Pandeya Ankit, Ojo Isoiza, Alegun Olaniyi, Wei Yinan
Department of Chemistry, University of Kentucky, Lexington, Kentucky 40506, United States.
ACS Infect Dis. 2020 Sep 11;6(9):2337-2354. doi: 10.1021/acsinfecdis.0c00384. Epub 2020 Aug 24.
Antibiotic resistance has emerged as a serious threat to global public health in recent years. Lack of novel antimicrobials, especially new classes of compounds, further aggravates the situation. For Gram-negative bacteria, their double layered cell envelope and an array of efflux pumps act as formidable barriers for antimicrobials to penetrate. While cytoplasmic targets are hard to reach, proteins in the periplasm are clearly more accessible, as the drug only needs to breach the outer membrane. In this review, we summarized recent efforts on the validation and testing of periplasmic proteins as potential antimicrobial targets and the development of related inhibitors that either inhibit the growth of a bacterial pathogen or reduce its virulence during interaction with host cells. We conclude that the periplasm contains a promising pool of novel antimicrobial targets that should be scrutinized more closely for the development of effective treatment against multidrug-resistant Gram-negative bacteria.
近年来,抗生素耐药性已成为对全球公共卫生的严重威胁。新型抗菌药物的缺乏,尤其是新类型化合物的缺乏,进一步加剧了这一情况。对于革兰氏阴性菌而言,其双层细胞膜和一系列外排泵构成了抗菌药物难以穿透的巨大屏障。虽然细胞质靶点难以触及,但周质中的蛋白质显然更容易接近,因为药物只需突破外膜即可。在本综述中,我们总结了近期关于验证和测试周质蛋白作为潜在抗菌靶点以及开发相关抑制剂的工作,这些抑制剂要么抑制细菌病原体的生长,要么在与宿主细胞相互作用期间降低其毒力。我们得出结论,周质中含有大量有前景的新型抗菌靶点,针对多重耐药革兰氏阴性菌开发有效治疗方法时应对其进行更深入的研究。