The goal of this research is to determine the mechanism by which Naegleria fowleri induces cytopathic effects in nerve cells in culture. The elucidation of the mechanism by which these effector cells cause target cell death would provide basic information as to the nature of effector-target cell interactions. Furthermore, recognition of the basic character of these cell-cell interactions would provide a basis for understanding the disease process caused by the pathogenic strains of N. fowleri, which induce primary amebic meningoencephalitis. In the first phase of this study, it is proposed to define whether pathogenic strains and low pathogenic strains of Naegleria induce cytopathology by a common mechanism. N. fowleri amebae exhibit a unique structure, the """"""""food-cup"""""""" or amebostome. It is proposed to determine whether """"""""food-cup"""""""" expression correlates with target cell destruction. Metabolic inhibitors such as cycloheximide and dinitrophenol, and microtubular and microfilament function inhibitors will be employed to study attachment and target cell killing. Scanning electron microscopy and a 51 Cr-release assay will be employed to monitor attachment and cytolysis, respectively. In the second phase, it is proposed to define which factors elicited by nerve cells and other mammalian cells serve as chemoattractants of Naegleria. Chemotaxis assays will include the use of Boyden chambers. In the third phase, the nature of Naegleria cytotoxin will be defined biologically, biochemically and immunologically. Sequential ammonium sulfate precipitation, gel filtration, and preparative isoelectrofocusing will be employed to purify the cytotoxic factor from crude lysates of N. fowleri. Characterization of the cytotoxic factor(s) will include determination of molecular weight, isoelectric points, reaction with reducing and alkylating agents, and inhibitors of proteases nd phospholipases. In the fourth phase, antiserum to the cytotoxic material will be prepred in rabbits. The antiserum will be used for determining the location of the cytotoxic factor on or within the amebae and for determining the location of the cytotoxin on or within the target nerve cell. We propose to study the mechanism of action of the cytotoxic factor on nerve cells by utilizing electron microscopy and radioisotope labeling techniques. We will label target cells with 86 Rb, 35 S-methionine, and 3 H-thymidine to determine if ion efflux occurs prior to cytoplasmic protein or nuclear content extrusion. In conducting these studies, the production of cytotoxins will be correlated to amebostome expression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI021055-01A1
Application #
3130968
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1984-12-01
Project End
1987-11-30
Budget Start
1984-12-01
Budget End
1985-11-30
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Type
Overall Medical
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Marciano-Cabral, F; Zoghby, K L; Bradley, S G (1990) Cytopathic action of Naegleria fowleri amoebae on rat neuroblastoma target cells. J Protozool 37:138-44
Zhang, L; Marciano-Cabral, F; Bradley, S G (1988) Effects of cyclophosphamide and a metabolite, acrolein, on Naegleria fowleri in vitro and in vivo. Antimicrob Agents Chemother 32:962-5
Marciano-Cabral, F (1988) Biology of Naegleria spp. Microbiol Rev 52:114-33
Marciano-Cabral, F; Cline, M (1987) Chemotaxis by Naegleria fowleri for bacteria. J Protozool 34:127-31
Marciano-Cabral, F; Cline, M L; Bradley, S G (1987) Specificity of antibodies from human sera for Naegleria species. J Clin Microbiol 25:692-7
Marciano-Cabral, F; Stanitski, S; Radhakrishna, V et al. (1987) Characterization of a neutral aminoacyl-peptide hydrolase from Naegleria fowleri. J Protozool 34:146-9
Whiteman, L Y; Marciano-Cabral, F (1987) Susceptibility of pathogenic and nonpathogenic Naegleria spp. to complement-mediated lysis. Infect Immun 55:2442-7
Fulford, D E; Marciano-Cabral, F (1986) Cytolytic activity of Naegleria fowleri cell-free extract. J Protozool 33:498-502
Cline, M; Carchman, R; Marciano-Cabral, F (1986) Movement of Naegleria fowleri stimulated by mammalian cells in vitro. J Protozool 33:10-3
Marciano-Cabral, F M; Fulford, D E (1986) Cytopathology of pathogenic and nonpathogenic Naegleria species for cultured rat neuroblastoma cells. Appl Environ Microbiol 51:1133-7