4.6 Article

Studies on the Transmission of a Tigecycline Resistance-Mediating tet(A) Gene Variant from Enterobacter hormaechei via a Two-Step Recombination Process

期刊

MICROBIOLOGY SPECTRUM
卷 10, 期 3, 页码 -

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/spectrum.00496-22

关键词

tigecycline; resistance; Enterobacter hormaechei; tet(A) variant; transmission; antibiotic resistance; antimicrobial agents; dissemination; plasmid-mediated resistance; resistance genes

资金

  1. National Natural Science Foundation of China [32172915]
  2. Henan outstanding foreign scientist studio [GZS2022010]
  3. German Federal Ministry of Education and Research (BMBF), Research Network Zoonotic Infectious Diseases [01KI1727D]

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This study investigates the transfer and recombination events of a tet(A) variant conferring tigecycline resistance in Enterobacter hormaechei. The results show that the tet(A) variant was present in E. hormaechei G17 and transferred between plasmids in a two-step recombination process. This transfer of resistance genes enhances the dissemination of tigecycline resistance and compromises the effectiveness of treatment for E. hormaechei infection.
To investigate the contribution of a tet(A) variant to tigecycline resistance in Enterobacter hormaechei and the recombination events that occurred during transmission of this variant. MICs were determined by broth microdilution. E. hormaechei G17 was characterized by PCR, transfer assay, S1-PFGE, Southern blot hybridization, and WGS analysis. A tet(A) variant conferring resistance to tigecycline was present in E. hormaechei G17. This strain harbored two resistance plasmids (pG17-1, 264,084 bp and pG17-Z 68,610 bp) and its E. coil transformant T-m-G17(TGC) one resistance plasmid (pTm-G17, 93,013 bp). The comparative analysis of pG17-1, pG17-2, and pTm-G17 showed that a tet(A) variant-carrying multiresistance gene cluster (similar to 23 kb) originating from pG17-1 had integrated into pG17-2, forming the novel plasmid pTm-G17. In a first step, this multiresistance gene cluster was excised from pG17-1 by recombination of homologous sequences, including Delta TnAs1 at both termini, thereby generating an unconventional circularizable structure (UCS). In a second step, this UCS integrated into pG17-2 via recombination between homologous sequences, including 1526 present on both, the UCS and pG17-2, thereby giving rise to the new plasmid pTm-G17. In summary, a tet(A) variant conferring resistance to tigecycline was reported in E. hormaechei. Transfer of a tet(A) variant-carrying multiresistance gene cluster between plasmids occurred in a two-step recombination process, in which homologous sequences, including either Delta TnAs1 or 1526, were involved. IMPORTANCE Tigecycline is an important last-resort broad spectrum antimicrobial agent. This study describes the two-step recombination processes resulting in the transfer of the tet(A) variant gene between different plasmids in E. hormaechei, which depicts the role of recombination processes in the generation of UCSs and new plasmids, both carrying a tet(A) variant conferring resistance to tigecycline. Such processes enhance the dissemination of resistance genes, which is of particular relevance for resistance genes, such as the tet(A) variant. The presence and transmission of a tet(A) variant in E. hormaechei will compromise the efficacy of tigecycline treatment for E. hormaechei associated infection.

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