Cargando…

Genomic and transcriptomic profiling of phoenix colonies

Pseudomonas aeruginosa is a Gram-negative bacterium responsible for numerous human infections. Previously, novel antibiotic tolerant variants known as phoenix colonies as well as variants similar to viable but non-culturable (VBNC) colonies were identified in response to high concentrations of amino...

Descripción completa

Detalles Bibliográficos
Autores principales: Sindeldecker, Devin, Dunn, Matthew, Zimmer, Aubree, Anderson, Matthew, Alfonzo, Juan, Stoodley, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374717/
https://www.ncbi.nlm.nih.gov/pubmed/35962051
http://dx.doi.org/10.1038/s41598-022-18059-1
_version_ 1784767848619442176
author Sindeldecker, Devin
Dunn, Matthew
Zimmer, Aubree
Anderson, Matthew
Alfonzo, Juan
Stoodley, Paul
author_facet Sindeldecker, Devin
Dunn, Matthew
Zimmer, Aubree
Anderson, Matthew
Alfonzo, Juan
Stoodley, Paul
author_sort Sindeldecker, Devin
collection PubMed
description Pseudomonas aeruginosa is a Gram-negative bacterium responsible for numerous human infections. Previously, novel antibiotic tolerant variants known as phoenix colonies as well as variants similar to viable but non-culturable (VBNC) colonies were identified in response to high concentrations of aminoglycosides. In this study, the mechanisms behind phoenix colony and VBNC-like colony emergence were further explored using both whole genome sequencing and RNA sequencing. Phoenix colonies were found to have a single nucleotide polymorphism (SNP) in the PA4673 gene, which is predicted to encode a GTP-binding protein. No SNPs were identified within VBNC-like colonies compared to the founder population. RNA sequencing did not detect change in expression of PA4673 but revealed multiple differentially expressed genes that may play a role in phoenix colony emergence. One of these differentially expressed genes, PA3626, encodes for a tRNA pseudouridine synthase which when knocked out led to a complete lack of phoenix colonies. Although not immediately clear whether the identified genes in this study may have interactions which have not yet been recognized, they may contribute to the understanding of how phoenix colonies are able to emerge and survive in the presence of antibiotic exposure.
format Online
Article
Text
id pubmed-9374717
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-93747172022-08-14 Genomic and transcriptomic profiling of phoenix colonies Sindeldecker, Devin Dunn, Matthew Zimmer, Aubree Anderson, Matthew Alfonzo, Juan Stoodley, Paul Sci Rep Article Pseudomonas aeruginosa is a Gram-negative bacterium responsible for numerous human infections. Previously, novel antibiotic tolerant variants known as phoenix colonies as well as variants similar to viable but non-culturable (VBNC) colonies were identified in response to high concentrations of aminoglycosides. In this study, the mechanisms behind phoenix colony and VBNC-like colony emergence were further explored using both whole genome sequencing and RNA sequencing. Phoenix colonies were found to have a single nucleotide polymorphism (SNP) in the PA4673 gene, which is predicted to encode a GTP-binding protein. No SNPs were identified within VBNC-like colonies compared to the founder population. RNA sequencing did not detect change in expression of PA4673 but revealed multiple differentially expressed genes that may play a role in phoenix colony emergence. One of these differentially expressed genes, PA3626, encodes for a tRNA pseudouridine synthase which when knocked out led to a complete lack of phoenix colonies. Although not immediately clear whether the identified genes in this study may have interactions which have not yet been recognized, they may contribute to the understanding of how phoenix colonies are able to emerge and survive in the presence of antibiotic exposure. Nature Publishing Group UK 2022-08-12 /pmc/articles/PMC9374717/ /pubmed/35962051 http://dx.doi.org/10.1038/s41598-022-18059-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sindeldecker, Devin
Dunn, Matthew
Zimmer, Aubree
Anderson, Matthew
Alfonzo, Juan
Stoodley, Paul
Genomic and transcriptomic profiling of phoenix colonies
title Genomic and transcriptomic profiling of phoenix colonies
title_full Genomic and transcriptomic profiling of phoenix colonies
title_fullStr Genomic and transcriptomic profiling of phoenix colonies
title_full_unstemmed Genomic and transcriptomic profiling of phoenix colonies
title_short Genomic and transcriptomic profiling of phoenix colonies
title_sort genomic and transcriptomic profiling of phoenix colonies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9374717/
https://www.ncbi.nlm.nih.gov/pubmed/35962051
http://dx.doi.org/10.1038/s41598-022-18059-1
work_keys_str_mv AT sindeldeckerdevin genomicandtranscriptomicprofilingofphoenixcolonies
AT dunnmatthew genomicandtranscriptomicprofilingofphoenixcolonies
AT zimmeraubree genomicandtranscriptomicprofilingofphoenixcolonies
AT andersonmatthew genomicandtranscriptomicprofilingofphoenixcolonies
AT alfonzojuan genomicandtranscriptomicprofilingofphoenixcolonies
AT stoodleypaul genomicandtranscriptomicprofilingofphoenixcolonies