细菌
化学
胆酸
抗菌剂
沙门氏菌
细胞内寄生虫
微生物学
细胞内
细菌外膜
抗生素
肠道菌群
两亲性
胃肠道
生物化学
大肠杆菌
生物
胆汁酸
遗传学
有机化学
基因
共聚物
聚合物
作者
Kavita Yadav,Prabhu Srinivas Yavvari,Sanjay Pal,Sandeep Kumar,Deepakkumar Mishra,Siddhi Gupta,Madhurima Mitra,Vijay Soni,Neha Khare,Priyanka Sharma,Chittur V. Srikanth,Arti Kapil,Archana Singh,Vinay Kumar Nandicoori,Avinash Bajaj
标识
DOI:10.1021/acs.bioconjchem.8b00880
摘要
A major impediment to developing effective antimicrobials against Gram-negative bacteria like Salmonella is the ability of the bacteria to develop resistance against existing antibiotics and the inability of the antimicrobials to clear the intracellular bacteria residing in the gastrointestinal tract. As the critical balance of charge and hydrophobicity is required for effective membrane-targeting antimicrobials without causing any toxicity to mammalian cells, herein we report the synthesis and antibacterial properties of cholic acid-derived amphiphiles conjugated with alkyl chains of varied hydrophobicity. Relative to other hydrophobic counterparts, a compound with hexyl chain (6) acted as an effective antimicrobial against different Gram-negative bacteria. Apart from its ability to permeate the outer and inner membranes of bacteria; compound 6 can cross the cellular and lysosomal barriers of epithelial cells and macrophages and kill the facultative intracellular bacteria without disrupting the mammalian cell membranes. Oral delivery of compound 6 was able to clear the Salmonella-mediated gut infection and inflammation, and was able to combat persistent, stationary, and multi-drug-resistant clinical strains. Therefore, our study reveals the ability of cholic acid-derived amphiphiles to clear intracellular bacteria and Salmonella-mediated gut infection and inflammation.
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