Gene expression of Porphyromonas gingivalis ATCC 33277 when growing in an in vitro multispecies biofilm
Porphyromonas gingivalis, an oral microorganism residing in the subgingival biofilm, may exert diverse pathogenicity depending on the presence of specific virulence factors, but its gene expression has not been completely established. This investigation aims to compare the transcriptomic profile of...
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description | Porphyromonas gingivalis, an oral microorganism residing in the subgingival biofilm, may exert diverse pathogenicity depending on the presence of specific virulence factors, but its gene expression has not been completely established. This investigation aims to compare the transcriptomic profile of this pathogen when growing within an in vitro multispecies biofilm or in a planktonic state.
P. gingivalis ATCC 33277 was grown in anaerobiosis within multi-well culture plates at 37°C under two conditions: (a) planktonic samples (no hydroxyapatite discs) or (b) within a multispecies-biofilm containing Streptococcus oralis, Actinomyces naeslundii, Veillonella parvula, Fusobacterium nucleatum and Aggregatibacter actinomycetemcomitans deposited on hydroxyapatite discs. Scanning Electron Microscopy (SEM) and Confocal Laser Scanning Microscopy (CLSM) combined with Fluorescence In Situ Hybridization (FISH) were used to verify the formation of the biofilm and the presence of P. gingivalis. Total RNA was extracted from both the multispecies biofilm and planktonic samples, then purified and, with the use of a microarray, its differential gene expression was analyzed. A linear model was used for determining the differentially expressed genes using a filtering criterion of two-fold change (up or down) and a significance p-value of |
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P. gingivalis ATCC 33277 was grown in anaerobiosis within multi-well culture plates at 37°C under two conditions: (a) planktonic samples (no hydroxyapatite discs) or (b) within a multispecies-biofilm containing Streptococcus oralis, Actinomyces naeslundii, Veillonella parvula, Fusobacterium nucleatum and Aggregatibacter actinomycetemcomitans deposited on hydroxyapatite discs. Scanning Electron Microscopy (SEM) and Confocal Laser Scanning Microscopy (CLSM) combined with Fluorescence In Situ Hybridization (FISH) were used to verify the formation of the biofilm and the presence of P. gingivalis. Total RNA was extracted from both the multispecies biofilm and planktonic samples, then purified and, with the use of a microarray, its differential gene expression was analyzed. A linear model was used for determining the differentially expressed genes using a filtering criterion of two-fold change (up or down) and a significance p-value of <0.05. Differential expression was confirmed by Reverse Transcription-quantitative Polymerase Chain Reaction (RT-qPCR).
SEM verified the development of the multispecies biofilm and FISH confirmed the incorporation of P. gingivalis. The microarray demonstrated that, when growing within the multispecies biofilm, 19.1% of P. gingivalis genes were significantly and differentially expressed (165 genes were up-regulated and 200 down-regulated), compared with planktonic growth. These genes were mainly involved in functions related to the oxidative stress, cell envelope, transposons and metabolism. The results of the microarray were confirmed by RT-qPCR.
Significant transcriptional changes occurred in P. gingivalis when growing in a multispecies biofilm compared to planktonic state.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0221234</identifier><identifier>PMID: 31437202</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Actinomyces ; Actinomyces - genetics ; Aggregatibacter actinomycetemcomitans - genetics ; Anaerobiosis ; Anaerobiosis - genetics ; Analysis ; Bacteria ; Biochemistry ; Biofilms ; Biofilms - growth & development ; Biology and Life Sciences ; Cell culture ; Confocal microscopy ; CRISPR ; Culture Media - chemistry ; Dental research ; Deoxyribonucleic acid ; DNA ; DNA microarrays ; Durapatite ; Electron microscopy ; Fluorescence ; Fluorescence in situ hybridization ; Fusobacterium nucleatum - genetics ; Gene expression ; Gene Expression Regulation, Bacterial ; Genes ; Genes, Bacterial ; Genetic aspects ; Genetic research ; Gram-negative bacteria ; Growth ; Humans ; Hydroxyapatite ; Hydroxyapatites ; Immunology ; Inflammation ; Laboratories ; Medicine and Health Sciences ; Metabolism ; Microscopy ; Odontology ; Oral microbiology ; Oxidative stress ; Pathogenicity ; Pathogens ; Plankton - genetics ; Plankton - growth & development ; Polymerase chain reaction ; Porphyromonas gingivalis ; Porphyromonas gingivalis - genetics ; Porphyromonas gingivalis - growth & development ; Research and Analysis Methods ; Reverse transcription ; Ribonucleic acid ; RNA ; RNA, Bacterial ; Scanning electron microscopy ; Scanning microscopy ; Streptococcus oralis - genetics ; Transcriptome ; Transposons ; Veillonella - genetics ; Virulence ; Virulence (Microbiology) ; Virulence factors</subject><ispartof>PloS one, 2019-08, Vol.14 (8), p.e0221234-e0221234</ispartof><rights>COPYRIGHT 2019 Public Library of Science</rights><rights>2019 Romero-Lastra et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 Romero-Lastra et al 2019 Romero-Lastra et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-5e2174290a00d73ce056b293bc78e72094cb827bc66db711d0c6d57a8ec7ed3</citedby><cites>FETCH-LOGICAL-c692t-5e2174290a00d73ce056b293bc78e72094cb827bc66db711d0c6d57a8ec7ed3</cites><orcidid>0000-0003-4421-7845</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706054/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706054/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,2915,23847,27903,27904,53769,53771,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31437202$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Roop, Roy Martin</contributor><creatorcontrib>Romero-Lastra, Patricia</creatorcontrib><creatorcontrib>Sánchez, María C</creatorcontrib><creatorcontrib>Llama-Palacios, Arancha</creatorcontrib><creatorcontrib>Figuero, Elena</creatorcontrib><creatorcontrib>Herrera, David</creatorcontrib><creatorcontrib>Sanz, Mariano</creatorcontrib><title>Gene expression of Porphyromonas gingivalis ATCC 33277 when growing in an in vitro multispecies biofilm</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Porphyromonas gingivalis, an oral microorganism residing in the subgingival biofilm, may exert diverse pathogenicity depending on the presence of specific virulence factors, but its gene expression has not been completely established. This investigation aims to compare the transcriptomic profile of this pathogen when growing within an in vitro multispecies biofilm or in a planktonic state.
P. gingivalis ATCC 33277 was grown in anaerobiosis within multi-well culture plates at 37°C under two conditions: (a) planktonic samples (no hydroxyapatite discs) or (b) within a multispecies-biofilm containing Streptococcus oralis, Actinomyces naeslundii, Veillonella parvula, Fusobacterium nucleatum and Aggregatibacter actinomycetemcomitans deposited on hydroxyapatite discs. Scanning Electron Microscopy (SEM) and Confocal Laser Scanning Microscopy (CLSM) combined with Fluorescence In Situ Hybridization (FISH) were used to verify the formation of the biofilm and the presence of P. gingivalis. Total RNA was extracted from both the multispecies biofilm and planktonic samples, then purified and, with the use of a microarray, its differential gene expression was analyzed. A linear model was used for determining the differentially expressed genes using a filtering criterion of two-fold change (up or down) and a significance p-value of <0.05. Differential expression was confirmed by Reverse Transcription-quantitative Polymerase Chain Reaction (RT-qPCR).
SEM verified the development of the multispecies biofilm and FISH confirmed the incorporation of P. gingivalis. The microarray demonstrated that, when growing within the multispecies biofilm, 19.1% of P. gingivalis genes were significantly and differentially expressed (165 genes were up-regulated and 200 down-regulated), compared with planktonic growth. These genes were mainly involved in functions related to the oxidative stress, cell envelope, transposons and metabolism. The results of the microarray were confirmed by RT-qPCR.
Significant transcriptional changes occurred in P. gingivalis when growing in a multispecies biofilm compared to planktonic state.</description><subject>Actinomyces</subject><subject>Actinomyces - genetics</subject><subject>Aggregatibacter actinomycetemcomitans - genetics</subject><subject>Anaerobiosis</subject><subject>Anaerobiosis - genetics</subject><subject>Analysis</subject><subject>Bacteria</subject><subject>Biochemistry</subject><subject>Biofilms</subject><subject>Biofilms - growth & development</subject><subject>Biology and Life Sciences</subject><subject>Cell culture</subject><subject>Confocal microscopy</subject><subject>CRISPR</subject><subject>Culture Media - chemistry</subject><subject>Dental research</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA microarrays</subject><subject>Durapatite</subject><subject>Electron microscopy</subject><subject>Fluorescence</subject><subject>Fluorescence in situ hybridization</subject><subject>Fusobacterium nucleatum - genetics</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genes</subject><subject>Genes, Bacterial</subject><subject>Genetic aspects</subject><subject>Genetic research</subject><subject>Gram-negative bacteria</subject><subject>Growth</subject><subject>Humans</subject><subject>Hydroxyapatite</subject><subject>Hydroxyapatites</subject><subject>Immunology</subject><subject>Inflammation</subject><subject>Laboratories</subject><subject>Medicine and Health Sciences</subject><subject>Metabolism</subject><subject>Microscopy</subject><subject>Odontology</subject><subject>Oral microbiology</subject><subject>Oxidative stress</subject><subject>Pathogenicity</subject><subject>Pathogens</subject><subject>Plankton - genetics</subject><subject>Plankton - growth & development</subject><subject>Polymerase chain reaction</subject><subject>Porphyromonas gingivalis</subject><subject>Porphyromonas gingivalis - genetics</subject><subject>Porphyromonas gingivalis - growth & development</subject><subject>Research and Analysis Methods</subject><subject>Reverse transcription</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA, Bacterial</subject><subject>Scanning electron microscopy</subject><subject>Scanning microscopy</subject><subject>Streptococcus oralis - genetics</subject><subject>Transcriptome</subject><subject>Transposons</subject><subject>Veillonella - genetics</subject><subject>Virulence</subject><subject>Virulence (Microbiology)</subject><subject>Virulence factors</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNk99r2zAQx83YWLtu_8HYDIOxPSTTL1v2yyCErQsUOtayVyHLZ0dBllLJTtv_fsrilnj0YQgkofvcV7rTXZK8xWiOKcdfNm7wVpr51lmYI0IwoexZcopLSmY5QfT50f4keRXCBqGMFnn-MjmhmFFOEDlN2nOwkMLd1kMI2tnUNelP57fre-86Z2VIW21bvZNGh3RxvVymlBLO09s12LT17jZaU21TaffzTvfepd1geh22oDSEtNKu0aZ7nbxopAnwZlzPkqvv366XP2YXl-er5eJipvKS9LMMCOaMlEgiVHOqAGV5RUpaKV5AfHHJVFUQXqk8ryuOcY1UXmdcFqA41PQseX9Q3RoXxJihIAjhBSIZYyQSqwNRO7kRW6876e-Fk1r8PXC-FdL3WhkQEgiQhvEiYxlThFagsqpWPM845pLQqPV1vG2oOqgV2N5LMxGdWqxei9btRM5RjjIWBT6NAt7dDBB60emgwBhpwQ37dxcZRozwMqIf_kGfjm6kWhkD0LZx8V61FxWLrOQ457zAkZo_QcVRQ6dVLKf4YTB1-DxxiEwPd30rhxDE6urX_7OXv6fsxyN2DdL06-DM0MdCDFOQHUDlXQgemsckYyT23fCQDbHvBjF2Q3R7d_xBj04P5U__AFEyBAA</recordid><startdate>20190822</startdate><enddate>20190822</enddate><creator>Romero-Lastra, Patricia</creator><creator>Sánchez, María C</creator><creator>Llama-Palacios, Arancha</creator><creator>Figuero, Elena</creator><creator>Herrera, David</creator><creator>Sanz, Mariano</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-4421-7845</orcidid></search><sort><creationdate>20190822</creationdate><title>Gene expression of Porphyromonas gingivalis ATCC 33277 when growing in an in vitro multispecies biofilm</title><author>Romero-Lastra, Patricia ; Sánchez, María C ; Llama-Palacios, Arancha ; Figuero, Elena ; Herrera, David ; Sanz, Mariano</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-5e2174290a00d73ce056b293bc78e72094cb827bc66db711d0c6d57a8ec7ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Actinomyces</topic><topic>Actinomyces - genetics</topic><topic>Aggregatibacter actinomycetemcomitans - genetics</topic><topic>Anaerobiosis</topic><topic>Anaerobiosis - genetics</topic><topic>Analysis</topic><topic>Bacteria</topic><topic>Biochemistry</topic><topic>Biofilms</topic><topic>Biofilms - growth & development</topic><topic>Biology and Life Sciences</topic><topic>Cell culture</topic><topic>Confocal microscopy</topic><topic>CRISPR</topic><topic>Culture Media - chemistry</topic><topic>Dental research</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA microarrays</topic><topic>Durapatite</topic><topic>Electron microscopy</topic><topic>Fluorescence</topic><topic>Fluorescence in situ hybridization</topic><topic>Fusobacterium nucleatum - genetics</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genes</topic><topic>Genes, Bacterial</topic><topic>Genetic aspects</topic><topic>Genetic research</topic><topic>Gram-negative bacteria</topic><topic>Growth</topic><topic>Humans</topic><topic>Hydroxyapatite</topic><topic>Hydroxyapatites</topic><topic>Immunology</topic><topic>Inflammation</topic><topic>Laboratories</topic><topic>Medicine and Health Sciences</topic><topic>Metabolism</topic><topic>Microscopy</topic><topic>Odontology</topic><topic>Oral microbiology</topic><topic>Oxidative stress</topic><topic>Pathogenicity</topic><topic>Pathogens</topic><topic>Plankton - genetics</topic><topic>Plankton - growth & development</topic><topic>Polymerase chain reaction</topic><topic>Porphyromonas gingivalis</topic><topic>Porphyromonas gingivalis - genetics</topic><topic>Porphyromonas gingivalis - growth & development</topic><topic>Research and Analysis Methods</topic><topic>Reverse transcription</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA, Bacterial</topic><topic>Scanning electron microscopy</topic><topic>Scanning microscopy</topic><topic>Streptococcus oralis - genetics</topic><topic>Transcriptome</topic><topic>Transposons</topic><topic>Veillonella - genetics</topic><topic>Virulence</topic><topic>Virulence (Microbiology)</topic><topic>Virulence factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Romero-Lastra, Patricia</creatorcontrib><creatorcontrib>Sánchez, María C</creatorcontrib><creatorcontrib>Llama-Palacios, Arancha</creatorcontrib><creatorcontrib>Figuero, Elena</creatorcontrib><creatorcontrib>Herrera, David</creatorcontrib><creatorcontrib>Sanz, Mariano</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Romero-Lastra, Patricia</au><au>Sánchez, María C</au><au>Llama-Palacios, Arancha</au><au>Figuero, Elena</au><au>Herrera, David</au><au>Sanz, Mariano</au><au>Roop, Roy Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gene expression of Porphyromonas gingivalis ATCC 33277 when growing in an in vitro multispecies biofilm</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2019-08-22</date><risdate>2019</risdate><volume>14</volume><issue>8</issue><spage>e0221234</spage><epage>e0221234</epage><pages>e0221234-e0221234</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Porphyromonas gingivalis, an oral microorganism residing in the subgingival biofilm, may exert diverse pathogenicity depending on the presence of specific virulence factors, but its gene expression has not been completely established. This investigation aims to compare the transcriptomic profile of this pathogen when growing within an in vitro multispecies biofilm or in a planktonic state.
P. gingivalis ATCC 33277 was grown in anaerobiosis within multi-well culture plates at 37°C under two conditions: (a) planktonic samples (no hydroxyapatite discs) or (b) within a multispecies-biofilm containing Streptococcus oralis, Actinomyces naeslundii, Veillonella parvula, Fusobacterium nucleatum and Aggregatibacter actinomycetemcomitans deposited on hydroxyapatite discs. Scanning Electron Microscopy (SEM) and Confocal Laser Scanning Microscopy (CLSM) combined with Fluorescence In Situ Hybridization (FISH) were used to verify the formation of the biofilm and the presence of P. gingivalis. Total RNA was extracted from both the multispecies biofilm and planktonic samples, then purified and, with the use of a microarray, its differential gene expression was analyzed. A linear model was used for determining the differentially expressed genes using a filtering criterion of two-fold change (up or down) and a significance p-value of <0.05. Differential expression was confirmed by Reverse Transcription-quantitative Polymerase Chain Reaction (RT-qPCR).
SEM verified the development of the multispecies biofilm and FISH confirmed the incorporation of P. gingivalis. The microarray demonstrated that, when growing within the multispecies biofilm, 19.1% of P. gingivalis genes were significantly and differentially expressed (165 genes were up-regulated and 200 down-regulated), compared with planktonic growth. These genes were mainly involved in functions related to the oxidative stress, cell envelope, transposons and metabolism. The results of the microarray were confirmed by RT-qPCR.
Significant transcriptional changes occurred in P. gingivalis when growing in a multispecies biofilm compared to planktonic state.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31437202</pmid><doi>10.1371/journal.pone.0221234</doi><tpages>e0221234</tpages><orcidid>https://orcid.org/0000-0003-4421-7845</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2019-08, Vol.14 (8), p.e0221234-e0221234 |
issn | 1932-6203 1932-6203 |
language | eng |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Free Full-Text Journals in Chemistry; Public Library of Science (PLoS) |
subjects | Actinomyces Actinomyces - genetics Aggregatibacter actinomycetemcomitans - genetics Anaerobiosis Anaerobiosis - genetics Analysis Bacteria Biochemistry Biofilms Biofilms - growth & development Biology and Life Sciences Cell culture Confocal microscopy CRISPR Culture Media - chemistry Dental research Deoxyribonucleic acid DNA DNA microarrays Durapatite Electron microscopy Fluorescence Fluorescence in situ hybridization Fusobacterium nucleatum - genetics Gene expression Gene Expression Regulation, Bacterial Genes Genes, Bacterial Genetic aspects Genetic research Gram-negative bacteria Growth Humans Hydroxyapatite Hydroxyapatites Immunology Inflammation Laboratories Medicine and Health Sciences Metabolism Microscopy Odontology Oral microbiology Oxidative stress Pathogenicity Pathogens Plankton - genetics Plankton - growth & development Polymerase chain reaction Porphyromonas gingivalis Porphyromonas gingivalis - genetics Porphyromonas gingivalis - growth & development Research and Analysis Methods Reverse transcription Ribonucleic acid RNA RNA, Bacterial Scanning electron microscopy Scanning microscopy Streptococcus oralis - genetics Transcriptome Transposons Veillonella - genetics Virulence Virulence (Microbiology) Virulence factors |
title | Gene expression of Porphyromonas gingivalis ATCC 33277 when growing in an in vitro multispecies biofilm |
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