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Lantibiotic production is a burden for the producing staphylococci
Lantibiotics are antimicrobial peptides that contain non-proteinogenic amino acids lanthionine and 3-methyllanthionine and are produced by Gram-positive bacteria. Here we addressed the pros and cons of lantibiotic production for its producing strains. Two staphylococcal strains, S. gallinarum Tü3928...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945643/ https://www.ncbi.nlm.nih.gov/pubmed/29749386 http://dx.doi.org/10.1038/s41598-018-25935-2 |
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author | Ebner, Patrick Reichert, Sebastian Luqman, Arif Krismer, Bernhard Popella, Peter Götz, Friedrich |
author_facet | Ebner, Patrick Reichert, Sebastian Luqman, Arif Krismer, Bernhard Popella, Peter Götz, Friedrich |
author_sort | Ebner, Patrick |
collection | PubMed |
description | Lantibiotics are antimicrobial peptides that contain non-proteinogenic amino acids lanthionine and 3-methyllanthionine and are produced by Gram-positive bacteria. Here we addressed the pros and cons of lantibiotic production for its producing strains. Two staphylococcal strains, S. gallinarum Tü3928 and S. epidermidis Tü3298 producing gallidermin and epidermin respectively were selected. In each of these parental strains, the structural genes gdmA and epiA were deleted; all the other biosynthetic genes including the immunity genes were left intact. Comparative analysis of the lantibiotic-producing strains with their non-producing mutants revealed that lantibiotic production is a burden for the cells. The production affected growth, caused release of ATP, lipids and increased the excretion of cytoplasmic proteins (ECP). The epidermin and gallidermin immunity genes were insufficient to protect the cells from their own product. Co-cultivation studies showed that the ΔgdmA mutant has an advantage over the parental strain; the latter was outcompeted. On the one hand, the production of staphylococcal lantibiotics is beneficial by suppressing competitors, but on the other hand they impose a burden on the producing-strains when they accumulate in higher amounts. Our observations explain why antibiotic-producing strains occur as a minority on our skin and other ecological niches, but retain corresponding antibiotic resistance. |
format | Online Article Text |
id | pubmed-5945643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59456432018-05-14 Lantibiotic production is a burden for the producing staphylococci Ebner, Patrick Reichert, Sebastian Luqman, Arif Krismer, Bernhard Popella, Peter Götz, Friedrich Sci Rep Article Lantibiotics are antimicrobial peptides that contain non-proteinogenic amino acids lanthionine and 3-methyllanthionine and are produced by Gram-positive bacteria. Here we addressed the pros and cons of lantibiotic production for its producing strains. Two staphylococcal strains, S. gallinarum Tü3928 and S. epidermidis Tü3298 producing gallidermin and epidermin respectively were selected. In each of these parental strains, the structural genes gdmA and epiA were deleted; all the other biosynthetic genes including the immunity genes were left intact. Comparative analysis of the lantibiotic-producing strains with their non-producing mutants revealed that lantibiotic production is a burden for the cells. The production affected growth, caused release of ATP, lipids and increased the excretion of cytoplasmic proteins (ECP). The epidermin and gallidermin immunity genes were insufficient to protect the cells from their own product. Co-cultivation studies showed that the ΔgdmA mutant has an advantage over the parental strain; the latter was outcompeted. On the one hand, the production of staphylococcal lantibiotics is beneficial by suppressing competitors, but on the other hand they impose a burden on the producing-strains when they accumulate in higher amounts. Our observations explain why antibiotic-producing strains occur as a minority on our skin and other ecological niches, but retain corresponding antibiotic resistance. Nature Publishing Group UK 2018-05-10 /pmc/articles/PMC5945643/ /pubmed/29749386 http://dx.doi.org/10.1038/s41598-018-25935-2 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ebner, Patrick Reichert, Sebastian Luqman, Arif Krismer, Bernhard Popella, Peter Götz, Friedrich Lantibiotic production is a burden for the producing staphylococci |
title | Lantibiotic production is a burden for the producing staphylococci |
title_full | Lantibiotic production is a burden for the producing staphylococci |
title_fullStr | Lantibiotic production is a burden for the producing staphylococci |
title_full_unstemmed | Lantibiotic production is a burden for the producing staphylococci |
title_short | Lantibiotic production is a burden for the producing staphylococci |
title_sort | lantibiotic production is a burden for the producing staphylococci |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5945643/ https://www.ncbi.nlm.nih.gov/pubmed/29749386 http://dx.doi.org/10.1038/s41598-018-25935-2 |
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