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High bacterial colonization and lipase activity in microcomedones
Background Although acne vulgaris has a multifactorial aetiology, comedogenesis and bacteria colonization of the pilosebaceous unit are known to play a major role in the onset of inflammatory acne lesions. However, many aspects remain poorly understood such as where and when is the early stage of th...
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Published in: | Experimental dermatology 2020-02, Vol.29 (2), p.168-176 |
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container_title | Experimental dermatology |
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creator | Josse, Gwendal Mias, Céline Le Digabel, Jimmy Filiol, Jérôme Ipinazar, Célia Villaret, Aurélie Gomiero, Caroline Bevilacqua, Marc Redoules, Daniel Nocera, Thérèse Saurat, Jean‐Hilaire Gontier, Etienne |
description | Background
Although acne vulgaris has a multifactorial aetiology, comedogenesis and bacteria colonization of the pilosebaceous unit are known to play a major role in the onset of inflammatory acne lesions. However, many aspects remain poorly understood such as where and when is the early stage of the Propionibacterium acnes colonization in follicular unit? Our research aimed at providing a precise analysis of microcomedone's structure to better understand the interplay between Propionibacterium acnes and follicular units, and therefore, the role of its interplay in the formation of acne lesions.
Methods
Microcomedones were sampled using cyanoacrylate skin surface stripping (CSSS). Their morphology was investigated with multiphoton imaging and their ultrastructure with scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Bacterial lipase activity in the microcomedones was quantified using a dedicated enzymatic test as well as a Fourier Transform Infra‐Red (FTIR) analysis. The porphyrin produced by bacteria was analysed with HPTLC and fluorescence spectroscopy.
Results
The imaging analysis showed that microcomedones' structure resembles a pouch, whose interior is mostly composed of lipids with clusters of bacteria and whose outer shell is made up of corneocyte layers. The extensive bacteria colonization is clearly visible using TEM. Even after sampling, clear lipase activity was still seen in the microcomedone. A high correlation, r = .85, was observed between porphyrin content measured with HPTLC and with fluorescence spectroscopy. These observations show that microcomedones, which are generally barely visible clinically, already contain a bacterial colonization. |
doi_str_mv | 10.1111/exd.14069 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7586799</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2348527967</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5099-2ddc3ca5ae03c6cc43e6ca929567b53c3f102c7d8b8580f86ba4803e1f8a5c743</originalsourceid><addsrcrecordid>eNp1kE1PAjEQhhujEUQP_gGziScPC-12-3UxIYhiYuJFE29Nt9uFkqXF7oLir7cKEj04lznMk2dmXgDOEeyjWAPzXvZRDqk4AF1EIUwhzcgh6EIBaUoZJB1w0jRzCBHDjByDDkac4lxkXTCc2OksKZRuTbCqTrSvvbMfqrXeJcqVSW2XqjFJBOzatpvEumRhdfDaL0zpnWlOwVGl6sac7XoPPN-On0aT9OHx7n40fEg1gUKkWVlqrBVRBmJNtc6xoVqJTBDKCoI1rhDMNCt5wQmHFaeFyjnEBlVcEc1y3APXW-9yVcTV2rg2qFoug12osJFeWfl34uxMTv1aMsIpEyIKLneC4F9Xpmnl3K-CizfLDOecZExQFqmrLRV_bJpgqv0GBOVX2jKmLb_TjuzF75P25E-8ERhsgTdbm83_Jjl-udkqPwECoYqS</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2348527967</pqid></control><display><type>article</type><title>High bacterial colonization and lipase activity in microcomedones</title><source>Wiley</source><creator>Josse, Gwendal ; Mias, Céline ; Le Digabel, Jimmy ; Filiol, Jérôme ; Ipinazar, Célia ; Villaret, Aurélie ; Gomiero, Caroline ; Bevilacqua, Marc ; Redoules, Daniel ; Nocera, Thérèse ; Saurat, Jean‐Hilaire ; Gontier, Etienne</creator><creatorcontrib>Josse, Gwendal ; Mias, Céline ; Le Digabel, Jimmy ; Filiol, Jérôme ; Ipinazar, Célia ; Villaret, Aurélie ; Gomiero, Caroline ; Bevilacqua, Marc ; Redoules, Daniel ; Nocera, Thérèse ; Saurat, Jean‐Hilaire ; Gontier, Etienne</creatorcontrib><description>Background
Although acne vulgaris has a multifactorial aetiology, comedogenesis and bacteria colonization of the pilosebaceous unit are known to play a major role in the onset of inflammatory acne lesions. However, many aspects remain poorly understood such as where and when is the early stage of the Propionibacterium acnes colonization in follicular unit? Our research aimed at providing a precise analysis of microcomedone's structure to better understand the interplay between Propionibacterium acnes and follicular units, and therefore, the role of its interplay in the formation of acne lesions.
Methods
Microcomedones were sampled using cyanoacrylate skin surface stripping (CSSS). Their morphology was investigated with multiphoton imaging and their ultrastructure with scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Bacterial lipase activity in the microcomedones was quantified using a dedicated enzymatic test as well as a Fourier Transform Infra‐Red (FTIR) analysis. The porphyrin produced by bacteria was analysed with HPTLC and fluorescence spectroscopy.
Results
The imaging analysis showed that microcomedones' structure resembles a pouch, whose interior is mostly composed of lipids with clusters of bacteria and whose outer shell is made up of corneocyte layers. The extensive bacteria colonization is clearly visible using TEM. Even after sampling, clear lipase activity was still seen in the microcomedone. A high correlation, r = .85, was observed between porphyrin content measured with HPTLC and with fluorescence spectroscopy. These observations show that microcomedones, which are generally barely visible clinically, already contain a bacterial colonization.</description><identifier>ISSN: 0906-6705</identifier><identifier>EISSN: 1600-0625</identifier><identifier>DOI: 10.1111/exd.14069</identifier><identifier>PMID: 31863492</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>Acne ; Acne vulgaris ; Acne Vulgaris - diagnostic imaging ; Acne Vulgaris - enzymology ; Acne Vulgaris - microbiology ; Bacteria ; Colonization ; electron microscopy ; fluorescence ; Fluorescence spectroscopy ; Fourier analysis ; fourier transform infrared ; hair follicle ; Hair Follicle - microbiology ; Humans ; Inflammation ; Lipase ; Lipase - metabolism ; Lipids ; Microscopy ; Microscopy, Electron, Scanning ; Microscopy, Electron, Transmission ; Microscopy, Fluorescence, Multiphoton ; multiphoton microscopy ; Original ; Porphyrins - metabolism ; Propionibacterium acnes ; Scanning electron microscopy ; Spectrum analysis ; Transmission electron microscopy ; Ultrastructure</subject><ispartof>Experimental dermatology, 2020-02, Vol.29 (2), p.168-176</ispartof><rights>2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>2019. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 John Wiley & Sons A/S . Published by John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5099-2ddc3ca5ae03c6cc43e6ca929567b53c3f102c7d8b8580f86ba4803e1f8a5c743</citedby><cites>FETCH-LOGICAL-c5099-2ddc3ca5ae03c6cc43e6ca929567b53c3f102c7d8b8580f86ba4803e1f8a5c743</cites><orcidid>0000-0001-8055-8255 ; 0000-0003-3375-5226</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31863492$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Josse, Gwendal</creatorcontrib><creatorcontrib>Mias, Céline</creatorcontrib><creatorcontrib>Le Digabel, Jimmy</creatorcontrib><creatorcontrib>Filiol, Jérôme</creatorcontrib><creatorcontrib>Ipinazar, Célia</creatorcontrib><creatorcontrib>Villaret, Aurélie</creatorcontrib><creatorcontrib>Gomiero, Caroline</creatorcontrib><creatorcontrib>Bevilacqua, Marc</creatorcontrib><creatorcontrib>Redoules, Daniel</creatorcontrib><creatorcontrib>Nocera, Thérèse</creatorcontrib><creatorcontrib>Saurat, Jean‐Hilaire</creatorcontrib><creatorcontrib>Gontier, Etienne</creatorcontrib><title>High bacterial colonization and lipase activity in microcomedones</title><title>Experimental dermatology</title><addtitle>Exp Dermatol</addtitle><description>Background
Although acne vulgaris has a multifactorial aetiology, comedogenesis and bacteria colonization of the pilosebaceous unit are known to play a major role in the onset of inflammatory acne lesions. However, many aspects remain poorly understood such as where and when is the early stage of the Propionibacterium acnes colonization in follicular unit? Our research aimed at providing a precise analysis of microcomedone's structure to better understand the interplay between Propionibacterium acnes and follicular units, and therefore, the role of its interplay in the formation of acne lesions.
Methods
Microcomedones were sampled using cyanoacrylate skin surface stripping (CSSS). Their morphology was investigated with multiphoton imaging and their ultrastructure with scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Bacterial lipase activity in the microcomedones was quantified using a dedicated enzymatic test as well as a Fourier Transform Infra‐Red (FTIR) analysis. The porphyrin produced by bacteria was analysed with HPTLC and fluorescence spectroscopy.
Results
The imaging analysis showed that microcomedones' structure resembles a pouch, whose interior is mostly composed of lipids with clusters of bacteria and whose outer shell is made up of corneocyte layers. The extensive bacteria colonization is clearly visible using TEM. Even after sampling, clear lipase activity was still seen in the microcomedone. A high correlation, r = .85, was observed between porphyrin content measured with HPTLC and with fluorescence spectroscopy. These observations show that microcomedones, which are generally barely visible clinically, already contain a bacterial colonization.</description><subject>Acne</subject><subject>Acne vulgaris</subject><subject>Acne Vulgaris - diagnostic imaging</subject><subject>Acne Vulgaris - enzymology</subject><subject>Acne Vulgaris - microbiology</subject><subject>Bacteria</subject><subject>Colonization</subject><subject>electron microscopy</subject><subject>fluorescence</subject><subject>Fluorescence spectroscopy</subject><subject>Fourier analysis</subject><subject>fourier transform infrared</subject><subject>hair follicle</subject><subject>Hair Follicle - microbiology</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Lipase</subject><subject>Lipase - metabolism</subject><subject>Lipids</subject><subject>Microscopy</subject><subject>Microscopy, Electron, Scanning</subject><subject>Microscopy, Electron, Transmission</subject><subject>Microscopy, Fluorescence, Multiphoton</subject><subject>multiphoton microscopy</subject><subject>Original</subject><subject>Porphyrins - metabolism</subject><subject>Propionibacterium acnes</subject><subject>Scanning electron microscopy</subject><subject>Spectrum analysis</subject><subject>Transmission electron microscopy</subject><subject>Ultrastructure</subject><issn>0906-6705</issn><issn>1600-0625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp1kE1PAjEQhhujEUQP_gGziScPC-12-3UxIYhiYuJFE29Nt9uFkqXF7oLir7cKEj04lznMk2dmXgDOEeyjWAPzXvZRDqk4AF1EIUwhzcgh6EIBaUoZJB1w0jRzCBHDjByDDkac4lxkXTCc2OksKZRuTbCqTrSvvbMfqrXeJcqVSW2XqjFJBOzatpvEumRhdfDaL0zpnWlOwVGl6sac7XoPPN-On0aT9OHx7n40fEg1gUKkWVlqrBVRBmJNtc6xoVqJTBDKCoI1rhDMNCt5wQmHFaeFyjnEBlVcEc1y3APXW-9yVcTV2rg2qFoug12osJFeWfl34uxMTv1aMsIpEyIKLneC4F9Xpmnl3K-CizfLDOecZExQFqmrLRV_bJpgqv0GBOVX2jKmLb_TjuzF75P25E-8ERhsgTdbm83_Jjl-udkqPwECoYqS</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Josse, Gwendal</creator><creator>Mias, Céline</creator><creator>Le Digabel, Jimmy</creator><creator>Filiol, Jérôme</creator><creator>Ipinazar, Célia</creator><creator>Villaret, Aurélie</creator><creator>Gomiero, Caroline</creator><creator>Bevilacqua, Marc</creator><creator>Redoules, Daniel</creator><creator>Nocera, Thérèse</creator><creator>Saurat, Jean‐Hilaire</creator><creator>Gontier, Etienne</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><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>7T5</scope><scope>H94</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8055-8255</orcidid><orcidid>https://orcid.org/0000-0003-3375-5226</orcidid></search><sort><creationdate>202002</creationdate><title>High bacterial colonization and lipase activity in microcomedones</title><author>Josse, Gwendal ; Mias, Céline ; Le Digabel, Jimmy ; Filiol, Jérôme ; Ipinazar, Célia ; Villaret, Aurélie ; Gomiero, Caroline ; Bevilacqua, Marc ; Redoules, Daniel ; Nocera, Thérèse ; Saurat, Jean‐Hilaire ; Gontier, Etienne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5099-2ddc3ca5ae03c6cc43e6ca929567b53c3f102c7d8b8580f86ba4803e1f8a5c743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acne</topic><topic>Acne vulgaris</topic><topic>Acne Vulgaris - diagnostic imaging</topic><topic>Acne Vulgaris - enzymology</topic><topic>Acne Vulgaris - microbiology</topic><topic>Bacteria</topic><topic>Colonization</topic><topic>electron microscopy</topic><topic>fluorescence</topic><topic>Fluorescence spectroscopy</topic><topic>Fourier analysis</topic><topic>fourier transform infrared</topic><topic>hair follicle</topic><topic>Hair Follicle - microbiology</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Lipase</topic><topic>Lipase - metabolism</topic><topic>Lipids</topic><topic>Microscopy</topic><topic>Microscopy, Electron, Scanning</topic><topic>Microscopy, Electron, Transmission</topic><topic>Microscopy, Fluorescence, Multiphoton</topic><topic>multiphoton microscopy</topic><topic>Original</topic><topic>Porphyrins - metabolism</topic><topic>Propionibacterium acnes</topic><topic>Scanning electron microscopy</topic><topic>Spectrum analysis</topic><topic>Transmission electron microscopy</topic><topic>Ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Josse, Gwendal</creatorcontrib><creatorcontrib>Mias, Céline</creatorcontrib><creatorcontrib>Le Digabel, Jimmy</creatorcontrib><creatorcontrib>Filiol, Jérôme</creatorcontrib><creatorcontrib>Ipinazar, Célia</creatorcontrib><creatorcontrib>Villaret, Aurélie</creatorcontrib><creatorcontrib>Gomiero, Caroline</creatorcontrib><creatorcontrib>Bevilacqua, Marc</creatorcontrib><creatorcontrib>Redoules, Daniel</creatorcontrib><creatorcontrib>Nocera, Thérèse</creatorcontrib><creatorcontrib>Saurat, Jean‐Hilaire</creatorcontrib><creatorcontrib>Gontier, Etienne</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Josse, Gwendal</au><au>Mias, Céline</au><au>Le Digabel, Jimmy</au><au>Filiol, Jérôme</au><au>Ipinazar, Célia</au><au>Villaret, Aurélie</au><au>Gomiero, Caroline</au><au>Bevilacqua, Marc</au><au>Redoules, Daniel</au><au>Nocera, Thérèse</au><au>Saurat, Jean‐Hilaire</au><au>Gontier, Etienne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High bacterial colonization and lipase activity in microcomedones</atitle><jtitle>Experimental dermatology</jtitle><addtitle>Exp Dermatol</addtitle><date>2020-02</date><risdate>2020</risdate><volume>29</volume><issue>2</issue><spage>168</spage><epage>176</epage><pages>168-176</pages><issn>0906-6705</issn><eissn>1600-0625</eissn><abstract>Background
Although acne vulgaris has a multifactorial aetiology, comedogenesis and bacteria colonization of the pilosebaceous unit are known to play a major role in the onset of inflammatory acne lesions. However, many aspects remain poorly understood such as where and when is the early stage of the Propionibacterium acnes colonization in follicular unit? Our research aimed at providing a precise analysis of microcomedone's structure to better understand the interplay between Propionibacterium acnes and follicular units, and therefore, the role of its interplay in the formation of acne lesions.
Methods
Microcomedones were sampled using cyanoacrylate skin surface stripping (CSSS). Their morphology was investigated with multiphoton imaging and their ultrastructure with scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Bacterial lipase activity in the microcomedones was quantified using a dedicated enzymatic test as well as a Fourier Transform Infra‐Red (FTIR) analysis. The porphyrin produced by bacteria was analysed with HPTLC and fluorescence spectroscopy.
Results
The imaging analysis showed that microcomedones' structure resembles a pouch, whose interior is mostly composed of lipids with clusters of bacteria and whose outer shell is made up of corneocyte layers. The extensive bacteria colonization is clearly visible using TEM. Even after sampling, clear lipase activity was still seen in the microcomedone. A high correlation, r = .85, was observed between porphyrin content measured with HPTLC and with fluorescence spectroscopy. These observations show that microcomedones, which are generally barely visible clinically, already contain a bacterial colonization.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31863492</pmid><doi>10.1111/exd.14069</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8055-8255</orcidid><orcidid>https://orcid.org/0000-0003-3375-5226</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acne Acne vulgaris Acne Vulgaris - diagnostic imaging Acne Vulgaris - enzymology Acne Vulgaris - microbiology Bacteria Colonization electron microscopy fluorescence Fluorescence spectroscopy Fourier analysis fourier transform infrared hair follicle Hair Follicle - microbiology Humans Inflammation Lipase Lipase - metabolism Lipids Microscopy Microscopy, Electron, Scanning Microscopy, Electron, Transmission Microscopy, Fluorescence, Multiphoton multiphoton microscopy Original Porphyrins - metabolism Propionibacterium acnes Scanning electron microscopy Spectrum analysis Transmission electron microscopy Ultrastructure |
title | High bacterial colonization and lipase activity in microcomedones |
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