Evidence map›Paper›PMID 25534905›Full record

ArticleBMC genomics2014

Susceptibility loci revealed for bovine respiratory disease complex in pre-weaned holstein calves.

Holly L Neibergs, Christopher M Seabury, Andrzej J Wojtowicz, Zeping Wang, Erik Scraggs, Jennifer N Kiser, Mahesh Neupane, James E Womack, Alison Van Eenennaam, Gerald Robert Hagevoort and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
6.6field-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

68 citing papers in PubMed, 113 citations in OpenAlex.

  1. Article
  2. Effects of the Prenatal Maternal Health Status on Calf Disease Prevalences and Respective Genetic Parameter Estimates in German Holstein Cattle.Journal of animal breeding and genetics = Zeitschrift fur Tierzuchtung und Zuchtungsbiologie · 2025
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  20. Detection ofFrontiers in microbiomes · 2022
    Article

8 more citing papers are in PubMed but not listed here.

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

15 authors at 5 institutions in 1 country.

Holly L NeibergsDepartment of Animal Sciences, Washington State University, P.O. Box 646310, Pullman, WA, 99164-6310, USA. Neibergs@wsu.edu.
Christopher M SeaburyDepartment of Veterinary Pathobiology, Texas A&M University, College Station, USA. CSeabury@cvm.tamu.edu.
Andrzej J WojtowiczDepartment of Animal Sciences, Washington State University, P.O. Box 646310, Pullman, WA, 99164-6310, USA. andrzej.wojtowicz@wsu.edu.
Zeping WangDepartment of Animal Sciences, Washington State University, P.O. Box 646310, Pullman, WA, 99164-6310, USA. zeping_wang@wsu.edu.
Erik ScraggsDepartment of Animal Sciences, Washington State University, P.O. Box 646310, Pullman, WA, 99164-6310, USA. erikscraggs@gmail.com.
Jennifer N KiserDepartment of Animal Sciences, Washington State University, P.O. Box 646310, Pullman, WA, 99164-6310, USA. Jennifer.kiser@email.wsu.edu.
Mahesh NeupaneDepartment of Animal Sciences, Washington State University, P.O. Box 646310, Pullman, WA, 99164-6310, USA. Mahesh.neupane@email.wsu.edu.
James E WomackDepartment of Veterinary Pathobiology, Texas A&M University, College Station, USA. jwomack@cvm.tamu.edu.
Alison Van EenennaamDepartment of Animal Sciences, University of California Davis, Davis, USA. alvaneenennaam@ucdavis.edu.
Gerald Robert HagevoortExtension Animal Sciences and Natural Resources Department, New Mexico State University, Las Cruces, USA. dairydoc@nmsu.edu.
Terry W LehenbauerDepartment of Population Health and Reproduction, University of California Davis, Davis, USA. tlehenbauer@vmtrc.ucdavis.edu.
Sharif AlyDepartment of Population Health and Reproduction, University of California Davis, Davis, USA. saly@vmtrc.ucdavis.edu.
Jessica DavisDepartment of Population Health and Reproduction, University of California Davis, Davis, USA. jdavis@vmtrc.ucdavis.edu.
Jeremy F TaylorDivision of Animal Sciences, University of Missouri, Columbia, USA. taylorjerr@missouri.edu.
Bovine Respiratory Disease Complex Coordinated Agricultural Project Research Team
Washington State University · USUniversity of California, Davis · USTexas A&M University · USNew Mexico State University · USUniversity of Missouri · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBovine respiratory disease complex (BRDC) is an infectious disease of cattle that is caused by a combination of viral and/or bacterial pathogens. Selection for cattle with reduced susceptibility to respiratory disease would provide a permanent tool for reducing the prevalence of BRDC. The objective of this study was to identify BRDC susceptibility loci in pre-weaned Holstein calves as a prerequisite to using genetic improvement as a tool for decreasing the prevalence of BRDC. High density SNP genotyping with the Illumina BovineHD BeadChip was conducted on 1257 male and 757 female Holstein calves from California (CA), and 767 calves identified as female from New Mexico (NM). Of these, 1382 were classified as BRDC cases, and 1396 were classified as controls, with all phenotypes assigned using the McGuirk health scoring system. During the acquisition of blood for DNA isolation, two deep pharyngeal and one mid-nasal diagnostic swab were obtained from each calf for the identification of bacterial and viral pathogens. Genome-wide association analyses were conducted using four analytical approaches (EIGENSTRAT, EMMAX-GRM, GBLUP and FvR). The most strongly associated SNPs from each individual analysis were ranked and evaluated for concordance. The heritability of susceptibility to BRDC in pre-weaned Holstein calves was estimated.

resultsThe four statistical approaches produced highly concordant results for 373 top ranked SNPs that defined 126 chromosomal regions for the CA population. Similarly, in NM, 370 SNPs defined 138 genomic regions that were identified by all four approaches. When the two populations were combined (i.e., CA + NM) and analyzed, 324 SNPs defined 116 genomic regions that were associated with BRDC across all analytical methods. Heritability estimates for BRDC were 21% for both CA and NM as individual populations, but declined to 13% when the populations were combined.

conclusionsFour analytical approaches utilizing both single and multi-marker association methods revealed common genomic regions associated with BRDC susceptibility that can be further characterized and used for genomic selection. Moderate heritability estimates were observed for BRDC susceptibility in pre-weaned Holstein calves, thereby supporting the application of genomic selection to reduce the prevalence of BRDC in U.S. Holsteins.

Indexed as

Genetic LociGenetic Predisposition to DiseaseWeaningAnimalsBovine Respiratory Disease ComplexBreedingCattleFemaleGenome-Wide Association StudyMale

Identifiers

PMID25534905
PMCPMC4445561
OpenAlexW2163746227

What OpenQuestion holds

Textmetadata
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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.