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Comparison of real time polymerase chain reaction quantification of changes in hilA and rpoS gene expression of a Salmonella typhimurium poultry isolate grown at fast versus slow dilution rates in an anaerobic continuous culture system

Permanent URL:
http://handle.nal.usda.gov/10113/57292
File:
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Abstract:
The objective of this study was to determine the genetic responses of a Salmonella enterica Typhimurium poultry isolate during low and high dilution rates (D) in steady state continuous culture (CC) incubations. Samples for genetic analyses were taken from a previous study where S. typhimurium cells had been grown in two chemostats operated concurrently, which were designated as Trials 1 and 2, with eight dilution rates sampled during steady state. Real-time PCR on two target genes (rpoS and hilA) were analyzed as changes in expression of the target gene relative to the reference gene (16S rRNA). At the lowest D (0.0125 h-1) in Trial 2, rpoS expression was more than 2-fold higher than the second highest relative expression. In Trial 1, hilA expression was 21.8- , 27.8-, and 21-fold higher in D 0.0125 h-1, 0.025 h-1, and 0.05 h-1, respectively, compared to D 0.1 h-1, 0.54 h-1, and 1.08 h-1. In Trial 2, D 0.025 h-1 and 0.27 h-1 showed no difference in hilA expression but were significantly higher compared to other D. From these results, low glucose conditions may play an essential role in triggering rpoS induction as well as contributing to potential virulence.
Author(s):
Kingsley D. Dunkley , Todd R. Callaway , Corliss A. O'Bryan , Megan M. Kundinger , Claudia S. Dunkley , Robin C. Anderson , David J. Nisbet , Philip G. Crandall , Steven C. Ricke
Subject(s):
Salmonella typhimurium , continuous systems , gene expression , gene expression regulation , genes , glucose , nutrient availability , polymerase chain reaction , poultry , ribosomal RNA , virulence
Source:
Food biotechnology 2012 8 1 v.23
Language:
English
Year:
2012
Collection:
Journal Articles, USDA Authors, Peer-Reviewed
Rights:
Works produced by employees of the U.S. Government as part of their official duties are not copyrighted within the U.S. The content of this document is not copyrighted.