Loading…

The Metallophore Staphylopine Enables italic toggle="yes">Staphylococcus aureus /italic> To Compete with the Host for Zinc and Overcome Nutritional Immunity

ABSTRACT During infection, the host sequesters essential nutrients, such as zinc, to combat invading microbes. Despite the ability of the immune effector protein calprotectin to bind zinc with subpicomolar affinity, Staphylococcus aureus is able to successfully compete with the host for zinc. Howeve...

Full description

Saved in:
Bibliographic Details
Published in:mBio 2017-11, Vol.8 (5)
Main Authors: Kyle P. Grim, Brian San Francisco, Jana N. Radin, Erin B. Brazel, Jessica L. Kelliher, Paola K. Párraga Solórzano, Philip C. Kim, Christopher A. McDevitt, Thomas E. Kehl-Fie
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page
container_issue 5
container_start_page
container_title mBio
container_volume 8
creator Kyle P. Grim
Brian San Francisco
Jana N. Radin
Erin B. Brazel
Jessica L. Kelliher
Paola K. Párraga Solórzano
Philip C. Kim
Christopher A. McDevitt
Thomas E. Kehl-Fie
description ABSTRACT During infection, the host sequesters essential nutrients, such as zinc, to combat invading microbes. Despite the ability of the immune effector protein calprotectin to bind zinc with subpicomolar affinity, Staphylococcus aureus is able to successfully compete with the host for zinc. However, the zinc importers expressed by S. aureus remain unknown. Our investigations have revealed that S. aureus possesses two importers, AdcABC and CntABCDF, which are induced in response to zinc limitation. While AdcABC is similar to known zinc importers in other bacteria, CntABCDF has not previously been associated with zinc acquisition. Concurrent loss of the two systems severely impairs the ability of S. aureus to obtain zinc and grow in zinc-limited environments. Further investigations revealed that the Cnt system is responsible for the ability of S. aureus to compete with calprotectin for zinc in culture and contributes to acquisition of zinc during infection. The cnt locus also enables S. aureus to produce the broad-spectrum metallophore staphylopine. Similarly to the Cnt transporter, loss of staphylopine severely impairs the ability of S. aureus to resist host-imposed zinc starvation, both in culture and during infection. Further investigations revealed that together staphylopine and the Cnt importer function analogously to siderophore-based iron acquisition systems in order to facilitate zinc acquisition by S. aureus. Analogous systems are found in a broad range of Gram-positive and Gram-negative bacterial pathogens, suggesting that this new type of zinc importer broadly contributes to the ability of bacteria to cause infection. IMPORTANCE A critical host defense against infection is the restriction of zinc availability. Despite the subpicomolar affinity of the immune effector calprotectin for zinc, Staphylococcus aureus can successfully compete for this essential metal. Here, we describe two zinc importers, AdcABC and CntABCDF, possessed by S. aureus, the latter of which has not previously been associated with zinc acquisition. The ability of S. aureus to compete with the host for zinc is dependent on CntABCDF and the metallophore staphylopine, both in culture and during infection. These results expand the mechanisms utilized by bacteria to obtain zinc, beyond Adc-like systems, and demonstrate that pathogens utilize strategies similar to siderophore-based iron acquisition to obtain other essential metals during infection. The staphylopine synthesis machin
doi_str_mv 10.1128/mBio.01281-17
format article
fullrecord <record><control><sourceid>doaj</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_8a26e45d09634efa9423ab852119bcc0</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_8a26e45d09634efa9423ab852119bcc0</doaj_id><sourcerecordid>oai_doaj_org_article_8a26e45d09634efa9423ab852119bcc0</sourcerecordid><originalsourceid>FETCH-doaj_primary_oai_doaj_org_article_8a26e45d09634efa9423ab852119bcc03</originalsourceid><addsrcrecordid>eNqtjbFOwzAQhi0kJCroyH7q3tZOmjYd6EBV1A7AQCaW6OpcGldOLrIdUN6FhyUq8Ab8y3d3-nS_EPdKzpSK0nn9aHgmh0lN1epKjCKVyOkqUepGjL0_yyFxrNJYjsRXVhE8U0Brua3YEbwFbKt-2ExDsGvwaMmDGQSjIfDpZOlh0pOfbP5EzVp3HrBzNGD-o24gY9hy3VIg-DShgjAU7dkHKNnBu2k0YFPA6wc5zTXBSxecCYYbtHCo664xob8T1yVaT-Nf3orD0y7b7qcF4zlvnanR9TmjyS8HdqccXTDaUp5itKRFUsj1Ml5QietFFOMxTSKl1ketZfyfv74B8Ll5xA</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The Metallophore Staphylopine Enables italic toggle="yes"&gt;Staphylococcus aureus /italic&gt; To Compete with the Host for Zinc and Overcome Nutritional Immunity</title><source>American Society for Microbiology</source><source>PubMed Central</source><creator>Kyle P. Grim ; Brian San Francisco ; Jana N. Radin ; Erin B. Brazel ; Jessica L. Kelliher ; Paola K. Párraga Solórzano ; Philip C. Kim ; Christopher A. McDevitt ; Thomas E. Kehl-Fie</creator><creatorcontrib>Kyle P. Grim ; Brian San Francisco ; Jana N. Radin ; Erin B. Brazel ; Jessica L. Kelliher ; Paola K. Párraga Solórzano ; Philip C. Kim ; Christopher A. McDevitt ; Thomas E. Kehl-Fie</creatorcontrib><description>ABSTRACT During infection, the host sequesters essential nutrients, such as zinc, to combat invading microbes. Despite the ability of the immune effector protein calprotectin to bind zinc with subpicomolar affinity, Staphylococcus aureus is able to successfully compete with the host for zinc. However, the zinc importers expressed by S. aureus remain unknown. Our investigations have revealed that S. aureus possesses two importers, AdcABC and CntABCDF, which are induced in response to zinc limitation. While AdcABC is similar to known zinc importers in other bacteria, CntABCDF has not previously been associated with zinc acquisition. Concurrent loss of the two systems severely impairs the ability of S. aureus to obtain zinc and grow in zinc-limited environments. Further investigations revealed that the Cnt system is responsible for the ability of S. aureus to compete with calprotectin for zinc in culture and contributes to acquisition of zinc during infection. The cnt locus also enables S. aureus to produce the broad-spectrum metallophore staphylopine. Similarly to the Cnt transporter, loss of staphylopine severely impairs the ability of S. aureus to resist host-imposed zinc starvation, both in culture and during infection. Further investigations revealed that together staphylopine and the Cnt importer function analogously to siderophore-based iron acquisition systems in order to facilitate zinc acquisition by S. aureus. Analogous systems are found in a broad range of Gram-positive and Gram-negative bacterial pathogens, suggesting that this new type of zinc importer broadly contributes to the ability of bacteria to cause infection. IMPORTANCE A critical host defense against infection is the restriction of zinc availability. Despite the subpicomolar affinity of the immune effector calprotectin for zinc, Staphylococcus aureus can successfully compete for this essential metal. Here, we describe two zinc importers, AdcABC and CntABCDF, possessed by S. aureus, the latter of which has not previously been associated with zinc acquisition. The ability of S. aureus to compete with the host for zinc is dependent on CntABCDF and the metallophore staphylopine, both in culture and during infection. These results expand the mechanisms utilized by bacteria to obtain zinc, beyond Adc-like systems, and demonstrate that pathogens utilize strategies similar to siderophore-based iron acquisition to obtain other essential metals during infection. The staphylopine synthesis machinery is present in a diverse collection of bacteria, suggesting that this new family of zinc importers broadly contributes to the ability of numerous pathogens to cause infection.</description><identifier>EISSN: 2150-7511</identifier><identifier>DOI: 10.1128/mBio.01281-17</identifier><language>eng</language><publisher>American Society for Microbiology</publisher><subject>calprotectin ; CntABCDF ; nutritional immunity ; siderophores ; Staphylococcus aureus ; staphylopine</subject><ispartof>mBio, 2017-11, Vol.8 (5)</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Kyle P. Grim</creatorcontrib><creatorcontrib>Brian San Francisco</creatorcontrib><creatorcontrib>Jana N. Radin</creatorcontrib><creatorcontrib>Erin B. Brazel</creatorcontrib><creatorcontrib>Jessica L. Kelliher</creatorcontrib><creatorcontrib>Paola K. Párraga Solórzano</creatorcontrib><creatorcontrib>Philip C. Kim</creatorcontrib><creatorcontrib>Christopher A. McDevitt</creatorcontrib><creatorcontrib>Thomas E. Kehl-Fie</creatorcontrib><title>The Metallophore Staphylopine Enables italic toggle="yes"&gt;Staphylococcus aureus /italic&gt; To Compete with the Host for Zinc and Overcome Nutritional Immunity</title><title>mBio</title><description>ABSTRACT During infection, the host sequesters essential nutrients, such as zinc, to combat invading microbes. Despite the ability of the immune effector protein calprotectin to bind zinc with subpicomolar affinity, Staphylococcus aureus is able to successfully compete with the host for zinc. However, the zinc importers expressed by S. aureus remain unknown. Our investigations have revealed that S. aureus possesses two importers, AdcABC and CntABCDF, which are induced in response to zinc limitation. While AdcABC is similar to known zinc importers in other bacteria, CntABCDF has not previously been associated with zinc acquisition. Concurrent loss of the two systems severely impairs the ability of S. aureus to obtain zinc and grow in zinc-limited environments. Further investigations revealed that the Cnt system is responsible for the ability of S. aureus to compete with calprotectin for zinc in culture and contributes to acquisition of zinc during infection. The cnt locus also enables S. aureus to produce the broad-spectrum metallophore staphylopine. Similarly to the Cnt transporter, loss of staphylopine severely impairs the ability of S. aureus to resist host-imposed zinc starvation, both in culture and during infection. Further investigations revealed that together staphylopine and the Cnt importer function analogously to siderophore-based iron acquisition systems in order to facilitate zinc acquisition by S. aureus. Analogous systems are found in a broad range of Gram-positive and Gram-negative bacterial pathogens, suggesting that this new type of zinc importer broadly contributes to the ability of bacteria to cause infection. IMPORTANCE A critical host defense against infection is the restriction of zinc availability. Despite the subpicomolar affinity of the immune effector calprotectin for zinc, Staphylococcus aureus can successfully compete for this essential metal. Here, we describe two zinc importers, AdcABC and CntABCDF, possessed by S. aureus, the latter of which has not previously been associated with zinc acquisition. The ability of S. aureus to compete with the host for zinc is dependent on CntABCDF and the metallophore staphylopine, both in culture and during infection. These results expand the mechanisms utilized by bacteria to obtain zinc, beyond Adc-like systems, and demonstrate that pathogens utilize strategies similar to siderophore-based iron acquisition to obtain other essential metals during infection. The staphylopine synthesis machinery is present in a diverse collection of bacteria, suggesting that this new family of zinc importers broadly contributes to the ability of numerous pathogens to cause infection.</description><subject>calprotectin</subject><subject>CntABCDF</subject><subject>nutritional immunity</subject><subject>siderophores</subject><subject>Staphylococcus aureus</subject><subject>staphylopine</subject><issn>2150-7511</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNqtjbFOwzAQhi0kJCroyH7q3tZOmjYd6EBV1A7AQCaW6OpcGldOLrIdUN6FhyUq8Ab8y3d3-nS_EPdKzpSK0nn9aHgmh0lN1epKjCKVyOkqUepGjL0_yyFxrNJYjsRXVhE8U0Brua3YEbwFbKt-2ExDsGvwaMmDGQSjIfDpZOlh0pOfbP5EzVp3HrBzNGD-o24gY9hy3VIg-DShgjAU7dkHKNnBu2k0YFPA6wc5zTXBSxecCYYbtHCo664xob8T1yVaT-Nf3orD0y7b7qcF4zlvnanR9TmjyS8HdqccXTDaUp5itKRFUsj1Ml5QietFFOMxTSKl1ketZfyfv74B8Ll5xA</recordid><startdate>20171101</startdate><enddate>20171101</enddate><creator>Kyle P. Grim</creator><creator>Brian San Francisco</creator><creator>Jana N. Radin</creator><creator>Erin B. Brazel</creator><creator>Jessica L. Kelliher</creator><creator>Paola K. Párraga Solórzano</creator><creator>Philip C. Kim</creator><creator>Christopher A. McDevitt</creator><creator>Thomas E. Kehl-Fie</creator><general>American Society for Microbiology</general><scope>DOA</scope></search><sort><creationdate>20171101</creationdate><title>The Metallophore Staphylopine Enables italic toggle="yes"&gt;Staphylococcus aureus /italic&gt; To Compete with the Host for Zinc and Overcome Nutritional Immunity</title><author>Kyle P. Grim ; Brian San Francisco ; Jana N. Radin ; Erin B. Brazel ; Jessica L. Kelliher ; Paola K. Párraga Solórzano ; Philip C. Kim ; Christopher A. McDevitt ; Thomas E. Kehl-Fie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-doaj_primary_oai_doaj_org_article_8a26e45d09634efa9423ab852119bcc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>calprotectin</topic><topic>CntABCDF</topic><topic>nutritional immunity</topic><topic>siderophores</topic><topic>Staphylococcus aureus</topic><topic>staphylopine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kyle P. Grim</creatorcontrib><creatorcontrib>Brian San Francisco</creatorcontrib><creatorcontrib>Jana N. Radin</creatorcontrib><creatorcontrib>Erin B. Brazel</creatorcontrib><creatorcontrib>Jessica L. Kelliher</creatorcontrib><creatorcontrib>Paola K. Párraga Solórzano</creatorcontrib><creatorcontrib>Philip C. Kim</creatorcontrib><creatorcontrib>Christopher A. McDevitt</creatorcontrib><creatorcontrib>Thomas E. Kehl-Fie</creatorcontrib><collection>DOAJ Directory of Open Access Journals</collection><jtitle>mBio</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kyle P. Grim</au><au>Brian San Francisco</au><au>Jana N. Radin</au><au>Erin B. Brazel</au><au>Jessica L. Kelliher</au><au>Paola K. Párraga Solórzano</au><au>Philip C. Kim</au><au>Christopher A. McDevitt</au><au>Thomas E. Kehl-Fie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Metallophore Staphylopine Enables italic toggle="yes"&gt;Staphylococcus aureus /italic&gt; To Compete with the Host for Zinc and Overcome Nutritional Immunity</atitle><jtitle>mBio</jtitle><date>2017-11-01</date><risdate>2017</risdate><volume>8</volume><issue>5</issue><eissn>2150-7511</eissn><abstract>ABSTRACT During infection, the host sequesters essential nutrients, such as zinc, to combat invading microbes. Despite the ability of the immune effector protein calprotectin to bind zinc with subpicomolar affinity, Staphylococcus aureus is able to successfully compete with the host for zinc. However, the zinc importers expressed by S. aureus remain unknown. Our investigations have revealed that S. aureus possesses two importers, AdcABC and CntABCDF, which are induced in response to zinc limitation. While AdcABC is similar to known zinc importers in other bacteria, CntABCDF has not previously been associated with zinc acquisition. Concurrent loss of the two systems severely impairs the ability of S. aureus to obtain zinc and grow in zinc-limited environments. Further investigations revealed that the Cnt system is responsible for the ability of S. aureus to compete with calprotectin for zinc in culture and contributes to acquisition of zinc during infection. The cnt locus also enables S. aureus to produce the broad-spectrum metallophore staphylopine. Similarly to the Cnt transporter, loss of staphylopine severely impairs the ability of S. aureus to resist host-imposed zinc starvation, both in culture and during infection. Further investigations revealed that together staphylopine and the Cnt importer function analogously to siderophore-based iron acquisition systems in order to facilitate zinc acquisition by S. aureus. Analogous systems are found in a broad range of Gram-positive and Gram-negative bacterial pathogens, suggesting that this new type of zinc importer broadly contributes to the ability of bacteria to cause infection. IMPORTANCE A critical host defense against infection is the restriction of zinc availability. Despite the subpicomolar affinity of the immune effector calprotectin for zinc, Staphylococcus aureus can successfully compete for this essential metal. Here, we describe two zinc importers, AdcABC and CntABCDF, possessed by S. aureus, the latter of which has not previously been associated with zinc acquisition. The ability of S. aureus to compete with the host for zinc is dependent on CntABCDF and the metallophore staphylopine, both in culture and during infection. These results expand the mechanisms utilized by bacteria to obtain zinc, beyond Adc-like systems, and demonstrate that pathogens utilize strategies similar to siderophore-based iron acquisition to obtain other essential metals during infection. The staphylopine synthesis machinery is present in a diverse collection of bacteria, suggesting that this new family of zinc importers broadly contributes to the ability of numerous pathogens to cause infection.</abstract><pub>American Society for Microbiology</pub><doi>10.1128/mBio.01281-17</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier EISSN: 2150-7511
ispartof mBio, 2017-11, Vol.8 (5)
issn 2150-7511
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_8a26e45d09634efa9423ab852119bcc0
source American Society for Microbiology; PubMed Central
subjects calprotectin
CntABCDF
nutritional immunity
siderophores
Staphylococcus aureus
staphylopine
title The Metallophore Staphylopine Enables italic toggle="yes">Staphylococcus aureus /italic> To Compete with the Host for Zinc and Overcome Nutritional Immunity
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T01%3A39%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-doaj&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Metallophore%20Staphylopine%20Enables%20italic%20toggle=%22yes%22%3EStaphylococcus%20aureus%20/italic%3E%20To%20Compete%20with%20the%20Host%20for%20Zinc%20and%20Overcome%20Nutritional%20Immunity&rft.jtitle=mBio&rft.au=Kyle%20P.%20Grim&rft.date=2017-11-01&rft.volume=8&rft.issue=5&rft.eissn=2150-7511&rft_id=info:doi/10.1128/mBio.01281-17&rft_dat=%3Cdoaj%3Eoai_doaj_org_article_8a26e45d09634efa9423ab852119bcc0%3C/doaj%3E%3Cgrp_id%3Ecdi_FETCH-doaj_primary_oai_doaj_org_article_8a26e45d09634efa9423ab852119bcc03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true