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Genome-wide association study of Mycobacterium avium subspecies Paratuberculosis infection in Chinese Holstein

BMC Genomics volume 19, Article number: 972 (2018) Cite this article

Abstract

Background

Paratuberculosis is a contagious, chronic and enteric disease in ruminants, which is caused by Mycobacterium avium subspecies paratuberculosis (MAP) infection, resulting in enormous economic losses worldwide. There is currently no effective cure for MAP infection or a vaccine, it is thus important to explore the genetic variants that contribute to host susceptibility to infection by MAP, which may provide a better understanding of the mechanisms of paratuberculosis and benefit animal genetic improvement. Herein we performed a genome-wide association study (GWAS) to identify genomic regions and candidate genes associated with susceptibility to MAP infection in dairy cattle.

Results

Using Illumina Bovine 50 K (54,609 SNPs) and GeneSeek HD (138,893 SNPs) chips, two analytical approaches were performed, GRAMMAR-GC and ROADTRIPS in 937 Chinese Holstein cows, among which individuals genotyped by the 50 K chip were imputed to HD SNPs with Beagle software. Consequently, 15 and 11 significant SNPs (P < 5 × 10− 5) were identified with GRAMMAR-GC and ROADTDRIPS, respectively. A total of 10 functional genes were in proximity to (i.e., within 1 Mb) these SNPs, including IL4, IL5, IL13, IRF1, MyD88, PACSIN1, DEF6, TDP2, ZAP70 and CSF2. Functional enrichment analysis showed that these genes were involved in immune related pathways, such as interleukin, T cell receptor signaling pathways and inflammatory bowel disease (IBD), implying their potential associations with susceptibility to MAP infection. In addition, by examining the publicly available cattle QTLdb, a previous QTL for MAP was found to be overlapped with one of regions detected currently at 32.5 Mb on BTA23, where the TDP2 gene was anchored.

Conclusions

In conclusion, we identified 26 SNPs located on 15 chromosomes in the Chinese Holstein population using two GWAS strategies with high density SNPs. Integrated analysis of GWAS, biological functions and the reported QTL information helps to detect positional candidate genes and the identification of regions associated with susceptibility to MAP traits in dairy cattle.

Background

Paratuberculosis, also known as Johne’s disease (JD), is a contagious, chronic and enteric disease in ruminants caused by Mycobacterium avium subspecies paratuberculosis (MAP) [1]. Symptoms of the disease include diarrhea and weight loss that eventually leads to death. This disease has a long period of incubation [2]. In cattle, JD cannot be diagnosed until symptoms are observed because animals can have MAP in their systems, but not have JD. It is always difficult to determine if an animal is at risk of contracting JD by screening for MAP. Once a cow shows symptoms of JD, there is no treatment so the only effective means to get rid of the disease is to cull. There is also no vaccine, so farmers cannot increase resistance to JD within their herds, which causes huge economic losses. The disease can easily be spread through the farm from contact with MAP infected feces or milk from infected cows. Changes in herd management could help to reduce JD, but understanding resistance in cattle will allow for better management of the disease. Genomic selection for disease-resistant animals may be a promising way to increase the ability of animals to resist MAP infection. Exploring the genetic variants that contribute to host susceptibility to infection by MAP is important both for animal genetic improvement programs and for a better understanding of the underlying mechanisms of disease.

Heritability estimates in Holstein and Jersey cows for infection with MAP range from 0.031 to 0.283 [3,4,5,6,7,8,9,10,11,12,13]. By employing a case-control design, several functional genes have been reported to be associated with susceptibility to MAP infection in cattle. This includes CLEC7A [14], IL10RA [15], IL12RB1, IL12RB2, IL23R, IFNGR2 [16], NOD2 [17,18,19], PGLYRP1 [20], SLC11A1 [21, 22], SP110 [23], TLR1 [24, 25], TLR2 [24,25,26] and TLR4 [24, 25]. Multiple QTLs are located on BTA7 [27] and BTA20 [28]. These studies indicated that genetic factors contribute to the susceptibility of MAP infection in cattle.

Nowadays, genome-wide association study (GWAS) is a popular strategy to identify candidate genes for specified traits. Earlier GWAS studies for MAP infection in Holstein cattle were based on serum ELISA, milk ELISA, fecal culture test or a comprehensive test for MAP infection [29,30,31,32,33,34,35,36,37]. Various SNPs associated with susceptibly to MAP infection are extensively distributed across all autosomes in different Holstein cattle populations. Several candidate genes for MAP infection were subsequently identified, such as EDN2, PRDM1, LAMB4, DLD, LDLRAD3, CACNA1B, TIMD4, ITK, C, BTN1A1 and TDP2 [29,30,31,32,33,34,35,36,37]. Zare et al. reported 9 SNPs on BTA3, BTA6, BTA17 and BTA23 in the US Jersey cattle population and suggested SLC17A1, UBD, HIVEP1, CCDC17, ZNF684, UBE2L3, UBE2K, FAM109A and FAM5C genes as candidates for susceptibly to MAP infection [35]. In the present study, the objectives were to identify genetic markers and genomic regions that are associated with susceptibility to MAP infection by performing a GWAS in Chinese Holsteins, and to provide further molecular information for the MAP resistance breeding program.

Methods

Data description

A total of 8214 Chinese Holstein cows from 7 dairy farms belonging to the Beijing Sanyuan Dairy Farm Center were fed under the same management throughout this study. We collected a 500 μL blood sample from the caudal vein of each cow and performed a regular quarantine inspection of the farms during September 2014. Serum extracted from blood samples were stored at 4 °C until testing; within 5 days after collection. The commercially available, ELISA kit (IDEXX Laboratories, Inc., Westbrook, ME, USA) was used according to the manufacturer instructions to measure the antibody levels of each serum sample. The MAP status of an animal was expressed as a percentage of the sample to positive ratio (S/P) with the formula: S/P ratio = [(optical density (OD) of the sample – OD of the negative control) / (OD of positive sample – OD of the negative control)], where ≤0.45 is negative; 0.45 < S/P < 0.55 is suspect; S/P ≥ 0.55 is positive. ELISA suspect results were excluded because of their uncertainty. Out of the 8214 detected cows, 185 positive individuals (case) and 760 negative individuals (control) from 6 herds were used for GWAS. ELISA results were employed as a binary trait (0 = negative, 1 = positive).

Genotyping

The individuals in this study were divided into 2 sub-groups for genotyping. Five hundred and thirty three cows belonging to the first sub-group were genotyped with the Illumina Bovine SNP50 BeadChip (54,609 SNPs, Illumina, San Diego, CA, USA) after extracting DNA from whole blood using routine procedures. DNA was isolated from whole blood with a commercially available kit, the DP318 Blood DNA Kit (Tiangen Biotech Co., China). The DNA of the remaining 412 cows in the second sub-group were extracted from hair by GeneSeek with QIAamp® DNA Mini Kit (QIAGEN Inc., Valencia, CA, USA) and then genotyped with the GeneSeek Genomic Profiler HD v2 (138,893 SNPs, GeneSeek, Lincoln, NE, USA). The genotype data were deposited in the Additional files (Additional files 1 and 2).

Imputation and quality control

To make full use of SNPs originating from the GeneSeek Genomic Profiler HD v2 (GeneSeek), individuals genotyped by the Illumina Bovine SNP50 BeadChip were imputed to GeneSeek Genomic Profiler HD v2. Imputation was performed using BEAGLE 3.3.2 [38] default options. Allelic R2 was estimated as an indicator of imputation accuracy based on the genotype probabilities.

To further evaluate imputation accuracy, we randomly selected 100 cows genotyped by the high-density chip, obtained the common SNPs between the two panels, and masked genotypes of SNPs left. We classified this small subset of cows as the study population, while the remaining cows genotyped by the high-density panel were classified as the reference population. After imputation, we compared the imputed and masked actual genotypes of the selected 100 cows to calculate the percentage of genotypes that are consistent between them.

Then we implemented PLINK [39] and removed SNPs with call rates < 95%, minor allele frequencies < 0.01, a deviation from Hardy-Weinburg equilibrium (HWE) P values < 10− 6 and > 5% missing genotypes. A dataset containing 109,607 SNPs and 937 animals (182 cases and 755 controls) was used for further analysis. All SNP positions were determined according to the Bos taurus UMD 3.1 assembly [40].

Population stratification

Differences in allele frequencies between subpopulations of admixed populations can lead to false association in a GWAS [41]. In order to determine whether stratification exists in our study population, a principle component analysis (PCA) was performed by GCTA 1.24 [42] and results were visualized by R 3.3.1 [43].

GWAS

GRAMMAR-GC

We performed a GWAS using the Genome-wide Rapid Association using Mixed Model and Regression-Genomic Control (GRAMMAR-GC) approach [44, 45], a single-marker method implemented within the GenABEL package [46] for R [43]. This approach can account for the potential population structure and infer relationships using SNP data without pedigree information. There have been multiple GWAS studies in cattle that utilized this approach [31, 34,35,36,37]. GRAMMAR-GC is comprised of three steps that use the regression of phenotypes on the genotypes of individuals for one SNP at a time. First, to account for familial dependence among individuals, phenotypes were corrected by conducting a polygenic analysis using a genomic kinship matrix based on the SNP genotypes. Residuals from the polygenic analysis were then used as dependent quantitative traits for association analysis of each SNP with a linear regression model. Finally, genomic control (GC) was applied to correct the test statistic using the genomic inflation factor (λ), which is the regression coefficient of the observed statistic on the expected statistic. We performed an association test for each SNP based on the following linear mixed model:

$$ \mathrm{y}=\mathrm{W}\upalpha +\mathrm{x}\upbeta +\mathrm{u}+\upvarepsilon, $$

where y is the liability vector for case/control observations; W is a matrix of covariates (fixed effects that contain herd and parity); α is a vector of the corresponding coefficients including the intercept; x is a vector of genotypes of a marker at the locus tested; β is the effect size of the marker; u is a vector of random polygenic effects with a covariance structure as β~N (0, Vg), Vg is the polygenic additive variance; ε is a vector of residual errors with ε~N (0, IVe), I is the identity matrix, and Ve is the residual variance component.

In general, for GRAMMAR-GC, the value \( {T}^2/\widehat{\zeta} \) of each SNP with one-degree freedom is compared with \( {\chi}_1^2 \) to determine whether the locus is significantly associated with the trait. Here \( {T}_k^2={\widehat{\beta}}_k^2/\operatorname{var}\left(\widehat{\beta_k}\right) \), where \( \widehat{\beta_k} \) is the effect of the kth SNP. The deflation factor ζ is estimated as ζ = median (\( {T}_1^2,{T}_2^2,\dots, {T}_k^2 \))/0.456.

ROADTRIPS

A second GWAS approach was implemented with ROADTRIPS 2.0 [47]. An important advantage of ROADTRIPS 2.0 is that it can analyze data with pedigree information and population admixture simultaneously. Based on the genome-wide SNP data, an empirical covariance matrix was constructed to adjust for potential population admixture and relatedness among individuals and maintain the advantage of utilizing known pedigree information when available. The ROADTRIPS 2.0 test statistic based on \( {\chi}_1^2 \) distribution for each SNP takes the form:

$$ \frac{{\left({\mathbf{V}}^T\mathbf{Y}\right)}^2}{{\widehat{\sigma}}^2{\mathbf{V}}^T\widehat{\boldsymbol{\Psi}}\mathbf{V}}\sim {\chi}_1^2 $$

Here Y = (Y1, Y2, …, Yn)T, is genotype vector at a test SNP for n individuals (coded using an allelic coding). V is a vector of length n coding for phenotype information (disease status) and known relationships.\( {\widehat{\sigma}}^2\widehat{\boldsymbol{\Psi}} \) is an estimate of the null variance/covariance matrix of Y.\( {\widehat{\sigma}}^2 \) is an estimate of Var(Y) in an outbred population and\( \widehat{\boldsymbol{\Psi}} \) is an estimated matrix used to simultaneously adjust for unknown relatedness/pedigree relationship errors and population stratification.

ROADTRIPS 2.0 provides three association tests named RM test, Rχ test and RW test. According to the authors’ recommendation, the RM test is the most powerful among the three tests when pedigree information is available. Compared with the Rχ test and the RW test, the RM test can use the phenotypic information of individuals with missing genotypes provided that they have a genotyped relative at the tested marker. Considering the features of the RM test and the data structure of this study being based on a corrected pedigree, we adopted the RM test for association analysis. P values of SNPs were derived from an asymptotic chi-square distribution with 1 degree of freedom. In addition, the fixed effects used here was the same as above.

Following the suggestion of the Welcome Trust Case Control Consortium [48], two P value thresholds of 5 × 10− 7 and 5 × 10− 5 were considered as genome-wide “strong” and “moderate” association respectively.

Gene contents and functional annotation

Using BioMart in the Ensembl database (Ensembl Genes 92), genes within 1 Mb of the significant SNPs were retrieved based on the UMD 3.1 assembly. To provide insight into the functional enrichment of genes identified, we carried out GO (Gene Ontology) and Pathway analysis using KOBAS 3.0 [49]. KOBAS annotates a set of genes with putative pathways and disease relationships by mapping to genes with a known annotation. In addition, we compared the regions within 1 Mb of the significant SNPs with the reported cattle to QTLs for JD tolerance and MAP susceptibility in the Animal QTL database (http://www.animalgenome.org/cgi-bin/QTLdb/index) [50].

Results

Imputation accuracy

After imputation, we discarded SNPs with allelic R2 < 0.85 and found an average allelic R2 of 96.7% for imputed genotypes. Then we took a small subset including 100 cows genotyped by the high-density chip for calculating the imputation accuracy. Finally, the percentage of consistent genotypes was 97.03%, which suggested a high accuracy of imputation.

GWAS based on GRAMMAR-GC

With GCTA 1.24, a slight population substructure was revealed (Additional file 3: Figure S1). The inflation factor (λ), estimated to be 0.9399 (SE = 0.0002), indicates population substructure was a minor issue and that our results can be accepted for further analysis. The GC-corrected P values for the majority of SNPs corresponded well to the expected P values under the null hypothesis of no association. However, a few departures which mean the P values of these SNPs were higher than the expected P values under the null hypothesis indicated associations with the trait being studied (Additional file 4: Figure S2). As shown in Tables 1, 2 SNPs passed the strong association threshold and 13 SNPs passed the moderate threshold (Fig. 1).

Table 1 Results of GRAMMAR-GC genome-wide association analysis for susceptibility to MAP infection (df = 1)
Full size table
Table 2 Results of ROADTRIPS genome-wide association analysis for susceptibility to MAP infection (df = 1)
Full size table
Fig. 1
figure 1

Manhattan plot of genome-wide SNPs obtained using GRAMMAR-GC. Each dot represents the result from the test of association for a single SNP. Minus log10 of the P value is indicated on the y-axis and map location of the SNP is indicated on the x-axis. Thresholds represent P values of 5E-05 and 5E-07 for moderate and strong associations, respectively

Full size image

GWAS based on ROADTRIPS

RM test was implemented for the association analysis. As shown in Additional file 5: Figure S3, the P values for the majority of SNPs exhibited a good correspondence to the expected values with a limited number of SNPs indicating their associations with the studied trait. In total, 4 and 7 SNPs passed the threshold of strong and moderate association, respectively (Fig. 2, Table 2).

Fig. 2
figure 2

Manhattan plot of genome-wide SNPs obtained using ROADTRIPS. Each dot represents the result from the test of association for a single SNP. Minus log10 of the P value is indicated on the y-axis and map location of the SNP is indicated on the x-axis. Thresholds represent P values of 5E-05 and 5E-07 for moderate and strong associations, respectively

Full size image

Gene contents and functional annotation

There were 15 significant SNPs detected by GRAMMAR-GC in total. Utilizing BioMart in the Ensembl database (Ensembl Genes 92), we obtained the 232 IDs for genes located within or overlapped with the regions nearby these SNPs (< 1 Mb) (Additional file 6: Table S1). Based on the 11 significant SNPs detected by ROADTRIPS, 123 functional gene IDs were identified (Additional file 7: Table S2). After the combination of results, a total of 343 genes were obtained, including 283 protein-coding genes, 21 miRNA genes, 6 pseudogenes, 12 snRNA, 15 snoRNA, 4 rRNA and 2 miscRNA (Additional file 8: Table S3).

GO and Pathway analysis were performed by KOBAS 3.0 to determine the biological functions of the 343 genes. Finally, 348 significant GO terms were detected, including those related to immune response (P < 0.05), such as immune response-regulating signaling pathway, regulation of leukocyte proliferation and immune response-activating signal transduction. Fifteen significant pathways were found, including those related to immune responses (P < 0.05) such as autoimmune thyroid disease and enrichment of the interleukin signaling pathway (Additional file 9: Table S4). In addition, T cell receptor signaling pathway [51] and inflammatory bowel disease (IBD) were detected but not significant.

Quantitative traits locus overlapped with SNPs

Until now, 6 JD tolerance and 161 MAP susceptibility QTLs have been reported in the cattle QTL database (http://www.animalgenome.org/cgi-bin/QTLdb/BT/index). After comparing these QTLs with the regions within 1 Mb of the 26 significant SNPs, 2 QTLs identified before [30, 37] located in BTA23 (~ 32.5 Mb) for MAP susceptibility were found. This implies the functional genes, such as TDP2 (tyrosyl-DNA phosphodiesterase 2) around these SNPs are likely candidates for MAP susceptibility traits.

Discussion

There have been multiple GWASs conducted in different cattle population [29,30,31,32,33,34,35,36,37], and some candidate loci and genes have been identified. Although these studies found evidence of genomic regions associated with MAP infection, the consistency was not high. The genomic regions and genes regarded as candidates for the target traits were variable among previous studies. The difference between genomic regions identified by different studies is because of different trait definitions except for statistical methodologies [52]. There were four main definitions for infection cases in previous studies: ELISA positive [27, 31, 33], fecal culture positive [29], tissue culture positive [29] and comprehensive testing. Comprehensive testing includes tissue culture positive and fecal culture positive [29], ELISA positive or fecal positive [30], and ELISA positive or tissue culture positive [34].

We found 15 SNPs passing the threshold (5 × 10− 5) using GRAMMAR-GC with BTA23 owning the most SNPs. The most significant SNP, BovineHD2200003382 (P = 1.13E-14) was identified on BTA22 (Table 1). Similarly, 11 SNPs passed the threshold (5 × 10− 5) using ROADTRIPS with the most significant SNP, BTB-01281916 (P = 1.21E-08) identified on BTA3 (Table 2). There was no common SNP sharing between these two methods because of some possible reasons. Firstly, different computational principles can cause different significant SNPs. It is common that the discrepancy caused by this reason, such as the report of Alpay et al. [36] and Sallam et al. [37]. Both ROADTRIPS and GRAMMAR-GC can correct sample structure. The ROADTRIPS program uses the quasi-likelihood methods (implemented in the MQLS and similar statistics), to obtain known kinship coefficients, which then together with the empirical covariance matrix estimated from genomic data to correct for known and unknown relatedness and population structure [47]. Instead of pedigree, GRAMMAR-GC program uses genomic kinship matrix estimated through genomic marker data to adjust for average allele sharing or relatedness among sample individuals and thus remove genetic stratification [44, 45].

Secondly, JD is affected by multiple genetic loci and SNPs identified using different methods were polygenic in present study. Those SNPs with large effect may be captured more easily by multiple GWAS methods. In addition, the size of study population may cause discrepancy. The more individuals, the higher the accuracy of GWAS result. So it seems normal that different methods identifying different SNPs in present study. Thus, it seems normal that different methods identify different SNPs.

While no SNPs were identified by two methods, but the SNPs between the two methods were located close to each other on the same chromosome. For example on BTA2 ~ 2.74 Mb was found between BovineHD0200036516 (GRAMMAR-GC) and BovineHD0200035709 (ROADTRIPS), on BTA7 ~ 14.81 Kb was found between BovineHD0700017491 (GRAMMAR-GC) and BTA-79476-no-rs (ROADTRIPS), on BTA7 ~ 1.91 Mb was found between BovineHD0700007000 (GRAMMAR-GC) and BovineHD0700006447 (ROADTRIPS) and ~ 0.76 Mb was found between BovineHD0700006647 (GRAMMAR-GC) and BovineHD0700006447 (ROADTRIPS). Combining the results of these two methods, 26 significant SNPs were obtained. The most SNPs were found on BTA7 followed by BTA23.

Among the 26 significant SNPs detected by two methods, BovineHD0700006447 (23.5 Mb) located on BTA7 in this study was close to SNPs detected by Pant et al. (20.6 Mb ~ 22.3 Mb) [27]. Genes nearby this SNP within less than 1 Mb were IL4, IL5, IL13 and IRF1. The genes, IL4 (interleukin 4), IL5 and IL13 are type 2 cytokines, that may be the predominant cytokines produced by CD4+ and other T cells in lymph nodes during the subclinical infection of MAP [53]. As previously reported [54,55,56], in the clinical infection, the bovine MAP infection disease was characterized by a gradual shift in the immune responses from cell-mediated immune response to antibody mediated immune response while IL4, IL5 and IL13 can promote the Th2 antibody-mediated immune response. Therefore, these three genes might play important roles in the pathogenesis of the disease [27]. IRF1, interferon regulatory factor 1, plays an important role in many immune responses including the Type 1 (Th1) cell-mediated immune response. Cell mediated immunity is an important host defense mechanism against intracellular pathogens including MAP [57]. In addition, it can regulate the expression of many immune genes such as IL6, IL12B, and inducible nitric oxide synthase (NOS2) that function in the pathogenesis of human IBD [58,59,60].

The most significant SNP, BovineHD2200003382 detected by GRAMMAR-GC was located at 11.3 Mb on BTA22. Genes within 1 Mb of this location includes MyD88 (myeloid differentiation primary response gene 88) which encodes a cytosolic adapter protein that plays a central role in the innate and adaptive immune response. MyD88 functions as an essential signal transducer in the interleukin-1 and Toll-like receptor signaling pathways [61].

SNP BovineHD4100015938 on BTA23 (8.98 Mb) was close to ARS-BFGL-NGS-109956 (7.84 Mb) and ARS-BFGL-NGS-115177 (7.87 Mb) reported by Zare et al. [35]. The genes near to these two SNPs included PACSIN1 and DEF6 that are related to immune response. PACSIN1 (protein kinase C and casein kinase substrate in neurons 1), belonging to a family of cytoplasmic phosphoproteins, participates in the regulation of endocytosis [62] and regulates the TLR7/9-mediated type I interferon response in plasmacytoid dendritic cells [63]. DEF6 (DEF6, guanine nucleotide exchange factor) is a guanine nucleotide exchange factor (GEF) for RAC (MIM 602048) and CDC42 (MIM 116952) that are highly expressed in B and T cells [64]. SNP BovineHD2300009447 (32.5 Mb) located on BTA23 was very close to ARS-BFGL-NGS-1938 (32.6 Mb) reported by Zare et al. in Jersey cattle [35], and close to ss105264543 (33.6 Mb) reported by Minozzi et al. in Holstein cattle [34]. Gene within 1 Mb of this region was TDP2 (tyrosyl-DNA phosphodiesterase 2). This gene encodes a member of a superfamily of divalent cation-dependent phosphodiesterases. The encoded protein associates with CD40, tumor necrosis factor (TNF) receptor-75 and TNF receptor associated factors (TRAFs) that inhibits nuclear factor-kappa-B activation. In addition, TDP2 has sequence and structural similarities with APE1 endonuclease, which is involved in both DNA repair and the activation of transcription factors [65].

Interleukin, T cell receptor signaling pathway and inflammatory bowel disease (IBD) pathways are related to immune or inflammatory response. Two genes including ZAP70 and SRF, except for IL4, IL5, IL13 and MyD88 stated above, were involved in the immune biological processes. ZAP70 (zeta chain of T-cell receptor associated protein kinase 70) encodes an enzyme belonging to the protein tyrosine kinase family that plays a role in T-cell development and lymphocyte activation. This enzyme, phosphorylated on tyrosine residues upon T-cell antigen receptor (TCR) stimulation, functions in the initial step of TCR-mediated signal transduction in combination with the Src family kinases, Lck and Fyn and plays an essential role in the process of thymocyte development [66]. In addition, mutations in this gene cause selective T-cell defect, a severe combined immunodeficiency disease characterized by a selective absence of CD8-positive T-cells [67]. Leite et al. investigated the expression of ZAP70 in cows naturally infected with MAP and revealed that the surface expression of ZAP70 was decreased in CD4+ T cells of both subclinical and clinical animals indicating a change in T cell phenotype with disease state [68]. CSF2 (colony stimulating factor 2), also known as CSF and GMCSF, encodes a cytokine that controls the production, differentiation, and function of granulocytes and macrophages. This gene has been localized to a cluster of related genes at chromosome region 5q31 that are known to be associated with interstitial deletions in the 5q- syndrome and acute myelogenous leukemia. Other genes in the cluster include those encoding interleukins 4, 5, and 13 [69].

Furthermore, we found a region nearby the BovineHD2300009447 (BTA23, 32.5 Mb) overlapped with one QTL associated with MAP susceptibility. Combing this information with related genes found above, the 32 ~ 33 Mb region of BTA23 may be a case of a genomic region associated with MAP infection, which corresponds to the report of Zare et al. [35].

The present study focused on the potential function of 10 candidate genes. Future analysis is necessary to investigate the biological processes and molecular mechanism of these genes to anchor immune alterations and possible triggers that result in clinical paratuberculosis.

Conclusions

We performed a case-control GWAS for MAP infection in Chinese Holstein cattle using two statistical approaches, GRAMMAR-GC and ROADTRIPS. Twenty-six significant SNPs located on 15 chromosomes were detected based on data after imputation. Ten genes within less than 1 Mb of these SNPs were involved in immune response pathways, implying their potential associations with susceptibility to MAP. These genes included IL4, IL5, IL13, IRF1, MyD88, PACSIN1, DEF6, TDP2, ZAP70 and CSF2. By examining the QTLdb, the 32 ~ 33 Mb region of BTA23 may be a genomic region associated with MAP infection.

Abbreviations

GC:

Genomic control

GRAMMAR-GC:

Genome-wide Rapid Association using Mixed Model and Regression-Genomic Control

GWAS:

Genome-wide association study

JD:

Johne’s disease

MAP:

Mycobacterium avium subspecies Paratuberculosis

PCA:

Principle component analysis

QQ:

Quantile-quantile

QTL:

Quantitative trait locus

SNP:

Single nucleotide polymorphisms

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Acknowledgements

Not applicable.

Funding

This work was supported financially by the National Natural Science Foundation (31472065, 31872330), Beijing Dairy Industry Innovation Team (BAIC06-2017/2018), Beijing Science and Technology Program (D171100002417001), earmarked fund for Modern Agro-industry Technology Research System (CARS-36), and the Program for Changjiang Scholar and Innovation Research Team in University (IRT_15R62IRT_15R62). Funding bodies did not have a role in the design of the study and collection, analysis, and interpretation of data, neither in writing the manuscript.

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Authors and Affiliations

  1. Key Laboratory of Animal Genetics and Breeding of Ministry of Agriculture, National Engineering Laboratory of Animal Breeding, College of Animal Science and Technology, China Agricultural University, Beijing, 100193, China

    Yahui Gao, Jianping Jiang, Shaohua Yang, Bo Han, Yachun Wang, Yi Zhang, Ying Yu, Shengli Zhang, Qin Zhang & Dongxiao Sun

  2. College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China

    Jie Cao

  3. Department of Animal and Avian Sciences, University of Maryland, College Park, MD, 20742, USA

    Lingzhao Fang

  4. Department of Animal and Veterinary Sciences, University of Vermont, Burlington, VT, 05405, USA

    Bonnie Cantrell

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  1. Yahui Gao
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Contributions

YG performed bioinformatics and statistical analysis, and also was a major contributor to manuscript preparation. JJ, SY, JC and BH performed experiments and sample collection. YW, YZ, YY, SZ and QZ participated in result interpretation, wrote, revised and approved the manuscript. LF and BC commented the manuscript and were major contribution to manuscript revision. DS conceived and designed the experiments and wrote the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Dongxiao Sun.

Ethics declarations

Ethics approval and consent to participate

All protocols for collection of the blood and hair samples of China Holstein cows were reviewed and approved by the Institutional Animal Care and Use Committee (IACUC) at China Agricultural University. Blood and hair samples were collected specifically for this study following standard procedures with the full agreement of the Beijing Dairy Cattle Center who owned the animals.

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Not applicable.

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The authors declare that they have no competing interests.

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Additional files

Additional file 1:

MAP file of SNP data. (MAP 3577 kb)

Additional file 2:

PED file of SNP data. (PARTIAL 776 kb)

Additional file 3:

Figure S1. PCA plot based on SNP data. (TIFF 175 kb)

Additional file 4:

Figure S2. Q-Q plot based on SNP data using GRAMMAR-GC. (TIFF 175 kb)

Additional file 5:

Figure S3. Q-Q plot based on SNP data using ROADTRIPS. (TIFF 179 kb)

Additional file 6:

Table S1. The features of genes based on GRAMMAR-GC. (XLSX 20 kb)

Additional file 7:

Table S2. The features of genes based on RODATRIPS. (XLSX 15 kb)

Additional file 8:

Table S3. The features of genes based on GRAMMAR-GC and RODATRIPS. (XLSX 26 kb)

Additional file 9:

Table S4. Functional enrichment of GO and Pathway analysis of 343 genes. (XLSX 32 kb)

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Gao, Y., Jiang, J., Yang, S. et al. Genome-wide association study of Mycobacterium avium subspecies Paratuberculosis infection in Chinese Holstein. BMC Genomics 19, 972 (2018). https://doi.org/10.1186/s12864-018-5385-3

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Keywords

BMC Genomics

ISSN: 1471-2164

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