| Literature DB >> 33373881 |
Chong Chen1, Chao-Yue Cui1, Xiao-Ting Wu1, Liang-Xing Fang2, Qian He1, Bing He1, Teng-Fei Long1, Xiao-Ping Liao2, Liang Chen3, Ya-Hong Liu2, Jian Sun4.
Abstract
The recent emergence of plasmid-mediated tigecycline resistance gene tet(X) has challenged the clinical effectiveness of tigecycline as a last-resort treatment option. During 2017-2018, 336 fecal samples from sick ducks, pigs, chickens and geese in Guangdong, China, were screened for tet(X)-positive Acinetobacter baumannii strains. Their activities on tetracyclines were determined by microbiological degradation and mass spectrometry, followed by susceptibility testing, sequence typing, gene transfer, molecular location and genomic DNA sequencing analyses. A total of 10 tet(X)-positive A. baumannii strains were isolated from ducks and chickens, including eight plasmid-borne tet(X5)-positive and two chromosomal tet(X6)-positive isolates. All of them exhibited good degradation activities on tetracyclines by hydroxylation at C11a and were multidrug-resistant to tigecycline, tetracycline, florfenicol, ciprofloxacin and trimethoprim/sulfamethoxazole. Genetically, they belonged to two sequence types (ST355, n = 8; ST1980, n = 2) that were consistent with their pulsotypes, revealing a clonal spread of ST355 A. baumannii. An ISCR2- or IS26-mediated tet(X) transposition structure, homologous to those of clinical A. baumannii strains, was also identified and ISCR2 could transfer tet(X5) into the recipient Acinetobacter baylyi ADP1 at a frequency of (1.8 ± 0.3)×10-6. Therefore, more efforts are needed to evaluate the clinical impact of these tigecycline resistance genes.Entities:
Keywords: A. baumannii; Clonal spread; IS26; ISCR2; Tet(X); Tigecycline resistance
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Year: 2020 PMID: 33373881 DOI: 10.1016/j.vetmic.2020.108954
Source DB: PubMed Journal: Vet Microbiol ISSN: 0378-1135 Impact factor: 3.293