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dc.contributor.authorChen, C. G.en_US
dc.contributor.authorYang, Y. L.en_US
dc.contributor.authorCheng, H. H.en_US
dc.contributor.authorSu, C. L.en_US
dc.contributor.authorHuang, S. F.en_US
dc.contributor.authorChen, C. T.en_US
dc.contributor.authorLiu, Y. T.en_US
dc.contributor.authorSu, I. J.en_US
dc.contributor.authorLo, H. J.en_US
dc.date.accessioned2019-04-03T06:45:09Z-
dc.date.available2019-04-03T06:45:09Z-
dc.date.issued2006-07-01en_US
dc.identifier.issn0394-6320en_US
dc.identifier.urihttp://dx.doi.org/10.1177/039463200601900312en_US
dc.identifier.urihttp://hdl.handle.net/11536/12084-
dc.description.abstractThe cph1/cph1 efg1/efg1andida albicans mutant cells were non-lethal in a mouse model of systemic infection. We investigated in vivo proliferation and invasion of C albicans cells in infected mice to elucidate the interaction between the host and the pathogen. Homogenates of kidneys from the mice infected with the wild-type and the mutant C albicans cells yielded a mean of 2.1 x 10(7)CFU/g and 2.2 x 10(6) CFU/g, respectively. The kidneys from the mice infected with the wild-type cells showed extensive renal cortical necrosis associated with neutrophilic infiltration. There were also wild-type hyphal cells present in abundance. Hence, tubular necrosis leading to renal failure in the mice may be the cause of death. Although the cph1/cph1 efg1/efg1 mutant cells were not lethal, they were capable of establishing restricted zones of infection and colonization near the renal pelvis instead of simply being cleared by the immune system in mice.en_US
dc.language.isoen_USen_US
dc.subjectCandida albicansen_US
dc.subjectfilamentous growthen_US
dc.subjectmouse modelen_US
dc.subjectvirulenceen_US
dc.titleNon-lethal Candida albicans cph1/cph1 efg1/efg1 transcription factor mutant establishing restricted zone of infection in a mouse model of systemic infectionen_US
dc.typeArticleen_US
dc.identifier.doi10.1177/039463200601900312en_US
dc.identifier.journalINTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGYen_US
dc.citation.volume19en_US
dc.citation.issue3en_US
dc.citation.spage561en_US
dc.citation.epage565en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000241176600012en_US
dc.citation.woscount22en_US
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