Lin J, Hogan J S, Aslam M, Smith K L
Department of Animal Sciences, Ohio State University, Ohio Agricultural Research and Development Center, Wooster 44691, USA.
J Dairy Sci. 1998 Aug;81(8):2151-8. doi: 10.3168/jds.S0022-0302(98)75792-3.
The serum and milk immunoglobulin (Ig) G responses of lactating dairy cows were determined following immunization with ferric enterobactin receptor FepA. Escherichia coli 471 was cultured in iron-depleted medium, and outer membrane proteins were extracted by 2% N-lauroylsarcosine sodium salt and 2% Triton X-100. The FepA was isolated from the outer membrane proteins by ion-exchange chromatography. Twenty cows were assigned to four treatment groups of 5 cows blocked by breed and days in milk. Treatment groups were vaccinated with 100 micrograms of FepA, 500 micrograms of FepA, Escherichia coli J5 bacterin, or sterile phosphate-buffered saline. Primary immunization was at approximately 200 d in milk, and booster immunizations were given 14 and 28 d later. Serum and whey IgG titers to FepA in cows vaccinated with FepA were significantly higher than those from cows vaccinated with either E. coli J5 bacterin or phosphate-buffered saline. Serum and whey IgG titers to FepA were elevated by 14 d in cows vaccinated with FepA. Significant differences were not observed between doses of FepA. The degree of cross-reactivity of purified IgG from cows vaccinated with FepA to E. coli and Klebsiella pneumoniae isolates was significantly higher than that to a control isolate that lacked FepA production. Immunization with FepA elicited an immunological response in serum and milk.
在用肠杆菌素铁受体FepA免疫后,测定了泌乳奶牛的血清和乳免疫球蛋白(Ig)G反应。将大肠杆菌471在缺铁培养基中培养,并用2%月桂酰肌氨酸钠盐和2% Triton X-100提取外膜蛋白。通过离子交换色谱从外膜蛋白中分离出FepA。将20头奶牛按品种和泌乳天数分为4个处理组,每组5头。处理组分别用100微克FepA、500微克FepA、大肠杆菌J5菌苗或无菌磷酸盐缓冲盐水进行疫苗接种。初次免疫在泌乳约200天时进行,分别在14天和28天后进行加强免疫。接种FepA的奶牛血清和乳清中针对FepA的IgG滴度显著高于接种大肠杆菌J5菌苗或磷酸盐缓冲盐水的奶牛。接种FepA的奶牛血清和乳清中针对FepA的IgG滴度在14天时升高。不同剂量的FepA之间未观察到显著差异。接种FepA的奶牛纯化IgG对大肠杆菌和肺炎克雷伯菌分离株的交叉反应程度显著高于对缺乏FepA产生的对照分离株的交叉反应程度。用FepA免疫可在血清和乳汁中引发免疫反应。