Department of Microbiology, Faculty of Medicine & Health Sciences, SGT Medical College, Hospital & Research Institute, Budhera, Gurugram-122505, Haryana, India.
Department of Microbiology, Vardhman Mahaveer Medical College and Safdarjung Hospital, New Delhi- 110029, India.
J Med Microbiol. 2021 Aug;70(8). doi: 10.1099/jmm.0.001398.
Fluoroquinolone (FQ) resistant are classified as high priority pathogens by WHO. FQ resistance among Typhi has emerged rapidly and is predominantly mediated by mutations in the topoisomerase genes , and . Mutations in GyrA result in classical FQ resistance (DCS-NAR) i.e. decreased susceptibility to ciprofloxacin (MIC of 0.12 to 0.5 µg ml) (DCS) and resistance to nalidixic acid (NAR). Previously a nalidixic acid disc test was proposed for detection of DCS. Recently isolates with non-classical FQ resistance caused by plasmid-mediated quinolone resistance (PMQR) and mutations in GyrB have emerged. These mechanisms also result in DCS but are nalidixic acid susceptible (NAS) and thus pose diagnostic challenges. CLSI and EUCAST have recommended use of 5 µg pefloxacin discs for detection of DCS in . The CLSI and EUCAST recommendations for use of 5 µg pefloxacin for detection of DCS has not been validated on typhoidal and resistance mediated by GyrB mutation in species. The aim of the present study was to validate the performance of the 5 µg pefloxacin discs to detect isolates of . Typhi with DCS with special reference to GyrB mutations. A total of 180 clinical isolates of Typhi (2005-2014) were investigated for genetic mechanisms of resistance. Zone diameters for nalidixic acid (30μg), ciprofloxacin (5μg) and pefloxacin (5µg) and minimum inhibitory concentration (MIC) for ciprofloxacin were determined using CLSI guidelines. Performance of the three discs was evaluated to detect FQ resistance in . Typhi. Topoisomerase mutations in GyrB +/ ParC and GyrB were detected in 112 and 34 isolates respectively. Different mutations have a varied effect on the MIC for ciprofloxacin. The current breakpoints for susceptible (≤0.06 µg ml) and non-susceptible (≥0.125 µg ml), failed to detect all isolates with a resistance mechanism. Performance of both ciprofloxacin and pefloxacin discs were excellent compared to nalidixic acid in differentiating isolates with non-classical resistance mediated by GyrB from wild-type. The pefloxacin disc can be used to detect FQ resistance among . Typhi. This is the first report of validation of pefloxacin for detection of FQ resistance in . Typhi mediated by GyrB mutation.
氟喹诺酮(FQ)耐药性被世界卫生组织列为高优先级病原体。伤寒沙门氏菌中的 FQ 耐药性迅速出现,主要由拓扑异构酶基因和的突变介导。GyrA 突变导致经典 FQ 耐药(DCS-NAR),即对环丙沙星(MIC 为 0.12 至 0.5 µg ml)的敏感性降低(DCS)和对萘啶酸(NAR)的耐药性。以前,提出了萘啶酸盘测试来检测 DCS。最近,出现了由质粒介导的喹诺酮耐药(PMQR)和 GyrB 突变引起的非经典 FQ 耐药的分离株。这些机制也导致 DCS,但对萘啶酸敏感(NAS),因此带来了诊断挑战。CLSI 和 EUCAST 建议使用 5µg 培氟沙星盘检测伤寒沙门氏菌中的 DCS。CLSI 和 EUCAST 推荐使用 5µg 培氟沙星检测 DCS 的建议尚未在伤寒沙门氏菌和物种的 GyrB 突变介导的耐药性上得到验证。本研究的目的是验证 5µg 培氟沙星盘检测 DCS 的性能,特别是针对 GyrB 突变的 DCS。总共研究了 180 株临床分离的伤寒沙门氏菌(2005-2014 年),以研究其耐药机制。使用 CLSI 指南确定萘啶酸(30μg)、环丙沙星(5μg)和培氟沙星(5µg)的药敏区直径和环丙沙星的最小抑菌浓度(MIC)。评估了三种圆盘检测伤寒沙门氏菌中 FQ 耐药性的性能。在 112 株和 34 株分离株中分别检测到 GyrB+ / ParC 和 GyrB 的拓扑异构酶突变。不同的突变对环丙沙星的 MIC 有不同的影响。目前的敏感(≤0.06µg ml)和不敏感(≥0.125µg ml)的断点无法检测到所有具有耐药机制的分离株。与萘啶酸相比,环丙沙星和培氟沙星盘在区分由 GyrB 介导的非经典耐药的分离株与野生型方面表现出色。培氟沙星盘可用于检测伤寒沙门氏菌中的 FQ 耐药性。这是首次报道培氟沙星用于检测由 GyrB 突变介导的伤寒沙门氏菌中的 FQ 耐药性。