Are molecular tools clarifying or confusing our understanding of the public health threat from zoonotic enteric protozoa in wildlife?
Status PubMed-not-MEDLINE Jazyk angličtina Země Anglie, Velká Británie Médium electronic-ecollection
Typ dokumentu časopisecké články, přehledy
PubMed
31338293
PubMed Central
PMC6626983
DOI
10.1016/j.ijppaw.2019.01.010
PII: S2213-2244(18)30184-6
Knihovny.cz E-zdroje
- Klíčová slova
- Emerging infection, Host specificity, Protozoa, Transmission, Wildlife, Zoonosis,
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Emerging infectious diseases are frequently zoonotic, often originating in wildlife, but enteric protozoa are considered relatively minor contributors. Opinions regarding whether pathogenic enteric protozoa may be transmitted between wildlife and humans have been shaped by our investigation tools, and have led to oscillations regarding whether particular species are zoonotic or have host-adapted life cycles. When the only approach for identifying enteric protozoa was morphology, it was assumed that many enteric protozoa colonized multiple hosts and were probably zoonotic. When molecular tools revealed genetic differences in morphologically identical species colonizing humans and other animals, host specificity seemed more likely. Parasites from animals found to be genetically identical - at the few genes investigated - to morphologically indistinguishable parasites from human hosts, were described as having zoonotic potential. More discriminatory molecular tools have now sub-divided some protozoa again. Meanwhile, some infection events indicate that, circumstances permitting, some "host-specific" protozoa, can actually infect various hosts. These repeated changes in our understanding are linked intrinsically to the investigative tools available. Here we review how molecular tools have assisted, or sometimes confused, our understanding of the public health threat from nine enteric protozoa and example wildlife hosts (Balantoides coli - wild boar; Blastocystis sp. - wild rodents; Cryptosporidium spp. - wild fish; Encephalitozoon spp. - wild birds; Entamoeba spp. - non-human primates; Enterocytozoon bieneusi - wild cervids; Giardia duodenalis - red foxes; Sarcocystis nesbitti - snakes; Toxoplasma gondii - bobcats). Molecular tools have provided evidence that some enteric protozoa in wildlife may infect humans, but due to limited discriminatory power, often only the zoonotic potential of the parasite is indicated. Molecular analyses, which should be as discriminatory as possible, are one, but not the only, component of the toolbox for investigating potential public health impacts from pathogenic enteric protozoa in wildlife.
Zobrazit více v PubMed
Abubakar S., Teoh B.T., Sam S.S., Chang L.Y., Johari J., Hooi P.S., Lakhbeer-Singh H.K., Italiano C.M., Omar S.F., Wong K.T., Ramli N., Tan C.T. Outbreak of human infection with Sarcocystis nesbitti, Malaysia, 2012. Emerg. Infect. Dis. 2013;19:1989–1991. PubMed PMC
Adamu H., Petros B., Zhang G., Kassa H., Amer S., Ye J., Feng Y., Xiao L. Distribution and clinical manifestations of Cryptosporidium species and subtypes in HIV/AIDS patients in Ethiopia. PLoS. Negl. Trop. Dis. 2014;8 e2831. PubMed PMC
Alexeieff A. Sur quelques particularités de structure de Balantioides (nom. nov.) coli (Malmsten) C.R. Séances Soc. Biol. Ses. Fil. 1931;107:210–211.
Alfellani M.A., Taner-Mulla D., Jacob A.S., Imeede C.A., Yoshikawa H., Stensvold C.R., Clark C.G. Genetic diversity of Blastocystis in livestock and zoo animals. Protist. 2013;164:497–509. PubMed
Alvarez-Pellitero P., Quiroga M.I., Sitjà-Bobadilla A., Redondo M.J., Palenzuela O., Padrós F., Vázquez S., Nieto J.M. Cryptosporidium scophthalmi n. sp. (Apicomplexa: Cryptosporidiidae) from cultured turbot Scophthalmus maximus. Light and electron microscope description and histopathological study. Dis. Aquat. Org. 2004;62:133–145. PubMed
Alvarez-Pellitero P., Sitjà-Bobadilla A. Cryptosporidium molnari n. sp. (Apicomplexa: Cryptosporidiidae) infecting two marine fish species, Sparus aurata L. and Dicentrarchus labrax L. Int. J. Parasitol. 2002;32:1007–1021. PubMed
Appelbee A.J., Thompson R.C., Olson M.E. Giardia and Cryptosporidium in mammalian wildlife--current status and future needs. Trends Parasitol. 2005;21:370–376. PubMed PMC
Arness M.K., Brown J.D., Dubey J.P., Neafie R.C., Granstrom D.E. An outbreak of acute eosinophilic myositis attributed to human Sarcocystis parasitism. Am. J. Trop. Med. Hyg. 1999;61:548–553. PubMed
Awakian A. Studies on the intestinal protozoa of rats. II. Rats as carriers of Balantidium. Trans. R. Soc. Trop. Med. Hyg. 1937;31:93–98.
Ballweber L.R., Xiao L., Bowman D.D., Kahn G., Cama V.A. Giardiasis in dogs and cats: update on epidemiology and public health significance. Trends Parasitol. 2010;26:180–189. PubMed
Barugahare R., Dennis M.M., Becker J.A., Šlapeta J. Detection of Cryptosporidium molnari oocysts from fish by fluorescent-antibody staining assays for Cryptosporidium spp. affecting humans. Appl. Environ. Microbiol. 2011;77:1878–1880. PubMed PMC
Beaver P.C., Gadgil K., Morera P. Sarcocystis in man: a review and report of five cases. Am. J. Trop. Med. Hyg. 1979;28:819–844. PubMed
Beck R., Sprong H., Lucinger S., Pozio E., Cacciò S.M. A large survey of Croatian wild mammals for Giardia duodenalis reveals a low prevalence and limited zoonotic potential. Vector Borne Zoonotic Dis. 2011;11:1049–1055. PubMed
Betts E.L., Gentekaki E., Thomasz A., Breakell V., Carpenter A.I., Tsaousis A.D. Genetic diversity of Blastocystis in non-primate animals. Parasitology. 2018;145:1228–1234. PubMed PMC
Buckholt M.A., Lee J.H., Tzipori S. Prevalence of Enterocytozoon bieneusi in swine: an 18-month survey at a slaughterhouse in Massachusetts. Appl. Environ. Microbiol. 2002;68:2595–2599. PubMed PMC
Burg J.L., Grover C.M., Pouletty P., Boothroyd J.C. Direct and sensitive detection of a pathogenic protozoan, Toxoplasma gondii, by polymerase chain reaction. J. Clin. Microbiol. 1989;27:1787–1792. PubMed PMC
Cacciò S.M., Lalle M., Svärd S.G. Host specificity in the Giardia duodenalis species comlex. Infect. Genet. Evol. 2018;66:335–345. PubMed
Cahill S., Llimona F., Cabañeros L., Calomardo F. Characteristics of wild boar (Sus scrofa) habituation to urban areas in the Collserola Natural Park (Barcelona) and comparison with other locations. Anim. Biodivers. Conserv. 2012;35:221–233.
Carme B., Demar M., Ajzenberg D., Dardé M.L. Severe acquired toxoplasmosis caused by wild cycle of Toxoplasma gondii, French Guiana. Emerg. Infect. Dis. 2009;15:656–658. PubMed PMC
Castellani A. Note on a liver abscess of amoebic origin in a monkey. Parasitology. 1908;1:101–102.
Certad G., Dupouy-Camet J., Gantois N., Hammouma-Ghelboun O., Pottier M., Guyot K., Benamrouz S., Osman M., Delaire B., Creusy C., Viscogliosi E., Dei-Cas E., Aliouat-Denis C.M., Follet J. Identification of Cryptosporidium species in fish from Lake Geneva (lac Leman) in France. PLoS One. 2015;10 PubMed PMC
Chistyakova L.V., Kostygov A.Y., Kornilova O.A., Yurchenko V. Reisolation and redescription of Balantidium duodenis, Stein, 1867 (Litostomatea, Trichostomatia) Parasitol. Res. 2014;113:4207–4215. PubMed
Cian A., El Safadi D., Osman M., Moriniere R., Gantois N., Benamrouz-Vanneste S., Delgado-Viscogliosi P., Guyot K., Li L.L., Monchy S., Noel C., Poirier P., Nourrisson C., Wawrzyniak I., Delbac F., Bosc S., Chabe M., Petit T., Certad G., Viscogliosi E. Molecular epidemiology of Blastocystis sp. in various animal groups from two French zoos and evaluation of potential zoonotic risk. PLoS One. 2017;12 PubMed PMC
Couso-Pérez S., Ares-Mazás E., Gómez-Couso H. Identification of a novel piscine Cryptosporidium genotype and Cryptosporidium parvum in cultured rainbow trout (Oncorhynchus mykiss) Parasitol. Res. 2018;117:2987–2996. PubMed
Da Silva Barbosa A., Ponce-Gordo F., Verdan Dib L., Antunes Uchôa C.M., Pereira Bastos O.M., Pissinatti A., Reis Amedoeira M.R. First molecular characterization of Balantioides coli (Malmsten, 1857) isolates maintained in vitro culture and from feces of captive animals, Rio de Janeiro, Brazil. Vet. Parasitol. Reg. Stud. Reports. 2017;10:102–113. PubMed
Debenham J.J., Landuyt H., Troell K., Tysnes K., Robertson L.J. Occurrence of Giardia in Swedish red foxes (Vulpes vulpes) J. Wildl. Dis. 2017;53:649–652. PubMed
Decraene V., Lebbad M., Botero-Kleiven S., Gustavsson A.M., Lofdahl M. First reported foodborne outbreak associated with microsporidia, Sweden, October 2009. Epidemiol. Infect. 2012;140:519–527. PubMed PMC
del Aguila C., Croppo G.P., Moura H., Da Silva A.J., Leitch G.J., Moss D.M., Wallace S., Slemenda S.B., Pieniazek N.J., Visvesvara G.S. Ultrastructure, immunofluorescence, western blot, and PCR analysis of eight isolates of Encephalitozoon (Septata) intestinalis established in culture from sputum and urine samples and duodenal aspirates of five patients with AIDS. J. Clin. Microbiol. 1998;36:1201–1208. PubMed PMC
Diamond L.S., Clark C.G. A redescription of Entamoeba histolytica Schaudinn, 1903 (emended Walker, 1911) separating it from Entamoeba dispar Brumpt, 1925. J. Eukaryot. Microbiol. 1993;40:340–344. PubMed
Didier E.S., Rogers L.B., Orenstein J.M., Baker M.D., Vossbrinck C.R., Van Gool T., Hartskeerl R., Soave R., Beaudet L.M. Characterization of Encephalitozoon (Septata) intestinalis isolates cultured from nasal mucosa and bronchoalveolar lavage fluids of two AIDS patients. J. Eukaryot. Microbiol. 1996;43:34–43. PubMed
Didier E.S., Weiss L.M. Microsporidiosis: not just in AIDS patients. Curr. Opin. Infect. Dis. 2011;24:490–495. PubMed PMC
Dobell C. J. Bale, Sons, and Danielson; London, UK: 1919. The Amoebae Living in Man. A Zoological Monograph.
Dowd S.E., Gerba C.P., Pepper I.L. Confirmation of the human-pathogenic microsporidia Enterocytozoon bieneusi, Encephalitozoon intestinalis, and Vittaforma corneae in water. Appl. Environ. Microbiol. 1998;64:3332–3335. PubMed PMC
Dubey J.P. Foodborne and waterborne zoonotic sarcocystosis. Food Water. Parasitol. 2015;1:2–11.
Dubey J.P., Jones J.L. Toxoplasma gondii infection in humans and animals in the United States. Int. J. Parasitol. 2008;38:1257–1278. PubMed
Dubey J.P., Velmurugan G.V., Rajendran C., Yabsley M.J., Thomas N.J., Beckmen K.B., Sinnett D., Ruid D., Hart J., Fair P.A., McFee W.E., Shearn-Bochsler V., Kwok O.C.H., Ferreira L.R., Choudhary S., Faria E.B., Zhou H., Felix T.A., Su C. Genetic characterisation of Toxoplasma gondii in wildlife from North America revealed widespread and high prevalence of the fourth clonal type. Int. J. Parasitol. 2011;41:1139–1147. PubMed
Dykes A.C., Juranek D.D., Lorenz R.A., Sinclair S., Jakubowski W., Davies R. Municipal waterborne giardiasis: an epidemilogic investigation. Beavers implicated as a possible reservoir. Ann. Intern. Med. 1980;92:165–170. PubMed
Eichhorn A., Gallagher B. Spontaneous amebic dysentery in monkeys. J. Infect. Dis. 1916;19:395–407.
Esposito D.H., Stich A., Epelboin L., Malvy D., Han P.V., Bottieau E., da Silva A., Zanger P., Slesak G., van Genderen P.J., Rosenthal B.M., Cramer J.P., Visser L.G., Munoz J., Drew C.P., Goldsmith C.S., Steiner F., Wagner N., Grobusch M.P., Plier D.A., Tappe D., Sotir M.J., Brown C., Brunette G.W., Fayer R., von Sonnenburg F., Neumayr A., Kozarsky P.E., Tioman Island Sarcocystosis Investigation Team Acute muscular sarcocystosis: an international investigation among ill travelers returning from Tioman Island, Malaysia, 2011-2012. Clin. Infect. Dis. 2014;59:1401–1410. PubMed PMC
Farah Haziqah M.T., Mohd Zain S.N., Chandrawathani P., Premaalatha B., Mohd Khairul Nizam M.K., Arutchelvan R., Suresh K. Genetic diversity of rodent Blastocystis sp from peninsular Malaysia. Trop. Biomed. 2018;25:586–592. PubMed
Fayer R., Esposito D.H., Dubey J.P. Human infections with Sarcocystis species. Clin. Microbiol. Rev. 2015;28:295–311. PubMed PMC
Feng M., Pandey K., Yanagi T., Wang T., Putaporntip C., Jongwutiwes S., Cheng X., Sherchand J.B., Pandey B.D., Tachibana H. Prevalence and genotypic diversity of Entamoeba species in inhabitants in Kathmandu, Nepal. Parasitol. Res. 2018;117:2467–2472. PubMed
Feng Y., Li N., Dearen T., Lobo M.L., Matos O., Cama V., Xiao L. Development of a multilocus sequence typing tool for high-resolution genotyping of Enterocytozoon bieneusi. Appl. Environ. Microbiol. 2011;77:4822–4828. PubMed PMC
Feng Y., Xiao L. Zoonotic potential and molecular epidemiology of Giardia species and giardiasis. Clin. Microbiol. Rev. 2011;24:110–140. PubMed PMC
Fournier S., Liguory O., Santillana-Hayat M., Guillot E., Sarfati C., Dumoutier N., Molina J., Derouin F. Detection of microsporidia in surface water: a one year follow-up study. FEMS Immunol. Med. Microbiol. 2000;29:95–100. PubMed
Galván A., Magnet A., Izquierdo F., Fenoy S., Henriques-Gi,l N., del Aguila C. Variability in minimal genomes: analysis of tandem repeats in the microsporidia Encephalitozoon intestinalis. Infect. Genet. Evol. 2013;20:26–33. PubMed
Gibson-Kueh S., Yang R., Thuy N.T., Jones J.B., Nicholls P.K., Ryan U. The molecular characterization of an Eimeria and Cryptosporidium detected in Asian seabass (Lates calcarifer) cultured in Vietnam. Vet. Parasitol. 2011;181:91–96. PubMed
Gjerde B. Phylogenetic relationships among Sarcocystis species in cervids, cattle and sheep inferred from the mitochondrial cytochrome c oxidase subunit I gene. Int. J. Parasitol. 2013;43:579–591. PubMed
Gjerde B. Molecular characterisation of Sarcocystis bovifelis, Sarcocystis bovini n. sp., Sarcocystis hirsuta and Sarcocystis cruzi from cattle (Bos taurus) and Sarcocystis sinensis from water buffaloes (Bubalus bubalis) Parasitol. Res. 2016;115:1473–1492. PubMed
Gou H., Guan G., Liu A., Ma M., Xu Z., Liu Z., Ren Q., Li Y., Yang J., Chen Z., Yin H., Luo J. A DNA barcode for Piroplasmea. Acta Trop. 2012;124:92–97. PubMed
Graczyk T.K., Majewska A.C., Schwab K.J. The role of birds in dissemination of human waterborne enteropathogens. Trends Parasitol. 2008;24:55–59. PubMed
Guan Y., Feng M., Cai J., Min X., Zhou X., Xu Q., Tan N., Cheng X., Tachibana H. Comparative analysis of genotypic diversity in Entamoeba nuttalli isolates from Tibetan macaques and rhesus macaques in China. Infect. Genet. Evol. 2016;38:126–131. PubMed
Hamnes I.S., Gjerde B.K., Forberg T., Robertson L.J. Occurrence of Giardia and Cryptosporidium in Norwegian red foxes (Vulpes vulpes) Vet. Parasitol. 2007;143:347–353. PubMed
Hampton J., Spencer P.B.S., Elliot A.D., Thompson R.C.A. Prevalence of zoonotic pathogens from feral pigs in major public drinking water catchments in Western Australia. EcoHealth. 2006;3:103–108.
Han J., Zhu Y., Chen X., Liao B., Yao H., Song J., Chen S., Meng F. The short ITS2 sequence serves as an efficient taxonomic sequence tag in comparison with the full-length ITS. BioMed Res. Int. 2013;2013:741476. PubMed PMC
Haro M., Del Aguila C., Fenoy S., Henriques-Gil N. Intraspecies genotype variability of the microsporidian parasite Encephalitozoon hellem. J. Clin. Microbiol. 2003;41:4166–4171. PubMed PMC
Haro M., Izquierdo F., Henriques-Gil N., Andrés I., Alonso F., Fenoy S., del Aguila C. First detection and genotyping of human-associated microsporidia in pigeons from urban parks. Appl. Environ. Microbiol. 2005;71:3153–3157. PubMed PMC
Hegner H. Specificity in the genus Balantidium based on size and shape of body and macronucleus, with descriptions of six new species. Am. J. Epidemiol. 1934;19:38–67.
Hinney B., Sak B., Joachim A., Kváč M. More than a rabbit's tale - Encephalitozoon spp. in wild mammals and birds. Int. J. Parasitol. Parasites. Wildl. 2016;5:76–87. PubMed PMC
Homan W.L., Vercammen M., De Braekeleer J., Verschueren H. Identification of a 200- to 300-fold repetitive 529 bp DNA fragment in Toxoplasma gondii, and its use for diagnostic and quantitative PCR. Int. J. Parasitol. 2000;30:69–75. PubMed
Howe D.K., Sibley L.D. Toxoplasma gondii comprises three clonal lineages: correlation of parasite genotype with human disease. J. Infect. Dis. 1995;172:1561–1566. PubMed
Huang J., Zhang Z., Yang Y., Wang R., Zhao J., Jian F., Ning C., Zhang L. New genotypes of Enterocytozoon bieneusi isolated from sika deer and red deer in China. Front. Microbiol. 2017;8:879. PubMed PMC
Italiano C.M., Wong K.T., AbuBakar S., Lau Y.L., Ramli N., Syed Omar S.F., Kahar Bador M., Tan C.T. Sarcocystis nesbitti causes acute, relapsing febrile myositis with a high attack rate: description of a large outbreak of muscular sarcocystosis in Pangkor Island, Malaysia, 2012. PLoS Negl. Trop. Dis. 2014;8 e2876. PubMed PMC
Jackson T.F., Sargeaunt P.G., Visser P.S., Gathiram V., Suparsad S., Anderson C.B. Entamoeba histolytica: naturally occurring infections in baboons. Arch. Invest. Med. 1990;21:153–156. PubMed
Jäkel T., Scharpfenecker M., Jitrawang P., Rückle J., Kliemt D., Mackenstedt U., Hongnark S., Khoprasert Y. Reduction of transmission stages concomitant with increased host immune responses to hypervirulent Sarcocystis singaporensis, and natural selection for intermediate virulence. Int. J. Parasitol. 2001;31:1639–1647. PubMed
Jiang T., Shwab E.K., Martin R.M., Gerhold R.W., Rosenthal B.M., Dubey J.P., Su C. A partition of Toxoplasma gondii genotypes across spatial gradients and among host species, and decreased parasite diversity towards areas of human settlement in North America. Int. J. Parasitol. 2018;48:611–619. PubMed
Jones K.E., Patel N.G., Levy M.A., Storeygard A., Balk D., Gittleman J.L., Daszak P. Global trends in emerging infectious diseases. Nature. 2008;451:990–993. PubMed PMC
Kan S.P., Pathmanathan R. Review of sarcocystosis in Malaysia. Southeast Asian J. Trop. Med. Publ. Health. 1991;22(Suppl. l):129–134. PubMed
Kašičková D., Sak B., Kváč M., Ditrich O. Sources of potentially infectious human microsporidia: molecular characterisation of microsporidia isolates from exotic birds in the Czech Republic, prevalence study and importance of birds in epidemiology of the human microsporidial infections. Vet. Parasitol. 2009;165:125–230. PubMed
Katsumata M., Yoshikawa H., Tokoro M., Mizuno T., Nagamoto T., Hendarto J., Asih P.B.S., Rozi I.E., Kimata I., Takami K., Syafruddin D. Molecular phylogeny of Blastocystis isolates from wild rodents captured in Indonesia and Japan. Parasitol. Res. 2018;117:2841–2846. PubMed
Khan A., Dubey J.P., Su C., Ajioka J.W., Rosenthal B.M., Sibley L.D. Genetic analyses of atypical Toxoplasma gondii strains reveal a fourth clonal lineage in North America. Int. J. Parasitol. 2011;41:645–655. PubMed PMC
Kikuchi Y., Chomel B.B., Kasten R.W., Martenson J.S., Swift P.K., O'Brien S.J. Seroprevalence of Toxoplasma gondii in American free-ranging or captive pumas (Felis concolor) and bobcats (Lynx rufus) Vet. Parasitol. 2004;120:1–9. PubMed
Koinari M., Karl S., Ng-Hublin J., Lymbery A.J., Ryan U.M. Identification of novel and zoonotic Cryptosporidium species in fish from Papua New Guinea. Vet. Parasitol. 2013;198:1–9. PubMed
Kváč M., Květoňová D., Sak B., Ditrich O. Cryptosporidium pig genotype II in immunocompetent man. Emerg. Infect. Dis. 2009;15:982–983. PubMed PMC
Kváč M., Tomanová V., Samková E., Koubová J., Kotková M., Hlásková L., McEvoy J., Sak B. Encephalitozoon cuniculi in raw cow's milk remains infectious after pasteurization. Foodb. Pathog. Dis. 2016;13:77–79. PubMed
Lau Y.L., Chang P.Y., Subramaniam V., Ng Y.H., Mahmud R., Ahmad A.F., Fong M.Y. Genetic assemblage of Sarcocystis spp. in Malaysian snakes. Parasit. Vectors. 2013;6:257. PubMed PMC
Lau Y.L., Chang P.Y., Tan C.T., Fong M.Y., Mahmud R., Wong K.T. Sarcocystis nesbitti infection in human skeletal muscle: possible transmission from snakes. Am. J. Trop. Med. Hyg. 2014;90:361–364. PubMed PMC
Levecke B., Dorny P., Vercammen F., Visser L.G., Van Esbroeck M., Vercruysse J., Verweij J.J. Transmission of Entamoeba nuttalli and Trichuris trichiura from nonhuman primates to humans. Emerg. Infect. Dis. 2015;21:1871–1872. PubMed PMC
Levine N.D. The ciliates. In: Levine N.D., editor. Protozoan Parasites of Domestic Animals and of Man. Burgess Publishing Company; Minneapolis: 1961. pp. 347–376.
Levine N.D. Ciliophora. In: Levine N.D., editor. Veterinary Protozoology. Iowa State University Press; Ames: 1985. pp. 334–364.
Li W., Deng L., Yu X., Zhong Z., Wang Q., Liu X., Niu L., Xie N., Deng J., Lei S., Wang L., Gong C., Zhou Z., Hu Y., Fu H., Xu H., Geng Y., Peng G. Multilocus genotypes and broad host-range of Enterocytozoon bieneusi in captive wildlife at zoological gardens in China. Parasit. Vectors. 2016;9:395. PubMed PMC
Liguory O., Fournier S., Sarfati C., Derouin F., Molina J.M. Genetic homology among thirteen Encephalitozoon intestinalis isolates obtained from human immunodeficiency virus-infected patients with intestinal microsporidiosis. J. Clin. Microbiol. 2000;38:2389–2391. PubMed PMC
Liu W., Nie C., Zhang L., Wang R., Liu A., Zhao W., Li H. First detection and genotyping of Enterocytozoon bieneusi in reindeers (Rangifer tarandus): a zoonotic potential of ITS genotypes. Parasit. Vectors. 2015;8:526. PubMed PMC
Lorenzi H., Khan A., Behnke M.S., Namasivayam S., Swapna L.S., Hadjithomas M., Karamycheva S., Pinney D., Brunk B.P., Ajioka J.W., Ajzenberg D., Boothroyd J.C., Boyle J.P., Dardé M.L., Diaz-Miranda M.A., Dubey J.P., Fritz H.M., Gennari S.M., Gregory B.D., Kim K., Saeij J.P., Su C., White M.W., Zhu X.Q., Howe D.K., Rosenthal B.M., Grigg M.E., Parkinson J., Liu L., Kissinger J.C., Roos D.S., Sibley L.D. Local admixture of amplified and diversified secreted pathogenesis determinants shapes mosaic Toxoplasma gondii genomes. Nat. Commun. 2016;7:e10147. PubMed PMC
Malmsten P.H. Infusorien als intestinal-thiere beim menschen. Arch. Pathol. Anat. Physiol. Klin. Med. 1857;12:902–909.
Mandour A.M. Sarcocystis nesbitti n. sp. from the rhesus monkey. J. Protozool. 1969;16:353–354. PubMed
Mateo M., de Mingo M.H., de Lucio A., Morales L., Balseiro A., Espí A., Barral M., Lima Barbero J.F., Habela M., Fernández-García J.L., Bernal R.C., Köster P.C., Cardona G.A., Carmena D. Occurrence and molecular genotyping of Giardia duodenalis and Cryptosporidium spp. in wild mesocarnivores in Spain. Vet. Parasitol. 2017;235:86–93. PubMed
Mathis A., Tanner I., Weber R., Deplazes P. Genetic and phenotypic intraspecific variation in the microsporidian Encephalitozoon hellem. Int. J. Parasitol. 1999;29:767–770. PubMed
Matos O., Lobo M.L., Xiao L. Epidemiology of Enterocytozoon bieneusi infection in humans. J. Parasitol. Res. 2012;2012:981424. PubMed PMC
McCarthy S., Ng J., Gordon C., Miller R., Wyber A., Ryan U.M. Prevalence of Cryptosporidium and Giardia species in animals in irrigation catchments in the southwest of Australia. Exp. Parasitol. 2007;118:596–599. PubMed
McDonald J.D. vol 20. University of California Publications in Zoology; 1922. pp. 243–300. (On Balantidium coli (Malmsten) and Balantidium suis (sp. nov.) with an Account of Their Neuromotor Apparatus).
Morine M., Yang R., Ng J., Kueh S., Lymbery A.J., Ryan U.M. Additional novel Cryptosporidium genotypes in ornamental fishes. Vet. Parasitol. 2012;190:578–582. PubMed
Mucker E.M., Dubey J.P., Lovallo M.J., Humphreys J.G. Seroprevalence of antibodies to Toxoplasma gondii in the Pennsylvania bobcat (Lynx rufus rufus) J. Wildl. Dis. 2006;42:188–191. PubMed
Mundim M.J.S., Mundim A.V., Santos A.L.Q., Cabral D.D., Faria E.S.M., Moraes F.M. Helmintos e protozoários em fezes de javalis (Sus scrofa scrofa) criados em cautiverio. Arq. Bras. Med. Vet. Zootec. 2004;56:792–795.
Murphy B.G., Bradway D., Walsh T., Sanders G.E., Snekvik K. Gastric cryptosporidiosis in freshwater angelfish (Pterophyllum scalare) J. Vet. Diagn. Invest. 2009;21:722–727. PubMed
Navarro-González N., Fernández-Llario P., Pérez-Martín J.E., Mentaberre G., López-Martín J.M., Lavín S., Serrano E. Supplemental feeding drives endoparasite infection in wild boar in Western Spain. Vet. Parasitol. 2013;196:114–123. PubMed
Neiva A., Marques Da Cunha A., Travassos L. Contribuçôes parazitolojicas I. Mem. Inst. Oswaldo Cruz. 1914;6:180–191.
Ng J., Yang R., Whiffin V., Cox P., Ryan U. Identification of zoonotic Cryptosporidium and Giardia genotypes infecting animals in Sydney's water catchments. Exp. Parasitol. 2011;128:138–144. PubMed
Nieves-Ramirez M.E., Partida-Rodriguez O., Laforest-Lapointe I., Reynolds L.A., Brown E.M., Valdez-Salazar A., Moran-Silva P., Rojas-Velazquez L., Morien E., Parfrey L.W., Jin M., Walter J., Torres J., Arrieta M.C., Ximenez-Garcia C., Finlay B.B. Asymptomatic intestinal colonization with protist Blastocystis is strongly associated with distinct microbiome ecological patterns. mSystems. 2018;3 PubMed PMC
Onac D., Oltean M., Mircean V., Jarca A., Cozma V. Occurrence of Giardia duodenalis zoonotic assemblages in red foxes from Romania. Sci. Parasitol. 2015;16:177–180.
Palenzuela O., Alvarez-Pellitero P., Sitjà-Bobadilla A. Molecular characterization of Cryptosporidium molnari reveals a distinct piscine clade. Appl. Environ. Microbiol. 2010;76:7646–7649. PubMed PMC
Palermo C. Murdoch University; 2016. Cryptosporidium in Fish: Morphological and Molecular Characterisation.http://researchrepository.murdoch.edu.au/id/eprint/35248/ Honours thesis.
Paparini A., Yang R.C., Chen L.D., Tong K.S., Gibson-Kueh S., Lymbery A., Ryan U.M. Cryptosporidium in fish: alternative sequencing approaches and analyses at multiple loci to resolve mixed infections. Parasitology. 2017;144:1811–1820. PubMed
Petrova M.S., Belova L.M., Gavrilova N.A., Loginova O.A., Shiryaeva V.A. Medications for treatment of pigs with mono- and mixed parasitic infections. Bulg. J. Vet. Med. 2017;20:359–361.
Pirestani M., Sadraei J., Forouzandeh M. Molecular characterization and genotyping of human related microsporidia in free-ranging and captive pigeons of Tehran. Iran. Infect. Genet. Evol. 2013;20:495–499. PubMed
Pomajbíková K., Oborník M., Horák A., Petrzelková K.J., Grim J.N., Levecke B., Todd A., Mulama M., Kiyang J., Modrý D. Novel insights into the genetic diversity of Balantidium and Balantidium-like cyst-forming ciliates. PLoS Negl. Trop. Dis. 2013;7:e2140. PubMed PMC
Pomares C., Devillard S., Holmes T.H., Olariu T.R., Press C.J., Ramirez R., Talucod J., Estran R., Su C., Dubey J.P., Ajzenberg D., Montoya J.G. Genetic characterization of Toxoplasma gondii DNA samples isolated from humans living in North America: an unexpected high prevalence of atypical genotypes. J. Infect. Dis. 2018;218:1783–1791. PubMed
Ponce-Gordo F., Jiménez-Ruiz E., Martínez-Díaz R.A. Tentative identification of Balantidium from ostriches (Struthio camelus) as Balantidium coli-like by analysis of polymorphic DNA. Vet. Parasitol. 2008;157:41–49. PubMed
Ponce-Gordo F., Fonseca-Salamanca F., Martínez-Díaz R.A. Genetic heterogeneity in internal transcribed spacer genes of Balantidium coli (Litostomatea, Ciliophora) Protist. 2011;162:774–794. PubMed
Ponce-Gordo F., Jirků-Pomajbíková K. Balantidium coli. In: Rose J.B., Jiménez-Cisneros B., editors. Global Water Pathogens Project. Michigan State University; E. Lansing, MI: 2018. p. 7. In Fayer, R. and Jakubowski, W. (Eds) Part 3. Protists. UNESCO.
Poulsen C.S., Stensvold C.R. Current status of epidemiology and diagnosis of human sarcocystosis. J. Clin. Microbiol. 2014;52:3524–3530. PubMed PMC
Reid A., Lymbery A., Ng J., Tweedle S., Ryan U. Identification of novel and zoonotic Cryptosporidium species in marine fish. Vet. Parasitol. 2010;168:190–195. PubMed
Riemann H.P., Howarth J.A., Ruppanner R., Franti C.E., Behymer D.E. Toxoplasma antibodies among bobcats and other carnivores of Northern California. J. Wildl. Dis. 1975;11:272–276. PubMed
Rinder H., Katzwinkel-Wladarsch S., Thomschke A., Loscher T. Strain differentiation in microsporidia. Tokai J. Exp. Clin. Med. 1999;23:433–437. PubMed
Rivera W.L., Yason J.A., Adao D.E. Entamoeba histolytica and E. dispar infections in captive macaques (Macaca fascicularis) in the Philippines. Primates. 2010;51:69–74. PubMed
Roberts N.M., Crimmins S.M. Bobcat population status and management in North America: evidence of large-scale population increase. J. Fish Wildlife Manag. 2010;1:169–174.
Roberts T., Barratt J., Harkness J., Ellis J., Stark D. Comparison of microscopy, culture, and conventional polymerase chain reaction for detection of Blastocystis sp. in clinical stool samples. Am. J. Trop. Med. Hyg. 2011;84:308–312. PubMed PMC
Ryan U., Paparini A., Tong K.S., Yang R.C., Gibson-Kueh S., O'Hara A., Lymbery A., Xiao L.H. Cryptosporidium huwi n. sp (Apicomplexa: Eimeriidae) from the guppy (Poecilia reticulata) Exp. Parasitol. 2015;150:31–35. PubMed
Sak B., Kašičková D., Kváč M., Květoňová D., Ditrich O. Microsporidia in exotic birds: intermittent spore excretion of Encephalitozoon spp. in naturally infected budgerigars (Melopsittacus undulatus) Vet. Parasitol. 2010;168:196–200. PubMed
Sak B., Kotková M., Hlásková L., Kváč M. Limited effect of adaptive immune response to control encephalitozoonosis. Parasite. Immunol. 2017;39 PubMed
Sak B., Kváč M., Kučerová Z., Květoňová D., Saková K. Latent microsporidial infection in immunocompetent individuals - a longitudinal study. PLoS Negl. Trop. Dis. 2011;5:e1162. PubMed PMC
Sak B., Kváč M., Květoňová D., Albrecht T., Piálek J. The first report on natural Enterocytozoon bieneusi and Encephalitozoon spp. infections in wild east-European house mice (Mus musculus musculus) and west-European house mice (M. m. domesticus) in a hybrid zone across the Czech Republic-Germany border. Vet. Parasitol. 2011;178:246–250. PubMed
Santín M., Fayer R. Enterocytozoon bieneusi genotype nomenclature based on the internal transcribed spacer sequence: a consensus. J. Eukaryot. Microbiol. 2009;56:34–38. PubMed
Santín M., Fayer R. Enterocytozoon bieneusi, Giardia, and Cryptosporidium infecting white-tailed deer. J. Eukaryot. Microbiol. 2015;62:34–43. PubMed
Sargeaunt P.G. The reliability of Entamoeba histolytica zymodemes in clinical diagnosis. Parasitol. Today. 1987;3:40–43. PubMed
Scamardella J.M. Not plants or animals: a brief history of the origin of Kingdoms Protozoa, Protista and Protoctista. Int. Microbiol. 1999;2:207–216. PubMed
Schuster F.L., Ramirez-Avila L. Current world status of Balantidium coli. Clin. Microbiol. Rev. 2008;28:626–638. PubMed PMC
Seifollahi Z., Sarkari B., Motazedian M.H., Asgari Q., Ranjbar M.J., Abdolahi Khabisi S. Protozoan parasites of rodents and their zoonotic significance in Boyer-Ahmad District, Southwestern Iran. Vet. Med. Int. 2016;2016:3263868. PubMed PMC
Selman M., Sak B., Kváč M., Farinelli L., Weiss L.M., Corradi N. Extremely reduced levels of heterozygosity in the vertebrate pathogen Encephalitozoon cuniculi. Eukaryot. Cell. 2013;12:496–502. PubMed PMC
Shahari S., Tengku-Idris T.I., Fong M.Y., Lau Y.L. Molecular evidence of Sarcocystis nesbitti in water samples of Tioman Island, Malaysia. Parasit. Vectors. 2016;9:598. PubMed PMC
Shwab E.K., Jiang T., Pena H.F.J., Gennari S.M., Dubey J.P., Su C. The ROP18 and ROP5 gene allele types are highly predictive of virulence in mice across globally distributed strains of Toxoplasma gondii. Int. J. Parasitol. 2016;46:141–146. PubMed
Shwab E.K., Zhu X.Q., Majumdar D., Pena H.F.J., Gennari S.M., Dubey J.P., Su C. Geographical patterns of Toxoplasma gondii genetic diversity revealed by multilocus PCR-RFLP genotyping. Parasitology. 2014;141:453–461. PubMed
Šlapeta J.R., Modrý D., Votýpka J., Jirků M., Lukeš J., Koudela B. Evolutionary relationships among cyst-forming coccidia Sarcocystis spp. (Alveolata: Apicomplexa: Coccidea) in endemic African tree vipers and perspective for evolution of heteroxenous life cycle. Mol. Phylogenet. Evol. 2003;27:464–475. PubMed
Smith J.M., Meerovitch E. Primates as a source of Entamoeba histolytica, their zymodeme status and zoonotic potential. J. Parasitol. 1985;71:751–756. PubMed
Sobottka I., Albrecht H., Visvesvara G.S., Pieniazek N.J., Deplazes P., Schwartz D.A., Laufs R., Elsner H.A. Inter- and intra-species karyotype variations among microsporidia of the genus Encephalitozoon as determined by pulsed field gel electrophoresis. Scand. J. Infect. Dis. 1999;31:555–558. PubMed
Solaymani-Mohammadi S., Rezaian M., Hooshyar H., Mowlavi G.R., Babaei Z., Anwar M.A. Intestinal protozoa in wild boars (Sus scrofa) in Western Iran. J. Wildl. Dis. 2004;40:801–803. PubMed
Sommer M.F., Beck R., Ionita M., Stefanovska J., Vasic A., Zdravkovic N., Hamel D., Rehbein S., Knaus M., Mitrea I.L., Shukullari E., Kirkova Z., Rapti D., Capari B., Silaghi C. Multilocus sequence typing of canine Giardia duodenalis from South Eastern European countries. Parasitol. Res. 2015;114:2165–2174. PubMed
Song Y., Li W., Liu H., Zhong Z., Luo Y., Wei Y., Fu W., Ren Z., Zhou Z., Deng L., Cheng J., Peng G. First report of Giardia duodenalis and Enterocytozoon bieneusi in forest musk deer (Moschus berezovskii) in China. Parasit. Vectors. 2018;11:204. PubMed PMC
Sprong H., Cacciò S.M., van der Giessen J.W., ZOOPNET Network, Partners Identification of zoonotic genotypes of Giardia duodenalis. Plos Negl. Trop. Dis. 2009;3:e558. PubMed PMC
Stein F. 1863. Über das Paramaecium (?) coli, Malmst. Amtlicher Bericht über die Sieben und Dreissigste Versammlung Deutscher Naturforscher und Aerzte in Karlsbad in September 1862; p. 165.
Stensvold C.R., Clark C.G. Current status of Blastocystis: a personal view. Parasitol. Int. 2016;65:763–771. PubMed
Stensvold C.R., Clark C.G. Molecular identification and subtype analysis of Blastocystis. Curr. Protoc. Microbiol. 2016;43 20A.2.1-20A.2.10. PubMed
Stojecki K., Sroka J., Cacciò S.M., Cencek T., Dutkiewicz J., Kusyk P. Prevalence and molecular typing of Giardia duodenalis in wildlife from eastern Poland. Folia Parasitol. (Praha) 2015;62 PubMed
Strüder-Kypke M.C., Wright A.-D.G., Foissner W., Chatzinotas A., Lynn D.H. Molecular phylogeny of litostome ciliates (Ciliophora, Litostomatea) with emphasis on free-living haptorian genera. Protist. 2006;157:261–278. PubMed
Su C., Asis A.K., Peng Z., Majumdar D., Ajzenberg D., Darde M.L., Zhu X.Q., Ajioka J.W., Rosenthal B.M., Dubey J.P., Sibley L.D. Globally diverse Toxoplasma gondii isolates comprise six major clades originating from a small number of distinct ancestral lineages. Proc. Natl. Acad. Sci. U.S.A. 2012;109:5844–5849. PubMed PMC
Su C., Shwab E.K., Zhou P., Zhu X.Q., Dubey J.P. Moving towards an integrated approach to molecular detection and identification of Toxoplasma gondii. Parasitology. 2010;137:1–11. PubMed
Supriadi, Fitria W.A., Nurcahyo R.W. Balantidium sp. infection in faeces samples of orangutan (Pongo pygmaeus) from Care center and Tanjung putting national park area, central Borneo. BIOMEDICH. 2012;1:47–52.
Suzuki J., Kobayashi S., Murata R., Yanagawa Y., Takeuchi T. Profiles of a pathogenic Entamoeba histolytica-like variant with variations in the nucleotide sequence of the small subunit ribosomal RNA isolated from a primate (De Brazza's guenon) J. Zoo Wildl. Med. 2007;38:471–474. PubMed
Tachibana H., Yanagi T., Pandey K., Cheng X.J., Kobayashi S., Sherchand J.B., Kanbara H. An Entamoeba sp. strain isolated from rhesus monkey is virulent but genetically different from Entamoeba histolytica. Mol. Biochem. Parasitol. 2007;153:107–114. PubMed
Takano J., Narita T., Tachibana H., Terao K., Fujimoto K. Comparison of Entamoeba histolytica DNA isolated from a cynomolgus monkey with human isolates. Parasitol. Res. 2007;101:539–546. PubMed
Tappe D., Abdullah S., Heo C.C., Kannan Kutty M., Latif B. Human and animal invasive muscular sarcocystosis in Malaysia - recent cases, review and hypotheses. Trop. Biomed. 2013;30:355–366. PubMed
Tappe D., Stich A., Langeheinecke A., von Sonnenburg F., Muntau B., Schafer J., Slesak G. Suspected new wave of muscular sarcocystosis in travellers returning from Tioman Island, Malaysia, May 2014. Euro Surveill. 2014;19:20816. PubMed
Tavalla M., Mardani-Kateki M., Abdizadeh R., Soltani S., Saki J. Molecular diagnosis of potentially human pathogenic Enterocytozoon bieneusi and Encephalitozoon species in exotic birds in Southwestern Iran. J. Infect. Public. Health. 2018;11:192–196. PubMed
Thompson R.C.A., Ash A. Molecular epidemiology of Giardia and Cryptosporidium infections. Infect. Genet. Evol. 2016;40:315–323. PubMed
Thompson R.C., Polley L. Parasitology and one health. Int. J. Parasitol. Parasites Wildl. 2014;3:A1–A2. PubMed PMC
Tian M., Chen Y., Wu L., Rosenthal B.M., Liu X., He Y., Dunams D.B., Cui L., Yang Z. Phylogenetic analysis of Sarcocystis nesbitti (Coccidia: Sarcocystidae) suggests a snake as its probable definitive host. Vet. Parasitol. 2012;183:373–376. PubMed
Tito R.Y., Chaffron S., Caenepeel C., Lima-Mendez G., Wang J., Vieira-Silva S., Falony G., Hildebrand F., Darzi Y., Rymenans L., Verspecht C., Bork P., Vermeire S., Joossens M., Raes J. Gut In press; 2018. Population-level Analysis of Blastocystis Subtype Prevalence and Variation in the Human Gut Microbiota. PubMed PMC
VanWormer E., Miller M.A., Conrad P.A., Grigg M.E., Rejmanek D., Carpenter T.E., Mazet J.A.K. Using molecular epidemiology to track Toxoplasma gondii from terrestrial carnivores to marine hosts: implications for public health and conservation. PLoS Negl. Trop. Dis. 2014;8:e2852. PubMed PMC
Verma S.K., Sweeny A.R., Lovallo M.J., Calero-Bernal R., Kwok O.C.H., Jiang T., Su C., Grigg M.E., Dubey J.P. Seroprevalence, isolation and co-infection of multiple Toxoplasma gondii strains in individual bobcats (Lynx rufus) from Mississippi, USA. Int. J. Parasitol. 2017;47:297–303. PubMed
Verweij J.J., Vermeer J., Brienen E.A., Blotkamp C., Laeijendecker D., van Lieshout L., Polderman A.M. Entamoeba histolytica infections in captive primates. Parasitol. Res. 2003;90:100–103. PubMed
Vlčková K., Kreisinger J., Pafčo B., Čížková D., Tagg N., Hehl A.B., Modrý D. Diversity of Entamoeba spp. in African great apes and humans: an insight from Illumina MiSeq high-throughput sequencing. Int. J. Parasitol. 2018;48:519–530. PubMed
Von Sonnenburg F., Cramer J.P., Freedman D.O., Plier D.A., Esposito D.H., Sotir M.J., Lankau E.W. Acute muscular sarcocystosis among returning travelers – Tioman Island, Malaysia, 2011. MMWR Morb. Mortal. Wkly. Rep. 2012;61:2. PubMed
Wagnerová P., Sak B., Květoňová D., Maršálek M., Langrová I., Kváč M. Humoral immune response and spreading of Encephalitozoon cuniculi infection in experimentally infected ponies. Vet. Parasitol. 2013;197:1–6. PubMed
Wang S.S., Wang R.J., Fan X.C., Liu T.L., Zhang L.X., Zhao G.H. Prevalence and genotypes of Enterocytozoon bieneusi in China. Acta Trop. 2018;183:142–152. PubMed
Wassermann M., Raisch L., Lyons J.A., Natusch D.J.D., Richter S., Wirth M., Preeprem P., Khoprasert Y., Ginting S., Mackenstedt U., Jakel T. Examination of Sarcocystis spp. of giant snakes from Australia and Southeast Asia confirms presence of a known pathogen - Sarcocystis nesbitti. PLoS One. 2017;12 PubMed PMC
Wawrzyniak I., Poirier P., Viscogliosi E., Dionigia M., Texier C., Delbac F., Alaoui H.E. Blastocystis, an unrecognized parasite: an overview of pathogenesis and diagnosis. Ther. Adv. Infect. Dis. 2013;1:167–178. PubMed PMC
Wong K.T., Pathmanathan R. High prevalence of human skeletal-muscle sarcocystosis in South-East Asia. Trans. R. Soc. Trop. Med. Hyg. 1992;86:631–632. PubMed
Xiao L. Molecular epidemiology of cryptosporidiosis: an update. Exp. Parasitol. 2010;124:80–89. PubMed
Xiao L., Li L., Moura H., Sulaiman I., Lal A.A., Gatti S., Scaglia M., Didier E.S., Visvesvara G.S. Genotyping Encephalitozoon hellem isolates by analysis of the polar tube protein gene. J. Clin. Microbiol. 2001;39:2191–2196. PubMed PMC
Xiao L., Li L., Visvesvara G.S., Moura H., Didier E.S., Lal A.A. Genotyping Encephalitozoon cuniculi by multilocus analyses of genes with repetitive sequences. J. Clin. Microbiol. 2001;39:2248–2253. PubMed PMC
Yaghoobi K., Sarkari B., Mansouri M., Motazedian M.H. Zoonotic intestinal protozoan of the wild boars, Sus scrofa, in Persian Gulf's coastal area (Bushehr province), Southwestern Iran. Vet. World. 2016;9:1047–1050. PubMed PMC
Yang R.C., Dorrestein G.M., Ryan U. Molecular characterisation of a disseminated Cryptosporidium infection in a Koi carp (Cyprinus carpio) Vet. Parasitol. 2016;226:53–56. PubMed
Yang R.C., Palermo C., Chen L.D., Edwards A., Paparini A., Tong K.S., Gibson-Kueh S., Lymbery A., Ryan U. Genetic diversity of Cryptosporidium in fish at the 18S and actin loci and high levels of mixed infections. Vet. Parasitol. 2015;214:255–263. PubMed
Yang Z.Q., Wei C.G., Zen J.S., Song J.L., Zuo Y.X., He Y.S., Zhang H.F., Attwood S.W., Chen X.W., Yang G.C., Zhou X., Quan X., Li C.Y., Han D., Liu A.W., Lin P. A taxonomic re-appraisal of Sarcocystis nesbitti (Protozoa: Sarcocystidae) from the monkey Macaca fascicularis in Yunnan, PR China. Parasitol. Int. 2005;54:75–81. PubMed
Yao H., Song J., Liu C., Luo K., Han H., Li Y., Pang X., Xu H., Zhu Y., Xiao P., Chen S. Use of ITS2 region as the universal DNA barcode for plants and animals. PLoS One. 2010;5:e13102. PubMed PMC
Ye J., Xiao L., Ma J., Guo M., Liu L., Feng Y. Anthroponotic enteric parasites in monkeys in public park, China. Emerg. Infect. Dis. 2012;18:1640–1643. PubMed PMC
Yoshikawa H., Koyama Y., Tsuchiya E., Takami K. Blastocystis phylogeny among various isolates from humans to insects. Parasitol. Int. 2016;65:750–759. PubMed
Yoshikawa H., Tokoro M., Nagamoto T., Arayama S., Asih P.B., Rozi I.E., Syafruddin D. Molecular survey of Blastocystis sp. from humans and associated animals in an Indonesian community with poor hygiene. Parasitol. Int. 2016;65:780–784. PubMed
Zanguee N., Lymbery J.A., Lau J., Suzuki A., Yang R., Ng J., Ryan U. Identification of novel Cryptosporidium species in aquarium fish. Vet. Parasitol. 2010;174:43–48. PubMed
Zhang X.X., Cong W., Liu G.H., Ni X.T., Ma J.G., Zheng W.B., Zhao Q., Zhu X.Q. Prevalence and genotypes of Enterocytozoon bieneusi in sika deer in Jilin province, Northeastern China. Acta Parasitol. 2016;61:382–388. PubMed
Zhang Y., Koehler A.V., Wang T., Haydon S.R., Gasser R.B. First detection and genetic characterisation of Enterocytozoon bieneusi in wild deer in Melbourne's water catchments in Australia. Parasit. Vectors. 2018;11:2. PubMed PMC
Zhang Z., Huang J., Karim M.R., Zhao J., Dong H., Ai W., Li F., Zhang L., Wang R. Zoonotic Enterocytozoon bieneusi genotypes in pere david's deer (Elaphurus davidianus) in Henan, China. Exp. Parasitol. 2015;155:46–48. PubMed
Zhao W., Wang J., Yang Z., Liu A. Dominance of the Enterocytozoon bieneusi genotype BEB6 in red deer (Cervus elaphus) and Siberian roe deer (Capreolus pygargus) in China and a brief literature review. Parasite. 2017;24:54. PubMed PMC
Zhao W., Zhang W., Wang R., Liu W., Liu A., Yang D., Yang F., Karim M.R., Zhang L. Enterocytozoon bieneusi in sika deer (Cervus nippon) and red deer (Cervus elaphus): deer specificity and zoonotic potential of ITS genotypes. Parasitol. Res. 2014;113:4243–4250. PubMed
Waterborne protozoan and microsporidian parasites in Eurasian beavers (Castor fiber)