首页> 美国卫生研究院文献>Infection and Immunity >A Recombinant Attenuated Salmonella enterica Serovar Typhimurium Vaccine Encoding Eimeria acervulina Antigen Offers Protection against E. acervulina Challenge
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A Recombinant Attenuated Salmonella enterica Serovar Typhimurium Vaccine Encoding Eimeria acervulina Antigen Offers Protection against E. acervulina Challenge

机译:编码小肠艾美球菌抗原的重组减毒小肠沙门氏菌鼠伤寒沙门氏菌疫苗可抵抗小肠埃希菌

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摘要

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 χ8879 (ΔphoP233 ΔsptP1033::xylEΔ asdA16). This strain is an attenuated derivative of the highly virulent strain UK-1. When strain χ8879(pYA3653) as the vector control and strain χ8879 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.
机译:球虫病是一种普遍存在的疾病,由属于艾美球虫属几个不同物种的肠道原生动物寄生虫引起。细胞介导的免疫(CMI)对于防御艾美尔球虫至关重要。因此,我们的方法利用细菌III型分泌系统(TTSS)将抗原直接传递到免疫宿主的细胞质中,并传递到主要的组织相容性复合体I类抗原加工途径中,以诱导CMI和抗原特异性细胞毒性T-特别是淋巴细胞反应。为了实现该目标,将编码子孢子抗原EASZ240和裂殖子抗原EAMZ250的艾美耳球虫基因与亲代pYA3653载体中的肠炎沙门氏菌血清鼠伤寒效应蛋白基因sptP融合,分别得到pYA3657和pYA3658。 SptP蛋白由沙门氏菌的TTSS分泌,并转移到免疫宿主细胞的细胞质中。 sptP基因的宿主菌株染色体拷贝被删除,并被报告基因xylE取代。将新构建的载体pYA3657和pYA3658引入宿主菌株χ8879(ΔphoP233ΔsptP1033::xylEΔasdA16)。该菌株是高毒力菌株UK-1的减毒衍生物。当使用χ8879(pYA3653)菌株作为载体对照和携带pYA3657或pYA3658的χ8879菌株对孵化日雏鸡进行口服免疫时,观察到了法氏囊,脾脏和肝脏的定殖,免疫后6到9天达到了最高滴度。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传递到Int-407细胞的细胞质中。体内实验表明,在用重组减毒沙门氏菌鼠伤寒沙门氏菌疫苗接种的鸡中,可诱导体液和细胞介导的免疫反应,从而对艾美球虫攻击具有显着的保护作用。

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