Microplate-based surface area assay for rapid phenotypic antibiotic susceptibility testing

被引:26
作者
Flentie, Kelly [1 ]
Spears, Benjamin R. [1 ]
Chen, Felicia [1 ]
Purmort, Nathan B. [1 ]
DaPonte, Kayla [1 ]
Viveiros, Emma [1 ]
Phelan, Nicholas [1 ]
Krebill, Cicely [1 ]
Flyer, Alec N. [1 ]
Hooper, David C. [2 ,3 ]
Smalley, David L. [4 ]
Ferraro, Mary Jane [2 ,3 ]
Vacic, Aleksandar [1 ]
Stern, Eric [1 ]
机构
[1] Selux Diagnost Inc, 56 Roland St,Suite 206, Charlestown, MA 02129 USA
[2] Massachusetts Gen Hosp, 55 Fruit St, Boston, MA 02114 USA
[3] Harvard Med Sch, 25 Shattuck St, Boston, MA 02115 USA
[4] Amer Esoter Labs, Century Ctr Cove 1701, Memphis, TN 38134 USA
关键词
IDENTIFICATION; INFECTIONS;
D O I
10.1038/s41598-018-35916-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Rapid delivery of proper antibiotic therapies to infectious disease patients is essential for improving patient outcomes, decreasing hospital lengths-of-stay, and combating the antibiotic resistance epidemic. Antibiotic stewardship programs are designed to address these issues by coordinating hospital efforts to rapidly deliver the most effective antibiotics for each patient, which requires bacterial identification and antimicrobial susceptibility testing (AST). Despite the clinical need for fast susceptibility testing over a wide range of antibiotics, conventional phenotypic AST requires overnight incubations, and new rapid phenotypic AST platforms restrict the number of antibiotics tested for each patient. Here, we introduce a novel approach to AST based on signal amplification of bacterial surfaces that enables phenotypic AST within 5 hours for non-fastidious bacteria. By binding bacterial surfaces, this novel method allows more accurate measurements of bacterial replication in instances where organisms filament or swell in response to antibiotic exposure. Further, as an endpoint assay performed on standard microplates, this method should enable parallel testing of more antibiotics than is currently possible with available automated systems. This technology has the potential to revolutionize clinical practice by providing rapid and accurate phenotypic AST data for virtually all available antibiotics in a single test.
引用
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页数:9
相关论文
共 27 条
[1]  
[Anonymous], MICROBE MAG
[2]  
[Anonymous], 2018, CDC FDA ANT RES IS B
[3]  
Brownson R.C., 2017, Evidence-Based Public Health
[4]   Beta-Lactam Antibiotics Induce a Lethal Malfunctioning of the Bacterial Cell Wall Synthesis Machinery [J].
Cho, Hongbaek ;
Uehara, Tsuyoshi ;
Bernhardt, Thomas G. .
CELL, 2014, 159 (06) :1300-1311
[5]   Direct, rapid antimicrobial susceptibility test from positive blood cultures based on microscopic imaging analysis [J].
Choi, Jungil ;
Jeong, Hyun Yong ;
Lee, Gi Yoon ;
Han, Sangkwon ;
Han, Shinhun ;
Jin, Bonghwan ;
Lim, Taegeun ;
Kim, Shin ;
Kim, Dong Young ;
Kim, Hee Chan ;
Kim, Eui-Chong ;
Song, Sang Hoon ;
Kim, Taek Soo ;
Kwon, Sunghoon .
SCIENTIFIC REPORTS, 2017, 7
[6]  
CLSI, 2018, M07 CLSI, V11th
[7]  
Crowther JR., 2000, Methods in Molecular Biology, V149, P1, DOI [10.1385/1592590497, DOI 10.1385/1592590497]
[8]   Balancing Enthusiasm for Innovative Technologies with Optimizing Value: An Approach to Adopt New Laboratory Tests for Infectious Diseases Using Bloodstream Infections as Exemplar [J].
Culbreath, Karissa ;
Petti, Cathy A. .
OPEN FORUM INFECTIOUS DISEASES, 2015, 2 (02)
[9]   Cellular Stress Induced by Resazurin Leads to Autophagy and Cell Death via Production of Reactive Oxygen Species and Mitochondrial Impairment [J].
Erikstein, Bjarte S. ;
Hagland, Hanne R. ;
Nikolaisen, Julie ;
Kulawiec, Mariola ;
Singh, Keshav K. ;
Gjertsen, Bjorn T. ;
Tronstad, Karl J. .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2010, 111 (03) :574-584
[10]   Clinical and economic impact of rapid reporting of bacterial identification and antimicrobial susceptibility results of the most frequently processed specimen types [J].
Galar, A. ;
Yuste, J. R. ;
Espinosa, M. ;
Guillen-Grima, F. ;
Hernaez-Crespo, S. ;
Leiva, J. .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2012, 31 (09) :2445-2452