Zhu Jiaying, Ju Yanmin, Zhou Xinyu, Chen Taoyu, Zhuge Xiangkai, Dai Jianjun
College of Pharmacy, China Pharmaceutical University, Nanjing, China.
Department of Nutrition and Food Hygiene, School of Public Health, Nantong University, Nantong, Jiangsu, China.
Front Microbiol. 2023 Jul 19;14:1219733. doi: 10.3389/fmicb.2023.1219733. eCollection 2023.
Carbapenem-resistant (CRKP), particularly those with high virulence, cause invasive disease in clinical settings. An epidemiological investigation was conducted on the evolution, virulence, and antimicrobial resistance of CRKP isolates in two tertiary teaching hospitals in Jiangsu, China from November 2020 to December 2021. There were 31 different CRKP strains discovered. We performed whole genome sequencing (WGS) on 13 and -producing CRKP to reveal molecular characteristics. Five ST15/ST11 isolates had CRISPR-Cas systems. By conjugation tests, can be transmitted horizontally to . A conjugative pHN7A8-related multi-resistance plasmid (, , , , , and ) was first discovered in CRKP clinical isolates. Using bacteriological testing, a serum killing assay, and an infection model with , three ST11-K64 generating carbapenem-resistant hypervirulent (CR-hvKP) were identified. These strains harbored a virulent plasmid and an IncFII-family pKPC/pHN7A8 conjugative plasmid, which led to hypervirulence and resistance. One of these CR-hvKPs, which co-harbored , , , and genes, was first discovered. Importantly, this CR-hvKP strain also produced biofilm and had non-inferior fitness. The widespread use of ceftazidime/avibactam might provide this CR-hvKP with a selective advantage; hence, immediate action is required to stop its dissemination. Another important finding is the novel ST6136 in . Finally, the sterilization efficiency rates of FeC nanoparticles in CRKP were more than 98%. Furthermore, our novel antibacterial FeC nanoparticles may also provide a therapeutic strategy for infections.
耐碳青霉烯类肺炎克雷伯菌(CRKP),尤其是那些具有高毒力的菌株,在临床环境中会引发侵袭性疾病。2020年11月至2021年12月,对中国江苏省两家三级教学医院的CRKP分离株的进化、毒力和抗菌药物耐药性进行了流行病学调查。共发现31种不同的CRKP菌株。我们对13株产碳青霉烯酶的CRKP进行了全基因组测序(WGS)以揭示其分子特征。5株ST15/ST11分离株具有CRISPR-Cas系统。通过接合试验,blaKPC-2可水平转移至blaNDM-1。在CRKP临床分离株中首次发现了一种与接合性质粒pHN7A8相关的多重耐药质粒(blaKPC-2、blaNDM-1、blaOXA-48、blaCTX-M-15、blaTEM-1和blaSHV-12)。通过细菌学检测、血清杀菌试验以及利用小鼠建立感染模型,鉴定出3株产碳青霉烯酶的高毒力肺炎克雷伯菌(CR-hvKP,ST11-K64)。这些菌株携带一个毒力质粒和一个IncFII家族的pKPC/pHN7A8接合质粒,这导致了高毒力和耐药性。其中一株CR-hvKP首次被发现同时携带blaKPC-2、blaNDM-1、blaOXA-48、blaCTX-M-15和blaTEM-1基因。重要的是,该CR-hvKP菌株还能产生生物膜且适应性不弱。头孢他啶/阿维巴坦的广泛使用可能为这种CR-hvKP提供了选择优势;因此,需要立即采取行动阻止其传播。另一个重要发现是肺炎克雷伯菌中的新型ST6136。最后,FeC纳米颗粒对CRKP的杀菌效率超过98%。此外,我们新型的抗菌FeC纳米颗粒可能也为感染提供一种治疗策略。