Genomic Understanding of an Infectious Brain Disease from the Desert.
Leandro Ferreira MorenoAbdalla A O AhmedBalázs BrankovicsChristina A CuomoSteph B J MenkenSaad J Taj-AldeenHani FaidahJ Benjamin StielowMarcus de M TeixeiraFrancesc Xavier Prenafeta-BoldúVania A VicenteSybren de HoogPublished in: G3 (Bethesda, Md.) (2018)
Rhinocladiella mackenziei accounts for the majority of fungal brain infections in the Middle East, and is restricted to the arid climate zone between Saudi Arabia and Pakistan. Neurotropic dissemination caused by this fungus has been reported in immunocompromised, but also immunocompetent individuals. If untreated, the infection is fatal. Outside of humans, the environmental niche of R. mackenziei is unknown, and the fungus has been only cultured from brain biopsies. In this paper, we describe the whole-genome resequencing of two R. mackenziei strains from patients in Saudi Arabia and Qatar. We assessed intraspecies variation and genetic signatures to uncover the genomic basis of the pathogenesis, and potential niche adaptations. We found that the duplicated genes (paralogs) are more susceptible to accumulating significant mutations. Comparative genomics with other filamentous ascomycetes revealed a diverse arsenal of genes likely engaged in pathogenicity, such as the degradation of aromatic compounds and iron acquisition. In addition, intracellular accumulation of trehalose and choline suggests possible adaptations to the conditions of an arid climate region. Specifically, protein family contractions were found, including short-chain dehydrogenase/reductase SDR, the cytochrome P450 (CYP) (E-class), and the G-protein β WD-40 repeat. Gene composition and metabolic potential indicate extremotolerance and hydrocarbon assimilation, suggesting a possible environmental habitat of oil-polluted desert soil.
Keyphrases
- genome wide
- climate change
- copy number
- saudi arabia
- resting state
- human health
- white matter
- genome wide identification
- functional connectivity
- end stage renal disease
- dna methylation
- newly diagnosed
- escherichia coli
- ejection fraction
- single cell
- high intensity
- multiple sclerosis
- prognostic factors
- genome wide analysis
- staphylococcus aureus
- intensive care unit
- tertiary care
- binding protein
- life cycle
- reactive oxygen species
- biofilm formation
- acute respiratory distress syndrome