Chlamydia pneumoniae causes chronic infections, which have been associated
with cardiovascular diseases. The antigenic structures of the organism have
been detected in atherosclerotic lesions by immunohistochemistry. We wante
d to further evaluate the presence and localization of C. pneumoniae in dif
ferent tissues by in situ hybridization. We established a new colorimetric
in situ hybridization method using a digoxigenin-labelled probe and studied
the localization of C. pneumoniae in formalin-fixed, paraffin-embedded lun
gs of infected mice. We also used the method to study its presence in 12 ab
dominal aortic aneurysms. In C. pneumoniae-infected mice, the organism was
first detected in bronchial epithelial cells, and later in pneumocytes and
endothelial cells. C. pneumoniae was also present in five of eight abdomina
l aortic aneurysms previously shown to be positive by immunohistochemistry.
The findings are in accordance with the invasive nature of C. pneumoniae,
and confirm its presence in abdominal aortic aneurysms.