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dc.contributor.authorRocha, Deisy M. G. C.es_ES
dc.contributor.authorMagalhães, Carloses_ES
dc.contributor.authorCá, Baltazares_ES
dc.contributor.authorRamos, Angelicaes_ES
dc.contributor.authorCarvalho, Teresaes_ES
dc.contributor.authorComas, Iñakies_ES
dc.contributor.authorGuimarães, João Tiagoes_ES
dc.contributor.authorBastos, Helder Novaises_ES
dc.contributor.authorSaraiva, Margaridaes_ES
dc.contributor.authorOsório, Nuno S.es_ES
dc.date.accessioned2021-06-29T10:58:52Z-
dc.date.available2021-06-29T10:58:52Z-
dc.date.issued2021-06-11-
dc.identifier.citationFrontiers in Microbiology 12:659545 (2021)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/244891-
dc.description12 páginas, 5 figuras.es_ES
dc.description.abstractWidespread and frequent resistance to the second-line tuberculosis (TB) medicine streptomycin, suggests ongoing transmission of low fitness cost streptomycin resistance mutations. To investigate this hypothesis, we studied a cohort of 681 individuals from a TB epidemic in Portugal. Whole-genome sequencing (WGS) analyses were combined with phenotypic growth studies in culture media and in mouse bone marrow derived macrophages. Streptomycin resistance was the most frequent resistance in the cohort accounting for 82.7% (n = 67) of the resistant Mycobacterium tuberculosis isolates. WGS of 149 clinical isolates identified 13 transmission clusters, including three clusters containing only streptomycin resistant isolates. The biggest cluster was formed by eight streptomycin resistant isolates with a maximum of five pairwise single nucleotide polymorphisms of difference. Interestingly, despite their genetic similarity, these isolates displayed different resistance levels to streptomycin, as measured both in culture media and in infected mouse bone marrow derived macrophages. The genetic bases underlying this phenotype are a combination of mutations in gid and other genes. This study suggests that specific streptomycin resistance mutations were transmitted in the cohort, with the resistant isolates evolving at the cluster level to allow low-to-high streptomycin resistance levels without a significative fitness cost. This is relevant not only to better understand transmission of streptomycin resistance in a clinical setting dominated by Lineage 4 M. tuberculosis infections, but mainly because it opens new prospects for the investigation of selection and spread of drug resistance in general.es_ES
dc.description.sponsorshipThis work has been funded by of the projects NORTE-01-0145- FEDER-000039, NORTE-01-0145-FEDER-000013, and NORTE01-0145-FEDER-00002, supported by Norte Portugal Regional Operational Program (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). It was also funded through the Foundation for Science and Technology (FCT) – project FCT IF/00474/2014, UIDB/50026/2020 and UIDP/50026/2020. DR and CM were funded by FCT Ph.D. scholarships (grant numbers SFRH/BD/135422/2017 and SFRH/BD/132797/2017, respectively). DR was partially funded by the PGCD – Graduate Program Science for Development. MS is supported by FCT through the Estimulo ao Emprego Científico.es_ES
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rightsopenAccesses_ES
dc.subjectEvolutiones_ES
dc.subjectResistancees_ES
dc.subjectStreptomycines_ES
dc.subjectTransmissiones_ES
dc.subjectTuberculosises_ES
dc.titleHeterogeneous Streptomycin Resistance Level Among Mycobacterium tuberculosis Strains From the Same Transmission Clusteres_ES
dc.typeartículoes_ES
dc.identifier.doi10.3389/fmicb.2021.659545-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://dx.doi.org/10.3389/fmicb.2021.659545es_ES
dc.identifier.e-issn1664-302X-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0/es_ES
dc.contributor.funderComissão de Coordenação e Desenvolvimento Regional do Norte (Portugal)es_ES
dc.contributor.funderEuropean Commissiones_ES
dc.contributor.funderFoundation for Science and Technologyes_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.contributor.orcidComas, Iñaki [0000-0001-5504-9408]es_ES
dc.identifier.pmid34177837-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.languageiso639-1en-
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