Screening of natural compounds identifies ferutinin as an antibacterial and anti-biofilm compound

被引:6
作者
Gilbert-Girard, Shella [1 ]
Reigada, Ines [1 ]
Savijoki, Kirsi [1 ]
Yli-Kauhaluoma, Jari [2 ]
Fallarero, Adyary [1 ]
机构
[1] Univ Helsinki, Fac Pharm, Div Pharmaceut Biosci, Drug Res Program, Helsinki, Finland
[2] Univ Helsinki, Fac Pharm, Div Pharmaceut Chem & Technol, Drug Res Program, Helsinki, Finland
关键词
Antibacterial screening; anti-biofilm; ferutinin; natural products; Staphylococcus aureus; STAPHYLOCOCCUS-AUREUS; IN-VITRO; ANTIMICROBIAL ACTIVITY; CYTOTOXIC ACTIVITIES; DAUCANE SESQUITERPENES; HONOKIOL; MAGNOLOL; ORIDONIN; CONSTITUENTS; ISOHEXENYLNAPHTHAZARINS;
D O I
10.1080/08927014.2021.1971655
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Antibacterial screenings are most commonly targeted at planktonic bacteria but less effort is dedicated to the exploration of agents acting on biofilms. Here, a natural compounds library was screened against Staphylococcus aureus using a 384-well plate platform to identify compounds preventing biofilm formation. Five structurally diverse hits were selected for follow-up studies: honokiol, tschimganidin, ferutinin, oridonin and deoxyshikonin. The compounds were evaluated against different bacterial species for their capacity to prevent and disrupt biofilms. The development of resistance and cytotoxicity were also investigated. Ferutinin displayed the best antibacterial activity, with a minimum inhibitory, bactericidal and biofilm preventive concentration of 25 mu M against S. aureus. It efficiently disrupted pre-formed biofilms (over 5-log reduction of viable cells) and reduced biofilm formation on a catheter in the presence of neutrophils. This work provides new information on the antibacterial activity of five natural compounds and identified ferutinin as a promising candidate against S. aureus biofilms.
引用
收藏
页码:791 / 807
页数:17
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