Yap G S, Scharton-Kersten T, Ferguson D J, Howe D, Suzuki Y, Sher A
Immunobiology Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Infect Immun. 1998 Sep;66(9):4382-8. doi: 10.1128/IAI.66.9.4382-4388.1998.
The virulent RH strain of Toxoplasma gondii is acutely lethal in mice and fails to establish chronic infection. Vaccination of BALB/c mice with a soluble tachyzoite antigen preparation, STAg, in combination with the immunostimulatory cytokine interleukin-12 results in partial protection against RH lethal challenge. Nevertheless, brain tissue obtained from surviving, vaccinated mice as late as 1 year after RH infection contained latent parasite forms as demonstrated by subinoculation into naive recipients. The tachyzoites arising in the subinoculated animals were genetically indistinguishable from the original RH inoculum. Microscopic examination revealed that the persistent parasite forms present in the brains of vaccinated and challenged mice have a tissue cyst-like morphology and express the bradyzoite antigen BAG-1 but not the tachyzoite-specific antigen SAG-2 but are different from the cysts formed by avirulent T. gondii strains in that the internal parasite stages display ultrastructural features intermediate between tachyzoites and bradyzoites. Moreover, the zoites within the RH tissue cysts are clearly distinct from conventional bradyzoites in their sensitivity to pepsin-HCl digestion. In contrast to the observations made with partially resistant STAg/interleukin-12-vaccinated animals, no latent forms could be detected in brain tissue after RH challenge of mice immunized with a live attenuated tachyzoite vaccine which confers total protection against this parasite isolate. The above findings demonstrate the potential of a virulent T. gondii strain to generate latent parasite stages, a process which may be promoted under conditions of incomplete vaccination.
刚地弓形虫的强毒株RH对小鼠具有急性致死性,无法建立慢性感染。用可溶性速殖子抗原制剂STAg与免疫刺激细胞因子白细胞介素-12联合接种BALB/c小鼠,可提供部分保护以抵抗RH致死性攻击。然而,在RH感染后长达1年从存活的接种疫苗小鼠获得的脑组织中,通过接种到未感染的受体动物中证实含有潜伏的寄生虫形式。在接种动物中产生的速殖子在基因上与原始的RH接种物无法区分。显微镜检查显示,接种疫苗并受到攻击的小鼠大脑中存在的持续寄生虫形式具有组织囊肿样形态,表达缓殖子抗原BAG-1但不表达速殖子特异性抗原SAG-2,但与无毒力的刚地弓形虫菌株形成的囊肿不同,因为内部寄生虫阶段显示出介于速殖子和缓殖子之间的超微结构特征。此外,RH组织囊肿内的虫体对胃蛋白酶-HCl消化的敏感性与传统缓殖子明显不同。与用部分抗性的STAg/白细胞介素-12接种动物的观察结果相反,在用活的减毒速殖子疫苗免疫的小鼠受到RH攻击后,在脑组织中未检测到潜伏形式,该疫苗可提供针对这种寄生虫分离株的完全保护。上述发现证明了强毒株刚地弓形虫产生潜伏寄生虫阶段的潜力,这一过程在不完全接种的条件下可能会被促进。