Department of Aquatic Life Medicine, Pukyong National University, Busan, Korea.
J Appl Microbiol. 2012 Aug;113(2):248-55. doi: 10.1111/j.1365-2672.2012.05328.x. Epub 2012 May 25.
The aim of this study was to generate temperature-sensitive Edwardsiella tarda mutant and to evaluate potential of the mutant as a vaccine in olive flounder (Paralichthys olivaceus).
A temperature-sensitive E. tarda mutant was generated by replacement of alr gene promoter with cI857-λP(R) promoter system plus another CI857 expression cassette that was driven by a constitutive promoter of E. tarda (EtPR C28-1). Growth of the mutant strain was not different to that of wild-type E. tarda under conditions of culture at 39°C. However, growth of the mutant strain was retarded by culturing at 25 or 20°C without d-alanine. To further inhibit leakage of λP(R) promoter, the mutant strain was transformed with a vector harbouring an EtPR C28-1-driven cI857 cassette (pEtPR-cI857), which resulted in more limited growth compared to the mutant without the plasmids. The level of alr gene transcription in the mutant E. tarda and the mutant harbouring pEtPR-cI857 was well coincided with the result of bacterial growth. Olive flounder fingerlings immunized with the E. tarda mutant showed decreased mortality, and a boost immunization induced 100% protection against E. tarda infection. The protection rate of fish was proportional to the serum agglutination titre against E. tarda.
An attenuated E. tarda mutant induced by shifting down temperature below 30°C was firstly generated. Immunization of fish with the mutant led to protection against virulent E. tarda challenge.
The results suggest that the present temperature-sensitive E. tarda mutant can be a good candidate for effective vaccines for prophylaxis of edwardsiellosis. Moreover, as the present E. tarda mutant can be cultured without supplementation of the specific nutrient and can be attenuated just by decreasing temperatures below 30°C, vaccines based on the present E. tarda mutant would be advantageous in an economical aspect.
本研究旨在构建温度敏感型迟钝爱德华氏菌突变株,并评估其作为橄榄斑鮐(Paralichthys olivaceus)疫苗的潜力。
通过用 cI857-λP(R)启动子系统取代 alr 基因启动子,并在另一个由迟钝爱德华氏菌组成型启动子(EtPR C28-1)驱动的 CI857 表达盒,构建了一株温度敏感型迟钝爱德华氏菌突变株。在 39°C 条件下培养时,突变株的生长与野生型迟钝爱德华氏菌无差异。然而,在 25 或 20°C 条件下培养时,突变株因缺乏 D-丙氨酸而生长受到抑制。为了进一步抑制 λP(R)启动子的渗漏,将携带 EtPR C28-1 驱动的 cI857 盒的质粒(pEtPR-cI857)转化至突变株,与未携带质粒的突变株相比,该突变株的生长受到更明显的抑制。突变型迟钝爱德华氏菌和携带 pEtPR-cI857 的突变株的 alr 基因转录水平与细菌生长结果一致。用迟钝爱德华氏菌突变株免疫的橄榄斑鮐鱼苗死亡率降低,加强免疫可 100%抵抗迟钝爱德华氏菌感染。鱼类的保护率与血清对迟钝爱德华氏菌的凝集效价成正比。
首次构建了一种通过降低温度至 30°C 以下诱导的减毒迟钝爱德华氏菌突变株。用该突变株免疫鱼类可抵抗强毒迟钝爱德华氏菌的攻击。
本研究结果表明,本研究构建的温度敏感型迟钝爱德华氏菌突变株可作为预防爱德华氏菌病的有效疫苗候选株。此外,由于本研究构建的迟钝爱德华氏菌突变株在不添加特定营养物质的情况下即可培养,且仅通过将温度降低至 30°C 以下即可减毒,因此基于本研究构建的迟钝爱德华氏菌突变株的疫苗在经济方面具有优势。