Imre A, Olasz F, Nagy B
Veterinary Medical Research Institute of the Hungarian Academy of Sciences, H-1581 Budapest, PO Box 18, Hungary.
Acta Vet Hung. 2005;53(2):163-72. doi: 10.1556/AVet.53.2005.2.2.
Analysis of flagellin genes was carried out on strains of Salmonella Typhimurium, Salmonella Hadar, Salmonella Abortusequi, Salmonella Enteritidis and Salmonella Gallinarum serovars, using a PCR system designed in this study. The purpose of these studies was to explore the flagellin genes of biphasic and monophasic Salmonellae for future targeted genetic interventions. The PCR primers were designed for two different structural genes of flagellin (fliC, fljB), for the repressor of fliC (fljA), for the operator region of fliC, and for the invertase system responsible for phase variation in Salmonella (hin, hixL, hixR). PCR analysis revealed that all of the examined genes (fliC, fliC-operator, fljB, fljA, hin, hixL, hixR) were present in all S. Typhimurium (n = 10) and S. Hadar (n = 10) strains tested. The results obtained on S. Typhimurium and S. Hadar strains confirmed their biphasic character at DNA level. However, the S. Enteritidis (n = 46) and S. Gallinarum (n = 5) strains lacked the invertase system (hin, hixL, hixR) as well as the fljA and fljB genes, while fliC and its operator were detectable. Consequently, the S. Enteritidis strains could only express fliC gene resulting in phase H1 flagellin. The examined S. Gallinarum strains were also demonstrated to have a cryptic flagellin gene (fliC). On the other hand, PCR results on S. Abortusequi (n = 2) indicated that both flagellin genes (fliC, fljB) and the whole phase variation system were present in both strains tested but only the H2 phase gene (fljB) was expressed. The phenotype of these strains could be clarified by motility test and/or by classical flagellar serology. The findings are also substantiated by the results of serovar-specific PCR for S. Typhimurium and S. Enteritidis. In conclusion, the PCR system developed in this study proved to be suitable for characterisation of Salmonella flagellin genes and confirmed serological results regarding all S. Typhimurium, S. Hadar and S. Enteritidis strains. This system could also identify cryptic flagellar genes of S. Abortusequi and S. Gallinarum.
使用本研究设计的PCR系统,对鼠伤寒沙门氏菌、哈达尔沙门氏菌、马流产沙门氏菌、肠炎沙门氏菌和鸡沙门氏菌血清型菌株的鞭毛蛋白基因进行了分析。这些研究的目的是探索双相和单相沙门氏菌的鞭毛蛋白基因,以便未来进行有针对性的基因干预。针对鞭毛蛋白的两个不同结构基因(fliC、fljB)、fliC的阻遏物(fljA)、fliC的操纵区以及负责沙门氏菌相变的转化酶系统(hin、hixL、hixR)设计了PCR引物。PCR分析显示,在所有测试的鼠伤寒沙门氏菌(n = 10)和哈达尔沙门氏菌(n = 10)菌株中均存在所有检测基因(fliC、fliC - 操纵区、fljB、fljA、hin、hixL、hixR)。在鼠伤寒沙门氏菌和哈达尔沙门氏菌菌株上获得的结果在DNA水平上证实了它们的双相特性。然而,肠炎沙门氏菌(n = 46)和鸡沙门氏菌(n = 5)菌株缺乏转化酶系统(hin、hixL、hixR)以及fljA和fljB基因,而fliC及其操纵区是可检测到的。因此,肠炎沙门氏菌菌株只能表达fliC基因,产生H1相鞭毛蛋白。所检测的鸡沙门氏菌菌株也被证明具有一个隐性鞭毛蛋白基因(fliC)。另一方面,马流产沙门氏菌(n = 2)的PCR结果表明,在测试的两个菌株中均存在两个鞭毛蛋白基因(fliC、fljB)和整个相变系统,但仅表达H2相基因(fljB)。这些菌株的表型可以通过运动性试验和/或经典鞭毛血清学来阐明。鼠伤寒沙门氏菌和肠炎沙门氏菌的血清型特异性PCR结果也证实了这些发现。总之,本研究开发的PCR系统被证明适用于沙门氏菌鞭毛蛋白基因的表征,并证实了关于所有鼠伤寒沙门氏菌、哈达尔沙门氏菌和肠炎沙门氏菌菌株的血清学结果。该系统还可以鉴定马流产沙门氏菌和鸡沙门氏菌的隐性鞭毛基因。