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Identification of multiple transfer units and novel subtypes of tmexCD-toprJ gene clusters in clinical carbapenem-resistant Enterobacter cloacae and Klebsiella oxytoca.
Sun, Shijun; Wang, Qi; Jin, Longyang; Guo, Yifan; Yin, Yuyao; Wang, Ruobing; Bi, Lei; Zhang, Renfei; Han, Yungang; Wang, Hui.
Afiliación
  • Sun S; Department of Clinical Laboratory, Peking University People's Hospital, Beijing, China.
  • Wang Q; Department of Clinical Laboratory, Peking University People's Hospital, Beijing, China.
  • Jin L; Department of Clinical Laboratory, Peking University People's Hospital, Beijing, China.
  • Guo Y; Department of Clinical Laboratory, Peking University People's Hospital, Beijing, China.
  • Yin Y; Department of Clinical Laboratory, Peking University People's Hospital, Beijing, China.
  • Wang R; Department of Clinical Laboratory, Peking University People's Hospital, Beijing, China.
  • Bi L; Department of Clinical Laboratory, Zibo Central Hospital, Shandong, China.
  • Zhang R; Department of Clinical Laboratory, The Third Hospital of Mianyang, Sichuan Mental Health Center, Sichuan, China.
  • Han Y; Department of Clinical Laboratory, Henan Provincial Chest Hospital, Henan, China.
  • Wang H; Department of Clinical Laboratory, Peking University People's Hospital, Beijing, China.
J Antimicrob Chemother ; 77(3): 625-632, 2022 02 23.
Article en En | MEDLINE | ID: mdl-34893837
ABSTRACT

OBJECTIVES:

Tigecycline is a last-resort antibiotic used to treat lethal infections caused by carbapenem-resistant Enterobacterales; however, plasmid-borne tigecycline resistance tmexCD-toprJ gene clusters can confer tigecycline resistance. The aim of the study was to identify novel subtypes and the spread of tmexCD-toprJ.

METHODS:

Five non-duplicate isolates of different species, carrying tmexCD-toprJ gene clusters or novel subtypes, were isolated from patients across China between November 2018 and June 2019. WGS was performed using Illumina and Nanopore platforms. A phylogenetic tree was constructed using a dataset of 77 sequences carrying the tmexCD-toprJ gene clusters, 72 of which were downloaded from NCBI with a blastn identity cut-off of 95%.

RESULTS:

We detected six different transfer units and two novel subtypes (tmexC1D1.2-toprJ1 and tmexC2D2.2-toprJ2) of the tmexCD-toprJ gene clusters. Among the six transfer units, three were mediated by IS26, while the rest were presumably mediated by Tn5393, hypothetical integrases (xerD-hp clusters-umuC-integrases-tnfxB2-tmexC2D2-toprJ2-umuC) and hypothetical units (hp-hp-hp-tnfxB2-tmexC2D2.2-toprJ2-ΔTn5393-Tn6292). Moreover, two tmexCD-toprJ-like gene clusters co-located on the same plasmid with blaNDM in five isolates. Phylogenetic analysis revealed that tmexCD-toprJ gene clusters may have originated in Pseudomonas spp., being mainly distributed in Pseudomonas spp. and Klebsiella spp. (64/77). Most tmexCD-toprJ gene clusters in Enterobacterales were located on plasmids, indicating that the gene clusters have a high inter-species transfer risk after transfer to Enterobacterales.

CONCLUSIONS:

In summary, to the best of our knowledge, this is the first report of tmexCD-toprJ gene clusters being isolated from Enterobacter cloacae and Klebsiella oxytoca, revealing that these multiple transfer units should be further studied because of their clinical significance.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enterobacter cloacae / Klebsiella oxytoca Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: J Antimicrob Chemother Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enterobacter cloacae / Klebsiella oxytoca Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: J Antimicrob Chemother Año: 2022 Tipo del documento: Article País de afiliación: China