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Sulfolobus acidocaldarius adhesion pili power twitching motility in the absence of a dedicated retraction ATPase
Type IV pili are ancient and widespread filamentous organelles found in most bacterial and archaeal phyla where they support a wide range of functions, including substrate adhesion, DNA uptake, self aggregation, and cell motility. In most bacteria, PilT-family ATPases disassemble adhesion pili, caus...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10418518/ https://www.ncbi.nlm.nih.gov/pubmed/37577505 http://dx.doi.org/10.1101/2023.08.04.552066 |
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author | Charles-Orszag, Arthur van Wolferen, Marleen Lord, Samuel J. Albers, Sonja-Verena Mullins, R. Dyche |
author_facet | Charles-Orszag, Arthur van Wolferen, Marleen Lord, Samuel J. Albers, Sonja-Verena Mullins, R. Dyche |
author_sort | Charles-Orszag, Arthur |
collection | PubMed |
description | Type IV pili are ancient and widespread filamentous organelles found in most bacterial and archaeal phyla where they support a wide range of functions, including substrate adhesion, DNA uptake, self aggregation, and cell motility. In most bacteria, PilT-family ATPases disassemble adhesion pili, causing them to rapidly retract and produce twitching motility, important for surface colonization. As archaea do not possess homologs of PilT, it was thought that archaeal pili cannot retract. Here, we employ live-cell imaging under native conditions (75°C and pH 2), together with automated single-cell tracking, high-temperature fluorescence imaging, and genetic manipulation to demonstrate that S. acidocaldarius exhibits bona fide twitching motility, and that this behavior depends specifically on retractable adhesion pili. Our results demonstrate that archaeal adhesion pili are capable of retraction in the absence of a PilT retraction ATPase and suggests that the ancestral type IV pilus machinery in the last universal common ancestor (LUCA) relied on such a bifunctional ATPase for both extension and retraction. |
format | Online Article Text |
id | pubmed-10418518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104185182023-08-12 Sulfolobus acidocaldarius adhesion pili power twitching motility in the absence of a dedicated retraction ATPase Charles-Orszag, Arthur van Wolferen, Marleen Lord, Samuel J. Albers, Sonja-Verena Mullins, R. Dyche bioRxiv Article Type IV pili are ancient and widespread filamentous organelles found in most bacterial and archaeal phyla where they support a wide range of functions, including substrate adhesion, DNA uptake, self aggregation, and cell motility. In most bacteria, PilT-family ATPases disassemble adhesion pili, causing them to rapidly retract and produce twitching motility, important for surface colonization. As archaea do not possess homologs of PilT, it was thought that archaeal pili cannot retract. Here, we employ live-cell imaging under native conditions (75°C and pH 2), together with automated single-cell tracking, high-temperature fluorescence imaging, and genetic manipulation to demonstrate that S. acidocaldarius exhibits bona fide twitching motility, and that this behavior depends specifically on retractable adhesion pili. Our results demonstrate that archaeal adhesion pili are capable of retraction in the absence of a PilT retraction ATPase and suggests that the ancestral type IV pilus machinery in the last universal common ancestor (LUCA) relied on such a bifunctional ATPase for both extension and retraction. Cold Spring Harbor Laboratory 2023-08-04 /pmc/articles/PMC10418518/ /pubmed/37577505 http://dx.doi.org/10.1101/2023.08.04.552066 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Charles-Orszag, Arthur van Wolferen, Marleen Lord, Samuel J. Albers, Sonja-Verena Mullins, R. Dyche Sulfolobus acidocaldarius adhesion pili power twitching motility in the absence of a dedicated retraction ATPase |
title | Sulfolobus acidocaldarius adhesion pili power twitching motility in the absence of a dedicated retraction ATPase |
title_full | Sulfolobus acidocaldarius adhesion pili power twitching motility in the absence of a dedicated retraction ATPase |
title_fullStr | Sulfolobus acidocaldarius adhesion pili power twitching motility in the absence of a dedicated retraction ATPase |
title_full_unstemmed | Sulfolobus acidocaldarius adhesion pili power twitching motility in the absence of a dedicated retraction ATPase |
title_short | Sulfolobus acidocaldarius adhesion pili power twitching motility in the absence of a dedicated retraction ATPase |
title_sort | sulfolobus acidocaldarius adhesion pili power twitching motility in the absence of a dedicated retraction atpase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10418518/ https://www.ncbi.nlm.nih.gov/pubmed/37577505 http://dx.doi.org/10.1101/2023.08.04.552066 |
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