| Literature DB >> 29509136 |
Bruna Fuga Araújo1, Melina Lorraine Ferreira1, Paola Amaral de Campos1, Sabrina Royer1, Iara Rossi Gonçalves1, Deivid William da Fonseca Batistão2, Miriam Rodriguez Fernandes3, Louise Teixeira Cerdeira3, Cristiane Silveira de Brito1, Nilton Lincopan3, Paulo Pinto Gontijo-Filho1, Rosineide Marques Ribas1.
Abstract
In this study, we describe the frequency of virulence genes in Klebsiella pneumoniae carbapenemase-2-producing Klebsiella pneumoniae (KPC-KP), including hypervirulent (hv) and hypermucoviscous (hm) strains by whole-genome sequencing. We also evaluate the capacity for biofilm formation by using phenotypic techniques. The occurrence of several virulence genes (fimABCDEFGHIK, mrkABCDFHJ, ecpA, wabG, entB, ugE, irp1, irp2, traT, iutA and ureADE) and a high frequency of hvhmKPC-KP isolates was found. Most hospital-associated lineages of KPC-KP belong to the international clonal group 258 (CG258). Biofilm formation was a constant feature among 90.9 % of KPC-KP strains. This report suggests a close relationship between ST437 and weak biofilm production, given that all weakly biofilm-producing strains belonged to this sequence type. This also supports the dissemination of KPC-KP containing numerous virulence determinants belonging to the biofilm-producing CG258 type in Brazil, including hv and hm strains. These factors allow this pathogen to cause infections, leading to its rapid expansion and persistence in hospital settings.Entities:
Keywords: KPC-2; Klebsiella pneumoniae; WGS; biofilm; hypervirulence
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Year: 2018 PMID: 29509136 DOI: 10.1099/jmm.0.000711
Source DB: PubMed Journal: J Med Microbiol ISSN: 0022-2615 Impact factor: 2.472