Rapid High-Throughput Discovery of Molecules With Antimicrobial Activity From Natural Products Enabled by a Nanoliter Matrix SlipChip

被引:0
作者
Wang, Qi [1 ,2 ]
Wang, Mengru [3 ,4 ]
Lyu, Weiyuan [2 ]
Li, Xiang [2 ]
Xu, Lei [2 ]
Qin, Yuyao [1 ]
Ren, Yan'an [2 ]
Deng, Zixin [1 ]
Tao, Meifeng [1 ]
Xiao, Weilie [3 ,4 ]
Shen, Feng [2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, State Key Lab Microbial Metab, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Biomed Engn, Shanghai 200030, Peoples R China
[3] Yunnan Univ, Yunnan Res & Dev Ctr Nat Prod, Key Lab Med Chem Nat Resource, Minist Educ,Yunnan Characterist Plant Extract Lab,, Kunming 650091, Peoples R China
[4] Yunnan Univ, Sch Chem Sci & Technol, Kunming 650091, Peoples R China
来源
SMALL METHODS | 2025年
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
antimicrobial resistance; high-throughput screening; lab on chip; microfluidics; MRSA; natural products; SlipChip; RESISTANCE;
D O I
10.1002/smtd.202402045
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Improper use of antibiotics has led to the development of antimicrobial resistance, or "superbugs," outpacing the discovery of new antibiotics. The lack of rapid, high-throughput screening methods is a major bottleneck in discovery novel antibiotics. Traditional methods consume significant amounts of samples, making it challenging to discover new antibiotics from limited natural product extracts. Here, a rapid, high-throughput screening method is reported for natural products with antimicrobial activity enabled by a nanoliter matrix SlipChip (nm-SlipChip). This nm-SlipChip creates a screening matrix with nanoliter droplets for 100 drug candidate-bacterium combinations. The effectiveness of candidate antibiotics is assessed by analyzing microbial phenotypic changes. This nm-SlipChip reduces sample consumption by over 5000-fold and shortens the detection time to three hours. Twenty compounds isolated from Callicarpa integerrima were tested against 10 pathogenic bacteria and identified two previously unreported clerodane diterpenes with activity against methicillin-resistant Staphylococcus aureus (MRSA). Molecular docking and fluorescence probe experiments reveals that their antimicrobial effect results from disruption of bacterial cell membranes and biofilms. The nm-SlipChip provides an effective method for discovering new antimicrobial drugs from natural sources, vital in combating antibiotic resistance.
引用
收藏
页数:11
相关论文
共 54 条
[1]   Massively multiplexed nucleic acid detection with Cas13 [J].
Ackerman, Cheri M. ;
Myhrvold, Cameron ;
Thakku, Sri Gowtham ;
Freije, Catherine A. ;
Metsky, Hayden C. ;
Yang, David K. ;
Ye, Simon H. ;
Boehm, Chloe K. ;
Kosoko-Thoroddsen, Tinna-Solveig F. ;
Kehe, Jared ;
Nguyen, Tien G. ;
Carter, Amber ;
Kulesa, Anthony ;
Barnes, John R. ;
Dugan, Vivien G. ;
Hung, Deborah T. ;
Blainey, Paul C. ;
Sabeti, Pardis C. .
NATURE, 2020, 582 (7811) :277-+
[2]   Organ-on-chip models for infectious disease research [J].
Alonso-Roman, Raquel ;
Mosig, Alexander S. ;
Figge, Marc Thilo ;
Papenfort, Kai ;
Eggeling, Christian ;
Schacher, Felix H. ;
Hube, Bernhard ;
Gresnigt, Mark S. .
NATURE MICROBIOLOGY, 2024, 9 (04) :891-904
[3]  
[Anonymous], 2021, Clinical and Laboratory Standards Institute (CLSI) guideline C64: quantitative measurement of proteins and peptides by mass spectrometry, V1st
[4]   Staphylococcus aureus biofilms Properties, regulation and roles in human disease [J].
Archer, Nathan K. ;
Mazaitis, Mark J. ;
Costerton, J. William ;
Leid, Jeff G. ;
Powers, Mary Elizabeth ;
Shirtliff, Mark E. .
VIRULENCE, 2011, 2 (05) :445-459
[5]   Natural products in drug discovery: advances and opportunities [J].
Atanasov, Atanas G. ;
Zotchev, Sergey B. ;
Dirsch, Verena M. ;
Supuran, Claudiu T. .
NATURE REVIEWS DRUG DISCOVERY, 2021, 20 (03) :200-216
[6]   Technologies to address antimicrobial resistance [J].
Baker, Stephen J. ;
Payne, David J. ;
Rappuoli, Rino ;
De Gregorio, Ennio .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (51) :12887-12895
[7]  
BAUER AW, 1966, AM J CLIN PATHOL, V45, P493
[8]   Callicarpanes A-L, Twelve New Clerodane Diterpenoids with NLRP3 Inflammasome Inhibitory Activity from Callicarpa integerrima [J].
Bi, De-Wen ;
Zhao, Ying-Xin ;
Qiu, Xiong ;
Zhang, Xue-Cong ;
Zhou, Ya-Ling ;
Zeb, Muhammad Aurang ;
Pang, Wen-Hui ;
Li, Rui ;
Wang, Meng-Ru ;
Cheng, Bin ;
Zhang, Jing-Jing ;
Zhang, Xing-Jie ;
Li, Xiao-Li ;
Zhang, Rui-Han ;
Xiao, Wei-Lie .
CHEMISTRY & BIODIVERSITY, 2023, 20 (01)
[9]   Visualization of metabolites and microbes at high spatial resolution using MALDI mass spectrometry imaging and in situ fluorescence labeling [J].
Bourceau, Patric ;
Geier, Benedikt ;
Suerdieck, Vincent ;
Bien, Tanja ;
Soltwisch, Jens ;
Dreisewerd, Klaus ;
Liebeke, Manuel .
NATURE PROTOCOLS, 2023, 18 (10) :3050-3079
[10]   A Clerodane Diterpene from Callicarpa americana Resensitizes Methicillin-Resistant Staphylococcus aureus to β-Lactam Antibiotics [J].
Dettweiler, Micah ;
Melander, Roberta J. ;
Porras, Gina ;
Risener, Caitlin ;
Marquez, Lewis ;
Samarakoon, Tharanga ;
Melander, Christian ;
Quave, Cassandra L. .
ACS INFECTIOUS DISEASES, 2020, 6 (07) :1667-1673