
Comparison of the Susceptibilities of C57BL/6 and A/J Mouse Strains toStreptococcus suisSerotype 2 Infection
Author(s) -
María de la Cruz Domínguez-Punaro,
Mariela Segura,
Danuta Radzioch,
Serge Rivest,
Marcelo Gottschalk
Publication year - 2008
Publication title -
infection and immunity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.508
H-Index - 220
eISSN - 1070-6313
pISSN - 0019-9567
DOI - 10.1128/iai.00350-08
Subject(s) - streptococcus suis , biology , serotype , immune system , immunology , pathogen , septic shock , microbiology and biotechnology , tumor necrosis factor alpha , meningitis , proinflammatory cytokine , virology , sepsis , inflammation , virulence , medicine , gene , genetics , psychiatry
Streptococcus suis is an important swine and human pathogen. Assessment of susceptibility toS. suis using animal models has been limited to monitoring mortality rates. We recently developed a hematogenous model ofS. suis infection in adult CD1 outbred mice to study the in vivo development of an early septic shock-like syndrome that leads to death and a late phase that clearly induces central nervous system damage, including meningitis. In the present study, we compared the severities of septic shock-like syndrome caused byS. suis between adult C57BL/6J (B6) and A/J inbred mice. Clinical parameters, proinflammatory mediators, and bacterial clearance were measured to dissect potential immune factors associated with genetic susceptibility toS. suis infection. Results showed that A/J mice were significantly more susceptible than B6 mice toS. suis infection, especially during the acute septic phase of infection (100% of A/J and 16% of B6 mice died before 24 h postinfection). The greater susceptibility of A/J mice was associated with an exaggerated inflammatory response, as indicated by their higher production of tumor necrosis factor alpha, interleukin-12p40/p70 (IL-12p40/p70), gamma interferon, and IL-1β, but not with different bacterial loads in the blood. In addition, IL-10 was shown to be responsible, at least in part, for the higher survival in B6 mice. Our findings demonstrate that A/J mice are very susceptible toS. suis infection and provide evidence that the balance between pro- and anti-inflammatory mediators is crucial for host survival during the septic phase.