Occurrence of a Hybrid Between Taenia saginata and Taenia asiatica Tapeworms in Cambodia

Article information

Korean J Parasito. 2021;59(2):179-182

Publication date (electronic) : 2021 April 30

doi : https://doi.org/10.3347/kjp.2021.59.2.179

Taehee Chang¹, Bong-Kwang Jung¹, Sooji Hong¹, Hyejoo Shin¹, Seungwan Ryoo¹, Jeonggyu Lee¹, Keon Hoon Lee¹, Hansol Park², Keeseon S. Eom², Virak Khieu³, Rekol Huy³, Woon-Mok Sohn⁴, Jong-Yil Chai^1,5,

¹Institute of Parasitic Diseases, Korea Association of Health Promotion, Seoul 07649, Korea

²Department of Parasitology and Medical Research Institute, Chungbuk National University College of Medicine, Cheongju 28644, Korea

³National Center for Parasitology, Entomology and Malaria Control, Ministry of Health, Phnom Penh, Cambodia

⁴Department of Parasitology and Tropical Medicine, and Institute of Health Sciences, Gyeongsang National University College of Medicine, Jinju 52727, Korea

⁵Department of Tropical Medicine and Parasitology, Seoul National University College of Medicine, Seoul 03080, Korea

^*Corresponding author (cjy@snu.ac.kr)

Received 2021 February 16; Revised 2021 March 17; Accepted 2021 March 17.

Taenia solium, Taenia saginata, and Taenia asiatica are 3 tapeworm species that can cause human intestinal infections. They have unique life cycles, taking humans as the only definitive host and pigs or cattle as the intermediate host [1]. T. asiatica, which is transmitted by swine (viscera), was first identified in Taiwan and then in South Korea and reported as a distinct species from T. saginata in 1993 [1,2]. The distribution of human taeniases by T. solium and T. saginata is worldwide, whereas T. asiatica is found mostly in Asian countries [3,4].

The possibility of hybridization between T. asiatica and T. saginata has been raised in previous studies that analyzed samples from several countries, including Thailand, China, the Philippines, and Lao PDR [5–8]. Although the 2 taxa have distinct biological characteristics, including host specificity, gene exchange between the 2 species was strongly suggested using allelic analysis on mitochondrial and nuclear genetic markers [5]. The existence of T. solium and T. saginata in Cambodia was confirmed by DNA sequencing of egg-positive fecal samples and adult worms expelled from residents [9,10]. However, there has been no report on the occurrence of T. asiatica or a hybrid between T. saginata and T. asiatica in humans despite its geographical location, surrounded by other countries where T. asiatica and hybrids between the 2 species have been found [5–8,11]. In this study, we report a hybrid individual between T. saginata and T. asiatica in a northern part of Cambodia, bordering Lao PDR, suggesting the occurrence of T. asiatica in this country.

Fecal samples were collected from total 1,156 people in 2 northern provinces (5 villages each), Preah Vihear and Stung Treng (Fig. 1), and examined by the Kato-Katz thick smear technique, as previously reported [10]. The fecal survey of people and worm collection after praziquantel medication were ethically approved by National Ethics Committee for Health Research, Cambodia (IRB no. 099NECHR). Twenty-six (2.4%) out of them were positive for Taenia spp. eggs, and 3 tapeworm strobilae were collected from 3 patients in Preah Vihear after praziquantel medication (15 mg/kg single dose) and purging with MgSO₄.

Fig. 1

Map of the areas for fecal surveys in Cambodia (A, Preah Vihear Province; B, Stung Treng Province) and the village (red, quadrangle) where the present hybrid case between Taenia saginata and Taenia asiatica was found.

Two of the 3 strobilae were diagnosed molecularly as ‘pure’ T. saginata based on the mitochondrial gene encoding cytochrome c oxidase subunit 1 (cox1), and 2 nuclear genes encoding elongation factor-1α (ef1) and ezrin-radixin-moesin (ERM)-like protein (elp) which were reported previously [10]. The remaining 1 strobila (75 cm in length, mostly gravid proglottids without a scolex) expelled from a 27-year-old man showed strange results that the elp allele type was different from ‘pure’ T. saginata. In this study, we further analyzed the allele type of the elp gene of this strobila. The sample preparation and genomic DNA extraction were conducted as described in our previous study [10]. The analyses of mitochondrial cox1 (1,620 bp) and 2 nuclear genes ef1 (1,090 bp) and elp (1,160 bp) were performed following conditions of Okamoto et al. [5]. A consistent sequence data of elp locus could not be obtained since double peaks were observed in electropherograms. Thus, to confirm the haploid genotype of elp locus, PCR amplification and sequencing were conducted at the single-allele level using T-Blunt PCR cloning kit (Solgent, Seoul, Korea).

Multiple sequences alignment was constructed with Clustal W [12]. A phylogenetic tree of elp locus sequences identified in this study and representative sequences of Taenia spp. available in the GenBank database were constructed using the maximum-likelihood (ML) method based on the Tamura-Nei model of nucleotide substitution. The tree was viewed by MEGA v6 [13]. Bootstrap values were calculated with 1,000 replications.

Our Taenia strobila sample showed a discrepancy in the diagnosis between the mitochondrial and nuclear genes. It possessed homozygous sequences typical of T. saginata cox1 (MT074050) and ef1 (MT075318) loci. However, at the elp locus, it was heterozygous with 1 allele (MT501760) matched with T. asiatica (elpA) and another (MT501761) with T. saginata (elpC) (Table 1; Fig. 2).

Table 1

Genotypes of the Taenia tapeworm sample from our patient

Fig. 2

A phylogenetic tree of our sample (alleles) in comparison with related Taenia spp. tapeworms drawn with elp DNA sequences using the maximum-likelihood method employing Tamura-Nei model of nucleotide substitution with 1,000 bootstrap replications. Black dots (●) indicate the sequences identified in this study. The allele MT501760 has been registered under the name T. saginata in GenBank; however, this allele is actually classified as a T. asiatica allele. Scale bar indicates nucleotide substitutions per site.

The homology between our allele sample elpA and T. asiatica (AB462829-AB462830) was 99.9–100%, whereas the homology between our sample elpA and T. saginata (AB462841-AB462842) or T. solium (AB505026) was lower than that, 99.1–99.2% or 94.7%, respectively. In addition, the homology between our allele sample elpC and T. saginata (AB462841-AB462842) was 99.9–100%, whereas the homology between our sample elpC and T. asiatica (AB462829-AB462830) or T. solium (AB505026) was lower than that, 99.1–99.2% or 94.8%, respectively. These results strongly suggest that our sample is a hybrid between the 2 Taenia species.

Hybridization between T. saginata and T. asiatica was reported recently in Asian countries [5–8] but not yet in Cambodia. In this study, we performed an allelic analysis of a Taenia tapeworm strobila collected from a human to rule out the hybrid issue in Cambodia and confirmed that our specimen is a hybrid between T. saginata and T. asiatica.

Human taeniases (by T. solium, T. asiatica, and T. saginata) are known to be endemic in East and Southeast Asia, including Thailand, Vietnam, Lao PDR, which neighbor with Cambodia, and also in Nepal and India [8,11,14]. However, in Cambodia, reports of human taeniasis due to T. asiatica have not yet been documented. Our present finding implies the possible existence of T. asiatica in the northern part of Cambodia, although it remains to be confirmed by further studies.

The transmission of tapeworms is closely related to the lifestyle and cultural characteristics of people, which involve the consumption of undercooked meat infected with viable metacestodes (i.e., cysticerci) [14]. In Cambodia, there is a traditional food habit of eating cattle or pig meat, for example raw beef salad (‘pleah sach ko’). However, as the intermediate host and life cycle of the hybrid between T. saginata and T. asiatica are unclear now, it is necessary to examine the metacestodes from domestic animals using genetic markers. Thus, the risk factors as well as the level of exposure of the people in Cambodia to the agents causing human taeniases, including the hybrid, should be evaluated.