Author
Listed:
- P. M. Ashton
(Oxford University Clinical Research Unit
University of Oxford)
- L. T. Thanh
(Oxford University Clinical Research Unit)
- P. H. Trieu
(Oxford University Clinical Research Unit)
- D. Anh
(Oxford University Clinical Research Unit)
- N. M. Trinh
(Oxford University Clinical Research Unit)
- J. Beardsley
(Oxford University Clinical Research Unit
University of Oxford
University of Sydney)
- F. Kibengo
(MRC/UVRI and LSHTM Uganda Research Unit)
- W. Chierakul
(Mahidol Oxford Tropical Medicine Research Unit)
- D. A. B. Dance
(University of Oxford
Lao–Oxford–Mahosot Hospital–Wellcome Trust Research Unit
London School of Hygiene and Tropical Medicine)
- S. Rattanavong
(Lao–Oxford–Mahosot Hospital–Wellcome Trust Research Unit)
- V. Davong
(Lao–Oxford–Mahosot Hospital–Wellcome Trust Research Unit)
- L. Q. Hung
(Cho Ray Hospital)
- N. V. V. Chau
(Hospital for Tropical Diseases)
- N. L. N. Tung
(Hospital for Tropical Diseases)
- A. K. Chan
(University of Toronto
Dignitas International)
- G. E. Thwaites
(Oxford University Clinical Research Unit
University of Oxford)
- D. G. Lalloo
(Liverpool School of Tropical Medicine)
- C. Anscombe
(Oxford University Clinical Research Unit
University of Oxford)
- L. T. H. Nhat
(Oxford University Clinical Research Unit)
- J. Perfect
(Duke University)
- G. Dougan
(Wellcome Trust-Cambridge Centre for Global Health Research
The Wellcome Trust Sanger Institute
University of Cambridge)
- S. Baker
(Oxford University Clinical Research Unit
University of Oxford
Wellcome Trust-Cambridge Centre for Global Health Research
University of Cambridge)
- S. Harris
(The Wellcome Trust Sanger Institute)
- J. N. Day
(Oxford University Clinical Research Unit
University of Oxford)
Abstract
Cryptococcus neoformans (C. neoformans var. grubii) is an environmentally acquired pathogen causing 181,000 HIV-associated deaths each year. We sequenced 699 isolates, primarily C. neoformans from HIV-infected patients, from 5 countries in Asia and Africa. The phylogeny of C. neoformans reveals a recent exponential population expansion, consistent with the increase in the number of susceptible hosts. In our study population, this expansion has been driven by three sub-clades of the C. neoformans VNIa lineage; VNIa-4, VNIa-5 and VNIa-93. These three sub-clades account for 91% of clinical isolates sequenced in our study. Combining the genome data with clinical information, we find that the VNIa-93 sub-clade, the most common sub-clade in Uganda and Malawi, was associated with better outcomes than VNIa-4 and VNIa-5, which predominate in Southeast Asia. This study lays the foundation for further work investigating the dominance of VNIa-4, VNIa-5 and VNIa-93 and the association between lineage and clinical phenotype.
Suggested Citation
P. M. Ashton & L. T. Thanh & P. H. Trieu & D. Anh & N. M. Trinh & J. Beardsley & F. Kibengo & W. Chierakul & D. A. B. Dance & S. Rattanavong & V. Davong & L. Q. Hung & N. V. V. Chau & N. L. N. Tung & , 2019.
"Three phylogenetic groups have driven the recent population expansion of Cryptococcus neoformans,"
Nature Communications, Nature, vol. 10(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-10092-5
DOI: 10.1038/s41467-019-10092-5
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