4.6 Article

Emergence of a NDM-1-producing ST25 Klebsiella pneumoniae strain causing neonatal sepsis in China

Journal

FRONTIERS IN MICROBIOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2022.980191

Keywords

CRKP; bla(NDM-1); ST25; neonatal sepsis; WGS

Categories

Funding

  1. National Natural Science Foundation of China
  2. Scientific Research Fund Project of Zhejiang Chinese Medical University
  3. Zhejiang Province Public Welfare Technology Application Research Project
  4. College Students Science and Technology Innovation Project (Xin Miao Talent Project) of Zhejiang Province
  5. [82072314]
  6. [2020ZG06]
  7. [LGN20H280002]
  8. [2021R410020]

Ask authors/readers for more resources

This study reports the first infection caused by bla(NDM-1)-positive ST25 Klebsiella pneumoniae in a neonatal unit. The strain was highly virulent and resistant to multiple antimicrobial agents. These findings highlight the need for stricter surveillance and more effective actions to prevent the dissemination of such K. pneumoniae strains in clinical settings, especially in neonatal wards.
Carbapenem-resistant Klebsiella pneumoniae (CRKP) seriously threaten the efficacy of modern medicine with a high associated mortality rate and unprecedented transmission rate. In this study, we isolated a clinical K. pneumoniae strain DY1928 harboring bla(NDM-1) from a neonate with blood infection. Antimicrobial susceptibility testing indicated that DY1928 was resistant to various antimicrobial agents, including meropenem, imipenem, ceftriaxone, cefotaxime, ceftazidime, cefepime, piperacillin-tazobactam, and amoxicillin-clavulanate. S1 nuclease-pulsed field gel electrophoresis (S1-PFGE), southern blot and conjugation experiment revealed that the bla(NDM-1) gene was located on a conjugative plasmid of IncA/C2 type with a 147.9 kb length. Whole-genome sequencing showed that there was a conservative structure sequence (bla(NDM-1)-ble-trpF-dsbD) located downstream of the bla(NDM-1) gene. Multilocus sequence typing (MLST) classified DY1928 as ST25, which was a hypervirulent K. pneumoniae type. Phylogenetic analysis of genomic data from all ST25 K. pneumoniae strains available in the NCBI database suggested that all bla(NDM-1) positive strains were isolated in China and had clinical origins. A mouse bloodstream infection model was constructed to test the virulence of DY1928, and 11 K. pneumoniae strains homologous to DY1928 were isolated from the feces of infected mice. Moreover, we found that DY1928 had a tendency to flow from the blood into the intestine in mice and caused multiple organ damage. To our knowledge, this is the first study to report an infection caused by bla(NDM-1)-positive ST25 K. pneumoniae in the neonatal unit. Our findings indicated that stricter surveillance and more effective actions were needed to reduce the risk of disseminating such K. pneumoniae strains in clinical settings, especially in neonatal wards.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available