Genomic and phenotypic characterisation of antimicrobial resistance in carbapenem-resistant Acinetobacter baumannii hyperendemic clones CC1, CC15, CC79 and CC25
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DC Field | Value | Language |
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dc.contributor | Centro de Biotecnologia | pt_BR |
dc.contributor | Lab. Bacteriologia | pt_BR |
dc.contributor.author | Camargo, Carlos Henrique | pt_BR |
dc.contributor.author | Cunha, Marcos Paulo Vieira | pt_BR |
dc.contributor.author | Barcellos, Thays Almeida Franco de | pt_BR |
dc.contributor.author | Bueno, Mariana Sardinha | pt_BR |
dc.contributor.author | Bertani, Amanda Maria de Jesus | pt_BR |
dc.contributor.author | Santos, Carla Adriana dos | pt_BR |
dc.contributor.author | Nagamori, Filipe Onishi | pt_BR |
dc.contributor.author | Takagi, Elizabeth Harummyy | pt_BR |
dc.contributor.author | Chimara, Erica | pt_BR |
dc.contributor.author | Carvalho, Eneas | pt_BR |
dc.contributor.author | Tiba-Casas, Monique Ribeiro | pt_BR |
dc.date.accessioned | 2020-10-15T18:28:20Z | - |
dc.date.available | 2020-10-15T18:28:20Z | - |
dc.date.issued | 2020 | pt_BR |
dc.identifier.citation | Camargo CH, Cunha MPV, Barcellos TAF, Bueno MS, Bertani AMJ, Santos CA, et al. Genomic and phenotypic characterisation of antimicrobial resistance in carbapenem-resistant Acinetobacter baumannii hyperendemic clones CC1, CC15, CC79 and CC25. Int. J. Antimicrob. Agents. Dec. 2020;(56)6:106195. doi:10.1016/j.ijantimicag.2020.106195. | pt_BR |
dc.identifier.uri | https://repositorio.butantan.gov.br/handle/butantan/3273 | - |
dc.description.abstract | Dissemination of carbapenem-resistant Acinetobacter baumannii (CRAB) is mainly driven by the spread of clonal lineages. High frequencies of CRAB are reported in South America, and clonal complexes CC1, CC15, CC79 and CC25 are predominant. A total of 79 non-redundant CRAB recovered from 26 Brazilian hospitals were selected to perform antimicrobial susceptibility test (AST) by microdilution and whole genome sequencing (WGS). MLST, acquired resistance genes and phylogeny based on high-quality SNPs were extracted from WGS. XDR (86.1%), MDR (12.7%) and one PDR isolate from CC15 (1.3%) were identified. Colistin resistance was more frequently on CC25 isolates (p<0.01). Prevalence of CC79 (n=22; 27.8%) CC1 (n=21; 26.6%), CC15 (n=21; 26.6%), and CC25 (n=12; 15.2%) was observed. Regarding the carbapenem-hydrolyzing class D β-lactamases (CHDL), blaOXA-23 gene was frequently detected in CC1, CC15, and CC25 isolates, but blaOXA-72 gene was the most frequent CHDL in CC79 isolates (n=12/22, 54.5%; p<0.01). High-quality SNPs analysis correlated well with the ST, and revealed that CRAB clones are highly conversed and present some clone-specific resistance determinants. This study provides essential information to understand the antimicrobial resistance patterns of CRAB in Brazilian hospitals, where hyperendemic XDR CRAB clones are disseminated. Phenotypic and genomic analysis of CRAB recovered from 26 Brazilian hospitals revealed the prevalence of XDR phenotype in the majority of international clonal complex CC79, CC1, CC15 and CC25. Dissemination of specific CRAB lineages in Brazil is suggested to be driven by their resistance determinants under antimicrobial selective pressure. | pt_BR |
dc.description.sponsorship | (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo | pt_BR |
dc.description.sponsorship | (CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico | pt_BR |
dc.format.extent | 106195 | pt_BR |
dc.language.iso | English | pt_BR |
dc.relation.ispartof | International Journal of Antimicrobial Agents | pt_BR |
dc.rights | Restricted access | pt_BR |
dc.title | Genomic and phenotypic characterisation of antimicrobial resistance in carbapenem-resistant Acinetobacter baumannii hyperendemic clones CC1, CC15, CC79 and CC25 | pt_BR |
dc.type | Article | pt_BR |
dc.identifier.doi | 10.1016/j.ijantimicag.2020.106195 | pt_BR |
dc.identifier.url | https://doi.org/10.1016/j.ijantimicag.2020.106195 | pt_BR |
dc.contributor.external | (IAL) Instituto Adolfo Lutz | pt_BR |
dc.contributor.external | (USP) Universidade de São Paulo | pt_BR |
dc.identifier.citationvolume | 56 | pt_BR |
dc.identifier.citationissue | 6 | pt_BR |
dc.subject.keyword | Illumina | pt_BR |
dc.subject.keyword | Polymyxin resistance | pt_BR |
dc.subject.keyword | Pan-drug resistance | pt_BR |
dc.subject.keyword | Molecular epidemiology | pt_BR |
dc.subject.keyword | Antimicrobial resistance | pt_BR |
dc.relation.ispartofabbreviated | Int J Antimicrob Agents | pt_BR |
dc.identifier.citationabnt | v. 56, n. 6, p. 106195, dez. 2020 | pt_BR |
dc.identifier.citationvancouver | Dec. 2020;(56)6:106195 | pt_BR |
dc.contributor.butantan | Carvalho, Eneas de|:Pesquisador|:Centro de Biotecnologia:Lab. Bacteriologia | pt_BR |
dc.sponsorship.butantan | (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2017/16988-6 | pt_BR |
dc.sponsorship.butantan | (CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦ | pt_BR |
dc.identifier.bvscc | BR78.1 | pt_BR |
dc.identifier.bvsdb | IBProd | pt_BR |
dc.description.dbindexed | Yes | pt_BR |
item.fulltext | Sem Texto completo | - |
item.openairetype | Article | - |
item.languageiso639-1 | English | - |
item.grantfulltext | none | - |
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