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Regulatory involvement of the PerR and SloR metalloregulators in the Streptococcus mutans oxidative stress response
is a commensal of the human oral microbiome that can promote dental caries under conditions of dysbiosis. This study investigates metalloregulators and their involvement in the oxidative stress response. Oxidative stress in the human mouth can derive from temporal increases in reactive oxygen specie...
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Published in: | Journal of bacteriology 2021-06, Vol.203 (11) |
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creator | Ruxin, Talia R Schwartzman, Julia A Davidowitz, Cleo R Peters, Zachary Holtz, Andrew Haney, Robet A Spatafora, Grace A |
description | is a commensal of the human oral microbiome that can promote dental caries under conditions of dysbiosis. This study investigates metalloregulators and their involvement in the
oxidative stress response. Oxidative stress in the human mouth can derive from temporal increases in reactive oxygen species (ROS) after meal consumption and from endogenous bacterial ROS-producers that colonize the dentition. We hypothesize that the
PerR (SMU.593) and SloR (SMU.186) metalloregulatory proteins contribute to the regulation of oxidative stress genes and their products. Expression assays with
UA159 wild type cultures exposed to H
O
reveal that H
O
upregulates
, and that PerR represses
transcription upon binding directly to Fur and PerR consensus sequences within the
operator. In addition, the results of Western blot experiments implicate the Clp proteolytic system in SloR degradation under conditions of H
O
-stress. To reveal a potential role for SloR in the H
O
-resistant phenotype of
GMS802 (a
-deficient strain), we generated a
/
double knockout mutant, GMS1386, where we observed upregulation of the
and
antioxidant genes. These results are consistent with GMS802 H
O
resistance and with a role for PerR as a transcriptional repressor. Cumulatively, these findings support a reciprocal relationship between PerR and SloR during the
oxidative stress response and begin to elucidate the fitness strategies that evolved to foster
persistence in the transient environments of the human oral cavity.
In 2020, untreated dental caries, especially in the permanent dentition, ranked among the most prevalent infectious diseases worldwide, disproportionately impacting individuals of low socioeconomic status. Untreated caries can lead to systemic health problems and has been associated with extended school and work absences, inappropriate use of emergency departments, and an inability for military forces to deploy. Together with public health policy, research aimed at alleviating
induced tooth decay is important because it can improve oral health (and overall health), especially in underserved populations. This research, focused on
metalloregulatory proteins and their gene targets, is significant because it can promote virulence gene control in an important oral pathogen, and contribute to the development of an anti-caries therapeutic that can reduce tooth decay. |
doi_str_mv | 10.1128/JB.00678-20 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8117520</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2543836211</sourcerecordid><originalsourceid>FETCH-LOGICAL-a442t-ec1fa813329fbaca0084bbe782e036f3b17c7cda729ad97b1f3ce61b3736aaf43</originalsourceid><addsrcrecordid>eNptkU1P3DAQhq2qCBbKqffKUi9IVcBjJ3FyqcSilg8hUS3t2Zo4EwhK4sV2VvDvSXeBUonL-DDPPDPWy9hnEIcAsji6mB8KkesikeIDm4EoiyTLlPjIZkJISEoo1Q7bDeFOCEjTTG6zHaV0ptJcz1hY0M3YYXT-kbfDynUr6mmI3DU83hL_RX7Bcaj5decWvKeIXef8y0iYRtbYdfS0jM46a8fA-zHiELh7aGuM7Yp4mNoh8Kks3RDoE9tqsAu0__zusT8_f_w-OUsur07PT44vE0xTGROy0GABSsmyqdCiEEVaVaQLSULljapAW21r1LLEutQVNMpSDpXSKkdsUrXHvm-8y7HqqbbTvzx2ZunbHv2jcdia_ztDe2tu3MoUADqTYhJ8fRZ4dz9SiObOjX6YbjYyS1WhcgkwUd82lPUuBE_N6wYQ5m9C5mJu1gmZtfNgQ2Po5T_f--iXt_e_al_SU0-QUpv5</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2543836211</pqid></control><display><type>article</type><title>Regulatory involvement of the PerR and SloR metalloregulators in the Streptococcus mutans oxidative stress response</title><source>American Society for Microbiology</source><source>Open Access: PubMed Central</source><creator>Ruxin, Talia R ; Schwartzman, Julia A ; Davidowitz, Cleo R ; Peters, Zachary ; Holtz, Andrew ; Haney, Robet A ; Spatafora, Grace A</creator><contributor>Henkin, Tina M ; Henkin, Tina M.</contributor><creatorcontrib>Ruxin, Talia R ; Schwartzman, Julia A ; Davidowitz, Cleo R ; Peters, Zachary ; Holtz, Andrew ; Haney, Robet A ; Spatafora, Grace A ; Henkin, Tina M ; Henkin, Tina M.</creatorcontrib><description>is a commensal of the human oral microbiome that can promote dental caries under conditions of dysbiosis. This study investigates metalloregulators and their involvement in the
oxidative stress response. Oxidative stress in the human mouth can derive from temporal increases in reactive oxygen species (ROS) after meal consumption and from endogenous bacterial ROS-producers that colonize the dentition. We hypothesize that the
PerR (SMU.593) and SloR (SMU.186) metalloregulatory proteins contribute to the regulation of oxidative stress genes and their products. Expression assays with
UA159 wild type cultures exposed to H
O
reveal that H
O
upregulates
, and that PerR represses
transcription upon binding directly to Fur and PerR consensus sequences within the
operator. In addition, the results of Western blot experiments implicate the Clp proteolytic system in SloR degradation under conditions of H
O
-stress. To reveal a potential role for SloR in the H
O
-resistant phenotype of
GMS802 (a
-deficient strain), we generated a
/
double knockout mutant, GMS1386, where we observed upregulation of the
and
antioxidant genes. These results are consistent with GMS802 H
O
resistance and with a role for PerR as a transcriptional repressor. Cumulatively, these findings support a reciprocal relationship between PerR and SloR during the
oxidative stress response and begin to elucidate the fitness strategies that evolved to foster
persistence in the transient environments of the human oral cavity.
In 2020, untreated dental caries, especially in the permanent dentition, ranked among the most prevalent infectious diseases worldwide, disproportionately impacting individuals of low socioeconomic status. Untreated caries can lead to systemic health problems and has been associated with extended school and work absences, inappropriate use of emergency departments, and an inability for military forces to deploy. Together with public health policy, research aimed at alleviating
induced tooth decay is important because it can improve oral health (and overall health), especially in underserved populations. This research, focused on
metalloregulatory proteins and their gene targets, is significant because it can promote virulence gene control in an important oral pathogen, and contribute to the development of an anti-caries therapeutic that can reduce tooth decay.</description><identifier>ISSN: 0021-9193</identifier><identifier>EISSN: 1098-5530</identifier><identifier>DOI: 10.1128/JB.00678-20</identifier><identifier>PMID: 33753467</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Antioxidants ; Bacteriology ; Biodegradation ; Decay ; Dental caries ; Dentition ; Dysbacteriosis ; Emergency medical care ; Gene expression ; Gene regulation ; Genes ; Health policy ; Health problems ; Hydrogen peroxide ; Infectious diseases ; Microbiomes ; Oral cavity ; Oxidation ; Oxidative stress ; Phenotypes ; Proteins ; Proteolysis ; Public health ; Reactive oxygen species ; Research Article ; Socioeconomics ; Streptococcus infections ; Streptococcus mutans ; Teeth ; Transcription ; Virulence ; Western blotting</subject><ispartof>Journal of bacteriology, 2021-06, Vol.203 (11)</ispartof><rights>Copyright © 2021 American Society for Microbiology.</rights><rights>Copyright American Society for Microbiology May 2021</rights><rights>Copyright © 2021 American Society for Microbiology. 2021 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a442t-ec1fa813329fbaca0084bbe782e036f3b17c7cda729ad97b1f3ce61b3736aaf43</citedby><cites>FETCH-LOGICAL-a442t-ec1fa813329fbaca0084bbe782e036f3b17c7cda729ad97b1f3ce61b3736aaf43</cites><orcidid>0000-0003-2043-4853 ; 0000-0003-4563-4835</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/JB.00678-20$$EPDF$$P50$$Gasm2$$H</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/JB.00678-20$$EHTML$$P50$$Gasm2$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3186,27923,27924,52750,52751,52752,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33753467$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Henkin, Tina M</contributor><contributor>Henkin, Tina M.</contributor><creatorcontrib>Ruxin, Talia R</creatorcontrib><creatorcontrib>Schwartzman, Julia A</creatorcontrib><creatorcontrib>Davidowitz, Cleo R</creatorcontrib><creatorcontrib>Peters, Zachary</creatorcontrib><creatorcontrib>Holtz, Andrew</creatorcontrib><creatorcontrib>Haney, Robet A</creatorcontrib><creatorcontrib>Spatafora, Grace A</creatorcontrib><title>Regulatory involvement of the PerR and SloR metalloregulators in the Streptococcus mutans oxidative stress response</title><title>Journal of bacteriology</title><addtitle>J Bacteriol</addtitle><addtitle>J Bacteriol</addtitle><description>is a commensal of the human oral microbiome that can promote dental caries under conditions of dysbiosis. This study investigates metalloregulators and their involvement in the
oxidative stress response. Oxidative stress in the human mouth can derive from temporal increases in reactive oxygen species (ROS) after meal consumption and from endogenous bacterial ROS-producers that colonize the dentition. We hypothesize that the
PerR (SMU.593) and SloR (SMU.186) metalloregulatory proteins contribute to the regulation of oxidative stress genes and their products. Expression assays with
UA159 wild type cultures exposed to H
O
reveal that H
O
upregulates
, and that PerR represses
transcription upon binding directly to Fur and PerR consensus sequences within the
operator. In addition, the results of Western blot experiments implicate the Clp proteolytic system in SloR degradation under conditions of H
O
-stress. To reveal a potential role for SloR in the H
O
-resistant phenotype of
GMS802 (a
-deficient strain), we generated a
/
double knockout mutant, GMS1386, where we observed upregulation of the
and
antioxidant genes. These results are consistent with GMS802 H
O
resistance and with a role for PerR as a transcriptional repressor. Cumulatively, these findings support a reciprocal relationship between PerR and SloR during the
oxidative stress response and begin to elucidate the fitness strategies that evolved to foster
persistence in the transient environments of the human oral cavity.
In 2020, untreated dental caries, especially in the permanent dentition, ranked among the most prevalent infectious diseases worldwide, disproportionately impacting individuals of low socioeconomic status. Untreated caries can lead to systemic health problems and has been associated with extended school and work absences, inappropriate use of emergency departments, and an inability for military forces to deploy. Together with public health policy, research aimed at alleviating
induced tooth decay is important because it can improve oral health (and overall health), especially in underserved populations. This research, focused on
metalloregulatory proteins and their gene targets, is significant because it can promote virulence gene control in an important oral pathogen, and contribute to the development of an anti-caries therapeutic that can reduce tooth decay.</description><subject>Antioxidants</subject><subject>Bacteriology</subject><subject>Biodegradation</subject><subject>Decay</subject><subject>Dental caries</subject><subject>Dentition</subject><subject>Dysbacteriosis</subject><subject>Emergency medical care</subject><subject>Gene expression</subject><subject>Gene regulation</subject><subject>Genes</subject><subject>Health policy</subject><subject>Health problems</subject><subject>Hydrogen peroxide</subject><subject>Infectious diseases</subject><subject>Microbiomes</subject><subject>Oral cavity</subject><subject>Oxidation</subject><subject>Oxidative stress</subject><subject>Phenotypes</subject><subject>Proteins</subject><subject>Proteolysis</subject><subject>Public health</subject><subject>Reactive oxygen species</subject><subject>Research Article</subject><subject>Socioeconomics</subject><subject>Streptococcus infections</subject><subject>Streptococcus mutans</subject><subject>Teeth</subject><subject>Transcription</subject><subject>Virulence</subject><subject>Western blotting</subject><issn>0021-9193</issn><issn>1098-5530</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNptkU1P3DAQhq2qCBbKqffKUi9IVcBjJ3FyqcSilg8hUS3t2Zo4EwhK4sV2VvDvSXeBUonL-DDPPDPWy9hnEIcAsji6mB8KkesikeIDm4EoiyTLlPjIZkJISEoo1Q7bDeFOCEjTTG6zHaV0ptJcz1hY0M3YYXT-kbfDynUr6mmI3DU83hL_RX7Bcaj5decWvKeIXef8y0iYRtbYdfS0jM46a8fA-zHiELh7aGuM7Yp4mNoh8Kks3RDoE9tqsAu0__zusT8_f_w-OUsur07PT44vE0xTGROy0GABSsmyqdCiEEVaVaQLSULljapAW21r1LLEutQVNMpSDpXSKkdsUrXHvm-8y7HqqbbTvzx2ZunbHv2jcdia_ztDe2tu3MoUADqTYhJ8fRZ4dz9SiObOjX6YbjYyS1WhcgkwUd82lPUuBE_N6wYQ5m9C5mJu1gmZtfNgQ2Po5T_f--iXt_e_al_SU0-QUpv5</recordid><startdate>20210601</startdate><enddate>20210601</enddate><creator>Ruxin, Talia R</creator><creator>Schwartzman, Julia A</creator><creator>Davidowitz, Cleo R</creator><creator>Peters, Zachary</creator><creator>Holtz, Andrew</creator><creator>Haney, Robet A</creator><creator>Spatafora, Grace A</creator><general>American Society for Microbiology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2043-4853</orcidid><orcidid>https://orcid.org/0000-0003-4563-4835</orcidid></search><sort><creationdate>20210601</creationdate><title>Regulatory involvement of the PerR and SloR metalloregulators in the Streptococcus mutans oxidative stress response</title><author>Ruxin, Talia R ; Schwartzman, Julia A ; Davidowitz, Cleo R ; Peters, Zachary ; Holtz, Andrew ; Haney, Robet A ; Spatafora, Grace A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a442t-ec1fa813329fbaca0084bbe782e036f3b17c7cda729ad97b1f3ce61b3736aaf43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antioxidants</topic><topic>Bacteriology</topic><topic>Biodegradation</topic><topic>Decay</topic><topic>Dental caries</topic><topic>Dentition</topic><topic>Dysbacteriosis</topic><topic>Emergency medical care</topic><topic>Gene expression</topic><topic>Gene regulation</topic><topic>Genes</topic><topic>Health policy</topic><topic>Health problems</topic><topic>Hydrogen peroxide</topic><topic>Infectious diseases</topic><topic>Microbiomes</topic><topic>Oral cavity</topic><topic>Oxidation</topic><topic>Oxidative stress</topic><topic>Phenotypes</topic><topic>Proteins</topic><topic>Proteolysis</topic><topic>Public health</topic><topic>Reactive oxygen species</topic><topic>Research Article</topic><topic>Socioeconomics</topic><topic>Streptococcus infections</topic><topic>Streptococcus mutans</topic><topic>Teeth</topic><topic>Transcription</topic><topic>Virulence</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ruxin, Talia R</creatorcontrib><creatorcontrib>Schwartzman, Julia A</creatorcontrib><creatorcontrib>Davidowitz, Cleo R</creatorcontrib><creatorcontrib>Peters, Zachary</creatorcontrib><creatorcontrib>Holtz, Andrew</creatorcontrib><creatorcontrib>Haney, Robet A</creatorcontrib><creatorcontrib>Spatafora, Grace A</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of bacteriology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ruxin, Talia R</au><au>Schwartzman, Julia A</au><au>Davidowitz, Cleo R</au><au>Peters, Zachary</au><au>Holtz, Andrew</au><au>Haney, Robet A</au><au>Spatafora, Grace A</au><au>Henkin, Tina M</au><au>Henkin, Tina M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulatory involvement of the PerR and SloR metalloregulators in the Streptococcus mutans oxidative stress response</atitle><jtitle>Journal of bacteriology</jtitle><stitle>J Bacteriol</stitle><addtitle>J Bacteriol</addtitle><date>2021-06-01</date><risdate>2021</risdate><volume>203</volume><issue>11</issue><issn>0021-9193</issn><eissn>1098-5530</eissn><abstract>is a commensal of the human oral microbiome that can promote dental caries under conditions of dysbiosis. This study investigates metalloregulators and their involvement in the
oxidative stress response. Oxidative stress in the human mouth can derive from temporal increases in reactive oxygen species (ROS) after meal consumption and from endogenous bacterial ROS-producers that colonize the dentition. We hypothesize that the
PerR (SMU.593) and SloR (SMU.186) metalloregulatory proteins contribute to the regulation of oxidative stress genes and their products. Expression assays with
UA159 wild type cultures exposed to H
O
reveal that H
O
upregulates
, and that PerR represses
transcription upon binding directly to Fur and PerR consensus sequences within the
operator. In addition, the results of Western blot experiments implicate the Clp proteolytic system in SloR degradation under conditions of H
O
-stress. To reveal a potential role for SloR in the H
O
-resistant phenotype of
GMS802 (a
-deficient strain), we generated a
/
double knockout mutant, GMS1386, where we observed upregulation of the
and
antioxidant genes. These results are consistent with GMS802 H
O
resistance and with a role for PerR as a transcriptional repressor. Cumulatively, these findings support a reciprocal relationship between PerR and SloR during the
oxidative stress response and begin to elucidate the fitness strategies that evolved to foster
persistence in the transient environments of the human oral cavity.
In 2020, untreated dental caries, especially in the permanent dentition, ranked among the most prevalent infectious diseases worldwide, disproportionately impacting individuals of low socioeconomic status. Untreated caries can lead to systemic health problems and has been associated with extended school and work absences, inappropriate use of emergency departments, and an inability for military forces to deploy. Together with public health policy, research aimed at alleviating
induced tooth decay is important because it can improve oral health (and overall health), especially in underserved populations. This research, focused on
metalloregulatory proteins and their gene targets, is significant because it can promote virulence gene control in an important oral pathogen, and contribute to the development of an anti-caries therapeutic that can reduce tooth decay.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>33753467</pmid><doi>10.1128/JB.00678-20</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0003-2043-4853</orcidid><orcidid>https://orcid.org/0000-0003-4563-4835</orcidid><oa>free_for_read</oa></addata></record> |
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source | American Society for Microbiology; Open Access: PubMed Central |
subjects | Antioxidants Bacteriology Biodegradation Decay Dental caries Dentition Dysbacteriosis Emergency medical care Gene expression Gene regulation Genes Health policy Health problems Hydrogen peroxide Infectious diseases Microbiomes Oral cavity Oxidation Oxidative stress Phenotypes Proteins Proteolysis Public health Reactive oxygen species Research Article Socioeconomics Streptococcus infections Streptococcus mutans Teeth Transcription Virulence Western blotting |
title | Regulatory involvement of the PerR and SloR metalloregulators in the Streptococcus mutans oxidative stress response |
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