Molecular Identification of Cryptosporidium Species from Pet Snakes in Thailand (2024)

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Korean J Parasitol. 2016 Aug; 54(4): 423–429.

Published online 2016 Aug 31. doi:10.3347/kjp.2016.54.4.423

PMCID: PMC5040075

PMID: 27658593

Benjarat Yimming,¹ Khampee Pattanatanang,¹ p*rnchai Sanyathitiseree,² Tawin Inpankaew,¹ Ketsarin Kamyingkird,¹ Nongnuch Pinyopanuwat,¹ Wissanuwat Chimnoi,¹ and Jumnongjit Phasuk^1,^*

Author information Article notes Copyright and License information PMC Disclaimer

Abstract

Cryptosporidium is an important pathogen causing gastrointestinal disease in snakes and is distributed worldwide. The main objectives of this study were to detect and identify Cryptosporidium species in captive snakes from exotic pet shops and snake farms in Thailand. In total, 165 fecal samples were examined from 8 snake species, boa constrictor (Boa constrictor constrictor), corn snake (Elaphe guttata), ball python (Python regius), milk snake (Lampropeltis triangulum), king snake (Lampropeltis getula), rock python (Python sebae), rainbow boa (Epicrates cenchria), and carpet python (Morelia spilota). Cryptosporidium oocysts were examined using the dimethyl sulfoxide (DMSO)-modified acid-fast staining and a molecular method based on nested-PCR, PCR-RFLP analysis, and sequencing amplification of the SSU rRNA gene. DMSO-modified acid-fast staining revealed the presence of Cryptosporidium oocysts in 12 out of 165 (7.3%) samples, whereas PCR produced positive results in 40 (24.2%) samples. Molecular characterization indicated the presence of Cryptosporidium parvum (mouse genotype) as the most common species in 24 samples (60%) from 5 species of snake followed by Cryptosporidium serpentis in 9 samples (22.5%) from 2 species of snake and Cryptosporidium muris in 3 samples (7.5%) from P. regius.

Keywords: Cryptosporidium parvum, Cryptosporidium serpentis, Cryptosporidium muris, snake, nested PCR, SSU rRNA, Thailand

INTRODUCTION

Cryptosporidium spp. are apicomplexan protozoan parasites that infect a wide variety of vertebrate hosts, including reptiles, birds, fish, amphibians, and mammals, and cause cryptosporidiosis [1]. Cryptosporidiosis is characterized by acute gastrointestinal disturbances, mucoid or hemorrhagic watery diarrhea, fever, lethargy, anorexia, and death in humans and mammals [2]. Cryptosporidium infections have been described in at least 57 reptilian species consisting of 40 species of snakes, 15 species of lizards, and 2 species of tortoises [3]. Unlike in other animals in which infection with Cryptosporidium spp. is usually self-limiting in immunocompetent individuals, cryptosporidiosis in reptiles is frequently chronic and sometimes lethal in snakes [4]. Two species, Cryptosporidium serpentis and Cryptosporidium varanii (syn. C. saurophilum) have been described in snakes and lizards to date [4,5]. C. serpentis is an important parasite in snakes and is usually found in the gastric epithelium [6]. Clinical signs of cryptosporidiosis in snakes have been described as anorexia, lethargy, postprandial regurgitation, midbody swelling, and weight loss [1]. The infection occurs more frequently in adults rather than in young reptiles, unlike in mammals and birds [7]. While C. varanii was originally described in lizards as causing weight loss, abdominal swelling and mortality, it can be found in snakes but has no significant signs [5].

Stressed animals, which have been raised in a limited living space together with various types of species, are more likely to contribute to the spread of the parasite [8]. The above factors have been reported to suppress the immune responses and increase the opportunity for pathogens to cause infections and consequently spread to other animals including humans [8,9]. Cryptosporidium infection in snakes is difficult to identify, especially in those with a subclinical infection [10]. Conventional methods for detection of Cryptosporidium oocysts (including microscopic examination of fecal smears with acid-fast stains) are not capable of identification to the species level. Therefore, molecular techniques have been developed to detect and differentiate Cryptosporidium at the species/genotype and subtype levels [11]. Previously, molecular analysis of Cryptosporidium infection in snakes has identified C. parvum, C. muris, and Cryptosporidium mouse genotype, which probably originated from the ingestion of infected rodents or other prey [4,6,12-14]. Likewise, molecular techniques will help ensure accurate species identification of Cryptosporidium oocysts in snakes.

The pet snake business has become popular in Thailand. However, there is a lack of information regarding Cryptosporidium infection in snakes in Thailand. The present study aimed to identify Cryptosporidium species in captive snake fecal samples using microscopic and molecular examinations. This study will be relevant to disease surveillance and to the improvement of the management of aliments in captive snakes in Thailand.

MATERIALS AND METHODS

Sample collection

In total, 165 fecal samples were collected from asymptomatic snakes of 8 species in 6 genera (Table 1). Of these, 34 snakes were housed in 5 exotic pet shops, and 131 were from 2 snake farms. Fecal samples were stored at 4˚C before analysis.

Table 1.

Detection of Cryptosporidium in snakes using microscopic and molecular methods

Scientific name	Common name	No. of samples		No. of positive samples				Species and/or genotype (no. of samples)
		No. of samples		Acid fast stain		PCR		Sequence analysis	RFLP
		Farm	Pet shop	Farm	Pet shop	Farm	Pet shop	Sequence analysis	RFLP
Boa constrictor constrictor	Boa constrictor	14	3	0	0	4	1	C. parvum (4)	C. parvum mouse genotype
								Cryptosporidium mouse genotype (1)	-
Elaphe guttata	Corn snake	71	5	7	2	17	2	C. parvum (10)	C. parvum mouse genotype
								C. serpentis (8)	-
								C. saurophilum (1)	-
Epicrates cenchria	Rainbow boa	0	1	0	0	0	0	-	-
Lampropeltis getula	King snake	19	2	0	0	1	0	C. serpentis (1)	-
Lampropeltis triangulum	Milk snake	4	3	0	0	1	1	C. parvum (2)	C. parvum mouse genotype
Morelia spilota	Carpet python	0	4	0	1	0	4	C. parvum (3)	C. parvum mouse genotype
								C. andersoni (1)	-
Python regius	Ball python	23	15	2	0	0	9	C. parvum (5)	C. parvum mouse genotype
								C. muris (3)	-
								Cryptosporidium mouse genotype (1)	-
Python sebae	Rock python	0	1	0	0	0	0	-	-
Total		131	34	9	3	23	17

Microscopy

Cryptosporidium oocysts were concentrated using Sheather’s sugar flotation technique [15]. One drop from the top of the supernatant was smeared on a slide followed by staining using DMSO-modified acid-fast stain as previously described [16].

DNA extraction

DNA was extracted from the supernatant produced using Sheather’s sugar flotation technique with a commercial kit (E.Z.N.A.^® Stool DNA Kit, Omega Biotek Inc., Norcross, GA, USA) following the manufacturer’s protocol. DNA was stored at -20˚C before molecular analysis.

Nested PCR amplification and PCR- RFLP analysis

Amplification of the 819-825 bp polymorphic fragment of the SSU rRNA using nested PCR was performed as previously described [17]. Briefly, the PCR conditions were composed of pre-denaturation at 94˚C for 5 min, then 35 cycles of denaturation at 94˚C for 45 sec, annealing at 55˚C for 45 sec, and extension at 72˚C for 1 min, followed by final extension at 72˚C for 10 min. RFLP of the secondary PCR products of C. parvum positive samples was performed using Vsp I (Thermo Fisher Scientific Inc., Rochester, New York, USA) for the genotyping of C. parvum [17]. The reaction mixture contained 0.5 µl of Vsp I (Thermo Fisher Scientific Inc.), 2.2 µl of restriction buffer, and 5 µl of PCR product at 37˚C for 30 min, under conditions recommended by the manufacturer. The digested products were analyzed using 2% agarose gel electrophoresis.

DNA sequencing and phylogenetic analysis

The positive Cryptosporidium samples were submitted for sequencing (1st Base Laboratory, Selangor, Malaysia). The DNA sequences were compared with those in the GenBank database using the basic local alignment search tool (BLAST) algorithm, and the species of Cryptosporidium present in the sample was determined. The nucleotide sequences of the partial SSU rRNA gene of the Cryptosporidium parasites were deposited in the GenBank^TM database under the accession nos. KM870564 - KM870603. Multiple alignments were done using the ClustalW program [18,19]. A neighbor-joining tree was constructed from the aligned sequences using the MEGA version 5 software [20].

Statistical analysis

Statistical analysis was performed using a chi-square (χ²) test in the Number Cruncher Statistical System (NCSS) version 2000 to determine the association between the prevalence of Cryptosporidium infection vs host genders and host locations. Values were tested for significance at P≤0.05.

RESULTS

Of the 165 fecal samples from captive snakes, 12 (7.3%) were detected as positive for Cryptosporidium oocysts using the DMSO-modified acid-fast stain, and 40 (24.2%) were positive using nested PCR (Table 1). Seventeen out of 34 samples (50.0%) from pet shops and 23 out of 131 samples (17.6%) from private farms were positive for Cryptosporidium. Among the positive results from nested PCR testing, sequencing analysis identified 24 (60.0%); 9 (22.5%); 3 (7.5%), 2 (5.0%), 1 (2.5%), and 1 (2.5%) as C. parvum, C. serpentis, C. muris, Cryptosporidium mouse genotype, C. andersoni, and C. saurophilum, respectively (Table 1). C. parvum was detected from Boa constrictor constrictor (4), Elaphe guttata (10), Lampropeltis triangulum (2), Python regius (5), and Morelia spilota (3). C. serpentis was detected from Lampropeltis getula (1) and Elaphe guttata (8). C. muris was detected from Python regius. Cryptosporidium mouse genotype was detected from B. constrictor constrictor (1) and P. regius. C. andersoni was detected from M. spilota. C. saurophilum was detected from E. guttata (Table 1).

Sequencing analysis indicated that C. parvum, C. serpentis, C. muris, Cryptosporidium mouse genotype, C. andersoni, and C. saurophilum were 99% identical to GenBank accession nos. DQ898158, AF093499, EU553588, EU553589, JX515549, and EU553551, respectively. Differentiation of the C. parvum genotype by PCR-RFLP showed that all 24 C. parvum positive samples were C. parvum mouse genotype (Fig. 1). This genotype is considered as nonpathogenic in snakes [21].

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Fig. 1.

PCR-RFLP analysis. Lane 1 is Cryptosporidium parvum without digestion showing a single 835 bp band and lanes 2-4 are C. parvum “mouse genotype” showing digested bands of 104, 175, and 457 bp. The molecular weight marker size, 100 bp ladder. Black arrow, the DNA marker size at 100 bp, 500 bp, and 1,000 bp.

Risk factor analysis showed that there were infection rates of 12.8% and 19.6% of Cryptosporidium spp. in male and female snakes (χ²=1.027, P =0.310), respectively, and the infection rates were 50.0% and 17.6% on pet shops and farms (χ²=17.470, P =0.00008), respectively. These results indicated that location was a statistically significant factor associated with Cryptosporidium spp. infection in snakes (Table 2). The neighbor-joining analysis results showed that 2 distinctive clades of intestinal and stomach Cryptosporidium species from this study were clearly separated (Fig. 2). Intestinal Cryptosporidium species consisted of C. parvum, Cryptosporidium mouse genotype, and C. saurophilum, while stomach Cryptosporidium species consisted of C. serpentis, C. muris, and C. andersoni.

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Fig. 2.

Phylogenetic relationships among Cryptosporidium species found in this study and other Cryptosporidium spp. performed using neighbor-joining analysis of the SSU rDNA fragment. The samples with local origin “Thailand” were in current study. Captive snake: B.c=Boa constrictor constrictor, E.g=Elaphe guttata, L.t=Lampropeltis triangulum, M.s=Morelia spilota, P.r=Python regius. Location: P1=Pet shop, P2=Pet shop, P4=Pet shop 4, P5=Pet shop 5, F1=Farm 1, F2=Farm 2.

Table 2.

Risk factors associated with Cryptosporidium spp. infection in snakes

Variable	No. (%) of infected snakes	No. (%) of non-infected snakes	Total sample	χ²	P-value^a
Sex^b	25 (17.4)	119 (82.6)	144	1.027 df = 1	0.310
Male	6 (12.8)	41 (87.2)	47
Female	19 (19.6)	78 (80.4)	97
Location	40 (24.2)	125 (75.8)	165	15.470 df = 1	0.00008
Pet shops	17 (50.0)	17 (50.0)	34
Farms	23 (17.6)	108 (82.4)	131

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^aP≤0.05 was considered statistically significant.

^bGender data were missing in 21 samples.

DISCUSSION

Cryptosporidiosis is a well-known cause of chronic hypertrophic gastritis, and is possibly lethal in captive snakes [5,22]. The present study was the first identification of Cryptosporidium infection in pet snakes in Thailand. We found 7.3% of the Cryptosporidium oocysts using the acid-fast stain technique and 24.2% of the Cryptosporidium DNA using a molecular method. The acid-fast staining technique is less sensitive for the detection of Cryptosporidium infection. However, it is the easiest and most effective method for veterinary clinical diagnosis [23]. Moreover, PCR is a sensitive and specific detection technique, which resulted in a much higher proportion of Cryptosporidium positive samples in comparison to acid-fast staining [24]. Additionally, PCR is an important method for the identification of Cryptosporidium species or genotypes in samples with low numbers of oocysts [25,26]. Thus, PCR is still hindered by its high cost and time-consuming DNA extraction, PCR amplification, and gel electrophoresis [27,28]. A combination of several diagnostic techniques for the detection of Cryptosporidium oocysts is still needed [29].

In the present study, sequencing analysis of the 18S rRNA gene revealed the presence of C. serpentis in the corn snake (E. guttata) and king snake (L. getula). These findings were similar to previous studies, which have found that C. serpentis is most common in snakes [4,6,9,12,14,30]. Additionally, we found C. saurophilum in the corn snake (E. guttata), which is similar to previous reports [4-6,13]. C. saurophilum was originally described as an intestinal parasite mainly in lizards [31]. The presence of C. saurophilum in reptiles other than lizards might have resulted from the fact that they were housed together [4-5]. Moreover, none of the infected animals showed any clinical signs of the disease in the present study, which was in agreement with previous reports [6,9]. However, the subclinical stage can last for years in these animals [32].

We have confirmed the presence of C. parvum, C. muris, and C. andersoni in captive snakes. C. parvum and C. muris were considered as Cryptosporidium from mammals. Therefore, they were not pathogenic in snakes [33,34]. On the other hand, we have also confirmed C. andersoni in captive snakes. Interestingly, C. andersoni was commonly found in infected cattle abomasum. Possibly, the finding of other Cryptospodium genotypes in snakes might be due to infection from infected prey animals [35]. This is the first report of C. andersoni in captive snakes.

The study of farm management found that the sanitary conditions on the farm and inadequate management influenced the rate of infection of Cryptospodium in dairy cows [36]. Farms with poor management and bad sanitary conditions present a high risk of Cryptospodium and other gastrointestinal protozoan infections. In this study, risk factor analysis indicated that location was significantly associated with Cryptospodium spp. infection. The risk of infection was higher in pet shops than in farms even though the former did not use for breeding, but only for selling snakes. However, our observation during sample collection found that some pet shops have many species of animals, and keep them at high densities in small cages. They also used contaminated equipment. The result is that pet shops tend to have a higher percentage of Cryptospodium spp. infection than private farms.

Phylogenetic analysis of SSU rRNA gene fragments within the genus Cryptospodium has proven to be a useful tool for both the systematic analysis of the presently recognized species and the possibility of definitive identification of new species or genotypes within this genus [4]. In this study, we identified 6 different Cryptospodium species or genotypes in reptiles. These results confirmed that C. serpentis and C. parvum are the main species found in snakes.

A high proportion of Cryptospodium species from mammals (75.0%) was detected in this study consisting of C. parvum, C. muris, Cryptospodium mouse genotype, and C. andersoni. However, these Cryptospodium are non-pathogenic in snakes but potentially zoonotic. Cryptosporidiosis causes mucoid or hemorrhagic diarrhea, fever, lethargy, anorexia, and death especially in immunocompromised patients [11,37-39]. Additionally, C. muris is probably the zoonotic Cryptospodium, which was reported in HIV patients in Perú, Thailand, Indonesia, France, and Kenya [40]. Recently, C. andersoni has been found in 21 diarrhea patients out of 232 outpatients in China, whereas Cryptospodium hominis (the human genotype) was found only in 2 patients [41]. In 2015, C. andersoni was first reported in a captured lesser panda in China [42]. Therefore, the present identification of C. andersoni might have a public health impact. Additionally, Cryptospodium has an environmentally resistant oocyst, which is a public health risk factor for handlers and owners, especially when they are children, elderly people, or immunocompromised patients. Consequently, feeding snakes with Cryptospodium infected mice or any other prey could possibly transmit the pathogen to humans via feces, water, and contaminated equipment. Although a substantial study of Cryptospodium transmission from reptiles to humans has not been reported yet, disinfection processes have been recommended as the best option for reducing the transmission risk by the application of 4-cholr-M-cresol, 5% ammonium solution, or hydrogen peroxide-based disinfectants [14,21,32]. The presence of Cryptospodium infection in snakes should not be ignored in snake collections because infection can be transmitted from animal to animal by the fecal-oral-route when animals are housed together. The lack of effective treatment for cryptosporidiosis almost always results in euthanasia of the infected snakes, which often leads to the loss of valuable animals in a collection [43]. Hyperimmune bovine colostrum (HBC) is recommended to combat clinical and subclinical C. serpentis infections in captive snakes [44].

In conclusion, applying a molecular method for the detection of the pathogen will probably prove the presence of the Cryptospodium species or genotype, because it is difficult to identify oocysts of pathogenic C. serpentis or C. saurophilum from those of non-pathogenic Cryptospodium species [45]. The study has shown that molecular techniques can separate different species and genotypes of Cryptospodium. The sequencing of the PCR products revealed that C. parvum, C. serpentis, C. muris, C. mouse genotype, C. andersoni, and C. saurophilum are different from each other. In addition, the PCR-RFLP technique can differentiate various C. parvum genotypes (e.g., C. parvum human, C. parvum mouse, and C. parvum bovine genotypes) [45]. This study found a high percentage of non-pathogenic Cryptospodium in snakes in Thailand. However, some species were zoonotic Cryptospodium, which might have been ingested from prey and passed through intestinal tract of the snake.

Cryptospodium oocysts from food items can cause the misidentification of cryptosporidiosis in snakes. In addition, paying more attention to cryptosporidiosis in snakes is required due to public health concerns. Moreover, the sanitary conditions associated with snake feeding should be improved along with avoiding the purchase of infected feeds. Thus, practicing good sanitation and hygiene, including at snake prey suppliers, should be considered, and these places tested for specific pathogens and to prevent the killing of snakes infected with non-pathogenic Cryptospodium.

Acknowledgments

This study was supported by a research grant from the Faculty of Veterinary Medicine, Kasetsart University, Thailand. Many thanks to the Kasetsart University Research and Development Institute (KURDI) for English editing of this manuscript.

Footnotes

The authors declare that there are no conflicts of interest.

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