|Publication Type||Journal Article|
|Year of Publication||2015|
|Authors||Farrer, RA, Desjardins, CA, Sakthikumar, S, Gujja, S, Saif, S, Zeng, Q, Chen, Y, Voelz, K, Heitman, J, May, RC, Fisher, MC, Cuomo, CA|
|Date Published||2015 Sep 01|
|Keywords||Animals, Cluster Analysis, Cryptococcosis, Cryptococcus gattii, DNA, Fungal, Environmental Microbiology, Evolution, Molecular, Genetic Variation, Genome, Fungal, Genotype, Humans, Molecular Sequence Annotation, Molecular Sequence Data, Phylogeography, Sequence Analysis, DNA, Synteny|
UNLABELLED: Cryptococcus gattii is a fungal pathogen of humans, causing pulmonary infections in otherwise healthy hosts. To characterize genomic variation among the four major lineages of C. gattii (VGI, -II, -III, and -IV), we generated, annotated, and compared 16 de novo genome assemblies, including the first for the rarely isolated lineages VGIII and VGIV. By identifying syntenic regions across assemblies, we found 15 structural rearrangements, which were almost exclusive to the VGI-III-IV lineages. Using synteny to inform orthology prediction, we identified a core set of 87% of C. gattii genes present as single copies in all four lineages. Remarkably, 737 genes are variably inherited across lineages and are overrepresented for response to oxidative stress, mitochondrial import, and metal binding and transport. Specifically, VGI has an expanded set of iron-binding genes thought to be important to the virulence of Cryptococcus, while VGII has expansions in the stress-related heat shock proteins relative to the other lineages. We also characterized genes uniquely absent in each lineage, including a copper transporter absent from VGIV, which influences Cryptococcus survival during pulmonary infection and the onset of meningoencephalitis. Through inclusion of population-level data for an additional 37 isolates, we identified a new transcontinental clonal group that we name VGIIx, mitochondrial recombination between VGII and VGIII, and positive selection of multidrug transporters and the iron-sulfur protein aconitase along multiple branches of the phylogenetic tree. Our results suggest that gene expansion or contraction and positive selection have introduced substantial variation with links to mechanisms of pathogenicity across this species complex.
IMPORTANCE: The genetic differences between phenotypically different pathogens provide clues to the underlying mechanisms of those traits and can lead to new drug targets and improved treatments for those diseases. In this paper, we compare 16 genomes belonging to four highly differentiated lineages of Cryptococcus gattii, which cause pulmonary infections in otherwise healthy humans and other animals. Half of these lineages have not had their genomes previously assembled and annotated. We identified 15 ancestral rearrangements in the genome and over 700 genes that are unique to one or more lineages, many of which are associated with virulence. In addition, we found evidence for recent transcontinental spread, mitochondrial genetic exchange, and positive selection in multidrug transporters. Our results suggest that gene expansion/contraction and positive selection are diversifying the mechanisms of pathogenicity across this species complex.
|PubMed Central ID||PMC4556806|
|Grant List||R37 AI039115 / AI / NIAID NIH HHS / United States |
U54 HG003067 / HG / NHGRI NIH HHS / United States
MR/K000373/1 / / Medical Research Council / United Kingdom
/ / Medical Research Council / United Kingdom
U54HG003067 / HG / NHGRI NIH HHS / United States
R01 AI050113 / AI / NIAID NIH HHS / United States
/ / Wellcome Trust / United Kingdom