Bei Weicheng, He Qigai, Zhou Rui, Yan Lin, Huang Hongliang, Chen Huanchun
Division of Animal Pathogens, State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, PR China.
Vet Microbiol. 2007 Nov 15;125(1-2):120-7. doi: 10.1016/j.vetmic.2007.05.013. Epub 2007 May 21.
Previously, we reported the construction and characterization of a genetically defined Actinobacillus pleuropneumoniae (A. pleuropneumoniae) apxIIC gene mutant, HB04C(-), which conferred protection to mice against infection with A. pleuropneumoniae. In this study, we further evaluated HB04C(-) for safety and its ability to elicit protective immunity in pigs. It was demonstrated that a dose of 2 x 10(8) CFU HB04C(-) was safe to the pigs via intranasal or intramuscular injection. Immunization with a dose of 2 x 10(8) HB04C(-) by both intranasal and intramuscular routine could yield equal protective efficacy and elicited significant protection against experiment challenge with homologous or heterologous serotypes of a virulent A. pleuropneumonia. Taken together, HB04C(-) might serve as a promising vaccine candidate against infection with A. pleuropneumoniae.
此前,我们报道了基因定义的胸膜肺炎放线杆菌(A. pleuropneumoniae)apxIIC基因突变体HB04C(-)的构建及特性,该突变体可使小鼠免受胸膜肺炎放线杆菌感染。在本研究中,我们进一步评估了HB04C(-)在猪体内的安全性及其引发保护性免疫的能力。结果表明,2×10(8) CFU的HB04C(-)通过鼻内或肌肉注射对猪是安全的。通过鼻内和肌肉常规途径用2×10(8) HB04C(-)剂量进行免疫可产生同等的保护效力,并对同源或异源血清型的强毒胸膜肺炎放线杆菌实验攻击引发显著保护。综上所述,HB04C(-)可能是一种有前景的抗胸膜肺炎放线杆菌感染疫苗候选物。