Enhanced Colorimetric Differentiation between Staphylococcus aureus and Pseudomonas aeruginosa Using a Shape-Encoded Sensor Hydrogel

被引:24
作者
Jia, Zhiyuan [1 ,2 ]
Gwynne, Lauren [3 ]
Sedgwick, Adam C. [4 ]
Mueller, Mareike [1 ,2 ]
Williams, George T. [3 ]
Jenkins, Andrew Toby A. [3 ]
James, Tony D. [3 ]
Schoenherr, Holger [1 ,2 ]
机构
[1] Univ Siegen, Dept Chem & Biol, Phys Chem 1, D-57076 Siegen, Germany
[2] Univ Siegen, Dept Chem & Biol, Res Ctr Micro & Nanochem & Engn C, D-57076 Siegen, Germany
[3] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
[4] Univ Texas Austin, Dept Chem, Austin, TX 78712 USA
基金
欧洲研究理事会; 英国工程与自然科学研究理事会; 英国医学研究理事会; 美国国家卫生研究院;
关键词
bacteria detection; bacteria differentiation; biosensors; fluorescent probe; hydrogels; N-SUCCINYL-CHITOSAN; PATHOGENIC BACTERIA; ELASTASE; IDENTIFICATION; ENZYMES; PROBE;
D O I
10.1021/acsabm.0c00403
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Herein, we demonstrate a combined fluorescent probe/shapeencoded hydrogel strategy for the fast, sensitive, and selective detection of bacterial species via their characteristic enzymes. A poly(vinyl alcohol) (PVA) hydrogel loaded with the fluorescent probe N,N'-(3-oxo-3H- spiro-[isobenzofuran-1,9'-xanthene]- 3',6'-diyl) bis(2,2,3,3,3-pentafluoropropanamide) (ACS-HNE) was designed for the detection of elastase, an enzyme produced by Pseudomonas aeruginosa. Likewise, a chitosan-derived hydrogel was loaded with the fluorescent probe 4-methylumbelliferyl-a-D-glucopyranoside (MUD) by entrapment for the selective detection of a-glucosidase, an enzyme produced by Staphylococcus aureus. For an observation time of 60 min, limits of detection (LODs) of <= 20 nM for elastase and <= 30 pM for alpha-glucosidase were obtained, which in the latter case is 3 orders of magnitude better than related chitosan systems with covalently coupled substrate. To illustrate the potential utility of these highly sensitive sensor hydrogels as a simple point-of-care test system, shaped hydrogel slabs representing the letters P and S were manufactured to detect P. aeruginosa and S. aureus, respectively. These shapes were shown to provide an additional unique color code under UV illumination corresponding to the characteristic enzyme produced by the corresponding bacteria. This study shows potential for the future development of an effective and simple point-of-care test for the rapid identification of bacterial species that can be operated by nonspecialists.
引用
收藏
页码:4398 / 4407
页数:10
相关论文
共 48 条
[11]   ACTIVATION OF AN ELASTASE PRECURSOR BY THE LASA GENE-PRODUCT OF PSEUDOMONAS-AERUGINOSA [J].
GOLDBERG, JB ;
OHMAN, DE .
JOURNAL OF BACTERIOLOGY, 1987, 169 (10) :4532-4539
[12]   Conventional and emerging detection techniques for pathogenic bacteria in food science: A review [J].
Hameed, Saima ;
Xie, Lijuan ;
Ying, Yibin .
TRENDS IN FOOD SCIENCE & TECHNOLOGY, 2018, 81 :61-73
[13]   GENETIC RECOMBINATION IN PSEUDOMONAS-AERUGINOSA [J].
HOLLOWAY, BW .
JOURNAL OF GENERAL MICROBIOLOGY, 1955, 13 (03) :572-581
[14]   Epidemiology and Treatment of Multidrug-Resistant and Extensively Drug-Resistant Pseudomonas aeruginosa Infections [J].
Horcajada, Juan P. ;
Montero, Milagro ;
Oliver, Antonio ;
Sorli, Luisa ;
Luque, Sonia ;
Gomez-Zorrilla, Silvia ;
Benito, Natividad ;
Grau, Santiago .
CLINICAL MICROBIOLOGY REVIEWS, 2019, 32 (04)
[15]   Multiplexed detection and differentiation of bacterial enzymes and bacteria by color-encoded sensor hydrogels [J].
Jia, Zhiyuan ;
Mueller, Mareike ;
Le Gall, Tony ;
Riool, Martijn ;
Mueller, Max ;
Zaat, Sebastian A. J. ;
Montier, Tristan ;
Schoenherr, Holger .
BIOACTIVE MATERIALS, 2021, 6 (12) :4286-4300
[16]   Protein Encapsulation: A Nanocarrier Approach to the Fluorescence Imaging of an Enzyme-Based Biomarker [J].
Jia, Zhiyuan ;
Han, Hai-Hao ;
Sedgwick, Adam C. ;
Williams, George T. ;
Gwynne, Lauren ;
Brewster, James T., II ;
Bull, Steven D. ;
Jenkins, A. Toby A. ;
He, Xiao-Peng ;
Schoenherr, Holger ;
Sessler, Jonathan L. ;
James, Tony D. .
FRONTIERS IN CHEMISTRY, 2020, 8
[17]   Cellular function of elastase in Pseudomonas aeruginosa:: role in the cleavage of nucleoside diphosphate kinase and in alginate synthesis [J].
Kamath, S ;
Kapatral, V ;
Chakrabarty, AM .
MOLECULAR MICROBIOLOGY, 1998, 30 (05) :933-941
[18]   Alkaline phosphatase-responsive fluorescent polymer probe coated surface for colorimetric bacteria detection [J].
Kang, Eun Bi ;
Mazrad, Zihnil Adha Islamy ;
Robby, Akhmad Irhas ;
In, Insik ;
Park, Sung Young .
EUROPEAN POLYMER JOURNAL, 2018, 105 :217-225
[19]   Detection of Pathogenic Biofilms with Bacterial Amyloid Targeting Fluorescent Probe, CDy11 [J].
Kim, Jun-Young ;
Sahu, Srikanta ;
Yau, Yin-Hoe ;
Wang, Xu ;
Shochat, Susana Geifman ;
Nielsen, Per Halkjaer ;
Dueholm, Morten Simonsen ;
Otzen, Daniel E. ;
Lee, Jungyeol ;
Delos Santos, May Margarette Salido ;
Yam, Joey Kuok Hoong ;
Kang, Nam-Young ;
Park, Sung-Jin ;
Kwon, Hawyoung ;
Seviour, Thomas ;
Yang, Liang ;
Givskov, Michael ;
Chang, Young-Tae .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (01) :402-407
[20]   FEATURES OF GOLD HAVING MICROMETER TO CENTIMETER DIMENSIONS CAN BE FORMED THROUGH A COMBINATION OF STAMPING WITH AN ELASTOMERIC STAMP AND AN ALKANETHIOL INK FOLLOWED BY CHEMICAL ETCHING [J].
KUMAR, A ;
WHITESIDES, GM .
APPLIED PHYSICS LETTERS, 1993, 63 (14) :2002-2004