脓肿分枝杆菌复合菌株的分子鉴定以及对大环内酯类和氨基糖苷类药物耐药性的测定。

Polish journal of microbiology Pub Date : 2023-12-16 eCollection Date: 2023-12-01 DOI:10.33073/pjm-2023-048
Katarzyna Kania, Katarzyna Wόjcik, Joanna Czekajewska, Magdalena Grzesiak, Karolina Klesiewicz
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引用次数: 0

摘要

脓肿分枝杆菌复合体(MABC)是快速生长分枝杆菌(RGM)中最重要的致病菌群之一,它包括三个亚种:脓肿分枝杆菌亚种、脓肿分枝杆菌亚种和脓肿分枝杆菌亚种。本研究的目的是分析2018年至2021年期间从波兰马洛波利斯卡地区患者体内分离出的其他非结核分枝杆菌中MABC的流行情况,并确定其亚种以及对大环内酯类和氨基糖苷类药物产生耐药性的分子机制。MABC的发病率为5.4%(12/223)。八株菌株被归类为脓肿疽杆菌亚种,三株为脓肿疽杆菌亚种,一株为脓肿疽杆菌亚种。分子分析表明,8 株脓肿 M. 亚种对大环内酯类药物产生抗药性,与 erm(41)T28 基因突变有关。一株脓肿霉菌亚种对大环内酯类(erm(41)T28 和 rrl 基因同时发生两个突变)和氨基糖苷类(rrs 基因发生点突变)产生耐药性。一株脓肿霉菌亚种对大环内酯类耐药(erm(41)T28 突变),而对氨基糖苷类没有突变。M. abscessus subsp. massiliense没有发现突变。脓肿霉菌对克拉霉素的耐药性很高,因此急需采用基于药敏性的治疗方法。通过分子测定氨基糖苷类和大环内酯类药物的耐药机制,可以快速准确地实施有针对性的治疗。
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Molecular Identification of Strains within the Mycobacterium abscessus Complex and Determination of Resistance to Macrolides and Aminoglycosides.

One of the most relevant and pathogenic groups among the rapidly growing mycobacteria (RGM) is Mycobacterium abscessus complex (MABC) that includes three subspecies: M. abscessus subsp. abscessus, M. abscessus subsp. bolletii, and M. abscessus subsp. massiliense. The aim of this study was the analysis of prevalence of MABC among other non-tuberculous mycobacteria isolated from patients in the Malopolska Region of Poland, between 2018 and 2021, as well as determination of their subspecies and molecular mechanisms of resistance to macrolides and aminoglycosides. The incidence of MABC was 5,4% (12/223). Eight strains were classified as M. abscessus subsp. abscessus, three as M. abscessus subsp. massiliense and one M. abscessus subsp. bolletii. Molecular analysis showed resistance to macrolides for eight strains of M. abscessus subsp. abscessus associated with erm(41)T28 gene mutations. One strain of M. abscessus subsp. abscessus showed resistance to macrolides (two mutations simultaneously: in erm(41)T28 and rrl genes) and aminoglycosides (point mutation in rrs gene). One strain of M. abscessus subs. bolletii was resistant to macrolides (erm(41)T28 mutation), whereas presented no mutations for aminoglycosides. M. abscessus subsp. massiliense reveal no mutations. High clarithromycin resistance of M. abscessus, determines the urgent need for susceptibility-based treatment. Molecular determination of resistance mechanisms to aminoglycosides and macrolides enables fast and accurate targeted treatment implementation.

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