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Effects of inoculating dose on the kinetics of Chlamydia muridarum genital infection in female mice
Author(s) -
Carey Alison J,
Cunningham Kelly A,
Hafner Louise M,
Timms Peter,
Beagley Kenneth W
Publication year - 2009
Publication title -
immunology and cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.999
H-Index - 104
eISSN - 1440-1711
pISSN - 0818-9641
DOI - 10.1038/icb.2009.3
Subject(s) - chlamydia trachomatis , chlamydia , infertility , infectious dose , pelvic inflammatory disease , genital tract , biology , immunology , sex organ , inoculation , infiltration (hvac) , chlamydiaceae , physiology , medicine , gynecology , pregnancy , virus , genetics , physics , thermodynamics
Chlamydia trachomatis infections have been implicated in problems such as pelvic inflammatory disease and infertility in females. Although there are some studies examining the kinetics of ascending infection, there is limited information on the kinetics of pathology development and cellular infiltrate into the reproductive tissues in relation to the effects of inoculating dose, and a better understanding of these is needed. The murine model of female genital tract Chlamydia muridarum infection is frequently used as a model of human C. trachomatis reproductive tract infection. To investigate the kinetics of ascending genital infection and associated pathology development, female BALB/c mice were intravaginally infected with C. muridarum at doses ranging from 5 × 10 2 to 2.6 × 10 6 inclusion forming units. We found that the inoculating dose affects the course of infection and the ascension of bacteria, with the highest dose ascending rapidly to the oviducts. By comparison, the lowest dose resulted in the greatest bacterial load in the lower reproductive tract. Interestingly, we found that the dose did not significantly affect inflammatory cell infiltrate in the various regions. Overall, this data show the effects of infectious dose on the kinetics of ascending chlamydial infection and associated inflammatory infiltration in BALB/c mice.