The halophilic bacteria Vibrio vulnificus and Vibrio damsela are found in marine and estuarine environments and are increasingly recognized etiological agents of severe wound infections and life-threatening septicemia in humans. The long-term objective of the research described in this application is to identify and characterize the potential extracellular virulence factors of the bacteria in order to aid the diagnosis, prevention, and treatment of the diseases they cause. Previous studies by the PI have focused on the purification and characterization of lethal, tissue-damaging cytolytic toxins (membrane-damaging toxins) produced by V. vulnificus and V. damsela, and a lethal, tissue-damaging elastolytic protease produced by V. vulnificus.
The specific aim of the research described in the application is to evaluate the importance of the previously isolated cytolysins and the elastase in the pathogenesis of experimental diseases caused by the bacteria. Studies to determine whether in vivo production and action of the three tissue-damaging substances are important virulence factors of the bacteria will include: (i) determining whether active and passive immunization against the isolated cytolysins and/or elastase protects mice against tissue damage or death after challenge with the bacteria, (ii) determining whether isogenic mutants specifically lacking the ability to express the putative virulence factors are less virulent for mice than are the parental, wild-type strains, (iii) determining whether parenteral administration of the isolated products enhances the virulence of the isogenic mutants for mice, (iv) using light and electron microscopy to determine whether the tissue damage elicited by the isolated products mimics that produced in mice by the replicating bacteria, and (v) determining whether the products are synthesized in vivo during the development of the infectious diseases in mice.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI018184-07
Application #
3127739
Study Section
Bacteriology and Mycology Subcommittee 1 (BM)
Project Start
1981-09-30
Project End
1990-12-31
Budget Start
1989-01-01
Budget End
1990-12-31
Support Year
7
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Type
Schools of Medicine
DUNS #
041418799
City
Winston-Salem
State
NC
Country
United States
Zip Code
27106
Cutter, D L; Kreger, A S (1990) Cloning and expression of the damselysin gene from Vibrio damsela. Infect Immun 58:266-8
Gray, L D; Kreger, A S (1989) Detection of Vibrio vulnificus cytolysin in V. vulnificus-infected mice. Toxicon 27:439-64
Kreger, A S; Kothary, M H; Gray, L D (1988) Cytolytic toxins of Vibrio vulnificus and Vibrio damsela. Methods Enzymol 165:176-89
Gray, L D; Kreger, A S (1987) Mouse skin damage caused by cytolysin from Vibrio vulnificus and by V. vulnificus infection. J Infect Dis 155:236-41
Kreger, A S; Bernheimer, A W; Etkin, L A et al. (1987) Phospholipase D activity of Vibrio damsela cytolysin and its interaction with sheep erythrocytes. Infect Immun 55:3209-12
Kothary, M H; Kreger, A S (1987) Purification and characterization of an elastolytic protease of Vibrio vulnificus. J Gen Microbiol 133:1783-91
Gray, L D; Kreger, A S (1986) Detection of anti-Vibrio vulnificus cytolysin antibodies in sera from mice and a human surviving V. vulnificus disease. Infect Immun 51:964-5
Kothary, M H; Kreger, A S (1985) Production and partial characterization of an elastolytic protease of Vibrio vulnificus. Infect Immun 50:534-40
Gray, L D; Kreger, A S (1985) Identification of Vibrio vulnificus by indirect immunofluorescence. Diagn Microbiol Infect Dis 3:461-8
Gray, L D; Kreger, A S (1985) Purification and characterization of an extracellular cytolysin produced by Vibrio vulnificus. Infect Immun 48:62-72

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