E. Tamburrini et al., Pneumocystis carinii infection in young non-immunosuppressed rabbits. Kinetics of infection and of the primary specific immune response, MED MICROBI, 188(1), 1999, pp. 1-7
The aim of this study was to determine the kinetics, the dissemination of t
he infection and the immunological response to Pneumocystis carinii primary
infection in a non-immunosuppressed rabbit model. For this purpose, we dev
eloped a nested PCR that amplified a portion of the mitochondrial large-sub
unit rRNA gene of rabbit-derived P. carinii. The PCR detected P. carinii DN
A in lung and bronchoalveolar lavage fluids from 14- to 45-day-old rabbits
but not in their serum. No P. carinii DNA was detected in extrapulmonary or
gans from 28-day-old rabbits with P. carinii pneumonia. ELISA and immunoblo
tting analysis showed that 5-day-old pups had elevated specific IgG. The Ig
G concentration sharply decreased, reaching a trough on day 21, and from th
en onwards progressively increased as the infection cleared. Conversely, th
e specific IgM concentration increased during the infection and peaked on d
ay 28. IgG mainly recognized a 50-kDa subunit of P. carinii organisms; IgM
recognized first a 45-kDa subunit on day 21, whereas from day 28 onwards it
also recognized the 50-kDa subunit. A P. carinii-specific splenocyte proli
ferative response was observed on day 45. These findings suggest that P. ca
rinii primary infection is a time-limited and a lung-limited event and cont
ribute new information on the relationship between the kinetics of primary
P. carinii infection and the immunological response in a model that mimics
the primary infections in humans.