首页> 美国卫生研究院文献>Infection and Immunity >Vaccination and Protection of Pigs against Pleuropneumonia with a Vaccine Strain of Actinobacillus pleuropneumoniae Produced by Site-Specific Mutagenesis of the ApxII Operon
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Vaccination and Protection of Pigs against Pleuropneumonia with a Vaccine Strain of Actinobacillus pleuropneumoniae Produced by Site-Specific Mutagenesis of the ApxII Operon

机译:用ApxII操纵子的位点特异性诱变产生的胸膜肺炎放线杆菌疫苗株对猪进行胸膜肺炎的疫苗接种和保护。

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摘要

The production of toxin (Apx)-neutralizing antibodies during infection plays a major role in the induction of protective immunity to Actinobacillus pleuropneumoniae reinfection. In the present study, the gene encoding the ApxII-activating protein, apxIIC, was insertionally inactivated on the chromosome of a serovar 7 strain, HS93. Expression of the structural toxin, ApxIIA, and of the two genes required for its secretion, apxIB and apxID, still occurs in this strain. The resulting mutant strain, HS93C Ampr, was found to secrete the unactivated toxin. Pigs vaccinated with live HS93C Ampr via the intranasal route were protected against a cross-serovar challenge with a virulent serovar 1 strain of A. pleuropneumoniae. This is the first reported vaccine strain of A. pleuropneumoniae which can be delivered live to pigs and offers cross-serovar protection against porcine pleuropneumonia.
机译:感染期间产生毒素(Apx)的中和抗体在诱导对胸膜肺炎放线杆菌再感染的保护性免疫中起主要作用。在本研究中,编码ApxII激活蛋白apxIIC的基因在血清型7株HS93的染色体上被插入失活。在该菌株中仍然发生结构毒素ApxIIA以及其分泌所需的两个基因apxIB和apxID的表达。发现所得突变株HS93C - Amp r 分泌了未激活的毒素。经鼻内途径接种活HS93C - Amp r 的猪用胸膜肺炎链球菌强毒血清型1株保护免受交叉血清攻击。这是首例报道的胸膜肺炎链球菌疫苗株,可活体递送给猪,并提供针对猪胸膜肺炎的跨血清保护。

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