Cytotoxins of the human pathogen Aeromonas hydrophila trigger, via the NLRP3 inflammasome, caspase-1 activation in macrophages.


Autoria(s): McCoy A.J.; Koizumi Y.; Toma C.; Higa N.; Dixit V.; Taniguchi S.; Tschopp J.; Suzuki T.
Data(s)

2010

Resumo

Aeromonas hydrophila is a Gram-negative pathogen that causes serious infectious disease in humans. A. hydrophila induces apoptosis in infected macrophages, but the host proinflammatory responses triggered by macrophage death are largely unknown. Here, we demonstrate that the infection of mouse macrophages with A. hydrophila triggers the activation of caspase-1 and release of IL-1β. Caspase-1 activation was abrogated in macrophages deficient in Nod-like receptor family, pyrin domain containing 3 (NLRP3) and apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC), but not NLR family, CARD domain containing 4 (NLRC4). The activation of the NLRP3 inflammasome was mediated by three cytotoxins (aerolysin, hemolysin and multifunctional repeat-in-toxin) produced by A. hydrophila. Our results indicated that the NLRP3 inflammasome senses A. hydrophila infection through the action of bacterial cytotoxins.

Identificador

http://serval.unil.ch/?id=serval:BIB_23D037FD20F7

isbn:1521-4141[electronic], 0014-2980[linking]

pmid:20722078

doi:10.1002/eji.201040490

isiid:000283387500018

Idioma(s)

en

Fonte

European Journal of Immunology, vol. 40, no. 10, pp. 2797-2803

Palavras-Chave #Aeromonas; Caspase-1; Nod-like receptor
Tipo

info:eu-repo/semantics/article

article