Cargando…

The Transcriptional Regulator SpxA1 Influences the Morphology and Virulence of Listeria monocytogenes

Listeria monocytogenes is a Gram-positive facultative anaerobe and an excellent model pathogen for investigating regulatory changes that occur during infection of a mammalian host. SpxA1 is a widely conserved transcriptional regulator that induces expression of peroxide-detoxifying genes in L. monoc...

Descripción completa

Detalles Bibliográficos
Autores principales: Cesinger, Monica R., Daramola, Oluwasegun I., Kwiatkowski, Lucy M., Reniere, Michelle L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584327/
https://www.ncbi.nlm.nih.gov/pubmed/36102657
http://dx.doi.org/10.1128/iai.00211-22
_version_ 1784813239718117376
author Cesinger, Monica R.
Daramola, Oluwasegun I.
Kwiatkowski, Lucy M.
Reniere, Michelle L.
author_facet Cesinger, Monica R.
Daramola, Oluwasegun I.
Kwiatkowski, Lucy M.
Reniere, Michelle L.
author_sort Cesinger, Monica R.
collection PubMed
description Listeria monocytogenes is a Gram-positive facultative anaerobe and an excellent model pathogen for investigating regulatory changes that occur during infection of a mammalian host. SpxA1 is a widely conserved transcriptional regulator that induces expression of peroxide-detoxifying genes in L. monocytogenes and is thus required for aerobic growth. SpxA1 is also required for L. monocytogenes virulence, although the SpxA1-dependent genes important in this context remain to be identified. Here, we sought to investigate the role of SpxA1 in a tissue culture model of infection and made the surprising discovery that ΔspxA1 cells are dramatically elongated during growth in the host cytosol. Quantitative microscopy revealed that ΔspxA1 cells also form elongated filaments extracellularly during early exponential phase in rich medium. Scanning and transmission electron microscopy analysis found that the likely cause of this morphological phenotype is aberrantly placed division septa localized outside cell midpoints. Quantitative mass spectrometry of whole-cell lysates identified SpxA1-dependent changes in protein abundance, including a significant number of motility and flagellar proteins that were depleted in the ΔspxA1 mutant. Accordingly, we found that both the filamentation and the lack of motility contributed to decreased phagocytosis of ΔspxA1 cells by macrophages. Overall, we identify a novel role for SpxA1 in regulating cell elongation and motility, both of which impact L. monocytogenes virulence.
format Online
Article
Text
id pubmed-9584327
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-95843272022-10-21 The Transcriptional Regulator SpxA1 Influences the Morphology and Virulence of Listeria monocytogenes Cesinger, Monica R. Daramola, Oluwasegun I. Kwiatkowski, Lucy M. Reniere, Michelle L. Infect Immun Molecular Pathogenesis Listeria monocytogenes is a Gram-positive facultative anaerobe and an excellent model pathogen for investigating regulatory changes that occur during infection of a mammalian host. SpxA1 is a widely conserved transcriptional regulator that induces expression of peroxide-detoxifying genes in L. monocytogenes and is thus required for aerobic growth. SpxA1 is also required for L. monocytogenes virulence, although the SpxA1-dependent genes important in this context remain to be identified. Here, we sought to investigate the role of SpxA1 in a tissue culture model of infection and made the surprising discovery that ΔspxA1 cells are dramatically elongated during growth in the host cytosol. Quantitative microscopy revealed that ΔspxA1 cells also form elongated filaments extracellularly during early exponential phase in rich medium. Scanning and transmission electron microscopy analysis found that the likely cause of this morphological phenotype is aberrantly placed division septa localized outside cell midpoints. Quantitative mass spectrometry of whole-cell lysates identified SpxA1-dependent changes in protein abundance, including a significant number of motility and flagellar proteins that were depleted in the ΔspxA1 mutant. Accordingly, we found that both the filamentation and the lack of motility contributed to decreased phagocytosis of ΔspxA1 cells by macrophages. Overall, we identify a novel role for SpxA1 in regulating cell elongation and motility, both of which impact L. monocytogenes virulence. American Society for Microbiology 2022-09-14 /pmc/articles/PMC9584327/ /pubmed/36102657 http://dx.doi.org/10.1128/iai.00211-22 Text en Copyright © 2022 Cesinger et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Molecular Pathogenesis
Cesinger, Monica R.
Daramola, Oluwasegun I.
Kwiatkowski, Lucy M.
Reniere, Michelle L.
The Transcriptional Regulator SpxA1 Influences the Morphology and Virulence of Listeria monocytogenes
title The Transcriptional Regulator SpxA1 Influences the Morphology and Virulence of Listeria monocytogenes
title_full The Transcriptional Regulator SpxA1 Influences the Morphology and Virulence of Listeria monocytogenes
title_fullStr The Transcriptional Regulator SpxA1 Influences the Morphology and Virulence of Listeria monocytogenes
title_full_unstemmed The Transcriptional Regulator SpxA1 Influences the Morphology and Virulence of Listeria monocytogenes
title_short The Transcriptional Regulator SpxA1 Influences the Morphology and Virulence of Listeria monocytogenes
title_sort transcriptional regulator spxa1 influences the morphology and virulence of listeria monocytogenes
topic Molecular Pathogenesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584327/
https://www.ncbi.nlm.nih.gov/pubmed/36102657
http://dx.doi.org/10.1128/iai.00211-22
work_keys_str_mv AT cesingermonicar thetranscriptionalregulatorspxa1influencesthemorphologyandvirulenceoflisteriamonocytogenes
AT daramolaoluwaseguni thetranscriptionalregulatorspxa1influencesthemorphologyandvirulenceoflisteriamonocytogenes
AT kwiatkowskilucym thetranscriptionalregulatorspxa1influencesthemorphologyandvirulenceoflisteriamonocytogenes
AT renieremichellel thetranscriptionalregulatorspxa1influencesthemorphologyandvirulenceoflisteriamonocytogenes
AT cesingermonicar transcriptionalregulatorspxa1influencesthemorphologyandvirulenceoflisteriamonocytogenes
AT daramolaoluwaseguni transcriptionalregulatorspxa1influencesthemorphologyandvirulenceoflisteriamonocytogenes
AT kwiatkowskilucym transcriptionalregulatorspxa1influencesthemorphologyandvirulenceoflisteriamonocytogenes
AT renieremichellel transcriptionalregulatorspxa1influencesthemorphologyandvirulenceoflisteriamonocytogenes