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Smartphone-operated affordable PCR thermal cycler for the detection of antimicrobial resistant bacterial genes
Antimicrobial resistance (AMR) is a global public health threat. Surveillance of AMR requires affordable, rapid, and user-friendly diagnostic methods. Our aim was to develop a low-cost thermocycler to perform polymerase chain reaction (PCR). We developed a smartphone-operated PCR thermal cycler usin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021165/ https://www.ncbi.nlm.nih.gov/pubmed/36962978 http://dx.doi.org/10.1371/journal.pgph.0001120 |
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author | Pudasaini, Sanam Thapa, Garima Marasini, Bishnu P. Giri, Basant |
author_facet | Pudasaini, Sanam Thapa, Garima Marasini, Bishnu P. Giri, Basant |
author_sort | Pudasaini, Sanam |
collection | PubMed |
description | Antimicrobial resistance (AMR) is a global public health threat. Surveillance of AMR requires affordable, rapid, and user-friendly diagnostic methods. Our aim was to develop a low-cost thermocycler to perform polymerase chain reaction (PCR). We developed a smartphone-operated PCR thermal cycler using locally available recycled materials. The thermal cycler was used for the amplification for three bacterial genes–bla-TEM, bla-CTXM and 16s rRNA in human urine samples. The performance of custom-built thermal cycler was compared with commercial thermal cycler. The thermal cycler was portable (<1kg weight), required 12 V power supply, 25 μL of solution, and cost only USD50.0. Temperature and time conditions were instructed using a custom-built smartphone application. The ramping rate of was 0.23°C for heating and 0.43°C for cooling. The reported temperatures were within ± 0.5°C of set temperature. The human urine samples were highly resistance and multi-resistant. Nearly 46% (n = 54) E. coli isolates were positive in ESBL screening test. The custom-built thermocycler was able to accurately predict the presence of bla-TEM, bla-CTXM genes, and 16s rRNA (n = 6). We developed and demonstrated a portable, low-cost, easy-to-use, and smartphone-operated PCR thermal cycler. Since it is portable, it can be used in remote location and field settings, including places without stable power supply. The use of the thermal cycler system can be extended, beyond the detection of AMR genes, e.g., in clinical diagnosis, genetics, forensic analysis, and environmental protection. |
format | Online Article Text |
id | pubmed-10021165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-100211652023-03-17 Smartphone-operated affordable PCR thermal cycler for the detection of antimicrobial resistant bacterial genes Pudasaini, Sanam Thapa, Garima Marasini, Bishnu P. Giri, Basant PLOS Glob Public Health Research Article Antimicrobial resistance (AMR) is a global public health threat. Surveillance of AMR requires affordable, rapid, and user-friendly diagnostic methods. Our aim was to develop a low-cost thermocycler to perform polymerase chain reaction (PCR). We developed a smartphone-operated PCR thermal cycler using locally available recycled materials. The thermal cycler was used for the amplification for three bacterial genes–bla-TEM, bla-CTXM and 16s rRNA in human urine samples. The performance of custom-built thermal cycler was compared with commercial thermal cycler. The thermal cycler was portable (<1kg weight), required 12 V power supply, 25 μL of solution, and cost only USD50.0. Temperature and time conditions were instructed using a custom-built smartphone application. The ramping rate of was 0.23°C for heating and 0.43°C for cooling. The reported temperatures were within ± 0.5°C of set temperature. The human urine samples were highly resistance and multi-resistant. Nearly 46% (n = 54) E. coli isolates were positive in ESBL screening test. The custom-built thermocycler was able to accurately predict the presence of bla-TEM, bla-CTXM genes, and 16s rRNA (n = 6). We developed and demonstrated a portable, low-cost, easy-to-use, and smartphone-operated PCR thermal cycler. Since it is portable, it can be used in remote location and field settings, including places without stable power supply. The use of the thermal cycler system can be extended, beyond the detection of AMR genes, e.g., in clinical diagnosis, genetics, forensic analysis, and environmental protection. Public Library of Science 2023-02-27 /pmc/articles/PMC10021165/ /pubmed/36962978 http://dx.doi.org/10.1371/journal.pgph.0001120 Text en © 2023 Pudasaini et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Pudasaini, Sanam Thapa, Garima Marasini, Bishnu P. Giri, Basant Smartphone-operated affordable PCR thermal cycler for the detection of antimicrobial resistant bacterial genes |
title | Smartphone-operated affordable PCR thermal cycler for the detection of antimicrobial resistant bacterial genes |
title_full | Smartphone-operated affordable PCR thermal cycler for the detection of antimicrobial resistant bacterial genes |
title_fullStr | Smartphone-operated affordable PCR thermal cycler for the detection of antimicrobial resistant bacterial genes |
title_full_unstemmed | Smartphone-operated affordable PCR thermal cycler for the detection of antimicrobial resistant bacterial genes |
title_short | Smartphone-operated affordable PCR thermal cycler for the detection of antimicrobial resistant bacterial genes |
title_sort | smartphone-operated affordable pcr thermal cycler for the detection of antimicrobial resistant bacterial genes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10021165/ https://www.ncbi.nlm.nih.gov/pubmed/36962978 http://dx.doi.org/10.1371/journal.pgph.0001120 |
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