...
首页> 外文期刊>The Journal of Veterinary Medical Science >Construction and Characterization of an Actinobacillus pleuropneumoniae Serotype 2 Mutant Lacking the Apx Toxin Secretion Protein Genes apxIIIB and apxIIID
【24h】

Construction and Characterization of an Actinobacillus pleuropneumoniae Serotype 2 Mutant Lacking the Apx Toxin Secretion Protein Genes apxIIIB and apxIIID

机译:缺乏Apx毒素分泌蛋白基因apxIIIB和apxIIID的胸膜肺炎放线杆菌血清型2突变体的构建和鉴定

获取原文
           

摘要

References(22) Cited-By(1) Apx toxins have been identified as important virulence factors of Actinobacillus pleuropneumoniae, the etiologic agent of porcine pleuropneumonia. In some A. pleuropneumoniae serotypes, Apx toxins are secreted by the cell membrane proteins encoded by apxIIIB and apxIIID genes. In an effort to develop a live vaccine strain against A. pleuropneumoniae, we inactivated the apxIIIB and apxIIID genes in A. pleuropneumoniae 1536, a serotype 2 strain, resulting in the ΔapxIIIB/DapxIIID mutant strain (1536ΔBΔD). Immunization of pigs with live 1536ΔBΔD A. pleuropneumoniae conferred protection against homologous challenge with wild-type A. pleuropneumoniae 1536. Thus, impaired Apx toxin secretion may decrease the virulence of A. pleuropneumoniae and may be an effective strategy for the development of a live-attenuated A. pleuropneumoniae vaccine.
机译:参考文献(22)被引用的By(1)Apx毒素已被确定为猪胸膜肺炎的病原体胸膜肺炎放线杆菌的重要毒力因子。在某些胸膜肺炎链球菌血清型中,Apx毒素由apxIIIB和apxIIID基因编码的细胞膜蛋白分泌。为了开发针对胸膜肺炎链球菌的活疫苗株,我们灭活了血清型2株胸膜肺炎链球菌1536中的apxIIIB和apxIIID基因,产生了ΔapxIIIB/ DapxIIID突变株(1536ΔBΔD)。用活的1536ΔBΔD胸膜肺炎链球菌对猪进行免疫可保护其免受野生型肺炎链球菌1536的同源性攻击。因此,受损的Apx毒素分泌可能会降低胸膜肺炎链球菌的毒力,并且可能是发展活猪肺炎的有效策略。减毒肺炎链球菌疫苗。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号