Genomic epidemiology and ceftazidime-avibactam high-level resistance mechanisms of Pseudomonas aeruginosa in China from 2010 to 2022.

IF 8.4 2区 医学 Q1 IMMUNOLOGY Emerging Microbes & Infections Pub Date : 2024-12-01 Epub Date: 2024-03-11 DOI:10.1080/22221751.2024.2324068
Xi Li, Longjie Zhou, Tailong Lei, Xiaofan Zhang, Jiayao Yao, Jintao He, Haiyang Liu, Heng Cai, Jingshu Ji, Yiwei Zhu, Yuexing Tu, Yunsong Yu, Hua Zhou
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Abstract

Ceftazidime-avibactam (CZA) resistance is a huge threat in the clinic; however, the underlying mechanism responsible for high-level CZA resistance in Pseudomonas aeruginosa (PA) isolates remains unknown. In this study, a total of 5,763 P. aeruginosa isolates were collected from 2010 to 2022 to investigate the ceftazidime-avibactam (CZA) high-level resistance mechanisms of Pseudomonas aeruginosa (PA) isolates in China. Fifty-six PER-producing isolates were identified, including 50 isolates carrying blaPER-1 in PA, and 6 isolates carrying blaPER-4. Of these, 82.1% (46/56) were classified as DTR-PA isolates, and 76.79% (43/56) were resistant to CZA. Importantly, blaPER-1 and blaPER-4 overexpression led to 16-fold and >1024-fold increases in the MICs of CZA, respectively. WGS revealed that the blaPER-1 gene was located in two different transferable IncP-2-type plasmids and chromosomes, whereas blaPER-4 was found only on chromosomes and was carried by a class 1 integron embedded in a Tn6485-like transposon. Overexpression of efflux pumps may be associated with high-level CZA resistance in blaPER-1-positive strains. Kinetic parameter analysis revealed that PER-4 exhibited a similar kcat/Km with ceftazidime and a high (∼3359-fold) IC50 value with avibactam compared to PER-1. Our study found that overexpression of PER-1 combined with enhanced efflux pump expression and the low affinity of PER-4 for avibactam contributes to high-level resistance to CZA. Additionally, the Tn6485-like transposon plays a significant role in disseminating blaPER. Urgent active surveillance is required to prevent the further spread of high-level CZA resistance in DTR-PA isolates.

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2010-2022年中国铜绿假单胞菌基因组流行病学及头孢他啶-阿维菌素高水平耐药机制。
头孢他啶-阿维巴坦(CZA)耐药性是临床上的一个巨大威胁;然而,铜绿假单胞菌(Pseudomonas aeruginosa,PA)分离株对头孢他啶-阿维巴坦(CZA)产生高水平耐药性的根本机制仍然未知。本研究从2010年至2022年共收集了5,763株铜绿假单胞菌分离株,调查了中国铜绿假单胞菌(PA)分离株对头孢他啶-阿维巴坦(CZA)的高水平耐药机制。研究发现了56株产生PER的分离株,包括50株携带blaPER-1的PA分离株和6株携带blaPER-4的PA分离株。其中,82.1%(46/56)被归类为 DTR-PA 分离物,76.79%(43/56)对 CZA 具有耐药性。重要的是,blaPER-1 和 blaPER-4 的过表达分别导致 CZA 的 MICs 增加了 16 倍和 >1024 倍。WGS显示,blaPER-1基因位于两个不同的可转移IncP-2型质粒和染色体上,而blaPER-4只存在于染色体上,由一个嵌入Tn6485类转座子的1类整合子携带。外排泵的过度表达可能与 blaPER-1 阳性菌株的高水平 CZA 抗性有关。动力学参数分析表明,与 PER-1 相比,PER-4 与头孢他啶的 kcat/Km 相似,与阿维菌素的 IC50 值较高(3359 倍)。我们的研究发现,PER-1的过表达加上外排泵表达的增强以及PER-4对阿维菌素的低亲和力导致了对CZA的高水平耐药性。此外,Tn6485 样转座子在传播 blaPER 方面发挥了重要作用。为防止 DTR-PA 分离物对 CZA 的高水平耐药性进一步扩散,需要进行紧急的积极监控。
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来源期刊
Emerging Microbes & Infections
Emerging Microbes & Infections IMMUNOLOGY-MICROBIOLOGY
CiteScore
26.20
自引率
2.30%
发文量
276
审稿时长
20 weeks
期刊介绍: Emerging Microbes & Infections is a peer-reviewed, open-access journal dedicated to publishing research at the intersection of emerging immunology and microbiology viruses. The journal's mission is to share information on microbes and infections, particularly those gaining significance in both biological and clinical realms due to increased pathogenic frequency. Emerging Microbes & Infections is committed to bridging the scientific gap between developed and developing countries. This journal addresses topics of critical biological and clinical importance, including but not limited to: - Epidemic surveillance - Clinical manifestations - Diagnosis and management - Cellular and molecular pathogenesis - Innate and acquired immune responses between emerging microbes and their hosts - Drug discovery - Vaccine development research Emerging Microbes & Infections invites submissions of original research articles, review articles, letters, and commentaries, fostering a platform for the dissemination of impactful research in the field.
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