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Signaling-Mediated Bacterial Persister Formation
Here we show that bacterial communication through indole signaling induces persistence, a phenomenon in which a subset of an isogenic bacterial population tolerates antibiotic treatment. We monitor indole-induced persister formation using microfluidics, and identify the role of oxidative stress and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329571/ https://www.ncbi.nlm.nih.gov/pubmed/22426114 http://dx.doi.org/10.1038/nchembio.915 |
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author | Vega, Nicole M. Allison, Kyle R. Khalil, Ahmad S. Collins, James J. |
author_facet | Vega, Nicole M. Allison, Kyle R. Khalil, Ahmad S. Collins, James J. |
author_sort | Vega, Nicole M. |
collection | PubMed |
description | Here we show that bacterial communication through indole signaling induces persistence, a phenomenon in which a subset of an isogenic bacterial population tolerates antibiotic treatment. We monitor indole-induced persister formation using microfluidics, and identify the role of oxidative stress and phage-shock pathways in this phenomenon. We propose a model in which indole signaling “inoculates” a bacterial sub-population against antibiotics by activating stress responses, leading to persister formation. |
format | Online Article Text |
id | pubmed-3329571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-33295712012-11-01 Signaling-Mediated Bacterial Persister Formation Vega, Nicole M. Allison, Kyle R. Khalil, Ahmad S. Collins, James J. Nat Chem Biol Article Here we show that bacterial communication through indole signaling induces persistence, a phenomenon in which a subset of an isogenic bacterial population tolerates antibiotic treatment. We monitor indole-induced persister formation using microfluidics, and identify the role of oxidative stress and phage-shock pathways in this phenomenon. We propose a model in which indole signaling “inoculates” a bacterial sub-population against antibiotics by activating stress responses, leading to persister formation. 2012-03-18 /pmc/articles/PMC3329571/ /pubmed/22426114 http://dx.doi.org/10.1038/nchembio.915 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Vega, Nicole M. Allison, Kyle R. Khalil, Ahmad S. Collins, James J. Signaling-Mediated Bacterial Persister Formation |
title | Signaling-Mediated Bacterial Persister Formation |
title_full | Signaling-Mediated Bacterial Persister Formation |
title_fullStr | Signaling-Mediated Bacterial Persister Formation |
title_full_unstemmed | Signaling-Mediated Bacterial Persister Formation |
title_short | Signaling-Mediated Bacterial Persister Formation |
title_sort | signaling-mediated bacterial persister formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3329571/ https://www.ncbi.nlm.nih.gov/pubmed/22426114 http://dx.doi.org/10.1038/nchembio.915 |
work_keys_str_mv | AT veganicolem signalingmediatedbacterialpersisterformation AT allisonkyler signalingmediatedbacterialpersisterformation AT khalilahmads signalingmediatedbacterialpersisterformation AT collinsjamesj signalingmediatedbacterialpersisterformation |