Cargando…

Extremophile Metal Resistance: Plasmid-Encoded Functions in Streptomyces mirabilis

The extreme metal tolerance of up to 130 mM NiSO(4) in Streptomyces mirabilis P16B-1 was investigated. Genome sequencing revealed the presence of a large linear plasmid, pI. To identify plasmid-encoded determinants of metal resistance, a newly established transformation system was used to characteri...

Descripción completa

Detalles Bibliográficos
Autores principales: Brangsch, Hanka, Höller, Marlene, Krauβe, Thomas, Waqas, Mohammed, Schroeckh, Volker, Brakhage, Axel A., Bunk, Boyke, Spröer, Cathrin, Overmann, Jörg, Kothe, Erika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195940/
https://www.ncbi.nlm.nih.gov/pubmed/35604229
http://dx.doi.org/10.1128/aem.00085-22
_version_ 1784727079205470208
author Brangsch, Hanka
Höller, Marlene
Krauβe, Thomas
Waqas, Mohammed
Schroeckh, Volker
Brakhage, Axel A.
Bunk, Boyke
Spröer, Cathrin
Overmann, Jörg
Kothe, Erika
author_facet Brangsch, Hanka
Höller, Marlene
Krauβe, Thomas
Waqas, Mohammed
Schroeckh, Volker
Brakhage, Axel A.
Bunk, Boyke
Spröer, Cathrin
Overmann, Jörg
Kothe, Erika
author_sort Brangsch, Hanka
collection PubMed
description The extreme metal tolerance of up to 130 mM NiSO(4) in Streptomyces mirabilis P16B-1 was investigated. Genome sequencing revealed the presence of a large linear plasmid, pI. To identify plasmid-encoded determinants of metal resistance, a newly established transformation system was used to characterize the predicted plasmid-encoded loci nreB, hoxN, and copYZ. Reintroduction into the plasmid-cured S. mirabilis ΔpI confirmed that the predicted metal transporter gene nreB constitutes a nickel resistance factor, which was further supported by its heterologous expression in Escherichia coli. In contrast, the predicted nickel exporter gene hoxN decreased nickel tolerance, while copper tolerance was enhanced. The predicted copper-dependent transcriptional regulator gene copY did not induce tolerance toward either metal. Since genes for transfer were identified on the plasmid, its conjugational transfer to the metal-sensitive Streptomyces lividans TK24 was checked. This resulted in acquired tolerance toward 30 mM nickel and additionally increased the tolerance toward copper and cobalt, while oxidative stress tolerance remained unchanged. Intracellular nickel concentrations decreased in the transconjugant strain. The high extracellular nickel concentrations allowed for biomineralization. Plasmid transfer could also be confirmed into the co-occurring actinomycete Kribbella spp. in soil microcosms. IMPORTANCE Living in extremely metal-rich environments requires specific adaptations, and often, specific metal tolerance genes are encoded on a transferable plasmid. Here, Streptomyces mirabilis P16B-1, isolated from a former mining area and able to grow with up to 130 mM NiSO(4), was investigated. The bacterial chromosome, as well as a giant plasmid, was sequenced. The plasmid-borne gene nreB was confirmed to confer metal resistance. A newly established transformation system allowed us to construct a plasmid-cured S. mirabilis as well as an nreB-rescued strain in addition to confirming nreB encoding nickel resistance if heterologously expressed in E. coli. The potential of intra- and interspecific plasmid transfer, together with the presence of metal resistance factors on that plasmid, underlines the importance of plasmids for transfer of resistance factors within a bacterial soil community.
format Online
Article
Text
id pubmed-9195940
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-91959402022-06-15 Extremophile Metal Resistance: Plasmid-Encoded Functions in Streptomyces mirabilis Brangsch, Hanka Höller, Marlene Krauβe, Thomas Waqas, Mohammed Schroeckh, Volker Brakhage, Axel A. Bunk, Boyke Spröer, Cathrin Overmann, Jörg Kothe, Erika Appl Environ Microbiol Environmental Microbiology The extreme metal tolerance of up to 130 mM NiSO(4) in Streptomyces mirabilis P16B-1 was investigated. Genome sequencing revealed the presence of a large linear plasmid, pI. To identify plasmid-encoded determinants of metal resistance, a newly established transformation system was used to characterize the predicted plasmid-encoded loci nreB, hoxN, and copYZ. Reintroduction into the plasmid-cured S. mirabilis ΔpI confirmed that the predicted metal transporter gene nreB constitutes a nickel resistance factor, which was further supported by its heterologous expression in Escherichia coli. In contrast, the predicted nickel exporter gene hoxN decreased nickel tolerance, while copper tolerance was enhanced. The predicted copper-dependent transcriptional regulator gene copY did not induce tolerance toward either metal. Since genes for transfer were identified on the plasmid, its conjugational transfer to the metal-sensitive Streptomyces lividans TK24 was checked. This resulted in acquired tolerance toward 30 mM nickel and additionally increased the tolerance toward copper and cobalt, while oxidative stress tolerance remained unchanged. Intracellular nickel concentrations decreased in the transconjugant strain. The high extracellular nickel concentrations allowed for biomineralization. Plasmid transfer could also be confirmed into the co-occurring actinomycete Kribbella spp. in soil microcosms. IMPORTANCE Living in extremely metal-rich environments requires specific adaptations, and often, specific metal tolerance genes are encoded on a transferable plasmid. Here, Streptomyces mirabilis P16B-1, isolated from a former mining area and able to grow with up to 130 mM NiSO(4), was investigated. The bacterial chromosome, as well as a giant plasmid, was sequenced. The plasmid-borne gene nreB was confirmed to confer metal resistance. A newly established transformation system allowed us to construct a plasmid-cured S. mirabilis as well as an nreB-rescued strain in addition to confirming nreB encoding nickel resistance if heterologously expressed in E. coli. The potential of intra- and interspecific plasmid transfer, together with the presence of metal resistance factors on that plasmid, underlines the importance of plasmids for transfer of resistance factors within a bacterial soil community. American Society for Microbiology 2022-05-23 /pmc/articles/PMC9195940/ /pubmed/35604229 http://dx.doi.org/10.1128/aem.00085-22 Text en Copyright © 2022 Brangsch 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 Environmental Microbiology
Brangsch, Hanka
Höller, Marlene
Krauβe, Thomas
Waqas, Mohammed
Schroeckh, Volker
Brakhage, Axel A.
Bunk, Boyke
Spröer, Cathrin
Overmann, Jörg
Kothe, Erika
Extremophile Metal Resistance: Plasmid-Encoded Functions in Streptomyces mirabilis
title Extremophile Metal Resistance: Plasmid-Encoded Functions in Streptomyces mirabilis
title_full Extremophile Metal Resistance: Plasmid-Encoded Functions in Streptomyces mirabilis
title_fullStr Extremophile Metal Resistance: Plasmid-Encoded Functions in Streptomyces mirabilis
title_full_unstemmed Extremophile Metal Resistance: Plasmid-Encoded Functions in Streptomyces mirabilis
title_short Extremophile Metal Resistance: Plasmid-Encoded Functions in Streptomyces mirabilis
title_sort extremophile metal resistance: plasmid-encoded functions in streptomyces mirabilis
topic Environmental Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195940/
https://www.ncbi.nlm.nih.gov/pubmed/35604229
http://dx.doi.org/10.1128/aem.00085-22
work_keys_str_mv AT brangschhanka extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis
AT hollermarlene extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis
AT kraubethomas extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis
AT waqasmohammed extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis
AT schroeckhvolker extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis
AT brakhageaxela extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis
AT bunkboyke extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis
AT sproercathrin extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis
AT overmannjorg extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis
AT kotheerika extremophilemetalresistanceplasmidencodedfunctionsinstreptomycesmirabilis