Published February 2016 | Version Supplemental Material
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Sunlight-Activated Propidium Monoazide Pretreatment for Differentiation of Viable and Dead Bacteria by Quantitative Real-Time Polymerase Chain Reaction

Abstract

Polymerase chain reaction (PCR)-based methods have been developed and increasingly used for rapid and sensitive detection of pathogens in water samples to better protect public health. A propidium monoazide (PMA) pretreatment can help to differentiate between viable and dead cells, but the photoactivation of PMA normally requires the use of an energy-consuming halogen light, which is not suitable for off-the-grid applications. Herein, we investigate sunlight as an alternative light source. Our results suggest that sunlight can successfully activate PMA, and the sunlight-activated PMA pretreatment can effectively reduce the amplification of DNA derived from dead cells in PCR assays. Potentially, a sunlight-activated PMA pretreatment unit can be integrated into a lab-on-a-chip PCR device for off-the-grid microbial detection and quantification.

Additional Information

© 2016 American Chemical Society. Received: December 15, 2015; Revised: December 30, 2015; Accepted: January 5, 2016; Publication Date (Web): January 5, 2016. The authors acknowledge the financial support of the Bill and Melinda Gates Foundation (BMGF OPP1111246). The authors declare no competing financial interest.

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Additional details

Identifiers

Eprint ID
63542
DOI
10.1021/acs.estlett.5b00348
Resolver ID
CaltechAUTHORS:20160111-103924491

Funding

Bill and Melinda Gates Foundation
OPP1111246

Dates

Created
2016-01-13
Created from EPrint's datestamp field
Updated
2021-11-10
Created from EPrint's last_modified field