Cargando…

Micron Scale Spatial Measurement of the O(2) Gradient Surrounding a Bacterial Biofilm in Real Time

Bacteria alter their local chemical environment through both consumption and the production of a variety of molecules, ultimately shaping the local ecology. Molecular oxygen (O(2)) is a key metabolite that affects the physiology and behavior of virtually all bacteria, and its consumption often resul...

Descripción completa

Detalles Bibliográficos
Autores principales: Klementiev, Alexander D., Jin, Zhaoyu, Whiteley, Marvin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587442/
https://www.ncbi.nlm.nih.gov/pubmed/33082251
http://dx.doi.org/10.1128/mBio.02536-20
_version_ 1783600175567077376
author Klementiev, Alexander D.
Jin, Zhaoyu
Whiteley, Marvin
author_facet Klementiev, Alexander D.
Jin, Zhaoyu
Whiteley, Marvin
author_sort Klementiev, Alexander D.
collection PubMed
description Bacteria alter their local chemical environment through both consumption and the production of a variety of molecules, ultimately shaping the local ecology. Molecular oxygen (O(2)) is a key metabolite that affects the physiology and behavior of virtually all bacteria, and its consumption often results in O(2) gradients within sessile bacterial communities (biofilms). O(2) plays a critical role in several bacterial phenotypes, including antibiotic tolerance; however, our understanding of O(2) levels within and surrounding biofilms has been hampered by the difficulties in measuring O(2) levels in real-time for extended durations and at the micron scale. Here, we developed electrochemical methodology based on scanning electrochemical microscopy to quantify the O(2) gradients present above a Pseudomonas aeruginosa biofilm. These results reveal that a biofilm produces a hypoxic zone that extends hundreds of microns from the biofilm surface within minutes and that the biofilm consumes O(2) at a maximum rate. Treating the biofilm with levels of the antibiotic ciprofloxacin that kill 99% of the bacteria did not affect the O(2) gradient, indicating that the biofilm is highly resilient to antimicrobial treatment in regard to O(2) consumption.
format Online
Article
Text
id pubmed-7587442
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-75874422020-12-01 Micron Scale Spatial Measurement of the O(2) Gradient Surrounding a Bacterial Biofilm in Real Time Klementiev, Alexander D. Jin, Zhaoyu Whiteley, Marvin mBio Observation Bacteria alter their local chemical environment through both consumption and the production of a variety of molecules, ultimately shaping the local ecology. Molecular oxygen (O(2)) is a key metabolite that affects the physiology and behavior of virtually all bacteria, and its consumption often results in O(2) gradients within sessile bacterial communities (biofilms). O(2) plays a critical role in several bacterial phenotypes, including antibiotic tolerance; however, our understanding of O(2) levels within and surrounding biofilms has been hampered by the difficulties in measuring O(2) levels in real-time for extended durations and at the micron scale. Here, we developed electrochemical methodology based on scanning electrochemical microscopy to quantify the O(2) gradients present above a Pseudomonas aeruginosa biofilm. These results reveal that a biofilm produces a hypoxic zone that extends hundreds of microns from the biofilm surface within minutes and that the biofilm consumes O(2) at a maximum rate. Treating the biofilm with levels of the antibiotic ciprofloxacin that kill 99% of the bacteria did not affect the O(2) gradient, indicating that the biofilm is highly resilient to antimicrobial treatment in regard to O(2) consumption. American Society for Microbiology 2020-10-20 /pmc/articles/PMC7587442/ /pubmed/33082251 http://dx.doi.org/10.1128/mBio.02536-20 Text en Copyright © 2020 Klementiev et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Observation
Klementiev, Alexander D.
Jin, Zhaoyu
Whiteley, Marvin
Micron Scale Spatial Measurement of the O(2) Gradient Surrounding a Bacterial Biofilm in Real Time
title Micron Scale Spatial Measurement of the O(2) Gradient Surrounding a Bacterial Biofilm in Real Time
title_full Micron Scale Spatial Measurement of the O(2) Gradient Surrounding a Bacterial Biofilm in Real Time
title_fullStr Micron Scale Spatial Measurement of the O(2) Gradient Surrounding a Bacterial Biofilm in Real Time
title_full_unstemmed Micron Scale Spatial Measurement of the O(2) Gradient Surrounding a Bacterial Biofilm in Real Time
title_short Micron Scale Spatial Measurement of the O(2) Gradient Surrounding a Bacterial Biofilm in Real Time
title_sort micron scale spatial measurement of the o(2) gradient surrounding a bacterial biofilm in real time
topic Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587442/
https://www.ncbi.nlm.nih.gov/pubmed/33082251
http://dx.doi.org/10.1128/mBio.02536-20
work_keys_str_mv AT klementievalexanderd micronscalespatialmeasurementoftheo2gradientsurroundingabacterialbiofilminrealtime
AT jinzhaoyu micronscalespatialmeasurementoftheo2gradientsurroundingabacterialbiofilminrealtime
AT whiteleymarvin micronscalespatialmeasurementoftheo2gradientsurroundingabacterialbiofilminrealtime