Department of Biotechnology, College of Pharmacy and Science, Chia Nan University of Pharmacy and Science, Jen-Te, Tainan, Taiwan, R.O.C.
Lett Appl Microbiol. 2010 Feb;50(2):168-72. doi: 10.1111/j.1472-765X.2009.02771.x. Epub 2009 Nov 12.
To investigate whether Vibrio vulnificus metalloprotease (VvpE) can induce the production of specific anti-VvpE antibody to confer effective protection against Vibrio vulnificus infection and to evaluate the possibility of VvpE as a potential vaccine candidate against disease caused by V. vulnificus.
The gene encoding the 65-kDa VvpE of V. vulnificus was amplified by PCR and cloned into the expression vector pET21(b). The recombinant VvpE of V. vulnificus was expressed in Escherichia coli BL21(DE3). This His(6)-tagged VvpE was purified and injected intramuscularly into mice to evaluate its ability to stimulate immune response. Specific antibody levels were measured by ELISA. The 75% protective efficacy of recombinant VvpE was evaluated by active immunization and intraperitoneal challenge with V. vulnificus in mice.
The recombinant His(6)-tagged VvpE of V. vulnificus is capable of inducing high antibody response in mice to confer effective protection against lethal challenge with V. vulnificus. VvpE might be a potential vaccine candidate to against V. vulnificus infection.
This study uses His(6)-tagged VvpE to act as vaccine that successfully induces effective and specific anti-VvpE antibody and offers an option for the potential vaccine candidate against V. vulnificus infection.
研究创伤弧菌金属蛋白酶(VvpE)是否能诱导产生特异性抗 VvpE 抗体,从而有效预防创伤弧菌感染,并评估 VvpE 作为预防创伤弧菌感染疾病的潜在疫苗候选物的可能性。
通过 PCR 扩增创伤弧菌 65kDa 的 VvpE 基因,并将其克隆到表达载体 pET21(b)中。在大肠杆菌 BL21(DE3)中表达重组创伤弧菌 VvpE。该 His(6)-标记的 VvpE 经纯化后肌肉内注射入小鼠,以评估其刺激免疫反应的能力。通过 ELISA 测量特异性抗体水平。通过主动免疫和腹腔内用创伤弧菌攻毒评估重组 VvpE 的 75%保护效力。
创伤弧菌重组 His(6)-标记的 VvpE 能够在小鼠中诱导高抗体反应,从而有效预防创伤弧菌的致死性攻击。VvpE 可能是预防创伤弧菌感染的潜在疫苗候选物。
本研究使用 His(6)-标记的 VvpE 作为疫苗,成功诱导出有效和特异性的抗 VvpE 抗体,为预防创伤弧菌感染提供了一种潜在的疫苗候选物。