Abstract

The relationship between parasite virulence and transmission is a pillar of evolutionary theory that has implications for public health. Part of this canon involves the idea that virulence and free-living survival (a key component of transmission) may have different relationships in different host–parasite systems. Most examinations of the evolution of virulence-transmission relationships—Theoretical or empirical in nature—Tend to focus on the evolution of virulence, with transmission being a secondary consideration. Even within transmission studies, the focus on free-living survival is a smaller subset, though recent studies have examined its importance in the ecology of infectious diseases. Few studies have examined the epidemic-scale consequences of variation in survival across different virulence–survival relationships. In this study, we utilize a mathematical model motivated by aspects of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) natural history to investigate how evolutionary changes in survival may influence several aspects of disease dynamics at the epidemiological scale. Across virulence–survival relationships (where these traits are either positively or negatively correlated), we found that small changes (5% above and below the nominal value) in survival can have a meaningful effect on certain outbreak features, including R0, and on the size of the infectious peak in the population. These results highlight the importance of properly understanding the mechanistic relationship between virulence and parasite survival, as the evolution of increased survival across different relationships with virulence may have considerably different epidemiological signatures.

Highlights

  • Interactions between the life history of a pathogen and the environment in which it is embedded drive the evolution of virulence

  • We find that the identity of the virulence–free-living survival relationship

  • The virulence–survival relationship drives the consequences of virus evolution on the trajectory of an outbreak

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Summary

Introduction

Interactions between the life history of a pathogen and the environment in which it is embedded drive the evolution of virulence. These interactions dictate both the experience of disease at the individual host level and the shape of disease dynamics in host populations [1,2]. The Curse of the Pharaoh hypothesis—Named after a tale about a mythical curse that torments individuals who dig up tombs of Egyptian pharaohs [11]—Suggests that, if a parasite has high free-living survival, it is far less dependent on its host for transmission and, will have no evolutionary incentive to decrease virulence [2,4,12]. Previous studies support a positive correlation between free-living survival and mortality per infection (a common proxy for virulence) [13]

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