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Published on: September 5, 2013
Emergence of mcr-8.1-bearing MDR-hypervirulent Klebsiella pneumoniae ST307
Jie Sheng1,2, Rory Cave3, Mary M Ter-Stepanyan4,5
1School of Basic Medical Sciences, Chongqing Medical University, Chongqing, China.
Abstract:
We report for the first time whole-genome sequencing of four multidrug-resistant sequence type (ST) 307 Klebsiella pneumoniae recovered from patients in two hospitals in Armenia. Comparative genomic analysis revealed that the isolates were closely related, with a maximum of 39 single nucleotide polymorphism (SNP) differences in the core genome. All Armenian isolates carried the integrative and conjugative element ICEKp4, which bears the yersiniabactin locus, and shared a common evolutionary origin, diverging around 2005 (95% CI: 1999 to 2011). Antibiotic susceptibility testing showed resistance to several antibiotics, including ampicillin, amoxicillin-clavulanic acid, cefepime, ceftazidime, norfloxacin, levofloxacin, and chloramphenicol. Specifically, isolates designated as ARM03 and ARM06 were resistant to piperacillin-tazobactam, ARM04 and ARM05 had intermediate resistance to both piperacillin-tazobactam and imipenem, and ARM03 showed intermediate resistance to amikacin. We further identified antimicrobial resistance (AMR) genes in four Armenian isolates, including blaOXA-1, blaTEM-1D, blaSHV-28, dfrA14, tet(A), sul2, qnrB1, aac(6´)-Ib-cr, strA, strB and the extended-spectrum β-lactamase gene blaCTX-M-15. Additionally, ARM03 and ARM06 also obtained dfrA5, sul1, sul3, cmlA1, mphA, aph3-Ia and the unique colistin resistance gene mcr-8.1, which was absent in all other publicly available ST307 isolates. These two isolates also acquired aerobactin siderophore-encoding gene clusters (iucABCD-iutA) and the hypermucoidy locus rmpADC (ARM06 had rmpA fragment). ARM04 and ARM05, as well as ARM03 and ARM06, had nearly identical AMR and virulence genes, along with similar plasmid replicon profiles, respectively. Our findings suggest that a transmission event occurred between the two hospitals in Armenia, likely facilitated by patients or community members, during which K. pneumoniae ST307 isolates acquired plasmids carrying AMR and virulence genes.IMPORTANCEMultidrug-resistant (MDR) Klebsiella pneumoniae sequence type (ST) 307 has emerged as a high-risk clone associated with hospital- and community-acquired infections, posing a major threat to global public health. We report in-depth comparative genomics analyses of K. pneumoniae ST307 isolates recovered from patients in Armenia. The unique colistin resistance gene mcr-8.1 identified in ARM03 and ARM06 was absent in all other ST307 isolates obtained from the publicly available data sets. ARM03 and ARM06 also acquired aerobactin siderophore-encoding gene clusters (iucABCD-iutA) and the hypermucoidy locus rmpADC (ARM06 possessed incomplete rmpA fragment). Our findings suggest that a transmission event has occurred between two hospitals in Armenia either through patients or community members. In addition, the Armenian isolates obtained plasmids carrying virulence and AMR genes during the transmission event. Our study emphasises the importance of genomic surveillance of this emerging MDR-hypervirulent pathogen to provide early interventions.
Insights
Whole-genome sequencing of multidrug-resistant Klebsiella pneumoniae ST307 in Armenia revealed a common origin and plasmid-mediated spread of antibiotic resistance genes, including a unique colistin resistance gene (mcr-8.1). This highlights the need for genomic surveillance of this high-risk pathogen.
Area of Science:
- Genomics
- Microbiology
- Infectious Diseases
Background:
- Multidrug-resistant (MDR) Klebsiella pneumoniae sequence type (ST) 307 is a significant global health threat, causing both hospital- and community-acquired infections.
- Understanding the genomic epidemiology of K. pneumoniae ST307 is crucial for effective control and intervention strategies.
Purpose of the Study:
- To perform whole-genome sequencing and comparative genomic analysis of MDR K. pneumoniae ST307 isolates from Armenia.
- To investigate the evolutionary origins, antimicrobial resistance (AMR) profiles, and virulence factors of these isolates.
- To identify potential transmission events and the role of plasmids in the spread of AMR and virulence genes.
Main Methods:
- Whole-genome sequencing of four K. pneumoniae ST307 isolates from Armenian hospitals.
- Comparative genomic analysis to determine genetic relatedness and identify key genetic elements.
- Antibiotic susceptibility testing and identification of antimicrobial resistance (AMR) and virulence genes.
Main Results:
- The Armenian K. pneumoniae ST307 isolates were closely related, sharing a common evolutionary origin around 2005.
- Isolates exhibited resistance to multiple antibiotics and carried various AMR genes, including the extended-spectrum beta-lactamase gene blaCTX-M-15.
- Two isolates (ARM03 and ARM06) uniquely harbored the colistin resistance gene mcr-8.1, aerobactin siderophore genes, and hypermucoid genes, suggesting acquisition via plasmids.
Conclusions:
- A transmission event likely occurred between two Armenian hospitals, facilitated by patients or community members.
- Plasmids carrying AMR and virulence genes played a significant role in the dissemination of K. pneumoniae ST307 in Armenia.
- Genomic surveillance of MDR-hypervirulent K. pneumoniae ST307 is essential for early detection and intervention.
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