Cargando…
Contrasting genes conferring short- and long-term biofilm adaptation in Listeria
Listeria monocytogenes is an opportunistic food-borne bacterium that is capable of infecting humans with high rates of hospitalization and mortality. Natural populations are genotypically and phenotypically variable, with some lineages being responsible for most human infections. The success of L. m...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Microbiology Society
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634452/ https://www.ncbi.nlm.nih.gov/pubmed/37850975 http://dx.doi.org/10.1099/mgen.0.001114 |
_version_ | 1785146213387993088 |
---|---|
author | Monteith, William Pascoe, Ben Mourkas, Evangelos Clark, Jack Hakim, Maliha Hitchings, Matthew D. McCarthy, Noel Yahara, Koji Asakura, Hiroshi Sheppard, Samuel K. |
author_facet | Monteith, William Pascoe, Ben Mourkas, Evangelos Clark, Jack Hakim, Maliha Hitchings, Matthew D. McCarthy, Noel Yahara, Koji Asakura, Hiroshi Sheppard, Samuel K. |
author_sort | Monteith, William |
collection | PubMed |
description | Listeria monocytogenes is an opportunistic food-borne bacterium that is capable of infecting humans with high rates of hospitalization and mortality. Natural populations are genotypically and phenotypically variable, with some lineages being responsible for most human infections. The success of L. monocytogenes is linked to its capacity to persist on food and in the environment. Biofilms are an important feature that allow these bacteria to persist and infect humans, so understanding the genetic basis of biofilm formation is key to understanding transmission. We sought to investigate the biofilm-forming ability of L. monocytogenes by identifying genetic variation that underlies biofilm formation in natural populations using genome-wide association studies (GWAS). Changes in gene expression of specific strains during biofilm formation were then investigated using RNA sequencing (RNA-seq). Genetic variation associated with enhanced biofilm formation was identified in 273 genes by GWAS and differential expression in 220 genes by RNA-seq. Statistical analyses show that the number of overlapping genes flagged by either type of experiment is less than expected by random sampling. This novel finding is consistent with an evolutionary scenario where rapid adaptation is driven by variation in gene expression of pioneer genes, and this is followed by slower adaptation driven by nucleotide changes within the core genome. |
format | Online Article Text |
id | pubmed-10634452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Microbiology Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106344522023-11-15 Contrasting genes conferring short- and long-term biofilm adaptation in Listeria Monteith, William Pascoe, Ben Mourkas, Evangelos Clark, Jack Hakim, Maliha Hitchings, Matthew D. McCarthy, Noel Yahara, Koji Asakura, Hiroshi Sheppard, Samuel K. Microb Genom Research Articles Listeria monocytogenes is an opportunistic food-borne bacterium that is capable of infecting humans with high rates of hospitalization and mortality. Natural populations are genotypically and phenotypically variable, with some lineages being responsible for most human infections. The success of L. monocytogenes is linked to its capacity to persist on food and in the environment. Biofilms are an important feature that allow these bacteria to persist and infect humans, so understanding the genetic basis of biofilm formation is key to understanding transmission. We sought to investigate the biofilm-forming ability of L. monocytogenes by identifying genetic variation that underlies biofilm formation in natural populations using genome-wide association studies (GWAS). Changes in gene expression of specific strains during biofilm formation were then investigated using RNA sequencing (RNA-seq). Genetic variation associated with enhanced biofilm formation was identified in 273 genes by GWAS and differential expression in 220 genes by RNA-seq. Statistical analyses show that the number of overlapping genes flagged by either type of experiment is less than expected by random sampling. This novel finding is consistent with an evolutionary scenario where rapid adaptation is driven by variation in gene expression of pioneer genes, and this is followed by slower adaptation driven by nucleotide changes within the core genome. Microbiology Society 2023-10-18 /pmc/articles/PMC10634452/ /pubmed/37850975 http://dx.doi.org/10.1099/mgen.0.001114 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License. This article was made open access via a Publish and Read agreement between the Microbiology Society and the corresponding author’s institution. |
spellingShingle | Research Articles Monteith, William Pascoe, Ben Mourkas, Evangelos Clark, Jack Hakim, Maliha Hitchings, Matthew D. McCarthy, Noel Yahara, Koji Asakura, Hiroshi Sheppard, Samuel K. Contrasting genes conferring short- and long-term biofilm adaptation in Listeria |
title | Contrasting genes conferring short- and long-term biofilm adaptation in Listeria
|
title_full | Contrasting genes conferring short- and long-term biofilm adaptation in Listeria
|
title_fullStr | Contrasting genes conferring short- and long-term biofilm adaptation in Listeria
|
title_full_unstemmed | Contrasting genes conferring short- and long-term biofilm adaptation in Listeria
|
title_short | Contrasting genes conferring short- and long-term biofilm adaptation in Listeria
|
title_sort | contrasting genes conferring short- and long-term biofilm adaptation in listeria |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634452/ https://www.ncbi.nlm.nih.gov/pubmed/37850975 http://dx.doi.org/10.1099/mgen.0.001114 |
work_keys_str_mv | AT monteithwilliam contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria AT pascoeben contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria AT mourkasevangelos contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria AT clarkjack contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria AT hakimmaliha contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria AT hitchingsmatthewd contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria AT mccarthynoel contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria AT yaharakoji contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria AT asakurahiroshi contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria AT sheppardsamuelk contrastinggenesconferringshortandlongtermbiofilmadaptationinlisteria |