Abstract

BackgroundDeep sequencing of viruses isolated from infected hosts is an efficient way to measure population-genetic variation and can reveal patterns of dispersal and natural selection. In this study, we mined existing Illumina sequence reads to investigate single-nucleotide polymorphisms (SNPs) within two RNA viruses of the Western honey bee (Apis mellifera), deformed wing virus (DWV) and Israel acute paralysis virus (IAPV). All viral RNA was extracted from North American samples of honey bees or, in one case, the ectoparasitic mite Varroa destructor.ResultsCoverage depth was generally lower for IAPV than DWV, and marked gaps in coverage occurred in several narrow regions (< 50 bp) of IAPV. These coverage gaps occurred across sequencing runs and were virtually unchanged when reads were re-mapped with greater permissiveness (up to 8% divergence), suggesting a recurrent sequencing artifact rather than strain divergence. Consensus sequences of DWV for each sample showed little phylogenetic divergence, low nucleotide diversity, and strongly negative values of Fu and Li’s D statistic, suggesting a recent population bottleneck and/or purifying selection. The Kakugo strain of DWV fell outside of all other DWV sequences at 100% bootstrap support. IAPV consensus sequences supported the existence of multiple clades as had been previously reported, and Fu and Li’s D was closer to neutral expectation overall, although a sliding-window analysis identified a significantly positive D within the protease region, suggesting selection maintains diversity in that region. Within-sample mean diversity was comparable between the two viruses on average, although for both viruses there was substantial variation among samples in mean diversity at third codon positions and in the number of high-diversity sites. FST values were bimodal for DWV, likely reflecting neutral divergence in two low-diversity populations, whereas IAPV had several sites that were strong outliers with very low FST.ConclusionsThis initial survey of genetic variation within honey bee RNA viruses suggests future directions for studies examining the underlying causes of population-genetic structure in these economically important pathogens.

Highlights

  • Deep sequencing of viruses isolated from infected hosts is an efficient way to measure populationgenetic variation and can reveal patterns of dispersal and natural selection

  • One run (BP) combined three tissues that exhibited gross pathologies or abnormalities after dissection from worker bees (DV, unpublished data). Another run (BRL) was of pupae intentionally inoculated with Israel acute paralysis virus (IAPV) and deformed wing virus (DWV) at the Beltsville Bee Research Laboratory

  • More directed sequencing efforts using virus-enriched samples and controlled study designs should provide even greater power to discern evolutionary forces acting on genomic variation

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Summary

Introduction

Deep sequencing of viruses isolated from infected hosts is an efficient way to measure populationgenetic variation and can reveal patterns of dispersal and natural selection. In addition to the recognized morbidity and mortality that can result from overt viral infections, lower viral loads that do not produce visible symptoms might impact colony health as well. Interactions have been identified between viruses and other parasites, the ectoparasitic mite Varroa destructor [6,7,8]. Recombination between co-infecting RNA viruses may facilitate adaptation or the emergence of novel viruses [9,10]. It has become a major goal to better understand the diversity of viral species in honey bee populations and how they may interact during co-infection

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