4.5 Article

Novel chromosomal insertions of ISEcp1-blaCTX-M-15 and diverse antimicrobial resistance genes in Zambian clinical isolates of Enterobacter cloacae and Escherichia coli

出版社

BMC
DOI: 10.1186/s13756-021-00941-8

关键词

ISEcp1; bla(CTX-M); Chromosomal insertion; Extended spectrum beta-lactamase; Zambia; AMR; Enterobacter cloacae; Escherichia coli

资金

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT) in Japan [17H01679, 18K19436, 18K14672]
  2. Japan Society for the Promotion of Science [17H01679, 18K19436, 18K14672]
  3. AMED (Japan Program for Infectious Diseases Research and Infrastructure) [JP21wm0125008]
  4. World-leading Innovative and Smart Education (WISE)
  5. Japan International Cooperation Agency (JICA) scholarship for Advanced Training Program for Fostering Global Leaders on Infectious Disease Control to Build Resilience against Public Health Emergencies
  6. Grants-in-Aid for Scientific Research [18K19436, 18K14672, 17H01679] Funding Source: KAKEN

向作者/读者索取更多资源

The study revealed the co-occurrence of ISEcp1-bla(CTX-M-15) and multiple antimicrobial resistance genes on chromosomal insertions in Enterobacter cloacae and Escherichia coli, potentially facilitating the propagation of multidrug-resistant clones. The chromosomal integration of bla(CTX-M) in certain strains may play a role in the dissemination of antimicrobial resistance genes compared to the plasmid location.
Background: The epidemiology of extended-spectrum beta-lactamases (ESBLs) has undergone dramatic changes, with CTX-M-type enzymes prevailing over other types. bla(CTX-M) genes, encoding CTX-M-type ESBLs, are usually found on plasmids, but chromosomal location is becoming common. Given that bla(CTX-M)-harboring strains often exhibit multidrug resistance (MDR), it is important to investigate the association between chromosomally integrated bla(CTX-M) and the presence of additional antimicrobial resistance (AMR) genes, and to identify other relevant genetic elements. Methods: A total of 46 clinical isolates of cefotaxime-resistant Enterobacteriaceae (1 Enterobacter cloacae, 9 Klebsiella pneumoniae, and 36 Escherichia coli) from Zambia were subjected to whole-genome sequencing (WGS) using MiSeq and MinION. By reconstructing nearly complete genomes, bla(CTX-M) genes were categorized as either chromosomal or plasmid-borne. Results: WGS-based genotyping identified 58 AMR genes, including four bla(CTX-M) alleles (i.e., bla(CTX-M-14), bla(CTX-M-15), bla(CTX-M-27), and bla(CTX-M-55)). Hierarchical clustering using selected phenotypic and genotypic characteristics suggested clonal dissemination of bla(CTX-M) genes. Out of 45 bla(CTX-M) gene-carrying strains, 7 harbored the gene in their chromosome. In one E. cloacae and three E. coli strains, chromosomal bla(CTX-M-15) was located on insertions longer than 10 kb. These insertions were bounded by ISEcp1 at one end, exhibited a high degree of nucleotide sequence homology with previously reported plasmids, and carried multiple AMR genes that corresponded with phenotypic AMR profiles. Conclusion: Our study revealed the co-occurrence of ISEcp1-bla(CTX-M-15) and multiple AMR genes on chromosomal insertions in E. cloacae and E. coli, suggesting that ISEcp1 may be responsible for the transposition of diverse AMR genes from plasmids to chromosomes. Stable retention of such insertions in chromosomes may facilitate the successful propagation of MDR clones among these Enterobacteriaceae species.

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