Khadke Sagar Kiran, Lee Jin-Hyung, Kim Yong-Guy, Raj Vinit, Lee Jintae
School of Chemical Engineering, Yeungnam University, Gyeongsan, South Korea.
Front Microbiol. 2022 Mar 16;13:818165. doi: 10.3389/fmicb.2022.818165. eCollection 2022.
Cinnamaldehyde has a broad range of biological activities, which include antibiofilm and anthelmintic activities. The ever-growing problem of drug resistance and limited treatment options have created an urgent demand for natural molecules with antibiofilm and anthelmintic properties. Hence, we hypothesized that molecules with a scaffold structurally similar to that of cinnamaldehyde might act as dual inhibitors against fungal biofilms and helminths. In this regard, eleven cinnamaldehyde analogs were tested to determine their effects on fungal biofilm and nematode . α-Methyl and -4-methyl cinnamaldehydes efficiently inhibited biofilm formation (>90% inhibition at 50 μg/mL) with minimum inhibitory concentrations (MICs) of ≥ 200 μg/mL and 4-bromo and 4-chloro cinnamaldehydes exhibited anthelmintic property at 20 μg/mL against . α-Methyl and -4-methyl cinnamaldehydes inhibited hyphal growth and cell aggregation. Scanning electron microscopy was employed to determine the surface architecture of biofilm and cuticle of , and confocal laser scanning microscopy was used to determine biofilm characteristics. The perturbation in gene expression of was investigated using qRT-PCR analysis and α-methyl and -4-methyl cinnamaldehydes exhibited down-regulation of , , , , and and up-regulation of and . Additionally, molecular interaction of these two molecules with UCF1 and YWP1 were revealed by molecular docking simulation. Our observations collectively suggest α-methyl and -4-methyl cinnamaldehydes are potent biofilm inhibitors and that 4-bromo and 4-chloro cinnamaldehydes are anthelmintic agents. Efforts are required to determine the range of potential therapeutic applications of cinnamaldehyde analogs.
肉桂醛具有广泛的生物活性,其中包括抗生物膜和驱虫活性。耐药性问题日益严重且治疗选择有限,这使得对具有抗生物膜和驱虫特性的天然分子产生了迫切需求。因此,我们推测,具有与肉桂醛结构相似支架的分子可能作为抗真菌生物膜和蠕虫的双重抑制剂。在这方面,测试了11种肉桂醛类似物,以确定它们对真菌生物膜和线虫的影响。α-甲基肉桂醛和4-甲基肉桂醛能有效抑制生物膜形成(在50μg/mL时抑制率>90%),最低抑菌浓度(MIC)≥200μg/mL,4-溴肉桂醛和4-氯肉桂醛在20μg/mL时对[具体对象未明确]表现出驱虫特性。α-甲基肉桂醛和4-甲基肉桂醛抑制菌丝生长和细胞聚集。采用扫描电子显微镜确定[具体对象未明确]生物膜和角质层的表面结构,并用共聚焦激光扫描显微镜确定生物膜特征。使用qRT-PCR分析研究[具体对象未明确]基因表达的扰动,α-甲基肉桂醛和4-甲基肉桂醛表现出[相关基因未明确]的下调以及[相关基因未明确]和[相关基因未明确]的上调。此外,通过分子对接模拟揭示了这两种分子与UCF1和YWP1的分子相互作用。我们的观察结果共同表明,α-甲基肉桂醛和4-甲基肉桂醛是有效的生物膜抑制剂,4-溴肉桂醛和4-氯肉桂醛是驱虫剂。需要努力确定肉桂醛类似物潜在治疗应用的范围。