Publication:
The primary target organ of cryptococcus gattii is different from that of cryptococcus neoformans in a murine model

dc.contributor.authorPopchai Ngamskulrungrojen_US
dc.contributor.authorYun Changen_US
dc.contributor.authorEdward Sionoven_US
dc.contributor.authorKyung J. Kwon-Chungaen_US
dc.contributor.otherNational Institute of Allergy and Infectious Diseasesen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-11T04:53:48Z
dc.date.available2018-06-11T04:53:48Z
dc.date.issued2012-05-01en_US
dc.description.abstractCryptococcosis 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.en_US
dc.identifier.citationmBio. Vol.3, No.3 (2012)en_US
dc.identifier.doi10.1128/mBio.00103-12en_US
dc.identifier.issn21507511en_US
dc.identifier.other2-s2.0-84863471593en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/14326
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84863471593&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.titleThe primary target organ of cryptococcus gattii is different from that of cryptococcus neoformans in a murine modelen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84863471593&origin=inwarden_US

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