Gil M T, de Souza C O, Asensi M, Buesa J
Department of Microbiology, Hospital Clinico Universitario, Facultad de Medicina, Universidad de Valencia, Spain.
Viral Immunol. 2000;13(2):187-200. doi: 10.1089/vim.2000.13.187.
The outer capsid proteins VP4 and VP7 induce neutralizing antibody against rotavirus. We have investigated in a mouse model the protection mediated by immunization with VP8*, the amino-terminal tryptic fragment of VP4. BALB/c female mice immunized with simian rotavirus SA11 VP6 and VP8* proteins expressed in Escherichia coli were mated with seronegative males. Litters were orally challenged with the SA11 strain (P5B[2], G3) or with the murine rotavirus strain EDIM (P10[16], G3) to verify the degree of protection against diarrhea induced in the newborns. Only those pups born to dams immunized with VP8* did not develop diarrhea after having been orally challenged with the SA11 strain. Pups born to naive dams but foster nursed by VP8*-immunized dams did not develop diarrhea after having been orally infected with the SA11 strain, but they suffered diarrhea when challenged with the EDIM strain. These results support the concepts that (1) VP8* is a highly immunogenic polypeptide that induces effective homotypic protection against disease in pups born to dams immunized with this antigen and (2) in newborn mice the protection against disease is mediated by neutralizing secretory antibodies present in the milk rather than by serum antibodies transferred through the placenta to the offspring.
外衣壳蛋白VP4和VP7可诱导针对轮状病毒的中和抗体。我们在小鼠模型中研究了用VP8*(VP4的氨基末端胰蛋白酶片段)免疫介导的保护作用。用在大肠杆菌中表达的猿猴轮状病毒SA11 VP6和VP8蛋白免疫的BALB/c雌性小鼠与血清阴性的雄性小鼠交配。用SA11毒株(P5B[2],G3)或鼠轮状病毒毒株EDIM(P10[16],G3)对幼崽进行口服攻击,以验证对新生儿诱导腹泻的保护程度。只有那些由用VP8免疫的母鼠所生的幼崽在用SA11毒株口服攻击后没有出现腹泻。由未免疫的母鼠所生但由用VP8免疫的母鼠哺乳的幼崽在用SA11毒株口服感染后没有出现腹泻,但在用EDIM毒株攻击时会出现腹泻。这些结果支持以下概念:(1)VP8是一种高度免疫原性的多肽,可诱导对用该抗原免疫的母鼠所生幼崽的疾病产生有效的同型保护;(2)在新生小鼠中,对疾病的保护是由乳汁中存在的中和分泌抗体介导的,而不是由通过胎盘转移给后代的血清抗体介导的。