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Caspase-11 Protects Against Bacteria That Escape the Vacuole
Author(s) -
Youssef Aachoui,
Irina A. Leaf,
Jon A. Hagar,
Mary F. Fontana,
Cristine G. Campos,
Daniel E. Zak,
Michael H. Tan,
Peggy A. Cotter,
Russell E. Vance,
Alan Aderem,
Edward A. Miao
Publication year - 2013
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1230751
Subject(s) - pyroptosis , caspase , microbiology and biotechnology , cytosol , caspase 1 , inflammasome , biology , immunity , bacteria , function (biology) , programmed cell death , chemistry , apoptosis , inflammation , enzyme , biochemistry , immunology , immune system , genetics
Caspases are either apoptotic or inflammatory. Among inflammatory caspases, caspase-1 and -11 trigger pyroptosis, a form of programmed cell death. Whereas both can be detrimental in inflammatory disease, only caspase-1 has an established protective role during infection. Here, we report that caspase-11 is required for innate immunity to cytosolic, but not vacuolar, bacteria. Although Salmonella typhimurium and Legionella pneumophila normally reside in the vacuole, specific mutants (sifA and sdhA, respectively) aberrantly enter the cytosol. These mutants triggered caspase-11, which enhanced clearance of S. typhimurium sifA in vivo. This response did not require NLRP3, NLRC4, or ASC inflammasome pathways. Burkholderia species that naturally invade the cytosol also triggered caspase-11, which protected mice from lethal challenge with B. thailandensis and B. pseudomallei. Thus, caspase-11 is critical for surviving exposure to ubiquitous environmental pathogens.

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