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Data from: The reference transcriptome of the adult female biting midge (Culicoides sonorensis) and differential gene expression profiling during teneral, blood, and sucrose feeding conditions
,Deep sequencing technologies were used to construct the first adult female Culicoides sonorensis reference transcriptome.,Genetic and genomic tools for Culicoides biting midges are lacking, despite the fact that they vector a large number of arboviruses and other pathogens impacting humans and domestic animals world-wide. Libraries of tissue-specific transcripts expressed in response to feeding and oral virus challenge in C. sonorensis have previously been reported, but extensive genome-wide expression profiling in the midge has not. Here, we successfully used deep sequencing technologies to construct the first adult female C. sonorensis reference transcriptome, and utilized genome-wide expression profiling to elucidate the genetic response to blood and sucrose feeding over time. The adult female midge unigene consists of 19,041 genes, of which less than 7% are differentially expressed during the course of a sucrose meal, while up to 52% of the genes respond significantly in blood-fed midges, indicating hematophagy induces complex physiological processes. Many genes that were differentially expressed during blood feeding were associated with digestion (e.g. proteases, lipases), hematophagy (e.g., salivary proteins), and vitellogenesis, revealing many major metabolic and biological factors underlying these critical processes. Additionally, key genes in the vitellogenesis pathway were identified, which provides the first glimpse into the molecular basis of anautogeny for C. sonorensis. This is the first extensive transcriptome for this genus, which will serve as a framework for future expression studies and in informing a reference genome assembly and annotation. Moreover, this study will serve as a foundation for subsequent studies of genome-wide expression analyses during early virus infection and dissecting the molecular mechanisms behind vector competence in midges.,
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Data from: Host associations of Culicoides biting midges in Northeastern Kansas, USA
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,Culicoides biting midges (Diptera: Ceratopogonidae) are hematophagous flies that transmit several viruses of veterinary concern to livestock. Understanding blood feeding behaviors is integral towards identification of putative vector species and preventing the transmission of these pathogens. PCR-based blood meal analysis was conducted on 440 blood-engorged Culicoides midges collected in northeastern Kansas, with 316 (71.8%) returning non-human vertebrate identifications at the ≥95% identity match level. Broadly, Culicoides sonorensis, Culicoides stellifer, and Culicoides variipennis were found to feed heavily on mammalian hosts, while Culicoides crepuscularis and Culicoides haematopotus fed on avian hosts. The blood meals in all specimens were graded prior to DNA extraction to determine whether blood meal size or digestion status significantly impacted the likelihood of a quality host match. Size had a significant impact on the likelihood of a quality match at grades 3–5, whereas digestion only significantly impacted outcomes at the most extreme grade. These vector–host dynamics have not previously been studied in Culicoides collected in Kansas, which represents a unique tallgrass prairie biome within the United States that is heavily interspersed with livestock operations. Based on these data, the highly abundant species C. crepuscularis and C. haematopotus are unlikely to be major vectors of mammalian viruses.,
Genetic detection of Lake Sinai Virus in honey bees (Apis mellifera) and other insects
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Lake Sinai Viruses (LSV) are common ribonucleic acid (RNA) viruses of honey bees (Apis mellifera) that frequently reach high abundance but are not linked to overt disease. LSVs are genetically heterogeneous and collectively widespread, but despite frequent detection in surveys, the ecological and geographic factors structuring their distribution in A. mellifera are not understood. Even less is known about their distribution in other species. Better understanding of LSV prevalence and ecology have been hampered by high sequence diversity within the LSV clade. We developed a new genetic assay that detects all currently known lineages. We also performed pilot metagenetic sequencing to quantify the diversity of LSV sequences. The resulting data are summarized herein.
Genetic detection of Lake Sinai Virus in honey bees (Apis mellifera) and other insects
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Lake Sinai Viruses (LSV) are common ribonucleic acid (RNA) viruses of honey bees (Apis mellifera) that frequently reach high abundance but are not linked to overt disease. LSVs are genetically heterogeneous and collectively widespread, but despite frequent detection in surveys, the ecological and geographic factors structuring their distribution in A. mellifera are not understood. Even less is known about their distribution in other species. Better understanding of LSV prevalence and ecology have been hampered by high sequence diversity within the LSV clade. We developed a new genetic assay that detects all currently known lineages. We also performed pilot metagenetic sequencing to quantify the diversity of LSV sequences. The resulting data are summarized herein.
Data from pathology of Lagovirus europaeus GI.2/RHDV2/b (rabbit hemorrhagic disease virus 2) in native North American lagomorphs
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Rabbit hemorrhagic disease, a notifiable foreign animal disease in the USA, was reported for the first time in wild native North American rabbits and hares in April 2020 in the southwestern USA. Affected species included the Desert Cottontail (Sylvilagus audubonii), Mountain Cottontail (S. nutallii), Black-tailed Jackrabbit (Lepus californicus), and Antelope Jackrabbit (L. alleni). Desert Cottontails (n=7) and Black-tailed Jackrabbits (n=7) collected in April and May 2020 were necropsied at the U.S. Geological Survey National Wildlife Health Center (NWHC) and tested positive for Lagovirus europaeus GI.2, also known as rabbit hemorrhagic disease virus 2 (GI.2/RHDV2/b), by real-time PCR at the U.S. Department of Agriculture’s Foreign Animal Disease Diagnostic Laboratory. Gross and microscopic lesions were similar to those reported in European rabbits (Oryctolagus cuniculus) and other hare (Lepus) species with GI.2/RHDV2/b infection and included epistaxis (12/13; 92%), massive hepatocellular dissociation (14/14; 100%) and necrosis/apoptosis (11/11; 100%), pulmonary congestion (12/12; 100%), edema (12/13; 92%), and hemorrhage (11/12; 92%), and acute renal tubular injury (3/8; 38%). As in previous reports and when compared to historical cases in the NWHC diagnostic database, massive hepatocellular dissociation and necrosis/apoptosis was the most diagnostically distinct finding in GI.2/RHDV2/b-positive rabbits and hares. Based on the apparent susceptibility of North American Sylvilagus and Lepus species to fatal GI.2/RHDV2/b infection, additional work is needed to understand the host range, pathogenicity, and potential population impacts of GI.2/RHDV2/b in North America.
Provenance, classification, and abundance of RNA sequence fragments used to assess virus infections in honey bees, Apis mellifera
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Deformed wing virus (DWV) is a major pathogen of concern to apiculture, and recent reports have indicated the local predominance and potential virulence of recombinants between DWV and a related virus, Varroa destructor virus 1 (VDV). However, little is known about the frequency and titer of VDV and recombinants relative to DWV generally. In this study, I assessed the relative occurrence and titer of DWV and VDV in public RNA-seq accessions of honey bee using a rapid, kmer-based approach. Three recombinant types were detectable graphically and corroborated by de novo assembly. Recombination breakpoints did not disrupt the capsid-encoding region, consistent with previous reports, and both VDV- and DWV-derived capsids were observed in recombinant backgrounds. High abundance of VDV kmers was largely restricted to recombinant forms. Non-metric multidimensional scaling identified genotypic clusters among DWV isolates, which was corroborated by read mapping and consensus generation. The recently described DWV-C lineage was not detected in the searched accessions. The data further highlight the utility of high-throughput sequencing to monitor viral polymorphisms and statistically test biological predictors of titer, and point to the need for consistent methodologies and sampling schemes.
Occurrences of Apis mellifera filamentous virus (AmFV) sequences in public accessions of Apis mellifera and Varroa destructor
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Honey bees (Apis mellifera), a critical agricultural pollinator in many areas, have a high rate of infection with a large DNA virus, Apis mellifera filamentous virus (AmFV), yet little is known about its ecology or impact on honey bee colonies, other than its ubiquity and apparent low virulence. This study scanned over 5,000 public data sets to detect AmFV sequences in honey bees as well as a parasitic mite of honey bees, Varroa destructor, that is a potential vector of AmFV. The data release consists of these files: 1. AmFV.genome.assemblies.aligned.fas, which contains new AmFV draft genome sequences generated by this study aligned with existing reference genome accessions downloaded from the National Center for Biotechnology Information (NCBI). 2. kmer.list.txt, a list of kmers that were extracted from reference sequences and searched for in Sequence Read Archive (SRA) accessions. 3. sample.metadata.txt, which lists all accessions of the SRA, and NCBI database of high-throughput sequence data, that were used in this study. The file also includes the raw occurrence counts of kmers listed in kmer.lists.txt, summed by category.
Viruses Promote Trophic Facilitation in Aphids - Feeding Behaviour Data
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The dataset includes three csv files: [1] effects of pre-inhabitation and viruses on the feeding behavior of Rhopalosiphum padi and R. maidis (min). [2] effects of pre-inhabitation and viruses on the fecundity of R. padi and R. maidis (total offspring in laboratory and field). [3] effect of pre-inhabitation and viruses on the host plant nutrient content (amino acids, total sterols, and simple sugars-mg/g). These data might be used by researchers studying positive interactions, effects of viruses on host plants and vectors, phytochemistry of the wheat plant, and feeding behavior of phloem-feeders.
Metagenomic detection and reconstruction of Lake Sinai Virus from honey bee sequence data
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A survey of public honey bee sequence data was performed to detect infections by Lake Sinai Virus (LSV). The Sequence Read Archive of the National Center for Biotechnology Information (NCBI) was queried to identify accessions of RNA sequence data derived from honey bee. These were filtered as described below and then up to 50 million reads or read pairs were downloaded and searched against a reference database of conserved LSV sequence. Accessions with matches above a specified threshold were downloaded in their entirety and assembled into longer contiguous sequences (contigs). The result contigs were searched against each open reading frame (ORF) of the reference LSV genome present in the NCBI database (accession NC_032433.1) and matching regions from each contig. These ORF sequences were aligned with additional sequences identified in NCBI databases through the BLAST web service. These alignments provide the basis for computing phylogenetic trees, rates of nucleotide substitution, codon usage bias, and other evolutionary parameters.
Mosquito Larval Habitat Along Five Altitudinal Transects in South Kona, Island of Hawai'i, 1995
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This data release provides information on mosquito larval habitat associated with tree ferns (Cibotium spp) that have been damaged by feral ungulates, ground pools, and tree holes on the SW slopes of Mauna Loa volcano. It also provides assessments of ground cover and habitat degradation by feral ungulates. Data was collected from five transects that fall within or immediately adjacent to the current boundaries of the Kona Unit of Hakalau Forest National Wildlife Refuge. Transects were sampled once between August 8 - August 10, 1995 with 10 m diameter circular plots spaced at 150 m intervals along each transect. Measurements included numbers of standing live and dead tree ferns (Cibotium spp.), numbers of fallen and animal damaged tree ferns, numbers of fallen feral pig damaged tree ferns with and without standing water, numbers of fallen tree ferns with standing water and mosquito larvae, abundance of tree holes and surface water, feral ungulate activity, and general vegetation characteristics of each plot. This XML describes two tabular CSV files: (i) Mosquito Larval Habitat - Habitat Characteristics.CSV, and (ii) Mosquito Larval Habitat - Transect Locations.CSV.