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Deskilled and Rapid Drug-Resistant Gene Detection by Centrifugal Force-Assisted Thermal Convection PCR Device

Here we report the improved Cyclo olefin polymer (COP) microfluidic chip and polymerase chain reaction (PCR) amplification system for point-of-care testing (POCT) in rapid detection of Carbapenem-resistant Enterobacteriaceae (CRE). The PCR solution and thermal cycling is controlled by the relative g...

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Autores principales: Espulgar, Wilfred Villariza, Saito, Masato, Takahashi, Kazuya, Ushiro, Sakiko, Yamamoto, Norihisa, Akeda, Yukihiro, Hamaguchi, Shigeto, Tomono, Kazunori, Tamiya, Eiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916093/
https://www.ncbi.nlm.nih.gov/pubmed/33572363
http://dx.doi.org/10.3390/s21041225
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author Espulgar, Wilfred Villariza
Saito, Masato
Takahashi, Kazuya
Ushiro, Sakiko
Yamamoto, Norihisa
Akeda, Yukihiro
Hamaguchi, Shigeto
Tomono, Kazunori
Tamiya, Eiichi
author_facet Espulgar, Wilfred Villariza
Saito, Masato
Takahashi, Kazuya
Ushiro, Sakiko
Yamamoto, Norihisa
Akeda, Yukihiro
Hamaguchi, Shigeto
Tomono, Kazunori
Tamiya, Eiichi
author_sort Espulgar, Wilfred Villariza
collection PubMed
description Here we report the improved Cyclo olefin polymer (COP) microfluidic chip and polymerase chain reaction (PCR) amplification system for point-of-care testing (POCT) in rapid detection of Carbapenem-resistant Enterobacteriaceae (CRE). The PCR solution and thermal cycling is controlled by the relative gravitational acceleration (7G) only and is expected to pose minimal problem in operation by non-expert users. Detection is based on identifying the presence of carbapenemase encoding gene through the corresponding fluorescence signal after amplification. For preliminary tests, the device has been demonstrated to detect bla(IMP-6) from patients stool samples. From the prepared samples, 96.4 fg/µL was detected with good certainty within 15 min (~106 thermocycles,) which is significantly faster than the conventional culture plate method. Moreover, the device is expected to detect other target genes in parallel as determination of the presence of bla(NDM-1) and bla(OXA-23) from control samples has also been demonstrated. With the rising threat of drug-resistant bacteria in global healthcare, this technology can greatly aid the health sector by enabling the appropriate use of antibiotics, accelerating the treatment of carriers, and suppressing the spread.
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spelling pubmed-79160932021-03-01 Deskilled and Rapid Drug-Resistant Gene Detection by Centrifugal Force-Assisted Thermal Convection PCR Device Espulgar, Wilfred Villariza Saito, Masato Takahashi, Kazuya Ushiro, Sakiko Yamamoto, Norihisa Akeda, Yukihiro Hamaguchi, Shigeto Tomono, Kazunori Tamiya, Eiichi Sensors (Basel) Article Here we report the improved Cyclo olefin polymer (COP) microfluidic chip and polymerase chain reaction (PCR) amplification system for point-of-care testing (POCT) in rapid detection of Carbapenem-resistant Enterobacteriaceae (CRE). The PCR solution and thermal cycling is controlled by the relative gravitational acceleration (7G) only and is expected to pose minimal problem in operation by non-expert users. Detection is based on identifying the presence of carbapenemase encoding gene through the corresponding fluorescence signal after amplification. For preliminary tests, the device has been demonstrated to detect bla(IMP-6) from patients stool samples. From the prepared samples, 96.4 fg/µL was detected with good certainty within 15 min (~106 thermocycles,) which is significantly faster than the conventional culture plate method. Moreover, the device is expected to detect other target genes in parallel as determination of the presence of bla(NDM-1) and bla(OXA-23) from control samples has also been demonstrated. With the rising threat of drug-resistant bacteria in global healthcare, this technology can greatly aid the health sector by enabling the appropriate use of antibiotics, accelerating the treatment of carriers, and suppressing the spread. MDPI 2021-02-09 /pmc/articles/PMC7916093/ /pubmed/33572363 http://dx.doi.org/10.3390/s21041225 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Espulgar, Wilfred Villariza
Saito, Masato
Takahashi, Kazuya
Ushiro, Sakiko
Yamamoto, Norihisa
Akeda, Yukihiro
Hamaguchi, Shigeto
Tomono, Kazunori
Tamiya, Eiichi
Deskilled and Rapid Drug-Resistant Gene Detection by Centrifugal Force-Assisted Thermal Convection PCR Device
title Deskilled and Rapid Drug-Resistant Gene Detection by Centrifugal Force-Assisted Thermal Convection PCR Device
title_full Deskilled and Rapid Drug-Resistant Gene Detection by Centrifugal Force-Assisted Thermal Convection PCR Device
title_fullStr Deskilled and Rapid Drug-Resistant Gene Detection by Centrifugal Force-Assisted Thermal Convection PCR Device
title_full_unstemmed Deskilled and Rapid Drug-Resistant Gene Detection by Centrifugal Force-Assisted Thermal Convection PCR Device
title_short Deskilled and Rapid Drug-Resistant Gene Detection by Centrifugal Force-Assisted Thermal Convection PCR Device
title_sort deskilled and rapid drug-resistant gene detection by centrifugal force-assisted thermal convection pcr device
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916093/
https://www.ncbi.nlm.nih.gov/pubmed/33572363
http://dx.doi.org/10.3390/s21041225
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