Bacterial infection tendentiously triggers inflammasome activation, whereas the roles of inflammasome activation in host defense against diverse infections remain unclear. Here, we identified that an ASC-dependent inflammasome activation played opposite roles in host defense against Francisella novicida wild-type (WT) U112 and mutant strain XWK4. Comparing with U112, XWK4 infection induced robust cytokine production, ASC-dependent inflammasome activation, and pyroptosis. Both AIM2 and NLRP3 were involved and played independent roles in XWK4-induced inflammasome activation. Type II interferon was partially required for XWK4-triggered inflammasome activation, which was different from type I interferon dependency in U112-induced inflammasome activation. Distinct from F. novicida U112 and Acinetobacter baumannii infection, Asc(-/-) mice were more resistant than WT mice response to XWK4 infection by limiting bacterial burden in vivo. The excessive inflammasome activation triggered by XWK4 infection caused dramatical cell death and pathological damage. Our study offers novel insights into mechanisms of inflammasome activation in host defense and provides potential therapeutic approach against bacterial infections and inflammatory diseases.
[1]Univ Sci & Technol China, Sch Life Sci, Hefei, Peoples R China.
[2]Chinese Acad Sci, Kunming Inst Zool, Key Lab Anim Models & Human Dis Mech, Key Lab Bioact Peptides Yunnan Prov, Kunming, Yunnan, Peoples R China.
[3]Shandong Univ, Cheeloo Coll Med, Adv Med Res Inst, Key Lab Expt Teratol,Minist Educ, Jinan, Peoples R China.
[4]Jiangnan Univ, State Key Lab Food Sci & Technol, Wuxi, Jiangsu, Peoples R China.
[5]Kunming Med Univ, Affiliated Hosp 1, Dept Clin Lab, Kunming, Yunnan, Peoples R China.
[6]Yunnan Key Lab Lab Med, Kunming, Yunnan, Peoples R China.
[7]Shandong Univ, Qilu Hosp, Dept Clin Lab, Jinan, Peoples R China.
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