首页> 外文期刊>Journal of food protection >Analysis Of Ciprofloxacin-resistant Salmonella Strains Fromswine, Chicken, And Their Carcasses In Taiwan And Detection Ofrnparc Resistance Mutations By A Mismatch Amplificationrnmutation Assay Pcr
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Analysis Of Ciprofloxacin-resistant Salmonella Strains Fromswine, Chicken, And Their Carcasses In Taiwan And Detection Ofrnparc Resistance Mutations By A Mismatch Amplificationrnmutation Assay Pcr

机译:台湾猪,鸡及其尸体对环丙沙星的沙门氏菌耐药性分析及错配扩增法

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One hundred thirty-three Salmonella strains isolated from the viscera of swine, chicken, and carcasses of swine and chicken in Taiwan from 2004 to 2006 were identified to serotype level and analyzed for their susceptibility to ciprofloxacin. In total, 76 (57%) strains of the Salmonella isolates exhibited high-level resistance to ciprofloxacin, having MICs ranging from 16 to 64 μg/ml. DNA sequence analysis revealed that mutations in the quinolone resistance-determining regions of gyrA (Ser83Phe, Asp87Gly or Asp87Asn), parC (Ser80Arg, or Ser80Ile or Glu84Lys), and parE (Ser458Pro) genes were associated with the Salmonella strains that demonstrated resistance to ciprofloxacin. A mismatch amplification mutation assay (MAMA)-PCR was developed to identify mutations in parC at codons 80 and 84. Specific PCR products were only recovered from ciprofloxacin-resistant Salmonella strains but not from the susceptible strains. MAMA-PCR targeting the mutations in parC correlated with what DNA sequencing revealed. In conclusion, monitoring ciprofloxacin-resistant Salmonella from animal sources should be performed on a regular basis. MAMA-PCR targeting parC could provide a fast method for those laboratories interested in quickly characterizing the resistance profile and with little access to DNA sequencing facilities.
机译:2004年至2006年,从台湾的猪,鸡的内脏以及猪和鸡的尸体中分离出的133株沙门氏菌被鉴定为血清型水平,并分析了它们对环丙沙星的敏感性。共有76株(57%)沙门氏菌菌株显示出对环丙沙星的高水平抗性,MIC范围为16至64μg/ ml。 DNA序列分析显示,gyrA(Ser83Phe,Asp87Gly或Asp87Asn),parC(Ser80Arg或Ser80Ile或Glu84Lys)和parE(Ser458Pro)的喹诺酮耐药性决定区域中的突变与沙门氏菌菌株有关,这些菌株对环丙沙星具有耐药性。开发了错配扩增突变测定(MAMA)-PCR以鉴定parC中80和84位密码子的突变。特异性PCR产物仅从耐环丙沙星的沙门氏菌菌株中回收,而从易感菌株中未回收。靶向parC中突变的MAMA-PCR与DNA测序揭示的结果相关。总之,应定期对动物来源的环丙沙星耐药沙门氏菌进行监测。靶向parC的MAMA-PCR可以为那些对快速鉴定耐药性特征并且几乎不需要DNA测序工具的实验室提供快速方法。

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