Increased genetic diversity and immigration after West Nile virus emergence in American crows: No evidence for a genetic bottleneck

Mol Ecol. 2023 Aug;32(15):4199-4208. doi: 10.1111/mec.17037. Epub 2023 Jun 5.

Abstract

Infectious diseases can cause steep declines in wildlife populations, leading to changes in genetic diversity that may affect the susceptibility of individuals to infection and the overall resilience of populations to pathogen outbreaks. Here, we examine evidence for a genetic bottleneck in a population of American crows (Corvus brachyrhynchos) before and after the emergence of West Nile virus (WNV). More than 50% of marked birds in this population were lost over the 2-year period of the epizootic, representing a 10-fold increase in adult mortality. Using analyses of single-nucleotide polymorphisms (SNPs) and microsatellite markers, we tested for evidence of a genetic bottleneck and compared levels of inbreeding and immigration in the pre- and post-WNV populations. Counter to expectations, genetic diversity (allelic diversity and the number of new alleles) increased after WNV emergence. This was likely due to increases in immigration, as the estimated membership coefficients were lower in the post-WNV population. Simultaneously, however, the frequency of inbreeding appeared to increase: Mean inbreeding coefficients were higher among SNP markers, and heterozygosity-heterozygosity correlations were stronger among microsatellite markers, in the post-WNV population. These results indicate that loss of genetic diversity at the population level is not an inevitable consequence of a population decline, particularly in the presence of gene flow. The changes observed in post-WNV crows could have very different implications for their response to future pathogen risks, potentially making the population as a whole more resilient to a changing pathogen community, while increasing the frequency of inbred individuals with elevated susceptibility to disease.

Keywords: West Nile virus; emerging infectious disease; genetic bottleneck; genetic diversity; immigration; inbreeding.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Bird Diseases*
  • Crows* / genetics
  • Emigration and Immigration
  • Genetic Variation
  • West Nile Fever* / epidemiology
  • West Nile Fever* / genetics
  • West Nile Fever* / veterinary
  • West Nile virus* / genetics

Associated data

  • RefSeq/GCA_000691975.1
  • RefSeq/GCA_000738735.5
  • Dryad/10.5061/dryad.5dv41nsbj