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首页> 外文期刊>Veterinary World >Prevalence and molecular detection of fluoroquinolone-resistant genes (qnrA and qnrS) in Escherichia coli isolated from healthy broiler chickens
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Prevalence and molecular detection of fluoroquinolone-resistant genes (qnrA and qnrS) in Escherichia coli isolated from healthy broiler chickens

机译:从健康肉鸡中分离出的大肠埃希菌中氟喹诺酮类耐药基因(qnrA和qnrS)的流行和分子检测

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Aim: The present study was carried out to determine the prevalence and molecular detection of fluoroquinolone-resistant Escherichia coli carrying qnrA and qnrS genes in healthy broiler chickens in Mymensingh, Bangladesh, and also to identify the genes responsible for such resistance. Materials and Methods: A total of 65 cloacal swabs were collected from apparently healthy chickens of 0-14 days (n=23) and 15-35 days (n=42) old. The samples were cultured onto Eosin Methylene Blue Agar, and the isolation and identification of the E. coli were performed based on morphology, cultural, staining, and biochemical properties followed by polymerase chain reaction (PCR) targeting E. coli 16S rRNA genes. The isolates were subjected to antimicrobial susceptibility test against five commonly used antibiotics under fluoroquinolone (quinolone) group, namely gatifloxacin, levofloxacin, moxifloxacin, ofloxacin, and pefloxacin by disk diffusion method. Detection of qnrA and qnrS genes was performed by PCR. Results: Among the 65 cloacal samples, 54 (83.08%) were found to be positive for E. coli. Antibiotic sensitivity test revealed that, of these 54 isolates, 18 (33.33%) were found to be resistant to at least one fluoroquinolone antibiotic. The highest resistance was observed against pefloxacin (61.11%). By PCR, of 18 E. coli resistant to fluoroquinolone, 13 (72.22%) were found to be positive for the presence of qnrS. None of the isolates were found positive for qnrA. Conclusion: Fluoroquinolone-resistant E. coli harboring qnrS genes is highly prevalent in apparently healthy broiler chickens and possesses a potential threat to human health.
机译:目的:本研究旨在确定孟加拉国迈门辛格健康肉鸡中携带qnrA和qnrS基因的耐氟喹诺酮类大肠杆菌的流行程度和分子检测,并鉴定引起这种抗性的基因。材料和方法:从0-14天(n = 23)和15-35天(n = 42)大的健康鸡身上收集了总共65株泄殖腔拭子。将样品培养到曙红亚甲蓝琼脂上,并根据形态,培养,染色和生化特性,然后针对大肠杆菌16S rRNA基因的聚合酶链反应(PCR),对大肠杆菌进行分离和鉴定。通过盘扩散法对分离的菌株进行了氟喹诺酮(喹诺酮)组下的五种常用抗生素的抗菌药敏试验,分别为加替沙星,左氧氟沙星,莫西沙星,氧氟沙星和培氟沙星。通过PCR检测qnrA和qnrS基因。结果:在65处泄殖腔样本中,有54份(83.08%)被发现为大肠杆菌阳性。抗生素敏感性测试表明,在这54个分离株中,有18个(33.33%)被发现对至少一种氟喹诺酮类抗生素具有抗药性。观察到对培氟沙星的最高耐药性(61.11%)。通过PCR,在18株对氟喹诺酮耐药的大肠杆菌中,发现13株(72.22%)对qnrS呈阳性。没有分离物被发现对qnrA呈阳性。结论:带有qnrS基因的耐氟喹诺酮类大肠杆菌在看似健康的肉鸡中高度流行,对人类健康具有潜在威胁。

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