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      Genome-Wide Association Study of Susceptibility to Infection by Mycobacterium avium Subspecies paratuberculosis in Holstein Cattle

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          Abstract

          Paratuberculosis, or Johne's disease, is a chronic, granulomatous, gastrointestinal tract disease of cattle and other ruminants caused by the bacterium Mycobacterium avium, subspecies paratuberculosis ( MAP). Control of Johne's disease is based on programs of testing and culling animals positive for infection with MAP while concurrently modifying management to reduce the likelihood of infection. The current study is motivated by the hypothesis that genetic variation in host susceptibility to MAP infection can be dissected and quantifiable associations with genetic markers identified. For this purpose, a case-control, genome-wide association study was conducted using US Holstein cattle phenotyped for MAP infection using a serum ELISA and/or fecal culture test. Cases included cows positive for either serum ELISA, fecal culture or both. Controls consisted of animals negative for the serum ELISA test or both serum ELISA and fecal culture when both were available. Controls were matched by herd and proximal birth date with cases. A total of 856 cows (451 cases and 405 controls) were used in initial discovery analyses, and an additional 263 cows (159 cases and 104 controls) from the same herds were used as a validation data set. Data were analyzed in a single marker analysis controlling for relatedness of individuals (GRAMMAR-GC) and also in a Bayesian analysis in which multiple marker effects were estimated simultaneously (GenSel). For the latter, effects of non-overlapping 1 Mb marker windows across the genome were estimated. Results from the two discovery analyses were generally concordant; however, discovery results were generally not well supported in analysis of the validation data set. A combined analysis of discovery and validation data sets provided strongest support for SNPs and 1 Mb windows on chromosomes 1, 2, 6, 7, 17 and 29.

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          Most cited references50

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          Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.

          A genome-wide association scan in individuals with Crohn's disease by the Wellcome Trust Case Control Consortium detected strong association at four novel loci. We tested 37 SNPs from these and other loci for association in an independent case-control sample. We obtained replication for the autophagy-inducing IRGM gene on chromosome 5q33.1 (replication P = 6.6 x 10(-4), combined P = 2.1 x 10(-10)) and for nine other loci, including NKX2-3, PTPN2 and gene deserts on chromosomes 1q and 5p13.
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            Human genetic susceptibility to infectious disease.

            Recent genome-wide studies have reported novel associations between common polymorphisms and susceptibility to many major infectious diseases in humans. In parallel, an increasing number of rare mutations underlying susceptibility to specific phenotypes of infectious disease have been described. Together, these developments have highlighted a key role for host genetic variation in determining the susceptibility to infectious disease. They have also provided insights into the genetic architecture of infectious disease susceptibility and identified immune molecules and pathways that are directly relevant to the human host defence.
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              Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.

              Genetic variation in both innate and adaptive immune systems is associated with Crohn's disease (CD) susceptibility, but much of the heritability to CD remains unknown. We performed a genome-wide association study (GWAS) in 896 CD cases and 3204 healthy controls all of Caucasian origin as defined by multidimensional scaling. We found supportive evidence for 21 out of 40 CD loci identified in a recent CD GWAS meta-analysis, including two loci which had only nominally achieved replication (rs4807569, 19p13; rs991804, CCL2/CCL7). In addition, we identified associations with genes involved in tight junctions/epithelial integrity (ASHL, ARPC1A), innate immunity (EXOC2), dendritic cell biology [CADM1 (IGSF4)], macrophage development (MMD2), TGF-beta signaling (MAP3K7IP1) and FUT2 (a physiological trait that regulates gastrointestinal mucosal expression of blood group A and B antigens) (rs602662, P=3.4x10(-5)). Twenty percent of Caucasians are 'non-secretors' who do not express ABO antigens in saliva as a result of the FUT2 W134X allele. We demonstrated replication in an independent cohort of 1174 CD cases and 357 controls between the four primary FUT2 single nucleotide polymorphisms (SNPs) and CD (rs602662, combined P-value 4.90x10(-8)) and also association with FUT2 W143X (P=2.6x10(-5)). Further evidence of the relevance of this locus to CD pathogenesis was demonstrated by the association of the original four SNPs and CD in the recently published CD GWAS meta-analysis (rs602662, P=0.001). These findings strongly implicate this locus in CD susceptibility and highlight the role of the mucus layer in the development of CD.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                4 December 2014
                : 9
                : 12
                : e111704
                Affiliations
                [1 ]Department of Animal Science, Faculty of Veterinary Medicine, Uludag University, Bursa, 16059, Turkey
                [2 ]Department of Animal Sciences, University of Wisconsin-Madison, Madison, Wisconsin, 53706, United States of America
                [3 ]Department of Animal Science, Faculty of Agriculture, Universiti Putra, UPM Serdang, Selangor, Malaysia
                [4 ]College of Animal Science, Xinjiang Agricultural University, Urumqi, Xinjiang, China
                [5 ]Department of Dairy Science, University of Wisconsin-Madison, Madison, Wisconsin, 53706, United States of America
                [6 ]Department of Pathobiological Science, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin, 53706, United States of America
                University of New South Wales, Australia
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: FA GES MTC BWK. Performed the experiments: FA YZ MHK XH XS. Analyzed the data: FA BWK YZ. Wrote the paper: FA YZ GES MTC BWK MHK XH. Identified cooperating dairy herds: GES MTC.

                [¤]

                Current address: ABS Global Inc., 1525 River Road, DeForest, Wisconsin, 53532, United States of America

                Article
                PONE-D-14-24575
                10.1371/journal.pone.0111704
                4256300
                25473852
                6c0d54c3-467b-477d-a722-cea8105fb3d3
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 4 June 2014
                : 26 August 2014
                Page count
                Pages: 14
                Funding
                This project was supported by grants from United States Department of Agriculture - National Institute of Food and Agriculture (grant #2010-65205-20442 and 2007-35205-17884). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Agriculture
                Livestock
                Cattle
                Genetics
                Animal Genetics
                Mammalian Genetics
                Genetics of Disease
                Genetic Predisposition
                Genomics
                Animal Genomics
                Mammalian Genomics
                Veterinary Science
                Veterinary Diseases
                Paratuberculosis
                Custom metadata
                The authors confirm that all data underlying the findings are fully available without restriction. The genotype data are available via the supporting information files. The phenotypic data are not owned by the authors, but are from the Johne's disease host genetics study and requests for data can be sent to Dr. Brian Kirkpatrick at bwkirkpa@ 123456wisc.edu .

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                Uncategorized

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