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Phylogenetic and Structural Diversity in the Feline Leukemia Virus Env Gene

Feline leukemia virus (FeLV) belongs to the genus Gammaretrovirus, and causes a variety of neoplastic and non-neoplastic diseases in cats. Alteration of viral env sequences is thought to be associated with disease specificity, but the way in which genetic diversity of FeLV contributes to the generat...

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Autores principales: Watanabe, Shinya, Kawamura, Maki, Odahara, Yuka, Anai, Yukari, Ochi, Haruyo, Nakagawa, So, Endo, Yasuyuki, Tsujimoto, Hajime, Nishigaki, Kazuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623909/
https://www.ncbi.nlm.nih.gov/pubmed/23593376
http://dx.doi.org/10.1371/journal.pone.0061009
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author Watanabe, Shinya
Kawamura, Maki
Odahara, Yuka
Anai, Yukari
Ochi, Haruyo
Nakagawa, So
Endo, Yasuyuki
Tsujimoto, Hajime
Nishigaki, Kazuo
author_facet Watanabe, Shinya
Kawamura, Maki
Odahara, Yuka
Anai, Yukari
Ochi, Haruyo
Nakagawa, So
Endo, Yasuyuki
Tsujimoto, Hajime
Nishigaki, Kazuo
author_sort Watanabe, Shinya
collection PubMed
description Feline leukemia virus (FeLV) belongs to the genus Gammaretrovirus, and causes a variety of neoplastic and non-neoplastic diseases in cats. Alteration of viral env sequences is thought to be associated with disease specificity, but the way in which genetic diversity of FeLV contributes to the generation of such variants in nature is poorly understood. We isolated FeLV env genes from naturally infected cats in Japan and analyzed the evolutionary dynamics of these genes. Phylogenetic reconstructions separated our FeLV samples into three distinct genetic clusters, termed Genotypes I, II, and III. Genotype I is a major genetic cluster and can be further classified into Clades 1–7 in Japan. Genotypes were correlated with geographical distribution; Genotypes I and II were distributed within Japan, whilst FeLV samples from outside Japan belonged to Genotype III. These results may be due to geographical isolation of FeLVs in Japan. The observed structural diversity of the FeLV env gene appears to be caused primarily by mutation, deletion, insertion and recombination, and these variants may be generated de novo in individual cats. FeLV interference assay revealed that FeLV genotypes did not correlate with known FeLV receptor subgroups. We have identified the genotypes which we consider to be reliable for evaluating phylogenetic relationships of FeLV, which embrace the high structural diversity observed in our sample. Overall, these findings extend our understanding of Gammaretrovirus evolutionary patterns in the field, and may provide a useful basis for assessing the emergence of novel strains and understanding the molecular mechanisms of FeLV transmission in cats.
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spelling pubmed-36239092013-04-16 Phylogenetic and Structural Diversity in the Feline Leukemia Virus Env Gene Watanabe, Shinya Kawamura, Maki Odahara, Yuka Anai, Yukari Ochi, Haruyo Nakagawa, So Endo, Yasuyuki Tsujimoto, Hajime Nishigaki, Kazuo PLoS One Research Article Feline leukemia virus (FeLV) belongs to the genus Gammaretrovirus, and causes a variety of neoplastic and non-neoplastic diseases in cats. Alteration of viral env sequences is thought to be associated with disease specificity, but the way in which genetic diversity of FeLV contributes to the generation of such variants in nature is poorly understood. We isolated FeLV env genes from naturally infected cats in Japan and analyzed the evolutionary dynamics of these genes. Phylogenetic reconstructions separated our FeLV samples into three distinct genetic clusters, termed Genotypes I, II, and III. Genotype I is a major genetic cluster and can be further classified into Clades 1–7 in Japan. Genotypes were correlated with geographical distribution; Genotypes I and II were distributed within Japan, whilst FeLV samples from outside Japan belonged to Genotype III. These results may be due to geographical isolation of FeLVs in Japan. The observed structural diversity of the FeLV env gene appears to be caused primarily by mutation, deletion, insertion and recombination, and these variants may be generated de novo in individual cats. FeLV interference assay revealed that FeLV genotypes did not correlate with known FeLV receptor subgroups. We have identified the genotypes which we consider to be reliable for evaluating phylogenetic relationships of FeLV, which embrace the high structural diversity observed in our sample. Overall, these findings extend our understanding of Gammaretrovirus evolutionary patterns in the field, and may provide a useful basis for assessing the emergence of novel strains and understanding the molecular mechanisms of FeLV transmission in cats. Public Library of Science 2013-04-11 /pmc/articles/PMC3623909/ /pubmed/23593376 http://dx.doi.org/10.1371/journal.pone.0061009 Text en © 2013 Watanabe et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Watanabe, Shinya
Kawamura, Maki
Odahara, Yuka
Anai, Yukari
Ochi, Haruyo
Nakagawa, So
Endo, Yasuyuki
Tsujimoto, Hajime
Nishigaki, Kazuo
Phylogenetic and Structural Diversity in the Feline Leukemia Virus Env Gene
title Phylogenetic and Structural Diversity in the Feline Leukemia Virus Env Gene
title_full Phylogenetic and Structural Diversity in the Feline Leukemia Virus Env Gene
title_fullStr Phylogenetic and Structural Diversity in the Feline Leukemia Virus Env Gene
title_full_unstemmed Phylogenetic and Structural Diversity in the Feline Leukemia Virus Env Gene
title_short Phylogenetic and Structural Diversity in the Feline Leukemia Virus Env Gene
title_sort phylogenetic and structural diversity in the feline leukemia virus env gene
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623909/
https://www.ncbi.nlm.nih.gov/pubmed/23593376
http://dx.doi.org/10.1371/journal.pone.0061009
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