首页> 外文期刊>Vaccine >Recombinant proteins containing the hypervariable region of the haemagglutinin protect chickens against challenge with Avibacterium paragallinarum .
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Recombinant proteins containing the hypervariable region of the haemagglutinin protect chickens against challenge with Avibacterium paragallinarum .

机译:含有血凝素高变区的重组蛋白可以保护鸡免受副鸡副球菌的攻击。

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The haemagglutinin (HA) protein plays a key role in the immunogenicity and pathogenicity of Avibacterium paragallinarum, but the domain organization and antigenicity exhibited by different domains of this protein remain unknown. This study reports the presence of a hypervariable region in the HA proteins of strains of serovars A and C of A. paragallinarum. This hypervariable region is located approximately at residues 1100-1600 of the HA protein. The sequence identity found in this hypervariable region was only 18.1%, whereas those upstream and downstream of this region were 83.8 and 97.8%, respectively. Western blot analyses using antisera against the whole-cell antigens of A. paragallinarum showed that the hypervariable region was more antigenic than other regions of the HA protein. Moreover, the antigenicity of the hypervariable region was serovar-specific. Chickens immunized with recombinant proteins that contained the hypervariable region were protected (83-100% protection rate) against challenge infection with A. paragallinarum of the homologous serovar. These results suggest that recombinant proteins containing the hypervariable region may be useful antigens for use in the development of a vaccine against A. paragallinarum.Digital Object Identifier http://dx.doi.org/10.1016/j.vaccine.2010.11.040
机译:血凝素(HA)蛋白在副鸡副杆菌的免疫原性和致病性中起着关键作用,但是该蛋白的不同结构域表现出的结构域组织和抗原性仍然未知。这项研究报告了iA血清型A和C的菌株HA蛋白中存在高变区。副乳。该高变区大约位于HA蛋白的残基1100-1600处。在该高变区中发现的序列同一性仅为18.1%,而在该区域的上游和下游分别为83.8和97.8%。使用针对A全细胞抗原的抗血清进行蛋白质印迹分析。副鞭毛蛋白显示高变区的抗原性高于HA蛋白的其他区域。此外,高变区的抗原性是血清型特异性的。用含有高变区的重组蛋白免疫的鸡受到保护(83-100%的保护率),以抵抗A感染。同源血清型的副鞭毛。这些结果表明,含有高变区的重组蛋白可能是有用的抗原,用于开发抗iA疫苗。 paragallinarum .Digital Object Identifier http://dx.doi.org/10.1016/j.vaccine.2010.11.040

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