Direct single-cell antimicrobial susceptibility testing of Escherichia coli in urine using a ready-to-use 3D microwell array chip

被引:13
|
作者
Wu, Wenshuai [1 ]
Cai, Gaozhe [2 ]
Liu, Yang [3 ]
Suo, Yuanjie [1 ]
Zhang, Boran [4 ]
Jin, Wei [1 ,5 ]
Yu, Yinghua [6 ]
Mu, Ying [1 ]
机构
[1] Zhejiang Univ, Inst Cyber Syst & Control, Res Ctr Analyt Instrumentat, State Key Lab Ind Control Technol, Hangzhou 310027, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, State Key Lab Transducer Technol, Shanghai 200050, Peoples R China
[3] Beijing Inst Technol, Sch Mechatron Engn, Beijing 102401, Peoples R China
[4] Zhejiang Univ, Coll Civil Engn & Architecture, Dept Hydraul Engn, Hangzhou 310058, Peoples R China
[5] Zhejiang Univ, Huzhou Inst, Huzhou 313002, Peoples R China
[6] Xuzhou Med Univ, Dept Pathogen Biol & Immunol, Jiangsu Key Lab Immun & Metab, Xuzhou 221004, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
ANTIBIOTIC SUSCEPTIBILITY; BACTERIAL-GROWTH; DIGITAL PCR; RESISTANCE; DEVICE;
D O I
10.1039/d2lc01095j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Empirical antibiotic therapies are prescribed for treating uncomplicated urinary tract infections (UTIs) due to the long turnaround time of conventional antimicrobial susceptibility testing (AST), leading to the prevalence of multi-drug resistant pathogens. We present a ready-to-use 3D microwell array chip to directly conduct comprehensive AST of pathogenic agents in urine at the single-cell level. The developed device features a highly integrated 3D microwell array, offering a dynamic range from 10(2) to 10(7) CFU mL(-1), and a capillary valve-based flow distributor for flow equidistribution in dispensing channels and uniform sample distribution. The chip with pre-loaded reagents and negative pressure inside only requires the user to initiate AST by loading samples (similar to 3 s) and can work independently. We demonstrate an accessible sample-to-result workflow, including syringe filter-based bacteria separation and rapid single-cell AST on chip, which enables us to bypass the time-consuming bacteria isolation and pre-culture, speeding up the AST in similar to 3 h from 2 days of conventional methods. Moreover, the bacterial concentration and AST with minimum inhibitory concentrations can be assessed simultaneously to provide comprehensive information on infections. With further development for multiple antibiotic conditions, the Dsc-AST assay could contribute to timely prescription of targeted drugs for better patient outcomes and mitigation of the threat of drug-resistant bacteria.
引用
收藏
页码:2399 / 2410
页数:12
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