Vandemaele Fréderic, Ververken Cedric, Bleyen Nele, Geys Jorina, D'Hulst Charlotte, Addwebi Tarek, van Empel Paul, Goddeeris Bruno Maria
Laboratory of Physiology and Immunology of Domestic Animals, Faculty of Applied Bioscience and Engineering, Catholic University Leuven, Kasteelpark Arenberg 30, 3001, Leuven, Belgium.
Avian Pathol. 2005 Jun;34(3):264-72. doi: 10.1080/03079450500112682.
The aim of this study was to investigate whether vaccination with the sugar-binding domain of FimH (FimH156) was able to protect chickens against avian pathogenic Escherichia coli (APEC). FimH156 was expressed and purified using Ni-NTA affinity chromatography. Binding of FimH156 to mannosylated bovine serum albumin demonstrated that the protein retained its biological activity. Moreover, anti-FimH156 antisera were able to inhibit in vitro binding of E. coli to mannosylated bovine serum albumin. In a first vaccination experiment, FimH156 was administered intramuscularly as a water-in-oil emulsion to specific pathogen free broiler chicks. A predisposing infection with the Newcastle disease virus strain Lasota was administered 3 weeks later, followed 3 days later by an aerosol challenge with the virulent APEC strain CH2. A good anti-FimH156 immunoglobulin (Ig)G immune response was detected in serum, but no protective effects of FimH156 against APEC were seen. In a second experiment, SPF chicks were vaccinated intramuscularly or intranasally with FimH156. Booster vaccinations were administered 20 days later. While the intramuscular immunization yielded a strong IgG response in the serum and trachea, no significant IgA response could be detected in tracheal washes. Intranasal immunization did not yield a significant IgG or IgA response in serum and trachea. No protective effects of the FimH156 could be detected, confirming the results of the first experiment. Thus, although the FimH156 induced a strong immune response, it was unable to protect chickens against APEC.
本研究的目的是调查用FimH的糖结合结构域(FimH156)进行疫苗接种是否能够保护鸡抵御禽致病性大肠杆菌(APEC)。使用镍-亚氨基二乙酸(Ni-NTA)亲和层析法表达并纯化了FimH156。FimH156与甘露糖基化牛血清白蛋白的结合表明该蛋白保留了其生物学活性。此外,抗FimH156抗血清能够在体外抑制大肠杆菌与甘露糖基化牛血清白蛋白的结合。在首次疫苗接种实验中,将FimH156作为油包水乳液肌内注射给无特定病原体的肉鸡雏鸡。3周后对其进行新城疫病毒Lasota株的诱发感染,3天后再用强毒APEC菌株CH2进行气溶胶攻击。在血清中检测到了良好的抗FimH156免疫球蛋白(Ig)G免疫反应,但未观察到FimH156对APEC的保护作用。在第二个实验中,用FimH156对无特定病原体(SPF)雏鸡进行肌内或鼻内接种。20天后进行加强免疫。虽然肌内免疫在血清和气管中产生了强烈的IgG反应,但在气管冲洗液中未检测到明显的IgA反应。鼻内免疫在血清和气管中未产生明显的IgG或IgA反应。未检测到FimH156的保护作用,证实了第一个实验的结果。因此,尽管FimH156诱导了强烈的免疫反应,但它无法保护鸡抵御APEC。