Boccardo G, Milne R G
J Virol Methods. 1981 Sep;3(2):109-13. doi: 10.1016/0166-0934(81)90007-0.
Injection into rabbits of native or glutaraldehyde (GA)-treated intact particles of the fijivirus maize rough dwarf virus (MRDV) failed to yield antibodies to the outer shell of the virus. After fixation of the particles with the cross-linking reagent dithiobis(succinimidyl)propionate (DSP), antisera were obtained reacting with the outer shell of MRDV (both DSP-fixed and unfixed) to a titre of 1/1024 in immunoelectron microscopic decoration tests, but giving no reaction with another fijivirus, oat sterile dwarf virus, whose subviral particles are known to be unrelated to those of MRDV. Further fixation of the DSP-fixed particles with GA did not appear to enhance immunogenicity. Stabilization with DSP could have further application with viruses the instability of which renders them poor immunogens.
将天然的或经戊二醛(GA)处理的斐济病毒玉米粗缩病毒(MRDV)完整颗粒注射到兔子体内,未能产生针对该病毒外壳的抗体。在用交联剂二硫代双(琥珀酰亚胺基)丙酸酯(DSP)固定颗粒后,获得了抗血清,该抗血清在免疫电子显微镜装饰试验中与MRDV的外壳(包括DSP固定的和未固定的)反应,效价达到1/1024,但与另一种斐济病毒燕麦不育矮化病毒没有反应,已知该病毒的亚病毒颗粒与MRDV的亚病毒颗粒无关。用GA对DSP固定的颗粒进行进一步固定似乎并没有增强免疫原性。用DSP进行稳定化处理可能对那些因不稳定而成为不良免疫原的病毒有进一步的应用价值。