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Development of single-cell-level microfluidic technology for long-term growth visualization of living cultures of Mycobacterium smegmatis

Analysis of growth and death kinetics at single-cell resolution is a key step in understanding the complexity of the nonreplicating growth phenotype of the bacterial pathogen Mycobacterium tuberculosis. Here, we developed a single-cell-resolution microfluidic mycobacterial culture device that allows...

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Autores principales: Wang, Han, Conover, Gloria M., Han, Song-I, Sacchettini, James C., Han, Arum
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433163/
https://www.ncbi.nlm.nih.gov/pubmed/34567751
http://dx.doi.org/10.1038/s41378-021-00262-1
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author Wang, Han
Conover, Gloria M.
Han, Song-I
Sacchettini, James C.
Han, Arum
author_facet Wang, Han
Conover, Gloria M.
Han, Song-I
Sacchettini, James C.
Han, Arum
author_sort Wang, Han
collection PubMed
description Analysis of growth and death kinetics at single-cell resolution is a key step in understanding the complexity of the nonreplicating growth phenotype of the bacterial pathogen Mycobacterium tuberculosis. Here, we developed a single-cell-resolution microfluidic mycobacterial culture device that allows time-lapse microscopy-based long-term phenotypic visualization of the live replication dynamics of mycobacteria. This technology was successfully applied to monitor the real-time growth dynamics of the fast-growing model strain Mycobacterium smegmatis (M. smegmatis) while subjected to drug treatment regimens during continuous culture for 48 h inside the microfluidic device. A clear morphological change leading to significant swelling at the poles of the bacterial membrane was observed during drug treatment. In addition, a small subpopulation of cells surviving treatment by frontline antibiotics was observed to recover and achieve robust replicative growth once regular culture media was provided, suggesting the possibility of identifying and isolating nonreplicative mycobacteria. This device is a simple, easy-to-use, and low-cost solution for studying the single-cell phenotype and growth dynamics of mycobacteria, especially during drug treatment.
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spelling pubmed-84331632021-09-24 Development of single-cell-level microfluidic technology for long-term growth visualization of living cultures of Mycobacterium smegmatis Wang, Han Conover, Gloria M. Han, Song-I Sacchettini, James C. Han, Arum Microsyst Nanoeng Article Analysis of growth and death kinetics at single-cell resolution is a key step in understanding the complexity of the nonreplicating growth phenotype of the bacterial pathogen Mycobacterium tuberculosis. Here, we developed a single-cell-resolution microfluidic mycobacterial culture device that allows time-lapse microscopy-based long-term phenotypic visualization of the live replication dynamics of mycobacteria. This technology was successfully applied to monitor the real-time growth dynamics of the fast-growing model strain Mycobacterium smegmatis (M. smegmatis) while subjected to drug treatment regimens during continuous culture for 48 h inside the microfluidic device. A clear morphological change leading to significant swelling at the poles of the bacterial membrane was observed during drug treatment. In addition, a small subpopulation of cells surviving treatment by frontline antibiotics was observed to recover and achieve robust replicative growth once regular culture media was provided, suggesting the possibility of identifying and isolating nonreplicative mycobacteria. This device is a simple, easy-to-use, and low-cost solution for studying the single-cell phenotype and growth dynamics of mycobacteria, especially during drug treatment. Nature Publishing Group UK 2021-05-20 /pmc/articles/PMC8433163/ /pubmed/34567751 http://dx.doi.org/10.1038/s41378-021-00262-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Han
Conover, Gloria M.
Han, Song-I
Sacchettini, James C.
Han, Arum
Development of single-cell-level microfluidic technology for long-term growth visualization of living cultures of Mycobacterium smegmatis
title Development of single-cell-level microfluidic technology for long-term growth visualization of living cultures of Mycobacterium smegmatis
title_full Development of single-cell-level microfluidic technology for long-term growth visualization of living cultures of Mycobacterium smegmatis
title_fullStr Development of single-cell-level microfluidic technology for long-term growth visualization of living cultures of Mycobacterium smegmatis
title_full_unstemmed Development of single-cell-level microfluidic technology for long-term growth visualization of living cultures of Mycobacterium smegmatis
title_short Development of single-cell-level microfluidic technology for long-term growth visualization of living cultures of Mycobacterium smegmatis
title_sort development of single-cell-level microfluidic technology for long-term growth visualization of living cultures of mycobacterium smegmatis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433163/
https://www.ncbi.nlm.nih.gov/pubmed/34567751
http://dx.doi.org/10.1038/s41378-021-00262-1
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