Konjufca Vjollca, Wanda Soo-Young, Jenkins Mark C, Curtiss Roy
Department of Biology, Washington University, St. Louis, MO 63130, USA.
Infect Immun. 2006 Dec;74(12):6785-96. doi: 10.1128/IAI.00851-06. Epub 2006 Sep 18.
Coccidiosis is a ubiquitous disease caused by intestinal protozoan parasites belonging to several distinct species of the genus Eimeria. Cell-mediated immunity (CMI) is critically important for protection against Eimeria; thus, our approach utilizes the bacterial type III secretion system (TTSS) to deliver an antigen directly into the cell cytoplasm of the immunized host and into the major histocompatibility complex class I antigen-processing pathway for induction of CMI and antigen-specific cytotoxic T-lymphocyte responses in particular. To accomplish this goal, Eimeria genes encoding the sporozoite antigen EASZ240 and the merozoite antigen EAMZ250 were fused to the Salmonella enterica serovar Typhimurium effector protein gene sptP in the parental pYA3653 vector, yielding pYA3657 and pYA3658, respectively. SptP protein is secreted by the TTSS of Salmonella and translocated into the cytoplasm of immunized host cells. The host strain chromosomal copy of the sptP gene was deleted and replaced by a reporter gene, xylE. The newly constructed vectors pYA3657 and pYA3658 were introduced into host strain chi8879 (DeltaphoP233 DeltasptP1033::xylEDelta asdA16). This strain is an attenuated derivative of the highly virulent strain UK-1. When strain chi8879(pYA3653) as the vector control and strain chi8879 harboring pYA3657 or pYA3658 were used to orally immunize day-of-hatch chicks, colonization of the bursa, spleen, and liver was observed, with peak titers 6 to 9 days postimmunization. In vitro experiments show that the EASZ240 antigen is secreted into the culture supernatant via the TTSS and that it is delivered into the cytoplasm of Int-407 cells by the TTSS. In vivo experiments indicate that both humoral and cell-mediated immune responses are induced in chickens vaccinated with a recombinant attenuated Salmonella serovar Typhimurium vaccine, which leads to significant protection against Eimeria challenge.
球虫病是一种由艾美耳属几个不同物种的肠道原生动物寄生虫引起的普遍疾病。细胞介导的免疫(CMI)对于抵抗艾美耳属寄生虫至关重要;因此,我们的方法利用细菌III型分泌系统(TTSS)将抗原直接递送至免疫宿主的细胞质中,并进入主要组织相容性复合体I类抗原加工途径,以诱导CMI,特别是抗原特异性细胞毒性T淋巴细胞反应。为实现这一目标,将编码子孢子抗原EASZ240和裂殖子抗原EAMZ250的艾美耳属基因与亲本pYA3653载体中的鼠伤寒沙门氏菌效应蛋白基因sptP融合,分别产生pYA3657和pYA3658。SptP蛋白由沙门氏菌的TTSS分泌并转运至免疫宿主细胞的细胞质中。宿主菌株染色体拷贝的sptP基因被删除,并用报告基因xylE取代。将新构建的载体pYA3657和pYA3658导入宿主菌株chi8879(DeltaphoP233 DeltasptP1033::xylEDelta asdA16)。该菌株是高毒力菌株UK-1的减毒衍生物。当使用chi8879(pYA3653)菌株作为载体对照以及携带pYA3657或pYA3658的chi8879菌株对出壳当天的雏鸡进行口服免疫时,观察到法氏囊、脾脏和肝脏的定植情况,免疫后6至9天达到滴度峰值。体外实验表明,EASZ240抗原通过TTSS分泌到培养上清液中,并通过TTSS递送至Int-407细胞的细胞质中。体内实验表明,用重组减毒鼠伤寒沙门氏菌疫苗接种的鸡会诱导体液免疫和细胞介导的免疫反应,从而对球虫病攻击产生显著保护作用。