Bailleul Geoffrey, Guabiraba Rodrigo, Virlogeux-Payant Isabelle, Lantier Isabelle, Trotereau Jérôme, Gilbert Florence B, Wiedemann Agnès, Trotereau Angélina, Velge Philippe, Schouler Catherine, Lalmanach Anne-Christine
ISP, INRA, Université de Tours, UMR 1282 Centre INRA Val de Loire, Nouzilly, France.
Front Microbiol. 2019 Mar 26;10:541. doi: 10.3389/fmicb.2019.00541. eCollection 2019.
Defensins are natural antimicrobial peptides. The avian beta-defensin AvBD7 isolated from the chicken bone marrow possess broad antibacterial spectrum and strong resistance to proteolysis. However, its ability to fight systemic infections of major concern for public health, such as salmonellosis, is unknown. As a first approach, fluorescence labeling of AvBD7 allowed to track its systemic distribution after intraperitoneal injection in mice using whole body live imaging. It was associated to peritoneal cells and to deeper organs such as the liver. In the next step, the use of labeled AvBD7 allowed to observe its interaction with murine macrophages in culture. After incubation, it was able to penetrate inside the cells through an endocytosis-like mechanism. Furthermore, natural AvBD7 contributed to the control of intracellular multiplication of a multidrug resistant strain, after incubation with infected macrophages. Finally, administration in a model of systemic lethal infection in mice led to significant improvement of mouse survival, consistently with significant reduction of the liver bacterial load. In conclusion, the results reveal a hitherto unknown intracellular antibacterial effect of AvBD7 in target cells and support AvBD7 as a candidate of interest for the treatment of infectious diseases caused by multidrug-resistant pathogenic
防御素是天然抗菌肽。从鸡骨髓中分离出的禽β-防御素AvBD7具有广谱抗菌活性且对蛋白水解具有较强抗性。然而,其对抗公众健康主要关注的全身感染(如沙门氏菌病)的能力尚不清楚。作为第一步,对AvBD7进行荧光标记,以便在小鼠腹腔注射后使用全身活体成像追踪其全身分布。它与腹膜细胞以及肝脏等更深层器官相关。在下一步中,使用标记的AvBD7能够观察其与培养中的小鼠巨噬细胞的相互作用。孵育后,它能够通过类似内吞作用的机制进入细胞内部。此外,天然AvBD7在与感染的巨噬细胞孵育后,有助于控制多重耐药菌株的细胞内增殖。最后,在小鼠全身致死性感染模型中给药导致小鼠存活率显著提高,同时肝脏细菌载量显著降低。总之,结果揭示了AvBD7在靶细胞中迄今未知的细胞内抗菌作用,并支持将AvBD7作为治疗由多重耐药病原体引起的传染病的有前景候选物。