Yang Guangyuan, Yang Ruotong, Zhu Xiaoxiao, Xu Qianwen, Niu Xiaojia, Miao Chengui, Wei Wenfan, Wang Changzhong, Wang Tianming, Wu Daqiang
Department of Pathogenic Biology and Immunology, College of Integrated Chinese and Western Medicine, Anhui University of Chinese Medicine, Hefei, Anhui, China.
Key laboratory of Xin'an Medicine, Ministry of Education, Research Institute of Integrated Traditional Chinese and Western Medicine, Anhui Academy of Chinese Medicine, Hefei, Anhui, China.
Microbiol Spectr. 2025 Jun 18:e0022225. doi: 10.1128/spectrum.00222-25.
is a rapidly spreading multidrug-resistant fungus that causes fatal infections under certain global conditions. Sodium houttuyfonate (SH) and sodium new houttuyfonate (SNH) are stable derivatives of houttuynin (decyl aldehyde) extracted from , both possessing antifungal and antibacterial pharmacological activities. However, the inhibitory effects of SH and SNH on remain unclear. Therefore, this study aims to evaluate the potential activity and possible mechanisms of SH and SNH as antifungal agents against . First, our results showed that SH and SNH exhibit significantly inhibitory activity against fluconazole-resistant strains, but do not possess effective fungicidal activity. In addition, transcriptome and RT-qPCR studies revealed that SH and SNH can repress the expression of genes related to adhesion, aggregation, and biofilm formation. Next, we observed that SH and SNH can disrupt the adhesion and aggregation of early-stage . Furthermore, using the XTT assay, crystal violet staining, and confocal laser scanning microscopy, we found that the biofilm formation ability of was disrupted by SH and SNH. We also found that SH and SNH can potentially increase chitin content and expose β-1,3-glucan in the cell wall. Finally, infection models using larvae and mice with systemic candidiasis demonstrated that SH and SNH significantly inhibited the colonization and pathological damage of . Therefore, our presented results suggest that SH and SNH can effectively inhibit the growth, adhesion, aggregation, and biofilm formation to treat its colonization and pathological damage to the host of .
Recently, the annual proportion of non- infections has been rising. The most notable characteristic of is its resistance to drugs, including multidrug resistance, which results in treatment failures and poses significant challenges in controlling its spread. Sodium houttuyfonate (SH) and sodium new houttuyfonate (SNH) are effective and stable derivatives of houttuynin (decyl aldehyde) extracted from traditional Chinese herbal medicine Houttuynia cordata, both possessing antifungal and antibacterial pharmacological activities. However, the inhibitory effects of SH and SNH on remain unclear. Through and approaches, we have demonstrated that SH and SNH can effectively inhibit the growth, adhesion, aggregation, and biofilm formation to treat its colonization and pathological damage to the host of . Thus, our findings provide new insights into possible options for clinical applications in the anti-.
是一种迅速传播的多重耐药真菌,在某些全球条件下会导致致命感染。鱼腥草素钠(SH)和新鱼腥草素钠(SNH)是从鱼腥草中提取的鱼腥草素(癸醛)的稳定衍生物,二者均具有抗真菌和抗菌药理活性。然而,SH和SNH对的抑制作用仍不清楚。因此,本研究旨在评估SH和SNH作为抗真菌剂对抗的潜在活性和可能机制。首先,我们的结果表明,SH和SNH对氟康唑耐药菌株表现出显著的抑制活性,但不具有有效的杀菌活性。此外,转录组和RT-qPCR研究表明,SH和SNH可抑制与黏附、聚集和生物膜形成相关基因的表达。接下来,我们观察到SH和SNH可破坏早期的黏附和聚集。此外,使用XTT测定、结晶紫染色和共聚焦激光扫描显微镜,我们发现SH和SNH破坏了的生物膜形成能力。我们还发现,SH和SNH可能会增加几丁质含量并使细胞壁中的β-1,3-葡聚糖暴露。最后,使用幼虫和系统性念珠菌病小鼠的感染模型表明,SH和SNH显著抑制了的定植和病理损伤。因此,我们呈现的结果表明,SH和SNH可有效抑制其生长、黏附、聚集和生物膜形成,从而治疗其对宿主的定植和病理损伤。
最近,非感染的年度比例一直在上升。最显著的特征是其耐药性,包括多重耐药性,这导致治疗失败,并在控制其传播方面带来重大挑战。鱼腥草素钠(SH)和新鱼腥草素钠(SNH)是从传统中药鱼腥草中提取的鱼腥草素(癸醛)的有效且稳定的衍生物,二者均具有抗真菌和抗菌药理活性。然而,SH和SNH对的抑制作用仍不清楚。通过和方法,我们证明了SH和SNH可有效抑制其生长、黏附、聚集和生物膜形成,从而治疗其对宿主的定植和病理损伤。因此,我们的发现为抗临床应用的可能选择提供了新见解。