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首页> 外文期刊>Berliner und Munchener Tierarztliche Wochenschrift >Identification of patterns of transmission of Salmonella within swine production systems using pulsed field gel electrophoresis (PFGE) and repetitive sequence polymerase chain reaction (REP-PCR): a quantitative analysis
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Identification of patterns of transmission of Salmonella within swine production systems using pulsed field gel electrophoresis (PFGE) and repetitive sequence polymerase chain reaction (REP-PCR): a quantitative analysis

机译:使用脉冲场凝胶电泳(PFGE)和重复序列聚合酶链反应(REP-PCR)鉴定猪生产系统中沙门氏菌的传播模式:定量分析

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摘要

Pulsed field gel electrophoresis (PFGE) using 3 enzymes (Spe I, Xba I, Avr II) and repetitive sequence polymerase chain reaction (REP-PCR) with 3 primers (BOX, ERIC, REP) were compared with respect to their validity as a method for identifying transmission of Salmonella on swine farms. Sixty-eight isolates of Salmonella were obtained from feces of swine, cats, mice, and birds, insect body parts, water and floor samples, and boot scrapings collected on 9 swine farms in Illinois USA. Genetic distances between isolates were calculated using the Dice matching coefficient. Cluster analysis of distance matrices was conducted using the UPGMA algorithm. There was no significant difference between PFGE and REP-PCR in the genetic diversity detected; however, REP-PCR differentiated between 14 pairs of isolates which PFGE identified as identical. There were no significant differences between PFGE and REP-PCR in identifying all or most close genetic links as isolates from the same farm, the same building, and from the same sampling visit, suggesting ecological validity for both methods. Thus, REP-PCR should be considered as an acceptable and perhaps preferable alternative to PFGE as a genotyping method for studies of Salmonella transmission.
机译:比较了使用3种酶(Spe I,Xba I,Avr II)的脉冲场凝胶电泳(PFGE)和使用3种引物(BOX,ERIC,REP)的重复序列聚合酶链反应(REP-PCR)的有效性猪场沙门氏菌传播的方法从美国伊利诺伊州的9个养猪场收集的猪,猫,小鼠和鸟类的粪便,昆虫的身体部位,水和地板样本以及靴子刮板中获得了68株沙门氏菌的分离株。使用Dice匹配系数计算分离株之间的遗传距离。距离矩阵的聚类分析是使用UPGMA算法进行的。 PFGE和REP-PCR在检测到的遗传多样性上没有显着差异。但是,REP-PCR区分了PFGE鉴定为相同的14对分离株。 PFGE和REP-PCR在鉴定所有或最紧密的遗传联系为同一农场,同一建筑物和同一采样访问的分离株方面没有显着差异,表明这两种方法的生态有效性。因此,对于沙门氏菌传播的研究,REP-PCR应该被认为是作为基因分型方法的PFGE的可接受且可能更好的选择。

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