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Same Species, Different Diseases: How and Why Typhoidal and Non-typhoidal Salmonella Enterica Serovars Differ

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2014 Aug 20
PMID 25136336
Citations 225
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Abstract

Human infections by the bacterial pathogen Salmonella enterica represent major disease burdens worldwide. This highly ubiquitous species consists of more than 2600 different serovars that can be divided into typhoidal and non-typhoidal Salmonella (NTS) serovars. Despite their genetic similarity, these two groups elicit very different diseases and distinct immune responses in humans. Comparative analyses of the genomes of multiple Salmonella serovars have begun to explain the basis of the variation in disease manifestations. Recent advances in modeling both enteric fever and intestinal gastroenteritis in mice will facilitate investigation into both the bacterial- and host-mediated mechanisms involved in salmonelloses. Understanding the genetic and molecular mechanisms responsible for differences in disease outcome will augment our understanding of Salmonella pathogenesis, host immunity, and the molecular basis of host specificity. This review outlines the differences in epidemiology, clinical manifestations, and the human immune response to typhoidal and NTS infections and summarizes the current thinking on why these differences might exist.

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References
1.
Raffatellu M, Santos R, Verhoeven D, George M, Wilson R, Winter S . Simian immunodeficiency virus-induced mucosal interleukin-17 deficiency promotes Salmonella dissemination from the gut. Nat Med. 2008; 14(4):421-8. PMC: 2901863. DOI: 10.1038/nm1743. View

2.
Girardin E, Grau G, Dayer J, Roux-Lombard P, Lambert P . Tumor necrosis factor and interleukin-1 in the serum of children with severe infectious purpura. N Engl J Med. 1988; 319(7):397-400. DOI: 10.1056/NEJM198808183190703. View

3.
Kent T, Formal S, Labrec E . Salmonella gastroenteritis in rhesus monkeys. Arch Pathol. 1966; 82(3):272-9. View

4.
Sztein M . Cell-mediated immunity and antibody responses elicited by attenuated Salmonella enterica Serovar Typhi strains used as live oral vaccines in humans. Clin Infect Dis. 2007; 45 Suppl 1:S15-9. DOI: 10.1086/518140. View

5.
Dutil L, Irwin R, Finley R, Ng L, Avery B, Boerlin P . Ceftiofur resistance in Salmonella enterica serovar Heidelberg from chicken meat and humans, Canada. Emerg Infect Dis. 2009; 16(1):48-54. PMC: 2874360. DOI: 10.3201/eid1601.090729. View