The rat model of Pneumocystis carinii pneumonia is frequently used to study
human P. carinii infection, but there are many differences between the rat
and human infections. We studied naturally acquired P. carinii in wild rat
s to examine the relevance of the rat model for human infection. P. carinii
DNA was detected in 47 of 51 wild rats and in 10 of 12 nonimmunosuppressed
laboratory rats. Evidence for three novel formae speciales of rat-derived
P. carinii was found, and these were provisionally named Pneumocystis carin
ii f. sp. rattus-secundi, Pneumocystis carinii f. sp. rattus-tertii, and Pn
eumocystis carinii f. sp. rattus-quarti. Our data suggest that low-level ca
rriage of P. carinii in wild rats and nonimmunosuppressed laboratory rats i
s common and that wild rats are frequently coinfected with more than one fo
rma specialis of P. carinii. We also examined the diversity in the internal
ly transcribed spacer (ITS) regions of the nuclear rRNA operon of Pneumocys
tis carini f. sp. carinii by using samples from wild rats and laboratory ra
ts and spore trap samples. We report a lack of variation in the ITS1 and IT
S2 regions that is consistent with an evolutionary bottleneck in the P. car
inii f. sp. carinii population. This study shows that human- and rat-derive
d P. carinii organisms are very different, not only in genetic composition
but also in population structure and natural history.