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Identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope
Diagnostics based on fluorescence imaging of biomolecules is typically performed in well-equipped laboratories and is in general not suitable for remote and resource limited settings. Here we demonstrate the development of a compact, lightweight and cost-effective smartphone-based fluorescence micro...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088845/ https://www.ncbi.nlm.nih.gov/pubmed/35558922 http://dx.doi.org/10.1039/c8ra06473c |
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author | Müller, Vilhelm Sousa, José M. Ceylan Koydemir, Hatice Veli, Muhammed Tseng, Derek Cerqueira, Laura Ozcan, Aydogan Azevedo, Nuno F. Westerlund, Fredrik |
author_facet | Müller, Vilhelm Sousa, José M. Ceylan Koydemir, Hatice Veli, Muhammed Tseng, Derek Cerqueira, Laura Ozcan, Aydogan Azevedo, Nuno F. Westerlund, Fredrik |
author_sort | Müller, Vilhelm |
collection | PubMed |
description | Diagnostics based on fluorescence imaging of biomolecules is typically performed in well-equipped laboratories and is in general not suitable for remote and resource limited settings. Here we demonstrate the development of a compact, lightweight and cost-effective smartphone-based fluorescence microscope, capable of detecting signals from fluorescently labeled bacteria. By optimizing a peptide nucleic acid (PNA) based fluorescence in situ hybridization (FISH) assay, we demonstrate the use of the smartphone-based microscope for rapid identification of pathogenic bacteria. We evaluated the use of both a general nucleic acid stain as well as species-specific PNA probes and demonstrated that the mobile platform can detect bacteria with a sensitivity comparable to that of a conventional fluorescence microscope. The PNA-based FISH assay, in combination with the smartphone-based fluorescence microscope, allowed us to qualitatively analyze pathogenic bacteria in contaminated powdered infant formula (PIF) at initial concentrations prior to cultivation as low as 10 CFU per 30 g of PIF. Importantly, the detection can be done directly on the smartphone screen, without the need for additional image analysis. The assay should be straightforward to adapt for bacterial identification also in clinical samples. The cost-effectiveness, field-portability and simplicity of this platform will create various opportunities for its use in resource limited settings and point-of-care offices, opening up a myriad of additional applications based on other fluorescence-based diagnostic assays. |
format | Online Article Text |
id | pubmed-9088845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90888452022-05-11 Identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope Müller, Vilhelm Sousa, José M. Ceylan Koydemir, Hatice Veli, Muhammed Tseng, Derek Cerqueira, Laura Ozcan, Aydogan Azevedo, Nuno F. Westerlund, Fredrik RSC Adv Chemistry Diagnostics based on fluorescence imaging of biomolecules is typically performed in well-equipped laboratories and is in general not suitable for remote and resource limited settings. Here we demonstrate the development of a compact, lightweight and cost-effective smartphone-based fluorescence microscope, capable of detecting signals from fluorescently labeled bacteria. By optimizing a peptide nucleic acid (PNA) based fluorescence in situ hybridization (FISH) assay, we demonstrate the use of the smartphone-based microscope for rapid identification of pathogenic bacteria. We evaluated the use of both a general nucleic acid stain as well as species-specific PNA probes and demonstrated that the mobile platform can detect bacteria with a sensitivity comparable to that of a conventional fluorescence microscope. The PNA-based FISH assay, in combination with the smartphone-based fluorescence microscope, allowed us to qualitatively analyze pathogenic bacteria in contaminated powdered infant formula (PIF) at initial concentrations prior to cultivation as low as 10 CFU per 30 g of PIF. Importantly, the detection can be done directly on the smartphone screen, without the need for additional image analysis. The assay should be straightforward to adapt for bacterial identification also in clinical samples. The cost-effectiveness, field-portability and simplicity of this platform will create various opportunities for its use in resource limited settings and point-of-care offices, opening up a myriad of additional applications based on other fluorescence-based diagnostic assays. The Royal Society of Chemistry 2018-10-29 /pmc/articles/PMC9088845/ /pubmed/35558922 http://dx.doi.org/10.1039/c8ra06473c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Müller, Vilhelm Sousa, José M. Ceylan Koydemir, Hatice Veli, Muhammed Tseng, Derek Cerqueira, Laura Ozcan, Aydogan Azevedo, Nuno F. Westerlund, Fredrik Identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope |
title | Identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope |
title_full | Identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope |
title_fullStr | Identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope |
title_full_unstemmed | Identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope |
title_short | Identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope |
title_sort | identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088845/ https://www.ncbi.nlm.nih.gov/pubmed/35558922 http://dx.doi.org/10.1039/c8ra06473c |
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