Department of Biotechnology and Animal Science, National Ilan University, Yilan 26047, Taiwan.
Institute of Cellular and Organismic Biology, Academia Sinica, Taipei 11529, Taiwan.
Int J Mol Sci. 2021 Apr 10;22(8):3926. doi: 10.3390/ijms22083926.
Post-weaning diarrhea due to enterotoxigenic (ETEC) is a common disease of piglets and causes great economic loss for the swine industry. Over the past few decades, decreasing effectiveness of conventional antibiotics has caused serious problems because of the growing emergence of multidrug-resistant (MDR) pathogens. Various studies have indicated that antimicrobial peptides (AMPs) have potential to serve as an alternative to antibiotics owing to rapid killing action and highly selective toxicity. Our previous studies have shown that AMP GW-Q4 and its derivatives possess effective antibacterial activities against the Gram-negative bacteria. Hence, in the current study, we evaluated the antibacterial efficacy of GW-Q4 and its derivatives against MDR ETEC and their minimal inhibition concentration (MIC) values were determined to be around 2~32 μg/mL. Among them, AMP Q4-15a-1 with the second lowest MIC (4 μg/mL) and the highest minimal hemolysis concentration (MHC, 256 μg/mL), thus showing the greatest selectivity (MHC/MIC = 64) was selected for further investigations. Moreover, Q4-15a-1 showed dose-dependent bactericidal activity against MDR ETEC in time-kill curve assays. According to the cellular localization and membrane integrity analyses using confocal microscopy, Q4-15a-1 can rapidly interact with the bacterial surface, disrupt the membrane and enter cytosol in less than 30 min. Minimum biofilm eradication concentration (MBEC) of Q4-15a-1 is 4× MIC (16 μg/mL), indicating that Q4-15a-1 is effective against MDR ETEC biofilm. Besides, we established an MDR ETEC infection model with intestinal porcine epithelial cell-1 (IPEC-1). In this infection model, 32 μg/mL Q4-15a-1 can completely inhibit ETEC adhesion onto IPEC-1. Overall, these results suggested that Q4-15a-1 may be a promising antibacterial candidate for treatment of weaned piglets infected by MDR ETEC.
断奶后仔猪腹泻由肠产毒性大肠杆菌(ETEC)引起,是一种常见疾病,给养猪业造成了巨大的经济损失。在过去的几十年中,由于多药耐药(MDR)病原体的不断出现,传统抗生素的效果逐渐降低,导致了严重的问题。各种研究表明,抗菌肽(AMPs)由于其快速的杀菌作用和高度的选择性毒性,有可能替代抗生素。我们之前的研究表明,AMP GW-Q4 及其衍生物对革兰氏阴性菌具有有效的抗菌活性。因此,在本研究中,我们评估了 GW-Q4 及其衍生物对 MDR ETEC 的抗菌功效,其最小抑菌浓度(MIC)值约为 2~32μg/mL。其中,MIC 值最低(4μg/mL)和最小溶血浓度(MHC,256μg/mL)最高的 AMP Q4-15a-1 显示出最大的选择性(MHC/MIC=64),因此被选为进一步研究的对象。此外,在时间杀伤曲线试验中,Q4-15a-1 对 MDR ETEC 表现出剂量依赖性杀菌活性。根据使用共聚焦显微镜进行的细胞定位和膜完整性分析,Q4-15a-1 可以在不到 30 分钟内迅速与细菌表面相互作用,破坏膜并进入细胞质。Q4-15a-1 的最小生物膜消除浓度(MBEC)为 4×MIC(16μg/mL),表明 Q4-15a-1 对 MDR ETEC 生物膜有效。此外,我们建立了一个含有肠上皮细胞-1(IPEC-1)的 MDR ETEC 感染模型。在该感染模型中,32μg/mL 的 Q4-15a-1 可完全抑制 ETEC 黏附在 IPEC-1 上。总的来说,这些结果表明,Q4-15a-1 可能是一种有前途的治疗 MDR ETEC 感染断奶仔猪的抗菌候选药物。