Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification?
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/239905 |
Resumo: | The surface envelope (SU) protein determines the cell tropism and consequently the pathogenesis of the feline leukemia virus (FeLV) in felids. Recombination of exogenous FeLV (exFeLV) with endogenous retroviruses (enFeLV) allows the emergence of more pathogenic variants. Currently, phenotypic testing through interference assays is the only method to distinguish among subgroups—namely, FeLV-A, -B, -C, -E, and -T. This study proposes a new method for FeLV classification based on molecular analysis of the SU gene. A total of 404 publicly available SU sequences were used to reconstruct a maximum likelihood tree. However, only 63 of these sequences had available information about phenotypic tests or subgroup assignments. Two major clusters were observed: (a) clade FeLV-A, which includes FeLV-A, FeLV-C, FeLV-E, and FeLV-T sequences, and (b) clade enFeLV, which includes FeLV-B and enFeLV strains. We found that FeLV-B, FeLV-C, FeLV-E, and FeLV-T SU sequences share similarities to FeLV-A viruses and most likely arose independently through mutation or recombination from this strain. FeLV-B and FeLV-C arose from recombination between FeLV-A and enFeLV viruses, whereas FeLV-T is a monophyletic subgroup that has probably originated from FeLV-A through combined events of deletions and insertions. Unfortunately, this study could not identify polymorphisms that are specifically linked to the FeLV-E subgroup. We propose that phylogenetic and recombination analysis together can explain the current phenotypic classification of FeLV viruses. |
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Ortiz, Lucía CanoTochetto, CarolineRoehe, Paulo MichelFranco, Ana ClaudiaJunqueira, Dennis Maletich2022-06-07T04:41:16Z20221999-4915http://hdl.handle.net/10183/239905001141066The surface envelope (SU) protein determines the cell tropism and consequently the pathogenesis of the feline leukemia virus (FeLV) in felids. Recombination of exogenous FeLV (exFeLV) with endogenous retroviruses (enFeLV) allows the emergence of more pathogenic variants. Currently, phenotypic testing through interference assays is the only method to distinguish among subgroups—namely, FeLV-A, -B, -C, -E, and -T. This study proposes a new method for FeLV classification based on molecular analysis of the SU gene. A total of 404 publicly available SU sequences were used to reconstruct a maximum likelihood tree. However, only 63 of these sequences had available information about phenotypic tests or subgroup assignments. Two major clusters were observed: (a) clade FeLV-A, which includes FeLV-A, FeLV-C, FeLV-E, and FeLV-T sequences, and (b) clade enFeLV, which includes FeLV-B and enFeLV strains. We found that FeLV-B, FeLV-C, FeLV-E, and FeLV-T SU sequences share similarities to FeLV-A viruses and most likely arose independently through mutation or recombination from this strain. FeLV-B and FeLV-C arose from recombination between FeLV-A and enFeLV viruses, whereas FeLV-T is a monophyletic subgroup that has probably originated from FeLV-A through combined events of deletions and insertions. Unfortunately, this study could not identify polymorphisms that are specifically linked to the FeLV-E subgroup. We propose that phylogenetic and recombination analysis together can explain the current phenotypic classification of FeLV viruses.application/pdfengViruses. Basel. Vol. 14, no. 2 (Feb. 2022), 249, 12 p.Vírus da leucemia felinaFilogeniaProteínas do envelope viralRecombinacao geneticaFeLVEnFeLVPhylogeneticsRecombinationCould phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification?Estrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001141066.pdf.txt001141066.pdf.txtExtracted Texttext/plain45719http://www.lume.ufrgs.br/bitstream/10183/239905/2/001141066.pdf.txt862689789ac92d91af7bd91c5ca477a6MD52ORIGINAL001141066.pdfTexto completo (inglês)application/pdf2180720http://www.lume.ufrgs.br/bitstream/10183/239905/1/001141066.pdf562a6b1dce1e7554654368f594ee16c9MD5110183/2399052022-06-08 04:40:52.097754oai:www.lume.ufrgs.br:10183/239905Repositório InstitucionalPUBhttps://lume.ufrgs.br/oai/requestlume@ufrgs.bropendoar:2022-06-08T07:40:52Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification? |
title |
Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification? |
spellingShingle |
Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification? Ortiz, Lucía Cano Vírus da leucemia felina Filogenia Proteínas do envelope viral Recombinacao genetica FeLV EnFeLV Phylogenetics Recombination |
title_short |
Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification? |
title_full |
Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification? |
title_fullStr |
Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification? |
title_full_unstemmed |
Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification? |
title_sort |
Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification? |
author |
Ortiz, Lucía Cano |
author_facet |
Ortiz, Lucía Cano Tochetto, Caroline Roehe, Paulo Michel Franco, Ana Claudia Junqueira, Dennis Maletich |
author_role |
author |
author2 |
Tochetto, Caroline Roehe, Paulo Michel Franco, Ana Claudia Junqueira, Dennis Maletich |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Ortiz, Lucía Cano Tochetto, Caroline Roehe, Paulo Michel Franco, Ana Claudia Junqueira, Dennis Maletich |
dc.subject.por.fl_str_mv |
Vírus da leucemia felina Filogenia Proteínas do envelope viral Recombinacao genetica |
topic |
Vírus da leucemia felina Filogenia Proteínas do envelope viral Recombinacao genetica FeLV EnFeLV Phylogenetics Recombination |
dc.subject.eng.fl_str_mv |
FeLV EnFeLV Phylogenetics Recombination |
description |
The surface envelope (SU) protein determines the cell tropism and consequently the pathogenesis of the feline leukemia virus (FeLV) in felids. Recombination of exogenous FeLV (exFeLV) with endogenous retroviruses (enFeLV) allows the emergence of more pathogenic variants. Currently, phenotypic testing through interference assays is the only method to distinguish among subgroups—namely, FeLV-A, -B, -C, -E, and -T. This study proposes a new method for FeLV classification based on molecular analysis of the SU gene. A total of 404 publicly available SU sequences were used to reconstruct a maximum likelihood tree. However, only 63 of these sequences had available information about phenotypic tests or subgroup assignments. Two major clusters were observed: (a) clade FeLV-A, which includes FeLV-A, FeLV-C, FeLV-E, and FeLV-T sequences, and (b) clade enFeLV, which includes FeLV-B and enFeLV strains. We found that FeLV-B, FeLV-C, FeLV-E, and FeLV-T SU sequences share similarities to FeLV-A viruses and most likely arose independently through mutation or recombination from this strain. FeLV-B and FeLV-C arose from recombination between FeLV-A and enFeLV viruses, whereas FeLV-T is a monophyletic subgroup that has probably originated from FeLV-A through combined events of deletions and insertions. Unfortunately, this study could not identify polymorphisms that are specifically linked to the FeLV-E subgroup. We propose that phylogenetic and recombination analysis together can explain the current phenotypic classification of FeLV viruses. |
publishDate |
2022 |
dc.date.accessioned.fl_str_mv |
2022-06-07T04:41:16Z |
dc.date.issued.fl_str_mv |
2022 |
dc.type.driver.fl_str_mv |
Estrangeiro info:eu-repo/semantics/article |
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001141066 |
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dc.language.iso.fl_str_mv |
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dc.relation.ispartof.pt_BR.fl_str_mv |
Viruses. Basel. Vol. 14, no. 2 (Feb. 2022), 249, 12 p. |
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info:eu-repo/semantics/openAccess |
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