4.4 Article

CTX-M-15-producing Klebsiella pneumoniae ST273 associated with nasal infection in a domestic cat

Journal

JOURNAL OF GLOBAL ANTIMICROBIAL RESISTANCE
Volume 28, Issue -, Pages 203-205

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jgar.2022.01.004

Keywords

Editor; Dr Marisa Haenni; Klebsiella pneumoniae; Extended-spectrum 13-lactamase; ESBL; CTX-M-15; Companion animals; Whole-genome sequencing

Funding

  1. Coordenacao de Aper-feicoamento de Pessoal de Nivel Superior -Brazil (CAPES) [001]
  2. CAPES-PrInt Project Omic sciences applied to the prevention of antimicrobial resistance at the human-animal-environment interface -a one health ap-proach [88881.311776/2018-01]
  3. Financeira de Estudos e Projetos (FINEP)
  4. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

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This study investigated the genetic context of expanded-spectrum 13-lactam resistance in a Klebsiella pneumoniae strain causing a hard-to-treat nasal infection in a domestic cat. The strain was found to carry multiple genes conferring resistance to various antimicrobial drugs. The results highlight the importance of horizontal gene transfer in the acquisition of antimicrobial resistance genes and emphasize the need for a One Health approach to understand the emergence and dissemination of antimicrobial resistance.
Objectives: The aim of this study was to investigate the genetic context of expanded-spectrum 13-lactam resistance in a Klebsiella pneumoniae strain causing a hard-to-treat nasal infection in a domestic cat. Methods: A K. pneumoniae isolate was recovered from a 4-year-old male cat hospitalised in a veterinary hospital in Paraiba, Northeastern Brazil. Following phenotypic confirmation of multidrug resistance by the disk diffusion method, the genome was sequenced using an Illumina MiSeq system. Multilocus sequence typing (MLST) and structural features related to antimicrobial resistance were determined by downstream bioinformatics analyses. Results: The strain was confirmed as sequence type 273 (ST273) K. pneumoniae harbouring a variety of genes conferring antimicrobial resistance to phenicols tetracyclines, aminoglycosides, 13-lactams, fosfomycin, sulfonamides and quinolones. Two plasmids were identified. Plasmid p114PB_I co-harboured a set of plasmid-borne resistance genes [ bla CTX-M -15 , bla TEM -1 , qnrS1, tetD, tetR, sul2, aph(6)-Id, aph(3 ') and cat2 ]. Notably, the multiresistance region was characterised as a chimeric plasmid structure sharing high sequence homology with several plasmids from Enterobacteriaceae. The second plasmid (p114PB_II) was characterised as a plasmid present in many genomes belonging to K. pneumoniae. Conclusion: The genetic context of the plasmid sequences harboured by a veterinary pathogenic K. pneumoniae isolate reveals the high complexity of horizontal gene transfer mechanisms in the acquisition of antimicrobial resistance genes. The emergence, dissemination and evolution of antimicrobial resistance must be investigated from a One Health perspective. (c) 2022 The Author(s). Published by Elsevier Ltd on behalf of International Society for Antimicrobial Chemotherapy. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )

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