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Biology subjects

Hay, J. A.

Publications and source records attributed to Hay, J. A..

3 recordsLinked to original sources

Tracking West Nile virus dynamics using viral loads from trapped mosquitoes

Mosquito-borne virus transmission is increasing globally. Due to a lack of effective vaccines or targeted treatments, mitigation relies on reducing human exposure to infectious mosquitoes. Entomological surveillance provides estimates of human risk by quantifying the prevalence of arboviruses in mosquito populations. Testing of pooled mosquitoes via RT-qPCR is often used to infer infection prevalence, however these data are often binarised and ignore semi-quantitative cycle threshold (Ct values) that may provide valuable information on virus kinetics, mosquito infectiousness, and ultimately human risk. West Nile virus (WNV) is a globally distributed arbovirus and endemic to the United States. In this study, we analysed pooled Ct values from retrospective mosquito surveillance and found substantial variation that could not be explained by laboratory factors alone. To understand how underlying viral load and epidemiological dynamics might explain this variation, we developed a multi-scale model linking pooled Ct values to heterogeneous within-host viral kinetics in mosquitoes and birds and seasonal transmission dynamics. Our modelling suggests that Ct values from positive pools might reflect a mixture of potentially infectious and non-infectious mosquitoes, indicating that a substantial proportion of PCR-positive mosquitoes might not contribute to transmission. We then developed a method to estimate mosquito infection prevalence using only pooled Ct values that distinguishes infectious from non-infectious prevalence. Estimates of overall prevalence were comparable to standard methods using binarised data and remained accurate at higher prevalences where standard approaches fail. Overall, these findings demonstrate that entomological viral load data reflect biologically meaningful variation in mosquito infection status that is lost through binarisation. Accounting for heterogeneous mosquito viral kinetics can improve interpretation of surveillance data and estimates of transmission risk, with implications for arbovirus surveillance beyond WNV.

ecology↗

Stabilizing selection of seasonal influenza receptor binding in populations with partial immunity

Mutations that alter cellular receptor binding of influenza hemagglutinin (HA) have profound effects on immune escape. Despite its high mutation rate, it is not fully understood why human influenza HA displays limited antigenic diversity across circulating viruses. We applied phylogenetic analysis and phylodynamic modeling to understand the evolutionary and epidemiological effects of binding avidity adaptation in humans using net charge as a marker for receptor binding avidity. Using 686 human influenza A/H3N2 HA sequences, we found that HA net charge followed an age-specific pattern. Phylogenetic analysis suggested that many binding variants have reduced fitness. Next, we developed an individual-based disease dynamic model embedded with within-host receptor binding adaptation and immune escape in a population with varied partial immunity. The model showed that mean binding avidity was unable to adapt to values that maximized transmissibility due to competing selective forces between within- and between-host levels. Overall, we demonstrated stabilizing selection of virus binding in a population with increasing partial immunity. These findings have potential implications in understanding the evolutionary mechanisms that determine the intensity of seasonal influenza epidemics.

evolutionary biology↗

Serosolver: an open source tool to infer epidemiological and immunological dynamics from serological data

We present a flexible, open source R package designed to obtain additional biological and epidemiological insights from commonly available serological datasets. Analysis of serological responses against pathogens with multiple strains such as influenza pose a specific statistical challenge because observed antibody responses measured in serological assays depend both on unobserved prior infections and the resulting cross-reactive antibody dynamics that these infections generate. We provide a general modelling framework to jointly infer these two typically confounded biological processes using antibody titres against current and historical strains. We do this by linking latent infection dynamics with a mechanistic model of antibody dynamics that generates expected antibody titres over time. This makes it possible to use observations of antibodies in serological assays to infer an individuals infection history as well as the parameters of the antibody process model. Our aim is to provide a flexible inference package that can be applied to a range of datasets studying different viruses over different timescales. We present two case studies to illustrate how our model can infer key immunological parameters, such as antibody titre boosting, waning and cross-reaction, and well as latent epidemiological processes such as attack rates and age-stratified infection risk.

immunology↗