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Genome Res DOI:10.1101/gr.218727.116

Population genomics and the evolution of virulence in the fungal pathogen.

Publication TypeJournal Article
Year of Publication2017
AuthorsDesjardins, CA, Giamberardino, C, Sykes, SM, Yu, C-H, Tenor, JL, Chen, Y, Yang, T, Jones, AM, Sun, S, Haverkamp, MR, Heitman, J, Litvintseva, AP, Perfect, JR, Cuomo, CA
JournalGenome Res
Volume27
Issue7
Pages1207-1219
Date Published2017 Jul
ISSN1549-5469
Abstract

is an opportunistic fungal pathogen that causes approximately 625,000 deaths per year from nervous system infections. Here, we leveraged a unique, genetically diverse population offrom sub-Saharan Africa, commonly isolated from mopane trees, to determine how selective pressures in the environment coincidentally adaptedfor human virulence. Genome sequencing and phylogenetic analysis of 387 isolates, representing the global VNI and African VNB lineages, highlighted a deep, nonrecombining split in VNB (herein, VNBI and VNBII). VNBII was enriched for clinical samples relative to VNBI, while phenotypic profiling of 183 isolates demonstrated that VNBI isolates were significantly more resistant to oxidative stress and more heavily melanized than VNBII isolates. Lack of melanization in both lineages was associated with loss-of-function mutations in thetranscription factor. A genome-wide association study across all VNB isolates revealed sequence differences between clinical and environmental isolates in virulence factors and stress response genes. Inositol transporters and catabolism genes, which process sugars present in plants and the human nervous system, were identified as targets of selection in all three lineages. Further phylogenetic and population genomic analyses revealed extensive loss of genetic diversity in VNBI, suggestive of a history of population bottlenecks, along with unique evolutionary trajectories for mating type loci. These data highlight the complex evolutionary interplay between adaptation to natural environments and opportunistic infections, and that selection on specific pathways may predispose isolates to human virulence.

DOI10.1101/gr.218727.116
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/28611159?dopt=Abstract

Alternate JournalGenome Res.
PubMed ID28611159
PubMed Central IDPMC5495072
Grant ListR37 AI039115 / AI / NIAID NIH HHS / United States
R01 AI073896 / AI / NIAID NIH HHS / United States
R01 AI093257 / AI / NIAID NIH HHS / United States
R01 AI050113 / AI / NIAID NIH HHS / United States
U19 AI110818 / AI / NIAID NIH HHS / United States