Epistasis and the Evolution of Antimicrobial Resistance

Эпистаз и эволюция устойчивости к противомикробным препаратам
Alex Wong
2017-02-17

antimicrobial resistanceepistasisgenetic backgroundmulti-drug resistanceresistance mutations
The fitness effects of a mutation can depend, sometimes dramatically, on genetic background; this phenomenon is often referred to as "epistasis." Epistasis can have important practical consequences in the context of antimicrobial resistance (AMR). For example, genetic background plays an important role in determining the costs of resistance, and hence in whether resistance will persist in the absence of antibiotic pressure. Furthermore, interactions between resistance mutations can have important implications for the evolution of multi-drug resistance. I argue that there is a need to better characterize the extent and nature of epistasis for mutations and horizontally transferred elements conferring AMR, particularly in clinical contexts. Furthermore, I suggest that epistasis should be an important consideration in attempts to slow or limit the evolution of AMR.
1
Accounting for epistasis should be an important component of strategies designed to slow or limit antimicrobial-resistance evolution.
2
Genetic background influences the fitness costs of resistance and therefore affects whether resistance persists without antibiotic pressure.
3
Interactions among resistance mutations can shape the evolution and emergence of multidrug resistance.
4
Mutation fitness effects can vary substantially across genetic backgrounds, making epistasis central to antimicrobial-resistance evolution.
5
The extent and nature of epistasis for antimicrobial-resistance mutations and horizontally transferred elements remain insufficiently characterized, especially in clinical contexts.

AMR-conferring mutations and horizontally transferred elements in clinical genetic backgrounds

The extent and nature of epistatic fitness effects, including resistance costs and interactions among resistance mutations influencing persistence and multidrug-resistance evolution

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2017-02-17
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Alex Wong
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