4.2 Article

Distinctive Mobile Genetic Elements Observed in the Clonal Expansion of Carbapenem-Resistant Klebsiella pneumoniae in India

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MICROBIAL DRUG RESISTANCE
卷 27, 期 8, 页码 1096-1104

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MARY ANN LIEBERT, INC
DOI: 10.1089/mdr.2020.0316

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K; pneumoniae; India; MLST; ST231; ST23; OXA48-like; colistin

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This study identified a high prevalence of multidrug-resistant K. pneumoniae in India, with OXA48-like carbapenemases being the main drivers of resistance. The predominant sequence type among OXA48-like producers was ST231, while NDM producers and NDM+OXA48-like producers were primarily associated with ST14. Additionally, a significant portion of CR K. pneumoniae exhibited colistin resistance, with plasmid analysis revealing diverse associations between carbapenemase-carrying genes and plasmid types.
Background: Klebsiella pneumoniae (Kp), a common multidrug-resistant pathogen, causes a wide spectrum of nosocomial infections with high rates of morbidity and mortality. The emergence of pan drug-resistant international high-risk clones such as ST258, ST14, ST15, ST147, and ST101 is a global concern. This study was performed to investigate the carbapenemases, the plasmid profile, and the clonal relationship among Indian K. pneumoniae. Materials and Methods: A total of 290 K. pneumoniae isolates from seven centers in India were characterized to determine sequence types (STs) and carbapenemases. A subset of isolates was subjected to whole genome sequencing and hybrid genome assembly to obtain the complete genome. Plasmids carrying carbapenemases were characterized to determine the dissemination of carbapenem-resistant (CR) K. pneumoniae. Results: From this study, 75 different STs were observed with ST231 being predominant. About 79% of the analyzed isolates were CR with 59% (n = 136) producing OXA48-like carbapenemases. While ST231 was the predominant clone among the OXA48-like producers; NDM producers and NDM+OXA48-like producers were mostly associated with ST14. Interestingly, 61% (n = 138) of the total CR K. pneumoniae were colistin resistant, belonging to 22 different STs. Plasmid profiling shows that bla(OXA48-like) was exclusively carried by ColKP3, whereas bla(NDM) was associated with IncFII-like plasmids. Conclusion: The highly mosaic genome of K. pneumoniae coupled with the diverse ecological niches in India makes it a hotspot for antimicrobial resistance, leading to increased morbidity and mortality. Extensive molecular surveillance of the clonal spread of K. pneumoniae could help in understanding AMR dynamics and thus rework therapeutic management.

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