After exposure to an enteropathogen, the manifestations of infectious diarrhea are variable and depend on host and pathogen factors. A variety of host factors modulate the likelihood of infection or severity of symptoms and can be categorized as those that mediate susceptibility (i.e. host genetic factors, pathogen receptors), and injury (i.e. stimulation of fluid and electrolyte channels, pro inflammatory cytokines). Resolution of infection is determined by factors that contribute to the phases of control and healing (i.e. anti-inflammatory cytokines and specific immunity). Our central hypothesis is that genetic polymorphisms that lead to qualitative or quantitative differences in one or several of these mediators are partially responsible for the development of infection and illness after exposure to enteric pathogens. To this end we will study two well-characterized populations of subjects with infectious diarrhea. The first study group will consist of healthy adults traveling from developed nations to areas of risk for infection with bacterial agents of diarrhea. The second study group will consist of healthy adults experimentally exposed to Cryptosporidium at the University of Texas - Houston Clinical Research Center. For both we propose to investigate host single nucleotide polymorphisms (SNPs) of genes that encode proteins that are associated with either susceptibility, modulation of disease manifestation (injury), eradication (control) and healing after infection. We will focus on three agents with potential for bioterrorism use by waterborne or food borne routes with distinct pathophysiology; enterotoxigenic E. coli a cause of secretory diarrhea, Enteroaggregative E. colia cause of inflammatory diarrhea and Cryptosporidium an intracellular pathogen. SNPs will be correlated with the isolation of an enteropathogen and clinical illness. The impact of SNPs will be examined in the context of different ethnic backgrounds. The understanding of the outcome of infection as they relate to host genetic factors will be of use in designing biodefense interventions that are directed towards improving risk assessment. The identification of populations that are more susceptible or vulnerable to the effects of enteric pathogens will be important in the design of strategies to decrease the impact that these agents may have in causing disease and defining the populations most likely to benefit from prevention, treatment and or vaccines.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI054948-05
Application #
7159398
Study Section
Special Emphasis Panel (ZRG1-BM-1 (02))
Program Officer
Schmitt, Clare K
Project Start
2003-09-30
Project End
2007-12-31
Budget Start
2007-01-01
Budget End
2007-12-31
Support Year
5
Fiscal Year
2007
Total Cost
$352,012
Indirect Cost
Name
University of Texas Health Science Center Houston
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
800771594
City
Houston
State
TX
Country
United States
Zip Code
77225
Mohamed, Jamal A; DuPont, Herbert L; Flores, Jose et al. (2011) Single nucleotide polymorphisms in the promoter of the gene encoding the lipopolysaccharide receptor CD14 are associated with bacterial diarrhea in US and Canadian travelers to Mexico. Clin Infect Dis 52:1332-41
Paredes-Paredes, Mercedes; Okhuysen, Pablo C; Flores, Jose et al. (2011) Seasonality of diarrheagenic Escherichia coli pathotypes in the US students acquiring diarrhea in Mexico. J Travel Med 18:121-5
Villa, Nicolas A; Okhuysen, Pablo C; Flores-Figueroa, Jose et al. (2011) Campylobacter jejuni is not an important pathogen as a cause of diarrhea in US travelers to Mexico. J Travel Med 18:56-8
Ajami, N; Koo, H; Darkoh, C et al. (2010) Characterization of norovirus-associated traveler's diarrhea. Clin Infect Dis 51:123-30
Koo, Hoonmo L; Ajami, Nadim J; Jiang, Zhi-Dong et al. (2010) Noroviruses as a cause of diarrhea in travelers to Guatemala, India, and Mexico. J Clin Microbiol 48:1673-6
Ouyang-Latimer, Jeannette; Ajami, Nadim J; Jiang, Zhi-Dong et al. (2010) Biochemical and genetic diversity of enterotoxigenic Escherichia coli associated with diarrhea in United States students in Cuernavaca and Guadalajara, Mexico, 2004-2007. J Infect Dis 201:1831-8
Flores, Jose; DuPont, Herbert L; Paredes-Paredes, Mercedes et al. (2010) Pilot study of whole-blood gamma interferon response to the Vibrio cholerae toxin B subunit and resistance to enterotoxigenic Escherichia coli-associated diarrhea. Clin Vaccine Immunol 17:879-81
Flores, Jose; Okhuysen, Pablo C (2009) Genetics of susceptibility to infection with enteric pathogens. Curr Opin Infect Dis 22:471-6
Flores, Jose; Okhuysen, Pablo C (2009) Enteroaggregative Escherichia coli infection. Curr Opin Gastroenterol 25:8-11
Mohamed, Jamal A; DuPont, Herbert L; Jiang, Zhi-Dong et al. (2009) A single-nucleotide polymorphism in the gene encoding osteoprotegerin, an anti-inflammatory protein produced in response to infection with diarrheagenic Escherichia coli, is associated with an increased risk of nonsecretory bacterial diarrhea in North Ame J Infect Dis 199:477-85

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