Non-specific interference of cobalt with siderophore-dependent iron uptake pathways
Much data shows that biological metals other than Fe 3+ can interfere with Fe 3+ acquisition by siderophores in bacteria. Siderophores are small Fe 3+ chelators produced by the microorganisms to obtain access to Fe 3+ . Here, we show that Co 2+ is imported into Pseudomonas aeruginosa cells in a comp...
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Veröffentlicht in: | Metallomics 2019-11, Vol.11 (11), p.1937-1951 |
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container_issue | 11 |
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container_title | Metallomics |
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creator | Carballido Lopez, Ana Cunrath, Olivier Forster, Anne Pérard, Julien Graulier, Gwenaëlle Legendre, Rachel Varet, Hugo Sismeiro, Odile Perraud, Quentin Pesset, Bénédicte Saint Auguste, Pamela Bumann, Dirk Mislin, Gaëtan L. A Coppee, Jean Yves Michaud-Soret, Isabelle Fechter, Pierre Schalk, Isabelle J |
description | Much data shows that biological metals other than Fe
3+
can interfere with Fe
3+
acquisition by siderophores in bacteria. Siderophores are small Fe
3+
chelators produced by the microorganisms to obtain access to Fe
3+
. Here, we show that Co
2+
is imported into
Pseudomonas aeruginosa
cells in a complex with the siderophore pyochelin (PCH) by the ferri-PCH outer membrane transporter FptA. Moreover, the presence of Co
2+
in the bacterial environment strongly affects the production of PCH. Proteomic and transcriptomic approaches showed that a decrease of PCH production is associated with repression of the expression of the genes involved in PCH biosynthesis. We used various molecular biology approaches to show that this repression is not Fur-(ferric uptake transcriptional regulator) dependent but due to competition of PCH-Co with PCH-Fe for PchR (transcriptional activator), thus inhibiting the formation of PchR-PCH-Fe and consequently the expression of the PCH genes. We observed a similar mechanism of repression of PCH production, but to a lesser extent, by Ni
2+
, but not for Zn
2+
, Cu
2+
, or Mn
2+
. Here, we show, for the first time at a molecular level, how the presence of a contaminant metal can interfere with Fe
3+
acquisition by the siderophores PCH and PVD.
Presence of Co
2+
affects the production of the siderophore Pyochelin in
Pseudomonas aeruginosa
. This repression is not Fur-dependent but due to competition of Pyochelin-Co
2+
with Pyochein-Fe
3+
for PchR (transcriptional activator). |
doi_str_mv | 10.1039/c9mt00195f |
format | Article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_proquest_miscellaneous_2307392900</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2307392900</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-3934aad4e637e5bbc13aba02af6515b1ded2f70456cd91b68c0d252ec07997b83</originalsourceid><addsrcrecordid>eNp90cFPFDEUBvDGYATRC3fJEC9IMvo6nU7pkWxATFY9iAm3ptO-Zouz06HtQPjvKS6uiQdPbfr98tKXj5ADCh8pMPnJyHUGoJK7F2SPCt7VXNLrne0d6C55ndINQNcC8Fdkl9GOMQFsj_z4FsY6TWi886byY8boMOJosAquMqHXQ67ufV5VyVuMYVqFiLXFCUeLY658DGM1T1n_wmrSeXWvH9Ib8tLpIeHb53Of_Lw4v1pc1svvn78szpa1aUWbayZZq7VtsWMCed8bynSvodGu45T31KJtnICWd8ZK2nenBmzDGzQgpBT9KdsnHzZzV3pQU_RrHR9U0F5dni3V0xs0kvNWyDta7PHGTjHczpiyWvtkcBj0iGFOqmEgmGwkQKHv_6E3YY5j2aQoyiQUJoo62SgTQ0oR3fYHFNRTLWohv179ruWi4MPnkXO_Rrulf3oo4N0GxGS26d9eS370v1xN1rFHE9Gcqg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2313909297</pqid></control><display><type>article</type><title>Non-specific interference of cobalt with siderophore-dependent iron uptake pathways</title><source>Oxford Academic Journals (OUP)</source><creator>Carballido Lopez, Ana ; Cunrath, Olivier ; Forster, Anne ; Pérard, Julien ; Graulier, Gwenaëlle ; Legendre, Rachel ; Varet, Hugo ; Sismeiro, Odile ; Perraud, Quentin ; Pesset, Bénédicte ; Saint Auguste, Pamela ; Bumann, Dirk ; Mislin, Gaëtan L. A ; Coppee, Jean Yves ; Michaud-Soret, Isabelle ; Fechter, Pierre ; Schalk, Isabelle J</creator><creatorcontrib>Carballido Lopez, Ana ; Cunrath, Olivier ; Forster, Anne ; Pérard, Julien ; Graulier, Gwenaëlle ; Legendre, Rachel ; Varet, Hugo ; Sismeiro, Odile ; Perraud, Quentin ; Pesset, Bénédicte ; Saint Auguste, Pamela ; Bumann, Dirk ; Mislin, Gaëtan L. A ; Coppee, Jean Yves ; Michaud-Soret, Isabelle ; Fechter, Pierre ; Schalk, Isabelle J</creatorcontrib><description>Much data shows that biological metals other than Fe
3+
can interfere with Fe
3+
acquisition by siderophores in bacteria. Siderophores are small Fe
3+
chelators produced by the microorganisms to obtain access to Fe
3+
. Here, we show that Co
2+
is imported into
Pseudomonas aeruginosa
cells in a complex with the siderophore pyochelin (PCH) by the ferri-PCH outer membrane transporter FptA. Moreover, the presence of Co
2+
in the bacterial environment strongly affects the production of PCH. Proteomic and transcriptomic approaches showed that a decrease of PCH production is associated with repression of the expression of the genes involved in PCH biosynthesis. We used various molecular biology approaches to show that this repression is not Fur-(ferric uptake transcriptional regulator) dependent but due to competition of PCH-Co with PCH-Fe for PchR (transcriptional activator), thus inhibiting the formation of PchR-PCH-Fe and consequently the expression of the PCH genes. We observed a similar mechanism of repression of PCH production, but to a lesser extent, by Ni
2+
, but not for Zn
2+
, Cu
2+
, or Mn
2+
. Here, we show, for the first time at a molecular level, how the presence of a contaminant metal can interfere with Fe
3+
acquisition by the siderophores PCH and PVD.
Presence of Co
2+
affects the production of the siderophore Pyochelin in
Pseudomonas aeruginosa
. This repression is not Fur-dependent but due to competition of Pyochelin-Co
2+
with Pyochein-Fe
3+
for PchR (transcriptional activator).</description><identifier>ISSN: 1756-5901</identifier><identifier>EISSN: 1756-591X</identifier><identifier>DOI: 10.1039/c9mt00195f</identifier><identifier>PMID: 31633703</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Biosynthesis ; Carbon dioxide ; Chelating agents ; Cobalt ; Contaminants ; Copper ; Gene expression ; Genes ; Heavy metals ; Iron ; Life Sciences ; Manganese ; Microbiology and Parasitology ; Microorganisms ; Molecular biology ; Proteomics ; Pseudomonas aeruginosa ; Siderophores ; Transcription ; Zinc</subject><ispartof>Metallomics, 2019-11, Vol.11 (11), p.1937-1951</ispartof><rights>Copyright Royal Society of Chemistry 2019</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-3934aad4e637e5bbc13aba02af6515b1ded2f70456cd91b68c0d252ec07997b83</citedby><cites>FETCH-LOGICAL-c474t-3934aad4e637e5bbc13aba02af6515b1ded2f70456cd91b68c0d252ec07997b83</cites><orcidid>0000-0003-3980-4463 ; 0000-0003-0102-5798 ; 0000-0001-9930-0748 ; 0000-0002-0097-8872 ; 0000-0001-7747-5731 ; 0000-0002-8936-4964 ; 0000-0003-3636-4239 ; 0000-0002-5646-3392 ; 0000-0002-8351-1679 ; 0000-0002-5196-9431 ; 0000-0001-5912-361X ; 0000-0001-8841-9030 ; 0000-0003-4113-4606</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,27926,27927</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31633703$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-02955479$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Carballido Lopez, Ana</creatorcontrib><creatorcontrib>Cunrath, Olivier</creatorcontrib><creatorcontrib>Forster, Anne</creatorcontrib><creatorcontrib>Pérard, Julien</creatorcontrib><creatorcontrib>Graulier, Gwenaëlle</creatorcontrib><creatorcontrib>Legendre, Rachel</creatorcontrib><creatorcontrib>Varet, Hugo</creatorcontrib><creatorcontrib>Sismeiro, Odile</creatorcontrib><creatorcontrib>Perraud, Quentin</creatorcontrib><creatorcontrib>Pesset, Bénédicte</creatorcontrib><creatorcontrib>Saint Auguste, Pamela</creatorcontrib><creatorcontrib>Bumann, Dirk</creatorcontrib><creatorcontrib>Mislin, Gaëtan L. A</creatorcontrib><creatorcontrib>Coppee, Jean Yves</creatorcontrib><creatorcontrib>Michaud-Soret, Isabelle</creatorcontrib><creatorcontrib>Fechter, Pierre</creatorcontrib><creatorcontrib>Schalk, Isabelle J</creatorcontrib><title>Non-specific interference of cobalt with siderophore-dependent iron uptake pathways</title><title>Metallomics</title><addtitle>Metallomics</addtitle><description>Much data shows that biological metals other than Fe
3+
can interfere with Fe
3+
acquisition by siderophores in bacteria. Siderophores are small Fe
3+
chelators produced by the microorganisms to obtain access to Fe
3+
. Here, we show that Co
2+
is imported into
Pseudomonas aeruginosa
cells in a complex with the siderophore pyochelin (PCH) by the ferri-PCH outer membrane transporter FptA. Moreover, the presence of Co
2+
in the bacterial environment strongly affects the production of PCH. Proteomic and transcriptomic approaches showed that a decrease of PCH production is associated with repression of the expression of the genes involved in PCH biosynthesis. We used various molecular biology approaches to show that this repression is not Fur-(ferric uptake transcriptional regulator) dependent but due to competition of PCH-Co with PCH-Fe for PchR (transcriptional activator), thus inhibiting the formation of PchR-PCH-Fe and consequently the expression of the PCH genes. We observed a similar mechanism of repression of PCH production, but to a lesser extent, by Ni
2+
, but not for Zn
2+
, Cu
2+
, or Mn
2+
. Here, we show, for the first time at a molecular level, how the presence of a contaminant metal can interfere with Fe
3+
acquisition by the siderophores PCH and PVD.
Presence of Co
2+
affects the production of the siderophore Pyochelin in
Pseudomonas aeruginosa
. This repression is not Fur-dependent but due to competition of Pyochelin-Co
2+
with Pyochein-Fe
3+
for PchR (transcriptional activator).</description><subject>Biosynthesis</subject><subject>Carbon dioxide</subject><subject>Chelating agents</subject><subject>Cobalt</subject><subject>Contaminants</subject><subject>Copper</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Heavy metals</subject><subject>Iron</subject><subject>Life Sciences</subject><subject>Manganese</subject><subject>Microbiology and Parasitology</subject><subject>Microorganisms</subject><subject>Molecular biology</subject><subject>Proteomics</subject><subject>Pseudomonas aeruginosa</subject><subject>Siderophores</subject><subject>Transcription</subject><subject>Zinc</subject><issn>1756-5901</issn><issn>1756-591X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp90cFPFDEUBvDGYATRC3fJEC9IMvo6nU7pkWxATFY9iAm3ptO-Zouz06HtQPjvKS6uiQdPbfr98tKXj5ADCh8pMPnJyHUGoJK7F2SPCt7VXNLrne0d6C55ndINQNcC8Fdkl9GOMQFsj_z4FsY6TWi886byY8boMOJosAquMqHXQ67ufV5VyVuMYVqFiLXFCUeLY658DGM1T1n_wmrSeXWvH9Ib8tLpIeHb53Of_Lw4v1pc1svvn78szpa1aUWbayZZq7VtsWMCed8bynSvodGu45T31KJtnICWd8ZK2nenBmzDGzQgpBT9KdsnHzZzV3pQU_RrHR9U0F5dni3V0xs0kvNWyDta7PHGTjHczpiyWvtkcBj0iGFOqmEgmGwkQKHv_6E3YY5j2aQoyiQUJoo62SgTQ0oR3fYHFNRTLWohv179ruWi4MPnkXO_Rrulf3oo4N0GxGS26d9eS370v1xN1rFHE9Gcqg</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Carballido Lopez, Ana</creator><creator>Cunrath, Olivier</creator><creator>Forster, Anne</creator><creator>Pérard, Julien</creator><creator>Graulier, Gwenaëlle</creator><creator>Legendre, Rachel</creator><creator>Varet, Hugo</creator><creator>Sismeiro, Odile</creator><creator>Perraud, Quentin</creator><creator>Pesset, Bénédicte</creator><creator>Saint Auguste, Pamela</creator><creator>Bumann, Dirk</creator><creator>Mislin, Gaëtan L. A</creator><creator>Coppee, Jean Yves</creator><creator>Michaud-Soret, Isabelle</creator><creator>Fechter, Pierre</creator><creator>Schalk, Isabelle J</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0003-3980-4463</orcidid><orcidid>https://orcid.org/0000-0003-0102-5798</orcidid><orcidid>https://orcid.org/0000-0001-9930-0748</orcidid><orcidid>https://orcid.org/0000-0002-0097-8872</orcidid><orcidid>https://orcid.org/0000-0001-7747-5731</orcidid><orcidid>https://orcid.org/0000-0002-8936-4964</orcidid><orcidid>https://orcid.org/0000-0003-3636-4239</orcidid><orcidid>https://orcid.org/0000-0002-5646-3392</orcidid><orcidid>https://orcid.org/0000-0002-8351-1679</orcidid><orcidid>https://orcid.org/0000-0002-5196-9431</orcidid><orcidid>https://orcid.org/0000-0001-5912-361X</orcidid><orcidid>https://orcid.org/0000-0001-8841-9030</orcidid><orcidid>https://orcid.org/0000-0003-4113-4606</orcidid></search><sort><creationdate>20191101</creationdate><title>Non-specific interference of cobalt with siderophore-dependent iron uptake pathways</title><author>Carballido Lopez, Ana ; Cunrath, Olivier ; Forster, Anne ; Pérard, Julien ; Graulier, Gwenaëlle ; Legendre, Rachel ; Varet, Hugo ; Sismeiro, Odile ; Perraud, Quentin ; Pesset, Bénédicte ; Saint Auguste, Pamela ; Bumann, Dirk ; Mislin, Gaëtan L. A ; Coppee, Jean Yves ; Michaud-Soret, Isabelle ; Fechter, Pierre ; Schalk, Isabelle J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-3934aad4e637e5bbc13aba02af6515b1ded2f70456cd91b68c0d252ec07997b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Biosynthesis</topic><topic>Carbon dioxide</topic><topic>Chelating agents</topic><topic>Cobalt</topic><topic>Contaminants</topic><topic>Copper</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Heavy metals</topic><topic>Iron</topic><topic>Life Sciences</topic><topic>Manganese</topic><topic>Microbiology and Parasitology</topic><topic>Microorganisms</topic><topic>Molecular biology</topic><topic>Proteomics</topic><topic>Pseudomonas aeruginosa</topic><topic>Siderophores</topic><topic>Transcription</topic><topic>Zinc</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carballido Lopez, Ana</creatorcontrib><creatorcontrib>Cunrath, Olivier</creatorcontrib><creatorcontrib>Forster, Anne</creatorcontrib><creatorcontrib>Pérard, Julien</creatorcontrib><creatorcontrib>Graulier, Gwenaëlle</creatorcontrib><creatorcontrib>Legendre, Rachel</creatorcontrib><creatorcontrib>Varet, Hugo</creatorcontrib><creatorcontrib>Sismeiro, Odile</creatorcontrib><creatorcontrib>Perraud, Quentin</creatorcontrib><creatorcontrib>Pesset, Bénédicte</creatorcontrib><creatorcontrib>Saint Auguste, Pamela</creatorcontrib><creatorcontrib>Bumann, Dirk</creatorcontrib><creatorcontrib>Mislin, Gaëtan L. A</creatorcontrib><creatorcontrib>Coppee, Jean Yves</creatorcontrib><creatorcontrib>Michaud-Soret, Isabelle</creatorcontrib><creatorcontrib>Fechter, Pierre</creatorcontrib><creatorcontrib>Schalk, Isabelle J</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Metallomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carballido Lopez, Ana</au><au>Cunrath, Olivier</au><au>Forster, Anne</au><au>Pérard, Julien</au><au>Graulier, Gwenaëlle</au><au>Legendre, Rachel</au><au>Varet, Hugo</au><au>Sismeiro, Odile</au><au>Perraud, Quentin</au><au>Pesset, Bénédicte</au><au>Saint Auguste, Pamela</au><au>Bumann, Dirk</au><au>Mislin, Gaëtan L. A</au><au>Coppee, Jean Yves</au><au>Michaud-Soret, Isabelle</au><au>Fechter, Pierre</au><au>Schalk, Isabelle J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Non-specific interference of cobalt with siderophore-dependent iron uptake pathways</atitle><jtitle>Metallomics</jtitle><addtitle>Metallomics</addtitle><date>2019-11-01</date><risdate>2019</risdate><volume>11</volume><issue>11</issue><spage>1937</spage><epage>1951</epage><pages>1937-1951</pages><issn>1756-5901</issn><eissn>1756-591X</eissn><abstract>Much data shows that biological metals other than Fe
3+
can interfere with Fe
3+
acquisition by siderophores in bacteria. Siderophores are small Fe
3+
chelators produced by the microorganisms to obtain access to Fe
3+
. Here, we show that Co
2+
is imported into
Pseudomonas aeruginosa
cells in a complex with the siderophore pyochelin (PCH) by the ferri-PCH outer membrane transporter FptA. Moreover, the presence of Co
2+
in the bacterial environment strongly affects the production of PCH. Proteomic and transcriptomic approaches showed that a decrease of PCH production is associated with repression of the expression of the genes involved in PCH biosynthesis. We used various molecular biology approaches to show that this repression is not Fur-(ferric uptake transcriptional regulator) dependent but due to competition of PCH-Co with PCH-Fe for PchR (transcriptional activator), thus inhibiting the formation of PchR-PCH-Fe and consequently the expression of the PCH genes. We observed a similar mechanism of repression of PCH production, but to a lesser extent, by Ni
2+
, but not for Zn
2+
, Cu
2+
, or Mn
2+
. Here, we show, for the first time at a molecular level, how the presence of a contaminant metal can interfere with Fe
3+
acquisition by the siderophores PCH and PVD.
Presence of Co
2+
affects the production of the siderophore Pyochelin in
Pseudomonas aeruginosa
. This repression is not Fur-dependent but due to competition of Pyochelin-Co
2+
with Pyochein-Fe
3+
for PchR (transcriptional activator).</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>31633703</pmid><doi>10.1039/c9mt00195f</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-3980-4463</orcidid><orcidid>https://orcid.org/0000-0003-0102-5798</orcidid><orcidid>https://orcid.org/0000-0001-9930-0748</orcidid><orcidid>https://orcid.org/0000-0002-0097-8872</orcidid><orcidid>https://orcid.org/0000-0001-7747-5731</orcidid><orcidid>https://orcid.org/0000-0002-8936-4964</orcidid><orcidid>https://orcid.org/0000-0003-3636-4239</orcidid><orcidid>https://orcid.org/0000-0002-5646-3392</orcidid><orcidid>https://orcid.org/0000-0002-8351-1679</orcidid><orcidid>https://orcid.org/0000-0002-5196-9431</orcidid><orcidid>https://orcid.org/0000-0001-5912-361X</orcidid><orcidid>https://orcid.org/0000-0001-8841-9030</orcidid><orcidid>https://orcid.org/0000-0003-4113-4606</orcidid><oa>free_for_read</oa></addata></record> |
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source | Oxford Academic Journals (OUP) |
subjects | Biosynthesis Carbon dioxide Chelating agents Cobalt Contaminants Copper Gene expression Genes Heavy metals Iron Life Sciences Manganese Microbiology and Parasitology Microorganisms Molecular biology Proteomics Pseudomonas aeruginosa Siderophores Transcription Zinc |
title | Non-specific interference of cobalt with siderophore-dependent iron uptake pathways |
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