Cargando…
Beyond the spore, the exosporium sugar anthrose impacts vegetative Bacillus anthracis gene regulation in cis and trans
The Bacillus anthracis exosporium nap is the outermost portion of spore that interacts with the environment and host systems. Changes to this layer have the potential to impact wide-ranging physiological and immunological processes. The unique sugar, anthrose, normally coats the exosporium nap at it...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050317/ https://www.ncbi.nlm.nih.gov/pubmed/36977718 http://dx.doi.org/10.1038/s41598-023-32162-x |
_version_ | 1785014623522521088 |
---|---|
author | Norris, Michael H. Bluhm, Andrew P. Metrailer, Morgan C. Jiranantasak, Treenate Kirpich, Alexander Hadfield, Ted Ponciano, Jose Miguel Blackburn, Jason K. |
author_facet | Norris, Michael H. Bluhm, Andrew P. Metrailer, Morgan C. Jiranantasak, Treenate Kirpich, Alexander Hadfield, Ted Ponciano, Jose Miguel Blackburn, Jason K. |
author_sort | Norris, Michael H. |
collection | PubMed |
description | The Bacillus anthracis exosporium nap is the outermost portion of spore that interacts with the environment and host systems. Changes to this layer have the potential to impact wide-ranging physiological and immunological processes. The unique sugar, anthrose, normally coats the exosporium nap at its most distal points. We previously identified additional mechanisms rendering B. anthracis anthrose negative. In this work, several new ant (−) B. anthracis strains are identified and the impact of anthrose negativity on spore physiology is investigated. We demonstrate that live-attenuated Sterne vaccines as well as culture filtrate anthrax vaccines generate antibodies targeting non-protein components of the spore. The role of anthrose as a vegetative B. anthracis Sterne signaling molecule is implicated by luminescent expression strain assays, RNA-seq experiments, and toxin secretion analysis by western blot. Pure anthrose and the sporulation-inducing nucleoside analogue decoyinine had similar effects on toxin expression. Co-culture experiments demonstrated gene expression changes in B. anthracis depend on intracellular anthrose status (cis) in addition to anthrose status of extracellular interactions (trans). These findings provide a mechanism for how a unique spore-specific sugar residue affects physiology, expression and genetics of vegetative B. anthracis with impacts on the ecology, pathogenesis, and vaccinology of anthrax. |
format | Online Article Text |
id | pubmed-10050317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100503172023-03-30 Beyond the spore, the exosporium sugar anthrose impacts vegetative Bacillus anthracis gene regulation in cis and trans Norris, Michael H. Bluhm, Andrew P. Metrailer, Morgan C. Jiranantasak, Treenate Kirpich, Alexander Hadfield, Ted Ponciano, Jose Miguel Blackburn, Jason K. Sci Rep Article The Bacillus anthracis exosporium nap is the outermost portion of spore that interacts with the environment and host systems. Changes to this layer have the potential to impact wide-ranging physiological and immunological processes. The unique sugar, anthrose, normally coats the exosporium nap at its most distal points. We previously identified additional mechanisms rendering B. anthracis anthrose negative. In this work, several new ant (−) B. anthracis strains are identified and the impact of anthrose negativity on spore physiology is investigated. We demonstrate that live-attenuated Sterne vaccines as well as culture filtrate anthrax vaccines generate antibodies targeting non-protein components of the spore. The role of anthrose as a vegetative B. anthracis Sterne signaling molecule is implicated by luminescent expression strain assays, RNA-seq experiments, and toxin secretion analysis by western blot. Pure anthrose and the sporulation-inducing nucleoside analogue decoyinine had similar effects on toxin expression. Co-culture experiments demonstrated gene expression changes in B. anthracis depend on intracellular anthrose status (cis) in addition to anthrose status of extracellular interactions (trans). These findings provide a mechanism for how a unique spore-specific sugar residue affects physiology, expression and genetics of vegetative B. anthracis with impacts on the ecology, pathogenesis, and vaccinology of anthrax. Nature Publishing Group UK 2023-03-28 /pmc/articles/PMC10050317/ /pubmed/36977718 http://dx.doi.org/10.1038/s41598-023-32162-x Text en © The Author(s) 2023 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 Norris, Michael H. Bluhm, Andrew P. Metrailer, Morgan C. Jiranantasak, Treenate Kirpich, Alexander Hadfield, Ted Ponciano, Jose Miguel Blackburn, Jason K. Beyond the spore, the exosporium sugar anthrose impacts vegetative Bacillus anthracis gene regulation in cis and trans |
title | Beyond the spore, the exosporium sugar anthrose impacts vegetative Bacillus anthracis gene regulation in cis and trans |
title_full | Beyond the spore, the exosporium sugar anthrose impacts vegetative Bacillus anthracis gene regulation in cis and trans |
title_fullStr | Beyond the spore, the exosporium sugar anthrose impacts vegetative Bacillus anthracis gene regulation in cis and trans |
title_full_unstemmed | Beyond the spore, the exosporium sugar anthrose impacts vegetative Bacillus anthracis gene regulation in cis and trans |
title_short | Beyond the spore, the exosporium sugar anthrose impacts vegetative Bacillus anthracis gene regulation in cis and trans |
title_sort | beyond the spore, the exosporium sugar anthrose impacts vegetative bacillus anthracis gene regulation in cis and trans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10050317/ https://www.ncbi.nlm.nih.gov/pubmed/36977718 http://dx.doi.org/10.1038/s41598-023-32162-x |
work_keys_str_mv | AT norrismichaelh beyondthesporetheexosporiumsugaranthroseimpactsvegetativebacillusanthracisgeneregulationincisandtrans AT bluhmandrewp beyondthesporetheexosporiumsugaranthroseimpactsvegetativebacillusanthracisgeneregulationincisandtrans AT metrailermorganc beyondthesporetheexosporiumsugaranthroseimpactsvegetativebacillusanthracisgeneregulationincisandtrans AT jiranantasaktreenate beyondthesporetheexosporiumsugaranthroseimpactsvegetativebacillusanthracisgeneregulationincisandtrans AT kirpichalexander beyondthesporetheexosporiumsugaranthroseimpactsvegetativebacillusanthracisgeneregulationincisandtrans AT hadfieldted beyondthesporetheexosporiumsugaranthroseimpactsvegetativebacillusanthracisgeneregulationincisandtrans AT poncianojosemiguel beyondthesporetheexosporiumsugaranthroseimpactsvegetativebacillusanthracisgeneregulationincisandtrans AT blackburnjasonk beyondthesporetheexosporiumsugaranthroseimpactsvegetativebacillusanthracisgeneregulationincisandtrans |