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肠杆菌科碳青霉烯类敏感临床分离株中异质性耐药的基因评估

Genetic Evaluation of Heteroresistance among Carbapenem-Susceptible Clinical Isolates of Enterobacterales.

作者信息

Koçer İpek, Eri Nmez Mehmet, Zer Yasemin

机构信息

Department of Medical Microbiology SANKO University School of Medicine, Gaziantep 27090, Türkiye.

Department of Medical Microbiology Gaziantep University School of Medicine, Gaziantep 27310, Türkiye.

出版信息

Can J Infect Dis Med Microbiol. 2024 Aug 26;2024:5014876. doi: 10.1155/2024/5014876. eCollection 2024.

Abstract

Carbapenems currently serve as the last line of defense when treating serious infections caused by multidrug-resistant Enterobacterale species; however, heteroresistance of these species is thought to cause failure in the treatment with these broad-spectrum antibiotics. This study was designed to determine the prevalence of carbapenem heteroresistance and associated genotypic modifications among phenotypically meropenem-susceptible and isolates. A total of 204 isolates of (: 118) and (: 86) from various clinical samples were included in this prospective experimental study. Identification and antimicrobial susceptibility testing of the isolates were performed by VITEK® (bioMérieux, France). Strains that were found susceptible to carbapenem group antibiotics (meropenem, imipenem, and ertapenem) with automated system were further investigated by disk diffusion method. The isolates with discrete colony growth within the clear inhibition zone among phenotypically meropenem-susceptible strains were tested for heteroresistance with the "gold standard" population analysis profile-area under the curve (PAP-AUC) method. In addition, heteroresistant isolates were analyzed for the presence of carbapenemase genes with in-house PCR method. The heteroresistance prevalence rate was 3.5% for and 18.1% for . The presence of heteroresistance in a total of 10 meropenem-susceptible isolates (, : 4; , : 6) was confirmed by the PAP-AUC method. The most frequently detected carbapenemase in heteroresistant isolates was OXA-48 (6/10), followed by NDM-1 (2/10). Meropenem is frequently preferred as initial empirical monotherapy in most of Gram-negative infections in adult and pediatric patients. The presence of heteroresistance against meropenem is too important to ignore, and for this reason, it seems beneficial to prefer combined treatment regimens in clinical practice.

摘要

碳青霉烯类药物目前是治疗由多重耐药肠杆菌科细菌引起的严重感染的最后一道防线;然而,这些细菌的异质性耐药被认为会导致这些广谱抗生素治疗失败。本研究旨在确定在表型对美罗培南敏感的 和 分离株中碳青霉烯类异质性耐药的流行情况及相关基因型改变。本前瞻性实验研究纳入了来自各种临床样本的总共204株 ( :118株)和 ( :86株)分离株。通过VITEK®(法国生物梅里埃公司)对分离株进行鉴定和抗菌药物敏感性测试。对自动系统检测显示对碳青霉烯类抗生素(美罗培南、亚胺培南和厄他培南)敏感的菌株,进一步采用纸片扩散法进行研究。在表型对美罗培南敏感的菌株中,对在清晰抑菌圈内有离散菌落生长的分离株,采用“金标准”群体分析谱-曲线下面积(PAP-AUC)法检测异质性耐药。此外,采用内部聚合酶链反应(PCR)方法分析异质性耐药分离株中碳青霉烯酶基因的存在情况。 的异质性耐药流行率为3.5%, 的为18.1%。通过PAP-AUC法证实了总共10株对美罗培南敏感的分离株( :4株; :6株)存在异质性耐药。在异质性耐药分离株中最常检测到的碳青霉烯酶是OXA-48(6/10),其次是NDM-1(2/10)。在大多数成人和儿童革兰阴性菌感染中,美罗培南常被优先用作初始经验性单药治疗。对美罗培南存在异质性耐药这一情况不容忽视,因此,在临床实践中选择联合治疗方案似乎是有益的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eea7/11368546/e0f9b27219ea/CJIDMM2024-5014876.001.jpg

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