Transferable mechanisms of quinolone resistance are more frequent among enterotoxigenic Escherichia coli isolates displaying low-level quinolone resistance.

IF 0.8 4区 医学 Q4 PARASITOLOGY
A M Medina, F P Rivera, M Riveros, T J Ochoa, M J Pons, J Ruiz
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引用次数: 0

Abstract

This study analysed the mechanisms of quinolone resistance among enterotoxigenic Escherichia coli (ETEC) in a periurban area of Lima, Peru. The susceptibility to nalidixic acid and ciprofloxacin, the role of Phe-Arg-b-Naphtylamyde inhibitable-(PAbN) efflux pumps, the presence of mutations in gyrA and parC as well as the presence of aac(6')Ib-cr, qepA, qnrA, qnrB, qnrC, qnrD, qnrVC and oqxAB were determined in 31 ETEC from previous case/control studies of children's diarrhoea. Discordances between disk diffusion, with all isolates showing intermediate or fully resistance to nalidixic acid, and minimal inhibitory concentration (MIC), with 7 isolates being below considered resistance breakpoint, were observed. Twenty-one isolates possessed gyrA mutations (19 S83L, 2 S83A). AAC(6') Ib-cr, QnrS, QnrB and QepA were found in 7, 6, 2 and 1 isolates respectively, with 3 isolates presenting 2 transferable mechanisms of quinolone resistance (TMQR) concomitantly. TMQR were more frequent among isolates with MIC to nalidixic acid ranging from 2 to 16 mg/L (p=0.03), while gyrA mutations were more frequent among isolates with nalidixic acid MIC >= 128 mg/L (p=0.0002). In summary, the mechanisms of quinolone resistance present in ETEC isolates in Peru have been described. Differences in the prevalence of underlying mechanisms associated with final MIC levels were observed. The results suggest two different evolutive strategies to survive in the presence of quinolones related to specific bacterial genetic background.

喹诺酮类药物耐药的可转移机制在表现出低水平喹诺酮类药物耐药性的产肠毒素大肠杆菌分离株中更为常见。
本研究分析了秘鲁利马城郊地区产肠毒素大肠杆菌(ETEC)喹诺酮类药物耐药的机制。在31例ETEC儿童腹泻病例/对照研究中,测定了对萘啶酸和环丙沙星的敏感性、ph - arg -b-萘胺抑制剂(PAbN)外排泵的作用、gyrA和parC突变的存在以及aac(6’)Ib-cr、qepA、qnrA、qnrB、qnrC、qnrD、qnrVC和oqxAB的存在。观察到磁盘扩散与最小抑制浓度(MIC)之间的不一致,所有分离株都对萘啶酸具有中等或完全抗性,其中7株低于考虑的抗性断点。21株分离株存在gyrA突变(19株S83L, 2株S83A)。AAC(6’)Ib-cr、QnrS、QnrB和QepA分别在7株、6株、2株和1株中检出,其中3株同时出现2种喹诺酮类药物耐药转移机制(TMQR)。MIC值为2 ~ 16 mg/L的分离株中TMQR突变较多(p=0.03), MIC >= 128 mg/L的分离株中gyrA突变较多(p=0.0002)。总之,秘鲁ETEC分离株喹诺酮类药物耐药的机制已经得到描述。观察到与最终MIC水平相关的潜在机制患病率的差异。结果表明,在喹诺酮类药物存在的情况下,两种不同的进化策略与特定的细菌遗传背景有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Tropical biomedicine
Tropical biomedicine 医学-寄生虫学
CiteScore
1.60
自引率
0.00%
发文量
63
审稿时长
6-12 weeks
期刊介绍: The Society publishes the Journal – Tropical Biomedicine, 4 issues yearly. It was first started in 1984. The journal is now abstracted / indexed by Medline, ISI Thompson, CAB International, Zoological Abstracts, SCOPUS. It is available free on the MSPTM website. Members may submit articles on Parasitology, Tropical Medicine and other related subjects for publication in the journal subject to scrutiny by referees. There is a charge of US$200 per manuscript. However, charges will be waived if the first author or corresponding author are members of MSPTM of at least three (3) years'' standing.
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