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首页> 外文期刊>Veterinary Microbiology >Sequence diversity of the immunogenic outer membrane lipoprotein PlpE from Mannheimia haemolytica serotypes 1, 2, and 6.
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Sequence diversity of the immunogenic outer membrane lipoprotein PlpE from Mannheimia haemolytica serotypes 1, 2, and 6.

机译:溶血曼海姆氏菌血清型1、2和6的免疫原性外膜脂蛋白PlpE的序列多样性。

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Mannheimia haemolytica serotype 1 (S1), S6 and S2 are the most common bacterial isolates 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. Recombinant PlpE (rPlpE) is highly immunogenic in cattle, and the acquired immunity markedly enhanced resistance to experimental challenge. We previously demonstrated that the immunodominant epitope (R2) is located between residues 26 and 76 on the N-terminus of PlpE from a reference S1 strain (Ayalew et al., 2004). This region consists of eight hexapeptide repeats. The potential of this epitope as a vaccine or supplement to commercial vaccines is dependant on its state of conservation amongst isolates of the three serotypes. To determine this, we sequenced plpE genes from 32 isolates. The sequences from S1 and S6 were identical with one exception. Substantial variation was observed among sequences from S2 strains, particularly in the R2 region of the protein. These variations in S2 isolates range from 3 to 28 hexapeptide repeats. Calculated molecular weight of PlpE from S1 and S6 isolates was 37 kDa, where as PlpE from S2 strains ranged from 30 to 50 kDa. These similarities and differences were demonstrated by western blot. Competitive binding assay was used to determine that antibody against rPlpE from S1 binds native PlpE on surfaces of both S1 and S2 cells..
机译:溶血性曼尼海姆氏菌血清型1(S1),S6和S2是肉牛在运送发烧性肺炎中发现的最常见细菌分离株。当前使用的针对溶血支原体的疫苗不能提供针对该疾病的完全保护。对溶血支原体外膜蛋白(OMP)的研究表明,针对S1的一种特定OMP的抗体PlpE在免疫中可能很重要。重组PlpE(rPlpE)在牛中具有高度免疫原性,并且获得的免疫力显着增强了对实验挑战的抵抗力。我们先前证明,免疫优势抗原决定簇(R2)位于参考S1菌株PlpE N末端的第26和第76位残基之间(Ayalew等,2004)。该区域由八个六肽重复序列组成。该表位作为疫苗或商业疫苗补充剂的潜力取决于其在三种血清型分离株中的保存状态。为了确定这一点,我们对32个分离株的plpE基因进行了测序。来自S1和S6的序列相同,但有一个例外。在来自S2菌株的序列之间,尤其是在蛋白质的R2区域中,观察到了很大的差异。 S2分离物中的这些变异范围为3到28个六肽重复序列。 S1和S6分离株的PlpE的计算分子量为37 kDa,而S2菌株的PlpE的分子量为30至50 kDa。这些相似性和差异通过蛋白质印迹证明。竞争性结合测定法用于确定来自S1的rPlpE抗体与S1和S2细胞表面上的天然PlpE结合。

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