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Fewell, J.

Publications and source records attributed to Fewell, J..

2 recordsLinked to original sources

Wolbachia-infected pharaoh ant colonies have higher egg production, metabolic rate, and worker survival

Wolbachia is a widespread endosymbiotic bacteria with diverse phenotypic effects on its insect hosts. Wolbachia also commonly infects social insects, where it faces unique challenges associated with its hosts caste-based reproductive division of labor and colony living. Here we dissect the benefits and costs of Wolbachia infection on life-history traits of pharaoh ants, Monomorium pharaonis. Pharaoh ants are relatively short-lived and show natural variation in Wolbachia infection between colonies, thereby making them an ideal model system for this study. We quantified effects on the lifespan of queen and worker castes, the egg-laying rate of queens across queen lifespan, and the metabolic rates of whole colonies and colony members. Newly-infected queens laid more eggs than uninfected queens but had similar metabolic rates and lifespans. Surprisingly, infected workers outlived uninfected workers. Infected colonies were more productive due to increased queen egg-laying rates and worker longevity, and infected colonies had higher metabolic rates during peak colony productivity. While some effects of infection, such as elevated colony-level metabolic rates may be detrimental in more stressful conditions, we did not find any costs of infection under laboratory conditions. Overall, our study emphasizes the beneficial effects of Wolbachia on colony-level growth and metabolism in this species.

evolutionary biology↗

Parallel genomic evolution of parasite tolerance in wild honey bee populations

Sudden biotic pressures, such as those from novel diseases and pathogens, require populations to respond rapidly or face potential extinction. How this response process takes place remains poorly understood, particularly in natural environments. In this study we take advantage of unique decade-long data sets of two wild honey bee (Apis mellifera) populations in the United States to reconstruct the evolution of tolerance to a novel parasite, the ectoparasitic mite Varroa destructor. Upon the arrival of Varroa, the two geographically isolated populations simultaneously suffered massive Varroa-induced mortality, but stabilized within two years. Here we sequenced and phased genomes of 465 bees sampled from both populations annually over the decade that spanned Varroas arrival. Remarkably, we found that genetic changes were strongly correlated between the populations, suggesting parallel selective responses to Varroa parasitization. The arrival of Varroa was also correlated with an influx of genes of African origin into both populations, though surprisingly it did not substantially contribute to the overall similarity of the evolutionary response between them. Genes involved in metabolic, protein processing and developmental pathways were under particularly strong selection. It is possible that interactions among highly connected gene groups in these pathways may help channelize selective responses to novel parasites, causing completely unrelated populations to exhibit parallel evolutionary trajectories when faced with the same biotic pressure. Our analyses illustrate that ecologically relevant traits emerge from highly polygenic selection involving thousands of genes contributing to complex patterns of evolutionary change.

evolutionary biology↗