Affiliation:
1. 1 Veterinary Medical Research Institute of the Hungarian Academy of Sciences H-1581 Budapest, P.O. Box 18, Hungary
2. 2 Agricultural Biotechnology Center Gödöllő, Hungary
3. 3 Veterinary Medical Research Institute of the Hungarian Academy of Sciences H-1581 Budapest, P.O. Box 18, Hungary
Abstract
Analysis of flagellin genes was carried out on strains ofSalmonellaTyphimurium,SalmonellaHadar,SalmonellaAbortusequi,SalmonellaEnteritidis andSalmonellaGallinarum 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 offliC (fljA), for the operator region offliC,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 allS. Typhimurium (n = 10)andS.Hadar (n = 10) strains tested. The results obtained onS. Typhimurium andS.Hadar strains confirmed their biphasic character at DNA level. However, theS. Enteritidis (n = 46) andS. Gallinarum (n = 5) strains lacked the invertase system(hin, hixL, hixR)as well as thefljAandfljBgenes, whilefliCand its operator were detectable. Consequently, theS. Enteritidis strains could only expressfliCgene resulting in phase H1 flagellin. The examinedS. Gallinarum strains were also demonstrated to have a cryptic flagellin gene(fliC). On the other hand, PCR results onS. 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 forS. Typhimurium andS. 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 allS. Typhimurium,S. Hadar andS. Enteritidis strains. This system could also identify cryptic flagellar genes ofS. Abortusequi andS. Gallinarum.
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11 articles.
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