Location: Egg Safety and Quality
2008 Annual Report
This research addresses National Program 108 (Food Safety), Component 1.1 Pathogens, Toxins and Chemical Contaminants Preharvest, Problem Statement 1.1.3 (Ecology, Host Pathoghen and Chemical Contaminants Relationships).2. Genes that vary between PT13a subpopulations also vary among other Salmonella spp. We determined that 14 genes of PT13a S. enteritidis have ORF-disrupting mutations that distinguish strains from each other, even if they at first appear clonal by DNA-DNA microarray hybridization. It is important to be able to tell bacterial strains from each other, because only some of them cause food borne illness. Analysis of the amino acid sequences of these 14 genes within other gram-negative bacteria and Salmonella spp. by BLAST analysis of public genomic databases available from National Center for Biotechnology Information and Sanger Institute indicate that they can vary greatly from serotype to serotype. In one gene, the introduction of a termination codon coincides with deletion of the 3’ end of the gene in other Salmonella serotypes, which suggests that introduction of small genetic mistakes might make DNA more fragile and prone to converting to a larger irreversible mistake. Another gene known to be important for survival of Salmonella in white blood cells is missing or has coding errors in 26 of 29 Salmonella genomes, which suggests that it is very hard for Salmonella to maintain this gene even though it facilitates disease potential. These results suggest that small genetic change (genetic drift) impacts the biology of Salmonella as much as does large genetic change (genetic shift). These results provide new epidemiological information about Salmonella serotypes that periodically emerge as food-borne pathogens.
This research addresses National Program 108 (Food Safety), Component 1.1 Pathogens, Toxins and Chemical Contaminants Preharvest, Problem Statements 1.1.2 (Epidemiology) and 1.1.3 (Ecology, Host Pathoghen and Chemical Contaminants Relationships).
Olson, A.B., Andrysiak, A.K., Tracz, D.M., Bouldin, J.G., Demzcuk, W., Ng, L., Maki, A., Jamieson, F., Gilmour, M.W. 2007. Limited genetic diversity in Salmonella enterica Serovar Enteritidis PT13. BMC Microbiology.(7)p.87.
Bouldin, J.G., Morales, C., Frye, J.G., Gast, R.K., Musgrove, M.T. 2007. Detection of Salmonella enterica subpopulations by phenotype microarray antibiotic resistance patterns. Applied and Environmental Microbiology. 73(23):7753-7756.
Gast, R.K. 2007. Serotype-specific and serotype-independent strategies for pre-harvest control of foodborne Salmonella in poultry. Avian Diseases. 51:817-828.
Gast, R.K. 2008. Paratyphoid Infections. Diseases of Poultry, 12 edition. Blackwell Publishing, Ames, iowa, pp.636-655.
Waltman, W.D., Gast, R.K., Mallinson, E.T. 2008. Salmonellosis. Isolation and Identification of Avian Pathogens, 5th edition. American Association of Avian Pathologists, Jacksonville, FL, pp.3-9.
Gast, R.K. 2008. Salmonella Infections: Diseases of Poultry, 12th edition. Blackwell Publishing, Ames, Iowa, pp.619.
Guard, J.G. 2008. Evolutionary trends in two strains of Salmonella enterica subsp. I serovar Enteritidis PT13a that vary in virulence potential: Version 5 NCBI database. National Center for Biotechnology Information (NCBI)Available:http://www.ncbi.nlm.nih.gov/Salmonella_SNPs.html
Bouldin, J.G., Morales, C. 2008. Nucleotide sequence of a predicted diguanylate cyclase unique to egg contaminating Salmonella enteritidis that does not form biofilm.. National Center for Biotechnology Information (NCBI). Available:http://www.ncbi.nlm.nih/entrez/viewer.fcgi?db=nuccore&id=170516891
Gast, R.K., Guraya, R., Bouldin, J.G., Holt, P.S. 2008. Multiplication of Salmonella Enteritidis on the yolk membrane and penetration to the yolk contents at 30 c in an in vitro egg contamination model. Journal of Food Protection. 71:1905-1909.