| Literature DB >> 30669829 |
Kavita Yadav1,2, Prabhu Srinivas Yavvari3, Sanjay Pal1,4, Sandeep Kumar1,2, Deepakkumar Mishra1, Siddhi Gupta1, Madhurima Mitra1, Vijay Soni5, Neha Khare1, Priyanka Sharma6, Chittur V Srikanth7, Arti Kapil6, Archana Singh8, Vinay Kumar Nandicoori5, Avinash Bajaj1.
Abstract
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.Entities:
Year: 2019 PMID: 30669829 DOI: 10.1021/acs.bioconjchem.8b00880
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774