Literature DB >> 21695551

Mannose-binding lectin 1 haplotypes influence serum MBL-A concentration, complement activity, and milk production traits in Chinese Holstein cattle.

Jianbo Liu1, Zhihua Ju, Qiuling Li, Jinming Huang, Rongling Li, Jiangbin Li, Lijuan Ma, Jifeng Zhong, Changfa Wang.   

Abstract

Mannose-binding lectin (MBL) is a member of the collectin protein family that binds a broad range of microorganisms and activates the lectin-complement pathway of innate immunity. MBL deficiency is associated with an increased risk for various infections and arises from five polymorphisms in the promoter and first exon of the MBL gene in humans. In this study, three novel single-nucleotide polymorphisms (SNPs) in the promoter region and two previously reported SNPs in exon 2 of the MBL1 gene were detected using PCR single-strand conformation polymorphism, restriction fragment length polymorphism, and DNA sequencing in 537 cattle from three Chinese breeds. Analysis of the genotypes and haplotypes was used to investigate the polymorphisms and their possible implications, especially their association with serum MBL-A levels, complement activity (CH50 and ACH50), and milk production traits was investigated. The g.2651G > A SNP in exon 2 affected the serum MBL-A concentrations and the serum CH50 values, whereas the g.-1330G > A SNP significantly affected CH50 and the somatic cell scores (SCSs). Statistical analysis revealed that cows with the ATGGC/ACAAC combined genotype and those with the AAGGT/ACGGT combined genotype exhibited the lowest and highest SCSs, respectively. Serum antibacterial activities were also conducted to verify the effect of the SNPs on resistance to mastitis pathogens. Results of real-time PCR showed that the liver of cows with clinical mastitis exhibited a higher MBL1 expression compared with healthy ones (P  <  0.05). Findings of this study indicate that the MBL1 gene possibly contributes to bacterial infection resistance and can be used as a molecular marker of milk production traits to control mastitis.

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Year:  2011        PMID: 21695551     DOI: 10.1007/s00251-011-0548-2

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  56 in total

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  6 in total

1.  Complement component 3 haplotypes influence serum complement activity and milk production traits in Chinese Holstein cattle.

Authors:  Yonghui Wang; Junyu Zhai; Chunhong Yang; Jingpeng Wang; Yan Sun; Yuhua Li; Zhihua Ju; Jingming Huang; Changfa Wang
Journal:  PLoS One       Date:  2022-06-30       Impact factor: 3.752

2.  A two-nucleotide deletion renders the mannose-binding lectin 2 (MBL2) gene nonfunctional in Danish Landrace and Duroc pigs.

Authors:  I M Bergman; K Edman; P van As; A Huisman; Helle Risdahl Juul-Madsen
Journal:  Immunogenetics       Date:  2014-01-31       Impact factor: 2.846

3.  SNPs identification and its correlation analysis with milk somatic cell score in bovine MBL1 gene.

Authors:  Zhengrong Yuan; Jiao Li; Junya Li; Xue Gao; Shangzhong Xu
Journal:  Mol Biol Rep       Date:  2012-11-01       Impact factor: 2.316

4.  Adjuvant effects of mannose-binding lectin ligands on the immune response to infectious bronchitis vaccine in chickens with high or low serum mannose-binding lectin concentrations.

Authors:  Rikke M Kjaerup; Tina S Dalgaard; Liselotte R Norup; Ingrid-Maria Bergman; Poul Sørensen; Helle R Juul-Madsen
Journal:  Immunobiology       Date:  2013-11-08       Impact factor: 3.144

5.  Transcriptomics of liver and muscle in Holstein cows genetically divergent for fertility highlight differences in nutrient partitioning and inflammation processes.

Authors:  Bruce Moran; Sean B Cummins; Christopher J Creevey; Stephen T Butler
Journal:  BMC Genomics       Date:  2016-08-11       Impact factor: 3.969

6.  Identification of polymorphisms in the bovine collagenous lectins and their association with infectious diseases in cattle.

Authors:  R S Fraser; J S Lumsden; B N Lillie
Journal:  Immunogenetics       Date:  2018-05-10       Impact factor: 2.846

  6 in total

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