Department of Microbiology, Institute of Translational Medicine, Medical College, Yangzhou University, Yangzhou, People's Republic of China.
Jiangsu Key Laboratory of Experimental & Translational Non-coding RNA Research, Yangzhou, People's Republic of China.
Microbiol Spectr. 2023 Jun 15;11(3):e0470222. doi: 10.1128/spectrum.04702-22. Epub 2023 Apr 18.
As multidrug-resistant pathogens emerge and spread rapidly, novel antibiotics urgently need to be discovered. With a dwindling antibiotic pipeline, antibiotic adjuvants might be used to revitalize existing antibiotics. In recent decades, traditional Chinese medicine has occupied an essential position in adjuvants of antibiotics. This study found that baicalein potentiates doxycycline against multidrug-resistant Gram-negative pathogens. Mechanism studies have shown that baicalein causes membrane disruption by attaching to phospholipids on the Gram-negative bacterial cytoplasmic membrane and lipopolysaccharides on the outer membrane. This process facilitates the entry of doxycycline into bacteria. Through collaborative strategies, baicalein can also increase the production of reactive oxygen species and inhibit the activities of multidrug efflux pumps and biofilm formation to potentiate antibiotic efficacy. Additionally, baicalein attenuates the lipopolysaccharide-induced inflammatory response . Finally, baicalein can significantly improve doxycycline efficacy in mouse lung infection models. The present study showed that baicalein might be considered a lead compound, and it should be further optimized and developed as an adjuvant that helps combat antibiotic resistance. Doxycycline is an important broad-spectrum tetracycline antibiotic used for treating multiple human infections, but its resistance rates are recently rising globally. Thus, new agents capable of boosting the effectiveness of doxycycline need to be discovered. In this study, it was found that baicalein potentiates doxycycline against multidrug-resistant Gram-negative pathogens and . Due to its low cytotoxicity and resistance, the combination of baicalein and doxycycline provides a valuable clinical reference for selecting more effective therapeutic strategies for treating infections caused by multidrug-resistant Gram-negative clinical isolates.
随着多药耐药病原体的出现和迅速传播,急需发现新的抗生素。由于抗生素管道日益减少,抗生素佐剂可能被用于使现有抗生素恢复活力。在最近几十年中,中药在抗生素佐剂中占据了重要地位。本研究发现,黄芩素增强了多西环素对多种耐药革兰氏阴性病原体的作用。机制研究表明,黄芩素通过附着在革兰氏阴性菌细胞质膜上的磷脂和外膜上的脂多糖来破坏细胞膜。这一过程促进了多西环素进入细菌。通过协同策略,黄芩素还可以增加活性氧的产生,抑制多药外排泵的活性和生物膜形成,从而增强抗生素的疗效。此外,黄芩素还可以减轻脂多糖诱导的炎症反应。最后,黄芩素可以显著提高多西环素在小鼠肺部感染模型中的疗效。本研究表明,黄芩素可能被认为是一种先导化合物,应进一步优化和开发为一种佐剂,以帮助对抗抗生素耐药性。多西环素是一种重要的广谱四环素抗生素,用于治疗多种人类感染,但近年来其耐药率在全球范围内呈上升趋势。因此,需要发现能够提高多西环素疗效的新药物。在本研究中,发现黄芩素增强了多西环素对多种耐药革兰氏阴性病原体的作用。由于其低细胞毒性和耐药性,黄芩素和多西环素的联合使用为选择更有效的治疗策略来治疗多药耐药革兰氏阴性临床分离株引起的感染提供了有价值的临床参考。