Cargando…

Metabolic profiling reveals nutrient preferences during carbon utilization in Bacillus species

The genus Bacillus includes species with diverse natural histories, including free-living nonpathogenic heterotrophs such as B. subtilis and host-dependent pathogens such as B. anthracis (the etiological agent of the disease anthrax) and B. cereus, a cause of food poisoning. Although highly similar...

Descripción completa

Detalles Bibliográficos
Autores principales: Chang, James D., Vaughan, Ellen E., Liu, Carmen Gu, Jelinski, Joseph W., Terwilliger, Austen L., Maresso, Anthony W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8669014/
https://www.ncbi.nlm.nih.gov/pubmed/34903830
http://dx.doi.org/10.1038/s41598-021-03420-7
_version_ 1784614703236907008
author Chang, James D.
Vaughan, Ellen E.
Liu, Carmen Gu
Jelinski, Joseph W.
Terwilliger, Austen L.
Maresso, Anthony W.
author_facet Chang, James D.
Vaughan, Ellen E.
Liu, Carmen Gu
Jelinski, Joseph W.
Terwilliger, Austen L.
Maresso, Anthony W.
author_sort Chang, James D.
collection PubMed
description The genus Bacillus includes species with diverse natural histories, including free-living nonpathogenic heterotrophs such as B. subtilis and host-dependent pathogens such as B. anthracis (the etiological agent of the disease anthrax) and B. cereus, a cause of food poisoning. Although highly similar genotypically, the ecological niches of these three species are mutually exclusive, which raises the untested hypothesis that their metabolism has speciated along a nutritional tract. Here, we developed a pipeline for quantitative total assessment of the use of diverse sources of carbon for general metabolism to better appreciate the “culinary preferences” of three distinct Bacillus species, as well as related Staphylococcus aureus. We show that each species has widely varying metabolic ability to utilize diverse sources of carbon that correlated to their ecological niches. This approach was applied to the growth and survival of B. anthracis in a blood-like environment and find metabolism shifts from sugar to amino acids as the preferred source of energy. Finally, various nutrients in broth and host-like environments are identified that may promote or interfere with bacterial metabolism during infection.
format Online
Article
Text
id pubmed-8669014
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-86690142021-12-15 Metabolic profiling reveals nutrient preferences during carbon utilization in Bacillus species Chang, James D. Vaughan, Ellen E. Liu, Carmen Gu Jelinski, Joseph W. Terwilliger, Austen L. Maresso, Anthony W. Sci Rep Article The genus Bacillus includes species with diverse natural histories, including free-living nonpathogenic heterotrophs such as B. subtilis and host-dependent pathogens such as B. anthracis (the etiological agent of the disease anthrax) and B. cereus, a cause of food poisoning. Although highly similar genotypically, the ecological niches of these three species are mutually exclusive, which raises the untested hypothesis that their metabolism has speciated along a nutritional tract. Here, we developed a pipeline for quantitative total assessment of the use of diverse sources of carbon for general metabolism to better appreciate the “culinary preferences” of three distinct Bacillus species, as well as related Staphylococcus aureus. We show that each species has widely varying metabolic ability to utilize diverse sources of carbon that correlated to their ecological niches. This approach was applied to the growth and survival of B. anthracis in a blood-like environment and find metabolism shifts from sugar to amino acids as the preferred source of energy. Finally, various nutrients in broth and host-like environments are identified that may promote or interfere with bacterial metabolism during infection. Nature Publishing Group UK 2021-12-13 /pmc/articles/PMC8669014/ /pubmed/34903830 http://dx.doi.org/10.1038/s41598-021-03420-7 Text en © The Author(s) 2021 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
Chang, James D.
Vaughan, Ellen E.
Liu, Carmen Gu
Jelinski, Joseph W.
Terwilliger, Austen L.
Maresso, Anthony W.
Metabolic profiling reveals nutrient preferences during carbon utilization in Bacillus species
title Metabolic profiling reveals nutrient preferences during carbon utilization in Bacillus species
title_full Metabolic profiling reveals nutrient preferences during carbon utilization in Bacillus species
title_fullStr Metabolic profiling reveals nutrient preferences during carbon utilization in Bacillus species
title_full_unstemmed Metabolic profiling reveals nutrient preferences during carbon utilization in Bacillus species
title_short Metabolic profiling reveals nutrient preferences during carbon utilization in Bacillus species
title_sort metabolic profiling reveals nutrient preferences during carbon utilization in bacillus species
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8669014/
https://www.ncbi.nlm.nih.gov/pubmed/34903830
http://dx.doi.org/10.1038/s41598-021-03420-7
work_keys_str_mv AT changjamesd metabolicprofilingrevealsnutrientpreferencesduringcarbonutilizationinbacillusspecies
AT vaughanellene metabolicprofilingrevealsnutrientpreferencesduringcarbonutilizationinbacillusspecies
AT liucarmengu metabolicprofilingrevealsnutrientpreferencesduringcarbonutilizationinbacillusspecies
AT jelinskijosephw metabolicprofilingrevealsnutrientpreferencesduringcarbonutilizationinbacillusspecies
AT terwilligeraustenl metabolicprofilingrevealsnutrientpreferencesduringcarbonutilizationinbacillusspecies
AT maressoanthonyw metabolicprofilingrevealsnutrientpreferencesduringcarbonutilizationinbacillusspecies