4.8 Article

PHYLOSCANNER: Inferring Transmission from Within- and Between-Host Pathogen Genetic Diversity

Journal

MOLECULAR BIOLOGY AND EVOLUTION
Volume 35, Issue 3, Pages 719-733

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msx304

Keywords

molecular epidemiology; pathogen transmission; multiple infection; pathogen genomics; phylogenetics; pathogen diversity

Funding

  1. ERC [PBDR-339251]
  2. Bill & Melinda Gates Foundation through PANGEA-HIV
  3. Medical Research Council [MR/K01532X/1, MR/L01632X/1]
  4. Medical Research Foundation
  5. Medical Research Council [MR/K010174/1B] Funding Source: researchfish
  6. National Institute for Health Research [NF-SI-0617-10139] Funding Source: researchfish
  7. MRC [MR/L01632X/1, MR/K01532X/1] Funding Source: UKRI

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A central feature of pathogen genomics is that different infectious particles (virions and bacterial cells) within an infected individual may be genetically distinct, with patterns of relatedness among infectious particles being the result of both within-host evolution and transmission from one host to the next. Here, we present a new software tool, phyloscanner, which analyses pathogen diversity from multiple infected hosts. phyloscanner provides unprecedented resolution into the transmission process, allowing inference of the direction of transmission from sequence data alone. Multiply infected individuals are also identified, as they harbor subpopulations of infectious particles that are not connected by within-host evolution, except where recombinant types emerge. Low-level contamination is flagged and removed. We illustrate phyloscanner on both viral and bacterial pathogens, namely HIV-1 sequenced on Illumina and Roche 454 platforms, HCV sequenced with the Oxford Nanopore MinION platform, and Streptococcus pneumoniae with sequences from multiple colonies per individual. phyloscanner is available from https://github.com/BDI-pathogens/phyloscanner.

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