Laboratorios de Investigación y Desarrollo, Universidad Peruana Cayetano Heredia (UPCH), Lima 34, Peru.
EA7417-BTSB, Université Fédérale Toulouse Midi-Pyrénées, INU Champollion, 81012 Albi, France.
Toxins (Basel). 2017 Dec 29;10(1):21. doi: 10.3390/toxins10010021.
The venom peptide bicarinalin, previously isolated from the ant , is an antimicrobial agent with a broad spectrum of activity. In this study, we investigate the potential of bicarinalin as a novel agent against , which causes several gastric diseases. First, the effects of synthetic bicarinalin have been tested against : one ATCC strain, and forty-four isolated from stomach ulcer biopsies of Peruvian patients. Then the cytoxicity of bicarinalin on human gastric cells and murine peritoneal macrophages was measured using XTT and MTT assays, respectively. Finally, the preventive effect of bicarinalin was evaluated by scanning electron microscopy using an adherence assay of on human gastric cells treated with bicarinalin. This peptide has a potent antibacterial activity at the same magnitude as four antibiotics currently used in therapies against . Bicarinalin also inhibited adherence of to gastric cells with an IC of 0.12 μg·mL and had low toxicity for human cells. Scanning electron microscopy confirmed that bicarinalin can significantly decrease the density of on gastric cells. We conclude that Bicarinalin is a promising compound for the development of a novel and effective anti- agent for both curative and preventive use.
先前从蚂蚁中分离出的毒液肽比卡林alin 是一种具有广谱活性的抗菌剂。在这项研究中,我们研究了比卡林alin 作为一种新型药物治疗的潜力,它可导致多种胃部疾病。首先,我们测试了合成比卡林alin 对:一个 ATCC 菌株和 44 株从秘鲁胃溃疡活检中分离出的菌株的作用。然后,我们分别使用 XTT 和 MTT 测定法测量了比卡林alin 对人胃细胞和鼠腹膜巨噬细胞的细胞毒性。最后,我们通过使用粘附测定法,用扫描电子显微镜评估了比卡林alin 对人胃细胞的预防作用。该肽具有与目前用于治疗的四种抗生素相当的强大的抗菌活性。比卡林alin 还能抑制与胃细胞的粘附,IC 为 0.12μg·mL,对人细胞的毒性低。扫描电子显微镜证实,比卡林alin 可显著降低胃细胞上的密度。我们得出结论,比卡林alin 是一种很有前途的化合物,可用于开发新型有效的治疗和预防用抗菌药物。