Department of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, NUHS, MD10, 4 Medical Drive, Singapore 117594, Singapore.
School of Biological Sciences, Campus Box 92, College of Natural and Health Sciences, University of Northern Colorado, 501 20th St., Greeley, CO 80639, USA.
Int J Mol Sci. 2023 Feb 22;24(5):4359. doi: 10.3390/ijms24054359.
Infections caused by multi-drug-resistant (MDR) bacteria are a global threat to human health. As venoms are the source of biochemically diverse bioactive proteins and peptides, we investigated the antimicrobial activity and murine skin infection model-based wound healing efficacy of a 13 kDa protein. The active component PaTx-II was isolated from the venom of (Australian King Brown or Mulga Snake). PaTx-II inhibited the growth of Gram-positive bacteria in vitro, with moderate potency (MICs of 25 µM) observed against , and . The antibiotic activity of PaTx-II was associated with the disruption of membrane integrity, pore formation, and lysis of bacterial cells, as evidenced by scanning and transmission microscopy. However, these effects were not observed with mammalian cells, and PaTx-II exhibited minimal cytotoxicity (CC > 1000 µM) toward skin/lung cells. Antimicrobial efficacy was then determined using a murine model of skin infection. Topical application of PaTx-II (0.5 mg/kg) cleared with concomitant increased vascularization and re-epithelialization, promoting wound healing. As small proteins and peptides can possess immunomodulatory effects to enhance microbial clearance, cytokines and collagen from the wound tissue samples were analyzed by immunoblots and immunoassays. The amounts of type I collagen in PaTx-II-treated sites were elevated compared to the vehicle controls, suggesting a potential role for collagen in facilitating the maturation of the dermal matrix during wound healing. Levels of the proinflammatory cytokines interleukin-1β (IL-1β), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α), cyclooxygenase-2 (COX-2) and interleukin-10 (IL-10), factors known to promote neovascularization, were substantially reduced by PaTx-II treatment. Further studies that characterize the contributions towards efficacy imparted by in vitro antimicrobial and immunomodulatory activity with PaTx-II are warranted.
耐多药(MDR)细菌引起的感染对人类健康构成全球性威胁。由于毒液是生物化学多样化的生物活性蛋白和肽的来源,我们研究了一种 13 kDa 蛋白的抗菌活性和基于鼠皮肤感染模型的伤口愈合功效。活性成分 PaTx-II 是从 (澳大利亚金棕色或 Mulga 蛇)的毒液中分离出来的。PaTx-II 在体外抑制革兰氏阳性菌的生长,对 、 和 观察到中等强度的效力(MIC 为 25 µM)。PaTx-II 的抗生素活性与膜完整性的破坏、孔形成和细菌细胞的裂解有关,这可以通过扫描和透射显微镜得到证明。然而,这些效应在哺乳动物细胞中没有观察到,并且 PaTx-II 对皮肤/肺细胞表现出最小的细胞毒性(CC > 1000 µM)。然后使用 皮肤感染的小鼠模型确定了抗菌功效。局部应用 PaTx-II(0.5 mg/kg)清除 ,同时增加血管生成和再上皮化,促进伤口愈合。由于小蛋白和肽可以具有免疫调节作用以增强微生物清除,因此通过免疫印迹和免疫测定分析了伤口组织样本中的细胞因子和胶原蛋白。与载体对照相比,在 PaTx-II 处理部位的 I 型胶原蛋白含量升高,表明胶原蛋白在促进伤口愈合过程中真皮基质的成熟中可能发挥作用。促炎细胞因子白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)、环加氧酶-2(COX-2)和白细胞介素-10(IL-10)的水平,这些因子已知可促进新血管生成,经 PaTx-II 处理后显著降低。进一步的研究需要表征 PaTx-II 的体外抗菌和免疫调节活性对功效的贡献。