At present the properties enabling Escherichia coli to act as one of the major opportunistic pathogens are not well understood. The E. coli cytolysin/hemolysin (hly) plays a contributory role in the virulence of extraintestinal disease, however, the nature of the interaction of the hly with host cells on a molecular levsel is unknown. The Hly polypeptide subunit is 110,000 daltons in molecular mass and its predicted amino acid sequence reveals domain-like elements based on hydropathy and isoelectric point characteristics. An objective of this project will be to delineate Hly-host cell interaction by use of genetically engineered forms of the hly protein, synthetic peptides, chemical cleavage fragments of the hly protein, and both specific polyclonal and monoclonal antibodies. We will develop the domain-specific reagents for use in in vitro and in vivo assays of the activities associated with the hemolysin. This type of analysis has been productively utilized in studies of diphtheria toxin and bacterial fimbriae and will enable an understanding of an important cytolysin. The second main objective of this project is the continued study of the function and regulation of transcription and translation of the four cistrons responsible for the E. coli hly. We will assay the altered function and cellular location of in vitro constructed mutations of each of the four cistrons. These will be made by either insertion of synthetic oligonucleotides or site-specific oligonucleotide-directed mutagenesis. We will quantitate and map the mRNAs by S-1 nuclease protection, Northern blotting and primer extension techniques. These genetic and physical studies will lead to an understanding of the factors affecting the expression of this virulence factor. Overall, the long term goal of this research program is to identify and characterize the genetic and physiological nature of bacterial factors influencing E. coli extraintestinal infections. This type of information is of great value in the development of selective strategies for the prevention and treatment of serious bacterial diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI020323-05
Application #
3129908
Study Section
Bacteriology and Mycology Subcommittee 1 (BM)
Project Start
1983-08-01
Project End
1991-07-31
Budget Start
1987-08-01
Budget End
1988-07-31
Support Year
5
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Ravindran, Sriram; Grys, Thomas E; Welch, Rodney A et al. (2004) Inhibition of plasma kallikrein by C1-inhibitor: role of endothelial cells and the amino-terminal domain of C1-inhibitor. Thromb Haemost 92:1277-83
Lathem, Wyndham W; Bergsbaken, Tessa; Welch, Rodney A (2004) Potentiation of C1 esterase inhibitor by StcE, a metalloprotease secreted by Escherichia coli O157:H7. J Exp Med 199:1077-87
Lathem, Wyndham W; Bergsbaken, Tessa; Witowski, Sarah E et al. (2003) Acquisition of stcE, a C1 esterase inhibitor-specific metalloprotease, during the evolution of Escherichia coli O157:H7. J Infect Dis 187:1907-14
Lathem, Wyndham W; Grys, Thomas E; Witowski, Sarah E et al. (2002) StcE, a metalloprotease secreted by Escherichia coli O157:H7, specifically cleaves C1 esterase inhibitor. Mol Microbiol 45:277-88
Lim, K B; Walker, C R; Guo, L et al. (2000) Escherichia coli alpha-hemolysin (HlyA) is heterogeneously acylated in vivo with 14-, 15-, and 17-carbon fatty acids. J Biol Chem 275:36698-702
Moayeri, M; Welch, R A (1997) Prelytic and lytic conformations of erythrocyte-associated Escherichia coli hemolysin. Infect Immun 65:2233-9
Serwecinska, L; Pytlos, M; Lukomski, S et al. (1997) The simultaneous production of both Hly- and Hpm-like hemolysins is characteristic of the Proteus penneri species. J Basic Microbiol 37:361-70
Leeds, J A; Welch, R A (1997) Enhancing transcription through the Escherichia coli hemolysin operon, hlyCABD: RfaH and upstream JUMPStart DNA sequences function together via a postinitiation mechanism. J Bacteriol 179:3519-27
Bauer, M E; Welch, R A (1997) Pleiotropic effects of a mutation in rfaC on Escherichia coli hemolysin. Infect Immun 65:2218-24
Leeds, J A; Welch, R A (1996) RfaH enhances elongation of Escherichia coli hlyCABD mRNA. J Bacteriol 178:1850-7

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