Murine Model of Clostridium difficile Infection with Aged Gnotobiotic C57BL/6 Mice and a BI/NAP1 Strain

SW Pawlowski, G Calabrese, GL Kolling… - The Journal of …, 2010 - academic.oup.com
SW Pawlowski, G Calabrese, GL Kolling, R Freire, C AlcantaraWarren, B Liu, RB Sartor…
The Journal of infectious diseases, 2010academic.oup.com
The increased incidence and severity of Clostridium difficile infection (CDI) in older adults
(age,⩾ 65 years) corresponds with the emergence of the BI/NAP1 strain, making elucidation
of the host immune response extremely important. We therefore infected germ-free C57BL/6
mice aged 7–14 months with a BI/NAP1 strain and monitored the mice for response. Infected
mice were moribund 48–72 h after infection and developed gross and histological cecitis
and colitis and elevated concentrations of keratinocyte chemoattractant, interleukin 1β …
Abstract
The increased incidence and severity of Clostridium difficile infection (CDI) in older adults (age, ⩾65 years) corresponds with the emergence of the BI/NAP1 strain, making elucidation of the host immune response extremely important. We therefore infected germ-free C57BL/6 mice aged 7–14 months with a BI/NAP1 strain and monitored the mice for response. Infected mice were moribund 48–72 h after infection and developed gross and histological cecitis and colitis and elevated concentrations of keratinocyte chemoattractant, interleukin 1β, monocyte chemotactic protein 1, and granulocyte colony-stimulating factor and decreased levels of interferon γ, interleukin 12 p40, interleukin 12 p70, and interleukin 10 compared with controls. We conclude that aged, germ-free C57BL/6 mice are susceptible to fulminant CDI from a BI/NAP1 strain and represent a novel model to further elucidate the host immune response to acute CDI.
Oxford University Press