This proposal involves an investigation of the molecular mechanism of enterotoxin B production and its control in Staphylococcus aureus. Enterotoxin are exoproteins produced by certain strains in culture media and in foods. They are known to be a major cause of food poisoning. It has been indicated that the enterotoxin B gene is chromosomal. The toxin gene is very labile, possibly a mobile genetic element, and is part of a unique and complex genetic system. The experimental approach involves the isolation of enterotoxin B gene(s) by molecular cloning E. coli and S. aureus. This consists of shotgun cloning of chromosomal restriction fragments onto a vector plasmid, transformation to a nontoxinogenic strain, and screening for the cloned toxin gene by a radioimmunoassay using anti-toxin serum. Once the toxin gene has been cloned and characterized by restriction mapping, an in vitro coupled transcription-translation system will be used to study the coding properties of the toxin gene. This system will also be used to identify the elements involved in the synthesis and regulation of enterotoxin B. The DNA sequence of the toxin gene(s) will be determined and the coding sequence for the toxin polypeptide identified. Sub-cloning experiments will be performed to determine if any regulatory sequences/gene are involved in enterotoxin B production. If a regulatory gene/polypeptide is involved, its precise role will be determined by using in vitro protein synthesis systems. The cloned toxin gene(s) will be used as a probe to localize the toxin genes in several enterotoxinogenic S. aureus strains by DNA-DNA hybridization. Preliminary studies will be carried out to determine the basis of the lability and mobility of the enterotoxin B gene and to see if the toxin gene is part of transposon system. Successful completion of these studies should reveal the molecular basis of enterotoxin B production and the molecular genetic processes underlying the public health problem of staphylococcal food poisoning.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI019783-04
Application #
3129201
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1982-08-01
Project End
1986-07-31
Budget Start
1985-08-01
Budget End
1986-07-31
Support Year
4
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Type
Schools of Medicine
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Compagnone-Post, P; Malyankar, U; Khan, S A (1991) Role of host factors in the regulation of the enterotoxin B gene. J Bacteriol 173:1827-30
Mahmood, R; Compagnone-Post, P; Khan, S A (1991) An in vitro coupled transcription-translation system from Staphylococcus aureus. Gene 106:29-34
Mahmood, R; Khan, S A (1990) Role of upstream sequences in the expression of the staphylococcal enterotoxin B gene. J Biol Chem 265:4652-6
Gaskill, M E; Khan, S A (1988) Regulation of the enterotoxin B gene in Staphylococcus aureus. J Biol Chem 263:6276-80
Johns Jr, M B; Khan, S A (1988) Staphylococcal enterotoxin B gene is associated with a discrete genetic element. J Bacteriol 170:4033-9
Jones, C L; Khan, S A (1986) Nucleotide sequence of the enterotoxin B gene from Staphylococcus aureus. J Bacteriol 166:29-33
Ranelli, D M; Jones, C L; Johns, M B et al. (1985) Molecular cloning of staphylococcal enterotoxin B gene in Escherichia coli and Staphylococcus aureus. Proc Natl Acad Sci U S A 82:5850-4