Different host defences are required to protect mice from primary systemic vs pulmonary infection with the facultative intracellular bacterial pathogen, Francisella tularensis LVS
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Conlan, JW
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Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, CanadaNatl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
Conlan, JW
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KuoLee, R
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Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, CanadaNatl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
KuoLee, R
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Shen, H
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Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, CanadaNatl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
Shen, H
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Webb, A
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Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, CanadaNatl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
Webb, A
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机构:
[1] Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
Francisella tularensis is a zoonotic, facultative intracellular bacterial pathogen capable of initiating infection, tularemia, via multiple routes including dermal micro-abrasions and inhalation. Mouse models of systemically-initiated infection with F tularensis LVS have been used extensively to reveal potential host defence mechanisms against the pathogen. Such studies have demonstrated the critical need for neutrophils and interferon-gamma (IFN-gamma) to combat the early stages of primary experimental tularaernia initiated by systemic routes. Surprisingly, however, the present study shows that these defences appear not to combat early pulmonary tularaernia initiated by inhalation of the pathogen into the lower airways. The results imply that the effectiveness of particular antibacterial host defences vary with invasion site. Thus, it is impossible to predict effective host defence mechanisms against inhalation-initiated tularaernia from current knowledge of anti-Francisella defences that have been shown to combat systemically-initiated infection.