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Molecular survey and genetic characterization of ‘Candidatus Mycoplasma haemolamae’ in llamas (Lama glama) and alpacas (Vicugna pacos) from Southern Chile.

dc.contributor.authorRamos, Patricio
dc.contributor.authorSepulveda-Garcia, Paulina
dc.contributor.authorAlabí, Amir [UNESP]
dc.contributor.authorRomero, Alex
dc.contributor.authorPinto, Teresa
dc.contributor.authorRojas, Alejandro
dc.contributor.authorBittencourt, Pedro
dc.contributor.authorMüller, Ananda
dc.contributor.institutionUniversidad Austral de Chile
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionRoss University School of Veterinary Medicine
dc.date.accessioned2022-04-29T08:30:45Z
dc.date.available2022-04-29T08:30:45Z
dc.date.issued2021-10-01
dc.description.abstractThis study aimed to perform a molecular survey and identification of hemotropic Mycoplasma spp. in domestic South American Camelids from Southern Chile. Conventional PCR (cPCR) for hemotropic Mycoplasma spp. based on 16S rRNA gene (620bp fragment) was performed in 87 EDTA-blood samples taken from 48 llamas (Lama glama) and 39 and alpacas (Vicugna pacos) from to Temuco, La Araucanía region and Valdivia, Los Rios region, Southern Chile. 16S rRNA hemotropic Mycoplasma PCR-positive were sequenced for species identification, phylogenetic and haplotype analyses, and further tested by cPCR targeting a fragment (160-210 bp) of the RNaseP (rnpB) gene. Based upon 16S rRNA cPCR results, the overall hemotropic Mycoplasma spp. occurrence in Southern camelids was 9.2% (8/87 [95% CI (4.0–17.3%)]), with five positive alpacas (12.8%; 5/39 [95% CI (4.3–27.4%)]) and three llamas (6.3%; 3/48 [95% CI (1.7–17.2%)]). All 16S rRNA PCR-positive samples were negative for the rnpB gene. Obtained 16S sequences presented high identity (99-100%) by BLASTn analysis to ‘Candidatus Mycoplasma haemolamae’ from an alpaca in the United Kingdom. Phylogenetic and haplotype analyses of the 16s rRNA gene showed high similarity among ‘Candidatus M. haemolamae’ sequences of this study and the ones from North America, Europe, and Asia evidencing a low diversity of Chilean samples, with only one haplotype detected (#1). Haplotype #1 from South American Camelids in Chile was worldwide distributed and observed in North America, Europe, and Asia. ‘Candidatus M. haemolamae’ detected for the first time in South American camelids in Southern Chile had low diversity and was worldwide spread.en
dc.description.affiliationInstitudo de Ciencias Clínicas Veterinarias Facultad de Ciencias Veterinarias Universidad Austral de Chile
dc.description.affiliationDepartamento de Patologia UNESP Teriogenologia e Saúde Única—Faculdade de Ciências Agrárias e Veterinarias Universidade Estadual Paulista (FCAV), Jaboticabal
dc.description.affiliationLaboratorio de Inmunología y Estrés de Organismos Acuáticos Instituto de Patología Animal Facultad de Ciencias Veterinarias Universidad Austral de Chile
dc.description.affiliationInstitute of Medicine and Center for Interdisciplinary Studies on the Nervous System CISNE Universidad Austral de Chile
dc.description.affiliationBiomedical Sciences Department Ross University School of Veterinary Medicine
dc.description.affiliationUnespDepartamento de Patologia UNESP Teriogenologia e Saúde Única—Faculdade de Ciências Agrárias e Veterinarias Universidade Estadual Paulista (FCAV), Jaboticabal
dc.identifierhttp://dx.doi.org/10.1016/j.actatropica.2021.106046
dc.identifier.citationActa Tropica, v. 222.
dc.identifier.doi10.1016/j.actatropica.2021.106046
dc.identifier.issn1873-6254
dc.identifier.issn0001-706X
dc.identifier.scopus2-s2.0-85110494853
dc.identifier.urihttp://hdl.handle.net/11449/229158
dc.language.isoeng
dc.relation.ispartofActa Tropica
dc.sourceScopus
dc.subjectCamelids
dc.subjectHemoplasma
dc.subjectHemotropic Mycoplasma spp.
dc.subjectPCR
dc.subjectSouth America
dc.titleMolecular survey and genetic characterization of ‘Candidatus Mycoplasma haemolamae’ in llamas (Lama glama) and alpacas (Vicugna pacos) from Southern Chile.en
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0002-1515-1341[5]
unesp.departmentPatologia Veterinária - FCAVpt

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