Abstract
Bluetongue virus (BTV) is an arthropod-borne pathogen that is associated with sometimes severe disease in both domestic and wild ruminants. Predominantly transmitted by Culicoides spp. biting midges, BTV is composed of a segmented, double-stranded RNA genome. Vector expansion and viral genetic changes, such as reassortment between BTV strains, have been implicated as potential drivers of ongoing BTV expansion into previously BTV-free regions. We used an in vitro system to investigate the extent and flexibility of reassortment that can occur between two BTV strains that are considered enzootic to the USA, BTV-2 and BTV-10. Whole genome sequencing (WGS) was coupled with plaque isolation and a novel, amplicon-based sequencing approach to quantitate the viral genetic diversity generated across multiple generations of in vitro propagation. We found that BTV-2 and BTV-10 were able to reassort across multiple segments, but that a preferred BTV-2 viral backbone emerged in later passages and that certain segments were more likely to be found in reassortant progeny. Our findings indicate that there may be preferred segment combinations that emerge during BTV reassortment. Moreover, our work demonstrates the usefulness of WGS and amplicon-based sequencing approaches to improve understanding of the dynamics of reassortment among segmented viruses such as BTV.
Highlights
Similar to our population level Whole genome sequencing (WGS) results, we found that no plaques had either segment 7 or 8 contributed by Bluetongue virus (BTV)-10 in passages 3 and 7, and that both parental strains of BTV were well-represented across plaques in segments 5 and 9
We found that certain segments that were well-represented in our metagenomic sequencing data were not detected by our plaque assay approach; in particular, BTV-10 contributed approximately 40% of segment 6 viral reads in passage 7 according to WGS, but not a single plaque with BTV-10 segment 6 was identified
BTV-2 and BTV-10 grow in cells, allowing us to sons. Both BTV-2 and BTV-10 grow in BHK 21 cells, allowing us to avoid avoid unfairly biasing our experiment with one virus outcompeting the other
Summary
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Bluetongue virus (BTV; genus Reoviridae, family Orbivirus) is associated with significant economic and animal health impacts worldwide. Composed of ten segments of double-stranded RNA (dsRNA) and transmitted by hematophagous Culicoides midges, BTV can cause severe disease in susceptible ruminants and has been identified as an important, re-emerging arbovirus with significant animal health implications [1,2]. BTV circulates year-round in tropical climates, and seasonally in more temperate and cooler environments [3]. Its range is defined by the presence of one or more competent vector species (Culicoides spp.) capable of transmitting the virus between ruminant hosts
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