Home Isolation and identification of Acanthamoeba spp. from thermal swimming pools and spas in Southern Brazil
Article
Licensed
Unlicensed Requires Authentication

Isolation and identification of Acanthamoeba spp. from thermal swimming pools and spas in Southern Brazil

  • Laura Fuhrich Fabres , Sayonara Peixoto Rosa dos Santos , Lisianne Brittes Benitez and Marilise Brittes Rott EMAIL logo
Published/Copyright: March 30, 2016
Become an author with De Gruyter Brill

Abstract

Free-living amoebae (FLA) are widely distributed in soil and water. A few number of them are implicated in human disease: Acanthamoeba spp., Naegleria fowleri, Balamuthia mandrillaris and Sappinia diploidea. Species of Acanthamoeba can cause keratitis and brain infections. In this study, 72 water samples were taken from both hot tubs and thermal swimming pools in the city of Porto Alegre, RS, Brazil, to determine the presence of Acanthamoeba in the water as well as perform the phenotypic and genotypic characterization of the isolates. The identification of the isolates was based on the cysts morphology and PCR amplification using genus-specific oligonucleotides. When the isolates were submitted to PCR reaction only 8 were confirmed as belonging to the genus Acanthamoeba. The sequences analysis when compared to the sequences in the GenBank, showed genotype distribution in group T3 (12,5%), T5 (12,5%), T4 (25%) and T15 (50%). The results of this study confirmed the presence of potentially pathogenic isolates of free living amoebae in hot swimming pool and spas which can present risks to human health.

Acknowledgements

The authors thank the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for financial support, the Microbiology, Immunology and Parasitology Department of the Universidade Federal do Rio Grande do Sul, Brazil

References

Alves J.M.P., Gusmão C.X., Teixeira M.M.G., Freitas D., Foronda A.S., Affonso H.T. 2000. Random amplified polymorphic DNA profiles as a tool for the characterization of Brazilian keratitis isolates of the genus Acanthamoeba. Brazilian Journal of Medical and Biological Research, 33, 19–26. DOI: http://dx.doi.org/10.1590/S0100-879X2000000100003http://dx.doi.org/10.1590/S0100-879X2000000100003Search in Google Scholar

Alves D.D., Moraes A.S., Nitz N., Oliveira M.G., Hecht M.M., Gurgel-Gonçalves R., Cuba C.A. 2012. Occurrence and characterization of Acanthamoeba similar to genotypes T4, T5, and T2/T6 isolated from environmental sources in Brasília, Federal District, Brazil. Experimental Parasitoly, 131, 239–244. DOI: 10.1016/j.exppara.2012.04.01110.1016/j.exppara.2012.04.011Search in Google Scholar PubMed

APHA 2005. Standard Methods for the Examination of Water and Wastewater. Washington, DC: APHA, WEF and AWWASearch in Google Scholar

Booton G.C., Rogerson A., Bonilla T.D., Seal D.V., Kelly D.J., Beat-tie T.K., Tomlinson A., Lares-Villa F., Fuerst P.A., Byers T.J. 2004. Molecular and physiological evaluation of subtropical environmental isolates of Acanthamoeba spp., causal agent of Acanthamoeba keratitis. Journal of Eukaryotic Microbiology, 51, 192–200. DOI: 10.1111/j.1550-7408.2004.tb00545.x10.1111/j.1550–7408.2004.tb00545.xSearch in Google Scholar

Booton G.C., Visvesvara G.S., Byers T.J., Kelly D.J., Fuerst P.A. 2005. Identification and Distribution of Acanthamoeba Species Genotypes Associated with nonkeratitis Infections. Journal of Clinical Microbiology, 43, 1689–1693. DOI: 10.1128/JCM.43.4.1689-1693.200510.1128/JCM.43.4.1689-1693.2005Search in Google Scholar PubMed PubMed Central

Booton, G.C., Joslin C.E., Shoff M., Ey T.U., Kelly D.J., Fuerst P.A. 2009. Genotypic identification of Acanthamoeba sp. isolates associated with an outbreak of Acanthamoeba keratitis. Cornea 28, 673–676. DOI: 10.1097/ICO.0b013e31819342a710.1097/ICO.0b013e31819342a7Search in Google Scholar PubMed PubMed Central

Carlesso A.M., Artuso G.L., Caumo K., Rott M.B. 2010. Potentially pathogenic Acanthamoeba isolated from a hospital in Brazil. Current Microbiology, 60, 185–190. DOI: 10.1007/s00284009-9523-710.1007/s00284-009-9523-7Search in Google Scholar PubMed

Caumo K., Frasson A.P., Pens C.J., Panatieri L.F., Frazzon A.P.G., Rott M.B. 2009. Potentially pathogenic Acanthamoeba in swimming pools: a survey in the southern Brazilian city of Porto Alegre. Annals of Tropical Medicine Parasitology, 103, 477–485. DOI: 10.1179/136485909X45182510.1179/136485909X451825Search in Google Scholar PubMed

Caumo K., Rott M.B. 2011. Acanthamoeba T3, T4 and T5 in swim-ming-pool waters from Southern Brazil. Acta Tropica, 117, 233–235. DOI: 10.1016/j.actatropica.2010.12.00810.1016/j.actatropica.2010.12.008Search in Google Scholar PubMed

Corsaro D., Venditti D. 2010. Phylogenetic evidence for a new genotype of Acanthamoeba (Amoebozoa Acanthamoebida). Parasitology Research, 7, 233–8. DOI: 10.1007/s00436-0101870-610.1007/s00436-010-1870–6Search in Google Scholar

Corsaro D., Walochnik J., Köhsler M., Rott M.B. 2015. Acanthamoeba misidentification and multiple labels: redefining genotypes T16, T19, and T20 and proposal for Acanthamoeba micheli sp. nov. (genotype T19). Parasitology Research, 114, 2481–2490. DOI: 10.1007/s00436-015-4445-810.1007/s00436-015-4445-8Search in Google Scholar PubMed

Di Cave D.D., Monno R., Bottalico P., Guerriero S., D’Amelio S., D’Orazi C., Berrilli F. 2009. Acanthamoeba T4 and T15 genotypes associated with keratitis infections in Italy. European Journal of Clinical Microbioly and Infectious Diseases, 28, 607–612. DOI: 10.1007/s10096-008-0682-410.1007/s10096-008-0682-4Search in Google Scholar PubMed

Di Cave D.D., D’alfonso R., Comlavi D., Orazi C.D., Monno R., Berrili F. 2014. Genotypic heterogeneity based on 18S-rRNA gene sequences among Acanthamoeba isolates from clinical samples in Italy. Experimental Parasitology, 145, 46–49. DOI: 10.1016/j.exppara.2014.05.00910.1016/j.exppara.2014.05.009Search in Google Scholar PubMed

Duarte J.L., Furst C., Klisiowicz D.R., Klassen G., Costa A.O. 2013. Morphological, genotypic, and physiological characterization of Acanthamoeba isolates from keratitis patients and the domestic environment in Vitoria, Espirito Santo, Brazil. Experimental Parasitology, 135, 9–14. DOI: 10.1016/j.exppara. 2013.05.01310.1016/j.exppara.2013.05.013Search in Google Scholar PubMed

Edagawa A., Kimura A., Kawabuchi-Kurata T., Kusuhara Y., Karanis P. 2009. Isolation and genotyping of potentially pathogenic Acanthamoeba and Naegleria species from tap-water sources in Osaka, Japan. Parasitology Research, 105, 1109– 1117. DOI: 10.1007/s00436-009-1528-410.1007/s00436-009-1528-4Search in Google Scholar PubMed

Flint J.A., Dobson P.J., Robinson B.S. 2003. Genetic analysis of forty isolates of Acanthamoeba group III by multilocus isoenzyme electrophoresis. Acta Protozoologica, 42, 317–324Search in Google Scholar

Gast R.J. 2001. Development of an Acanthamoeba-specific reverses dot-blot and the discovery of a new ribotype. Journal of Eukaryotic Microbiology, 48, 609–15. DOI: 10.1111/j.15507408.2001.tb00199.x10.1111/j.15507408.2001.tb00199.xSearch in Google Scholar

Gianinazzi C., Schild M., Zumkehr B., Wuthrich F., Nuesch I., Ryter R., Schurch N., Gottstein B., Muller N. 2010. Screening of Swiss hot spring resorts for potentially pathogenic free-living amoebae. Experimental Parasitology, 126, 45–53. DOI: 10.1016/j.exppara.2009.12.00810.1016/j.exppara.2009.12.008Search in Google Scholar PubMed

Greub G., Raoult D. 2004. Microorganisms resistant to free-living amoebae. Clinical Microbiology Reviews, Washington 17, 413–433. DOI: 10.1128/CMR.17.2.413-43310.1128/CMR.17.2.413-433Search in Google Scholar

Hewett M.K., Robinson B.S., Monis P.T., Saint C.P. 2003. Identification of a new Acanthamoeba 18S rRNA gene sequence type, corresponding to the species Acanthamoeba jacobsi Sawyer. Acta Protozoologica, 42, 325–9Search in Google Scholar

Horn M., Fritsche T.R., Gautom R.K., Schleifer K.H., Wagner M. 1999. Novel bacterial endosymbionts of Acanthamoeba spp. related to the Paramecium caudatum symbiont Caedibacter caryophilus. Environmental Microbiology, 1, 357–67. DOI: 10. 1046/j.1462-2920.1999.00045.x10. 1046/j.1462-2920.1999.00045.xSearch in Google Scholar

Huang S.W., Hsu B.M. 2010. Isolation and identification of Acanthamoeba from Taiwan spring recreation areas using culture enrichment combined with PCR. Acta Tropica, 115, 282–287. DOI: 10.1016/j.actatropica.2010.04.01210.1016/j.actatropica.2010.04.012Search in Google Scholar PubMed

Kao P.M., Hsu B.M., Chen N.H., Huang K.H., Huang S.W., King K.L., Chiu Y.C. 2012a. Isolation and identification of Acanthamoeba species from thermal spring environmental in southern Taiwan. Experimental Parasitology, 130, 354–358. DOI: 10.1016/j.exppara.2012.02.00810.1016/j.exppara.2012.02.008Search in Google Scholar PubMed

Kao P.M., Hsu B.M., Chen N.H., Huang K.H., Huang C.C., Ji D.D., Chen J.S., Lin W.C., Huang S.W., Chiu Y.C. 2012b. Molecular detection and comparison of Acanthamoeba genotypes in different functions of watersheds in Taiwan. Environmental Monitoring and Assessment, 184, 4335–4344. DOI: 10.1007/s10661-011-2267-410.1007/s10661-011-2267-4Search in Google Scholar PubMed

Khan N.A., Jarroll E.L., Paget T.A. 2001. Acanthamoeba can be differentiated by the polymerase chain reaction and simple plating assays. Current Microbiology, 43, 204–208. DOI: 10.1007/s00284001028810.1007/s002840010288Search in Google Scholar PubMed

Khan N.A., Tareen N.K. 2003. Genotypic, phenotypic, biochemical, physiological and pathogenicity-based categorization of Acanthamoeba strains. Folia Parasitology, 50, 97–104. DOI: 10.14411/fp.2003.01710.14411/fp.2003.017Search in Google Scholar PubMed

Khan N.A. 2006. Acanthamoeba: Biology and increasing importance in human health. FEMS Microbiological Reviews, 30, 564–595. DOI: 10.1111/j.1574-6976.2006.00023.x10.1111/j.1574-6976.2006.00023.xSearch in Google Scholar PubMed

Kiss C., Barna Z., Vargha M., Torok J.K. 2014. Incidence and molecular diversity of Acanthamoeba species isolated from public baths in Hungary. Parasitology Research, 113, 2551–2557. DOI: 10.1007/s00436-014-3905-x10.1007/s00436-014-3905-xSearch in Google Scholar PubMed

Koehsler M., Leitsch D., Ducheˆne M., Nagl M., Walochnik J. 2009. Acanthamoeba castellanii, growth on human cell layers reactivates attenuated properties after prolonged axenic culture. FEMS Microbiology Letters, 299, 121–127. DOI, 10.1111/ j.1574-6968.2009.01680.x10.1111/j.1574-6968.2009.01680.xSearch in Google Scholar PubMed PubMed Central

Ledee D.R., Hay J., Byers T.J., Seal D.V., Kirkness C.M. 1996. Acanthamoeba griffini. Molecular characterization of a new corneal pathogen. Investigative Ophthalmology & Visual Science, 37, 544–550Search in Google Scholar

Ledee D.R., Iovieno A., Miller D., Mandal N., Diaz M., Fell J., Fini M.E., Alfonso E.C. 2009. Molecular identification of T4 and T5 genotypes in isolates from Acanthamoeba keratitis patients. Journal of Clinical Microbiology, 47, 1458–1462. DOI: 10.1128/JCM.02365-0810.1128/JCM.02365-08Search in Google Scholar PubMed PubMed Central

Liang S.Y., Ji D.R., Hsia K.T., Hung C.C., Sheng W.H., Hsu B.M., Chen J.S., Wu M.H., Lai C.H., Ji D.D. 2010. Isolation and identification of Acanthamoeba species related to amoebic encephalitis and nonpathogenic free-living amoeba species from the rice field. Journal of Applied Microbiology, 109, 1422– 1429. DOI: 10.1111/j.1365-2672.2010.04779.x10.1111/j.1365-2672.2010.04779.xSearch in Google Scholar PubMed

Maghsood A.H., Sissons J., Rezaian M., Nolder D., Warhurst D., Khan N.A. 2005. Acanthamoeba genotype T4 from the UK and Iran and isolation of the T2 genotype from clinical isolates. Journal of Medical Microbiology, 54, 755–759. DOI: 10.1099/jmm.0.45970-010.1099/jmm.0.45970-0Search in Google Scholar PubMed

Magliano A.C.M., Silva F.M., Teixeira M.M.G., Alfieri S.C. 2009. Genotyping, physiological features and proteolytic activities of a potentially pathogenic Acanthamoeba sp. isolated from tap water in Brazil. Experimental Parasitology, 12, 231–235. DOI: 10.1016/j.exppara.2009.07.00610.1016/j.exppara.2009.07.006Search in Google Scholar PubMed

Magliano A.C., Teixeira M.M., Alfier, S.C. 2012. Revisiting the Acanthamoeba species that form star-shaped cysts (genotypes T7, T8, T9, and T17): characterization of seven new Brazilian environmental isolates and phylogenetic inferences. Parasitology, 139, 45–52. DOI: 10.1017/S003118201100164810.1017/S0031182011001648Search in Google Scholar PubMed

Magnet A., Henriques-Gil N., Galván-Diaz A.L., Izquiedo F., Fenoy S., Del Aguila C. 2014. Novel Acanthamoeba 18S rRNA gene sequence type from an envirionmental isolate. Parasitology Research, 113, 2845–2850. DOI: 10.1007/s00436014-3945-210.1007/s00436-014-3945-2Search in Google Scholar PubMed

Marciano-Cabral F., Cabral G. 2003 Acanthamoeba spp. as agents of disease in humans. Clinical Microbiology Reviews, 16, 273–307. DOI: 10.1128/CMR.16.2.273-307.200310.1128/CMR.16.2.273-307.2003Search in Google Scholar PubMed PubMed Central

Mathers W.D., Nelson S.E., Scott N.E., Lane J.L., Wilson M.E., Allen R.C. Folberg R. 2000. Confirmation of confocal microscopy diagnosis of Acanthamoeba keratitis using polymerase chain reaction analysis. Archives of Ophthalmology, 118, 178–183. DOI:10.1001/archopht.118.2.17810.1001/archopht.118.2.178Search in Google Scholar PubMed

Nagyová V., Nagy A., Timko J. 2010. Morphological, physiological and molecular biological characterisation of isolates from first cases of Acanthamoeba keratitis in Slovakia. Parasitology Research, 106, 861–872. DOI: 10.1007/s00436-010-1731-310.1007/s00436-010-1731-3Search in Google Scholar PubMed

Nuprasert W., Putaporntip C., Pariyakanok L., Jongwutiwes S. 2010. Identification of a novel T17 genotype of Acanthamoeba from environmental isolates and T10 genotype causing keratitis in Thailand. Journal of Clinical Microbiology, 48, 4636–40. DOI: 10.1128/JCM.01090-1010.1128/JCM.01090-10Search in Google Scholar PubMed PubMed Central

Page F.C. 1967. Re-definition of the genus Acanthamoeba with descriptions of three species. The Journal of Protozoology, 14, 709–724. DOI: 10.1111/j.1550-7408.1967.tb02066.x10.1111/j.1550–7408.1967.tb02066.xSearch in Google Scholar

Page FC 1988. A New Key to Freshwater and Soil Amoebae. Freshwater Biological Association Scientific Publications, Cumbria. DOI: 10.1002/iroh.1978063023110.1002/iroh.19780630231Search in Google Scholar

Pussard M., Pons R. 1977. Morphologie de la paroi kystique et taxonomie du genre Acanthamoeba (Protozoa, Amoebida). Protistologica, 13, 557–598Search in Google Scholar

Qvarnstrom Y., Nerad T.A., Visvesvara G.S. 2013. Characterization of a new pathogenic Acanthamoeba Species, A. byersi n. sp., isolated from a human with fatal amoebic encephalitis. Journal of Eukaryotic Microbiology, 60, 626–633. DOI: 10.1111/ jeu.1206910.1111/ jeu.12069Search in Google Scholar

Salah M., Iciar M. 1997. Universal and rapid salt-extraction of high quality genomic DNA for PCR-based techniques. Nucleic Acids Research, Oxford, 25, 4692–4693. DOI: 10.1093/nar/ 25.22.469210.1093/nar/ 25.22.4692Search in Google Scholar

Schroeder J.M., Booton G.C., Hay J., Niszl I.A., Seal D.V., Markus M.B., Fuerst P.A., Byers T.J. 2001. Use of subgenic 18S ribosomal DNA PCR and sequencing for genus and genotype identification of Acanthamoebae from humans with keratitis and from sewage sludge. Journal of Clinical Microbiology, 39, 1903–1911. DOI: 10.1128/JCM.39.5.1903-1911.200110.1128/JCM.39.5.1903-1911.2001Search in Google Scholar PubMed PubMed Central

Schuster F.L., Visvesvara G.S. 2004. Free-living amoebae as opportunistic and non-opportunistic pathogens of humans and animals. International Journal of Parasitology, 34, 1001–1027. DOI: 10.1016/j.ijpara.2004.06.00410.1016/j.ijpara.2004.06.004Search in Google Scholar PubMed

Stothard D.R., Schroeder-Diedrich J.M., Awwad M.H., Gast R.J., Ledee D.R., Rodriguez-Zaragoza S. Dean C.L., Fuerst P.A., Byers T.J. 1998. The evolutionary history of the genus Acanthamoeba and the identification of eight new 18S rRNA gene sequence types. Journal Eukaryotic Microbiology, 45, 45–5410.1111/j.1550-7408.1998.tb05068.xSearch in Google Scholar PubMed PubMed Central

Tanveer T., Hameed A., Muazzam A.G., Jung S.Y., Gul A., Matin A. 2013. Isolation and molecular characterization of potentially pathogenic Acanthamoeba genotypes from diverse resources including household driking water from Khyber Paktunkhwa, Pakistan. Parasitology Research, 112, 2925–2932. DOI: 10.1007/s00436-013-3465-510.1007/s00436-013-3465-5Search in Google Scholar PubMed

Trabelsi H., Dendana F., Sellami A., Sellami H., Cheikhrouhou F., Neji S., Makni F., Ayadi A. 2012. Pathogenic free-living amoebae: Epidemiology and clinical review. Pathologie Biologie, 60, 399–405. DOI: 10.1016/j.patbio.2012.03.00210.1016/j.patbio.2012.03.002Search in Google Scholar PubMed

Tsvetkova N., Schild M., Panaiotv S., Kurdova-Mintcheva R., Gottstein B., Walochnik J. 2004. The identification of free-living environmental isolates of amoebae from Bulgaria. Parasitology Research, 92, 405–413. DOI: 10.1007/s00436-0031052-x10.1007/s00436-0031052-xSearch in Google Scholar

Visvesvara G.S., Moura H., Schuster F.L. 2007. Pathogenic and opportunistic free-living amoebae: Acanthamoeba spp., Balamuthia mandrillaris, Naegleria fowleri and Sappinia diploidea. FEMS Immunology and Medical Microbiology, 50, 1–26. DOI: http://dx.doi.org/10.1111/j.1574-695X.2007.00232.xhttp://dx.doi.org/10.1111/j.1574-695X.2007.00232.xSearch in Google Scholar PubMed

Visvesvara G., Schuster F. 2008a. Opportunistic free-living amebae, Part I. Clinical Microbiology Newsletter, 30, 151–158. DOI: 10.1016/j.clinmicnews.2008.09.00410.1016/j.clinmicnews.2008.09.004Search in Google Scholar

Visvesvara G., Schuster F. 2008b Opportunistic free-living amebae, Part II. Clinical Microbiology Newsletter, 30, 159–166. DOI: 10.1016/j.clinmicnews.2008.10.00110.1016/j.clinmicnews.2008.10.001Search in Google Scholar

Walochnik J., Obwaller A., Aspöck H. 2000. Correlations between morphological, molecular, biological and physiological characteristics in clinical and nonclinical isolates of Acanthamoeba spp. Applied Environmental Microbiology, 66, 4408–4413. DOI: 10.1128/AEM.66.10.4408-4413.200010.1128/AEM.66.10.4408-4413.2000Search in Google Scholar PubMed PubMed Central

Winck M.A., Caumo K., Rott M.B. 2011. Prevalence of Acanthamoeba from tap water in Rio Grande do Sul, Brazil. Current Microbiology, 63, 464–469. DOI: 10.1007/s00284-011-0003-510.1007/s00284-011-0003-5Search in Google Scholar PubMed

Zhang Y., Sun X., Wang Z., Li R., Luo S., Jin X., Deng S., Chen W. 2004. Identification of 18S ribosomal DNA genotype of Acanthamoeba from patients with keratitis in North China. Investigative Ophthalmology & Visual Science, 45, 1904–1907. DOI: 10.1167/iovs.03-107310.1167/iovs.03-1073Search in Google Scholar PubMed

Received: 2015-4-4
Revised: 2015-9-29
Accepted: 2015-11-25
Published Online: 2016-3-30
Published in Print: 2016-6-1

© W. Stefański Institute of Parasitology, PAS

Articles in the same Issue

  1. Research Article
  2. Human Trichinella infection outbreaks in Slovakia, 1980-2008
  3. Research Article
  4. Immune responses in rats and sheep induced by a DNA vaccine containing the phosphoglycerate kinase gene of Fasciola hepatica and liver fluke infection
  5. Research Article
  6. Isolation and identification of Acanthamoeba spp. from thermal swimming pools and spas in Southern Brazil
  7. Research Article
  8. First report and spore ultrastructure of Vairimorpha plodiae (Opisthokonta: Microspora) from Plodia interpunctella (Lepidoptera: Pyralidae) in Turkey
  9. Research Article
  10. Evaluation of immuno diagnostic assay for the exposure of stage specific filarial infection
  11. Research Article
  12. Morphological, molecular and developmental characterization of the thelastomatid nematode Thelastoma bulhoesi (de Magalhães, 1900) (Oxyuridomorpha: Thelastomatidae) parasite of Periplaneta americana (Linnaeus, 1758) (Blattodea: Blattidae) in Japan
  13. Research Article
  14. Wild boar (Sus scrofa) – reservoir host of Toxoplasma gondii, Neospora caninum and Anaplasma phagocytophilum in Slovakia
  15. Research Article
  16. Prevalence of Giardia spp. in young dogs using a combination of two diagnostic methods
  17. Research Article
  18. CIAS detection of Fasciola hepatica/F. gigantica intermediate forms in bovines from Bangladesh
  19. Research Article
  20. Redescription of two species of cystidicolid nematodes (Spirurina: Cystidicolidae) from Notopterus notopterus (Osteichthyes) in Thailand
  21. Research Article
  22. Paradiplozoon iraqensis n. sp. (Monogenea: Diplozoinae) from Cyprinion macrostomum (Cyprinidae) in the Tigris River, Iraq
  23. Research Article
  24. Genetic diversity of Diplomonadida in fish of the genus Coregonus from Southeastern Siberia
  25. Research Article
  26. Dynamics and effects of Ligula intestinalis (L.) infection in the native fish Barbus callensis Valenciennes, 1842 in Algeria
  27. Research Article
  28. Bioinformatics analysis and expression of a novel protein ROP48 in Toxoplasma gondii
  29. Research Article
  30. Vertical transmission of Trypanosoma evansi in dromedary camels and studies on fetal pathology, diagnosis and treatment
  31. Research Article
  32. Molecular detection and prevalence of Theileria equi and Babesia caballi in horses of central Balkan
  33. Research Article
  34. Two new species of the genus Pterygosoma (Acariformes: Pterygosomatidae) parasitizing agamid lizards (Sauria: Agamidae) from the Indian subcontinent
  35. Research Article
  36. A new species of Spauligodon (Nematoda; Oxyuroidea; Pharyngodonide) and other Helminths in Ptychozoon Kuhli (Squamata: Gekkonidae) from East Malaysia
  37. Research Article
  38. Molecular characterization and phylogeny of some mazocraeidean monogeneans from carangid fish
  39. Research Article
  40. Validation of the TrichinEasy® digestion system for the detection of Anisakidae larvae in fish products
  41. Research Article
  42. Evaluation of the in vitro activity of ceragenins against Trichomonas vaginalis
  43. Research Article
  44. Prevalence and genotypes of Enterocytozoon bieneusi in sika deer in Jilin province, Northeastern China
  45. Research Article
  46. Endoparasitic fauna of red foxes (Vulpes vulpes) and golden jackals (Canis aureus) in Serbia
  47. Research Article
  48. Molecular characterization of Giardia duodenalis from white yaks in China
  49. Research Article
  50. Seroprevalence of Toxoplasma gondii among turkeys on family farms in the state of Northeastern Brazil
  51. Research Article
  52. First report of molecular identification of Cystoisospora suis in piglets with lethal diarrhea in Japan
  53. Research Article
  54. Determination of PCT on admission is a useful tool for the assessment of disease severity in travelers with imported Plasmodium falciparum malaria
  55. Research Article
  56. Dynamics of Theileria orientalis genotype population in cattle in a year-round grazing system
  57. Research Article
  58. A new isosporoid coccidia (Apicomplexa: Eimeriidae)from the southern house wren Troglodytes musculus Naumann, 1823 (Passeriformes: Troglodytidae) from Brazil
  59. Research Article
  60. Mass spectrometry analysis of the excretory-secretory (E-S) products of the model cestode Hymenolepis diminut a reveals their immunogenic properties and the presence of new E-S proteins in cestodes
Downloaded on 29.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/ap-2016-0031/html
Scroll to top button