Cryptococcal cell morphology affects host cell interactions and pathogenicity.
dc.contributor.author | Okagaki, Laura H | |
dc.contributor.author | Strain, Anna K | |
dc.contributor.author | Nielsen, Judith N | |
dc.contributor.author | Charlier, Caroline | |
dc.contributor.author | Baltes, Nicholas J | |
dc.contributor.author | Chrétien, Fabrice | |
dc.contributor.author | Heitman, Joseph | |
dc.contributor.author | Dromer, Françoise | |
dc.contributor.author | Nielsen, Kirsten | |
dc.contributor.editor | Mitchell, Aaron P | |
dc.coverage.spatial | United States | |
dc.date.accessioned | 2011-06-21T17:32:23Z | |
dc.date.issued | 2010-06-17 | |
dc.description.abstract | Cryptococcus neoformans is a common life-threatening human fungal pathogen. The size of cryptococcal cells is typically 5 to 10 microm. Cell enlargement was observed in vivo, producing cells up to 100 microm. These morphological changes in cell size affected pathogenicity via reducing phagocytosis by host mononuclear cells, increasing resistance to oxidative and nitrosative stress, and correlated with reduced penetration of the central nervous system. Cell enlargement was stimulated by coinfection with strains of opposite mating type, and ste3aDelta pheromone receptor mutant strains had reduced cell enlargement. Finally, analysis of DNA content in this novel cell type revealed that these enlarged cells were polyploid, uninucleate, and produced daughter cells in vivo. These results describe a novel mechanism by which C. neoformans evades host phagocytosis to allow survival of a subset of the population at early stages of infection. Thus, morphological changes play unique and specialized roles during infection. | |
dc.description.version | Version of Record | |
dc.identifier | ||
dc.identifier.eissn | 1553-7374 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.language.iso | en_US | |
dc.publisher | Public Library of Science (PLoS) | |
dc.relation.ispartof | PLoS Pathog | |
dc.relation.isversionof | 10.1371/journal.ppat.1000953 | |
dc.relation.journal | Plos Pathogens | |
dc.subject | Animals | |
dc.subject | Blood-Brain Barrier | |
dc.subject | Blotting, Western | |
dc.subject | Brain | |
dc.subject | Bronchoalveolar Lavage | |
dc.subject | Cell Adhesion | |
dc.subject | Cell Proliferation | |
dc.subject | Cryptococcosis | |
dc.subject | Cryptococcus neoformans | |
dc.subject | Female | |
dc.subject | Flow Cytometry | |
dc.subject | Humans | |
dc.subject | Lung Diseases, Fungal | |
dc.subject | Mice | |
dc.subject | Mice, Inbred A | |
dc.subject | Oxidative Stress | |
dc.subject | Phagocytosis | |
dc.subject | Ploidies | |
dc.subject | RNA, Messenger | |
dc.subject | Receptors, Pheromone | |
dc.subject | Reverse Transcriptase Polymerase Chain Reaction | |
dc.title | Cryptococcal cell morphology affects host cell interactions and pathogenicity. | |
dc.title.alternative | ||
dc.type | Journal article | |
duke.contributor.orcid | Heitman, Joseph|0000-0001-6369-5995 | |
duke.date.pubdate | 2010-6-0 | |
duke.description.issue | 6 | |
duke.description.volume | 6 | |
pubs.author-url | ||
pubs.begin-page | e1000953 | |
pubs.issue | 6 | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Medicine, Infectious Diseases | |
pubs.organisational-group | Molecular Genetics and Microbiology | |
pubs.organisational-group | Pharmacology & Cancer Biology | |
pubs.organisational-group | School of Medicine | |
pubs.publication-status | Published online | |
pubs.volume | 6 |