Chemical Compositions of Houttuynia cordata Thunb. Volatile Oil and Its Analogues Attenuate Staphylococcus aureus Virulence by Targeting α-Hemolysin

金黄色葡萄球菌 鱼腥草 溶血素 传统医学 化学 生物有机化学 微生物学 毒力 生物 色谱法 生物化学 细菌 萃取(化学) 医学 基因 遗传学
作者
Yingxue Yang,Lihong V. Wang,Bing Zhao,Zi-Wei Lin,Zhengmin Fan,Ye Hang,Pan Li,Chunli Wu
出处
期刊:Russian Journal of Bioorganic Chemistry [Pleiades Publishing]
卷期号:48 (S1): S166-S177 被引量:3
标识
DOI:10.1134/s1068162023010284
摘要

Houttuynia cordata Thunb. is a medicinal and edible plant that has been used to treat phlegm, asthma, cough, carbuncle, swelling, and sore in China for thousands of years. Many previous studies have reported the chemical compositions and pharmacological acivities of hydrodistillation extracted Houttuynia volatile oil. However, no scientific studies on the inhibition activity against virulence factors of Staphylococcus aureus (S. aureus) have been published. So this article analyze the chemical compositions of Houttuynia volatile oil, and evaluate the anti-α-hemolysin (Hla) activity of Houttuynia volatile oil, its three compositions (nonanol, α-terpineol, 4-terpineol) and eleven analogues. In addition, inhibition activity of three compositions to the A549 cells infection of S. aureus was evaluated in vitro. The results is thirty-four ion chromatographic peaks with matching degree ≥90% were identified, and main chemical compositions of Houttuynia volatile oil were β-myrcene (24.48%) and β-phellandrene (11.28%). The MIC of lauraldehyde against S. aureus ATCC 29213 was found to be 8 μg/mL, and houttuynin showed the strongest inhibition activity against the six S. aureus strains with the MIC of 64 or 128 μg/mL. Besides, growth curve analysis revealed the non-bactericidal activity of nonanol, α-terpilenol, and 4-terpineol at sub-MIC. The result of anti-virulence study demonstrated that dodecanol, undecanol, and decanol showed the strongest anti-Hla activity by significantly inhibiting hemolysis of rabbit blood. Nonanol, α-terpilenol, and 4-terpineol can obviously protect A549 cells from α-Hla-mediated injury at 8, 16, and 32 μg/mL in vitro, respectively.
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