Pugh G W, Tabatabai L B
National Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Ames, Iowa 50010.
Infect Immun. 1994 Dec;62(12):5327-34. doi: 10.1128/iai.62.12.5327-5334.1994.
A study was conducted to determine whether the covalent chemical modification of Brucella abortus 19 salt-extractable proteins (BCSP) and BCSP derivatives would modulate the immune responses in BALB/c mice. Salt-extractable proteins BCSP 0-70 and BCSP 70-100 were modified with acetoacetic anhydride, and recombinant proteins rBCSP20 (20 kDa), rBCSP31 (31 kDa), and rBCSP45 (45 kDa) were modified with succinic and dodecanoyl anhydrides. Four weeks after mice were vaccinated with the different preparations, principal and control mice were challenge exposed with a virulent culture of B. abortus 2308, and mice were necropsied 2 weeks later. Serum samples were obtained immediately before mice were challenge exposed and at necropsy. Sera were tested for specific immunoglobulin M (IgM) and G (IgG) antibodies by using an enzyme-linked immunosorbent assay. Acylation decreased the immune responses (increased IgG antibodies and reduced spleen CFU and splenomegaly) induced by both BCSP 0-70 and BCSP 70-100. Modification of the recombinant proteins by dodecanoyl and succinic anhydrides had no effect on the protection induced; however, the IgG serologic responses to the homologous and heterologous proteins were altered. Monophosphoryl lipid A markedly enhanced the immunogenicity of BCSP 0-70.
开展了一项研究,以确定对流产布鲁氏菌19盐提取蛋白(BCSP)及其衍生物进行共价化学修饰是否会调节BALB/c小鼠的免疫反应。用乙酰乙酸酐修饰盐提取蛋白BCSP 0 - 70和BCSP 70 - 100,并用琥珀酸酐和十二烷酰酐修饰重组蛋白rBCSP20(20 kDa)、rBCSP31(31 kDa)和rBCSP45(45 kDa)。在用不同制剂对小鼠进行疫苗接种4周后,用流产布鲁氏菌2308的强毒株对主要组和对照组小鼠进行攻击暴露,并在2周后对小鼠进行尸检。在小鼠攻击暴露前和尸检时立即采集血清样本。通过酶联免疫吸附测定法检测血清中的特异性免疫球蛋白M(IgM)和G(IgG)抗体。酰化作用降低了BCSP 0 - 70和BCSP 70 - 100诱导的免疫反应(IgG抗体增加,脾脏菌落形成单位和脾肿大减少)。用十二烷酰酐和琥珀酸酐对重组蛋白进行修饰对诱导的保护作用没有影响;然而,对同源和异源蛋白的IgG血清学反应发生了改变。单磷酰脂质A显著增强了BCSP 0 - 70的免疫原性。