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Dynamic Transcriptional Landscape of Mycobacterium smegmatis under Cold Stress

Bacterial adaptation to cold stress requires wide transcriptional reprogramming. However, the knowledge of molecular mechanisms underlying the cold stress response of mycobacteria is limited. We conducted comparative transcriptomic analysis of Mycobacterium smegmatis subjected to cold shock. The gro...

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Autores principales: Grigorov, Artem S., Skvortsova, Yulia V., Bychenko, Oksana S., Aseev, Leonid V., Koledinskaya, Ludmila S., Boni, Irina V., Azhikina, Tatyana L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454040/
https://www.ncbi.nlm.nih.gov/pubmed/37628885
http://dx.doi.org/10.3390/ijms241612706
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author Grigorov, Artem S.
Skvortsova, Yulia V.
Bychenko, Oksana S.
Aseev, Leonid V.
Koledinskaya, Ludmila S.
Boni, Irina V.
Azhikina, Tatyana L.
author_facet Grigorov, Artem S.
Skvortsova, Yulia V.
Bychenko, Oksana S.
Aseev, Leonid V.
Koledinskaya, Ludmila S.
Boni, Irina V.
Azhikina, Tatyana L.
author_sort Grigorov, Artem S.
collection PubMed
description Bacterial adaptation to cold stress requires wide transcriptional reprogramming. However, the knowledge of molecular mechanisms underlying the cold stress response of mycobacteria is limited. We conducted comparative transcriptomic analysis of Mycobacterium smegmatis subjected to cold shock. The growth of M. smegmatis cultivated at 37 °C was arrested just after exposure to cold (acclimation phase) but later (by 24 h) was resumed at a much slower rate (adaptation phase). Transcriptomic analyses revealed distinct gene expression patterns corresponding to the two phases. During the acclimation phase, differential expression was observed for genes associated with cell wall remodeling, starvation response, and osmotic pressure stress, in parallel with global changes in the expression of transcription factors and the downregulation of ribosomal genes, suggesting an energy-saving strategy to support survival. At the adaptation phase, the expression profiles were recovered, indicating restoration of the processes repressed earlier. Comparison of transcriptional responses in M. smegmatis with those in other bacteria revealed unique adaptation strategies developed by mycobacteria. Our findings shed light on the molecular mechanisms underlying M. smegmatis survival under cold stress. Further research should clarify whether the discovered transcriptional mechanisms exist in other mycobacterial species, including pathogenic Mycobacterium tuberculosis, which could be important for transmission control.
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spelling pubmed-104540402023-08-26 Dynamic Transcriptional Landscape of Mycobacterium smegmatis under Cold Stress Grigorov, Artem S. Skvortsova, Yulia V. Bychenko, Oksana S. Aseev, Leonid V. Koledinskaya, Ludmila S. Boni, Irina V. Azhikina, Tatyana L. Int J Mol Sci Article Bacterial adaptation to cold stress requires wide transcriptional reprogramming. However, the knowledge of molecular mechanisms underlying the cold stress response of mycobacteria is limited. We conducted comparative transcriptomic analysis of Mycobacterium smegmatis subjected to cold shock. The growth of M. smegmatis cultivated at 37 °C was arrested just after exposure to cold (acclimation phase) but later (by 24 h) was resumed at a much slower rate (adaptation phase). Transcriptomic analyses revealed distinct gene expression patterns corresponding to the two phases. During the acclimation phase, differential expression was observed for genes associated with cell wall remodeling, starvation response, and osmotic pressure stress, in parallel with global changes in the expression of transcription factors and the downregulation of ribosomal genes, suggesting an energy-saving strategy to support survival. At the adaptation phase, the expression profiles were recovered, indicating restoration of the processes repressed earlier. Comparison of transcriptional responses in M. smegmatis with those in other bacteria revealed unique adaptation strategies developed by mycobacteria. Our findings shed light on the molecular mechanisms underlying M. smegmatis survival under cold stress. Further research should clarify whether the discovered transcriptional mechanisms exist in other mycobacterial species, including pathogenic Mycobacterium tuberculosis, which could be important for transmission control. MDPI 2023-08-11 /pmc/articles/PMC10454040/ /pubmed/37628885 http://dx.doi.org/10.3390/ijms241612706 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Grigorov, Artem S.
Skvortsova, Yulia V.
Bychenko, Oksana S.
Aseev, Leonid V.
Koledinskaya, Ludmila S.
Boni, Irina V.
Azhikina, Tatyana L.
Dynamic Transcriptional Landscape of Mycobacterium smegmatis under Cold Stress
title Dynamic Transcriptional Landscape of Mycobacterium smegmatis under Cold Stress
title_full Dynamic Transcriptional Landscape of Mycobacterium smegmatis under Cold Stress
title_fullStr Dynamic Transcriptional Landscape of Mycobacterium smegmatis under Cold Stress
title_full_unstemmed Dynamic Transcriptional Landscape of Mycobacterium smegmatis under Cold Stress
title_short Dynamic Transcriptional Landscape of Mycobacterium smegmatis under Cold Stress
title_sort dynamic transcriptional landscape of mycobacterium smegmatis under cold stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454040/
https://www.ncbi.nlm.nih.gov/pubmed/37628885
http://dx.doi.org/10.3390/ijms241612706
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