37
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Genome-wide association study identifies novel loci associated with resistance to bovine tuberculosis

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Tuberculosis (TB) caused by Mycobacterium bovis is a re-emerging disease of livestock that is of major economic importance worldwide, as well as being a zoonotic risk. There is significant heritability for host resistance to bovine TB (bTB) in dairy cattle. To identify resistance loci for bTB, we undertook a genome-wide association study in female Holstein–Friesian cattle with 592 cases and 559 age-matched controls from case herds. Cases and controls were categorised into distinct phenotypes: skin test and lesion positive vs skin test negative on multiple occasions, respectively. These animals were genotyped with the Illumina BovineHD 700K BeadChip. Genome-wide rapid association using linear and logistic mixed models and regression (GRAMMAR), regional heritability mapping (RHM) and haplotype-sharing analysis identified two novel resistance loci that attained chromosome-wise significance, protein tyrosine phosphatase receptor T ( PTPRT; P=4.8 × 10 −7) and myosin IIIB ( MYO3B; P=5.4 × 10 −6). We estimated that 21% of the phenotypic variance in TB resistance could be explained by all of the informative single-nucleotide polymorphisms, of which the region encompassing the PTPRT gene accounted for 6.2% of the variance and a further 3.6% was associated with a putative copy number variant in MYO3B. The results from this study add to our understanding of variation in host control of infection and suggest that genetic marker-based selection for resistance to bTB has the potential to make a significant contribution to bTB control.

          Related collections

          Most cited references28

          • Record: found
          • Abstract: found
          • Article: not found

          Genome-wide association studies for complex traits: consensus, uncertainty and challenges.

          The past year has witnessed substantial advances in understanding the genetic basis of many common phenotypes of biomedical importance. These advances have been the result of systematic, well-powered, genome-wide surveys exploring the relationships between common sequence variation and disease predisposition. This approach has revealed over 50 disease-susceptibility loci and has provided insights into the allelic architecture of multifactorial traits. At the same time, much has been learned about the successful prosecution of association studies on such a scale. This Review highlights the knowledge gained, defines areas of emerging consensus, and describes the challenges that remain as researchers seek to obtain more complete descriptions of the susceptibility architecture of biomedical traits of interest and to translate the information gathered into improvements in clinical management.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls

            Copy number variants (CNVs) account for a major proportion of human genetic polymorphism and have been predicted to play an important role in genetic susceptibility to common disease. To address this we undertook a large direct genome-wide study of association between CNVs and eight common human diseases. Using a purpose-designed array we typed ~19,000 individuals into distinct copy-number classes at 3,432 polymorphic CNVs, including an estimated ~50% of all common CNVs larger than 500bp. We identified several biological artefacts that lead to false-positive associations, including systematic CNV differences between DNAs derived from blood and cell-lines. Association testing and follow-up replication analyses confirmed three loci where CNVs were associated with disease, IRGM for Crohn's disease, HLA for Crohn's disease, rheumatoid arthritis, and type 1 diabetes, and TSPAN8 for type 2 diabetes, though in each case the locus had previously been identified in SNP-based studies, reflecting our observation that the majority of common CNVs which are well-typed on our array are well tagged by SNPs and so have been indirectly explored through SNP studies. We conclude that common CNVs which can be typed on existing platforms are unlikely to contribute greatly to the genetic basis of common human diseases.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Classification of worldwide bovine tuberculosis risk factors in cattle: a stratified approach

              The worldwide status of bovine tuberculosis (bTB) as a zoonosis remains of great concern. This article reviews the main risk factors for bTB in cattle based on a three-level classification: animal, herd and region/country level. A distinction is also made, whenever possible, between situations in developed and developing countries as the difference of context might have consequences in terms of risk of bTB. Recommendations are suggested to animal health professionals and scientists directly involved in the control and prevention of bTB in cattle. The determination of Millenium Development Goals for bTB is proposed to improve the control/eradication of the disease worldwide.
                Bookmark

                Author and article information

                Journal
                Heredity (Edinb)
                Heredity (Edinb)
                Heredity
                Nature Publishing Group
                0018-067X
                1365-2540
                May 2014
                05 February 2014
                1 May 2014
                : 112
                : 5
                : 543-551
                Affiliations
                [1 ]The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh , Edinburgh, UK
                [2 ]Agri-Food and Biosciences Institute Stormont , Belfast, UK
                [3 ]Queen's University Belfast, School of Biological Sciences, Medical Biology Centre , Belfast, UK
                Author notes
                [* ]MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital , Crewe Road, Edinburgh EH4 2XU, UK. E-mail: mairead.bermingham@ 123456igmm.ed.ac.uk
                [4]

                Current Address: Department of Biosciences, University of Exeter, Devon, UK.

                [5]

                Current Address: Centre for Public Health, Institute of Clinical Sciences—Block B, Queen's University Belfast, Royal Victoria Hospital, Belfast, UK.

                Article
                hdy2013137
                10.1038/hdy.2013.137
                3998787
                24496092
                f056741d-379e-4a18-9459-facc19a90b24
                Copyright © 2014 The Genetics Society

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/

                History
                : 17 June 2013
                : 03 October 2013
                : 16 October 2013
                Categories
                Original Article

                Human biology
                genome-wide association study,bovine tuberculosis,novel resistance loci
                Human biology
                genome-wide association study, bovine tuberculosis, novel resistance loci

                Comments

                Comment on this article