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Abstract During infectious disease outbreaks, estimates of time‐varying pathogen transmissibility, such as the instantaneous reproduction number or epidemic growth rate , are used to inform decision‐making by public health authorities. For directly transmitted infectious diseases, the renewal equation framework is a widely used method for measuring time‐varying transmissibility. The framework uses information on the typical time elapsing between an infection and the offspring infections (quantified by the generation time distribution), and , to describe the rate at which currently infected individuals generate new infections, if conditions affecting human transmission were to remain the same as at time . For diseases with transmission cycles involving hosts and vectors, however, renewal equation models have been far less used. This is likely due to difficulties in mechanistically defining generation times that can capture the complexity of multi‐stage, human‐vector relationships. Here, using dengue as an example, we provide general renewal equations that are derived from first principles using age‐structured systems of coupled partial differential equations across human and vector sub‐populations. Our framework tracks the multi‐stage transmission cycle over calendar time and across stage‐specific ages, resulting in governing renewal equations that quantify how the rate at which new infections are generated from existing infections depends on stage‐specific processes. In a numerical application to real‐world temperature data, we show how the generation time distribution depends on both current and historical conditions. The framework provides a foundation on which to base inferential frameworks for estimating and for infectious diseases with multiple stages in the transmission cycle.

More information Original publication

DOI

10.1111/2041-210x.70110

Type

Journal article

Publisher

Wiley

Publication Date

2025-11-01T00:00:00+00:00

Volume

16

Pages

2653 - 2666

Total pages

13