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N Ceré

Publications and source records attributed to N Ceré.

5 recordsLinked to original sources
PubMed1997

Natural transmission of Pneumocystis carinii in nonimmunosuppressed animals: early contagiousness of experimentally infected rabbits (Oryctolagus cuniculus).

Airborne transmission of Pneumocystis carinii has been established, but the infective form and the sources of infection remain unknown. Animal models for studies of P. carinii have previously been limited to immunosuppressed rodents; however, this study was performed with nonimmunodepressed P. carinii-free rabbits. This study was aimed at determining (i) the delay between inoculation of animals (day zero [D0]) and the onset of contagiousness and (ii) the end of contagiousness of these animals (donors). Five-week-old rabbits were used as contact animals and were housed with the donors. The cohabitation periods were for 4 or 5 days from D0 to D4, D4 to D8, D8 to D13, D13 to D18, and D18 to D22. The highest parasite burdens were observed in contact animals housed with donors from D8 to D13 or D13 to D18. This period (8th to 18th day following the day of inoculation of donors) might correspond to the highest phase of contagiousness of donors.

Animals↗
PubMedDate not supplied

Cultivation of rabbit Pneumocystis carinii on cells derived from rabbit (Oryctolagus cuniculus).

Cultivation of Pneumocystis carinii from rabbit onto cell monolayers was intended. Three cell types were used: rat lung derived cell line L2 and canine kidney derived cell line MDCK, and primary epithelial rabbit lung cells derived from 20 days old foetuses. These primary cells were also immortalized by transfection of the coding sequences for the large and small T antigens of the SV40 virus. P. carinii were extracted from lungs of corticoid treated young rabbits and were purified on Ficoll. In vitro development of P. carinii was assessed by counting the number of attached parasites on cells after staining. No development was observed on L2 nd MDCK cell lines. On the contrary, a development was observed on rabbit derived cells with a threefold increase of attached parasites on the third day of culture. Immortalized cells allowed also multiplication of attached P. carinii. These results are similar to those obtained with culture of rodent P. carinii onto cell monolayers.

Animals↗
PubMedDate not supplied

Animal pneumocystosis: a model for man.

Pneumocystis carinii is an important pulmonary pathogen responsible for morbidity and mortality in patients with AIDS. Apart from AIDS, cases of pneumocystosis have been reported in patients receiving immunosuppressive therapy associated with organ transplantation without chemoprophylaxis and in malignant blood diseases. In vitro models are only of limited interest because there is no continuous in vitro culture. The in vivo models have contributed a great deal to the understanding of human Pneumocystis carinii pneumonia. Indeed, animal models remain of prime interest for many purposes, principally comparative medicine, pathogenesis, epidemiology and immunology. Among animal models, the rabbit is a very susceptible host to P. carinii infection, and does not need glucocorticoid treatment. Moreover, antigenic and genomic data suggest that rabbit-derived Pneumocystis strains are more closely related to human Pneumocystis than those of mice or rats. We have therefore shown that the rabbit model permits the study of the pulmonary surfactant modification due to P. carinii infection. This model should be a very interesting model for pathogenesis or immune response studies in immunocompetent animals. The rabbit model could also be used for epidemiological studies. P. carinii transmission appears to be very rapid via contact of Pneumocystis-free rabbits with infected rabbits. These Pneumocystis-free animals could be helpful for characterizing the source and the reservoir and studying parasite transmission.

AIDS-Related Opportunistic Infections↗