| Literature DB >> 32122894 |
Chao-Yue Cui1,2, Chong Chen1,2, Bao-Tao Liu3, Qian He1,2, Xiao-Ting Wu1,2, Ruan-Yang Sun1,2, Yan Zhang1,2, Ze-Hua Cui1,2, Wen-Ying Guo1,2, Qiu-Lin Jia1,2, Cang Li1,2, Barry N Kreiswirth4, Xiao-Ping Liao1,2,5, Liang Chen4, Ya-Hong Liu1,2,5, Jian Sun6,2,5.
Abstract
Tigecycline serves as one of the antibiotics of last resort to treat multidrug-resistant (including carbapenem-resistant) pathogens. However, the recently emerged plasmid-mediated tigecycline resistance mechanism, Tet(X), challenges the clinical efficacy of this class of antibiotics. In this study, we detected 180 tet(X)-harboring Acinetobacter isolates (8.9%, n = 180) from 2,018 samples collected from avian farms and adjacent environments in China. Eighteen tet(X)-harboring isolates (10.0%) were found to cocarry the carbapenemase gene bla NDM-1, mostly from waterfowl samples (94.4%, 17/18). Interestingly, among six Acinetobacter strains, tet(X) and bla NDM-1 were found to colocalize on the same plasmids. Moreover, whole-genome sequencing (WGS) revealed a novel orthologue of tet(X) in the six isolates coharboring tet(X) and bla NDM-1 Inverse PCR suggested that the two tet(X) genes form a single transposable unit and may be cotransferred. Sequence comparison between six tet(X)- and bla NDM-1-coharboring plasmids showed that they shared a highly homologous plasmid backbone even though they were isolated from different Acinetobacter species (three from Acinetobacter indicus, two from Acinetobacter schindleri, and one from Acinetobacter lwoffii) from various sources and from different geological regions, suggesting the horizontal genetic transfer of a common tet(X)- and bla NDM-1-coharboring plasmid among Acinetobacter species in China. Emergence and spread of such plasmids and strains are of great clinical concern, and measures must be implemented to avoid their dissemination.Entities:
Keywords: Acinetobacter spp.; blaNDM-1zzm321990; coharboring plasmid; tet(X); tigecycline resistance; waterfowls
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Year: 2020 PMID: 32122894 PMCID: PMC7179582 DOI: 10.1128/AAC.02502-19
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191