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Monitoring food pathogens: Novel instrumentation for cassette PCR testing

In this manuscript, we report the design and development of a fast, reliable instrument to run gel-based cassette polymerase chain reactions (PCR). Here termed the GelCycler Mark II, our instrument is a miniaturized molecular testing system that is fast, low cost and sensitive. Cassette PCR utilizes...

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Detalles Bibliográficos
Autores principales: Hunt, Darin, Figley, Curtis, Manage, Dammika P., Lauzon, Jana, Figley, Rachel, Pilarski, Linda M., McMullen, Lynn M., Pilarski, Patrick M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945031/
https://www.ncbi.nlm.nih.gov/pubmed/29746561
http://dx.doi.org/10.1371/journal.pone.0197100
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author Hunt, Darin
Figley, Curtis
Manage, Dammika P.
Lauzon, Jana
Figley, Rachel
Pilarski, Linda M.
McMullen, Lynn M.
Pilarski, Patrick M.
author_facet Hunt, Darin
Figley, Curtis
Manage, Dammika P.
Lauzon, Jana
Figley, Rachel
Pilarski, Linda M.
McMullen, Lynn M.
Pilarski, Patrick M.
author_sort Hunt, Darin
collection PubMed
description In this manuscript, we report the design and development of a fast, reliable instrument to run gel-based cassette polymerase chain reactions (PCR). Here termed the GelCycler Mark II, our instrument is a miniaturized molecular testing system that is fast, low cost and sensitive. Cassette PCR utilizes capillary reaction units that carry all reagents needed for PCR, including primers and Taq polymerase, except the sample, which is loaded at the time of testing. Cassette PCR carries out real time quantitative PCR followed by melt curve analysis (MCA) to verify amplicon identity at the expected melt temperature (T(m)). The cassette PCR technology is well developed, particularly for detecting pathogens, and has been rigorously validated for detecting pathogenic Escherichia coli in meat samples. However, the work has been hindered by the lack of a robust and stable instrument to carry out the PCR, which requires fast and accurate temperature regulation, improved light delivery and fluorescent recording, and faster PCR reactions that maintain a high sensitivity of detection. Here, we report design and testing of a new instrument to address these shortcomings and to enable standardized testing by cassette PCR and commercial manufacture of a robust and accurate instrument that can be mass produced to deliver consistent performance. As a corollary to our new instrument development, we also report the use of an improved design approach using a machined aluminum cassette to meet the new instrument standards, prevent any light bleed across different trenches in each cassette, and allow testing of a larger number of samples for more targets in a single run. The GelCycler Mark II can detect and report E. coli contamination in 41 minutes. Sample positives are defined in as having a melt curve comparable to the internal positive control, with peak height exceeding that of the internal negative control. In a fractional analysis, as little as 1 bacterium per capillary reaction unit is directly detectable, with no enrichment step, in 35 cycles of PCR/MCA, in a total time of 53 minutes, making this instrument and technology among the very best for speed and sensitivity in screening food for pathogenic contamination.
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spelling pubmed-59450312018-05-25 Monitoring food pathogens: Novel instrumentation for cassette PCR testing Hunt, Darin Figley, Curtis Manage, Dammika P. Lauzon, Jana Figley, Rachel Pilarski, Linda M. McMullen, Lynn M. Pilarski, Patrick M. PLoS One Research Article In this manuscript, we report the design and development of a fast, reliable instrument to run gel-based cassette polymerase chain reactions (PCR). Here termed the GelCycler Mark II, our instrument is a miniaturized molecular testing system that is fast, low cost and sensitive. Cassette PCR utilizes capillary reaction units that carry all reagents needed for PCR, including primers and Taq polymerase, except the sample, which is loaded at the time of testing. Cassette PCR carries out real time quantitative PCR followed by melt curve analysis (MCA) to verify amplicon identity at the expected melt temperature (T(m)). The cassette PCR technology is well developed, particularly for detecting pathogens, and has been rigorously validated for detecting pathogenic Escherichia coli in meat samples. However, the work has been hindered by the lack of a robust and stable instrument to carry out the PCR, which requires fast and accurate temperature regulation, improved light delivery and fluorescent recording, and faster PCR reactions that maintain a high sensitivity of detection. Here, we report design and testing of a new instrument to address these shortcomings and to enable standardized testing by cassette PCR and commercial manufacture of a robust and accurate instrument that can be mass produced to deliver consistent performance. As a corollary to our new instrument development, we also report the use of an improved design approach using a machined aluminum cassette to meet the new instrument standards, prevent any light bleed across different trenches in each cassette, and allow testing of a larger number of samples for more targets in a single run. The GelCycler Mark II can detect and report E. coli contamination in 41 minutes. Sample positives are defined in as having a melt curve comparable to the internal positive control, with peak height exceeding that of the internal negative control. In a fractional analysis, as little as 1 bacterium per capillary reaction unit is directly detectable, with no enrichment step, in 35 cycles of PCR/MCA, in a total time of 53 minutes, making this instrument and technology among the very best for speed and sensitivity in screening food for pathogenic contamination. Public Library of Science 2018-05-10 /pmc/articles/PMC5945031/ /pubmed/29746561 http://dx.doi.org/10.1371/journal.pone.0197100 Text en © 2018 Hunt et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hunt, Darin
Figley, Curtis
Manage, Dammika P.
Lauzon, Jana
Figley, Rachel
Pilarski, Linda M.
McMullen, Lynn M.
Pilarski, Patrick M.
Monitoring food pathogens: Novel instrumentation for cassette PCR testing
title Monitoring food pathogens: Novel instrumentation for cassette PCR testing
title_full Monitoring food pathogens: Novel instrumentation for cassette PCR testing
title_fullStr Monitoring food pathogens: Novel instrumentation for cassette PCR testing
title_full_unstemmed Monitoring food pathogens: Novel instrumentation for cassette PCR testing
title_short Monitoring food pathogens: Novel instrumentation for cassette PCR testing
title_sort monitoring food pathogens: novel instrumentation for cassette pcr testing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945031/
https://www.ncbi.nlm.nih.gov/pubmed/29746561
http://dx.doi.org/10.1371/journal.pone.0197100
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