Genetically, C. parvum are largely divided into 2 distinct groups; genotypes 1 and 2. The genotype 1 (transmitted anthroponotically), so far, has been known to be associated only with human and primate infections (Spano et al., 1998; Widmer et al., 2000), with the exception of a report of its presence in a dugong (Morgan et al., 2000). Recently, the genotype 1 was proposed to be a new species, C. hominis n. sp., based on biological and molecular data (Morgan et al., 2002). The genotype 2 (transmitted zoonotically) has been found to infect a wide range of mammals, including humans (McLauchlin et al., 2000). Despite worldwide reports, no information on the genotypes of C. parvum occurring in Korean people has been reported (Chai et al., 2001); isolates from humans have never been successfully propagated in the laboratory.

The major clinical characteristics of the genotype 1 include a longer duration of oocyst excretion and a greater number of oocysts produced, compared with the genotype 2 (Xiao et al., 2001). Although the transmission cycles of both genotypes may overlap (e. g., water-borne), mixtures of the genotypes 1 and 2 have rarely been identified in a single isolate from humans (Spano et al., 1998; McLauchlin et al., 2000; Widmer et al., 2002). With regard to mixtures of the genotypes 1 and 2 in human isolates, there have been no experimental studies on the biological characteristics, virulence, and laboratory maintenance. The present paper reports, for the first time in the Republic of Korea, a human isolate of C. parvum having the mixed genotypes 1 and 2 (designated hereafter SNU-H1), and a successful laboratory propagation of the SNU-H1 in a calf and 3 strains of mice.

The SNU-H1 was isolated from an 8-year-old boy, suffering from acute gastroenteritis due to cryptosporidiosis, at the Seoul National University Hospital, Seoul, Republic of Korea. The oocysts were purified by the discontinuous sucrose gradient method and confirmed by the modified acid-fast stain. Because the oocysts isolated from the patient were small in number, the first passage of this isolate was performed using specific-pathogen-free (SPF), immunosuppressed (ImSP), female C57BL/6 mice. The passage using these mice was successful, and the oocysts obtained from the first passage were used in the subsequent experiments.

To observe the animal infectivity, the SNU-H1 was experimentally infected to ICR, BALB/c, and C57BL/6 mice (SPF, 4-wk-old females) which were purchased from the Daehan Laboratory Animal Center, Ltd. (Jinju, Korea). Five mice in each group were supplied with food and water sterilized by irradiation and autoclaving. To increase the parasite load by immunosuppression of the host (Chai et al., 1990), the mice were each injected with 0.2 mg prednisolone intramuscularly every other day, from 7 days prior to infection, until the end of the experiment. Each mouse was infected orally with 10⁶ oocysts, and the oocyst production in the feces was quantified by collection and pooling of the fecal pellets (Chai et al., 1999).

Two newborn calves were purchased from a farm and transported to the laboratory of the National Veterinary Research and Quarantine Services within a few hrs after birth. To reduce the possibility of contamination with exogenous genotypes of C. parvum, only the parasites propagated in the SPF mice were used to infect the 2 calves. Each newborn calf was infected orally with 2 x 10⁷ oocysts, and the oocyst production in the feces was measured by collection and pooling of the fecal pellets (Guk et al., 2003).

The oocysts were purified by the method previously described (Guk et al., 2003). DNA extraction was performed following the procedure previously described (Caccio et al., 2000). The purified DNA was stored at 4℃. Amplification of a locus containing the GAG microsatellite (GenBank accession number: G35358) was performed using the forward primer, 5'-CTAAAAATGGTGGAGAATATTC, and the reverse primer, 5'-CAACAAAATCTATATCCTC, to obtain the expected 238 base pair (bp) product. The PCR mix consisted of 1x buffer (50 mM KCl, 10 mM Tris-HCl, pH 9.0, 0.1% Triton X-100), 1.5 mM MgCl₂, 200 µM each dNTP, 50 pmol of each primer, 2.5 units of Taq polymerase (Promega, Madison, Wisconsin), and 1~5 µl of the purified DNA in a final volume of 50 µl. The PCR was performed as follows: after an initial denaturation for 5 min at 94℃ a set of 40 cycles was run, each consisting of 30 sec at 94℃ 30 sec at 50℃ and 60 sec at 72℃ followed by a final extension of 5 min at 72℃ The PCR products were separated by electrophoresis on a 1.2% agarose gel.

On the basis of the sequence difference between the genotypes 1 and 2, previously designed human-specific and animal-specific reverse primers were used (Morgan et al., 1997). The human-specific primer, CPHR (5'-CCTCTTTCCAATTAAAGTTGATG-3'), was designed to amplify a 411 bp product from the human isolates of C. parvum. The animal-specific primer, CPCR (5'-TCCAAATTATTGTAACCTGGAAG-3'), was designed to amplify a 312 bp product from the animal isolates. The forward primer, 021F (5'-GGTACTGGATAGATAGTGGA-3'), was annealed into both the human and animal isolates (Morgan et al., 1997). The PCR mix consisted of 1x buffer (50 mM KCl, 10 mM Tris-HCl, pH 9.0, 0.1% Triton X-100), 1.5 mM MgCl₂, 200µM each dNTP, 1.75 pmol of CP-HR and 2.5 pmol of CP-CR, 0.5 units of Taq polymerase (Promega), and 1~5µl of the purified DNA in a final volume of 50µl. The PCR was performed as follows: after an initial denaturation for 2 min at 94 C, a set of 45 cycles was run, each consisting of 30 sec at 94℃, 30 sec at 58℃, and 30 sec at 72℃, followed by a final extension of 5 min at 72℃. The PCR products were separated by electrophoresis on a 1.2% agarose gel.

All 3 ImSP mouse strains appeared to be successfully infected with the SNU-H1, a C. parvum human isolate, with excretion of oocysts in the feces from days 2-3 post-infection (PI) (Fig. 1). Prolonged infections were observed in ImSP ICR mice, but not in ImSP BALB/c and C57BL/6 mice. ImSP BALB/c mice excreted only a small number of oocysts over a shorter period, with no oocysts detected at day 27 PI. ImSP C57BL/6 mice excreted a large number of oocysts from day 5 to 12 PI, but the oocyst numbers decreased thereafter. In ImSP ICR mice, until day 10 PI, the numbers of oocysts excreted were less than in ImSP C57BL/6 mice, but were elevated abruptly after day 10 PI and peaked at day 13 PI; the peak value was maintained longer than in the other mouse strains (Fig. 1).

The infection and propagation of the SNU-H1 was successful in one of the 2 calves, which were infected with 2 x 10⁷ oocysts harvested from the first passage. From day 4 PI, severe watery diarrhea was observed in the infected calf. A great number of oocysts were excreted from day 5 to 9 PI. After day 9 PI, the oocyst excretion decreased, and the calf recovered from the severe diarrhea. In contrast, the other newborn calf died on day 2 PI for an unknown reason.

When the locus containing the microsatellite (tandem repeats of the GAG trinucleotide) of the SNU-H1 was amplified by PCR, a 238 bp fragment was obtained (Fig. 2-A), which indicates that the SNU-H1 belongs to C. parvum (Caccio et al., 2000). To identify its specific genotype, the previously confirmed method of Morgan et al. (1997) was applied. Analyses of the oocysts isolated from the original specimen from the patient, as well as oocysts from the first passage in ImSP C57BL/6 mice and second passage in the calf, showed amplified fragments of both 411 bp (genotype 1-specific) and 312 bp (genotype 2-specific) (Fig. 2-B).

The results of the present study have shown that the SNU-H1 is a mixture of the genotypes 1 and 2 of C. parvum. Moreover, this human isolate was successfully propagated in 3 mouse strains and a calf, and both genotypes were preserved. The DNA extracted from the oocysts collected after several passages showed no changes in the genetic profiles from that of the original isolate.

With regard to the animal susceptibility to C. parvum infection, no reports are currently available on the natural infections of animals (other than man) with the genotype 1, with the exception of a report on a dugong (Morgan et al., 2000). However, the successful experimental propagation of the genotype 1 has been achieved using animal models, such as captive primates, gnotobiotic piglets, lambs, and calves (Widmer et al., 2000; Giles et al., 2001; Widmer et al., 2002; Akiyoshi et al., 2002). The present study agrees that calves are susceptible to an experimental infection with the genotype 1.

Mice have never previously been included in the animals susceptible to the experimental infection with the genotype 1. Even the gamma-interferon knock-out mice and rodents showed no susceptibility to infection with the oocysts of the genotype 1 (Widmer et al., 2000; Akiyoshi et al., 2002). The present study, however, showed that immunosuppressed mice by steroid injection could be infected with both the genotypes 1 and 2. Therefore, immunosuppressed mice are suggested to be useful in evaluating the infectivity of the genotype 1.

Prior to the present study, natural infections of humans, or animals, with a mixture of the genotypes 1 and 2 of C. parvum have rarely been reported (Widmer et al., 2002). The present study confirms the presence of a mixed human infection with the genotypes 1 and 2 in the Republic of Korea. However, mixed human infections with the genotypes 1 and 2 seem to be a common characteristic in the Republic of Korea; for example, in a recent survey of Koreans infected with C. parvum, 6 of 7 positive samples were identified to be mixed-infected with both the genotypes 1 and 2 (unpublished observation). The present study, together with this communication, suggests that there may be unique transmission patterns of C. parvum in the Republic of Korea. A peculiar epidemiological feature reported was that, unlike the general tendency for cryptosporidial infections to occur predominantly among children, it was highly prevalent among aged people (Chai et al., 2001). Further studies are required to understand the transmission cycles of the mixed genotypes 1 and 2 in the Republic of Korea.

It is of considerable interest to note that the passage of the human genotype 1 to gnotobiotic piglets frequently results in the emergence of the genotype 2 (Widmer et al., 2002). Two possibilities were suggested for the reason; the genotype 2 subpopulations could have either accidentally contaminated, or originally resided in the genotype 1, with the resultant genotype 2 overgrowing the genotype 1. In the present study, we used the isolate from a natural mixed infection with the genotypes 1 and 2, and both genotypes were preserved with no changes in the genetic profiles during several passages in different animal hosts.

In the experimental genetic cross between 2 distinct isolates of the genotype 2, mixed infections produced a recombinant progeny, and it is suggested that outcrossing between genotypes may occur in nature (Feng et al., 2002). Experimental co-infections have shown that the development of different genetic subpopulations is not synchronous, and it may explain the rarity of mixed infections with different genotypes (Widmer et al., 2002).

In the present study, the oocyst shedding patterns of the mixed genotypes 1 and 2 were significantly different between the mouse strains. A delayed-onset, but a prolonged excretion of oocysts was observed in ImSP ICR mice, whereas ImSP C57BL/6 mice excreted a large number of oocysts during the early stages of the infection. ImSP BALB/c mice shed the smallest number of oocysts. Further studies are required to elucidate the immunophysiological mechanisms responsible for these differences.