Evidence map›Paper›PMID 27643611›Full record

ArticlePloS one2016

Transcriptomic Analysis of Persistent Infection with Foot-and-Mouth Disease Virus in Cattle Suggests Impairment of Apoptosis and Cell-Mediated Immunity in the Nasopharynx.

Michael Eschbaumer, Carolina Stenfeldt, George R Smoliga, Juan M Pacheco, Luis L Rodriguez, Robert W Li, James Zhu, Jonathan Arzt

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
8.4field-weighted citation impact, top 3% of its field
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

24 citing papers in PubMed, 32 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Michael EschbaumerPlum Island Animal Disease Center (PIADC), Foreign Animal Disease Research Unit (FADRU), United States Department of Agriculture (USDA)-Agricultural Research Service (ARS), Greenport, NY, United States of America.ORCID http://orcid.org/0000-0002-1104-0695
Carolina StenfeldtPlum Island Animal Disease Center (PIADC), Foreign Animal Disease Research Unit (FADRU), United States Department of Agriculture (USDA)-Agricultural Research Service (ARS), Greenport, NY, United States of America.
George R SmoligaPlum Island Animal Disease Center (PIADC), Foreign Animal Disease Research Unit (FADRU), United States Department of Agriculture (USDA)-Agricultural Research Service (ARS), Greenport, NY, United States of America.
Juan M PachecoPlum Island Animal Disease Center (PIADC), Foreign Animal Disease Research Unit (FADRU), United States Department of Agriculture (USDA)-Agricultural Research Service (ARS), Greenport, NY, United States of America.
Luis L RodriguezPlum Island Animal Disease Center (PIADC), Foreign Animal Disease Research Unit (FADRU), United States Department of Agriculture (USDA)-Agricultural Research Service (ARS), Greenport, NY, United States of America.
Robert W LiAnimal Genomics and Improvement Laboratory (AGIL), USDA-ARS, Beltsville, MD, United States of America.
James ZhuPlum Island Animal Disease Center (PIADC), Foreign Animal Disease Research Unit (FADRU), United States Department of Agriculture (USDA)-Agricultural Research Service (ARS), Greenport, NY, United States of America.
Jonathan ArztPlum Island Animal Disease Center (PIADC), Foreign Animal Disease Research Unit (FADRU), United States Department of Agriculture (USDA)-Agricultural Research Service (ARS), Greenport, NY, United States of America.
Agricultural Research Service · USOak Ridge Associated Universities · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to investigate the mechanisms of persistent foot-and-mouth disease virus (FMDV) infection in cattle, transcriptome alterations associated with the FMDV carrier state were characterized using a bovine whole-transcriptome microarray. Eighteen cattle (8 vaccinated with a recombinant FMDV A vaccine, 10 non-vaccinated) were challenged with FMDV A24 Cruzeiro, and the gene expression profiles of nasopharyngeal tissues collected between 21 and 35 days after challenge were compared between 11 persistently infected carriers and 7 non-carriers. Carriers and non-carriers were further compared to 2 naïve animals that had been neither vaccinated nor challenged. At a controlled false-discovery rate of 10% and a minimum difference in expression of 50%, 648 genes were differentially expressed between FMDV carriers and non-carriers, and most (467) had higher expression in carriers. Among these, genes associated with cellular proliferation and the immune response-such as chemokines, cytokines and genes regulating T and B cells-were significantly overrepresented. Differential gene expression was significantly correlated between non-vaccinated and vaccinated animals (biological correlation +0.97), indicating a similar transcriptome profile across these groups. Genes related to prostaglandin E2 production and the induction of regulatory T cells were overexpressed in carriers. In contrast, tissues from non-carrier animals expressed higher levels of complement regulators and pro-apoptotic genes that could promote virus clearance. Based on these findings, we propose a working hypothesis for FMDV persistence in nasopharyngeal tissues of cattle, in which the virus may be maintained by an impairment of apoptosis and the local suppression of cell-mediated antiviral immunity by inducible regulatory T cells.

Indexed as

Immunity, CellularTranscriptomeAnimalsApoptosisCattleCattle DiseasesFoot-and-Mouth DiseaseFoot-and-Mouth Disease VirusGene Expression ProfilingImmunity, HumoralImmunity, InnateNasopharynxVaccinationVaccines, SyntheticViral VaccinesVaccines, SyntheticViral Vaccines

Identifiers

PMID27643611
PMCPMC5028045
OpenAlexW2521059898

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

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.