Patterns of RNA virus infection and transmission within a wild simian zoonotic reservoir in Uganda



Patterns of RNA virus infection and transmission within a wild simian zoonotic reservoir in Uganda

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Pres_WT


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Patterns of RNA virus infection and transmission within a wild simian zoonotic reservoir in Uganda

James Lester

The context of viral transmission in Kibale National Park

  • KNP a 776 km2 area of protected forest
  • Diverse primate community
  • Of great conservation, and potential zoonosis interest

(Figure: Lessons about parks and poverty from a decade of forest loss and economic growth around Kibale National Park, Uganda, Naughton-Treves et al, 2011)

Our reservoir of interest - Kibale red colobus

  • Especially sensitive to environmental change
  • Live in multi-male groups of 19-80 individuals
  • Predated by chimps
  • Known hosts of SIV, SFV, SPgV and SHFV1/2

Viruses of interest: SIV and SFV

  • SIV
    • Considerable variation in prevalence between populations, fluid transmission
    • Relatively low prevalences identified within Kibale RCB, as opposed to Taï and others

    • Associated with dominance rank in sooty mangabeys
  • SFV
    • Consistently observed at high prevalence within RCB populations, salivary transmission
    • Maternal clustering identified within chimpanzees

Viruses of interest: SHFV(1/2) and SPgV

  • SHFV(1/2)
    • Only recently identified in the wild, no previous epidemiology
    • Previously involved in research facility outbreaks, able to readily spread amongst infected hosts, not airborne
  • SPgV
    • Similarly, only recently identified within wild-living primates, no previous epidemiology
    • Has a human analog - HPgV
    • Associated with presence of other blood-borne or sexually transmitted infections
    • Vertical transmission, either prenatal or during birth

Our approach

  • Deep sequencing of blood samples from two red colobus troops
    • Allowing us to obtain full-length genomes for SHFV(1/2) and SPgV
    • Alongside clear identification of coinfections
    • Able to use sequencing not just as a diagnostic tool, but also to cluster infections
  • Monthly behavioural scans for one of these groups over several consecutive days, with one focal red colobus troop
  • Microsatellite data for each sampled individual

Our approach (cont.)

Key questions

  • What are the demographic correlates of infection with these viruses?
  • Do they associate with each other?
  • Does infection with these viruses relate to patterns of behaviour?
  • Can viral clustering be related to this?

Correlates of infection

Patterns of coinfection

Patterns of infection clustering

Behavioural correlates of infection

Behavioural correlates of infection clustering

Conclusions

  • Indications of age-associated accumulation of infection in certain contexts - Particularly females
  • Indications of both horizontal and (more tentatively) vertical transmission
  • Co-infection with only the SHFV viruses indicated
  • Association between agonistic, copulatory and associative behaviour and SHFV infection, not so for SPgV and SIV

Remaining questions and further work

  • Low prevalence of SIV, and lack of association with dominance
  • High SPgV prevalence with no association with dominance - Patterns of recovery and immunity?
  • Why SHFV relates so strongly to patterns of agonism and other indications of social dominance?
  • Requires further analysis of within-sample viral diversity
  • Longitudinal viral sampling, for molecular clock calibration and potential dating of divergence

Acknowledgements

University of Cambridge

  • Simon Frost
  • Bethany Dearlove

University of Madison-Wisconsin

  • Tony Goldberg
  • Sam Sibley

Stanford University

  • James Holland Jones

CDC

  • William M. Switzer

McGill University

  • Colin Chapman

University of Oregon

  • Nelson Ting
  • Maria Jose Ruiz-Lopez

Makerere University

  • Geoffrey Weny
  • David Hyeroba
  • Alex Tumukunde

Funding

  • ESRC
  • NIH