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通过免疫印迹法对溶血巴斯德氏菌A和T生物型中铁调节蛋白进行抗原分析,揭示了生物型特异性表位。

Antigenic analysis of iron-regulated proteins in Pasteurella haemolytica A and T biotypes by immunoblotting reveals biotype-specific epitopes.

作者信息

Murray J E, Davies R C, Lainson F A, Wilson C F, Donachie W

机构信息

Moredum Research Institute, Edinburgh, UK.

出版信息

J Gen Microbiol. 1992 Feb;138(2):283-8. doi: 10.1099/00221287-138-2-283.

DOI:10.1099/00221287-138-2-283
PMID:1373434
Abstract

The antigenic relationships of the iron-regulated proteins (IRPs) in Pasteurella haemolytica A and T biotype strains were examined by SDS-PAGE and immunoblotting. P. haemolytica cells of the A biotype, grown under conditions of iron-limitation, expressed two IRPs, of 35 and 70 kDa. All T biotype strains expressed IRPs with slightly different molecular masses of 37 and 78 kDa. Immunoblotting of all 16 P. haemolytica serotypes was carried out using a panel of polyclonal and monoclonal antibodies raised against serotype A2 antigens. Polyclonal antibodies revealed inter-serotype cross-reactivity towards the 35 and 70 kDa IRPs within the A biotype but no cross-reactivity against a T biotype protein in the 78 kDa region. Monoclonal antibody against the 35 kDa antigen reacted only with the A biotype 35 kDa IRP. Identical profiles were obtained for 10 field isolates of serotype A2, further emphasizing the antigen conservation within the A biotype. These findings reinforce the view that the A and T biotypes of P. haemolytica should be considered as separate species and suggest that IRPs from single A and T biotype strains incorporated into a vaccine might provide cross-protection against all P. haemolytica serotypable strains. Similar studies on the IRPs of 10 untypable strains revealed some of these to have different antigenic reactivities from those observed within the A and T biotypes.

摘要

通过SDS - PAGE和免疫印迹法检测了溶血巴斯德菌A和T生物型菌株中铁调节蛋白(IRPs)的抗原关系。在铁限制条件下生长的A生物型溶血巴斯德菌细胞表达了两种IRPs,分子量分别为35 kDa和70 kDa。所有T生物型菌株表达的IRPs分子量略有不同,为37 kDa和78 kDa。使用一组针对A2血清型抗原产生的多克隆和单克隆抗体对所有16种溶血巴斯德菌血清型进行了免疫印迹分析。多克隆抗体显示A生物型内不同血清型之间对35 kDa和70 kDa的IRPs存在交叉反应,但对78 kDa区域的T生物型蛋白无交叉反应。针对35 kDa抗原的单克隆抗体仅与A生物型的35 kDa IRP发生反应。10株A2血清型田间分离株获得了相同的图谱,进一步强调了A生物型内的抗原保守性。这些发现强化了溶血巴斯德菌的A和T生物型应被视为不同物种的观点,并表明将单一A和T生物型菌株的IRPs纳入疫苗可能为所有可分型的溶血巴斯德菌菌株提供交叉保护。对10株不可分型菌株的IRPs进行的类似研究表明,其中一些菌株的抗原反应性与A和T生物型中观察到的不同。

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