Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiro

Detalhes bibliográficos
Autor(a) principal: Enrico Giovanelli Tacconi Gimenez
Data de Publicação: 2023
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFMG
Texto Completo: http://hdl.handle.net/1843/74376
Resumo: Corynebacterium pseudotuberculosis is the causative agent of caseous lymphadenitis (CLA) in several animals, including camelids, ruminants, horses and humans. CLA can result in severe economic losses, especially in camelids, which are highly valued as companion animals. Little is known about the mechanisms involved in tropism for different hosts. Cp162 strain isolated from camel is the only one of this host that had its genome sequenced. This study aimed to evaluate the evolution of genome assemblies of the Cp162 lineage, identify possible genes related to host tropism and understand the genomic diversity of C. pseudotuberculosis through comparative genomics and phylogeny analyses. Since the first assembly, there was an increase of 88 kb, 121 protein coding genes, a reduction in the number of pseudogenes and correction of two inversions and one rearrangement. Compared to 129 other genomes of the species, Cp162 has four unique genes, which encode two transposases and two truncated genes. Three genes uniquely missing from this lineage are lysG and two that encode “NUDIX domain protein”, and a hypothetical protein. No genes could be associated with the camel host tropism, which suggests that the tropism could be associated with sequence polymorphisms rather than the presence and absence of genes, and more genomes from this host need to be analyzed. The analysis showed that the C. pseudotuberculosis pangenome is closed, but there are many unknown genes in this genome that may be associated with tropism for other hosts.
id UFMG_56e57d99d50bac44c0aa3378ad5b64c3
oai_identifier_str oai:repositorio.ufmg.br:1843/74376
network_acronym_str UFMG
network_name_str Repositório Institucional da UFMG
repository_id_str
spelling Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiroSequenciamento de nova geraçãoCorynebacterium pseudotuberculosisMontagem ab initiopangenômicaBioinformáticaSequenciamento de Nucleotídeos em Larga EscalaCorynebacterium pseudotuberculosisGenômicaCorynebacterium pseudotuberculosis is the causative agent of caseous lymphadenitis (CLA) in several animals, including camelids, ruminants, horses and humans. CLA can result in severe economic losses, especially in camelids, which are highly valued as companion animals. Little is known about the mechanisms involved in tropism for different hosts. Cp162 strain isolated from camel is the only one of this host that had its genome sequenced. This study aimed to evaluate the evolution of genome assemblies of the Cp162 lineage, identify possible genes related to host tropism and understand the genomic diversity of C. pseudotuberculosis through comparative genomics and phylogeny analyses. Since the first assembly, there was an increase of 88 kb, 121 protein coding genes, a reduction in the number of pseudogenes and correction of two inversions and one rearrangement. Compared to 129 other genomes of the species, Cp162 has four unique genes, which encode two transposases and two truncated genes. Three genes uniquely missing from this lineage are lysG and two that encode “NUDIX domain protein”, and a hypothetical protein. No genes could be associated with the camel host tropism, which suggests that the tropism could be associated with sequence polymorphisms rather than the presence and absence of genes, and more genomes from this host need to be analyzed. The analysis showed that the C. pseudotuberculosis pangenome is closed, but there are many unknown genes in this genome that may be associated with tropism for other hosts.Corynebacterium pseudotuberculosis é o agente causador da linfadenite caseosa (CLA) em vários animais, incluindo camelídeos, ruminantes, cavalos e humanos. A CLA pode resultar em perdas econômicas graves, especialmente em camelídeos, que são muito valorizados como animais de companhia. Pouco se sabe sobre os mecanismos envolvidos no tropismo por diferentes hospedeiros. A linhagem Cp162 isolada de camelo é a única deste hospedeiro que teve o seu genoma sequenciado. Este estudo teve como objetivo avaliar a evolução das montagens do genoma da linhagem Cp162, identificar possíveis genes relacionados ao tropismo por seu hospedeiro e compreender a diversidade genômica de C. pseudotuberculosis por meio de análises de genômica comparativa e filogenia. Desde a primeira montagem, houve um aumento de 88 Kb, 121 genes codificadores de proteínas, redução no número de pseudogenes e a correção de duas inversões e um rearranjo. Em comparação com 129 outros genomas da espécie, Cp162 possui quatro genes exclusivos, que codificam duas transposases e dois genes truncados. Três genes exclusivamente ausentes desta linhagem são lysG e dois que codificam “NUDIX domain protein”, e uma proteína hipotética. Nenhum gene pôde ser associado ao tropismo ao hospedeiro camelo, o que sugere que o tropismo poderia estar associado a polimorfismos de sequência ao invés de presença e ausência de genes, e mais genomas deste hospedeiro precisam ser analisados. A análise mostrou que o pangenoma de C. pseudotuberculosis é fechado, mas existem muitos genes desconhecidos neste genoma que podem estar associados ao tropismo para outros hospedeiros.Universidade Federal de Minas GeraisBrasilICB - INSTITUTO DE CIÊNCIAS BIOLOGICASPrograma de Pós-Graduação em BioinformaticaUFMGVasco Ariston de Carvalho Azevedohttp://lattes.cnpq.br/1020477751003832Marcus VInícius Canário VianaBruno Silva AndradeSandeep TiwariEnrico Giovanelli Tacconi Gimenez2024-08-20T18:09:49Z2024-08-20T18:09:49Z2023-09-29info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/1843/74376porhttp://creativecommons.org/licenses/by-nc-nd/3.0/pt/info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMG2024-08-20T18:09:50Zoai:repositorio.ufmg.br:1843/74376Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2024-08-20T18:09:50Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false
dc.title.none.fl_str_mv Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiro
title Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiro
spellingShingle Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiro
Enrico Giovanelli Tacconi Gimenez
Sequenciamento de nova geração
Corynebacterium pseudotuberculosis
Montagem ab initio
pangenômica
Bioinformática
Sequenciamento de Nucleotídeos em Larga Escala
Corynebacterium pseudotuberculosis
Genômica
title_short Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiro
title_full Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiro
title_fullStr Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiro
title_full_unstemmed Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiro
title_sort Re-sequenciamento de Corynebacterium pseudotuberculosis e a busca por mecanismos de tropismo pelo hospedeiro
author Enrico Giovanelli Tacconi Gimenez
author_facet Enrico Giovanelli Tacconi Gimenez
author_role author
dc.contributor.none.fl_str_mv Vasco Ariston de Carvalho Azevedo
http://lattes.cnpq.br/1020477751003832
Marcus VInícius Canário Viana
Bruno Silva Andrade
Sandeep Tiwari
dc.contributor.author.fl_str_mv Enrico Giovanelli Tacconi Gimenez
dc.subject.por.fl_str_mv Sequenciamento de nova geração
Corynebacterium pseudotuberculosis
Montagem ab initio
pangenômica
Bioinformática
Sequenciamento de Nucleotídeos em Larga Escala
Corynebacterium pseudotuberculosis
Genômica
topic Sequenciamento de nova geração
Corynebacterium pseudotuberculosis
Montagem ab initio
pangenômica
Bioinformática
Sequenciamento de Nucleotídeos em Larga Escala
Corynebacterium pseudotuberculosis
Genômica
description Corynebacterium pseudotuberculosis is the causative agent of caseous lymphadenitis (CLA) in several animals, including camelids, ruminants, horses and humans. CLA can result in severe economic losses, especially in camelids, which are highly valued as companion animals. Little is known about the mechanisms involved in tropism for different hosts. Cp162 strain isolated from camel is the only one of this host that had its genome sequenced. This study aimed to evaluate the evolution of genome assemblies of the Cp162 lineage, identify possible genes related to host tropism and understand the genomic diversity of C. pseudotuberculosis through comparative genomics and phylogeny analyses. Since the first assembly, there was an increase of 88 kb, 121 protein coding genes, a reduction in the number of pseudogenes and correction of two inversions and one rearrangement. Compared to 129 other genomes of the species, Cp162 has four unique genes, which encode two transposases and two truncated genes. Three genes uniquely missing from this lineage are lysG and two that encode “NUDIX domain protein”, and a hypothetical protein. No genes could be associated with the camel host tropism, which suggests that the tropism could be associated with sequence polymorphisms rather than the presence and absence of genes, and more genomes from this host need to be analyzed. The analysis showed that the C. pseudotuberculosis pangenome is closed, but there are many unknown genes in this genome that may be associated with tropism for other hosts.
publishDate 2023
dc.date.none.fl_str_mv 2023-09-29
2024-08-20T18:09:49Z
2024-08-20T18:09:49Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1843/74376
url http://hdl.handle.net/1843/74376
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv http://creativecommons.org/licenses/by-nc-nd/3.0/pt/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-nd/3.0/pt/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Minas Gerais
Brasil
ICB - INSTITUTO DE CIÊNCIAS BIOLOGICAS
Programa de Pós-Graduação em Bioinformatica
UFMG
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
Brasil
ICB - INSTITUTO DE CIÊNCIAS BIOLOGICAS
Programa de Pós-Graduação em Bioinformatica
UFMG
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMG
instname:Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
instname_str Universidade Federal de Minas Gerais (UFMG)
instacron_str UFMG
institution UFMG
reponame_str Repositório Institucional da UFMG
collection Repositório Institucional da UFMG
repository.name.fl_str_mv Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)
repository.mail.fl_str_mv repositorio@ufmg.br
_version_ 1816829580620595200