Evidence map›Paper›PMID 28646863›Full record

ArticleBMC genomics2017

Fine-mapping host genetic variation underlying outcomes to Mycobacterium bovis infection in dairy cows.

S Wilkinson, S C Bishop, A R Allen, S H McBride, R A Skuce, M Bermingham, J A Woolliams, E J Glass

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Can We Breed Cattle for Lower Bovine TB Infectivity?Frontiers in veterinary science · 2018
    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

8 authors at 4 institutions in 1 country.

S WilkinsonThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush EH25 9RG, Edinburgh, UK. samantha.wilkinson@roslin.ed.ac.uk.
S C BishopThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush EH25 9RG, Edinburgh, UK.
A R AllenAgri-Food and Biosciences Institute, Stormont, Belfast, Northern Ireland, BT4 3SD, UK.
S H McBrideAgri-Food and Biosciences Institute, Stormont, Belfast, Northern Ireland, BT4 3SD, UK.
R A SkuceAgri-Food and Biosciences Institute, Stormont, Belfast, Northern Ireland, BT4 3SD, UK.
M BerminghamThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush EH25 9RG, Edinburgh, UK.
J A WoolliamsThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush EH25 9RG, Edinburgh, UK.
E J GlassThe Roslin Institute and R(D)SVS, University of Edinburgh, Easter Bush EH25 9RG, Edinburgh, UK.
University of Edinburgh · GBAgri Food and Biosciences Institute · GBQueen's University Belfast · GBWestern General Hospital · GB

Funding

Biotechnology and Biological Sciences Research Council BB/E018335/1Biotechnology and Biological Sciences Research Council BB/E018335/2Biotechnology and Biological Sciences Research Council BB/E018386/1Biotechnology and Biological Sciences Research Council BB/J004227/1Biotechnology and Biological Sciences Research Council BB/J004235/1Biotechnology and Biological Sciences Research Council BB/L004054/1Biotechnology and Biological Sciences Research Council BB/P013740/1Biotechnology and Biological Sciences Research Council BBS/E/D/20211553
6 · The paper itself

Abstract

backgroundSusceptibility to Mycobacterium bovis infection in cattle is governed in part by host genetics. However, cattle diagnosed as infected with M. bovis display varying signs of pathology. The variation in host response to infection could represent a continuum since time of exposure or distinct outcomes due to differing pathogen handling. The relationships between host genetics and variation in host response and pathological sequelae following M. bovis infection were explored by genotyping 1966 Holstein-Friesian dairy cows at 538,231 SNPs with three distinct phenotypes. These were: single intradermal cervical comparative tuberculin (SICCT) test positives with visible lesions (VLs), SICCT-positives with undetected visible lesions (NVLs) and matched controls SICCT-negative on multiple occasions.

resultsRegional heritability mapping identified three loci associated with the NVL phenotype on chromosomes 17, 22 and 23, distinct to the region on chromosome 13 associated with the VL phenotype. The region on chromosome 23 was at genome-wide significance and candidate genes overlapping the mapped window included members of the bovine leukocyte antigen class IIb region, a complex known for its role in immunity and disease resistance. Chromosome heritability analysis attributed variance to six and thirteen chromosomes for the VL and NVL phenotypes, respectively, and four of these chromosomes were found to explain a proportion of the phenotypic variation for both the VL and NVL phenotype. By grouping the M. bovis outcomes (VLs and NVLs) variance was attributed to nine chromosomes. When contrasting the two M. bovis infection outcomes (VLs vs NVLs) nine chromosomes were found to harbour heritable variation. Regardless of the case phenotype under investigation, chromosome heritability did not exceed 8% indicating that the genetic control of bTB resistance consists of variants of small to moderate effect situated across many chromosomes of the bovine genome.

conclusionsThese findings suggest the host genetics of M. bovis infection outcomes is governed by distinct and overlapping genetic variants. Thus, variation in the pathology of M. bovis infected cattle may be partly genetically determined and indicative of different host responses or pathogen handling. There may be at least three distinct outcomes following M. bovis exposure in dairy cattle: resistance to infection, infection resulting in pathology or no detectable pathology.

Indexed as

Chromosome MappingDairyingGenetic VariationAnimalsCattleChromosomes, MammalianFemaleGenome-Wide Association StudyMycobacterium bovisPolymorphism, Single NucleotideTuberculosis, Osteoarticular

Identifiers

PMID28646863
PMCPMC5483290
OpenAlexW2700580565

What Socratic 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 Socratic graph.