Genomic insights into blaNDM-carrying carbapenem-resistant Klebsiella pneumoniae clinical isolates from a university hospital in Thailand

被引:14
作者
Chukamnerd, Arnon [1 ]
Pomwised, Rattanaruji [2 ]
Jeenkeawpiam, Kongpop [3 ]
Sakunrang, Chanida [3 ]
Chusri, Sarunyou [1 ,4 ]
Surachat, Komwit [1 ,3 ]
机构
[1] Prince Songkla Univ, Fac Med, Dept Biomed Sci & Biomed Engn, Hat Yai, Thailand
[2] Prince Songkla Univ, Fac Sci, Div Biol Sci, Hat Yai, Thailand
[3] Prince Songkla Univ, Fac Sci, Mol Evolut & Computat Biol Res Unit, Hat Yai, Thailand
[4] Prince Songkla Univ, Fac Med, Dept Internal Med, Div Infect Dis, Hat Yai, Thailand
关键词
Carbapenem-resistant Klebsiella pneumoniae; bla(NDM); Bioinformatics tool; Antimicrobial resistance; Whole-genome sequencing; RESTRICTION-MODIFICATION SYSTEMS; QUINOLONE RESISTANCE; INCFII PLASMID; EFFLUX PUMPS; ENTEROBACTERIACEAE; SUSCEPTIBILITY; IDENTIFICATION; MECHANISMS; EVOLUTION; OXA-232;
D O I
10.1016/j.micres.2022.127136
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The emergence of carbapenem-resistant Klebsiella pneumoniae (CRKP) isolates is a serious threat to global health. Here, we elucidate the genetic features of blaNDM-carrying CRKP clinical isolates from a university hospital in Thailand. The entire genomes of 19 CRKP isolates were extracted and then sequenced using the MGISEQ200 platform. Using various bioinformatics tools, we analyzed the antimicrobial resistance (AMR), virulence factors, gene transfer, bacterial defense mechanisms, and genomic diversity of the CRKP isolates. The sequence type (ST) 16 was found in most of the isolates, along with carriages of the blaNDM-1, blaOXA-232, and blaCTX-M-15 genes. The IncFIB(pQil), Col440II, and ColKP3 plasmids were identified with high frequency. The CRKP isolates harbored genes encoding for virulence factors such as adherence, biofilm formation, immune evasion, and iron uptake. The CRISPR-Cas region in the CRKP9 isolate consisted of 28 distinct spacer sequences. The genomes of the CRKP isolates presented restriction-modification (R-M) sites (M.Kpn34618Dcm and M.Kpn928I) and integrated bacteriophage genomes (Klebsiella phage ST16-OXA48phi5.4 and Enterobacteria phage mEp390). Bottromycin and sactipeptides were also identified. The isolates could be separated into three clades according to STs and pairwise single nucleotide polymorphism (SNP) distance. Pairwise average nucleotide identity (ANI) values revealed intra-species. These findings support the importance of whole-genome sequencing (WGS) to the rapid and accurate genomic analysis of clinical isolates of CRKP.
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页数:12
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