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The Burkholderia pseudomallei intracellular ‘TRANSITome’
Prokaryotic cell transcriptomics has been limited to mixed or sub-population dynamics and individual cells within heterogeneous populations, which has hampered further understanding of spatiotemporal and stage-specific processes of prokaryotic cells within complex environments. Here we develop a ‘TR...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998038/ https://www.ncbi.nlm.nih.gov/pubmed/33772012 http://dx.doi.org/10.1038/s41467-021-22169-1 |
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author | Heacock-Kang, Yun McMillan, Ian A. Norris, Michael H. Sun, Zhenxin Zarzycki-Siek, Jan Bluhm, Andrew P. Cabanas, Darlene Norton, Robert E. Ketheesan, Natkunam Miller, Jeff F. Schweizer, Herbert P. Hoang, Tung T. |
author_facet | Heacock-Kang, Yun McMillan, Ian A. Norris, Michael H. Sun, Zhenxin Zarzycki-Siek, Jan Bluhm, Andrew P. Cabanas, Darlene Norton, Robert E. Ketheesan, Natkunam Miller, Jeff F. Schweizer, Herbert P. Hoang, Tung T. |
author_sort | Heacock-Kang, Yun |
collection | PubMed |
description | Prokaryotic cell transcriptomics has been limited to mixed or sub-population dynamics and individual cells within heterogeneous populations, which has hampered further understanding of spatiotemporal and stage-specific processes of prokaryotic cells within complex environments. Here we develop a ‘TRANSITomic’ approach to profile transcriptomes of single Burkholderia pseudomallei cells as they transit through host cell infection at defined stages, yielding pathophysiological insights. We find that B. pseudomallei transits through host cells during infection in three observable stages: vacuole entry; cytoplasmic escape and replication; and membrane protrusion, promoting cell-to-cell spread. The B. pseudomallei ‘TRANSITome’ reveals dynamic gene-expression flux during transit in host cells and identifies genes that are required for pathogenesis. We find several hypothetical proteins and assign them to virulence mechanisms, including attachment, cytoskeletal modulation, and autophagy evasion. The B. pseudomallei ‘TRANSITome’ provides prokaryotic single-cell transcriptomics information enabling high-resolution understanding of host-pathogen interactions. |
format | Online Article Text |
id | pubmed-7998038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79980382021-04-16 The Burkholderia pseudomallei intracellular ‘TRANSITome’ Heacock-Kang, Yun McMillan, Ian A. Norris, Michael H. Sun, Zhenxin Zarzycki-Siek, Jan Bluhm, Andrew P. Cabanas, Darlene Norton, Robert E. Ketheesan, Natkunam Miller, Jeff F. Schweizer, Herbert P. Hoang, Tung T. Nat Commun Article Prokaryotic cell transcriptomics has been limited to mixed or sub-population dynamics and individual cells within heterogeneous populations, which has hampered further understanding of spatiotemporal and stage-specific processes of prokaryotic cells within complex environments. Here we develop a ‘TRANSITomic’ approach to profile transcriptomes of single Burkholderia pseudomallei cells as they transit through host cell infection at defined stages, yielding pathophysiological insights. We find that B. pseudomallei transits through host cells during infection in three observable stages: vacuole entry; cytoplasmic escape and replication; and membrane protrusion, promoting cell-to-cell spread. The B. pseudomallei ‘TRANSITome’ reveals dynamic gene-expression flux during transit in host cells and identifies genes that are required for pathogenesis. We find several hypothetical proteins and assign them to virulence mechanisms, including attachment, cytoskeletal modulation, and autophagy evasion. The B. pseudomallei ‘TRANSITome’ provides prokaryotic single-cell transcriptomics information enabling high-resolution understanding of host-pathogen interactions. Nature Publishing Group UK 2021-03-26 /pmc/articles/PMC7998038/ /pubmed/33772012 http://dx.doi.org/10.1038/s41467-021-22169-1 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Heacock-Kang, Yun McMillan, Ian A. Norris, Michael H. Sun, Zhenxin Zarzycki-Siek, Jan Bluhm, Andrew P. Cabanas, Darlene Norton, Robert E. Ketheesan, Natkunam Miller, Jeff F. Schweizer, Herbert P. Hoang, Tung T. The Burkholderia pseudomallei intracellular ‘TRANSITome’ |
title | The Burkholderia pseudomallei intracellular ‘TRANSITome’ |
title_full | The Burkholderia pseudomallei intracellular ‘TRANSITome’ |
title_fullStr | The Burkholderia pseudomallei intracellular ‘TRANSITome’ |
title_full_unstemmed | The Burkholderia pseudomallei intracellular ‘TRANSITome’ |
title_short | The Burkholderia pseudomallei intracellular ‘TRANSITome’ |
title_sort | burkholderia pseudomallei intracellular ‘transitome’ |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998038/ https://www.ncbi.nlm.nih.gov/pubmed/33772012 http://dx.doi.org/10.1038/s41467-021-22169-1 |
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