Genome Diversity, Recombination, and Virulence across the Major Lineages of Paracoccidioides

Author:

Muñoz José F.123,Farrer Rhys A.3ORCID,Desjardins Christopher A.3,Gallo Juan E.14,Sykes Sean3,Sakthikumar Sharadha3,Misas Elizabeth12,Whiston Emily A.5,Bagagli Eduardo6,Soares Celia M. A.7,Teixeira Marcus de M.89,Taylor John W.5,Clay Oliver K.110,McEwen Juan G.111,Cuomo Christina A.3ORCID

Affiliation:

1. Cellular and Molecular Biology Unit, Corporación para Investigaciones Biológicas, Medellín, Colombia

2. Institute of Biology, Universidad de Antioquia, Medellín, Colombia

3. Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA

4. Doctoral Program in Biomedical Sciences, Universidad del Rosario, Bogotá, Colombia

5. Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, California, USA

6. Instituto de Biociências, Universidade Estadual Paulista, Botucatu, São Paulo, Brazil

7. Laboratório de Biología Molecular, Instituto de Ciências Biológicas, ICBII, Goiânia, Brazil

8. Instituto de Ciências Biológicas, Universidade de Brasília, Brasília, Distrito Federal, Brazil

9. Division of Pathogen Genomics, Translational Genomics Research Institute North, Flagstaff, Arizona, USA

10. School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia

11. School of Medicine, Universidad de Antioquia, Medellín, Colombia

Abstract

Characterization of genetic differences between lineages of the dimorphic human-pathogenic fungus Paracoccidioides can identify changes linked to important phenotypes and guide the development of new diagnostics and treatments. In this article, we compared genomes of 31 diverse isolates representing the major lineages of Paracoccidioides spp. and completed the first annotated genome sequences for the PS3 and PS4 lineages. We analyzed the population structure and characterized the genetic diversity among the lineages of Paracoccidioides , including a deep split of S1 into two lineages (S1a and S1b), and differentiated S1b, associated with most clinical cases, as the more highly recombining and diverse lineage. In addition, we found patterns of positive selection in surface proteins and secreted enzymes among the lineages, suggesting diversifying mechanisms of pathogenicity and adaptation across this species complex. These genetic differences suggest associations with the geographic range, pathogenicity, and ecological niches of Paracoccidioides lineages.

Funder

Colciencias

HHS | NIH | National Institute of Allergy and Infectious Diseases

Wellcome Trust

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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