Doran J L, Collinson S K, Kay C M, Banser P A, Burian J, Munro C K, Lee S H, Somers J M, Todd E C, Kay W W
Department of Microbiology and Biochemistry, University of Victora, British Columbia, Canada.
Mol Cell Probes. 1994 Aug;8(4):291-310. doi: 10.1006/mcpr.1994.1041.
Immunochemical analyses of 85 isolates of 17 Salmonella serovars using polyclonal antiserum to SEF21, the type 1 fimbriae of Salmonella enteritidis, demonstrated antigenic relatedness among both type 1 and type 2 fimbriae of Salmonella. However, anti-SEF21 antiserum was not entirely suitable as a Salmonella diagnostic probe due either to a variability of, or a rare deficiency of, detectable fimbriae. Partial amino acid sequence analyses of the SEF21 structural fimbrin protein revealed 99% homology to Salmonella typhimurium FimA. Therefore, oligonucleotide probes for Salmonella detection were designed following sequencing of S. enteritidis fimA and comparison to the corresponding genes of S. typhimurium, Escherichia coli, Klebsiella pneumoniae and Serratia marcescens. One oligonucleotide probe hybridized to all 612 Salmonella isolates of 89 serovars tested while two other probes detected 97.5% and 99.7% of the isolates. Three consistently weak positive reactions were obtained, therefore, inclusivity was optimized by identification of a Salmonella-specific tctC DNA probe that detected 609 of 612 Salmonella isolates. No hybridization of these Salmonella probes was detected to 250 other Enterobacteriaceae isolates or to 14 other eubacterial species. Therefore, in combination, DNA probes to fimA and tctC proved to be highly reliable diagnostics for Salmonella bacteria. Accordingly, PCR assays targeting fimA and tctC were developed.
利用针对肠炎沙门氏菌1型菌毛SEF21的多克隆抗血清,对17种沙门氏菌血清型的85个分离株进行免疫化学分析,结果表明沙门氏菌1型和2型菌毛之间存在抗原相关性。然而,抗SEF21抗血清并不完全适合作为沙门氏菌诊断探针,这是因为可检测到的菌毛存在变异性或罕见的缺陷。对SEF21结构菌毛蛋白进行的部分氨基酸序列分析显示,其与鼠伤寒沙门氏菌FimA的同源性为99%。因此,在对肠炎沙门氏菌fimA进行测序并与鼠伤寒沙门氏菌、大肠杆菌、肺炎克雷伯菌和粘质沙雷氏菌的相应基因进行比较之后,设计了用于检测沙门氏菌的寡核苷酸探针。一种寡核苷酸探针与所检测的89个血清型的所有612个沙门氏菌分离株杂交,而另外两种探针分别检测到97.5%和99.7%的分离株。获得了三个始终呈弱阳性的反应,因此,通过鉴定一种沙门氏菌特异性tctC DNA探针来优化包容性,该探针检测到612个沙门氏菌分离株中的609个。未检测到这些沙门氏菌探针与250个其他肠杆菌科分离株或14个其他真细菌物种发生杂交。因此,fimA和tctC的DNA探针组合被证明是沙门氏菌细菌的高度可靠诊断方法。据此,开发了针对fimA和tctC的PCR检测方法。