Nano-biofilm Arrays as a Novel Universal Platform for Microscale Microbial Culture and High-Throughput Downstream Applications
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Published:2019-07-24
Issue:14
Volume:26
Page:2529-2535
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ISSN:0929-8673
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Container-title:Current Medicinal Chemistry
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language:en
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Short-container-title:CMC
Author:
Srinivasan Anand1, Ramasubramanian Anand K.2, Lopez-Ribot José L.3
Affiliation:
1. BioBridge Global, San Antonio, TX, 78201, United States 2. Department of Biomedical, Chemical and Materials Engineering, San Jos�© State University, San Jos�©, CA, 95192, United States 3. Department of Biology and South Texas Center for Emerging Infectious Diseases, The University of Texas at San Antonio, San Antonio, TX, 78249, United States
Abstract
Biofilms are the predominant mode of microbial growth and it is now fully accepted that a
majority of infections in humans are associated with a biofilm etiology. Biofilms are defined as attached
and structured microbial communities surrounded by a protective exopolymeric matrix. Importantly,
sessile microorganisms growing within a biofilm are highly resistant to antimicrobial agents.
Thus, there is an urgent need to develop new and improved anti-biofilm therapies. Unfortunately, most
of the current techniques for in-vitro biofilm formation are not compatible with high throughput screening
techniques that can speed up discovery of new drugs with anti-biofilm activity. To try to overcome
this major impediment, our group has developed a novel technique consisting of micro-scale culture of
microbial biofilms on a microarray platform. Using this technique, hundreds to thousands of microbial
biofilms, each with a volume of approximately 30-50 nanolitres, can be simultaneously formed on a
standard microscope slide. Despite more than three orders of magnitude of miniaturization over conventional
biofilms, these nanobiofilms display similar growth, structural and phenotypic properties,
including antibiotic drug resistance. These nanobiofilm chips are amenable to automation, drastically
reducing assay volume and costs. This technique platform allows for true high-throughput screening in
search for new anti-biofilm drugs.
Funder
National Institute of Dental and Craniofacial Research University of Texas at San Antonio; UTSA American Heart Association National Institutes of Health
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology,Molecular Medicine,Drug Discovery,Biochemistry,Organic Chemistry
Reference33 articles.
1. Costerton JW, Cheng KJ, Geesey GG, Ladd TI, Nickel JC, Dasgupta M, Marrie TJ. Annu Rev Microbiol, Bacterial biofilms in nature and disease.,, 1987, 41,, 435-464,[http://dx.doi.org/10.1146/annurev.mi.41.100187.002251]. [PMID: 3318676]. 2. Donlan RM. Emerg Infect Dis, Biofilms: Microbial life on surfaces.,, 2002, 8,, 881-890,[http://dx.doi.org/10.3201/eid0809.020063]. [PMID: 12194761]. 3. Costerton JW, Stewart PS, Greenberg EP. Science, Bacterial biofilms: a common cause of persistent infections.,, 1999, 284,, 1318-1322,[http://dx.doi.org/10.1126/science.284.5418.1318]. [PMID: 10334980]. 4. Donlan RM, Costerton JW. Clin Microbiol Rev, Biofilms: Survival mechanisms of clinically relevant microorganisms.,, 2002, 15,, 167-193,[http://dx.doi.org/10.1128/CMR.15.2.167-193.2002]. [PMID: 11932229]. 5. Darouiche RO. N Engl J Med, Treatment of infections associated with surgical implants.,, 2004, 350,, 1422-1429,[http://dx.doi.org/10.1056/NEJMra035415]. [PMID: 15070792].
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