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Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water

Drinking water can be exposed to different biological contaminants from the source, through the pipelines, until reaching the final consumer or industry. Some of these are pathogenic bacteria and viruses which may cause important gastrointestinal or systemic diseases. The microbiological quality of...

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Autores principales: Gutiérrez-del-Río, Ignacio, Marín, Laura, Fernández, Javier, Álvarez San Millán, María, Ferrero, Francisco Javier, Valledor, Marta, Campo, Juan Carlos, Cobián, Natalia, Méndez, Ignacio, Lombó, Felipe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755745/
https://www.ncbi.nlm.nih.gov/pubmed/29304041
http://dx.doi.org/10.1371/journal.pone.0184277
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author Gutiérrez-del-Río, Ignacio
Marín, Laura
Fernández, Javier
Álvarez San Millán, María
Ferrero, Francisco Javier
Valledor, Marta
Campo, Juan Carlos
Cobián, Natalia
Méndez, Ignacio
Lombó, Felipe
author_facet Gutiérrez-del-Río, Ignacio
Marín, Laura
Fernández, Javier
Álvarez San Millán, María
Ferrero, Francisco Javier
Valledor, Marta
Campo, Juan Carlos
Cobián, Natalia
Méndez, Ignacio
Lombó, Felipe
author_sort Gutiérrez-del-Río, Ignacio
collection PubMed
description Drinking water can be exposed to different biological contaminants from the source, through the pipelines, until reaching the final consumer or industry. Some of these are pathogenic bacteria and viruses which may cause important gastrointestinal or systemic diseases. The microbiological quality of drinking water relies mainly in monitoring three indicator bacteria of faecal origin, Escherichia coli, Enterococcus faecalis and Clostridium perfringens, which serve as early sentinels of potential health hazards for the population. Here we describe the analysis of three chimeric fluorescent protein bullets as biosensor candidates for fast detection of E. coli in drinking water. Two of the chimeric proteins (based on GFP-hadrurin and GFP-pb5 chimera proteins) failed with respect to specificity and/or sensitivity, but the GFP-colS4 chimera protein was able to carry out specific detection of E. coli in drinking water samples in a procedure encompassing about 8 min for final result and this biosensor protein was able to detect in a linear way between 20 and 10(3) CFU of this bacterium. Below 20 CFU, the system cannot differentiate presence or absence of the target bacterium. The fluorescence in this biosensor system is provided by the GFP subunit of the chimeric protein, which, in the case of the better performing sensor bullet, GFP-colS4 chimera, is covalently bound to a flexible peptide bridge and to a bacteriocin binding specifically to E. coli cells. Once bound to the target bacteria, the excitation step with 395 nm LED light causes emission of fluorescence from the GFP domain, which is amplified in a photomultiplier tube, and finally this signal is converted into an output voltage which can be associated with a CFU value and these data distributed along mobile phone networks, for example. This method, and the portable fluorimeter which has been developed for it, may contribute to reduce the analysis time for detecting E. coli presence in drinking water.
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spelling pubmed-57557452018-01-26 Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water Gutiérrez-del-Río, Ignacio Marín, Laura Fernández, Javier Álvarez San Millán, María Ferrero, Francisco Javier Valledor, Marta Campo, Juan Carlos Cobián, Natalia Méndez, Ignacio Lombó, Felipe PLoS One Research Article Drinking water can be exposed to different biological contaminants from the source, through the pipelines, until reaching the final consumer or industry. Some of these are pathogenic bacteria and viruses which may cause important gastrointestinal or systemic diseases. The microbiological quality of drinking water relies mainly in monitoring three indicator bacteria of faecal origin, Escherichia coli, Enterococcus faecalis and Clostridium perfringens, which serve as early sentinels of potential health hazards for the population. Here we describe the analysis of three chimeric fluorescent protein bullets as biosensor candidates for fast detection of E. coli in drinking water. Two of the chimeric proteins (based on GFP-hadrurin and GFP-pb5 chimera proteins) failed with respect to specificity and/or sensitivity, but the GFP-colS4 chimera protein was able to carry out specific detection of E. coli in drinking water samples in a procedure encompassing about 8 min for final result and this biosensor protein was able to detect in a linear way between 20 and 10(3) CFU of this bacterium. Below 20 CFU, the system cannot differentiate presence or absence of the target bacterium. The fluorescence in this biosensor system is provided by the GFP subunit of the chimeric protein, which, in the case of the better performing sensor bullet, GFP-colS4 chimera, is covalently bound to a flexible peptide bridge and to a bacteriocin binding specifically to E. coli cells. Once bound to the target bacteria, the excitation step with 395 nm LED light causes emission of fluorescence from the GFP domain, which is amplified in a photomultiplier tube, and finally this signal is converted into an output voltage which can be associated with a CFU value and these data distributed along mobile phone networks, for example. This method, and the portable fluorimeter which has been developed for it, may contribute to reduce the analysis time for detecting E. coli presence in drinking water. Public Library of Science 2018-01-05 /pmc/articles/PMC5755745/ /pubmed/29304041 http://dx.doi.org/10.1371/journal.pone.0184277 Text en © 2018 Gutiérrez-del-Río 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
Gutiérrez-del-Río, Ignacio
Marín, Laura
Fernández, Javier
Álvarez San Millán, María
Ferrero, Francisco Javier
Valledor, Marta
Campo, Juan Carlos
Cobián, Natalia
Méndez, Ignacio
Lombó, Felipe
Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water
title Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water
title_full Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water
title_fullStr Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water
title_full_unstemmed Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water
title_short Development of a biosensor protein bullet as a fluorescent method for fast detection of Escherichia coli in drinking water
title_sort development of a biosensor protein bullet as a fluorescent method for fast detection of escherichia coli in drinking water
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5755745/
https://www.ncbi.nlm.nih.gov/pubmed/29304041
http://dx.doi.org/10.1371/journal.pone.0184277
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