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Quinolone resistance mechanisms among extended-spectrum beta-lactamase (ESBL) producing Escherichia coli isolated from rivers and lakes in Switzerland

机译:从瑞士河流和湖泊中分离出的产广谱β-内酰胺酶(ESBL)大肠杆菌中的喹诺酮耐药机制

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摘要

Sixty extended-spectrum β-lactamase (ESBL)-producing Escherichia coli isolated from rivers and lakes in Switzerland were screened for individual strains additionally exhibiting a reduced quinolone susceptibility phenotype. Totally, 42 such isolates were found and further characterized for their molecular (fluoro)quinolone resistance mechanisms. PCR and sequence analysis were performed to identify chromosomal mutations in the quinolone resistance-determining regions (QRDR) of gyrA, gyrB, parC and parE and to describe the occurrence of the following plasmid-mediated quinolone resistance genes: qepA, aac-6'-Ib-cr, qnrA, qnrB, qnrC, qnrD and qnrS. The contribution of efflux pumps to the resistance phenotype of selected strains was further determined by the broth microdilution method in the presence and absence of the efflux pump inhibitor phe-arg-β-naphthylamide (PAβN). Almost all strains, except two isolates, showed at least one mutation in the QRDR of gyrA. Ten strains showed only one mutation in gyrA, whereas thirty isolates exhibited up to four mutations in the QRDR of gyrA, parC and/or parE. No mutations were detected in gyrB. Most frequently the amino-acid substitution Ser83→Leu was detected in GyrA followed by Asp87→Asn in GyrA, Ser80→Ile in ParC, Glu84→Val in ParC and Ser458→Ala in ParE. Plasmid-mediated quinolone resistance mechanisms were found in twenty isolates bearing QnrS1 (4/20), AAC-6'-Ib-cr (15/20) and QepA (1/20) determinants, respectively. No qnrA, qnrB, qnrC and qnrD were found. In the presence of PAβN, the MICs of nalidixic acid were decreased 4- to 32-fold. (Fluoro) quinolone resistance is due to various mechanisms frequently associated with ESBL-production in E. coli from surface waters in Switzerland.
机译:筛选了从瑞士河流和湖泊中分离出的60株产广谱β-内酰胺酶(ESBL)的大肠杆菌,以筛选另外表现出降低的喹诺酮敏感性表型的菌株。总共发现了42种这样的分离株,并进一步对其分子(氟)喹诺酮耐药机制进行了表征。进行PCR和序列分析以鉴定gyrA,gyrB,parC和parE的喹诺酮抗性决定区(QRDR)中的染色体突变,并描述以下质粒介导的喹诺酮抗性基因的出现:qepA,aac-6'- Ib-cr,qnrA,qnrB,qnrC,qnrD和qnrS。在存在和不存在外排泵抑制剂phe-arg-β-萘酰胺(PAβN)的情况下,通过肉汤微量稀释法进一步确定外排泵对所选菌株抗性表型的贡献。除两个分离株外,几乎所有菌株都在gyrA的QRDR中显示至少一个突变。十个菌株在gyrA中仅显示一个突变,而三十个分离株在gyrA,parC和/或parE的QRDR中显示最多四个突变。在gyrB中未检测到突变。最常见的是在GyrA中检测到氨基酸取代Ser83→Leu,然后在GyrA中检测到Asp87→Asn,在ParC中检测到Ser80→Ile,在ParC中检测到Glu84→Val,在ParE中检测到Ser458→Ala。在分别带有QnrS1(4/20),AAC-6'-Ib-cr(15/20)和QepA(1/20)决定簇的20个分离物中发现了质粒介导的喹诺酮抗性机制。找不到qnrA,qnrB,qnrC和qnrD。在PAβN存在下,萘啶酸的MIC降低了4到32倍。 (氟)喹诺酮耐药性归因于瑞士从地表水在大肠杆菌中生产ESBL经常引起的各种机制。

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