a Center for Experimental and Molecular Medicine, Academic Medical Center, University of Amsterdam , Amsterdam , the Netherlands.
b Department of Pathology , Academic Medical Center, University of Amsterdam , Amsterdam , the Netherlands.
Virulence. 2017 Nov 17;8(8):1683-1694. doi: 10.1080/21505594.2017.1307485. Epub 2017 Apr 19.
Melioidosis is a severe infectious disease with a high mortality that is endemic in South-East Asia and Northern Australia. The causative pathogen, Burkholderia pseudomallei, is listed as potential bioterror weapon due to its high virulence and potential for easy dissemination. Currently, there is no licensed vaccine for prevention of melioidosis. Here, we explore the use of rapid plasmid DNA vaccination against B. pseudomallei flagellin for protection against respiratory challenge. We tested three flagellin DNA vaccines with different subcellular targeting designs. C57BL/6 mice were vaccinated via skin tattoo on day 0, 3 and 6 before intranasal challenge with B. pseudomallei on day 21. Next, the most effective construct was used as single vaccination on day 0 by tattoo or intranasal formulation. Mice were sacrificed 72 hours post-challenge to assess bacterial loads, cytokine responses, inflammation and microscopic lesions. A construct encoding a cellular secretion signal resulted in the most effective protection against melioidosis via tattooing, with a 10-fold reduction in bacterial loads in lungs and distant organs compared to the empty vector. Strikingly, a single intranasal administration of the same vaccine resulted in >1000-fold lower bacterial loads and increased survival. Pro-inflammatory cytokine responses were significantly diminished and strong reductions in markers for distant organ damage were observed. A rapid vaccination scheme using flagellin DNA tattoo provides significant protection against intranasal challenge with B. pseudomallei, markedly improved by a single administration via airway mucosa. Hence intranasal vaccination with flagellin-encoding DNA may be applicable when acute mass vaccination is indicated and warrants further testing.
类鼻疽是一种严重的传染病,死亡率很高,在东南亚和澳大利亚北部流行。病原体是类鼻疽伯克霍尔德菌,由于其高毒性和易于传播的潜力,被列为潜在的生物恐怖武器。目前,尚无预防类鼻疽的许可疫苗。在这里,我们探讨了使用快速质粒 DNA 疫苗接种针对类鼻疽鞭毛蛋白来预防呼吸道挑战的方法。我们测试了三种具有不同亚细胞靶向设计的鞭毛蛋白 DNA 疫苗。C57BL/6 小鼠在第 0、3 和 6 天通过皮肤纹身接种疫苗,然后在第 21 天通过鼻腔内接种 B. pseudomallei 进行挑战。接下来,使用最有效的构建体通过纹身或鼻腔配方进行单次接种。在挑战后 72 小时处死小鼠,以评估细菌负荷、细胞因子反应、炎症和微观病变。编码细胞分泌信号的构建体通过纹身可有效预防类鼻疽,与空载体相比,肺部和远处器官的细菌负荷降低了 10 倍。引人注目的是,单次鼻腔内给予相同疫苗可使细菌负荷降低 1000 倍以上,并提高存活率。促炎细胞因子反应明显减弱,远处器官损伤的标志物明显减少。使用鞭毛蛋白 DNA 纹身进行快速疫苗接种方案可显著预防鼻腔内接种 B. pseudomallei 的挑战,通过气道黏膜进行单次给药可显著改善。因此,当需要急性大规模接种疫苗时,鼻内接种鞭毛蛋白编码 DNA 可能是可行的,并值得进一步研究。