Paper-based PCR method development, validation and application for microbial detection

Abstract Background The analysis of the quality of food is important to protect humans from food-borne or food-based illnesses caused by pathogens, such as bacteria, fungi, viruses, and protozoa. Rapid identification of these pathogens is critical to ensure food safety. Various detection and identif...

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Main Authors: Amruta Patil-Joshi, B. E. Rangaswamy, Anjali Apte-Deshpande
Format: Article
Language:English
Published: SpringerOpen 2021-03-01
Series:Journal of Genetic Engineering and Biotechnology
Subjects:
PCR
Online Access:https://doi.org/10.1186/s43141-020-00110-1
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spelling doaj-5ff99d7ff1654995a1f08fdcd2c2f1572021-03-11T12:46:59ZengSpringerOpenJournal of Genetic Engineering and Biotechnology2090-59202021-03-0119111010.1186/s43141-020-00110-1Paper-based PCR method development, validation and application for microbial detectionAmruta Patil-Joshi0B. E. Rangaswamy1Anjali Apte-Deshpande2Department of Biotechnology, BIETDepartment of Biotechnology, BIETCentral Dogma Pvt Ltd.Abstract Background The analysis of the quality of food is important to protect humans from food-borne or food-based illnesses caused by pathogens, such as bacteria, fungi, viruses, and protozoa. Rapid identification of these pathogens is critical to ensure food safety. Various detection and identification strategies exist; however, they are laborious and time consuming and hence the detection takes longer time. The aim of this study was to develop the specific and fast method for the detection of contaminants in milk. Results In this study, we have developed a simple paper-based PCR method with minimum sample preparation process. The 16S rDNA universal primers were used for the detection of bacterial contaminants. LacZ primers were used for coliform detection which causes serious illness and hence their detection is crucial. ITS region primers were used for fungal detection. The most unique thing about this study is use of Whatman paper no. 1 as sample carrier material. We developed and validated the paper-based PCR method and used it for the detection of microbes and coliforms using milk as a representative sample. Conclusion We evaluated this method for its suitability in the detection of contaminant microbes using different milk samples. The paper-based method could successfully detect contaminants in the milk samples and the results were comparable to the traditional microbial detection method. The traditional microbiological method takes at least 18–20 h for detecting the presence of microbes in any sample but the developed paper-based PCR method can confirm the microbial presence in 2–3 h. This is very promising especially in the testing where sample sterility is crucial.https://doi.org/10.1186/s43141-020-00110-1ColiformsMilk samplePCRRapid testWhatman paper
collection DOAJ
language English
format Article
sources DOAJ
author Amruta Patil-Joshi
B. E. Rangaswamy
Anjali Apte-Deshpande
spellingShingle Amruta Patil-Joshi
B. E. Rangaswamy
Anjali Apte-Deshpande
Paper-based PCR method development, validation and application for microbial detection
Journal of Genetic Engineering and Biotechnology
Coliforms
Milk sample
PCR
Rapid test
Whatman paper
author_facet Amruta Patil-Joshi
B. E. Rangaswamy
Anjali Apte-Deshpande
author_sort Amruta Patil-Joshi
title Paper-based PCR method development, validation and application for microbial detection
title_short Paper-based PCR method development, validation and application for microbial detection
title_full Paper-based PCR method development, validation and application for microbial detection
title_fullStr Paper-based PCR method development, validation and application for microbial detection
title_full_unstemmed Paper-based PCR method development, validation and application for microbial detection
title_sort paper-based pcr method development, validation and application for microbial detection
publisher SpringerOpen
series Journal of Genetic Engineering and Biotechnology
issn 2090-5920
publishDate 2021-03-01
description Abstract Background The analysis of the quality of food is important to protect humans from food-borne or food-based illnesses caused by pathogens, such as bacteria, fungi, viruses, and protozoa. Rapid identification of these pathogens is critical to ensure food safety. Various detection and identification strategies exist; however, they are laborious and time consuming and hence the detection takes longer time. The aim of this study was to develop the specific and fast method for the detection of contaminants in milk. Results In this study, we have developed a simple paper-based PCR method with minimum sample preparation process. The 16S rDNA universal primers were used for the detection of bacterial contaminants. LacZ primers were used for coliform detection which causes serious illness and hence their detection is crucial. ITS region primers were used for fungal detection. The most unique thing about this study is use of Whatman paper no. 1 as sample carrier material. We developed and validated the paper-based PCR method and used it for the detection of microbes and coliforms using milk as a representative sample. Conclusion We evaluated this method for its suitability in the detection of contaminant microbes using different milk samples. The paper-based method could successfully detect contaminants in the milk samples and the results were comparable to the traditional microbial detection method. The traditional microbiological method takes at least 18–20 h for detecting the presence of microbes in any sample but the developed paper-based PCR method can confirm the microbial presence in 2–3 h. This is very promising especially in the testing where sample sterility is crucial.
topic Coliforms
Milk sample
PCR
Rapid test
Whatman paper
url https://doi.org/10.1186/s43141-020-00110-1
work_keys_str_mv AT amrutapatiljoshi paperbasedpcrmethoddevelopmentvalidationandapplicationformicrobialdetection
AT berangaswamy paperbasedpcrmethoddevelopmentvalidationandapplicationformicrobialdetection
AT anjaliaptedeshpande paperbasedpcrmethoddevelopmentvalidationandapplicationformicrobialdetection
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