Genetic characterization of fluoroquinolone-resistant Escherichia coli associated with bovine mastitis in India

被引:6
作者
Balakrishnan, Sangeetha [1 ]
Antony, Prabhakar Xavier [1 ]
Mukhopadhyay, Hirak Kumar [1 ]
Pillai, Raghavan Madhusoodanan [1 ]
Thanislass, Jacob [2 ]
Padmanaban, Vijayalakshmi [3 ]
Srinivas, Mouttou Vivek [1 ]
机构
[1] Rajiv Gandhi Inst Vet Educ & Res, Dept Vet Microbiol, Pondicherry 605009, India
[2] Rajiv Gandhi Inst Vet Educ & Res, Dept Vet Biochem, Pondicherry 605009, India
[3] Rajiv Gandhi Inst Vet Educ & Res, Dept Vet Med, Pondicherry 605009, India
关键词
Escherichia coli; fluoroquinolones; gyrA; parC; quinolone resistance determining region;
D O I
10.14202/vetworld.2016.705-709
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Aim: The present study was undertaken to characterize the mutation in gyrA (DNA gyrase) and parC (topoisomerase IV) genes responsible for fluoroquinolone resistance in Escherichia coli isolates associated with the bovine mastitis. Materials and Methods: A total of 92 milk samples from bovine mastitis cases were sampled in and around Puducherry (Southern India). Among these samples, 30 isolates were bacteriologically characterized as E. coli. Minimum inhibitory concentrations (MIC) of fluoroquinolones of these 30 E. coli isolates were evaluated by resazurin microtiter assay. Then, the quinolone resistance determining region (QRDR) (gyrA and parC genes) of these E. coli isolates was genetically analyzed for determining the chromosomal mutation causing fluoroquinolone resistance. Results: E. coli isolates showed a resistance rate of 63.33%, 23.33% and 30.03% to nalidixic acid, ciprofloxacin and enrofloxacin, respectively. Mutations were found at 83rd and 87th amino acid position of gyrA gene, and at 80th and 108th amino acid position of parC gene in our study isolates. Among these five isolates, one had a single mutation at 83 amino acid position of gyrA with reduced susceptibility (0.5 mu g/ml) to ciprofloxacin. Then, in remaining four isolates, three isolates showed triple mutation (at gyrA: S83 -> L and D87 -> N; at parC: S80 -> I) and the fifth isolate showed an additional mutation at codon 108 of parC (A108 -> T) with the increased ciprofloxacin MIC of 16-128 mu g/ml. The most common mutation noticed were at S83 -> L and D87 -> N of gyrA and S80 I of ParC. Conclusion: The study confirms the presence of mutation/s responsible for fluoroquinolone resistance in QRDR of gyrA and parC genes of E. coli isolates of animal origin, and there is increased rate of fluoroquinolone resistance with high-level of MIC. The mutations observed in this study were similar to that of human isolates.
引用
收藏
页码:705 / 709
页数:5
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