The Mooney Lab

The University of Edinburgh

Malaria-Associated l-Arginine Deficiency Induces Mast Cell-Associated Disruption to Intestinal Barrier Defenses against Nontyphoidal Salmonella Bacteremia


Journal article


J. Chau, Caitlin M Tiffany, Shilpa Nimishakavi, Jessica A. Lawrence, N. Pakpour, Jason P Mooney, Kristen L Lokken, G. Caughey, R. Tsolis, S. Luckhart
Infection and Immunity, 2013

Semantic Scholar DOI PubMed
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APA   Click to copy
Chau, J., Tiffany, C. M., Nimishakavi, S., Lawrence, J. A., Pakpour, N., Mooney, J. P., … Luckhart, S. (2013). Malaria-Associated l-Arginine Deficiency Induces Mast Cell-Associated Disruption to Intestinal Barrier Defenses against Nontyphoidal Salmonella Bacteremia. Infection and Immunity.


Chicago/Turabian   Click to copy
Chau, J., Caitlin M Tiffany, Shilpa Nimishakavi, Jessica A. Lawrence, N. Pakpour, Jason P Mooney, Kristen L Lokken, G. Caughey, R. Tsolis, and S. Luckhart. “Malaria-Associated l-Arginine Deficiency Induces Mast Cell-Associated Disruption to Intestinal Barrier Defenses against Nontyphoidal Salmonella Bacteremia.” Infection and Immunity (2013).


MLA   Click to copy
Chau, J., et al. “Malaria-Associated l-Arginine Deficiency Induces Mast Cell-Associated Disruption to Intestinal Barrier Defenses against Nontyphoidal Salmonella Bacteremia.” Infection and Immunity, 2013.


BibTeX   Click to copy

@article{j2013a,
  title = {Malaria-Associated l-Arginine Deficiency Induces Mast Cell-Associated Disruption to Intestinal Barrier Defenses against Nontyphoidal Salmonella Bacteremia},
  year = {2013},
  journal = {Infection and Immunity},
  author = {Chau, J. and Tiffany, Caitlin M and Nimishakavi, Shilpa and Lawrence, Jessica A. and Pakpour, N. and Mooney, Jason P and Lokken, Kristen L and Caughey, G. and Tsolis, R. and Luckhart, S.}
}

Abstract

ABSTRACT Coinfection with malaria and nontyphoidal Salmonella serotypes (NTS) can cause life-threatening bacteremia in humans. Coinfection with malaria is a recognized risk factor for invasive NTS, suggesting that malaria impairs intestinal barrier function. Here, we investigated mechanisms and strategies for prevention of coinfection pathology in a mouse model. Our findings reveal that malarial-parasite-infected mice, like humans, develop l-arginine deficiency, which is associated with intestinal mastocytosis, elevated levels of histamine, and enhanced intestinal permeability. Prevention or reversal of l-arginine deficiency blunts mastocytosis in ileal villi as well as bacterial translocation, measured as numbers of mesenteric lymph node CFU of noninvasive Escherichia coli Nissle and Salmonella enterica serotype Typhimurium, the latter of which is naturally invasive in mice. Dietary supplementation of malarial-parasite-infected mice with l-arginine or l-citrulline reduced levels of ileal transcripts encoding interleukin-4 (IL-4), a key mediator of intestinal mastocytosis and macromolecular permeability. Supplementation with l-citrulline also enhanced epithelial adherens and tight junctions in the ilea of coinfected mice. These data suggest that increasing l-arginine bioavailability via oral supplementation can ameliorate malaria-induced intestinal pathology, providing a basis for testing nutritional interventions to reduce malaria-associated mortality in humans.


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