Cryptococcus gattii in North American Pacific Northwest: Whole-Population Genome Analysis Provides Insights into Species Evolution and Dispersal

Author:

Engelthaler David M.1,Hicks Nathan D.1,Gillece John D.1,Roe Chandler C.1,Schupp James M.1,Driebe Elizabeth M.1,Gilgado Felix2,Carriconde Fabian23,Trilles Luciana24,Firacative Carolina25,Ngamskulrungroj Popchai26,Castañeda Elizabeth5,Lazera Marcia dos Santos4,Melhem Marcia S. C.7,Pérez-Bercoff Åsa28,Huttley Gavin8,Sorrell Tania C.2,Voelz Kerstin910,May Robin C.910,Fisher Matthew C.11,Thompson George R.12,Lockhart Shawn R.13,Keim Paul114,Meyer Wieland2

Affiliation:

1. Translational Genomics Research Institute, Flagstaff, Arizona, USA

2. Molecular Mycology Research Laboratory, Center for Infectious Diseases and Microbiology, Sydney Medical School, Westmead Hospital, Marie Bashir Institute for Infectious Diseases and Biosecurity, The University of Sydney, Westmead Millennium Institute, Sydney, Australia

3. Institut Agronomique Néo-Calédonien (IAC), Noumea, New Caledonia

4. Laboratório de Micologia, Instituto de Pesquisa Clínica Evandro Chagas, FIOCRUZ, Rio de Janeiro, Brazil

5. Microbiology Group, Instituto Nacional de Salud, Bogotá, Colombia

6. Department of Microbiology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand

7. Public Health Reference Laboratory, Institute Adolfo Lutz, São Paulo, SP, Brazil

8. John Curtin School of Medical Research, Australian National University, Canberra, Australia

9. Institute of Microbiology and Infection and School of Biosciences, University of Birmingham, Birmingham, United Kingdom

10. National Institute for Health Research Surgical Reconstruction and Microbiology Research Centre, Queen Elizabeth Hospital, Birmingham, United Kingdom

11. Department of Infectious Disease Epidemiology, Imperial College London, London, United Kingdom

12. University of California, Davis, Davis, California, USA

13. Centers for Disease Control and Prevention, Atlanta, Georgia, USA

14. Microbial Genetics and Genomics Center, Northern Arizona University, Flagstaff, Arizona, USA

Abstract

ABSTRACT The emergence of distinct populations of Cryptococcus gattii in the temperate North American Pacific Northwest (PNW) was surprising, as this species was previously thought to be confined to tropical and semitropical regions. Beyond a new habitat niche, the dominant emergent population displayed increased virulence and caused primary pulmonary disease, as opposed to the predominantly neurologic disease seen previously elsewhere. Whole-genome sequencing was performed on 118 C. gattii isolates, including the PNW subtypes and the global diversity of molecular type VGII, to better ascertain the natural source and genomic adaptations leading to the emergence of infection in the PNW. Overall, the VGII population was highly diverse, demonstrating large numbers of mutational and recombinational events; however, the three dominant subtypes from the PNW were of low diversity and were completely clonal. Although strains of VGII were found on at least five continents, all genetic subpopulations were represented or were most closely related to strains from South America. The phylogenetic data are consistent with multiple dispersal events from South America to North America and elsewhere. Numerous gene content differences were identified between the emergent clones and other VGII lineages, including genes potentially related to habitat adaptation, virulence, and pathology. Evidence was also found for possible gene introgression from Cryptococcus neoformans var. grubii that is rarely seen in global C. gattii but that was present in all PNW populations. These findings provide greater understanding of C. gattii evolution in North America and support extensive evolution in, and dispersal from, South America. IMPORTANCE Cryptococcus gattii emerged in the temperate North American Pacific Northwest (PNW) in the late 1990s. Beyond a new environmental niche, these emergent populations displayed increased virulence and resulted in a different pattern of clinical disease. In particular, severe pulmonary infections predominated in contrast to presentation with neurologic disease as seen previously elsewhere. We employed population-level whole-genome sequencing and analysis to explore the genetic relationships and gene content of the PNW C. gattii populations. We provide evidence that the PNW strains originated from South America and identified numerous genes potentially related to habitat adaptation, virulence expression, and clinical presentation. Characterization of these genetic features may lead to improved diagnostics and therapies for such fungal infections. The data indicate that there were multiple recent introductions of C. gattii into the PNW. Public health vigilance is warranted for emergence in regions where C. gattii is not thought to be endemic.

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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