Cargando…

Changes in Transcriptome of Yersinia pseudotuberculosis IP32953 Grown at 3 and 28°C Detected by RNA Sequencing Shed Light on Cold Adaptation

Yersinia pseudotuberculosis is a bacterium that not only survives, but also thrives, proliferates, and remains infective at cold-storage temperatures, making it an adept foodborne pathogen. We analyzed the differences in gene expression between Y. pseudotuberculosis IP32953 grown at 3 and 28°C to in...

Descripción completa

Detalles Bibliográficos
Autores principales: Virtanen, Jussa-Pekka, Keto-Timonen, Riikka, Jaakkola, Kaisa, Salin, Noora, Korkeala, Hannu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277586/
https://www.ncbi.nlm.nih.gov/pubmed/30538955
http://dx.doi.org/10.3389/fcimb.2018.00416
_version_ 1783378183566917632
author Virtanen, Jussa-Pekka
Keto-Timonen, Riikka
Jaakkola, Kaisa
Salin, Noora
Korkeala, Hannu
author_facet Virtanen, Jussa-Pekka
Keto-Timonen, Riikka
Jaakkola, Kaisa
Salin, Noora
Korkeala, Hannu
author_sort Virtanen, Jussa-Pekka
collection PubMed
description Yersinia pseudotuberculosis is a bacterium that not only survives, but also thrives, proliferates, and remains infective at cold-storage temperatures, making it an adept foodborne pathogen. We analyzed the differences in gene expression between Y. pseudotuberculosis IP32953 grown at 3 and 28°C to investigate which genes were significantly more expressed at low temperature at different phases of growth. We isolated and sequenced the RNA from six distinct corresponding growth points at both temperatures to also outline the expression patterns of the differentially expressed genes. Genes involved in motility, chemotaxis, phosphotransferase systems (PTS), and ATP-binding cassette (ABC) transporters of different nutrients such as fructose and mannose showed higher levels of transcripts at 3°C. At the beginning of growth, especially genes involved in securing nutrients, glycolysis, transcription, and translation were upregulated at 3°C. To thrive as well as it does at low temperature, Y. pseudotuberculosis seems to require certain cold shock proteins, especially those encoded by yptb3585, yptb3586, yptb2414, yptb2950, and yptb1423, and transcription factors, like Rho, IF-1, and RbfA, to maintain its protein synthesis. We also found that genes encoding RNA-helicases CsdA (yptb0468), RhlE (yptb1214), and DbpA (yptb1652), which unwind frozen secondary structures of nucleic acids with cold shock proteins, were significantly more expressed at 3°C, indicating that these RNA-helicases are important or even necessary during cold. Genes involved in excreting poisonous spermidine and acquiring compatible solute glycine betaine, by either uptake or biosynthesis, showed higher levels of transcripts at low temperatures. This is the first finding of a strong connection between the aforementioned genes and the cold adaptation of Y. pseudotuberculosis. Understanding the mechanisms behind the cold adaptation of Y. pseudotuberculosis is crucial for controlling its growth during cold storage of food, and will also shed light on microbial cold adaptation in general.
format Online
Article
Text
id pubmed-6277586
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-62775862018-12-11 Changes in Transcriptome of Yersinia pseudotuberculosis IP32953 Grown at 3 and 28°C Detected by RNA Sequencing Shed Light on Cold Adaptation Virtanen, Jussa-Pekka Keto-Timonen, Riikka Jaakkola, Kaisa Salin, Noora Korkeala, Hannu Front Cell Infect Microbiol Cellular and Infection Microbiology Yersinia pseudotuberculosis is a bacterium that not only survives, but also thrives, proliferates, and remains infective at cold-storage temperatures, making it an adept foodborne pathogen. We analyzed the differences in gene expression between Y. pseudotuberculosis IP32953 grown at 3 and 28°C to investigate which genes were significantly more expressed at low temperature at different phases of growth. We isolated and sequenced the RNA from six distinct corresponding growth points at both temperatures to also outline the expression patterns of the differentially expressed genes. Genes involved in motility, chemotaxis, phosphotransferase systems (PTS), and ATP-binding cassette (ABC) transporters of different nutrients such as fructose and mannose showed higher levels of transcripts at 3°C. At the beginning of growth, especially genes involved in securing nutrients, glycolysis, transcription, and translation were upregulated at 3°C. To thrive as well as it does at low temperature, Y. pseudotuberculosis seems to require certain cold shock proteins, especially those encoded by yptb3585, yptb3586, yptb2414, yptb2950, and yptb1423, and transcription factors, like Rho, IF-1, and RbfA, to maintain its protein synthesis. We also found that genes encoding RNA-helicases CsdA (yptb0468), RhlE (yptb1214), and DbpA (yptb1652), which unwind frozen secondary structures of nucleic acids with cold shock proteins, were significantly more expressed at 3°C, indicating that these RNA-helicases are important or even necessary during cold. Genes involved in excreting poisonous spermidine and acquiring compatible solute glycine betaine, by either uptake or biosynthesis, showed higher levels of transcripts at low temperatures. This is the first finding of a strong connection between the aforementioned genes and the cold adaptation of Y. pseudotuberculosis. Understanding the mechanisms behind the cold adaptation of Y. pseudotuberculosis is crucial for controlling its growth during cold storage of food, and will also shed light on microbial cold adaptation in general. Frontiers Media S.A. 2018-11-27 /pmc/articles/PMC6277586/ /pubmed/30538955 http://dx.doi.org/10.3389/fcimb.2018.00416 Text en Copyright © 2018 Virtanen, Keto-Timonen, Jaakkola, Salin and Korkeala. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Virtanen, Jussa-Pekka
Keto-Timonen, Riikka
Jaakkola, Kaisa
Salin, Noora
Korkeala, Hannu
Changes in Transcriptome of Yersinia pseudotuberculosis IP32953 Grown at 3 and 28°C Detected by RNA Sequencing Shed Light on Cold Adaptation
title Changes in Transcriptome of Yersinia pseudotuberculosis IP32953 Grown at 3 and 28°C Detected by RNA Sequencing Shed Light on Cold Adaptation
title_full Changes in Transcriptome of Yersinia pseudotuberculosis IP32953 Grown at 3 and 28°C Detected by RNA Sequencing Shed Light on Cold Adaptation
title_fullStr Changes in Transcriptome of Yersinia pseudotuberculosis IP32953 Grown at 3 and 28°C Detected by RNA Sequencing Shed Light on Cold Adaptation
title_full_unstemmed Changes in Transcriptome of Yersinia pseudotuberculosis IP32953 Grown at 3 and 28°C Detected by RNA Sequencing Shed Light on Cold Adaptation
title_short Changes in Transcriptome of Yersinia pseudotuberculosis IP32953 Grown at 3 and 28°C Detected by RNA Sequencing Shed Light on Cold Adaptation
title_sort changes in transcriptome of yersinia pseudotuberculosis ip32953 grown at 3 and 28°c detected by rna sequencing shed light on cold adaptation
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277586/
https://www.ncbi.nlm.nih.gov/pubmed/30538955
http://dx.doi.org/10.3389/fcimb.2018.00416
work_keys_str_mv AT virtanenjussapekka changesintranscriptomeofyersiniapseudotuberculosisip32953grownat3and28cdetectedbyrnasequencingshedlightoncoldadaptation
AT ketotimonenriikka changesintranscriptomeofyersiniapseudotuberculosisip32953grownat3and28cdetectedbyrnasequencingshedlightoncoldadaptation
AT jaakkolakaisa changesintranscriptomeofyersiniapseudotuberculosisip32953grownat3and28cdetectedbyrnasequencingshedlightoncoldadaptation
AT salinnoora changesintranscriptomeofyersiniapseudotuberculosisip32953grownat3and28cdetectedbyrnasequencingshedlightoncoldadaptation
AT korkealahannu changesintranscriptomeofyersiniapseudotuberculosisip32953grownat3and28cdetectedbyrnasequencingshedlightoncoldadaptation