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Identification of the Extracytoplasmic Function σ Factor σ(P) Regulon in Bacillus thuringiensis
Bacillus thuringiensis and other members of the Bacillus cereus family are resistant to many β-lactams. Resistance is dependent upon the extracytoplasmic function sigma factor σ(P). We used label-free quantitative proteomics to identify proteins whose expression was dependent upon σ(P). We compared...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Microbiology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791391/ https://www.ncbi.nlm.nih.gov/pubmed/35080471 http://dx.doi.org/10.1128/msphere.00967-21 |
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author | Ho, Theresa D. Nauta, Kelsie M. Luhmann, Emma K. Radoshevich, Lilliana Ellermeier, Craig D. |
author_facet | Ho, Theresa D. Nauta, Kelsie M. Luhmann, Emma K. Radoshevich, Lilliana Ellermeier, Craig D. |
author_sort | Ho, Theresa D. |
collection | PubMed |
description | Bacillus thuringiensis and other members of the Bacillus cereus family are resistant to many β-lactams. Resistance is dependent upon the extracytoplasmic function sigma factor σ(P). We used label-free quantitative proteomics to identify proteins whose expression was dependent upon σ(P). We compared the protein profiles of strains which either lacked σ(P) or overexpressed σ(P). We identified 8 members of the σ(P) regulon which included four β-lactamases as well as three penicillin-binding proteins (PBPs). Using transcriptional reporters, we confirmed that these genes are induced by β-lactams in a σ(P)-dependent manner. These genes were deleted individually or in various combinations to determine their role in resistance to a subset of β-lactams, including ampicillin, methicillin, cephalexin, and cephalothin. We found that different combinations of β-lactamases and PBPs are involved in resistance to different β-lactams. Our data show that B. thuringiensis utilizes a suite of enzymes to protect itself from β-lactam antibiotics. IMPORTANCE Antimicrobial resistance is major concern for public health. β-Lactams remain an important treatment option for many diseases. However, the spread of β-lactam resistance continues to rise. Many pathogens acquire antibiotic resistance from environmental bacteria. Thus, understanding β-lactam resistance in environmental strains may provide insights into additional mechanisms of antibiotic resistance. Here, we describe how a single regulatory system, σ(P), in B. thuringiensis controls expression of multiple genes involved in resistance to β-lactams. Our findings indicate that some of these genes are partially redundant. Our data also suggest that the large number of genes controlled by σ(P) results in increased resistance to a wider range of β-lactam classes than any single gene could provide. |
format | Online Article Text |
id | pubmed-8791391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-87913912022-02-09 Identification of the Extracytoplasmic Function σ Factor σ(P) Regulon in Bacillus thuringiensis Ho, Theresa D. Nauta, Kelsie M. Luhmann, Emma K. Radoshevich, Lilliana Ellermeier, Craig D. mSphere Research Article Bacillus thuringiensis and other members of the Bacillus cereus family are resistant to many β-lactams. Resistance is dependent upon the extracytoplasmic function sigma factor σ(P). We used label-free quantitative proteomics to identify proteins whose expression was dependent upon σ(P). We compared the protein profiles of strains which either lacked σ(P) or overexpressed σ(P). We identified 8 members of the σ(P) regulon which included four β-lactamases as well as three penicillin-binding proteins (PBPs). Using transcriptional reporters, we confirmed that these genes are induced by β-lactams in a σ(P)-dependent manner. These genes were deleted individually or in various combinations to determine their role in resistance to a subset of β-lactams, including ampicillin, methicillin, cephalexin, and cephalothin. We found that different combinations of β-lactamases and PBPs are involved in resistance to different β-lactams. Our data show that B. thuringiensis utilizes a suite of enzymes to protect itself from β-lactam antibiotics. IMPORTANCE Antimicrobial resistance is major concern for public health. β-Lactams remain an important treatment option for many diseases. However, the spread of β-lactam resistance continues to rise. Many pathogens acquire antibiotic resistance from environmental bacteria. Thus, understanding β-lactam resistance in environmental strains may provide insights into additional mechanisms of antibiotic resistance. Here, we describe how a single regulatory system, σ(P), in B. thuringiensis controls expression of multiple genes involved in resistance to β-lactams. Our findings indicate that some of these genes are partially redundant. Our data also suggest that the large number of genes controlled by σ(P) results in increased resistance to a wider range of β-lactam classes than any single gene could provide. American Society for Microbiology 2022-01-26 /pmc/articles/PMC8791391/ /pubmed/35080471 http://dx.doi.org/10.1128/msphere.00967-21 Text en Copyright © 2022 Ho et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Ho, Theresa D. Nauta, Kelsie M. Luhmann, Emma K. Radoshevich, Lilliana Ellermeier, Craig D. Identification of the Extracytoplasmic Function σ Factor σ(P) Regulon in Bacillus thuringiensis |
title | Identification of the Extracytoplasmic Function σ Factor σ(P) Regulon in Bacillus thuringiensis |
title_full | Identification of the Extracytoplasmic Function σ Factor σ(P) Regulon in Bacillus thuringiensis |
title_fullStr | Identification of the Extracytoplasmic Function σ Factor σ(P) Regulon in Bacillus thuringiensis |
title_full_unstemmed | Identification of the Extracytoplasmic Function σ Factor σ(P) Regulon in Bacillus thuringiensis |
title_short | Identification of the Extracytoplasmic Function σ Factor σ(P) Regulon in Bacillus thuringiensis |
title_sort | identification of the extracytoplasmic function σ factor σ(p) regulon in bacillus thuringiensis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791391/ https://www.ncbi.nlm.nih.gov/pubmed/35080471 http://dx.doi.org/10.1128/msphere.00967-21 |
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