1. Hypervirulence and biofilm production in KPC-2-producing Klebsiella pneumoniae CG258 isolated in Brazil.
- Author
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Araújo BF, Ferreira ML, Campos PA, Royer S, Gonçalves IR, da Fonseca Batistão DW, Fernandes MR, Cerdeira LT, Brito CS, Lincopan N, Gontijo-Filho PP, and Ribas RM
- Subjects
- Bacterial Proteins genetics, Brazil, Humans, Klebsiella pneumoniae genetics, Klebsiella pneumoniae physiology, Microbial Sensitivity Tests, beta-Lactamases genetics, Bacterial Proteins metabolism, Biofilms, Klebsiella Infections microbiology, Klebsiella pneumoniae enzymology, Klebsiella pneumoniae pathogenicity, beta-Lactamases metabolism
- 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.
- Published
- 2018
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