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dc.contributor.author
Polat, Meripet  
dc.contributor.author
Takeshima, Shin-nosuke  
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Hosomichi, Kazuyoshi  
dc.contributor.author
Kim, Jiyun  
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Miyasaka, Taku  
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Yamada, Kazunori  
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Arainga, Mariluz  
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Murakami, Tomoyuki  
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Matsumoto, Yuki  
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de la Barra Diaz, Verónica  
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Panei, Carlos Javier  
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Gonzalez, Ester Teresa  
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Kanemaki, Misao  
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Onuma, Misao  
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Giovambattista, Guillermo  
dc.contributor.author
Aida, Yoko  
dc.date.available
2018-08-02T20:27:57Z  
dc.date.issued
2016-01  
dc.identifier.citation
Polat, Meripet; Takeshima, Shin-nosuke; Hosomichi, Kazuyoshi; Kim, Jiyun; Miyasaka, Taku; et al.; A new genotype of bovine leukemia virus in South America identified by NGS-based whole genome sequencing and molecular evolutionary genetic analysis; BioMed Central; Retrovirology; 13; 1; 1-2016; 1-23  
dc.identifier.issn
1742-4690  
dc.identifier.uri
http://hdl.handle.net/11336/53978  
dc.description.abstract
Background: Bovine leukemia virus (BLV) is a member of retroviridae family, together with human T cell leukemia virus types 1 and 2 (HTLV-1 and -2) belonging to the genes deltaretrovirus, and infects cattle worldwide. Previous studies have classified the env sequences of BLV provirus from different geographic locations into eight genetic groups. To investigate the genetic variability of BLV in South America, we performed phylogenetic analyses of whole genome and partial env gp51 sequences of BLV strains isolated from Peru, Paraguay and Bolivia, for which no the molecular characteristics of BLV have previously been published, and discovered a novel BLV genotype, genotype-9, in Bolivia. Results: In Peru and Paraguay, 42.3 % (139/328) and over 50 % (76/139) of samples, respectively, were BLV positive. In Bolivia, the BLV infection rate was up to 30 % (156/507) at the individual level. In Argentina, 325/420 samples were BLV positive, with a BLV prevalence of 77.4 % at the individual level and up to 90.9 % at herd level. By contrast, relatively few BLV positive samples were detected in Chile, with a maximum of 29.1 % BLV infection at the individual level. We performed phylogenetic analyses using two different approaches, maximum likelihood (ML) tree and Bayesian inference, using 35 distinct partial env gp51 sequences from BLV strains isolated from Peru, Paraguay, and Bolivia, and 74 known BLV strains, representing eight different BLV genotypes from various geographical locations worldwide. The results indicated that Peruvian and Paraguayan BLV strains were grouped into genotypes-1, -2, and -6, while those from Bolivia were clustered into genotypes-1, -2, and -6, and a new genotype, genotype-9. Interestingly, these results were confirmed using ML phylogenetic analysis of whole genome sequences obtained by next generation sequencing of 25 BLV strains, assigned to four different genotypes (genotypes-1, -2, -6, and -9) from Peru, Paraguay, and Bolivia. Comparative analyses of complete genome sequences clearly showed some specific substitutions, in both structural and non-structural BLV genes, distinguishing the novel genotype-9 from known genotypes. Conclusions: Our results demonstrate widespread BLV infection in South American cattle and the existence of a new BLV genotype-9 in Bolivia. We conclude that at least seven BLV genotypes (genotypes-1, -2, -4, -5, -6, -7, and -9) are circulating in South America.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
BioMed Central  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/  
dc.subject
Blv Whole Genome Analysis  
dc.subject
Bovine Leukemia Virus (Blv)  
dc.subject
Gp51 Env Sequencing  
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Next Generation Sequencing  
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Phylogenetic Analysis  
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South America  
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Virología  
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Ciencias Biológicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
A new genotype of bovine leukemia virus in South America identified by NGS-based whole genome sequencing and molecular evolutionary genetic analysis  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-07-31T17:20:25Z  
dc.journal.volume
13  
dc.journal.number
1  
dc.journal.pagination
1-23  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Polat, Meripet. University of Tokyo; Japón. RIKEN; Japón  
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Fil: Takeshima, Shin-nosuke. University of Tokyo; Japón. RIKEN; Japón  
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Fil: Hosomichi, Kazuyoshi. Kanazawa University; Japón  
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Fil: Kim, Jiyun. RIKEN; Japón  
dc.description.fil
Fil: Miyasaka, Taku. RIKEN; Japón  
dc.description.fil
Fil: Yamada, Kazunori. RIKEN; Japón  
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Fil: Arainga, Mariluz. RIKEN; Japón  
dc.description.fil
Fil: Murakami, Tomoyuki. RIKEN; Japón  
dc.description.fil
Fil: Matsumoto, Yuki. RIKEN; Japón  
dc.description.fil
Fil: de la Barra Diaz, Verónica. Laboratorio Veterinario Lavet; Chile  
dc.description.fil
Fil: Panei, Carlos Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico - CONICET - La Plata. Instituto de Genética Veterinaria Ing. Fernando Noel Dulout; Argentina. Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Departamento de Microbiología. Cátedra de Virología; Argentina  
dc.description.fil
Fil: Gonzalez, Ester Teresa. Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Departamento de Microbiología. Cátedra de Virología; Argentina  
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Fil: Kanemaki, Misao. Institute for Animal Science; Japón  
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Fil: Onuma, Misao. RIKEN; Japón  
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Fil: Giovambattista, Guillermo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico - CONICET - La Plata. Instituto de Genética Veterinaria Ing. Fernando Noel Dulout; Argentina  
dc.description.fil
Fil: Aida, Yoko. University of Tokyo; Japón. RIKEN; Japón  
dc.journal.title
Retrovirology  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://retrovirology.biomedcentral.com/articles/10.1186/s12977-016-0239-z  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1186/s12977-016-0239-z