福氏志贺氏菌2a和3a o型抗原在沙门氏菌口服活疫苗Ty21a中的稳定染色体表达

Q2 Biochemistry, Genetics and Molecular Biology
Clinical and Vaccine Immunology Pub Date : 2017-12-05 Print Date: 2017-12-01 DOI:10.1128/CVI.00181-17
Madushini N Dharmasena, Manuel Osorio, Kazuyo Takeda, Scott Stibitz, Dennis J Kopecko
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引用次数: 16

摘要

我们一直在探索使用减毒伤寒沙门氏菌血清型Ty21a活疫苗株作为多种外源抗原(包括志贺氏菌o型抗原)的表达和递送的多功能口服疫苗载体。在这项研究中,我们分别克隆了生物合成福氏志贺氏菌血清型2a和3a o抗原所需的基因,这两种抗原已被证明对多种主要疾病的福氏志贺氏菌血清型提供广泛的交叉保护。克隆的S. flexneri 2a rfb操纵子与SfII噬菌体上的bgt和gtrII在Ty21a中足以表达含有3,4个抗原决定因子的异源S. flexneri 2a o抗原。此外,该rfb操纵子与Sfx噬菌体上含有的gtrA、gtrB和gtrX以及Sf6噬菌体上含有的oac一起足以表达含有6、7和8抗原决定因子的flexneri 3a o抗原。这些质粒携带或染色体插入基因的Ty21a同时稳定地表达了同源伤寒沙门氏菌o型抗原和异源福氏沙门氏菌o型抗原。表达外源S. flexneri 2a或3a脂多糖(LPS)的候选Ty21a疫苗株对同源S. Typhi和外源志贺氏菌脂多糖均产生显著的血清抗体应答,并保护小鼠免受S. flexneri 2a或3a毒力攻击。这些新的表达福氏梭菌2a和3a o -抗原的Ty21a疫苗菌株,以及我们之前构建的表达sonneshigella或痢疾志贺氏菌1 o -抗原的Ty21a菌株,有可能同时用于预防全球志贺氏菌病的主要原因以及伤寒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Stable Chromosomal Expression of Shigella flexneri 2a and 3a O-Antigens in the Live Salmonella Oral Vaccine Vector Ty21a.

Stable Chromosomal Expression of Shigella flexneri 2a and 3a O-Antigens in the Live Salmonella Oral Vaccine Vector Ty21a.

Stable Chromosomal Expression of Shigella flexneri 2a and 3a O-Antigens in the Live Salmonella Oral Vaccine Vector Ty21a.

We have been exploring the use of the live attenuated Salmonella enterica serovar Typhi Ty21a vaccine strain as a versatile oral vaccine vector for the expression and delivery of multiple foreign antigens, including Shigella O-antigens. In this study, we separately cloned genes necessary for the biosynthesis of the Shigella flexneri serotype 2a and 3a O-antigens, which have been shown to provide broad cross-protection to multiple disease-predominant S. flexneri serotypes. The cloned S. flexneri 2a rfb operon, along with bgt and gtrII, contained on the SfII bacteriophage, was sufficient in Ty21a to express the heterologous S. flexneri 2a O-antigen containing the 3,4 antigenic determinants. Further, this rfb operon, along with gtrA, gtrB, and gtrX contained on the Sfx bacteriophage and oac contained on the Sf6 bacteriophage, was sufficient to express S. flexneri 3a O-antigen containing the 6, 7, and 8 antigenic determinants. Ty21a, with these plasmid-carried or chromosomally inserted genes, demonstrated simultaneous and stable expression of homologous S Typhi O-antigen plus the heterologous S. flexneri O-antigen. Candidate Ty21a vaccine strains expressing heterologous S. flexneri 2a or 3a lipopolysaccharide (LPS) elicited significant serum antibody responses against both homologous S Typhi and heterologous Shigella LPS and protected mice against virulent S. flexneri 2a or 3a challenges. These new S. flexneri 2a and 3a O-antigen-expressing Ty21a vaccine strains, together with our previously constructed Ty21a strains expressing Shigella sonnei or Shigella dysenteriae 1 O-antigens, have the potential to be used together for simultaneous protection against the predominant causes of shigellosis worldwide as well as against typhoid fever.

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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
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