Evidence map›Paper›PMID 27070316›Full record

ArticlePLoS computational biology2016

Molecular Infectious Disease Epidemiology: Survival Analysis and Algorithms Linking Phylogenies to Transmission Trees.

Eben Kenah, Tom Britton, M Elizabeth Halloran, Ira M Longini

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
13.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Evaluation of Phylogenetic Methods for Inferring the Direction of Human Immunodeficiency Virus (HIV) Transmission: HIV Prevention Trials Network (HPTN) 052.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Article
  11. Bayesian reconstruction of transmission trees from genetic sequences and uncertain infection times.Statistical applications in genetics and molecular biology · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. The Puzzle of HIV Neutral and Selective Evolution.Molecular biology and evolution · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 2 countries.

Eben KenahBiostatistics Department and Emerging Pathogens Institute, University of Florida, Gainesville, Florida, United States of America.
Tom BrittonDepartment of Mathematics, Stockholm University, Stockholm, Sweden.
M Elizabeth HalloranCenter for Inference and Dynamics of Infectious Diseases, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Ira M LonginiBiostatistics Department and Emerging Pathogens Institute, University of Florida, Gainesville, Florida, United States of America.
University of Florida · USFred Hutch Cancer Center · USStockholm University · SE

Funding

Understanding Transmission with Integrated Genetic and Epidemiologic InferenceU54GM111274 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPMAN, JAMES STEPHEN · 2014 to 2018
$12.5M
Regression, Phylogenetics, and Study Design in Infectious Disease EpidemiologyR01AI116770 · NIAID · UNIVERSITY OF FLORIDA · PI KENAH, EBEN · 2016 to 2020
$1.8M
Survival analysis and regression in infectious disease epidemiologyR00AI095302 · NIAID · UNIVERSITY OF FLORIDA · PI KENAH, EBEN · 2012 to 2013
$445k
Survival analysis and regression in infectious disease epidemiologyK99AI095302 · NIAID · UNIVERSITY OF WASHINGTON · PI KENAH, EBEN · 2011 to 2011
$120k
NIAID NIH HHS K99 AI095302NIAID NIH HHS R00 AI095302NIAID NIH HHS R01 AI116770NIGMS NIH HHS U54 GM111274
6 · The paper itself

Abstract

Recent work has attempted to use whole-genome sequence data from pathogens to reconstruct the transmission trees linking infectors and infectees in outbreaks. However, transmission trees from one outbreak do not generalize to future outbreaks. Reconstruction of transmission trees is most useful to public health if it leads to generalizable scientific insights about disease transmission. In a survival analysis framework, estimation of transmission parameters is based on sums or averages over the possible transmission trees. A phylogeny can increase the precision of these estimates by providing partial information about who infected whom. The leaves of the phylogeny represent sampled pathogens, which have known hosts. The interior nodes represent common ancestors of sampled pathogens, which have unknown hosts. Starting from assumptions about disease biology and epidemiologic study design, we prove that there is a one-to-one correspondence between the possible assignments of interior node hosts and the transmission trees simultaneously consistent with the phylogeny and the epidemiologic data on person, place, and time. We develop algorithms to enumerate these transmission trees and show these can be used to calculate likelihoods that incorporate both epidemiologic data and a phylogeny. A simulation study confirms that this leads to more efficient estimates of hazard ratios for infectiousness and baseline hazards of infectious contact, and we use these methods to analyze data from a foot-and-mouth disease virus outbreak in the United Kingdom in 2001. These results demonstrate the importance of data on individuals who escape infection, which is often overlooked. The combination of survival analysis and algorithms linking phylogenies to transmission trees is a rigorous but flexible statistical foundation for molecular infectious disease epidemiology.

Indexed as

AlgorithmsAnimalsCommunicable DiseasesComputational BiologyComputer SimulationDisease Transmission, InfectiousFoot-and-Mouth DiseaseFoot-and-Mouth Disease VirusHumansModels, StatisticalMolecular EpidemiologyPhylogenyStochastic ProcessesSurvival Analysis

Identifiers

PMID27070316
PMCPMC4829193
OpenAlexW2336199538

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.