Laboratory of Genetic Technology, Department of Ecology, Genetics and Evolution, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Center for Gastrointestinal Biology, Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
J Appl Microbiol. 2020 Nov;129(5):1389-1401. doi: 10.1111/jam.14695. Epub 2020 Jun 22.
To investigate the anti-inflammatory activity of an invasive and Hp65-producing strain Lactococcus lactis NCDO2118 FnBPA+ (pXYCYT:Hsp65) in acute 2,4,6-trinitrobenzene sulphonic acid (TNBS)-induced colitis in mice as an innovative therapeutic strategy against Crohn's disease (CD).
The pXYCYT:Hsp65 plasmid was transformed into the L. lactis NCDO2118 FnBPA+ strain, resulting in the L. lactis NCDO2118 FnBPA+ (pXYCYT:Hsp65) strain. Then, the functionality of the strain was evaluated in vitro for Hsp65 production by Western blotting and for invasion into Caco-2 cells. The results demonstrated that the strain was able to produce Hsp65 and efficiently invade eukaryotic cells. Subsequently, in vivo, the anti-inflammatory capacity of the recombinant strain was evaluated in colitis induced with TNBS in BALB/c mice. Oral administration of the recombinant strain was able to attenuated the severity of colitis by mainly reducing IL-12 and IL-17 levels and increasing IL-10 and secretory immunoglobulin A levels.
The L. lactis NCDO2118 FnBPA+ (pXYCYT:Hsp65) strain contributed to a reduction in inflammatory damage in experimental CD.
This study, which used L. lactis for the production and delivery of Hsp65, has scientific relevance because it shows the efficacy of this new strategy based on therapeutic protein delivery into mammalian enterocytes.
研究产侵袭性和 Hp65 的乳球菌 Lactococcus lactis NCDO2118 FnBPA+(pXYCYT:Hsp65)在急性 2,4,6-三硝基苯磺酸(TNBS)诱导的小鼠结肠炎中的抗炎活性,作为一种针对克罗恩病(CD)的创新治疗策略。
将 pXYCYT:Hsp65 质粒转化到乳球菌 Lactococcus lactis NCDO2118 FnBPA+菌株中,得到乳球菌 Lactococcus lactis NCDO2118 FnBPA+(pXYCYT:Hsp65)菌株。然后,通过 Western blot 检测 Hsp65 的产生和对 Caco-2 细胞的侵袭来评估该菌株的体外功能。结果表明,该菌株能够产生 Hsp65 并有效地入侵真核细胞。随后,在体内,用 TNBS 诱导 BALB/c 小鼠结肠炎来评估重组菌株的抗炎能力。重组菌株的口服给药能够通过主要降低 IL-12 和 IL-17 水平以及增加 IL-10 和分泌型免疫球蛋白 A 水平来减轻结肠炎的严重程度。
乳球菌 Lactococcus lactis NCDO2118 FnBPA+(pXYCYT:Hsp65)菌株有助于减少实验性 CD 中的炎症损伤。
本研究使用乳球菌生产和递呈 Hsp65,具有科学意义,因为它展示了基于治疗性蛋白递送至哺乳动物肠细胞的这种新策略的疗效。