Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/168391
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dc.titleRapid and in-situ detection of fecal indicator bacteria in water using simple DNA extraction and portable loop-mediated isothermal amplification (LAMP) PCR methods
dc.contributor.authorBAE SUNG WOO
dc.contributor.authorSeunguk Lee
dc.contributor.authorValerie Khoo Si Ling
dc.contributor.authorCarl Angelo Dulatre Medriano
dc.contributor.authorTaewoo Lee
dc.contributor.authorSung-Yong Park
dc.date.accessioned2020-05-22T02:32:47Z
dc.date.available2020-05-22T02:32:47Z
dc.date.issued2019-05-21
dc.identifier.citationBAE SUNG WOO, Seunguk Lee, Valerie Khoo Si Ling, Carl Angelo Dulatre Medriano, Taewoo Lee, Sung-Yong Park (2019-05-21). Rapid and in-situ detection of fecal indicator bacteria in water using simple DNA extraction and portable loop-mediated isothermal amplification (LAMP) PCR methods. ScholarBank@NUS Repository.
dc.identifier.issn0043-1354
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/168391
dc.description.abstractContamination of water by fecal matter and potential human enteric pathogens is a serious health concern. Microbiological water quality has been assessed by conventional culture-based methods of fecal indicator bacteria (FIB). Recently, molecular techniques for FIB have been introduced as alternative tools for rapid detection. However, such molecular techniques require a modern laboratory setting, expensive equipment, and skilled personnel. In this study, we developed a simple and rapid DNA extraction method based on a syringe filter without any specialized equipment. Furthermore, loop-mediated isothermal amplification (LAMP) PCR for fecal indicator bacteria (FIB) (i.e. E. coli and E. faecalis) was carried out using the DNA extracts from the syringe-filter based DNA extraction method. The efficiency of the extracted DNA from the syringe-filter based method was comparable to the results of the commercial kit method. We also tested fresh and marine-water collected directly from different locations in Singapore that were spiked with E. coli or E. faecalis. The LAMP assays combined with our DNA extraction method showed higher sensitivity and more tolerance to PCR inhibitors than that of conventional PCR methods. We further developed a portable LAMP device to conduct isothermal PCR reactions for rapid on-site measurement of FIB. As the color changes in the end point of the LAMP reaction can be observed with the naked eye, the portable LAMP device was easily operated and quick, obtaining results in 30 min. The simple, portable and user-friendly platform can be used as an initial screening for the rapid detection of the presence FIB in lower-resource settings. In conclusion, the portable LAMP device coupled with a syringe-filter based DNA extraction method enables us to detect the presence of FIB for assessing microbial water quality within 1 h without any sophisticated laboratory equipment or highly trained personne
dc.description.urihttps://www.sciencedirect.com/science/article/abs/pii/S0043135419304373
dc.publisherElsevier
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.typeArticle
dc.contributor.departmentCIVIL AND ENVIRONMENTAL ENGINEERING
dc.contributor.departmentMECHANICAL ENGINEERING
dc.published.statePublished
dc.grant.idMSRDP-P01
dc.grant.fundingagencyNational Research Foundation
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