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Importance of Lipopolysaccharide and Cyclic β-1,2-Glucans in Brucella-Mammalian Infections

Overview
Journal Int J Microbiol
Publisher Wiley
Specialty Microbiology
Date 2010 Dec 15
PMID 21151694
Citations 26
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Abstract

Brucella species are the causative agents of one of the most prevalent zoonotic diseases: brucellosis. Infections by Brucella species cause major economic losses in agriculture, leading to abortions in infected animals and resulting in a severe, although rarely lethal, debilitating disease in humans. Brucella species persist as intracellular pathogens that manage to effectively evade recognition by the host's immune system. Sugar-modified components in the Brucella cell envelope play an important role in their host interaction. Brucella lipopolysaccharide (LPS), unlike Escherichia coli LPS, does not trigger the host's innate immune system. Brucella produces cyclic β-1,2-glucans, which are important for targeting them to their replicative niche in the endoplasmic reticulum within the host cell. This paper will focus on the role of LPS and cyclic β-1,2-glucans in Brucella-mammalian infections and discuss the use of mutants, within the biosynthesis pathway of these cell envelope structures, in vaccine development.

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References
1.
Ciocchini A, Guidolin L, Casabuono A, Couto A, Inon de Iannino N, Ugalde R . A glycosyltransferase with a length-controlling activity as a mechanism to regulate the size of polysaccharides. Proc Natl Acad Sci U S A. 2007; 104(42):16492-7. PMC: 2034269. DOI: 10.1073/pnas.0708025104. View

2.
Briones G, Inon de Iannino N, Roset M, Vigliocco A, Paulo P, Ugalde R . Brucella abortus cyclic beta-1,2-glucan mutants have reduced virulence in mice and are defective in intracellular replication in HeLa cells. Infect Immun. 2001; 69(7):4528-35. PMC: 98529. DOI: 10.1128/IAI.69.7.4528-4535.2001. View

3.
Godfroid F, Taminiau B, Danese I, Denoel P, Tibor A, Weynants V . Identification of the perosamine synthetase gene of Brucella melitensis 16M and involvement of lipopolysaccharide O side chain in Brucella survival in mice and in macrophages. Infect Immun. 1998; 66(11):5485-93. PMC: 108687. DOI: 10.1128/IAI.66.11.5485-5493.1998. View

4.
Bryant C, Spring D, Gangloff M, Gay N . The molecular basis of the host response to lipopolysaccharide. Nat Rev Microbiol. 2009; 8(1):8-14. DOI: 10.1038/nrmicro2266. View

5.
Scholz H, Hubalek Z, Sedlacek I, Vergnaud G, Tomaso H, Al Dahouk S . Brucella microti sp. nov., isolated from the common vole Microtus arvalis. Int J Syst Evol Microbiol. 2008; 58(Pt 2):375-82. DOI: 10.1099/ijs.0.65356-0. View