Ayalew Sahlu, Confer Anthony W, Blackwood Emily R
Department of Veterinary Pathobiology, College of Veterinary Medicine, Oklahoma State University, Stillwater, OK 74078, USA.
Infect Immun. 2004 Dec;72(12):7265-74. doi: 10.1128/IAI.72.12.7265-7274.2004.
Mannheimia haemolytica serotype 1 (S1) is the most common bacterial isolate found in shipping fever pneumonia in beef cattle. Currently used vaccines against M. haemolytica do not provide complete protection against the disease. Research with M. haemolytica outer membrane proteins (OMPs) has shown that antibodies to one particular OMP from S1, PlpE, may be important in immunity. In a recently published work, members of our laboratory showed that recombinant PlpE (rPlpE) is highly immunogenic when injected subcutaneously into cattle and that the acquired immunity markedly enhanced resistance to experimental challenge (A. W. Confer, S. Ayalew, R. J. Panciera, M. Montelongo, L. C. Whitworth, and J. D. Hammer, Vaccine 21:2821-2829, 2003). The objective of this work was to identify epitopes of PlpE that are responsible for inducing the immune response. Western blot analysis of a series of rPlpE with nested deletions on both termini with bovine anti-PlpE hyperimmune sera showed that the immunodominant region is located close to the N terminus of PlpE. Fine epitope mapping, in which an array of overlapping 13-mer synthetic peptides attached to a derivatized cellulose membrane was probed with various affinity-purified anti-PlpE antibodies, identified eight highly reactive regions, of which region 2 (R2) was identified as the specific epitope. The R2 region is comprised of eight imperfect repeats of a hexapeptide (QAQNAP) and is located between residues 26 and 76. Complement-mediated bactericidal activity of affinity-purified anti-PlpE bovine antibodies confirmed that antibodies directed against the R2 region are effective in killing M. haemolytica.
溶血曼氏杆菌1型(S1)是肉牛运输热肺炎中最常见的分离细菌。目前使用的针对溶血曼氏杆菌的疫苗不能提供对该疾病的完全保护。对溶血曼氏杆菌外膜蛋白(OMPs)的研究表明,针对S1中一种特定OMP(PlpE)的抗体可能在免疫中起重要作用。在最近发表的一项工作中,我们实验室的成员表明,重组PlpE(rPlpE)皮下注射到牛体内时具有高度免疫原性,并且获得的免疫力显著增强了对实验性攻击的抵抗力(A.W.Confer、S.Ayalew、R.J.Panciera、M.Montelongo、L.C.Whitworth和J.D.Hammer,《疫苗》21:2821 - 2829,2003)。这项工作的目的是确定负责诱导免疫反应的PlpE表位。用牛抗PlpE超免疫血清对一系列在两端具有嵌套缺失的rPlpE进行蛋白质印迹分析表明,免疫显性区域位于PlpE的N端附近。精细表位定位,即用附着在衍生化纤维素膜上的一系列重叠13肽合成肽阵列与各种亲和纯化的抗PlpE抗体进行检测,确定了八个高反应性区域,其中区域2(R2)被确定为特异性表位。R2区域由六肽(QAQNAP)的八个不完全重复组成,位于第26和76位残基之间。亲和纯化的抗PlpE牛抗体的补体介导杀菌活性证实,针对R2区域的抗体在杀死溶血曼氏杆菌方面是有效的。