To investigate the pathogenesis of acute Mycoplasma pneumoniae infecti
on, BALB/c mice were anesthetized with metofane, and M. pneumoniae was
introduced intranasally on days 0, 1, and 2, Mice were sacrificed on
days 0-15. A histopathologic scoring system defined;inflammatory chang
es in the lungs on a scale of 0-26 (least to most severe). Broth cultu
res were positive for all nasal passage and bronchoalveolar lavage (BA
L) specimens. Histopathologic scores ranged from 0 to 21, The mean log
(10) (cfu/mL) were 4.1-6.4 on days 1-10 and greater than or equal to 1
.7 on days 13-15 for nasal passage and BAL specimens, Serum polymerase
chain reaction was negative. ELISA for serum IgM and immunoblots for
M. pneumoniae antibody were positive in 21 (62%) of 34 and 33 (97%) of
34 infected animals, respectively, at days 8-15. ELISA for IgG antibo
dy was negative. This mouse pneumonia model can be used to study the i
mmunologic and therapeutic responses to acute M. pneumoniae infection.