,
E. robustum, and
E. lindoense in the absolute sizes of collar spines, and from
E. ralli in the arrangement of collar spines [
171]. Interestingly, intra-redial encystment of the cercariae (i.e., metacercariae) was observed within the rediae of
E. nudicaudatum, which means precocious encystment in snails [
172,
173], as observed similarly in
E. trivolvis [
6].
During the experimental life cycle, production of at least 3 redial generations was observed [
172]. A year after the discovery of
E. nudicaudatum,
E. pinnicaudatum (the name came from the cercariae having a well-developed dorso-ventral fin-fold) was reported as a new species, from the same place where
E. nudicaudatum was discovered [
174]. In adult flukes, only a minor difference was found in the arrangement of collar spines between
E. nudicaudatum and
E. pinnicaudatum; in the former there were 7 unalternating lateral spines but in the latter there were 5 unalternating collar spines [
174]. The cercariae of these 2 species were recorded among the cercarial fauna from British freshwater molluscs [
175]. However, taxonomic attention has seldom been paid to these 2 species of
Echinostoma spp., and further studies to evaluate their taxonomic validity through molecular analysis are needed.
This species was originally described from Brazil based on experimentally obtained adults from mammalian hosts, including hamsters, mice, and rats infected with the metacercariae from
B. glabrata snails [
176]. Later, this fluke was detected from naturally infected water rats,
Nectomys squamipes, in Brazil [
89,
90]. It is of note that the eggs of
E. paraensei (less probably
E. luisreyi) were detected in the coprolite of a mummified human body in Brazil using molecular techniques [
15].
The adult
E. paraensei resembled adults of
E. revolutum,
E. lindoense, and
E. barbosai; however, the minute size of 5–11 dorsalmost collar spines was characteristic for
E. paraensei [
176] (
Table 5). Kanev [
20] considered
E. paraensei a synonym of
E. caproni based mainly on the fact that
E. paraensei also uses species of
Biomphalaria as the 1st intermediate host. Huffman and Fried [
7] accepted this concept, and Kanev [
4] listed only 5 species in the 37-collar-spined group, which included
E. revolutum (sensu stricto),
E. trivolvis,
E. caproni,
E. jurini, and
E. echinatum excluding
E. paraensei. However,
E. paraensei was acknowledged as a distinct species because of its unique isoenzymatic patterns [
34], DNA sequences [
35], patterns of random amplification of polymorphic DNA (RAPD) [
177], host-parasite relationships [
178], and unique metacercarial excystation patterns and morphological features [
179]. The validity of
E. paraensei was agreed by Fried and Huffman [
85], Kostadinova and Gibson [
26], Fried and Graczyk [
8], and Toledo et al. [
9].
Molecular data of
E. paraensei have been available since Morgan and Blair [
35,
41,
105] who analyzed the ITS region,
cox1, and
nad1 of
E. paraensei (from Australia) and other 37-collar-spined
Echinostoma spp. The results evidenced that
E. paraensei (PCer-1) is distinct from
E. caproni and phylogenetically rather close to
E. trivolvis [
35,
41,
105]. In addition, Morgan and Blair [
41] found an isolate (cercariae from
Glyptophysa sp. snails; AF026282) of
E. paraensei from Townsville, Australia, which diverged from the Brazilian species (AF025834) by only 2 nucleotide substitution out of 530 sequenced. Georgieva et al. [
10] further reported that
E. paraensei was grouped with
E. nasincovae (under the name
Echinostoma n. sp.) and
E. trivolvis forming a second clade among the 37-collar-spined
Echinostoma group. Recently,
cytochrome B gene was found to be useful to differentiate
E. paraensei from Asian
E. revolutum and African
E. caproni [
75].
This species was originally described from the bird
Colymbus cristatus and several species of ducks from Central Europe, including Austria and Russia [
4,
16,
17,
19]. Miller [
180] described this species in North America (Canada) and synonymized
Echinostoma columbae Zunker, 1925 with
E. paraulum. However, Kanev et al. [
6] regarded Miller’s specimens as
E. trivolvis, whereas Beaver [
19] synonymized
E. columbae with
E. revolutum. Human infection with
E. paraulum was reported from Russia in 1938 [
181] and also from Yunnan Province, China in 1979 [
14]. The rediae and cercariae were found in
P. corneus, and the metacercariae were found in
Planorbis carinatus snails [
182]. This host selection was different in
E. revolutum; rediae and cercariae developed in
Lymnaea palustris and metacercariae in
P. corneus [
182]. The metacercariae of
E. revolutum were bigger having a thick cyst wall but those of
E. paraulum were smaller having a thin cyst wall [
182].
Skrjabin [
183], Sprehn [
184], Skrjabin and Bashikirova [
32], and Iskova [
185] supported the taxonomic validity of
E. paraulum; however, Beaver [
19], Yamaguti [
1,
97], and Kanev [
4,
20] denied the validity and synonymized it with
E. revolutum. Beaver [
19] mentioned that 37 collar spines of
E. paraulum were arranged exactly as in
E. revolutum, its relative size of various organs was identical with that of
E. revolutum, and there was not a single character by which
E. paraulum can be separated from
E. revolutum. Yamaguti [
1,
97] synonymized various species with
E. revolutum, including
E. echinatum,
E. armatum,
E. revolutum var.
japonicum,
E. miyagawai, and
E. paraulum. Kanev [
4,
20] confirmed its complete life cycle from Europe, including Austria where
E. paraulum was originally described and concluded that
E. paraulum corresponded completely with
E. revolutum. Thereafter, Huffman and Fried [
7], Kostadinova and Gibson [
26], Fried and Graczyk [
8], and Toledo et al. [
9] did not recognize
E. paraulum as a distinct species.
Georgieva et al. [
10] was the first who molecularly confirmed the unique status of
E. paraulum. They obtained 5 isolates from cercariae (4;
L. stagnalis) and an adult (1;
Aythya fuligula) originating from Germany and Czech Republic, respectively, and analyzed
nad1 and 28S rDNA sequences together with other 37-collar-spined
Echinostoma spp. The phylogenetic tree of
nad1 showed that
E. paraulum was distinct from all other species analyzed and included within the 1st clade where
E. revolutum (sensu lato),
E. miyagawai,
E. novaezealandense (as
Echinostoma sp. NZ-Ad), and
E. robustum/
friedi are located [
10]. The phylogenetic tree of 28S rDNA supported this showing similar findings [
10]. They also mentioned that although
E. paraulum and
E. revolutum use the same snail species (
L. stagnalis) as their 1st intermediate host, the cercariae of
E. paraulum were dissimilar to those of
E. revolutum in the pattern of paraesophageal gland-cells [
10]. Subsequently, the morphology and life cycle of
E. paraulum were redescribed by Faltýnková et al. [
11]. According to them, the cercariae of
E. paraulum were much larger in size with a much longer tail than those of
E. revolutum, possessing a larger number of paraesophageal gland-cell outlets than the cercariae of
E. revolutum. The adults of
E. paraulum were in comparison with the same age of
E. revolutum much smaller in size, with a more robust body, longer forebody, and distinctly wider head collar, and notably their testes had a characteristic median constriction [
11] (
Table 5). Nagataki et al. [
72] supported the validity of
E. paraulum using
nad1 analysis of 37-collar-spined
Echinostoma spp. and mentioned that
E. paraulum formed a sister group with
E. robustum and
E. miyagawai. Mohanta et al. [
46] also established a phylogenetic tree based on
nad1 which supported the taxonomic validity of
E. paraulum. Adult
E. paraulum was reported from the house crow in Pakistan [
67] and ducks in Bangladesh [
66]. However, the specimen from Pakistan showed testes with no distinct median constriction, and thus the specific diagnosis needs reconfirmation.
This species was described as a new species from the naturally infected
B. glabrata snails in Guadeloupe, French West Indies [
38]. This snail host served as both the 1st and 2nd intermediate host (metacercariae also in
P. marmorata snails and tadpoles of
Bufo marinus), and birds (ducklings of
Cairina moschata and canaries) served as the experimental definitive host [
38]. The adults morphologically resembled
E. trivolvis (under the name
E. multispinosum reported from birds in Cuba),
E. revolutum (under the name
E. mendax reported from birds in Brazil), and
E. barbosai (from birds in Brazil) but differed in body length, size of oral and ventral suckers, pharynx, and other organs [
38]. In the cercariae of
E. parvocirrus, the number of penetration gland-cell pores was 6 (4 in
E. barbosai), and the number of paraesophageal gland-cell pores at the cephalic portion was 8 ventral and 4 dorsal (11 ventral and 6 dorsal in
E. barbosai) [
38]. This species has been listed among the 37-collar spined ‘
E. revolutum’ spp. by Kostadinova and Gibson [
26], Fried and Graczyk [
8], Maldonado and Lanfredi [
92], Toledo et al. [
9], Nagataki et al. [
72], and Le et al. [
112]. However, taxonomic attention on this species has been scarce, and there has been no information on molecular characteristics.
This species was described based on adult flukes obtained from a laboratory-raised pigeon experimentally fed the metacercariae in
L. stagnalis snails from Birmingham, UK [
174]. The snails had both cercarial and metacercarial stages, and collected in the same locality where
E. nudicaudatum was discovered [
171,
174]. The adults of
E. pinnicaudatum were morphologically close to
E. nudicaudatum with only a recognizable difference in the arrangement of collar spines; in the former there were 5 unalternating lateral spines, whereas in the latter there were 7 of these [
174]. However, the morphology of cercariae was distinctly different. In the cercaria of
E. pinnicaudatum there was a well-developed, dorso-ventral fin-fold (as the name ‘
pinnicaudatum’ indicates) but in the cercaria of
E. nudicaudatum the fin-fold was totally absent [
174]. The cercariae of
E. pinnicaudatum was recorded among the cercarial fauna from British freshwater molluscs [
175]. However, taxonomic attention has never been paid to
E. pinnicuadatum, and further studies to evaluate its taxonomic validity through molecular analysis should be performed.
This species was originally described from the small intestine of a waterfowl,
Rallus aquaticus indicus in Aichi, Shiga, and Shizuoka Prefecture, Japan [
68]. Later, this species was found again in the same species of birds in Fukuoka Prefecture, Japan [
186] and in the bird
Fulica atra in Azerbaidzhan [
1]. The adult worms had total 37 collar spines with 4 end group spines on each side, cup-shaped ventral sucker, and vitellaria beginning at the level of the posterior end of the ventral sucker [
68]. It resembled
E. revolutum (including synonyms
E. mendax,
E. erraticum,
E. microrchis, and
E. neglectum),
E. paraulum, and
E. acuticauda but differed in the number of end group spines, size of eggs, and others [
68]. No further information is available on this species, and its taxonomic validity should be re-evaluated providing molecular data.
E. robustum (
Fig. 3) was first described from the small intestine of 2 naturally infected avian species,
Streptopelia chinensis formosa and
Columba livia domestica, in Taiwan [
187]. Domestic pigeons, chickens, and ducks, wild ducks, and wild geese were also found to be definitive hosts [
1,
97]. This species is morphologically close to
E. miyagawai (and
E. friedi) but can be differentiated in several features, including the morphology of testes, irregularly and deeply lobed and horizontally extended in
E. robustum whereas subglobular with irregular margins or 3 lobed in
E. miyagawai [
46,
98,
187] (
Table 5). In addition, the size of the ventral sucker in comparison to the body width is smaller in
E. miyagawai [
21] than in
E. robustum [
187]. The existence of this species has been extended to Japan [
18], China [
188], Bangladesh [
46,
66,
70], Russia [
78,
79], Uzbekistan, Azerbaidzhan, Georgia, Estonia, Bulgaria [
1], Poland [
77], UK [
76], USA [
31,
42], and Brazil [
31] (
Table 4). Cercariae develop in freshwater snails (
Radix lagotis,
R. auricularia, and
Planorbis sp.), and encyst in the same or different snails (
Radix spp. or
Cristaria plicata), fish (
Hemiculter leucisculus, Acheilognathus chankaensis, or
Gobio gobio), or frogs (
Rana temporaria) [
79].
This species was synonymized with
E. revolutum by Bezubik in 1956, but soon acknowledged as a distinct species by Rayski and Fahmy [
76] in 1962 and listed in Skrjabin and Bashikirova [
32] and Yamaguti [
1,
97]. However, Huffman and Fried [
7], Kanev [
4], Kostadinova and Gibson [
26], Fried and Graczyk [
8], and Toledo et al. [
9] did not recognize this as a valid species. Kanev [
4] synonymized this species with
E. echinatum; however, it appeared to be inappropriate since
E. echinatum itself needs revalidation [
10,
11,
45]. The validity of
E. robustum was supported by Detwiler et al. [
31,
42] through molecular analyses (
cox1,
nad1, and ITS) of isolates from Indiana and Minnesota, USA and Minas Gerais, Brazil. Georgieva et al. [
45] indicated that
E. friedi sensu Marcilla et al. (unpublished, in GenBank only, AJ564379) and
E. revolutum of Morgan and Blair [
35,
41,
105] (AF025832) from Europe had strong association with
E. robustum sensu Detwiler et al. [
31] from USA (GQ463053, GQ463054) and Brazil (GQ463055). The clade comprising of these 5 isolates exhibited a complex structure suggesting the existence of at least 3 different species [
45]. Further studies are needed to back up this suggestion.
In addition, the clones of
E. robustum sensu Detwiler et al. [
31] and
E. friedi (Marcilla et al., unpublished) showed almost identical
nad1 sequences and formed together subclades ‘a-d’ (
E. robustum/
E. friedi lineage). However,
E. friedi was synonymized with
E. miyagawai based on morphological analyses [
11]. Mohanta et al. [
46] suggested a synonymy between
E. robustum,
E. miyagawai, and
E. friedi based on analysis of
nad1 sequences; however, Heneberg [
47] did not agree to this synonymy but suggested that the G1-G11 isolates designated as
E. robustum by Mohanta et al. [
46] were in fact
E. miyagawai. In this respect, whether
E. miyagawai and
E. robustum are taxonomically distinct species, despite several morphological differences [
46], needs additional studies. Moreover, whether the specimens from Indiana and Minnesota (USA) and Brazil [
31] are conspecific with the original
E. robustum from Taiwan requires reconfirmation.
Adults of this species were originally reported from experimental chicks, pigeons, hamsters, and mice fed the metacercariae in laboratory-raised
B. glabrata snails in California, USA; the cercariae were originally obtained from
Physa rivalis snails in Minas Gerais, Brazil and the infected snails were shipped to California [
37].
P. rivalis also served as the 2nd intermediate host [
37]. In adults of
E. rodriguesi, the arrangement of collar spines resembled those of
E. revolutum,
E. lindoense,
E. barbosai, and
E. paraensei, and the size and shape of collar spines and testes were indistinguishable from those of
E. audyi (synonym of
E. revolutum) and
E. barbosai [
37]. However, the number of flame cells on the cercariae was 21 pairs in
E. rodriguesi,
E. lindoense, and
E. paraensei but
E. barbosai had 24 pairs, and
E. revolutum (under the name
E. audyi) had 27 pairs [
37]. This species was also reported from rodents in Argentina [
189,
190].
Regarding its taxonomic validity, Kanev [
20] was of opinion that
E. rodriguesi may be a synonym of
E. trivolvis, and Kostadinova and Gibson [
26] did not list this species as a distinct species. Fried and Graczyk [
8] and Toledo et al. [
9] also excluded
E. rodriguesi from the list of 37-collar-spined
Echinostoma group. However, Kanev et al. [
6] suggested that
E. trivolvis occurred only in North America and did not include
E. rodriguesi among the synonyms of
E. trivolvis. In addition, Kanev et al. [
18] used the name
E. rodriguesi and mentioned about the migration of sporocysts within the snail body as a characteristic feature. Thereafter,
E. rodriguesi has been acknowledged as a distinct species and mentioned by various researchers, including Latin American workers [
27,
44,
89,
90,
120,
189–
191]. However, molecular data have not been provided for
E. rodriguesi, and thus further validation of this species is needed.
[syn. Echinostoma armigerum Barker and Irvine, 1915; Echinostoma callawayensis Barker and Noll, 1915; Echinostoma coalitum Barker and Beaver, 1915; Echinoparyphium contiguum Barker and Bastron, 1915; Echinostoma multispinosum Pérez Vigueras, 1944]
This species originated from
Cercaria trivolvis, its rediae, and metacercariae in the North American planorbid snail,
Helisoma trivolvis (under the name
Planorbis trivolvis) from Urbana, Illinois, USA [
192,
193]. The adult flukes of this species were described earlier in North America under the name
E. echinatum by Leidy from musk rats in 1888 [
106] followed by Stiles and Hassall from cotton rabbits in 1895 [
107] and Hassall from chickens in 1896 [
108]. They were also described under different names
E. armigerum and
E. coalitum by Barker on the specimens from muskrats in Nebraska in 1915 [
194] and from muskrats in Ontario, Canada by Law and Kennedy in 1932 [
19,
195].
Beaver [
19] studied on
C. trivolvis shed from
Helisoma trivolvis snails, obtained adult flukes in the laboratory, and assigned them as
E. revolutum. Later, however, Kanev [
20] and Kanev et al. [
6] pointed out that the
E. revolutum of Beaver [
19] was actually
E. trivolvis, and many of the articles published from North America until 1988 under the name
E. revolutum should be reconsidered as having been
E. trivolvis. Later, the true existence of
E. revolutum in North America was morphologically as well as molecularly confirmed by Sorensen et al. [
86,
87]; it was transmitted by
L. elodes snails in Indiana, USA. In addition, based on
nad1 gene sequences, the American
E. revolutum was shown to be genetically different from European populations [
10,
31].
The morphological details of
E. trivolvis larvae and adults were described by Kanev et al. [
6]. He used the
C. trivolvis shed from
H. trivolvis snails collected from Douglas Lake, Michigan, USA as the starting point and obtained metacercariae from the pericardial sac of laboratory-raised
P. acuta and
P. fontinalis snails and adults from golden hamsters, rats, mice, ducks, geese, chickens, pigeons, turkeys, partridges, and guinea fowls. The first intermediate host also included
Physa gyrina snails at St. Joseph, Illinois, USA [
196]. Metacercariae developed also in the pericardial sac and posterior kidney region of mussels (
Anodonta cygnea) and various freshwater snails, including
Viviparus viviparus,
V. contectus,
L. stagnalis,
L. tomentosa,
L. truncatula,
L. palustris,
L. peregra,
L. auricularia,
P. corneus,
B. glabrata,
B. alexandriana,
Bithynia tentaculata and
B. leachi, and kidney and eye socket of tadpoles and frogs and freshwater turtles [
6]. Precocious encystment of metacercariae within rediae was observed [
6].
C. trivolvis has 37 collar spines, 7 fin-folds on the tail, 2 pairs of 3 flame cells at the level of the pharynx and total 36 flame cells, 6 pores of penetration gland-cells along the esophagus, and 4–6 pores of paraesophageal gland-cells on the oral sucker [
6]. The cercariae were also described under different names,
C. trisolenata Faust, 1917,
C. acanthostoma Faust, 1918, and
C. complexa Faust, 1919 [
6]. The metacercariae were 135–170 μm in diameter, having a thick outer cyst wall and a thin inner cyst wall [
6]. The adult flukes had a variable body size, from 3–5 mm to 20–30 mm, variable body shape, from elongate, flattened dorso-ventrally, and tapering posteriorly, to broad, with a tapering anterior end and a bluntly rounded posterior end [
6].
E. trivolvis is different from
E. revolutum in various points, including the number and arrangement of protein fractions in adult worm homogenates, number and distribution of argentophilic structures [
197], number and position of paraesophageal gland-cell ducts in cercariae (4–6 on the oral sucker only in the former and 12 on the oral sucker and body in the latter), and geographical distribution [
4,
6,
11] (
Table 5). Sloss et al. [
34] showed different electrophoretic patterns between
E. trivolvis,
E. caproni, and
E. paraensei.
Kanev et al. [
6] synonymized
E. armigerum,
E. callawayensis,
E. coalitum,
E. multispinosum, and
Echinoparyphium contiguum with
E. trivolvis. Kanev [
20] also considered
E. rodriguesi a synonym of
E. trivolvis but later Kanev et al. [
6] denied the presence of
E. trivolvis in South America and did not list
E. rodriguesi among the synonyms of
E. trivolvis. The distinct taxonomic status of
E. trivolvis has been acknowledged by Huffman and Fried [
7], Kostadinova and Gibson [
26], Fried and Graczyk [
8], Maldonado and Lanfredi [
92], Toledo et al. [
9], Detwiler et al. [
31,
42], and Georgieva et al. [
10,
24,
45].
The molecular data of
E. trivolvis have been available after Morgan and Blair [
35] who compared the nucleotide sequences of ITS region (ITS1-5.8S-ITS2) with those of
E. revolutum,
E. paraensei,
E. caproni (including
E. liei and
Echinostoma sp. II), and
Echinostoma sp. I (
E. deserticum). They concluded that
E. trivolvis was phylogenetically close to
E. revolutum and
E. paraensei but distinct from one another and far from
E. caproni and
Echinostoma sp. I (
E. deserticum). Sorensen et al. [
87] notified intraspecific variation in ITS loci among isolates of
E. trivolvis (different localities in Indiana) and
E. revolutum (North American and European). The
nad1 and
cox1 sequences became available after Morgan and Blair [
41] and Detwiler et al. [
31,
42]. The clones used were 3 from the cercariae of
E. trivolvis from
H. trivolvis and
L. elodes snails in Indiana and Minnesota and 1 from the adult worm recovered in muskrats in Wisconsin [
31]. The
nad1 phylogeny demonstrated that the muskrats were infected with 5 echinostome lineages; 3
E. trivolvis lineages, 1
E. revolutum, and 1
Echinoparyphium lineage 1 [
31]. High levels of intraspecific variation with 3 lineages of
E. trivolvis suggested the existence of multiple cryptic species within
E. trivolvis [
31,
42].
[syn. Echinostoma cf. friedi of Kostadinova et al. (2003)]
Echinostoma sp. IG is a tentative name of a unique species but not yet formally described [
45]. It was based on a larval stage (cercariae) from
Radix peregra in Iceland and
R. auricularia in Germany [
11,
45]. Its molecular information has been available for
nad1 and 28S rDNA sequences [
10,
45]. Cercariae and rediae ex.
Planorbis sp. snails found in Wales, UK showing unique molecular characteristics [
40] were also assigned to this species [
11]. The cercariae of this species were unique having distal dorsal fin-fold and 12 paraesophageal gland-cell outlets restricted to the region of the oral sucker [
11]. The adult stage has not yet been found [
11].
CONCLUSION
A total of 26 Echinostoma species are recognized as valid (16 species) or validity-retained (10) among the 37-collar-spined Echinostoma spp. around the world. The morphology of the cercarial stage as well as the size and shape of adult flukes, including the relative size of the oral and ventral suckers, size, shape, and arrangement of collar spines, and morphology of testes and cirrus sac as well as arrangement of vitelline follicles are important criteria for species differentiation. However, some of these species are difficult to distinguish one from the other only by morphology. Molecular techniques, in particular, gene sequencing of mitochondrial cox1 and nad1, is a highly useful technique for discriminating the species and seems to be essential to determine the taxonomic validity of 37-collar-spined Echinostoma spp. group.
Notes
-
CONFLICT OF INTEREST
We have no conflict of interest related to this study.
ACKNOWLEDGMENT
We are grateful to the staff of Institute of Parasitic Diseases, Korea Association of Health Promotion, Seoul, Korea who helped echinostome studies.
Fig. 1A phylogenetic tree of Echinostoma revolutum (Southeast Asian and American lineages) and 6 other 37-collar-spined Echinostoma group constructed based on 184 bp of mitochondrial cox1 sequences by maximum-likelihood method using the MEGA-X program employing Tamura-nei model of nucleotide substitution with 1,000 bootstrap replications. Opisthorchis viverrini was used as an outgroup.
Fig. 2A phylogenetic tree of Echinostoma revolutum (Eurasian and American lineages) and 13 other 37-collar-spined Echinostoma spp. constructed based on 472 bp of mitochondrial nad1 sequences by maximum-likelihood method using the MEGA-X program employing Tamura-nei model of nucleotide substitution with 1,000 bootstrap replications. O. viverrini was used as an outgroup.
Fig. 3Adult specimens of Echinostoma revolutum (A) from Thailand (courtesy of Prof. Chalobol Wongsawad, Chiang Mai University), E. cinetorchis (B) from South Korea, E. mekongi (C) from Cambodia, and E. robustum (D) from India under the same magnification. Scale bar=2 mm.
Table 1List of 16 valid and 10 validity-retained species of 37-collar-spined Echinostoma group
Table 1
|
Species and nominator |
Size of adults (mm) |
Size of eggs (μm) |
Country of first report |
Reference no. |
Validity |
|
E. revolutum (Froelich, 1802) Dietz, 1909 |
9.5–11.8×1.5–2.1 |
108–125×57–75 |
Germany |
[11] |
valid (type species) |
|
E. acuticauda Nicoll, 1914 |
9.0–12.0×0.9–1.0 |
112–126×63–75 |
Australia |
[93] |
retained |
|
E. barbosai Lie & Basch, 1966 |
3.6–7.8×0.46–0.96 |
111–131×62–66 |
Brazil |
[117] |
retained |
|
E. bolschewense (Kotova, 1939) Nasincova, 1991 |
7.4–12.5×0.99–1.6 |
138–162×75–85 |
Russia |
[122] |
valid |
|
E. caproni Richard, 1964 |
5.7×1.5 (av.) |
105–120×50–60 |
Madagascar |
[80] |
valid |
|
E. chloephagae Sutton & Lunaschi, 1980 |
5.1–6.9×0.82–0.99 |
100–120×60–70 |
Argentina |
[131] |
retained |
|
E. cinetorchis Ando & Ozaki, 1923 |
9.5–14.6×1.7–2.2 |
96–100×61–70 |
Japan |
[59] |
valid |
|
E. deserticum Kechemir et al., 2002 |
5.6–15.2×0.75–3.1 |
58–74×36–46 |
Niger |
[43] |
valid |
|
E. echinatum (Zeder, 1803) de Blainville, 1828 |
8.1–11.1×0.77–1.5 |
? |
Germany |
[99] |
retained |
|
E. jurini (Skvortsov, 1924) Kanev, 1985 |
6.6–14.0×0.58–1.3 |
96–132×72–88 |
Russia |
[5] |
retained |
|
E. lindoense Sandground & Bonne, 1940 |
13.0–15.0×2.5–3.0 |
92–124×65–76 |
Indonesia |
[63] |
valid |
|
E. luisreyi Maldonado et al., 2003 |
5.3–9.3×1.1–2. 3 |
89–113×65–82 |
Brazil |
[44] |
valid |
|
E. mekongi Cho et al., 2020 |
9.0–13.1×1.3–2.5 |
98–132×62–90 |
Cambodia |
[49] |
valid |
|
E. miyagawai Ishii, 1932 |
9.2–11.0×1.2–1.5 |
94–96×59–60 |
Japan |
[11] |
valid |
|
E. nasincovae Georgieva et al., 2014 |
4.3–4.8×0.99–1.1 |
100–105×61–70 |
Czech Republic |
[11] |
valid |
|
E. novaezealandense Georgieva et al., 2017 |
9.6–10.5×0.7–1.1 |
81–87×42–53 |
New Zealand |
[24] |
valid |
|
E. nudicaudatum Nasir, 1960 |
6.8–7.6×0.98–1.3 |
97–115×67–72 |
UK |
[171] |
retained |
|
E. paraensei Lie & Basch, 1967 |
7.5–16.0×0.79–2.0 |
104–122×74–86 |
Brazil |
[176] |
valid |
|
E. paraulum Dietz, 1909 |
5.6–6.9×1.2–1.7 |
104–122×53–70 |
Austria/Russia |
[11] |
valid |
|
E. parvocirrus Nassi & Dupouy, 1988 |
6.7–8.4×1.3–1.5 |
105–120×64–71 |
Guadeloupe |
[38] |
retained |
|
E. pinnicaudatum Nasir, 1961 |
5.5–7.1×0.8–1.1 |
97–115×67–72 |
UK |
[174] |
retained |
|
E. ralli Yamaguti, 1934 |
8.6×1.1 (av.) |
110–130×68–81 |
Japan |
[68] |
retained |
|
E. robustum Yamaguti, 1935 |
7.8–9.8×1.3–2.2 |
111–129×60–69 |
Taiwan |
[187] |
valid |
|
E. rodriguesi Hsu et al., 1968 |
3.9–6.8×0.5–1.3 |
96–128×56–68 |
Brazil |
[37] |
retained |
|
E. trivolvis (Cort, 1914) Kanev, 1985 |
5.5–21.0×0.5–1.5 |
90–130×60–70 |
USA |
[6] |
valid |
|
Echinostoma sp. IG Georgieva et al., 2013 |
- |
- |
Germany |
[45] |
valida
|
Table 2List of 37-collar-spined Echinostoma spp. (30 species) synonymized with other species
Table 2
|
Species and nominator |
Country of first report |
Synonymized with |
Synonymy proposed by |
|
E. armatum (Mollin, 1858) Yamaguti, 1971 |
South America |
E. revolutum
|
Beaver [19] |
|
E. armigerum Barker and Irvine, 1915 |
North America |
E. trivolvis
|
Kanev [4,20] |
|
E. audyi Lie and Umathevy, 1965 |
Malaysia |
E. revolutum
|
Kanev [20] |
|
E. callawayensis Barker and Noll, 1915 |
North America |
E. trivolvis
|
Kanev [4,20] |
|
E. coalitum Barker and Beaver, 1915 |
North America |
E. trivolvis
|
Kanev [4,20] |
|
E. columbae Zunker, 1925 |
Germany |
E. revolutum
|
Beaver [19] |
|
Echinoparyphium contiguum Barker and Bastron, 1915 |
USA |
E. trivolvis
|
Kanev et al. [6] |
|
E. dilatatum (Miram, 1840) Cobbold, 1860 |
Russia |
E. revolutum
|
Beaver [19] |
|
E. equinatus gigas Marco del Pont, 1926 |
Argentina |
Echinoparyphium recurvatum
|
Lunaschi et al. [29] |
|
E. echinocephalum (Rudolphi, 1819) Cobbold, 1860 |
Egypt |
E. revolutum
|
Beaver [19] |
|
E. erraticum Lutz, 1924 |
Brazil |
E. revolutum
|
Beaver [19] |
|
E. friedi Toledo et al., 2000 |
Spain |
E. miyagawai
|
Faltýnková et al. [11] |
|
E. ivaniosi Mohandas, 1973 |
India |
E. revolutum
|
Kanev [4] |
|
E. liei Jeyarasasingam et al., 1972 |
Egypt |
E. caproni
|
Huffman and Fried [7] |
|
E. limicoli Johnson, 1920 |
Europe |
E. revolutum
|
Beaver [19] |
|
E. londonensis Khan, 1961 |
UK |
E. jurini
|
Kanev [4] |
|
E. mendax Dietz, 1909 |
Brazil |
E. revolutum
|
Beaver [19] |
|
E. microrchis Lutz, 1924 |
Brazil |
E. revolutum
|
Beaver [19] |
|
E. multispinosum Pérez Vigueras, 1944 |
Cuba |
E. trivolvis
|
Kanev et al. [6] |
|
E. neglectum Lutz, 1924 |
Brazil |
E. revolutum
|
Beaver [19] |
|
E. nephrocystis Lutz, 1924 |
Brazil |
E. revolutum
|
Beaver [19] |
|
E. orlovi Romashov, 1966 |
Russia |
E. jurini
|
Kanev et al. [5] |
|
E. oxycephalum (Rudolphi, 1819) Railliet, 1896 |
Europe |
E. revolutum
|
Beaver [19] |
|
E. revolutum tenuicollis Bashikirova, 1941 |
Azerbaidzhan |
E. revolutum
|
This review |
|
E. revolutum var. japonicum Kurisu, 1932 |
Japan |
E. revolutum
|
Yamaguti [1] |
|
E. sisjakowi (Skvortsov, 1935) Yamaguti, 1971a
|
Russia |
E. jurini
|
Kanev et al. [5] |
|
E. spiniferum (La Valette, 1855) sensu Nasincova, 1992 |
Czechoslovakia |
E. nasincovae
|
Faltýnková et al. [11] |
|
E. stromi Bashkirova, 1946 |
Azerbaidzhan |
E. revolutum
|
Yamaguti [1] |
|
E. sudanense Odhner, 1910 |
Sudan |
E. revolutum
|
Beaver [19] |
|
E. togoensis Jourdan and Kulo, 1981 |
Togo |
E. caproni
|
Huffman and Fried [7] |
Table 3Continental distribution of 37-collar-spined Echinostoma spp.
Table 3
|
Asia |
Europe |
Africa |
North/Central America |
South America |
Oceania |
|
E. revolutum
|
E. revolutum
|
E. caproni
|
E. revolutum
|
E. revolutum
|
E. revolutum
|
|
E. cinetorchis
|
E. bolschewense
|
E. deserticum
|
E. parvocirrus
|
E. barbosai
|
E. acuticauda
|
|
E. lindoense
|
E. echinatum
|
|
E. robustum
|
E. chloephagae
|
E. miyagawai
|
|
E. mekongi
|
E. jurini
|
|
E. trivolvis
|
E. luisreyi
|
E. novaezealnadense
|
|
E. miyagawai
|
E. miyagawai
|
|
|
E. paraensei
|
E. paraensei
|
|
E. paraulum
|
E. nasincovae
|
|
|
E. robustum
|
|
|
E. ralli
|
E. nudicaudatum
|
|
|
E. rodriguesi
|
|
|
E. robustum
|
E. paraulum
|
|
|
|
|
|
E. pinnicaudatum
|
|
|
|
|
|
E. robustum
|
|
|
|
|
|
Echinostoma sp. IG |
|
|
|
|
Table 4Geographical distribution of 26 valid or validity-retained 37-collar-spined Echinostoma species
Table 4
|
Species and nominator |
Continent and country where this species has been reported |
|
E. revolutuma
|
Asia, Europe, North America, South America, Oceania |
|
E. acuticauda
|
Australia |
|
E. barbosai
|
Brazil |
|
E. bolschewense
|
Czech Republic, Russia, Slovak Republic |
|
E. caproni
|
Cameroon, Congo, Egypt, Madagascar, Togo |
|
E. chloephagae
|
Argentina |
|
E. cinetorchis
|
China, Indonesia, Japan, South Korea, Taiwan, Vietnam |
|
E. deserticum
|
Algeria, Niger |
|
E. echinatum
|
Europe (Germany and other countries) |
|
E. jurini
|
Europe (Bulgaria, Russia, and other countries) |
|
E. lindoense
|
Indonesia, Malaysia, The Philippines, Thailand |
|
E. luisreyi
|
Brazil |
|
E. mekongi
|
Cambodia |
|
E. miyagawaib
|
Asia, Europe, Oceania |
|
E. nasincovae
|
Czech Republic, Slovak Republic |
|
E. novaezealandense
|
New Zealand |
|
E. nudicaudatum
|
UK |
|
E. paraensei
|
Australia, Brazil |
|
E. paraulum
|
Austria, Bangladesh, China, Czech Republic, Germany, Pakistan, Russia |
|
E. parvocirrus
|
Guadeloupe (West Indies) |
|
E. pinnicaudatum
|
UK |
|
E. ralli
|
Japan |
|
E. robustumc
|
Asia, Europe, North America, South America |
|
E. rodriguesi
|
Argentina, Brazil |
|
E. trivolvis
|
North America (Canada, USA) |
|
Echinostoma sp. IG Georgieva et al., 2013 |
Germany, Iceland, UK |
Table 5Characteristics of
Echinostoma revolutum in comparison with closely related species
a
Table 5
|
E. revolutum |
E. lindoense |
E. miyagawai |
E. robustum |
E. trivolvis |
|
Definitive host |
birds, mammals |
mammals |
birds, mammals |
birds |
birds, mammals |
|
1st intermediate host |
lymnaeid and planorbid snails |
lymnaeid and planorbid snails |
lymnaeid and planorbid snails |
lymnaeid snails |
lymnaeid and planorbid snails |
|
No. of outlets of penetration gland-cells (cercaria) |
6 |
6 |
6 |
? |
6 |
|
No. of outlets of paraesophageal gland-cells (cercaria) |
12 |
60–64 |
42–46 |
? |
4–6 |
|
Size of metacercariae (μm) |
132–152 (diameter) |
120–130 (in diameter) |
144–154 (in diameter) |
? |
135–170 (in diameter) |
|
Collar spines (adult) |
slender and sharply pointed |
short and less sharply pointed |
small with sharply pointed ends |
innermost end group spines smaller than others |
very sharply pointed |
|
Body constriction near the ventral sucker level (adult) |
no constriction |
constricted at middle level of ventral sucker |
constricted at posterior end level of ventral sucker |
constricted at posterior end level of ventral sucker |
no constriction |
|
Shape of testes (adult) |
smooth or slightly lobed |
deeply lobed |
subglobular and indented, 3 lobed |
irregularly lobed and horizontally extended |
smooth, oval orslightly irregular |
|
Vitellaria confluence near the posterior end of body (adult) |
not confluent |
confluent |
confluent |
confluent |
confluent |
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