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Emergence and Pathogenicity of Highly Virulent Cryptococcus gattii Genotypes in the Northwest United States

Cryptococcus gattii causes life-threatening disease in otherwise healthy hosts and to a lesser extent in immunocompromised hosts. The highest incidence for this disease is on Vancouver Island, Canada, where an outbreak is expanding into neighboring regions including mainland British Columbia and the...

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Autores principales: Byrnes, Edmond J., Li, Wenjun, Lewit, Yonathan, Ma, Hansong, Voelz, Kerstin, Ren, Ping, Carter, Dee A., Chaturvedi, Vishnu, Bildfell, Robert J., May, Robin C., Heitman, Joseph
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858702/
https://www.ncbi.nlm.nih.gov/pubmed/20421942
http://dx.doi.org/10.1371/journal.ppat.1000850
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author Byrnes, Edmond J.
Li, Wenjun
Lewit, Yonathan
Ma, Hansong
Voelz, Kerstin
Ren, Ping
Carter, Dee A.
Chaturvedi, Vishnu
Bildfell, Robert J.
May, Robin C.
Heitman, Joseph
author_facet Byrnes, Edmond J.
Li, Wenjun
Lewit, Yonathan
Ma, Hansong
Voelz, Kerstin
Ren, Ping
Carter, Dee A.
Chaturvedi, Vishnu
Bildfell, Robert J.
May, Robin C.
Heitman, Joseph
author_sort Byrnes, Edmond J.
collection PubMed
description Cryptococcus gattii causes life-threatening disease in otherwise healthy hosts and to a lesser extent in immunocompromised hosts. The highest incidence for this disease is on Vancouver Island, Canada, where an outbreak is expanding into neighboring regions including mainland British Columbia and the United States. This outbreak is caused predominantly by C. gattii molecular type VGII, specifically VGIIa/major. In addition, a novel genotype, VGIIc, has emerged in Oregon and is now a major source of illness in the region. Through molecular epidemiology and population analysis of MLST and VNTR markers, we show that the VGIIc group is clonal and hypothesize it arose recently. The VGIIa/IIc outbreak lineages are sexually fertile and studies support ongoing recombination in the global VGII population. This illustrates two hallmarks of emerging outbreaks: high clonality and the emergence of novel genotypes via recombination. In macrophage and murine infections, the novel VGIIc genotype and VGIIa/major isolates from the United States are highly virulent compared to similar non-outbreak VGIIa/major-related isolates. Combined MLST-VNTR analysis distinguishes clonal expansion of the VGIIa/major outbreak genotype from related but distinguishable less-virulent genotypes isolated from other geographic regions. Our evidence documents emerging hypervirulent genotypes in the United States that may expand further and provides insight into the possible molecular and geographic origins of the outbreak.
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spelling pubmed-28587022010-04-26 Emergence and Pathogenicity of Highly Virulent Cryptococcus gattii Genotypes in the Northwest United States Byrnes, Edmond J. Li, Wenjun Lewit, Yonathan Ma, Hansong Voelz, Kerstin Ren, Ping Carter, Dee A. Chaturvedi, Vishnu Bildfell, Robert J. May, Robin C. Heitman, Joseph PLoS Pathog Research Article Cryptococcus gattii causes life-threatening disease in otherwise healthy hosts and to a lesser extent in immunocompromised hosts. The highest incidence for this disease is on Vancouver Island, Canada, where an outbreak is expanding into neighboring regions including mainland British Columbia and the United States. This outbreak is caused predominantly by C. gattii molecular type VGII, specifically VGIIa/major. In addition, a novel genotype, VGIIc, has emerged in Oregon and is now a major source of illness in the region. Through molecular epidemiology and population analysis of MLST and VNTR markers, we show that the VGIIc group is clonal and hypothesize it arose recently. The VGIIa/IIc outbreak lineages are sexually fertile and studies support ongoing recombination in the global VGII population. This illustrates two hallmarks of emerging outbreaks: high clonality and the emergence of novel genotypes via recombination. In macrophage and murine infections, the novel VGIIc genotype and VGIIa/major isolates from the United States are highly virulent compared to similar non-outbreak VGIIa/major-related isolates. Combined MLST-VNTR analysis distinguishes clonal expansion of the VGIIa/major outbreak genotype from related but distinguishable less-virulent genotypes isolated from other geographic regions. Our evidence documents emerging hypervirulent genotypes in the United States that may expand further and provides insight into the possible molecular and geographic origins of the outbreak. Public Library of Science 2010-04-22 /pmc/articles/PMC2858702/ /pubmed/20421942 http://dx.doi.org/10.1371/journal.ppat.1000850 Text en Byrnes et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Byrnes, Edmond J.
Li, Wenjun
Lewit, Yonathan
Ma, Hansong
Voelz, Kerstin
Ren, Ping
Carter, Dee A.
Chaturvedi, Vishnu
Bildfell, Robert J.
May, Robin C.
Heitman, Joseph
Emergence and Pathogenicity of Highly Virulent Cryptococcus gattii Genotypes in the Northwest United States
title Emergence and Pathogenicity of Highly Virulent Cryptococcus gattii Genotypes in the Northwest United States
title_full Emergence and Pathogenicity of Highly Virulent Cryptococcus gattii Genotypes in the Northwest United States
title_fullStr Emergence and Pathogenicity of Highly Virulent Cryptococcus gattii Genotypes in the Northwest United States
title_full_unstemmed Emergence and Pathogenicity of Highly Virulent Cryptococcus gattii Genotypes in the Northwest United States
title_short Emergence and Pathogenicity of Highly Virulent Cryptococcus gattii Genotypes in the Northwest United States
title_sort emergence and pathogenicity of highly virulent cryptococcus gattii genotypes in the northwest united states
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2858702/
https://www.ncbi.nlm.nih.gov/pubmed/20421942
http://dx.doi.org/10.1371/journal.ppat.1000850
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