Untangling the effects of within-host and between-host natural selection in viruses with applications to evolution of HIV-1 co-receptor usage

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Abstract
The fitness of a pathogen can be characterised at multiple levels corresponding to different stages of its life cycle, including replication within target cells (replicative capacity), immune evasion, and the capacity to infect new hosts (transmissibility). Pathogens evolve towards greater fitness within hosts, which can potentially compromise transmissibility. Typically, epidemiological studies for measuring pathogen fitness compute a single selection coefficient for pathogen variants that encompasses all stages of the pathogen life cycle. To address this problem, we develop a population-genetic model and software for the inference of multi-level selection coefficients which represent relative within-host fitness and transmissibility. Our approach builds on population genetic models previously applied to macro-evolution, whereby speciation and extinction rates are state-dependent. We relate the state-dependence in speciation and extinction rates to competing within- and between-host selection. Evolution of beneficial phenotypes within hosts may occur rapidly (higher ‘speciation’), but reduce rates of dispersal between hosts (higher ‘extinction’). This new coalescent-based method also accounts for highly nonlinear-population dynamics and variable sampling through time making it suitable for epidemiological studies. We derive the equilibrium proportion of a variant with multi-level selection under mutation-selection balance and show how this can be used in combination with the coalescent to greatly increase accuracy and precision of estimated selection coefficients. We characterise the accuracy of this method using a variety of birth-death and coalescent simulations before analysing a real dataset of HIV-1 genetic sequences from a large population-based sample of 4056 people living with HIV in Zambia. We quantified the multi-level relative fitness underlying HIV-1 ‘co-receptor switching’. In accordance with previous observations, we estimate that the relative transmissibility of X4-tropic virus is 9%, while within-host switching to X4-tropism is approximately seven-fold higher than switching to R5-tropism, indicating a strong within-host and between-host tradeoff of co-receptor usage. Our methods are available in an open-source R package musseco, providing a general-purpose tool for inferring multi-level selection coefficients for epidemiological sequence data. Author Summary The fitness of a pathogen can be characterised at each stage of its life cycle. However, epidemiological studies measuring pathogen fitness typically estimate a single value encompassing the entire life cycle. Pathogens evolve towards greater fitness within hosts, but this can compromise the capacity to infect new hosts. Our new method quantifies relative fitness at both levels. This method accounts for rapidly changing pathogen populations and variable sampling through time making it suitable for epidemiological studies. We tested our method using simulations and demonstrate its application by analysing real HIV-1 genetic sequences from people living with HIV in Zambia. This method sheds new light on long-standing questions about the relative fitness of HIV-1 variants which utilise different host-cell co-receptors. Using our new method, we estimate that the capacity of X4 variants to infect new people is just 9% of that of R5 variants, while within-host switching from R5 to X4 usage is seven times greater than the reverse switch. This indicates a strong within-host and between-host trade-off in co-receptor usage.
Funding Information
  • Wellcome Trust (220885/Z/20/Z)

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