Publication: The primary target organ of cryptococcus gattii is different from that of cryptococcus neoformans in a murine model
Issued Date
2012-05-01
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21507511
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2-s2.0-84863471593
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Mahidol University
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SCOPUS
Bibliographic Citation
mBio. Vol.3, No.3 (2012)
Suggested Citation
Popchai Ngamskulrungroj, Yun Chang, Edward Sionov, Kyung J. Kwon-Chunga The primary target organ of cryptococcus gattii is different from that of cryptococcus neoformans in a murine model. mBio. Vol.3, No.3 (2012). doi:10.1128/mBio.00103-12 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/14326
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Title
The primary target organ of cryptococcus gattii is different from that of cryptococcus neoformans in a murine model
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Abstract
Cryptococcosis is caused by the opportunistic pathogen Cryptococcus neoformans or by the primary pathogen Cryptococcus gattii. Epidemiological studies suggest that patients infected with C. gattii mainly present with pulmonary disease, while those infected with C. neoformans commonly manifest meningoencephalitis. We compared the pathogenesis of the two species using the C. neoformans H99 and C. gattii R265 strains in a murine inhalation model. C. neoformans grew faster in the brain and caused death by meningoencephalitis, while C. gattii grew faster in the lungs and caused death without roducing fulminating meningoencephalitis. Despite the consistent failure to recover R265 cells from blood, a fraction of the R265 population was detected in the extrapulmonary organs, including the brain. Upon intravenous (i.v.) inoculation of 104 cells via the tail vein, however, C. gattii produced severe meningoencephalitis, demonstrating that C. gattii cells can efficiently cross the blood-brain barrier. Interestingly, i.v. inoculation with five cells caused brain infection in only 10% of C. gattii-infected mice, compared to 60% of mice infected with C. neoformans. In mice that had been initially inoculated via the pulmonary route and subsequently challenged intravenously, a protective effect was observed only in mice infected with C. gattii. C. neoformans cells grew 10 to 100 times faster than C. gattii cells in blood or serum collected from naive mice. The paucity of meningoencephalitis upon inhalation of C. gattii, therefore, may be partly due to an unknown factor(s) in the host's blood coupled with immune protection that reduces dissemination to the brain and fosters lung infection. © 2012 Ngamskulrungroj et al.