Genome-wide changes in genetic diversity in a population of Myotis lucifugus affected by white-nose syndrome
Document Type
Article
Publication Date
2020
Department/School
Biology
Publication Title
G3: Genes, Genomes, Genetics
Abstract
Copyright © 2020 Lilley et al. Novel pathogens can cause massive declines in populations, and even extirpation of hosts. But disease can also act as a selective pressure on survivors, driving the evolution of resistance or tolerance. Bat white-nose syndrome (WNS) is a rapidly spreading wildlife disease in North America. The fungus causing the disease invades skin tissues of hibernating bats, resulting in disruption of hibernation behavior, premature energy depletion, and subsequent death. We used whole-genome sequencing to investigate changes in allele frequencies within a population of Myotis lucifugus in eastern North America to search for genetic resistance to WNS. Our results show low FST values within the population across time, i.e., prior to WNS (Pre-WNS) compared to the population that has survived WNS (Post-WNS). However, when dividing the population with a geographical cut-off between the states of Pennsylvania and New York, a sharp increase in values on scaffold GL429776 is evident in the Post-WNS samples. Genes present in the diverged area are associated with thermoregulation and promotion of brown fat production. Thus, although WNS may not have subjected the entire M. lucifugus population to selective pressure, it may have selected for specific alleles in Pennsylvania through decreased gene flow within the population. However, the persistence of remnant sub-populations in the aftermath of WNS is likely due to multiple factors in bat life history.
Link to Published Version
Recommended Citation
Lilley, T. M., Wilson, I. W., Field, K. A., Reeder, D. M., Vodzak, M. E., Turner, G. G., Kurta, A., Blomberg, A. S., Hoff, S., Herzog, C. J., Sewall, B. J., & Paterson, S. (2020). Genome-wide changes in genetic diversity in a population of Myotis lucifugus affected by white-nose syndrome. G3 & Genes|Genomes|Genetics, 10(6), 2007–2020. https://doi.org/10.1534/g3.119.400966