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Estimating the reproduction number and transmission heterogeneity from the size distribution of clusters of identical pathogen sequences
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Abstract
Quantifying transmission intensity and heterogeneity is crucial to ascertain the threat posed by infectious diseases and inform the design of interventions. Methods that jointly estimate the reproduction number
R
and the dispersion parameter
k
have however mainly remained limited to the analysis of epidemiological clusters or contact tracing data, whose collection often proves difficult. Here, we show that clusters of identical sequences are imprinted by the pathogen offspring distribution, and we derive an analytical formula for the distribution of the size of these clusters. We develop and evaluate a novel inference framework to jointly estimate the reproduction number and the dispersion parameter from the size distribution of clusters of identical sequences. We then illustrate its application across a range of epidemiological situations. Finally, we develop a hypothesis testing framework relying on clusters of identical sequences to determine whether a given pathogen genetic subpopulation is associated with increased or reduced transmissibility. Our work provides new tools to estimate the reproduction number and transmission heterogeneity from pathogen sequences without building a phylogenetic tree, thus making it easily scalable to large pathogen genome datasets.
Significance statement
For many infectious diseases, a small fraction of individuals has been documented to disproportionately contribute to onward spread. Characterizing the extent of superspreading is a crucial step towards the implementation of efficient interventions. Despite its epidemiological relevance, it remains difficult to quantify transmission heterogeneity. Here, we present a novel inference framework harnessing the size of clusters of identical pathogen sequences to estimate the reproduction number and the dispersion parameter. We also show that the size of these clusters can be used to estimate the transmission advantage of a pathogen genetic variant. This work provides crucial new tools to better characterize the spread of pathogens and evaluate their control.
Title: Estimating the reproduction number and transmission heterogeneity from the size distribution of clusters of identical pathogen sequences
Description:
Abstract
Quantifying transmission intensity and heterogeneity is crucial to ascertain the threat posed by infectious diseases and inform the design of interventions.
Methods that jointly estimate the reproduction number
R
and the dispersion parameter
k
have however mainly remained limited to the analysis of epidemiological clusters or contact tracing data, whose collection often proves difficult.
Here, we show that clusters of identical sequences are imprinted by the pathogen offspring distribution, and we derive an analytical formula for the distribution of the size of these clusters.
We develop and evaluate a novel inference framework to jointly estimate the reproduction number and the dispersion parameter from the size distribution of clusters of identical sequences.
We then illustrate its application across a range of epidemiological situations.
Finally, we develop a hypothesis testing framework relying on clusters of identical sequences to determine whether a given pathogen genetic subpopulation is associated with increased or reduced transmissibility.
Our work provides new tools to estimate the reproduction number and transmission heterogeneity from pathogen sequences without building a phylogenetic tree, thus making it easily scalable to large pathogen genome datasets.
Significance statement
For many infectious diseases, a small fraction of individuals has been documented to disproportionately contribute to onward spread.
Characterizing the extent of superspreading is a crucial step towards the implementation of efficient interventions.
Despite its epidemiological relevance, it remains difficult to quantify transmission heterogeneity.
Here, we present a novel inference framework harnessing the size of clusters of identical pathogen sequences to estimate the reproduction number and the dispersion parameter.
We also show that the size of these clusters can be used to estimate the transmission advantage of a pathogen genetic variant.
This work provides crucial new tools to better characterize the spread of pathogens and evaluate their control.
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