Cargando…

Transcriptional Landscape of Waddlia chondrophila Aberrant Bodies Induced by Iron Starvation

Chronic infections caused by obligate intracellular bacteria belonging to the Chlamydiales order are related to the formation of persistent developmental forms called aberrant bodies (ABs), which undergo DNA replication without cell division. These enlarged bacteria develop and persist upon exposure...

Descripción completa

Detalles Bibliográficos
Autores principales: Ardissone, Silvia, Scherler, Aurélie, Pillonel, Trestan, Martin, Virginie, Kebbi-Beghdadi, Carole, Greub, Gilbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760296/
https://www.ncbi.nlm.nih.gov/pubmed/33255276
http://dx.doi.org/10.3390/microorganisms8121848
_version_ 1783627299424305152
author Ardissone, Silvia
Scherler, Aurélie
Pillonel, Trestan
Martin, Virginie
Kebbi-Beghdadi, Carole
Greub, Gilbert
author_facet Ardissone, Silvia
Scherler, Aurélie
Pillonel, Trestan
Martin, Virginie
Kebbi-Beghdadi, Carole
Greub, Gilbert
author_sort Ardissone, Silvia
collection PubMed
description Chronic infections caused by obligate intracellular bacteria belonging to the Chlamydiales order are related to the formation of persistent developmental forms called aberrant bodies (ABs), which undergo DNA replication without cell division. These enlarged bacteria develop and persist upon exposure to different stressful conditions such as β-lactam antibiotics, iron deprivation and interferon-γ. However, the mechanisms behind ABs biogenesis remain uncharted. Using an RNA-sequencing approach, we compared the transcriptional profile of ABs induced by iron starvation to untreated bacteria in the Chlamydia-related species Waddlia chondrophila, a potential agent of abortion in ruminants and miscarriage in humans. Consistent with the growth arrest observed following iron depletion, our results indicate a significant reduction in the expression of genes related to energy production, carbohydrate and amino acid metabolism and cell wall/envelope biogenesis, compared to untreated, actively replicating bacteria. Conversely, three putative toxin-antitoxin modules were among the most up-regulated genes upon iron starvation, suggesting that their activation might be involved in growth arrest in adverse conditions, an uncommon feature in obligate intracellular bacteria. Our work represents the first complete transcriptomic profile of a Chlamydia-related species in stressful conditions and sets the grounds for further investigations on the mechanisms underlying chlamydial persistence.
format Online
Article
Text
id pubmed-7760296
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-77602962020-12-26 Transcriptional Landscape of Waddlia chondrophila Aberrant Bodies Induced by Iron Starvation Ardissone, Silvia Scherler, Aurélie Pillonel, Trestan Martin, Virginie Kebbi-Beghdadi, Carole Greub, Gilbert Microorganisms Article Chronic infections caused by obligate intracellular bacteria belonging to the Chlamydiales order are related to the formation of persistent developmental forms called aberrant bodies (ABs), which undergo DNA replication without cell division. These enlarged bacteria develop and persist upon exposure to different stressful conditions such as β-lactam antibiotics, iron deprivation and interferon-γ. However, the mechanisms behind ABs biogenesis remain uncharted. Using an RNA-sequencing approach, we compared the transcriptional profile of ABs induced by iron starvation to untreated bacteria in the Chlamydia-related species Waddlia chondrophila, a potential agent of abortion in ruminants and miscarriage in humans. Consistent with the growth arrest observed following iron depletion, our results indicate a significant reduction in the expression of genes related to energy production, carbohydrate and amino acid metabolism and cell wall/envelope biogenesis, compared to untreated, actively replicating bacteria. Conversely, three putative toxin-antitoxin modules were among the most up-regulated genes upon iron starvation, suggesting that their activation might be involved in growth arrest in adverse conditions, an uncommon feature in obligate intracellular bacteria. Our work represents the first complete transcriptomic profile of a Chlamydia-related species in stressful conditions and sets the grounds for further investigations on the mechanisms underlying chlamydial persistence. MDPI 2020-11-24 /pmc/articles/PMC7760296/ /pubmed/33255276 http://dx.doi.org/10.3390/microorganisms8121848 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ardissone, Silvia
Scherler, Aurélie
Pillonel, Trestan
Martin, Virginie
Kebbi-Beghdadi, Carole
Greub, Gilbert
Transcriptional Landscape of Waddlia chondrophila Aberrant Bodies Induced by Iron Starvation
title Transcriptional Landscape of Waddlia chondrophila Aberrant Bodies Induced by Iron Starvation
title_full Transcriptional Landscape of Waddlia chondrophila Aberrant Bodies Induced by Iron Starvation
title_fullStr Transcriptional Landscape of Waddlia chondrophila Aberrant Bodies Induced by Iron Starvation
title_full_unstemmed Transcriptional Landscape of Waddlia chondrophila Aberrant Bodies Induced by Iron Starvation
title_short Transcriptional Landscape of Waddlia chondrophila Aberrant Bodies Induced by Iron Starvation
title_sort transcriptional landscape of waddlia chondrophila aberrant bodies induced by iron starvation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760296/
https://www.ncbi.nlm.nih.gov/pubmed/33255276
http://dx.doi.org/10.3390/microorganisms8121848
work_keys_str_mv AT ardissonesilvia transcriptionallandscapeofwaddliachondrophilaaberrantbodiesinducedbyironstarvation
AT scherleraurelie transcriptionallandscapeofwaddliachondrophilaaberrantbodiesinducedbyironstarvation
AT pilloneltrestan transcriptionallandscapeofwaddliachondrophilaaberrantbodiesinducedbyironstarvation
AT martinvirginie transcriptionallandscapeofwaddliachondrophilaaberrantbodiesinducedbyironstarvation
AT kebbibeghdadicarole transcriptionallandscapeofwaddliachondrophilaaberrantbodiesinducedbyironstarvation
AT greubgilbert transcriptionallandscapeofwaddliachondrophilaaberrantbodiesinducedbyironstarvation