Institute of Biomedical Sciences, Mackay Medical College, New Taipei City, Taiwan, ROC.
Institute of Molecular and Cellular Biology, National Taiwan University, Taipei, Taiwan, ROC.
Fish Shellfish Immunol. 2019 Dec;95:606-616. doi: 10.1016/j.fsi.2019.10.052. Epub 2019 Nov 1.
To develop an alternative to conventional antibiotics used in the aquaculture and livestock industries, we employed Bacillus subtilis, considered a biosafe microorganism, to express the degradable antimicrobial peptide lactoferricin. An expression plasmid pP43-6LFBII-GFP, in which reporter GFP cDNA was fused downstream of lactoferricin cDNA driven by an endogenous constitutive P43 promoter was electroporated into B. subtilis, followed by regeneration and cultivation. The putative colonies harboring plasmids were primarily screened by PCR-amplification of lactoferricin cDNA. Four transformants which were stable inheritance of plasmid containing lactoferricin cDNA included strains T1, T4, T7 and T13. Based on Western blot and Southern blot analyses, we found that transgenic strains T1 and T13 not only highly expressed exogenous recombinant lactoferricin, but also exhibited more stable inheritance of plasmids with 931 and 647 copies per cell, respectively. In the antibacterial in vitro experiment, the bactericidal activity of each microliter of cell lysate from transgenic strains T1 and T13 (5 × 10 CFU) for Escherichia coli was equivalent to 56 and 53 ng of Ampicillin dosage, respectively, while for Staphylococcus epidermidis, the equivalency T1 and T13 was 154 and 130 ng of Ampicillin dosage, respectively. Equivalencies of bacterial activity for Vibrio parahaemolyticus and Edwardsiella tarda followed suit. In the antibacterial in vivo experiment, we oral-in-tube fed tilapia fry (Oreochromis mossambicus X O. niloticus) with cell lysate from transgenic strain T1 and T13 individually. After 1-h of incubation, we immersed these treated fish fry in a water tank containing E. tarda (5 × 10 CFU) for a 5-hr bacterial challenge. After one month cultivation, an average survival rate of 63 and 67% was observed after having fed the fish fry with transgenic strains T1 and T13, respectively. However, the average survival rate of fish fry fed with B. subtilis WT strain and transgenic strain T19 without expressing recombinant lactoferricin reached only 5 and 9%, respectively. These data indicate that the survival of fish fry infected by the intestinal pathogen tested could be significantly enhanced by feeding transgenic B. subtilis containing antibacterial peptide. Therefore, we suggest that this strategy could be applied to both aquaculture and livestock industries to (i) reduce the dependency on conventional antibiotics during seasonal outbreaks and (ii) eliminate the problem of antibiotic resistance.
为了开发替代水产养殖和畜牧业中传统抗生素的方法,我们利用枯草芽孢杆菌来表达可降解的抗菌肽乳铁蛋白。我们构建了表达质粒 pP43-6LFBII-GFP,其中报告基因 GFP 的 cDNA 下游融合了乳铁蛋白 cDNA,由内源性组成型 P43 启动子驱动。将该质粒电转入枯草芽孢杆菌,然后进行再生和培养。通过 PCR 扩增检测乳铁蛋白 cDNA,初步筛选出含有质粒的假定菌落。含有乳铁蛋白 cDNA 的质粒在四个转化株(T1、T4、T7 和 T13)中稳定遗传。通过 Western blot 和 Southern blot 分析,我们发现转染株 T1 和 T13 不仅能高水平表达外源性重组乳铁蛋白,而且质粒的遗传也更稳定,拷贝数分别为每个细胞 931 和 647 个。在体外抗菌实验中,每个微升细胞裂解物(5×10 CFU)对大肠杆菌的杀菌活性相当于 56 和 53ng 的氨苄西林剂量,而对表皮葡萄球菌,T1 和 T13 的等效性分别为 154 和 130ng 的氨苄西林剂量。副溶血弧菌和迟缓爱德华氏菌的细菌活性等效性也类似。在体内抗菌实验中,我们分别用转染株 T1 和 T13 的细胞裂解物经口投喂奥利亚罗非鱼(奥利亚罗非鱼 X 尼罗罗非鱼)鱼苗。孵育 1 小时后,将这些处理过的鱼苗浸入含有 5×10 CFU 的爱德华氏菌的水箱中进行 5 小时的细菌攻毒。一个月后培养,分别用转染株 T1 和 T13 喂养的鱼苗的平均存活率为 63%和 67%。然而,用枯草芽孢杆菌 WT 株和不表达重组乳铁蛋白的转染株 T19 喂养的鱼苗的平均存活率仅为 5%和 9%。这些数据表明,通过喂食含有抗菌肽的转基因枯草芽孢杆菌,可显著提高感染肠道病原体的鱼苗的存活率。因此,我们建议将这种策略应用于水产养殖和畜牧业,以(i)减少季节性爆发时对抗生素的依赖,(ii)消除抗生素耐药性问题。