Could phylogenetic analysis be used for feline Leukemia Virus (FeLV) classification?

Detalhes bibliográficos
Autor(a) principal: Ortiz, Lucía Cano
Data de Publicação: 2022
Outros Autores: Tochetto, Caroline, Roehe, Paulo Michel, Franco, Ana Claudia, Junqueira, Dennis Maletich
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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spelling 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
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dc.language.iso.fl_str_mv eng
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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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