Evidence map›Paper›PMID 41564144›Full record

ArticlePLoS neglected tropical diseases2026

Genomic characterization of a severe West Nile Virus transmission season using a single reaction amplicon sequencing approach.

Shawn Freed, Sarah Chandler, Sarah Uhm, Zach Pella, Dikchha Gurung, Hallie Smith, Tammy Dowdy, Amanda M Bartling, Ava Butz, Michael R Wiley and 8 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Shawn FreedUniversity of Nebraska Medical Center, College of Public Health, Department of Epidemiology, Omaha, Nebraska, United States of America.
Sarah ChandlerUniversity of Nebraska Medical Center, College of Medicine, Omaha, Nebraska, United States of America.
Sarah UhmUniversity of Nebraska Medical Center, College of Public Health, Department of Epidemiology, Omaha, Nebraska, United States of America.
Zach PellaUniversity of Nebraska Medical Center, College of Public Health, Department of Epidemiology, Omaha, Nebraska, United States of America.
Dikchha GurungUniversity of Nebraska Medical Center, College of Public Health, Department of Epidemiology, Omaha, Nebraska, United States of America.
Hallie SmithNebraska Department of Health and Human Services, Lincoln, Nebraska, United States of America.
Tammy DowdyNebraska Department of Health and Human Services, Lincoln, Nebraska, United States of America.
Amanda M BartlingNebraska Public Health Laboratory, Omaha, Nebraska, United States of America.
Ava ButzUniversity of Nebraska Medical Center, College of Public Health, Department of Epidemiology, Omaha, Nebraska, United States of America.
Michael R WileyNebraska Public Health Laboratory, Omaha, Nebraska, United States of America.
M Jana BroadhurstUniversity of Nebraska Medical Center, College of Medicine, Department of Pathology, Microbiology, and Immunology, Omaha, Nebraska, United States of America.
Sydney SteinNebraska Department of Health and Human Services, Lincoln, Nebraska, United States of America.
Emily L McCutchenNebraska Public Health Laboratory, Omaha, Nebraska, United States of America.
Jeff HamikNebraska Department of Health and Human Services, Lincoln, Nebraska, United States of America.
Peter C IwenNebraska Public Health Laboratory, Omaha, Nebraska, United States of America.
Nick DowneyIntegrated DNA Technologies, Coralville, Iowa, United States of America.
Kaylee S HerzogUniversity of Nebraska Medical Center, College of Public Health, Department of Epidemiology, Omaha, Nebraska, United States of America.
Joseph R FauverUniversity of Nebraska Medical Center, College of Public Health, Department of Epidemiology, Omaha, Nebraska, United States of America.ORCID https://orcid.org/0000-0001-8099-2991

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

West Nile virus (WNV) is an endemic arthropod-borne virus that has routinely caused seasonal outbreaks in the United States since it was first detected in 1999. While phylogenetic studies have shown how WNV has diversified and undergone genotype replacement since introduction, more geographically focused studies are needed to understand intricate transmission dynamics at local and regional scales. In this study, we validate the IDT xGen WNV panel, a novel single reaction amplicon-based Next-Generation Sequencing approach, to generate high-quality WNV genomes and compare it to the "Primal Scheme" assay for WNV, a common amplicon sequencing strategy. By generating >250 genomes from mosquito pools, we show that the IDT xGen WNV panel generated coding-complete and accurate WNV genomes when compared to the current sequencing approaches. Additionally, we used this approach to generate 100 coding-complete WNV genomes from surveillance pools of mosquitoes collected in Nebraska during the 2023 outbreak. Our discrete phylogeographic analysis revealed substantial genetic diversity in WNV genomes from 2023 with minimal clustering across the state. This study demonstrated the utility of a single reaction amplicon-based sequencing approach to generate quality WNV genomes from routine surveillance samples and characterize WNV transmission dynamics in a high-incidence setting.

Indexed as

Genome, ViralWest Nile FeverWest Nile virusAnimalsCulicidaeGenetic VariationHigh-Throughput Nucleotide SequencingHumansMosquito VectorsPhylogenyPhylogeographySeasons

Identifiers

PMID41564144
PMCPMC12844533

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.