Evidence map›Paper›PMID 39970184›Full record

ArticlePLoS computational biology2025

Quantifying infectious disease epidemic risks: A practical approach for seasonal pathogens.

Alexander R Kaye, Giorgio Guzzetta, Michael J Tildesley, Robin N Thompson

Abstract read
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Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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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.

Alexander R KayeMathematics Institute, University of Warwick, Coventry, United Kingdom.ORCID 0000-0002-0665-9047
Giorgio GuzzettaCentre for Health Emergencies, Bruno Kessler Foundation, Trento, Italy.
Michael J TildesleyMathematics Institute, University of Warwick, Coventry, United Kingdom.
Robin N ThompsonMathematical Institute, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-8545-5212

Funding

Wellcome Trust
6 · The paper itself

Abstract

For many infectious diseases, the risk of outbreaks varies seasonally. If a pathogen is usually absent from a host population, a key public health policy question is whether the pathogen's arrival will initiate local transmission, which depends on the season in which arrival occurs. This question can be addressed by estimating the "probability of a major outbreak" (the probability that introduced cases will initiate sustained local transmission). A standard approach for inferring this probability exists for seasonal pathogens (involving calculating the Case Epidemic Risk; CER) based on the mathematical theory of branching processes. Under that theory, the probability of pathogen extinction is estimated, neglecting depletion of susceptible individuals. The CER is then one minus the extinction probability. However, as we show, if transmission cannot occur for long periods of the year (e.g., over winter or over summer), the pathogen will most likely go extinct, leading to a CER that is equal (or very close) to zero even if seasonal outbreaks can occur. This renders the CER uninformative in those scenarios. We therefore devise an alternative approach for inferring outbreak risks for seasonal pathogens (involving calculating the Threshold Epidemic Risk; TER). Estimation of the TER involves calculating the probability that introduced cases will initiate a local outbreak in which a threshold number of cumulative infections is exceeded before outbreak extinction. For simple seasonal epidemic models, such as the stochastic Susceptible-Infectious-Removed model, the TER can be calculated numerically (without model simulations). For more complex models, such as stochastic host-vector models, the TER can be estimated using model simulations. We demonstrate the application of our approach by considering chikungunya virus in northern Italy as a case study. In that context, transmission is most likely in summer, when environmental conditions promote vector abundance. We show that the TER provides more useful assessments of outbreak risks than the CER, enabling practically relevant risk quantification for seasonal pathogens.

Indexed as

Communicable DiseasesDisease OutbreaksEpidemicsEpidemiological ModelsModels, BiologicalSeasonsAnimalsComputational BiologyComputer SimulationHumansModels, StatisticalProbabilityRisk Assessment

Identifiers

PMID39970184
PMCPMC11867399

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LicenceCC BY
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Registered trials

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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.