Guimarães Valéria Dellaretti, Innocentin Silvia, Lefèvre François, Azevedo Vasco, Wal Jean-Michel, Langella Philippe, Chatel Jean-Marc
Unité de Virologie et Immunologie Moléculaire, INRA, Domaine de Vilvert, 78352 Jouy en Josas Cedex, France.
Appl Environ Microbiol. 2006 Nov;72(11):7091-7. doi: 10.1128/AEM.01325-06. Epub 2006 Sep 8.
The use of the food-grade bacterium Lactococcus lactis as a DNA delivery vehicle at the mucosal level is an attractive DNA vaccination strategy. Previous experiments showed that recombinant L. lactis expressing the Listeria monocytogenes inlA gene can deliver a functional gene into mammalian cells. Here, we explored the potential use of noninvasive L. lactis strains as a DNA delivery vehicle. We constructed two Escherichia coli-L. lactis shuttle plasmids, pLIG:BLG1 and pLIG:BLG2, containing a eukaryotic expression cassette with the cDNA of bovine beta-lactoglobulin (BLG). The greatest BLG expression after transfection of Cos-7 cells was obtained with pLIG:BLG1, which was then used to transform L. lactis MG1363. The resulting L. lactis strain MG1363(pLIG:BLG1) was not able to express BLG. The potential of L. lactis as a DNA delivery vehicle was analyzed by detection of BLG in Caco-2 human colon carcinoma cells after 3 h of coincubation with (i) purified pLIG:BLG1, (ii) MG1363(pLIG:BLG1), (iii) a mix of MG1363(pLIG) and purified pLIG:BLG1, and (iv) MG1363. Both BLG cDNA and BLG expression were detected only in Caco-2 cells coincubated with MG1363(pLIG:BLG1). There was a decrease in the BLG cDNA level in Caco-2 cells between 24 and 48 h after coincubation. BLG expression by Caco-2 cells started at 24 h and increased between 24 and 72 h. BLG secretion by Caco-2 cells started 48 h after coincubation with MG1363(pLIG:BLG1). We conclude that lactococci can deliver BLG cDNA into mammalian epithelial cells, demonstrating their potential to deliver in vivo a DNA vaccine.
将食品级细菌乳酸乳球菌用作黏膜水平的DNA递送载体是一种有吸引力的DNA疫苗接种策略。先前的实验表明,表达单核细胞增生李斯特菌inlA基因的重组乳酸乳球菌能够将功能性基因递送至哺乳动物细胞。在此,我们探索了非侵袭性乳酸乳球菌菌株作为DNA递送载体的潜在用途。我们构建了两个大肠杆菌-乳酸乳球菌穿梭质粒,pLIG:BLG1和pLIG:BLG2,它们含有一个带有牛β-乳球蛋白(BLG)cDNA的真核表达盒。用pLIG:BLG1转染Cos-7细胞后获得了最高的BLG表达,随后用其转化乳酸乳球菌MG1363。所得的乳酸乳球菌菌株MG1363(pLIG:BLG1)无法表达BLG。通过在与以下物质共孵育3小时后检测Caco-2人结肠癌细胞中的BLG,分析了乳酸乳球菌作为DNA递送载体的潜力:(i) 纯化的pLIG:BLG1,(ii) MG1363(pLIG:BLG1),(iii) MG1363(pLIG)和纯化的pLIG:BLG1的混合物,以及(iv) MG1363。仅在与MG1363(pLIG:BLG1)共孵育的Caco-2细胞中检测到了BLG cDNA和BLG表达。共孵育后24至48小时,Caco-2细胞中的BLG cDNA水平有所下降。Caco-2细胞的BLG表达在24小时开始,并在24至72小时之间增加。Caco-2细胞与MG1363(pLIG:BLG1)共孵育48小时后开始分泌BLG。我们得出结论,乳球菌能够将BLG cDNA递送至哺乳动物上皮细胞,证明了它们在体内递送DNA疫苗的潜力。