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Identification of Hidden Population Structure in Time-Scaled Phylogenies.
Volz, Erik M; Carsten, Wiuf; Grad, Yonatan H; Frost, Simon D W; Dennis, Ann M; Didelot, Xavier.
Afiliação
  • Volz EM; Department of Infectious Disease Epidemiology and MRC Centre for Global Infectious Disease Analysis, Imperial College London, Norfolk Place, W2 1PG London, UK.
  • Carsten W; Department of Mathematical Sciences, University of Copenhagen, Universitetsparken 5, DK-2100 Copenhagen, Denmark.
  • Grad YH; Department of Immunology and Infectious Diseases, TH Chan School of Public Health, Harvard University, 677 Huntington Ave, Boston, MA 02115, USA.
  • Frost SDW; Department of Veterinary Medicine, University of Cambridge, Madingley Rd, Cambridge CB3 0ES, UK.
  • Dennis AM; The Alan Turing Institute, 96 Euston Rd, London NW1 2DB, London, UK.
  • Didelot X; Department of Medicine, University of North Carolina Chapel Hill, 321 S Columbia St, Chapel Hill, NC 27516, USA.
Syst Biol ; 69(5): 884-896, 2020 09 01.
Article em En | MEDLINE | ID: mdl-32049340
ABSTRACT
Population structure influences genealogical patterns, however, data pertaining to how populations are structured are often unavailable or not directly observable. Inference of population structure is highly important in molecular epidemiology where pathogen phylogenetics is increasingly used to infer transmission patterns and detect outbreaks. Discrepancies between observed and idealized genealogies, such as those generated by the coalescent process, can be quantified, and where significant differences occur, may reveal the action of natural selection, host population structure, or other demographic and epidemiological heterogeneities. We have developed a fast non-parametric statistical test for detection of cryptic population structure in time-scaled phylogenetic trees. The test is based on contrasting estimated phylogenies with the theoretically expected phylodynamic ordering of common ancestors in two clades within a coalescent framework. These statistical tests have also motivated the development of algorithms which can be used to quickly screen a phylogenetic tree for clades which are likely to share a distinct demographic or epidemiological history. Epidemiological applications include identification of outbreaks in vulnerable host populations or rapid expansion of genotypes with a fitness advantage. To demonstrate the utility of these methods for outbreak detection, we applied the new methods to large phylogenies reconstructed from thousands of HIV-1 partial pol sequences. This revealed the presence of clades which had grown rapidly in the recent past and was significantly concentrated in young men, suggesting recent and rapid transmission in that group. Furthermore, to demonstrate the utility of these methods for the study of antimicrobial resistance, we applied the new methods to a large phylogeny reconstructed from whole genome Neisseria gonorrhoeae sequences. We find that population structure detected using these methods closely overlaps with the appearance and expansion of mutations conferring antimicrobial resistance. [Antimicrobial resistance; coalescent; HIV; population structure.].
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Filogenia / Epidemiologia Molecular Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Filogenia / Epidemiologia Molecular Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article