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Characterization of Eight Bacterial Biosensors for Microbial Diagnostic and Therapeutic Applications
[Image: see text] The engineering of microbial cells to produce and secrete therapeutics directly in the human body, known as advanced microbial therapeutics, is an exciting alternative to current drug delivery routes. These living therapeutics can be engineered to sense disease biomarkers and, in r...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764412/ https://www.ncbi.nlm.nih.gov/pubmed/36449712 http://dx.doi.org/10.1021/acssynbio.2c00491 |
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author | Vaaben, Troels Holger Vazquez-Uribe, Ruben Sommer, Morten Otto Alexander |
author_facet | Vaaben, Troels Holger Vazquez-Uribe, Ruben Sommer, Morten Otto Alexander |
author_sort | Vaaben, Troels Holger |
collection | PubMed |
description | [Image: see text] The engineering of microbial cells to produce and secrete therapeutics directly in the human body, known as advanced microbial therapeutics, is an exciting alternative to current drug delivery routes. These living therapeutics can be engineered to sense disease biomarkers and, in response, deliver a therapeutic activity. This strategy allows for precise and self-regulating delivery of a therapeutic that adapts to the disease state of the individual patient. Numerous sensing systems have been characterized for use in prokaryotes, but a very limited number of advanced microbial therapeutics have incorporated such sensors. We characterized eight different sensors that respond to physiologically relevant conditions and molecules found in the human body in the probiotic strain Escherichia coli Nissle 1917. The resulting sensors were characterized under aerobic and anaerobic conditions and were demonstrated to be functional under gut-like conditions using the nematode Caenorhabditis elegans as an in vivo model. We show for the first time how a biosensor is able to detect in vivo the bile acid-like molecule Δ(4)-dafachronic acid, a small molecule in C. elegans that regulates lifespan. Furthermore, we exemplify how bacterial sensors can be used to dynamically report on changes in the intestinal environment of C. elegans, by demonstrating the use of a biosensor able to detect changes in lactate concentrations in the gut lumen of individual C. elegans. The biosensors presented in this study allow for dynamic control of expression in vivo and represent a valuable tool in further developing advanced microbiome therapeutics. |
format | Online Article Text |
id | pubmed-9764412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97644122022-12-21 Characterization of Eight Bacterial Biosensors for Microbial Diagnostic and Therapeutic Applications Vaaben, Troels Holger Vazquez-Uribe, Ruben Sommer, Morten Otto Alexander ACS Synth Biol [Image: see text] The engineering of microbial cells to produce and secrete therapeutics directly in the human body, known as advanced microbial therapeutics, is an exciting alternative to current drug delivery routes. These living therapeutics can be engineered to sense disease biomarkers and, in response, deliver a therapeutic activity. This strategy allows for precise and self-regulating delivery of a therapeutic that adapts to the disease state of the individual patient. Numerous sensing systems have been characterized for use in prokaryotes, but a very limited number of advanced microbial therapeutics have incorporated such sensors. We characterized eight different sensors that respond to physiologically relevant conditions and molecules found in the human body in the probiotic strain Escherichia coli Nissle 1917. The resulting sensors were characterized under aerobic and anaerobic conditions and were demonstrated to be functional under gut-like conditions using the nematode Caenorhabditis elegans as an in vivo model. We show for the first time how a biosensor is able to detect in vivo the bile acid-like molecule Δ(4)-dafachronic acid, a small molecule in C. elegans that regulates lifespan. Furthermore, we exemplify how bacterial sensors can be used to dynamically report on changes in the intestinal environment of C. elegans, by demonstrating the use of a biosensor able to detect changes in lactate concentrations in the gut lumen of individual C. elegans. The biosensors presented in this study allow for dynamic control of expression in vivo and represent a valuable tool in further developing advanced microbiome therapeutics. American Chemical Society 2022-11-30 2022-12-16 /pmc/articles/PMC9764412/ /pubmed/36449712 http://dx.doi.org/10.1021/acssynbio.2c00491 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Vaaben, Troels Holger Vazquez-Uribe, Ruben Sommer, Morten Otto Alexander Characterization of Eight Bacterial Biosensors for Microbial Diagnostic and Therapeutic Applications |
title | Characterization
of Eight Bacterial Biosensors for
Microbial Diagnostic and Therapeutic Applications |
title_full | Characterization
of Eight Bacterial Biosensors for
Microbial Diagnostic and Therapeutic Applications |
title_fullStr | Characterization
of Eight Bacterial Biosensors for
Microbial Diagnostic and Therapeutic Applications |
title_full_unstemmed | Characterization
of Eight Bacterial Biosensors for
Microbial Diagnostic and Therapeutic Applications |
title_short | Characterization
of Eight Bacterial Biosensors for
Microbial Diagnostic and Therapeutic Applications |
title_sort | characterization
of eight bacterial biosensors for
microbial diagnostic and therapeutic applications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764412/ https://www.ncbi.nlm.nih.gov/pubmed/36449712 http://dx.doi.org/10.1021/acssynbio.2c00491 |
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