Evidence map›Paper›PMID 41078497›Full record

ArticleFrontiers in veterinary science2025

Bovine viral diarrhea virus 2 strains generate deletion viral genomes primarily in the NS2 region of the viral genome.

David J Holthausen, Darrell O Bayles, John D Neill, Rohana P Dassanayake, Shollie M Falkenberg, Daniel W Nielsen, Anna K Goldkamp, Harish Menghwar, Eduardo Casas

Abstract read
In one paragraph

Article in Frontiers in veterinary science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

9 authors.

David J HolthausenRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA, United States.
Darrell O BaylesInfectious Bacterial Diseases Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA, United States.
John D NeillRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA, United States.
Rohana P DassanayakeRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA, United States.
Shollie M FalkenbergDepartment of Pathobiology, Animal Health Research, College of Veterinary Medicine, Auburn University, Auburn, AL, United States.
Daniel W NielsenRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA, United States.
Anna K GoldkampRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA, United States.
Harish MenghwarRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA, United States.
Eduardo CasasRuminant Diseases and Immunology Research Unit, National Animal Disease Center, USDA, Agricultural Research Service, Ames, IA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bovine viral diarrhea virus (BVDV) is a significant economic concern for the global cattle industry. This is attributed to the increased risk of transplacental BVDV infection during pregnancy, before sufficient maturation of the fetal immune system. This results in significant reproductive losses via spontaneous abortion as well as the birth of offspring that are persistently infected and immunotolerant to the non-cytopathic BVDV strain. These persistently infected cattle act as reservoirs and are the major source of BVDV transmission within the herd. Previously, we reported bioinformatic analyses showing that BVDV1a and 1b genotypes generate distinct sets of diverse deletion viral genomes (DelVGs) during the natural viral life cycle. DelVGs are generated by skipping events that occur during genome synthesis by the error-prone viral replication machinery. These replication-deficient genomes play many roles in host-pathogen interactions, contributing to the establishment of viral persistence. A total of 21 field isolates of the BVDV2 genotype were analyzed for the presence and characterization of DelVGs using Illumina MiSeq BVDV2 genome sequencing reads. BVDV2 strains generate significantly more Nonstructural protein 2 (NS2) DelVGs than any other region of the genome, with over 90% of those deletions having both 5` and 3` junctions within the NS2 region. BVDV2c strains produce approximately 150 times as many DelVG reads as BVDV2a strains. Of the BVDV2a isolates queried, cytopathic BVDV2a strains generated two times as many NS2 DelVG reads as compared to non-cytopathic BVDV2a strains.

Indexed as

bovine viral diarrhea virus 2deletion viral genomesnon-standard viral genomespestivirusviral evolution

Identifiers

PMID41078497
PMCPMC12507611

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Registered trials

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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.