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Using genetic data to identify transmission risk factors: Statistical assessment and application to tuberculosis transmission

  • Isaac H. Goldstein
    ,
  • Damon Bayer
    ,
  • Ivan Barilar
    ,
  • Balladiah Kizito
    ,
  • Ogopotse Matsiri
    ,
  • Chawangwa Modongo
*Corresponding author for this work
  • University of California at Irvine
    ,
  • Research Center Borstel - Leibniz Lung Center
    ,
  • Victus Global Botswana Organisation
    ,
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Identifying host factors that influence infectious disease transmission is an important step toward developing interventions to reduce disease incidence. Recent advances in methods for reconstructing infectious disease transmission events using pathogen genomic and epidemiological data open the door for investigation of host factors that affect onward transmission. While most transmission reconstruction methods are designed to work with densely sampled outbreaks, these methods are making their way into surveillance studies, where the fraction of sampled cases with sequenced pathogens could be relatively low. Surveillance studies that use transmission event reconstruction then use the reconstructed events as response variables (i.e., infection source status of each sampled case) and use host characteristics as predictors (e.g., presence of HIV infection) in regression models. We use simulations to study estimation of the effect of a host factor on probability of being an infection source via this multi-step inferential procedure. Using TransPhylo—a widely-used method for Bayesian estimation of infectious disease transmission events—and logistic regression, we find that low sensitivity of identifying infection sources leads to dilution of the signal, biasing logistic regression coefficients toward zero. We show that increasing the proportion of sampled cases improves sensitivity and some, but not all properties of the logistic regression inference. Application of these approaches to real world data from a population-based TB study in Botswana fails to detect an association between HIV infection and probability of being a TB infection source. We conclude that application of a pipeline, where one first uses TransPhylo and sparsely sampled surveillance data to infer transmission events and then estimates effects of host characteristics on probabilities of these events, should be accompanied by a realistic simulation study to better understand biases stemming from imprecise transmission event inference.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

e1010696

Journal (Volume, Issue Number)

PLoS Computational Biology (Volume 18, Issue 12)

Publication milestones

  • Published - 12/2022

Publication status

Published - 12/2022

ISSN

1553-734X

Publication IDs

  • Scopus: 85144587363
  • PubMed: 36469509

Publication metrics

Metrics

Scopus
citations
Fractional count
1
Fractional count
0.10
Fractional count
9
Fractional count
0.90
Fractional count
1
Fractional count
1

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28
Citation count
10

Funding Details

This work was supported by the National Institutes of Health (R01AI147336 to IG, BK, OM, CM, SN, VMN, SSS; R01AI097045 to NMZ). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. We thank Xavier Didelot for helping us resolve issues using TransPhylo and Paul Bastide and Sebastian Lequime for their help using nosoi. We also thank Caroline Colijn, Jessica Stockdale and Vijay Jeevanantham Naidu for sharing their code using TransPhylo and BEAST2.
FundersFunding numbers
NIH
R01AI147336
NIAID
R01AI097045