2013
DOI: 10.3201/eid1912.121506
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Distinct Lineage of Vesiculovirus from Big Brown Bats, United States

Abstract: We identified a novel rhabdovirus, American bat vesiculovirus, from postmortem tissue samples from 120 rabies-negative big brown bats with a history of human contact. Five percent of the tested bats were infected with this virus. The extent of zoonotic exposure and possible health effects in humans from this virus are unknown.

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Cited by 22 publications
(25 citation statements)
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“…In the absence of a definitive diagnosis for the skin lesions, metagenomic sequencing was performed on seven lip lesions and one nonlesioned lip, according to previously described protocols, to further investigate a potential underlying viral etiology (21)(22)(23)(24). In brief, a tissue homogenate was centrifuged through a 0.22-m filter to enrich viral particles by size and then treated with nucleases to deplete host nucleic acids.…”
Section: Methodsmentioning
confidence: 99%
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“…In the absence of a definitive diagnosis for the skin lesions, metagenomic sequencing was performed on seven lip lesions and one nonlesioned lip, according to previously described protocols, to further investigate a potential underlying viral etiology (21)(22)(23)(24). In brief, a tissue homogenate was centrifuged through a 0.22-m filter to enrich viral particles by size and then treated with nucleases to deplete host nucleic acids.…”
Section: Methodsmentioning
confidence: 99%
“…Tissues from 40 bluegills, three related Lepomis species, and one largemouth bass were extracted using Qiagen DNA extraction kits. Screening for BGHBV was accomplished by traditional PCR, targeting the polymerase with the primer set BGHBV-PolF (5=-TGTGGACAAAAATCCACGAA-3=) and BGHBV-PolR (5=-CGTAAAGCACCTATGGGCAT-3=), using a previously described touchdown protocol (21). Additional primers targeting the polymerase, capsid, and core proteins were also designed and verified (Table 2).…”
Section: Methodsmentioning
confidence: 99%
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“…Briefly, deep sequencing using Illumina Miseq and the 454 Genome Sequencer FLX platform was performed on enriched viral particles from the tissue according to previously described protocols in which both viral DNA and RNA were randomly amplified and sequenced [16, 18]. Sequences were analyzed by a customized pipeline in which de novo assembly was performed, and the resulting contigs and the unassembled singlets were compared against the GenBank database using BLASTx and BLASTn [16, 17]. Over 1,800 Miseq sequences and 30 pyrosequences were mapped to a picornavirus coding sequence.…”
mentioning
confidence: 99%
“…Three sets of overlapping consensus primers covering the 5′ NTR-VP1, VP1−2C, and 2C-3′NTR regions (TTAAAACAGCYTTGGGGTTGT [1 to 21] and GCTGATTTATCACTGTGCGAGTT [2544 to 2522]; AACTTGGTGTGGTCCCTAGC [2446 to 2465] and CCTTTCTTTTGGCAATAATCC [5134 to 5114]; and TCTCAAGAAGTTAGGGATTATTGC [5100 to 5123] and GGCCCCCAAGTGACCAAAAT [7333 to 7314] [coordinates per GenBank KT285485]) were used to amplify the genome of EV-D68. Three RT-PCRs were performed, using the One-Step RT-PCR Kit (Qiagen) on each RNA sample with a “touch-down” protocol (4). For each sample the three amplicons were pooled, purified, and subjected to Nextera XT (Illumina) library preparation, followed by sequencing using the Illumina MiSeq platform.…”
Section: Genome Announcementmentioning
confidence: 99%