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SadA, a Trimeric Autotransporter from Salmonella enterica Serovar Typhimurium, Can Promote Biofilm Formation and Provides Limited Protection against Infection

Authors :
Robin C. May
Calman A. MacLennan
John Pravin
Duncan J. Maskell
Sarah Peters
Claudia T. P. Moraes
Karina Tveen Jensen
Douglas F. Browning
Ian R. Henderson
Dhaarini Raghunathan
Adriana Flores-Langarica
Roxane M. F. Piazza
Jessica Hitchcock
Laura J. V. Piddock
Mark A. Webber
Timothy J. Wells
Faye C. Morris
Gavin K. Paterson
Denisse L. Leyton
Saeeda Bobat
Jessica M A Blair
Adam F. Cunningham
Robert K. Shaw
Source :
Infection and Immunity. 79:4342-4352
Publication Year :
2011
Publisher :
American Society for Microbiology, 2011.

Abstract

Salmonella enterica is a major cause of morbidity worldwide and mortality in children and immunocompromised individuals in sub-Saharan Africa. Outer membrane proteins of Salmonella are of significance because they are at the interface between the pathogen and the host, they can contribute to adherence, colonization, and virulence, and they are frequently targets of antibody-mediated immunity. In this study, the properties of SadA, a purported trimeric autotransporter adhesin of Salmonella enterica serovar Typhimurium, were examined. We demonstrated that SadA is exposed on the Salmonella cell surface in vitro and in vivo during infection of mice. Expression of SadA resulted in cell aggregation, biofilm formation, and increased adhesion to human intestinal Caco-2 epithelial cells. Immunization of mice with folded, full-length, purified SadA elicited an IgG response which provided limited protection against bacterial challenge. When anti-SadA IgG titers were enhanced by administering alum-precipitated protein, a modest additional protection was afforded. Therefore, despite SadA having pleiotropic functions, it is not a dominant, protective antigen for antibody-mediated protection against Salmonella .

Details

ISSN :
10985522 and 00199567
Volume :
79
Database :
OpenAIRE
Journal :
Infection and Immunity
Accession number :
edsair.doi.dedup.....d43872cef5673c8b4c7954a146b0bdcd