Evidence map›Paper›PMID 26121276›Full record

ArticlePloS one2015

Immunological Response to Single Pathogen Challenge with Agents of the Bovine Respiratory Disease Complex: An RNA-Sequence Analysis of the Bronchial Lymph Node Transcriptome.

Polyana C Tizioto, JaeWoo Kim, Christopher M Seabury, Robert D Schnabel, Laurel J Gershwin, Alison L Van Eenennaam, Rachel Toaff-Rosenstein, Holly L Neibergs, Bovine Respiratory Disease Complex Coordinated Agricultural Project Research Team, Jeremy F Taylor

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

56 citing papers in PubMed, 73 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

10 authors at 5 institutions in 2 countries.

Polyana C TiziotoEmbrapa Southeast Livestock, São Carlos, São Paulo, Brazil; Division of Animal Sciences, University of Missouri, Columbia, Missouri, United States of America.
JaeWoo KimDivision of Animal Sciences, University of Missouri, Columbia, Missouri, United States of America.
Christopher M SeaburyDepartment of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, Texas, United States of America.
Robert D SchnabelDivision of Animal Sciences, University of Missouri, Columbia, Missouri, United States of America.
Laurel J GershwinDepartment of Pathology, Microbiology & Immunology, School of Veterinary Medicine, University of California Davis, Davis, California, United States of America.
Alison L Van EenennaamDepartment of Animal Science, College of Agriculture, University of California Davis, Davis, California, United States of America.
Rachel Toaff-RosensteinDepartment of Animal Science, College of Agriculture, University of California Davis, Davis, California, United States of America.
Holly L NeibergsDepartment of Animal Sciences, College of Veterinary Medicine, Washington State University, Pullman, Washington, United States of America.
Bovine Respiratory Disease Complex Coordinated Agricultural Project Research Team
Jeremy F TaylorDivision of Animal Sciences, University of Missouri, Columbia, Missouri, United States of America.
University of California, Davis · USUniversity of Missouri · USBrazilian Agricultural Research Corporation · BRTexas A&M University · USWashington State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Susceptibility to bovine respiratory disease (BRD) is multi-factorial and is influenced by stress in conjunction with infection by both bacterial and viral pathogens. While vaccination is broadly used in an effort to prevent BRD, it is far from being fully protective and cases diagnosed from a combination of observed clinical signs without any attempt at identifying the causal pathogens are usually treated with antibiotics. Dairy and beef cattle losses from BRD are profound worldwide and genetic studies have now been initiated to elucidate host loci which underlie susceptibility with the objective of enabling molecular breeding to reduce disease prevalence. In this study, we employed RNA sequencing to examine the bronchial lymph node transcriptomes of controls and beef cattle which had individually been experimentally challenged with bovine respiratory syncytial virus, infectious bovine rhinotracheitis, bovine viral diarrhea virus, Pasteurella multocida, Mannheimia haemolytica or Mycoplasma bovis to identify the genes that are involved in the bovine immune response to infection. We found that 142 differentially expressed genes were located in previously described quantitative trait locus regions associated with risk of BRD. Mutations affecting the expression or amino acid composition of these genes may affect disease susceptibility and could be incorporated into molecular breeding programs. Genes involved in innate immunity were generally found to be differentially expressed between the control and pathogen-challenged animals suggesting that variation in these genes may lead to a heritability of susceptibility that is pathogen independent. However, we also found pathogen-specific expression profiles which suggest that host genetic variation for BRD susceptibility is pathogen dependent.

Indexed as

Sequence Analysis, RNAAnimalsBovine Respiratory Disease ComplexBronchiCattleCattle DiseasesCluster AnalysisDown-RegulationGene Expression ProfilingLymph NodesMolecular Sequence AnnotationPrincipal Component AnalysisProtein IsoformsQuality ControlRespiratory Tract InfectionsRNA, MessengerProtein IsoformsRNA, MessengerToll-Like Receptors

Identifiers

PMID26121276
PMCPMC4484807
OpenAlexW1544271909

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.