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Protocol for detecting Yersinia pseudotuberculosis nitric oxide exposure during in vitro growth

Yersinia pseudotuberculosis (Yptb) is a bacterial pathogen that causes foodborne illness. Defense against the host antimicrobial gas, nitric oxide (NO), by the bacterial NO-detoxifying gene, hmp, promotes Yptb replication in mouse models of infection. Here, we detail the use of fluorescent signals a...

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Detalles Bibliográficos
Autores principales: Braza, Rezia Era D., Cotten, Katherine L., Davis, Kimberly M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563189/
https://www.ncbi.nlm.nih.gov/pubmed/36219561
http://dx.doi.org/10.1016/j.xpro.2022.101760
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author Braza, Rezia Era D.
Cotten, Katherine L.
Davis, Kimberly M.
author_facet Braza, Rezia Era D.
Cotten, Katherine L.
Davis, Kimberly M.
author_sort Braza, Rezia Era D.
collection PubMed
description Yersinia pseudotuberculosis (Yptb) is a bacterial pathogen that causes foodborne illness. Defense against the host antimicrobial gas, nitric oxide (NO), by the bacterial NO-detoxifying gene, hmp, promotes Yptb replication in mouse models of infection. Here, we detail the use of fluorescent signals as readouts for NO exposure within individual cells and subsequent detection of heterogeneity within a population, using single-cell imaging and analysis. This protocol quantifies NO exposure in culture, without capturing the full complexity of the host environment. For complete details on the use and execution of this protocol, please refer to Patel et al. (2021).
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spelling pubmed-95631892022-10-15 Protocol for detecting Yersinia pseudotuberculosis nitric oxide exposure during in vitro growth Braza, Rezia Era D. Cotten, Katherine L. Davis, Kimberly M. STAR Protoc Protocol Yersinia pseudotuberculosis (Yptb) is a bacterial pathogen that causes foodborne illness. Defense against the host antimicrobial gas, nitric oxide (NO), by the bacterial NO-detoxifying gene, hmp, promotes Yptb replication in mouse models of infection. Here, we detail the use of fluorescent signals as readouts for NO exposure within individual cells and subsequent detection of heterogeneity within a population, using single-cell imaging and analysis. This protocol quantifies NO exposure in culture, without capturing the full complexity of the host environment. For complete details on the use and execution of this protocol, please refer to Patel et al. (2021). Elsevier 2022-10-09 /pmc/articles/PMC9563189/ /pubmed/36219561 http://dx.doi.org/10.1016/j.xpro.2022.101760 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Braza, Rezia Era D.
Cotten, Katherine L.
Davis, Kimberly M.
Protocol for detecting Yersinia pseudotuberculosis nitric oxide exposure during in vitro growth
title Protocol for detecting Yersinia pseudotuberculosis nitric oxide exposure during in vitro growth
title_full Protocol for detecting Yersinia pseudotuberculosis nitric oxide exposure during in vitro growth
title_fullStr Protocol for detecting Yersinia pseudotuberculosis nitric oxide exposure during in vitro growth
title_full_unstemmed Protocol for detecting Yersinia pseudotuberculosis nitric oxide exposure during in vitro growth
title_short Protocol for detecting Yersinia pseudotuberculosis nitric oxide exposure during in vitro growth
title_sort protocol for detecting yersinia pseudotuberculosis nitric oxide exposure during in vitro growth
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563189/
https://www.ncbi.nlm.nih.gov/pubmed/36219561
http://dx.doi.org/10.1016/j.xpro.2022.101760
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