Cargando…

A CRISPR interference screen reveals a role for cell wall teichoic acids in conjugation in Bacillus subtilis

Conjugative elements are widespread in bacteria and include plasmids and integrative and conjugative elements (ICEs). They transfer from donor to recipient cells via an element‐encoded type IV secretion system. These elements interact with and utilize host functions for their lifecycles. We sought t...

Descripción completa

Detalles Bibliográficos
Autores principales: Harden, M. Michael, Anderson, Mary E., Grossman, Alan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324163/
https://www.ncbi.nlm.nih.gov/pubmed/35490406
http://dx.doi.org/10.1111/mmi.14914
_version_ 1784756739949723648
author Harden, M. Michael
Anderson, Mary E.
Grossman, Alan D.
author_facet Harden, M. Michael
Anderson, Mary E.
Grossman, Alan D.
author_sort Harden, M. Michael
collection PubMed
description Conjugative elements are widespread in bacteria and include plasmids and integrative and conjugative elements (ICEs). They transfer from donor to recipient cells via an element‐encoded type IV secretion system. These elements interact with and utilize host functions for their lifecycles. We sought to identify essential host genes involved in the lifecycle of the integrative and conjugative element ICEBs1 of Bacillus subtilis. We constructed a library of strains for inducible knockdown of essential B. subtilis genes using CRISPR interference. Each strain expressed one guide RNA in ICEBs1. We induced partial interference of essential genes and identified those that caused an acute defect in acquisition of ICEBs1 by recipient cells. This screen revealed that reducing expression of genes needed for synthesis of cell wall teichoic acids caused a decrease in conjugation. Using three different ways to reduce their synthesis, we found that wall teichoic acids were necessary in both donors and recipients for efficient conjugative transfer of ICEBs1. Further, we found that depletion of wall teichoic acids caused cells involved in ICEBs1 conjugation to die, most likely from damage to the cell envelope. Our results indicate that wall teichoic acids help protect against envelope stress caused by active conjugation machines.
format Online
Article
Text
id pubmed-9324163
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-93241632022-07-30 A CRISPR interference screen reveals a role for cell wall teichoic acids in conjugation in Bacillus subtilis Harden, M. Michael Anderson, Mary E. Grossman, Alan D. Mol Microbiol Research Articles Conjugative elements are widespread in bacteria and include plasmids and integrative and conjugative elements (ICEs). They transfer from donor to recipient cells via an element‐encoded type IV secretion system. These elements interact with and utilize host functions for their lifecycles. We sought to identify essential host genes involved in the lifecycle of the integrative and conjugative element ICEBs1 of Bacillus subtilis. We constructed a library of strains for inducible knockdown of essential B. subtilis genes using CRISPR interference. Each strain expressed one guide RNA in ICEBs1. We induced partial interference of essential genes and identified those that caused an acute defect in acquisition of ICEBs1 by recipient cells. This screen revealed that reducing expression of genes needed for synthesis of cell wall teichoic acids caused a decrease in conjugation. Using three different ways to reduce their synthesis, we found that wall teichoic acids were necessary in both donors and recipients for efficient conjugative transfer of ICEBs1. Further, we found that depletion of wall teichoic acids caused cells involved in ICEBs1 conjugation to die, most likely from damage to the cell envelope. Our results indicate that wall teichoic acids help protect against envelope stress caused by active conjugation machines. John Wiley and Sons Inc. 2022-05-21 2022-06 /pmc/articles/PMC9324163/ /pubmed/35490406 http://dx.doi.org/10.1111/mmi.14914 Text en © 2022 The Authors. Molecular Microbiology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Harden, M. Michael
Anderson, Mary E.
Grossman, Alan D.
A CRISPR interference screen reveals a role for cell wall teichoic acids in conjugation in Bacillus subtilis
title A CRISPR interference screen reveals a role for cell wall teichoic acids in conjugation in Bacillus subtilis
title_full A CRISPR interference screen reveals a role for cell wall teichoic acids in conjugation in Bacillus subtilis
title_fullStr A CRISPR interference screen reveals a role for cell wall teichoic acids in conjugation in Bacillus subtilis
title_full_unstemmed A CRISPR interference screen reveals a role for cell wall teichoic acids in conjugation in Bacillus subtilis
title_short A CRISPR interference screen reveals a role for cell wall teichoic acids in conjugation in Bacillus subtilis
title_sort crispr interference screen reveals a role for cell wall teichoic acids in conjugation in bacillus subtilis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324163/
https://www.ncbi.nlm.nih.gov/pubmed/35490406
http://dx.doi.org/10.1111/mmi.14914
work_keys_str_mv AT hardenmmichael acrisprinterferencescreenrevealsaroleforcellwallteichoicacidsinconjugationinbacillussubtilis
AT andersonmarye acrisprinterferencescreenrevealsaroleforcellwallteichoicacidsinconjugationinbacillussubtilis
AT grossmanaland acrisprinterferencescreenrevealsaroleforcellwallteichoicacidsinconjugationinbacillussubtilis
AT hardenmmichael crisprinterferencescreenrevealsaroleforcellwallteichoicacidsinconjugationinbacillussubtilis
AT andersonmarye crisprinterferencescreenrevealsaroleforcellwallteichoicacidsinconjugationinbacillussubtilis
AT grossmanaland crisprinterferencescreenrevealsaroleforcellwallteichoicacidsinconjugationinbacillussubtilis