首页> 外文期刊>Journal of applied microbiology >Analysis of gyrA mutations in quinolone-resistant and -susceptible Campylobacter jejuni isolates from retail poultry and human clinical isolates by non-radioactive single-strand conformation polymorphism analysis and DNA sequencing
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Analysis of gyrA mutations in quinolone-resistant and -susceptible Campylobacter jejuni isolates from retail poultry and human clinical isolates by non-radioactive single-strand conformation polymorphism analysis and DNA sequencing

机译:通过非放射性单链构象多态性分析和DNA测序分析零售家禽和人类临床分离株对喹诺酮耐药和易感空肠弯曲杆菌分离株的gyrA突变

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Aims: The aims of this study were to characterize the molecular variations in the quinolone resistance-determining region (QRDR) of gyrA among quinolone-resistant and -susceptible Campylobacter jejuni isolates originating from foods of animal origin and human infections and to evaluate the suitability of the single-strand conformation polymorphism (SSCP) method as a screening method for molecular characterization of fluoroquinolone resistance. Methods and Results: Alterations in QRDR of gyrA from 182 C. jejuni isolates were determined by nonradioisotopic SSCP analysis and direct sequencing. A total of 13 types of nucleic acid sequence combinations within the QRDR of the gyrA gene resulted in 11 different SSCP patterns. All nalidixic acid resistant strains possessed nucleotide substitution at either codon Thr-86 or Asp-90. Silent mutations were detected additionally. Thr-86 to Ile mutation was detected in all 139 ciprofloxacin resistant strains, which showed cross-resistance to nalidixic acid. Conclusions: The SSCP method is suitable for a molecular screening of quinolone resistant C. jejuni isolates and in combination with DNA sequencing suitable to detect genetic variations of the QRDR of gyrA. Significance and Impact of Study: This study provides data of the genetic variations of the QRDR of gyrA from C. jejuni isolates of foods and human beings.
机译:目的:本研究的目的是鉴定源自动物源性食物和人类感染食品的对喹诺酮耐药和易感的空肠弯曲杆菌菌株中gyrA的喹诺酮耐药决定区(QRDR)的分子变异,并评估其适应性。单链构象多态性(SSCP)方法作为氟喹诺酮耐药性分子表征的筛选方法。方法和结果:通过非放射性同位素SSCP分析和直接测序,确定了182个空肠弯曲杆菌菌株gyrA的QRDR改变。 gyrA基因的QRDR内共有13种类型的核酸序列组合,产生11种不同的SSCP模式。所有耐萘啶酸的菌株均在密码子Thr-86或Asp-90处具有核苷酸取代。另外检测到沉默突变。在所有139个对环丙沙星耐药的菌株中均检测到Thr-86到Ile突变,这些菌株显示出与萘啶酸的交叉耐药性。结论:SSCP方法适用于对喹诺酮抗性空肠弯曲杆菌分离株的分子筛查,并与适合检测gyrA QRDR遗传变异的DNA测序相结合。研究的意义和影响:该研究提供了来自空肠弯曲杆菌食物和人类分离株的gyrA QRDR的遗传变异数据。

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