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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Veröffentlicht in:PloS one 2019-08, Vol.14 (8), p.e0221234-e0221234
Hauptverfasser: Romero-Lastra, Patricia, Sánchez, María C, Llama-Palacios, Arancha, Figuero, Elena, Herrera, David, Sanz, Mariano
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container_title PloS one
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creator Romero-Lastra, Patricia
Sánchez, María C
Llama-Palacios, Arancha
Figuero, Elena
Herrera, David
Sanz, Mariano
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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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 &lt;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. 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Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Meteorological &amp; Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - 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 &lt;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>
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1932-6203
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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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