Gastrointestinal apicomplexan parasites of captive reptiles: diversity, causes, consequences

. 2025 Oct 16 ; 21 (1) : 614. [epub] 20251016

Jazyk angličtina Země Anglie, Velká Británie Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid41102773
Odkazy

PubMed 41102773
PubMed Central PMC12532844
DOI 10.1186/s12917-025-05029-8
PII: 10.1186/s12917-025-05029-8
Knihovny.cz E-zdroje

BACKGROUND: Captive reptiles frequently suffer from gastrointestinal parasites, which stem from their breeding conditions such as limited space and frequent contact with faeces, high numbers of individuals in inadequate conditions, stress, but also from extensive exports and imports in recent years. In particular, parasites with single-host life cycles are common as they can easily complete their development. This study focused on extensive sampling across a variety of captive reptiles groups including lizards (agamas, chameleons, geckos, iguanas, monitors, skinks), snakes, tortoises, and also crocodiles, originating from various resources (pet trades, private breeders, and zoos). RESULTS: Examination of faecal samples revealed that 17.9% (55/308) of captive reptiles were infected with coccidia, namely Eimeria (7.1%), Choleoeimeria (5.5%), Isospora (3.9%), and Caryospora (0.3%), and that 3.2% (10/308) were infected with Cryptosporidium. These apicomplexans, which have monoxenous life cycles, may easily be maintained in breedings, and commonly transmitted to the breedings of new owners via trades and expos. While Choleoeimeria spp. were most prevalent in snake hosts, Isospora amphiboluri was recorded as the most common parasite of bearded dragons; however, its host specificity was shown to be relatively low, as it was also able to infect veiled chameleons. In addition, other representatives of coccidia, as well as pseudoparasites from prey items, were also recorded. Although the treatment of coccidiosis in reptiles remains debatable, our findings revealed that it was more effective to treat infected animals with anticoccidials than to leave them untreated. CONCLUSIONS: This is a comprehensive study on a variety of genera of gastrointestinal apicomplexan protists in captive reptiles that considers not only their detection and identification based on a robust combination of morphological and molecular data, but also their host specificity, evolutionary relationships, clinical status, and possible pseudoinfections with parasites of prey items that cannot be proven without the use of molecular methods. The study highlights the frequent occurrence and importance of gastrointestinal parasites in the health of captive reptiles, the need for their examination and consideration, and the application of proper management strategies.

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CITES. Full CITES trade database download, version 2024.1. Cambridge, UK: UNEP-WCMC; 2024. https://trade.cites.org/#. Accessed 06 Jan 2025.

Altherr S, Lameter K. The rush for the rare: reptiles and amphibians in the European pet trade. Animals. 2020;10:2085. 10.3390/ani10112085. PubMed DOI PMC

Nijman V, Shepherd CR, Sanders KL. Over-exploitation and illegal trade of reptiles in Indonesia. Herpetol J. 2012;22:83–9.

Toland E, Bando M, Hamers M, Cadenas V, Laidlaw R, Martínez-Silvestre A, et al. Turning negatives into positives for pet trading and keeping: a review of positive lists. Animals. 2020;10:2371. 10.3390/ani10122371. PubMed DOI PMC

Taylor MA, Coop RL, Wall RL. Veterinary parasitology. 3rd ed. Oxford: Blackwell Publishing; 2007.

Mennerat A, Nilsen F, Ebert D, Skorping A. Intensive farming: evolutionary implications for parasites and pathogens. Evol Biol. 2010;37:59–67. 10.1007/s11692-010-9089-0. PubMed DOI PMC

Hofmannová L, Kvičerová J, Bízková K, Modrý D. Intranuclear coccidiosis in tortoises - discovery of its causative agent and transmission. Eur J Protistol. 2019;67:71–6. 10.1016/j.ejop.2018.11.002. PubMed DOI

Jacobson ER, Garner MM. Infectious diseases and pathology of reptiles: color atlas and text. 2nd ed. New York: CRC Press; 2021.

Rataj AV, Lindtner-Knific R, Vlahović K, Mavri U, Dovč A. Parasites in pet reptiles. Acta Vet Scand. 2011;53:33. 10.1186/1751-0147-53-33. PubMed DOI PMC

McAllister CT, Upton SJ, Jacobson ER, Kopit W. A description of PubMed DOI

Modrý D, Koudela B. Description of

Modrý D, Šlapeta JR, Koudela B. Six new species of coccidia (Apicomplexa: Eimeriidae) from East African chameleons (Sauria: Chamaeleonidae). J Parasitol. 2000;86:373–9. 10.1645/0022-3395(2000)086[0373:SNSOCA]2.0.CO;2. PubMed DOI

Modrý D, Daszak P, Volf J, Veselý M, Ball SJ, Koudela B. Five new species of coccidia (Apicomplexa: Eimeriidae) from Madagascan chameleons (Sauria: Chamaeleonidae). Syst Parasitol. 2001;48:117–23. 10.1023/a:1006476325181. PubMed DOI

Asmundsson IM, Upton SJ, Freed PS. Five new species of coccidia (Apicomplexa: Eimeriidae) from colubrid snakes of Ecuador. J Parasitol. 2001;87:1077–81. 10.1645/0022-3395(2001)087[1077:FNSOCA]2.0.CO;2. PubMed DOI

Maupin RS, Diong CH, Mcquistion TE. Two new coccian parasites from the grand anglehead lizard, PubMed DOI

Megía-Palma R, Martínez J, Acevedo I, Martín J, García-Roa R, Ortega J, et al. Phylogeny of the reptilian DOI

Phisalix M. Coccidiose des serpentes. Bull Soc Pathol Exot. 1921;14:82–4.

Duszynski DW, Upton SJ. The Biology of the Coccidia (Apicomplexa) of Snakes of the World. 1st ed. USA: CreateSpace Independent Publishing Platform; 2009.

Anderson DR, Duszynski DW, Marquardt WC. Three new coccidia (Protozoa: Telosporea) from kingsnakes, DOI

Asmundsson IM, Duszynski DW, Campbell JA. Seven new species of PubMed DOI

Upton SJ, McAllister CT, Trauth SE. Description of the oöcysts of two new species of DOI

Abdel-Baki AS, Al-Quraishy S, Duszynski DW. PubMed DOI

Levine ND, Ivens V. The Coccidian Parasites of Rodents. FL, Boca Raton: CRC Press; 1990. p. 5–183.

Ernst JV, Chobotar B, Hammond DM. The oocysts of PubMed DOI

Sibert GJ, Clarence AS. Fine structure of zygotes and oocysts of PubMed DOI

Barbosa AS, Bastos OMP, Dib LV, de Siqueira MP, Cardozo ML, Ferreira LC, et al. Gastrointestinal parasites of swine raised in different management systems in the State of Rio de Janeiro. Pesq Vet Bras. 2015;35:941–6. DOI

Rom B, Kornaś S, Basiaga M. Endoparasites of pet reptiles based on coproscopic methods. Ann Parasitol. 2018;64:115–20. 10.17420/ap6402.142. PubMed DOI

Mitchell MA, Tully TN, editors. Manual of exotic pets practice. Missouri: Saunders Elsevier; 2008. Chapters 6–9.

Veterinary Information Network, Inc. 2025. https://www.vin.com/vin. Accessed 06 Jan 2025.

Jacobson ER, Kollias GV, Peters LJ. Dosages for antibiotics and parasiticides used in exotic animals. Compend Contin Educ Vet. 1983;5:315–24.

Jacobson ER. Use of Chemotherapeutics in Reptile Medicine. In: Jacobson ER, Kollias GV, editors. Exotic Animals. New York: Churchill Livingstone; 1988. p. 35–48.

Willette-Frahm M, Wright KM, Thode BC. Select protozoal diseases in amphibians and reptiles: a report for the Infectious Diseases Committee, American Association of Zoo Veterinarians. Bull Assoc Reptilian Amphibian Vet. 1995;5:19–29.

Wilson SC, Carpenter JW. Endoparasitic diseases of reptiles. Semin Avian Exot Pet Med. 1996;5:64–74. DOI

Funk RS. Herp hints and husbandry: parasiticide dosages for captive amphibians and reptiles. Bull Chic Herpetol Soc. 1988;23:30.

Koudela B, Modrý D. New species of

Hallinger MJ, Taubert A, Hermosilla C, Mutschmann F. Captive agamid lizards in Germany: prevalence, pathogenicity and therapy of gastrointestinal protozoan and helminth infections. Comp Immunol Microbiol Infect Dis. 2019;63:74–80. 10.1016/j.cimid.2019.01.005. PubMed DOI

Gałȩcki R, Sokoł R. Treatment of cryptosporidiosis in captive green iguanas ( PubMed DOI

Szczepaniak KO, Tomczuk K, Lojszczyk-Szczepaniak A, Lopuszynski W. Reclassification of PubMed DOI PMC

Schmidt-Ukaj S, Hochleithner M, Richter B, Hochleithner C, Brandstetter D, Knotek Z. A survey of diseases in captive bearded dragons: a retrospective study of 529 patients. Vet Med. 2017;62:508–15. DOI

Duszynski DW, Wilber PG. A guideline for the preparation of species descriptions in the Eimeriidae. J Parasitol. 1997;83:333–6. PubMed DOI

Pasmans F, Blahak S, Martel A, Pantchev N. Introducing reptiles into a captive collection: the role of the veterinarian. Vet J. 2008;175:53–68. 10.1016/j.tvjl.2006.12.009. PubMed DOI

Brownstein DG, Strandberg JD, Montali RJ, Bush M, Fortner J. PubMed DOI

Terrell SP, Uhl EW, Funk RS. Proliferative enteritis in leopard geckos ( PubMed DOI

Graczyk TK, Cranfield MR, Fayer R. Oocysts of PubMed DOI

Teixeira M, Albuquerque GR, Lopes CW, Florentino MV. An adeleid coccidia, a pseudoparasite of

Berto BP, Lopes BDB, Flausino W, Teixeira Filho WL, Lopes CWG. Contribution on the study of PubMed DOI

Ghimire TR. Redescription of genera of family Eimeriidae Minchin, 1903. Int J Life Sci. 2010;4:26–47. 10.3126/IJLS.V4I0.3285. DOI

Pellérdy L. Coccidia and coccidiosis. Budapest: Akadémiai Kiadó; 1974.

Long PL. The biology of the Coccidia. Baltimore, Maryland: University Park Press; 1982.

Levine ND. The Protozoan Phylum Apicomplexa, vol. 2. FL, Boca Raton: CRC Press; 1988. p. 154.

Trefancová A, Mácová A, Kvičerová J. Isosporan oocysts in the faeces of bank voles ( PubMed DOI

Modrý D, Pafčo B, Petrželková KJ, Hasegawa H. Parasites of Apes. an atlas of coproscopic diagnostics. Frankfurt: Edition Chimaira; 2018.

Berto BP, McIntosh D, Lopez CWG. Studies on coccidian oocysts (Apicomplexa: Eucoccidiorida). Braz J Vet Parasitol. 2014;23:1–15. 10.1590/S1984-29612014001. PubMed DOI

Kvičerová J, Pakandl M, Hypša V. Phylogenetic relationships among Eimeria spp. (Apicomplexa, Eimeriidae) infecting rabbits: evolutionary significance of biological and morphological features. Parasitology. 2008;135:443–52. 10.1017/S0031182007004106. PubMed DOI

Schwarz RS, Jenkins MC, Klopp S, Miska KB. Genomic analysis of PubMed DOI

Xiao L, Escalante L, Yang C, Sulaiman I, Escalante AA, Montali RJ, et al. Phylogenetic analysis of PubMed DOI PMC

Sulaiman IM, Lal AA, Xiao L. Molecular phylogeny and evolutionary relationships of PubMed DOI

Peng MM, Matos O, Gatei W, Das P, Stantic-Pavlinic M, Bern C, Sulaiman IM, Glaberman S, Lal AA, Xiao L. A comparison of PubMed

BLAST. National Library of Medicine, Bethesda. 2025. https://blast.ncbi.nlm.nih.gov/Blast.cgi. Accessed 06 Jan 2025.

Hall TA. Bioedit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucleic Acids Symp Ser. 2003;41:95–8.

Guindon S, Gascuel O. A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol. 2003;52:696–704. 10.1080/10635150390235520. PubMed DOI

Huelsenbeck JP, Ronquist F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics. 2001;17:754–5. 10.1093/bioinformatics/17.8.754. PubMed DOI

SMS: Smart Model Selection in PhyML. http://www.atgc-montpellier.fr/sms/. Accessed 06 Jan 2025.

Lefort V, Longueville JE, Gascuel O. SMS: smart model selection in PhyML. Mol Biol Evol. 2017;34:2422–4. 10.1093/molbev/msx149. PubMed DOI PMC

Page RD. Treeview: an application to display phylogenetic trees on personal computers. Bioinformatics. 1996;12:357–8. 10.1093/bioinformatics/12.4.357. PubMed DOI

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