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Pathogenic diversity amongst serotype C VGIII and VGIV Cryptococcus gattii isolates

Journal Article · · Scientific Reports
DOI:https://doi.org/10.1038/srep11717· OSTI ID:1624776
 [1];  [2];  [3];  [4];  [5];  [6];  [6];  [3];  [3];  [3];  [3];  [7]
  1. Federal Univ. of Rio de Janeiro (Brazil). Inst. de Microbiologia de Goes; DOE/OSTI
  2. Centro de Desenvolvimento Tecnológico em Saúde (CDTS), Rio de Janeiro (Brazil). Fundação Oswaldo Cruz – Fiocruz
  3. Federal Univ. of Rio Grande do Sul, Porto Alegre (Brazil). Centro de Biotecnologia
  4. Federal Univ. of Rio de Janeiro (Brazil). Inst. de Microbiologia de Goes
  5. Univ. of Sydney, NSW (Australia). Sydney Medical School Westmead Hospital. Marie Bashir Inst. for Infectious Diseases and Biosecurity. Centre for Infectious Diseases and Microbiology. Molecular Mycology Research Lab.; Instituto Nacional de Salud, Bogotá (Colombia). Grupo de Microbiología
  6. Univ. of Sydney, NSW (Australia). Sydney Medical School Westmead Hospital. Marie Bashir Inst. for Infectious Diseases and Biosecurity. Centre for Infectious Diseases and Microbiology. Molecular Mycology Research Lab.
  7. Federal Univ. of Rio de Janeiro (Brazil). Inst. de Microbiologia de Goes; Centro de Desenvolvimento Tecnológico em Saúde (CDTS), Rio de Janeiro (Brazil). Fundação Oswaldo Cruz – Fiocruz
Cryptococcus gattii is one of the causative agents of human cryptococcosis. Highly virulent strains of serotype B C. gattii have been studied in detail, but little information is available on the pathogenic properties of serotype C isolates. In this study, we analyzed pathogenic determinants in three serotype C C. gattii isolates (106.97, ATCC 24066 and WM 779). Isolate ATCC 24066 (molecular type VGIII) differed from isolates WM 779 and 106.97 (both VGIV) in capsule dimensions, expression of CAP genes, chitooligomer distribution, and induction of host chitinase activity. Isolate WM 779 was more efficient than the others in producing pigments and all three isolates had distinct patterns of reactivity with antibodies to glucuronoxylomannan. This great phenotypic diversity reflected in differential pathogenicity. VGIV isolates WM 779 and 106.97 were similar in their ability to cause lethality and produced higher pulmonary fungal burden in a murine model of cryptococcosis, while isolate ATCC 24066 (VGIII) was unable to reach the brain and caused reduced lethality in intranasally infected mice. These results demonstrate a high diversity in the pathogenic potential of isolates of C. gattii belonging to the molecular types VGIII and VGIV.
Research Organization:
Univ. of Sydney, NSW (Australia)
Sponsoring Organization:
USDOE Office of Science (SC)
Grant/Contract Number:
SC0010687
OSTI ID:
1624776
Journal Information:
Scientific Reports, Journal Name: Scientific Reports Journal Issue: 1 Vol. 5; ISSN 2045-2322
Publisher:
Nature Publishing GroupCopyright Statement
Country of Publication:
United States
Language:
English

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Cited By (2)

The Anti-helminthic Compound Mebendazole Has Multiple Antifungal Effects against Cryptococcus neoformans journal March 2017
Differential In Vitro Cytokine Induction by the Species of Cryptococcus gattii Complex journal January 2018

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