Classification of Cutibacterium acnes at phylotype level by MALDI-MS proteotyping

Cutibacterium acnes is a major commensal human skin bacteria. It is a producer of propionic acids that maintain skin acidic pH to inhibit the growth of pathogens. On the other hand, it is also associated with diseases such as acne vulgaris and sarcoidosis. C. acnes strains have been classified into...

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Veröffentlicht in:Proceedings of the Japan Academy Series B, 2019/12/11, Vol.95(10), pp.612-623
Hauptverfasser: TERAMOTO, Kanae, OKUBO, Tatsuki, YAMADA, Yoshihiro, SEKIYA, Sadanori, IWAMOTO, Shinichi, TANAKA, Koichi
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container_title Proceedings of the Japan Academy
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creator TERAMOTO, Kanae
OKUBO, Tatsuki
YAMADA, Yoshihiro
SEKIYA, Sadanori
IWAMOTO, Shinichi
TANAKA, Koichi
description Cutibacterium acnes is a major commensal human skin bacteria. It is a producer of propionic acids that maintain skin acidic pH to inhibit the growth of pathogens. On the other hand, it is also associated with diseases such as acne vulgaris and sarcoidosis. C. acnes strains have been classified into six phylotypes using DNA-based approaches. Because several characteristic features of C. acnes vary according to the phylotype, the development of a practical method to identify these phylotypes is needed. For rapid identification of phylotypes for C. acnes strains, a matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) fingerprinting technique has been applied; however, some phylotypes have not been discriminated. We developed a high-throughput protein purification method to detect biomarker proteins by ultrafiltration. MALDI-MS proteotyping using profiling of identified biomarker peaks was applied for the classification of 24 strains of C. acnes, and these were successfully classified into the correct phylotypes. This is a promising method that allows the discrimination of C. acnes phylotypes independent of a DNA-based approach.
doi_str_mv 10.2183/pjab.95.042
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It is a producer of propionic acids that maintain skin acidic pH to inhibit the growth of pathogens. On the other hand, it is also associated with diseases such as acne vulgaris and sarcoidosis. C. acnes strains have been classified into six phylotypes using DNA-based approaches. Because several characteristic features of C. acnes vary according to the phylotype, the development of a practical method to identify these phylotypes is needed. For rapid identification of phylotypes for C. acnes strains, a matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) fingerprinting technique has been applied; however, some phylotypes have not been discriminated. We developed a high-throughput protein purification method to detect biomarker proteins by ultrafiltration. MALDI-MS proteotyping using profiling of identified biomarker peaks was applied for the classification of 24 strains of C. acnes, and these were successfully classified into the correct phylotypes. 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Jpn. Acad., Ser. B</addtitle><description>Cutibacterium acnes is a major commensal human skin bacteria. It is a producer of propionic acids that maintain skin acidic pH to inhibit the growth of pathogens. On the other hand, it is also associated with diseases such as acne vulgaris and sarcoidosis. C. acnes strains have been classified into six phylotypes using DNA-based approaches. Because several characteristic features of C. acnes vary according to the phylotype, the development of a practical method to identify these phylotypes is needed. For rapid identification of phylotypes for C. acnes strains, a matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) fingerprinting technique has been applied; however, some phylotypes have not been discriminated. We developed a high-throughput protein purification method to detect biomarker proteins by ultrafiltration. 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This is a promising method that allows the discrimination of C. acnes phylotypes independent of a DNA-based approach.</description><subject>Acne</subject><subject>Amino Acid Sequence</subject><subject>Amino acids</subject><subject>antitoxin</subject><subject>Bacteria</subject><subject>Bioinformatics</subject><subject>Biological products</subject><subject>Biomarkers</subject><subject>Biomarkers - analysis</subject><subject>Classification</subject><subject>Cutibacterium acnes</subject><subject>Deoxyribonucleic acid</subject><subject>Discrimination</subject><subject>DNA</subject><subject>Drug resistance</subject><subject>Fingerprinting</subject><subject>Genomes</subject><subject>High-Throughput Screening Assays</subject><subject>Identification</subject><subject>Instrument industry (Equipment)</subject><subject>Ionization</subject><subject>Ions</subject><subject>MALDI-MS proteotyping</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Methods</subject><subject>Mutation</subject><subject>Original</subject><subject>Pathogens</subject><subject>phylotype</subject><subject>Propionibacteriaceae - classification</subject><subject>Propionibacteriaceae - genetics</subject><subject>Propionic acid</subject><subject>Protein purification</subject><subject>Proteins</subject><subject>ribosomal protein</subject><subject>Ribosomal Proteins - analysis</subject><subject>Ribosomal Proteins - genetics</subject><subject>Sarcoidosis</subject><subject>Scientific imaging</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Strains (organisms)</subject><subject>Ultrafiltration</subject><issn>0386-2208</issn><issn>0021-4280</issn><issn>1349-2896</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkt-L1DAQgIMo3nr65LsUfBGka340afMirOt5nuyhoj6HNJ3uZmmbmqQH-99fyt6tnkgggeSbb8jMIPSS4CUlFXs37nW9lHyJC_oILQgrZE4rKR6jBWaVyCnF1Rl6FsIeY0Z5RZ6iM0YqWmIiF-j7utMh2NYaHa0bMtdm6ynaWpsI3k59ps0AIdMxG3eHzsXDCFkHN9Bl9SG7Xm0-XuXXP7LRuwjzox22z9GTVncBXtyd5-jXp4uf68_55uvl1Xq1yU3Jq5gXtSBlwUTNDdOmlYw3NU-HgZKbGriEijWixLwmTArcNpgXuigLTFtBwAh2jt4fveNU99AYGKLXnRq97bU_KKetevgy2J3auhslJMW4wknw5k7g3e8JQlS9DQa6Tg_gpqBoqhZLNSvKhL7-B927yQ_pe4limEuanH-ore5A2aF1Ka-ZpWolCipSI8hMLf9DpdVAb40boLXp_kHA22OA8S4ED-3pjwSreQLUPAFKcpUmINGv_i7Lib1veQIuj8A-RL2FE6B9tCZlvpcledq_fVlJTvCH5D4RZqe9goHdAkzlw_I</recordid><startdate>20191211</startdate><enddate>20191211</enddate><creator>TERAMOTO, Kanae</creator><creator>OKUBO, Tatsuki</creator><creator>YAMADA, Yoshihiro</creator><creator>SEKIYA, Sadanori</creator><creator>IWAMOTO, Shinichi</creator><creator>TANAKA, Koichi</creator><general>The Japan Academy</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>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BVBZV</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20191211</creationdate><title>Classification of Cutibacterium acnes at phylotype level by MALDI-MS proteotyping</title><author>TERAMOTO, Kanae ; 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We developed a high-throughput protein purification method to detect biomarker proteins by ultrafiltration. MALDI-MS proteotyping using profiling of identified biomarker peaks was applied for the classification of 24 strains of C. acnes, and these were successfully classified into the correct phylotypes. This is a promising method that allows the discrimination of C. acnes phylotypes independent of a DNA-based approach.</abstract><cop>Japan</cop><pub>The Japan Academy</pub><pmid>31827019</pmid><doi>10.2183/pjab.95.042</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Acne
Amino Acid Sequence
Amino acids
antitoxin
Bacteria
Bioinformatics
Biological products
Biomarkers
Biomarkers - analysis
Classification
Cutibacterium acnes
Deoxyribonucleic acid
Discrimination
DNA
Drug resistance
Fingerprinting
Genomes
High-Throughput Screening Assays
Identification
Instrument industry (Equipment)
Ionization
Ions
MALDI-MS proteotyping
Mass spectrometry
Mass spectroscopy
Methods
Mutation
Original
Pathogens
phylotype
Propionibacteriaceae - classification
Propionibacteriaceae - genetics
Propionic acid
Protein purification
Proteins
ribosomal protein
Ribosomal Proteins - analysis
Ribosomal Proteins - genetics
Sarcoidosis
Scientific imaging
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Strains (organisms)
Ultrafiltration
title Classification of Cutibacterium acnes at phylotype level by MALDI-MS proteotyping
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