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Three phylogenetic groups have driven the recent population expansion of Cryptococcus neoformans

  • P. M. Ashton
  • , L. T. Thanh
  • , P. H. Trieu
  • , D. Van 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
  • , A. K. Chan
  • , G. E. Thwaites
  • , D. G. Lalloo
  • , C. Anscombe
  • , L. T.H. Nhat
  • , J. Perfect
  • G. Dougan, S. Baker, S. Harris, J. N. Day
  • Oxford University Clinical Research Unit
  • Nuffield Department of Medicine
  • University of Sydney
  • London School of Hygiene and Tropical Medicine
  • Mahidol University
  • Laos-Oxford-Mahosot-Wellcome Research Unit
  • Cho Ray Hospital
  • Hospital for Tropical Diseases
  • Sunnybrook Health Sciences Centre
  • Dignitas International
  • Liverpool School of Tropical Medicine
  • Duke University School of Medicine
  • Wellcome Trust
  • Wellcome Trust Sanger Institute
  • Department of Medicine

Research output: Contribution to journalArticlepeer-review

48 Citations (Scopus)

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.

Original languageEnglish
Article number2035
JournalNature Communications
Volume10
Issue number1
DOIs
Publication statusPublished - 1 Dec 2019
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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