Award Abstract # 1133746
Development of aptamer nanosensors for detection of Staphylococcus aureus

NSF Org: CBET
Division of Chemical, Bioengineering, Environmental, and Transport Systems
Recipient: VIRGINIA POLYTECHNIC INSTITUTE & STATE UNIVERSITY
Initial Amendment Date: August 4, 2011
Latest Amendment Date: August 24, 2013
Award Number: 1133746
Award Instrument: Continuing Grant
Program Manager: William Cooper
CBET
 Division of Chemical, Bioengineering, Environmental, and Transport Systems
ENG
 Directorate for Engineering
Start Date: September 1, 2011
End Date: August 31, 2015 (Estimated)
Total Intended Award Amount: $346,134.00
Total Awarded Amount to Date: $396,134.00
Funds Obligated to Date: FY 2011 = $165,566.00
FY 2012 = $88,963.00

FY 2013 = $141,605.00
History of Investigator:
  • Peter Vikesland (Principal Investigator)
    pvikes@vt.edu
  • Amy Pruden (Co-Principal Investigator)
Recipient Sponsored Research Office: Virginia Polytechnic Institute and State University
300 TURNER ST NW
BLACKSBURG
VA  US  24060-3359
(540)231-5281
Sponsor Congressional District: 09
Primary Place of Performance: Virginia Polytechnic Institute and State University
VA  US  24061-0001
Primary Place of Performance
Congressional District:
09
Unique Entity Identifier (UEI): QDE5UHE5XD16
Parent UEI: X6KEFGLHSJX7
NSF Program(s): SSA-Special Studies & Analysis,
EnvE-Environmental Engineering,
International Research Collab
Primary Program Source: 01001112DB NSF RESEARCH & RELATED ACTIVIT
01001213DB NSF RESEARCH & RELATED ACTIVIT

01001314DB NSF RESEARCH & RELATED ACTIVIT
Program Reference Code(s): 015E, 021E, 145E, 5946, 5979
Program Element Code(s): 138500, 144000, 729800
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.041

ABSTRACT

PI:Vikesland
Proposal Number:1133746
Nanoparticle based assays are of growing interest for the in vitro and in vivo detection of pathogens because of their potential utility in highly sensitive and rapid field monitoring. Recently aptamers oligonucleotide strands that bind to biological targets with high affinity and selectivity, have been proposed as alternative recognition elements for biomolecules, pharmaceuticals, and whole cells. Although aptamer functionalized nanomaterials have shown great utility for detection of these and other analytes there are few reports of the use of aptamer-functionalized nanoparticles for intact pathogen detection. This project will produce aptamer functionalized gold nanoparticles Apt AuNPs for quantification of Staphylococcus aureus as a model emerging environmental pathogen of concern. It is the PI's hypothesis that coupling of the specificity imparted by an aptamer with the sensitivity achieved via surface plasmon facilitated signal transduction will produce sensor platforms that will be robust and readily translatable to field applications. To this end, they have proposed a design for Apt-AuNP constructs such that their sensitivity and specificity is maximized. It is noted that past studies illustrating the underlying fundamental applicability of aptamer functionalized nanoparticles for sensor applications have not necessarily produced nanoparticles that fully retain the specificity of the aptamer. In particular the PI contends that aptamer binding density is often not considered, even though it is well established that aptamer conformation must change in response to a recognition event. They propose a systematic approach to evaluate the role of surface density on aptamer specificity. Four research tasks have been identified: Task 1: Apt-AuNP of varying aptamer identity and surface density will be produced and characterized. Task 2: Apt-AuNP specificity will be assessed using a colorimetric screening assay. Task 3: Apt-AuNP sensitivity will be determined using a surface enhanced Raman spectroscopic assay. Task 4: The field capabilities of Apt-AuNP will be evaluated using a portable Raman spectrophotometer.
This project is novel in that it will be the first to develop an aptamer functionalized
nanoparticle for pathogen detection. Prior to this effort, nanomaterial enabled biosensors for pathogens have relied almost exclusively on antibodies to provide assay specificity. The PI's strategy for the design of the Apt-AuNP particles utilizes a fundamental approach that will systematically consider how the different components of the Apt-AuNP construct affect aptamer sensitivity. The researchers believe this systematic engineering-science based approach will be emulated by others when they undertake the design of aptamer functionalized nanoparticles and as such has significant transformative potential.
Methicillin resistant S. aureus MRSA is the causative agent for a growing number of deadly disease outbreaks both within the United States as well as worldwide. Although this organism is historically associated with hospitals, recently, environmental outbreaks of MRSA as well as its detection in wastewater effluent have inaugurated MRSA as an emerging environmental pathogen of concern. Unfortunately existing protocols for detection of MRSA and other S. aureus strains are slow and not easily translatable to field applications. The proposed biosensor will address the global need for improved S. aureus detection specifically while providing a framework for the development of other aptamer based probes in the future.
Beyond a contribution to pressing research needs in nanotechnology environmental health and
safety, the project will build upon an existing educational outreach component, the Nanotechnology Educational and Environmental Outreach NEEO Program, that has been designed to train the next generation of environmental professionals in understanding and quantifying the effects of emerging technologies on human and environmental health. In this program, members of the Virginia Tech Environmental BioNanotechnology Laboratory research team are working in partnership with the Western Virginia Public Education Consortium to develop a series of extramurally funded internships that enable middle school educators and students to shadow the research team and learn about new methods for observing nanoscale phenomena occurring at biological and environmental interfaces. These internships are intended to provide opportunities for the development of new technology inspired curricula for educators as well as training and professional preparation for students.

PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH

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Haoran Wei,Seyyed M. Hossein Abtahi, and Peter J. Vikesland "Plasmonic Colorimetric and SERS Sensors for Environmental Analysis" Environmental Science: Nano , v.2 , 2015 , p.120 10.1039/C4EN00211C
Leng, W.L. and Vikesland, P.J. "MGITC Facilitated Formation of AuNP Multimers" Langmuir , v.30 , 2014 , p.8342 10.1021/la501807n
Weinan Leng and Peter Vikesland "MGITC Facilitated Formation of AuNP Multimers" Langmuir , v.30 , 2014 , p.8342 10.1021/la501807n
Weinan Leng and Peter Vikesland "Nanoclustered gold honeycombs for surface-enhanced Raman scattering" Analytical Chemistry , 2013 , p.1342 10.1021/ac301028w
Weinan Leng, Paramjeet Pati, and Peter Vikesland "Room Temperature Seed Mediated Growth of Gold Nanoparticles: Mechanistic Investigations and Life Cycle Assessment" Environmental Science: Nano , v.2 , 2015 , p.440 10.1039/C5EN00026B

PROJECT OUTCOMES REPORT

Disclaimer

This Project Outcomes Report for the General Public is displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed in this Report are those of the PI and do not necessarily reflect the views of the National Science Foundation; NSF has not approved or endorsed its content.

Staphylococcus aureus is one of the leading causes of a wide range of opportunistic infections in humans. Because of its increased resistance to multiple antibiotics and frequent detection in environmental matrices such as wastewater, S. aureus is considered an emerging environmental pathogen of concern. In this project we sought to develop rapid detection approaches for both S. aureus as well as the antibiotic resistance gene mecA. These detection strategies combine the sensitivity enabled by nanotechnology (i.e., the capacity to find a needle in a haystack) with the specificity of DNA (i.e., the capacity to identify the composition of the needle). By using gold nanoparticles that are surface functionalized either with aptamers (sequences of single strand DNA (ssDNA) that produce 3D structures that specifically bind to surface groups on S. aureus) or ssDNA specifically designed to bind to mecA we are able to detect these analytes quickly. Our nanoparticle probes interact with the target and we then utilize either light or Raman spectroscopy to quantify the target.

 

The intellectual outcomes of this effort can be summarized as follows:

1)    We illustrate that aptamer based nanotechnology approaches have merit for use in environmental matrices. Challenges in probe production and non-specific (i.e., off-target) binding, however, must be fully addressed prior to widespread use of these types of probes.

2)    Antibiotic resistance gene (ARG) detection is possible using nanoparticle based probes. To date we have illustrated the capacity for these probes to detect the ARG mecA and this approach should be extended to additional ARG types.

3)    We have developed alternative room-temperature based approaches for the synthesis of gold nanoparticles that have a smaller environmental footprint than syntheses performed at elevated temperature.

The broader impacts of this effort are our illustration of the potential utility of these probes for environmental application. In addition, this project supported the research and training of two female graduate students and one female undergraduate student.

 


Last Modified: 11/28/2015
Modified by: Peter J Vikesland

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