4.7 Article

Comparative phylogenomics of ESBL-, AmpC- and carbapenemase-producing Klebsiella pneumoniae originating from companion animals and humans

Journal

JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Volume 77, Issue 5, Pages 1263-1271

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jac/dkac041

Keywords

-

Funding

  1. Institut Pasteur
  2. ANSES
  3. MedVetKlebs project, a component of One Health European Joint Programme EJP - European Union's Horizon 2020 research and innovation program [773830]
  4. Pasteur-Roux fellowship from Institut Pasteur

Ask authors/readers for more resources

This study performed comparative phylogenomics on a large collection of multidrug-resistant K. pneumoniae recovered from companion animals in France. The results showed the transmission of K. pneumoniae clones between animals and humans, suggesting the circulation of clones at the country level.
Background WHO considers ESBL- and carbapenemase-producing Klebsiella pneumoniae a major global concern. In animals, ESBL- and carbapenemase-producing K. pneumoniae of human-related ST11, ST15 and ST307 have been reported, but not in the context of large WGS-based One Health investigations. Objectives To perform comparative phylogenomics on a large collection of multidrug-resistant (MDR) K. pneumoniae recovered from diseased companion animals and humans. Methods MDR K. pneumoniae (n = 105) recovered from companion animals in France during 2010-18 were phenotypically characterized. All isolates were whole-genome sequenced using the NovaSeq technology and phylogenomic analysis across animal and human K. pneumoniae was performed using appropriate pipelines. Results bla (CTX-M-15), bla(DHA-1) and bla(OXA-48) were strongly associated with IncFIIk, IncR and IncL plasmids, respectively. When compared with human K. pneumoniae genomes, four groups of closely related French human and animal isolates belonging to ST11, ST15 and ST307 were detected, suggesting the circulation of clones between the human and animal sectors at country level. A large cluster of 31 ST11-KL105 animal isolates from France and Switzerland suggested it corresponds to a sub-lineage that is particularly well-adapted to the animal host. Conclusions This study demonstrates the spread of bla(CTX-M-15)-carrying ST15 and ST307, and bla(DHA-1)-carrying ST11 K. pneumoniae clones in animal populations. ST11 was the main vector of bla(OXA-48)/IncL, despite the absence of carbapenem use in French animals. Comparative phylogenomics suggests cross-transmission of K. pneumoniae sub-lineages more prone than others to colonize/infect the animal host. Our data also evidenced the emergence of convergent hypervirulent and MDR K. pneumoniae in animals.

Authors

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

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available