金黄色葡萄球菌黏附素ClfA等抗体抑制该菌黏附牛乳腺上皮细胞效果的比较
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  • 英文篇名:Adhesive inhibition comparison of Staphylococcus aureus to bovine mammary epithelial cells by antibodies against 3 different adhesins
  • 作者:马鹏睿 ; 王彩蝶 ; 张宝江 ; 苏艳
  • 英文作者:Pengrui Ma;Caidie Wang;Baojiang Zhang;Yan Su;College of Veterinary Medicine, Xinjiang Agricultural University;
  • 关键词:金黄色葡萄球菌 ; 黏附素分子 ; 抗体 ; 牛乳腺上皮细胞 ; 黏附抑制
  • 英文关键词:Staphylococcus aureus;;adhesin;;antibody;;bovine mammary epithelial cell;;adhesion inhibition
  • 中文刊名:WSXB
  • 英文刊名:Acta Microbiologica Sinica
  • 机构:新疆农业大学动物医学学院;
  • 出版日期:2017-07-10 14:22
  • 出版单位:微生物学报
  • 年:2018
  • 期:v.58;No.334
  • 基金:乌鲁木齐市科技局科技应用项目(Y141210011);; 新疆维吾尔自治区科技人才培养项目(qn2015yx013);; 国家自然科学基金(31260222)~~
  • 语种:中文;
  • 页:WSXB201802012
  • 页数:10
  • CN:02
  • ISSN:11-1995/Q
  • 分类号:109-118
摘要
【目的】为从免疫的角度比较和分析黏附素分子细胞外纤维蛋白原结合蛋白(Extracellular fibrinogen-binding protein,EfB)和纤维连接蛋白结合蛋A(Fibronection binding protein,FnBP)对聚集因子A(Clumping factor A,ClfA)抑制牛源金黄色葡萄球菌(Staphylococcus aureus,SA)黏附牛乳腺原代上皮细胞作用的增强效果。【方法】本试验分离培养牛乳腺上皮细胞并鉴定;将真核重组质粒EfB和FnBPA分别与ClfA组合免疫新西兰大白兔,并利用免疫后抗体体外抑制2株SA分离株侵染牛乳腺上皮细胞,采用平板计数法定量检测与比较不同免疫组合诱导抗体对黏附的抑制作用;对SA和乳腺上皮细胞分别进行荧光染色,观察不同免疫组合诱导的抗体对黏附抑制效果的差异。【结果】成功分离培养了牛乳腺原代上皮细胞;证明了构建的ClfA、FnBPA和EfB真核重组表达质粒均可在细胞中表达,且在免疫实验兔后可诱导特异性抗体的产生;细菌平板计数和荧光染色观察的结果表明,黏附素分子单独和组合免疫的抗体对该菌不同菌株(GY278和GY309)的黏附抑制能力不同,ClfA抗体的黏附抑制能力最强,FnBPA分子A区的黏附抑制能力优于D区。FnBPA、EfB分别与ClfA联合免疫抗体对黏附的抑制程度高于黏附素分子单独免疫组,FnBPA分子A区对ClfA黏附抑制的增强作用优于D区,FnBPA-A区与Efb相比对ClfA的黏附抑制增强差异不显著。【结论】FnBPA-A、FnBPA-D和EfB分别与ClfA联合免疫可不同程度地影响ClfA的黏附抑制效果,该结果为以黏附素分子为靶点的牛乳腺炎疫苗的研究提供了实验数据。
        [Objective] To compare the inhibition effects of antibodies against extracellular fibrinogen-binding protein(Ef B) and fibronection binding protein(FnBPA) to clumping factor A(ClfA) of Staphylococcus aureus(SA) to bovine mammary epithelial cells(b MEC) by immunization method. [Methods] The antibodies were obtained by immunizing rabbits with the recombinant plasmids Efb or FnBPA in-combination with ClfA. The antibodies inhibition effects on adereing of 2 SA strains to bMEC were tested using plate counting method and observed by fluorescent staining of SA and bMEC, respectively. [Results] Our results indicated that the antibodies had different inhibition effects on adhesion of SA(GY278 and GY309). ClfA antibody showed the highest inhibition ability. FnBPA-A showed greater inhibition enhancement to ClfA than FnBPA-D. [Conclusion] The in-combination immunization of FnBPA-A, FnBPA-D and EfB with ClfA could affect the antibodies inhibition to various degrees and this result provided experiment basis for the development of bovine mastitis vaccine.
引文
[1]De Vliegher S,Fox LK,Piepers S,Mc Dougall S,Barkema HW.Invited review:Mastitis in dairy heifers:nature of the disease,potential impact,prevention,and control.Journal of Dairy Science,2012,95(3):1025–1040.
    [2]Zhou H,Xiong ZY,Li HP,Zheng YL,Jiang YQ.An immunogenicity study of a newly fusion protein Cna-Fn BP vaccinated against Staphylococcus aureus infections in a mice model.Vaccine,2006,24(22):4830–4837.
    [3]Patti JM,Allen BL,Mc Gavin MJ,H??k M.MSCRAMM-mediated adherence of microorganisms to host tissues.Annual Review of Microbiology,1994,48:585–617.
    [4]Josefsson E,Hartford O,O’Brien L,Patti JM,Foster T.Protection against Experimental Staphylococcus aureus arthritis by vaccination with clumping factor A,a novel virulence determinant.The Journal of Infectious Diseases,2001,184(12):1572–1580.
    [5]Zhang X,Gao YP,Dong J,Liu Y,Wu N,Shao NS,Yang G.Expression,purification of Staphylococcus aureus Efb protein and preparation of its functional antibody.Bulletin of the Academy of Military Medical Sciences,2009,33(6):531–534.(in Chinese)张鑫,高亚萍,董洁,刘玉,吴娜,邵宁生,杨光.金黄色葡萄球菌Efb蛋白的表达、纯化及功能抗体的制备.军事医学科学院院刊,2009,33(6):531–534.
    [6]Mc Devitt D,Francois P,Vaudaux P,Foster TJ.Molecular characterization of the clumping factor(fibrinogen receptor)of Staphylococcus aureus.Molecular Microbiology,1994,11(2):237–248.
    [7]Hettinga KA,van Valenberg HJF,Lam TJGM,van Hooijdonk ACM.Detection of mastitis pathogens by analysis of volatile bacterial metabolites.Journal of Dairy Science,2008,91(10):3834–3839.
    [8]Shao JG,Zhang BJ,Li SC,Wang CD,Wang GQ,Su Y.Comparison and analysis of the biological activity of antiserum after immunizing with expressed different domains of Staphylococus aureus adhesin Fn BPA isolated from bovine milk.Acta Veterinaria et Zootechnica Sinica,2015,46(7):1208–1214.(in Chinese)邵俊高,张宝江,李善春,王彩蝶,王国勤,苏艳.牛乳源金黄色葡萄球菌黏附素分子Fn BPA不同功能区生物学活性的比较分析.畜牧兽医学报,2015,46(7):1208–1214.
    [9]Wang SM,Su Y.Bioinformatic analysis on Staphylococcus aureus fibronectin-binding protein A(Fn BPA)signal peptide and its eukaryotic secret expression.Journal of Xinjiang Agricultural University,2012,35(3):212–216.(in Chinese)王世民,苏艳.金黄色葡萄球菌纤连结合蛋白信号肽的生物信息学分析及其真核分泌表达.新疆农业大学学报,2012,35(3):212–216.
    [10]Hammel M,Sfyroera G,Ricklin D,Magotti P,Lambris JD,Geisbrecht BV.A structural basis for complement inhibition by Staphylococcus aureus.Nature Immunology,2007,8(4):430–437.
    [11]Lee LYL,Liang XW,H??k M,Brown EL.Identification and characterization of the C3 binding domain of the Staphylococcus aureus extracellular fibrinogen-binding protein(Efb).Journal of Biological Chemistry,2004,279(49):50710–50716.
    [12]Garcia BL,Ramyar KX,Ricklin D,Lambris JD,Geisbrecht BV.Advances in understanding the structure,function,and mechanism of the SCIN and Efb families of Staphylococcal immune evasion proteins//Lambris JD,Hajishengallis G.Current Topics in Innate Immunity II.New York:Springer,2012:113–133.
    [13]Chen Z,Liu SN,Mou K,Cao BL,Zhao HK.Prokaryotic expression of Staphylococcus aureus Clf A and assay for its antisera bioactivity.Chinese Veterinary Science,2010,30(1):29–31,46.(in Chinese)陈智,刘少宁,牟凯,曹丙蕾,赵宏坤.金黄色葡萄球菌聚集因子A蛋白的原核表达及抗血清活性分析.中国兽医学报,2010,30(1):29–31,46.
    [14]Castagliuolo I,Piccinini R,Beggiao E,PalùG,Mengoli C,Ditadi F,Vicenzoni G,Zecconi A.Mucosal genetic immunization against four adhesins protects against Staphylococcus aureus-induced mastitis in mice.Vaccine,2006,24(20):4393–4402.
    [15]Cui XJ,Hu QL,Li YP,Tao L,Xiu L,Liu BC,Chen Y,Wang X.The apoptosis of bovine primary mammary epithelial cells induced by Staphylococcus aureus.Scientia Agricultura Sinaca,2013,46(15):3212–3219.(in Chinese)崔新洁,胡庆亮,李奕平,陶琳,修磊,刘秉春,陈媛,王潇.金黄色葡萄球菌诱导牛原代乳腺上皮细胞的凋亡.中国农业科学,2013,46(15):3212–3219.
    [16]Bouchard DS,Rault L,Berkova N,Le Loir Y,Even S.Inhibition of Staphylococcus aureus invasion into bovine mammary epithelial cells by contact with live Lactobacillus casei.Applied and Environmental Microbiology,2013,79(3):877–885.
    [17]Jiang XJ,Hao YQ,Zhang AR,Fan X,Chen XJ.Cloning and expression of the region A of clumping factor A gene of Staphylococcus aureus and its immunological characteristics.Chinese Veterinary Science,2009,39(7):626–631.(in Chinese)姜晓娟,郝永清,张爱荣,范鑫,陈晓杰.金黄色葡萄球菌凝聚因子A区基因的克隆表达及表达产物的免疫学特性.中国兽医科学,2009,39(7):626–631.
    [18]Li X,Wang X G,Thompson CD,Park S,Park WB,Lee JC.Preclinical efficacy of clumping factor A in prevention of Staphylococcus aureus infection.m Bio,2016,7(1):e02232-15.
    [19]Delfani S,Imani Fooladi AA,Mobarez AM,Emaneini M,Amani J,Sedighian H.In silico analysis for identifying potential vaccine candidates against Staphylococcus aureus.Clinical and Experimental Vaccine Research,2015,4(1):99–106.
    [20]Hall AE,Domanski PJ,Patel PR,Vernachio JH,Syribeys PJ,Gorovits EL,Johnson MA,Ross JM,Hutchins JT,Patti JM.Characterization of a protective monoclonal antibody recognizingStaphylococcus aureus MSCRAMM protein clumping factor A.Infection and Immunity,2003,71(12):6864–6870.
    [21]Liu YT,Su Y,Zhang BJ,Su LL,Jiang HJ.Immunological comparison of Efb and Clf A of Staphylococcus aureus isolated from bovine.Chinese Journal of Biotechnology,2015,31(9):1335–1343.(in Chinese)刘云涛,苏艳,张宝江,苏玲玲,姜慧娇.牛源金黄色葡萄球菌粘附因子Efb与Clf A的免疫生物学特性比较.生物工程学报,2015,31(9):1335–1343.
    [22]Jiang HJ,Su Y,Shen Y.Characterization of antiserum after co-immunized with adhesins expressing Clf A,Fn BPA-A and Fn BPA-BCD of Staphylococus aureus.Acta Microbiologica Sinica,2015,55(10):1343–1349.(in Chinese)姜慧娇,苏艳,申煜.金黄色葡萄球菌黏附素Clf A,Fn BPA-A,Fn BPA-BCD联合免疫的免疫生物学特性.微生物学报,2015,55(10):1343–1349.
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