中国城乡蝇源耐替加环素细菌的出现和基因组流行病学研究

IF 10.3 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Environment International Pub Date : 2024-11-01 DOI:10.1016/j.envint.2024.109099
Zelin Yan , Panpan Wang , Hanyu Wang , Jing Zhang , Yanyan Zhang , Yuchen Wu , Hongwei Zhou , Yan Li , Zhangqi Shen , Gongxiang Chen , Ruichao Li , Rong Zhang
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引用次数: 0

摘要

质粒介导的替加环素耐药基因,特别是 tet(X4) 和 tmexCD-toprJ 基因,因其可转移性而备受关注。本研究旨在调查作为抗菌素耐药基因重要储存库的苍蝇中与 tet(X) 和 tmexCD-toprJ 相关的耐药机制。研究共收集了 52 个对替加环素耐药的细菌分离物,其中 40 个(76.9%)和 12 个(23.1%)分别对 tet(X) 和 tmexCD-toprJ 呈阳性。耐替加环素细菌分离自中国不同的地理位置,其中以 tet(X4) 阳性的大肠埃希菌和 tmexCD1-toprJ1 阳性的肺炎克雷伯菌为主。农村地区的 tet(X) 阳性率明显高于城市地区(2.7% 对 0.3%;P <;0.001),而 tmexCD1-toprJ1 阳性率在城市和农村地区没有明显差异(0.2% 对 0.6%;P >;0.05)。大多数 tet(X) 阳性菌株(n = 40,100.0 %)和 11 株 tmexCD1-toprJ1 阳性菌株(91.7 %)表现出多重耐药性。通过全基因组测序分析确定了携带 tmexCD1-toprJ1 的 IncFIB(Mar)/IncHI1B 杂交质粒,该质粒主导了 tmexCD1-toprJ1 在肺炎双球菌中的传播。遗传背景分析表明,tmexCD1-toprJ1与IS26局部相关,IS26可能会加剧tmexCD1-toprJ1在不同细菌中的传播。此外,tmexCD1-toprJ1的基因结构中还含有多个抗菌药耐药基因,包括aph(3′)-Ic、sul1、blaDHA-1、blaCTX-M-5等,可赋予氨基糖苷类、磺胺类和碳青霉烯类耐药性。这项研究有助于深入了解替加环素耐药基因的流行病学和传播动态,为制定有针对性的干预策略提供信息,从而减少抗菌素耐药性的传播。
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Emergence and genomic epidemiology of tigecycline resistant bacteria of fly origin across urban and rural China
Plasmid-mediated tigecycline resistance genes, notably the tet(X) and tmexCD-toprJ genes, have garnered considerable attention due to their transferability. This study aims to investigate the prevalence and resistance mechanisms associated with tet(X) and tmexCD-toprJ in flies, which are important reservoirs of antimicrobial resistance genes. A total of 52 tigecycline resistant bacterial isolates were collected, among which 40 (76.9 %) and 12 (23.1 %) were positive for tet(X) and tmexCD-toprJ, respectively. Tigecycline resistant bacteria were isolated from diverse geographical locations in China, with tet(X4)-positive Escherichia coli and tmexCD1-toprJ1-positive Klebsiella pneumoniae dominant among the isolates. The prevalence of tet(X) in rural area was significantly higher than that in urban area (2.7 % vs. 0.3 %; P < 0.001), while the prevalence of tmexCD1-toprJ1 shows no significant difference between urban and rural areas (0.2 % vs. 0.6 %; P > 0.05). Most tet(X)-positive strains (n = 40, 100.0 %), and 11(91.7 %) of the tmexCD1-toprJ1-positive strains exhibited multi-drug resistance. The IncFIB(Mar)/IncHI1B hybrid plasmid carrying tmexCD1-toprJ1 was identified by whole-genome sequencing analysis, which dominated the transmission of tmexCD1-toprJ1 in K. pneumoniae. Genetic context analysis showed that tmexCD1-toprJ1 was related locally to IS26, and IS26 may exacerbate the spread of tmexCD1-toprJ1 in different bacteria. In addition, the genetic structure of tmexCD1-toprJ1 also contains several antimicrobial resistance genes, including aph(3′)-Ic, sul1, blaDHA-1, blaCTX-M−5, etc., conferring resistance to aminoglycosides, sulfonamides, and carbapenems. This study provides insights into the epidemiology and transmission dynamics of tigecycline resistance genes, informing targeted intervention strategies to mitigate antimicrobial resistance dissemination.
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来源期刊
Environment International
Environment International 环境科学-环境科学
CiteScore
21.90
自引率
3.40%
发文量
734
审稿时长
2.8 months
期刊介绍: Environmental Health publishes manuscripts focusing on critical aspects of environmental and occupational medicine, including studies in toxicology and epidemiology, to illuminate the human health implications of exposure to environmental hazards. The journal adopts an open-access model and practices open peer review. It caters to scientists and practitioners across all environmental science domains, directly or indirectly impacting human health and well-being. With a commitment to enhancing the prevention of environmentally-related health risks, Environmental Health serves as a public health journal for the community and scientists engaged in matters of public health significance concerning the environment.
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