Host adaptation of a bacterial toxin from the human pathogen salmonella typhi.

Bibliographic Collection: 
CARTA-Inspired Publication
Publication Type: Journal Article
Authors: Deng, L.; Song, J.; Gao, X.; Wang, J.; Yu, H.; Chen, X.; Nissi M Varki; Naito-Matsui, Y.; Galan, J.E.; Ajit Varki
Year of Publication: 2014
Journal: Cell
Volume: 159
Number: 6
Pagination: 1290-9
Date Published: 12/2014
Publisher: United States
Publication Language: eng
Accession Number: 25480294
Abstract:

Salmonella Typhi is an exclusive human pathogen that causes typhoid fever. Typhoid toxin is a S. Typhi virulence factor that can reproduce most of the typhoid fever symptoms in experimental animals. Toxicity depends on toxin binding to terminally sialylated glycans on surface glycoproteins. Human glycans are unusual because of the lack of CMAH, which in other mammals converts N-acetylneuraminic acid (Neu5Ac) to N-glycolylneuraminic acid (Neu5Gc). Here, we report that typhoid toxin binds to and is toxic toward cells expressing glycans terminated in Neu5Ac (expressed by humans) over glycans terminated in Neu5Gc (expressed by other mammals). Mice constitutively expressing CMAH thus displaying Neu5Gc in all tissues are resistant to typhoid toxin. The atomic structure of typhoid toxin bound to Neu5Ac reveals the structural bases for its binding specificity. These findings provide insight into the molecular bases for Salmonella Typhi's host specificity and may help the development of therapies for typhoid fever.

Notes:

Copyright (c) 2014 Elsevier Inc. All rights reserved.Cell. 2014 Dec 4;159(6):1290-9. doi: 10.1016/j.cell.2014.10.057. PMID:25480294 [PubMed - in process] PMCID:PMC4258231 [Available on 2015/12/4] 

Author Address:

Glycobiology Research and Training Center, University of California, San Diego, La Jolla, CA 92093, USA; Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA; Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093, USA. Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06536, USA. Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06536, USA. School of Life Sciences, Tsinghua University, Beijing 100084, PRC. Department of Chemistry, University of California, Davis, Davis, CA 95616, USA. Department of Chemistry, University of California, Davis, Davis, CA 95616, USA. Glycobiology Research and Training Center, University of California, San Diego, La Jolla, CA 92093, USA; Department of Pathology, University of California, San Diego, La Jolla, CA 92093, USA. Glycobiology Research and Training Center, University of California, San Diego, La Jolla, CA 92093, USA; Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA; Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093, USA. Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06536, USA. Electronic address: jorge.galan@yale.edu. Glycobiology Research and Training Center, University of California, San Diego, La Jolla, CA 92093, USA; Department of Medicine, University of California, San Diego, La Jolla, CA 92093, USA; Department of Pathology, University of California, San Diego, La Jolla, CA 92093, USA; Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093, USA. Electronic address: a1varki@ucsd.edu.

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