Bodunova Natalia, Tsapkova Larisa, Polyakova Vera, Baratova Irina, Rumyantsev Konstantin, Dekhnich Natalia, Nikolskaya Karina, Chebotareva Margarita, Voynovan Irina, Parfenchikova Elena, Pronina Galina, Chernikova Ekaterina, Bordin Dmitry
A.S. Loginov Moscow Clinical Scientific Center, 111123 Moscow, Russia.
Department of Faculty Therapy, Smolensk State Medical University of the Ministry of Health of Russia, 214019 Smolensk, Russia.
Curr Issues Mol Biol. 2024 Jun 29;46(7):6665-6674. doi: 10.3390/cimb46070397.
The Maastricht VI/Florence consensus recommends, as one of the measures to enhance the efficacy of infection eradication, a personalized treatment approach involving the selection of an antimicrobial agent based on the pre-determined resistance of To address the need to develop test systems for personalized drug selection, this study was designed to analyze the molecular resistance of using a newly developed Sanger sequencing test platform. The characteristics of the test system were determined on 25 pure culture samples of with known resistance. Sensitivity and specificity for detecting resistance to clarithromycin was 100% and those to levofloxacin were 93% and 92%, respectively. The test system has been tested in real clinical practice on 112 -positive patients who had not previously received proton pump inhibitors (PPIs) or antibacterial drugs. Mutations indicating resistance to clarithromycin were found in 27 (24%) samples and those indicating resistance to levofloxacin were found in 26 (23%) samples. Double resistance was observed in 16 (14%) samples. The most common mutations leading to clarithromycin resistance were 2143G and 2142G and to levofloxacin resistance-261A and 271A in the gene, which account for 69% of all identified genetic determinants in levofloxacin-resistant bacteria. Thus, a personalized approach to the selection of eradication therapy based on the detection of bacterial resistance before prescribing first-line therapy could help to avoid the prescription of ineffective eradication therapies and, overall, contribute to the control of antibiotic resistance of .
马斯特里赫特VI/佛罗伦萨共识建议,作为提高根除感染疗效的措施之一,采用个性化治疗方法,即根据预先确定的耐药性选择抗菌药物。为满足开发个性化药物选择测试系统的需求,本研究旨在使用新开发的桑格测序测试平台分析[细菌名称]的分子耐药性。在25份已知耐药性的[细菌名称]纯培养样本上确定了该测试系统的特性。检测克拉霉素耐药性的敏感性和特异性分别为100%,检测左氧氟沙星耐药性的敏感性和特异性分别为93%和92%。该测试系统已在112例此前未接受过质子泵抑制剂(PPI)或抗菌药物的[细菌名称]阳性患者的实际临床实践中进行了测试。在27份(24%)样本中发现了表明对克拉霉素耐药的突变,在26份(23%)样本中发现了表明对左氧氟沙星耐药的突变。在16份(14%)样本中观察到双重耐药。导致克拉霉素耐药的最常见突变是[细菌名称]基因中的2143G和2142G,导致左氧氟沙星耐药的是261A和271A,它们占左氧氟沙星耐药细菌中所有已鉴定遗传决定因素的69%。因此,在开一线治疗药物之前基于检测细菌耐药性来选择[细菌名称]根除治疗的个性化方法,有助于避免开具无效的[细菌名称]根除治疗药物,并总体上有助于控制[细菌名称]的抗生素耐药性。