The evolutionary emergence of new pathogens via mutation poses a considerable risk to human and animal populations. Most previous studies have investigated cases where a potentially pandemic strain emerges though mutation from an initial maladapted strain (i.e., its basic reproductive ratio R-0 < 1). However, an alternative (and arguably more likely) cause of novel pathogen emergence is where a "weakly adapted" strain (with R-0 approximate to 1) mutates into a strongly adapted strain (with R-0 >> 1). In this case, a proportion of the host susceptible population is removed as the first strain spreads, but the impact this feedback has on emergence of mutated strains has yet to be quantified. We produce a model of pathogen emergence that takes into account changes in the susceptible population over time and find that the ongoing depletion of susceptible individuals by the first strain has a drastic effect on the emergence probability of the mutated strain, above that assumed by just scaling the reproductive ratio. Finally, we apply our model to the documented emergence of Chikungunya virus on La Reunion Island and demonstrate that the emergence probability of the mutated strain was reduced approximately 10 fold, compared to models assuming that susceptible depletion would not affect outbreak probability. These results highlight the importance of taking population feedbacks into account when predicting disease emergence.
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BIST, Bioinformat & Genom Programme, Ctr Genom Regulat CRG, Barcelona 08003, Spain
UPF, Barcelona 08003, SpainBIST, Bioinformat & Genom Programme, Ctr Genom Regulat CRG, Barcelona 08003, Spain
Ksiezopolska, Ewa
Gabaldon, Toni
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BIST, Bioinformat & Genom Programme, Ctr Genom Regulat CRG, Barcelona 08003, Spain
UPF, Barcelona 08003, Spain
ICREA, Barcelona 08010, SpainBIST, Bioinformat & Genom Programme, Ctr Genom Regulat CRG, Barcelona 08003, Spain
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Univ Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90095 USA
Park, Miran
Loverdo, Claude
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Univ Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90095 USA
Loverdo, Claude
Schreiber, Sebastian J.
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Univ Calif Davis, Dept Evolut & Ecol, Davis, CA 95616 USA
Univ Calif Davis, Grad Grp Appl Math, Davis, CA 95616 USAUniv Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90095 USA
Schreiber, Sebastian J.
Lloyd-Smith, James O.
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Univ Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90095 USA
NIH, Fogarty Int Ctr, Bethesda, MD 20892 USAUniv Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90095 USA
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Stellenbosch Univ, Dept Bot & Zool, Ctr Invas Biol, Matieland, South AfricaStellenbosch Univ, Dept Bot & Zool, Ctr Invas Biol, Matieland, South Africa
Gallien, Laure
Landi, Pietro
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Stellenbosch Univ, Dept Math Sci, Ctr Invas Biol, Matieland, South AfricaStellenbosch Univ, Dept Bot & Zool, Ctr Invas Biol, Matieland, South Africa
Landi, Pietro
Hui, Cang
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Stellenbosch Univ, Dept Math Sci, Ctr Invas Biol, Matieland, South Africa
African Inst Math Sci, Math & Phys Biosci, Cape Town, South AfricaStellenbosch Univ, Dept Bot & Zool, Ctr Invas Biol, Matieland, South Africa
Hui, Cang
Richardson, David M.
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Stellenbosch Univ, Dept Bot & Zool, Ctr Invas Biol, Matieland, South AfricaStellenbosch Univ, Dept Bot & Zool, Ctr Invas Biol, Matieland, South Africa