ISCR1 associated with blaCTX-M-1 y blaCTX-M-2 genes in IncN and IncFIIA plasmids isolated from Klebsiella pneumoniae of nosocomial origin in Mérida, Venezuela
Introduction: Insertion sequences such as ISCR1 promote capture, transposition and expression of blaCTX-M genes. Thus, gene dissemination in bacterial populations occurs rapidly. Objective: To determine the presence of ISCR1 sequence genes and their association with blaCTX-M-1 and blaCTX-M-2 on plas...
| Autores: | , , , , |
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| Tipo de documento: | artigo |
| Estado: | Versão publicada |
| Data de publicação: | 2013 |
| País: | Argentina |
| Recursos: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositório: | CONICET Digital (CONICET) |
| Idioma: | inglês |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/1503 |
| Acesso em linha: | http://hdl.handle.net/11336/1503 |
| Access Level: | Acceso aberto |
| Palavra-chave: | Klebsiella pneumoniae Plasmidos Infeccion hospitalaria https://purl.org/becyt/ford/3.3 https://purl.org/becyt/ford/3 |
| Resumo: | Introduction: Insertion sequences such as ISCR1 promote capture, transposition and expression of blaCTX-M genes. Thus, gene dissemination in bacterial populations occurs rapidly. Objective: To determine the presence of ISCR1 sequence genes and their association with blaCTX-M-1 and blaCTX-M-2 on plasmids IncN and IncFIIA from K. pneumoniae of nosocomial origin, was determined. Materials and methods: Three strains of K. pneumoniae with reduced susceptibility to extendedspectrum cephalosporins were isolated from neonatal sepsis cases of nosocomial origin. Phenotypic tests showed the presence of ESBLs. Plasmids were isolated and classified according to incompatibility groups by PCR replicon typing. Detection and association of ISCR1 with blaCTX-M genes were determined by PCR and direct sequencing through the use of several sets of PCR primers. Results: All strains showed phenotypic profile consistent with ESBL-producing transferred by conjugation. PCR amplification assay for CTX-M together with sequencing analysis revealed thatstrains carrying blaCTX-M-1 y blaCTX-M-2 genes were localized in plasmids of approximately 150 kb related to IncN and IncFIIA groups, respectively. ISCR1 was found upstream and associated with blaCTX-M-1 y blaCTX-M genes. Conclusion. Thus far, this is the first Venezuelan report, in which ISCR1 presence is closely related to blaCTX-M-1 y blaCTX-M-2 gene mobilization in IncN and IncFIIA conjugative plasmids located in K. pneumonaiae strains circulating at a neonatal high risk unit. |
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