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Detection of sef14, sef17 and sef21 Fimbrial Virulence Genes of Salmonella enteritidis by Multiplex PCR

机译:多重PCR检测肠炎沙门氏菌sef14,sef17和sef21菌性毒力基因

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Salmonella serovars show their diverse effects by joining the gastrointestinal epithelia. The infectious trait of this bacterium depends on colonization in GI epithelial surfaces. Fimbirae play the main role in this junction. Three kinds of fimbrial genes are more important and responsible for the pathogenecity and the attachment of Salmonella enteritidis to intestinal epithelium (sef14, 17, 21). Therefore, researchers have attempted to study the significance of fimbriae genes by the molecular method. In first of all, the molecular method has to be optimized for investigating the presence of these genes in the confirmed isolates of S. enteritidis. About 45 isolates of S. enteritidis collected from 60 diarrheic feces of both livestock and avian population with clinical sign of diarrhea were considered. In order to trace the most important fimbrial genes, the multiplex PCR method was designed and optimized. The optimal primers, annealing temperature of primers and concentration of DNA template, MgCl2 and Taq DNA polymerase were determined.
机译:沙门氏菌血清通过加入胃肠道上皮细胞显示出不同的作用。该细菌的感染性取决于胃肠道上皮表面的定殖。 Fimbirae在此交汇处起主要作用。三种纤维基因更为重要,它们负责肠炎沙门氏菌的致病性和附着性(sef14、17、21)。因此,研究人员试图通过分子方法研究菌毛基因的重要性。首先,必须对分子方法进行优化,以调查确认的肠炎链球菌分离物中这些基因的存在。考虑了从牲畜和禽类的60个腹泻粪便中收集到的约45株肠炎链球菌的分离株,它们具有腹泻的临床症状。为了追踪最重要的纤维基因,设计并优化了多重PCR方法。确定了最佳引物,引物的退火温度以及DNA模板的浓度,MgCl2和Taq DNA聚合酶。

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