Complete genome and gene expression analyses of Asaia bogorensis reveal unique responses to culture with mammalian cells as a potential opportunistic human pathogen
Asaia bogorensis, a member of acetic acid bacteria (AAB), is an aerobic bacterium isolated from flowers and fruits, as well as an opportunistic pathogen that causes human peritonitis and bacteraemia. Here, we determined the complete genomic sequence of the As. bogorensis type strain NBRC 16594, and...
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Veröffentlicht in: | DNA research 2015-10, Vol.22 (5), p.357-366 |
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description | Asaia bogorensis, a member of acetic acid bacteria (AAB), is an aerobic bacterium isolated from flowers and fruits, as well as an opportunistic pathogen that causes human peritonitis and bacteraemia. Here, we determined the complete genomic sequence of the As. bogorensis type strain NBRC 16594, and conducted comparative analyses of gene expression under different conditions of co-culture with mammalian cells and standard AAB culture. The genome of As. bogorensis contained 2,758 protein-coding genes within a circular chromosome of 3,198,265 bp. There were two complete operons encoding cytochrome bo3-type ubiquinol terminal oxidases: cyoABCD-1 and cyoABCD-2. The cyoABCD-1 operon was phylogenetically common to AAB genomes, whereas the cyoABCD-2 operon belonged to a lineage distinctive from the cyoABCD-1 operon. Interestingly, cyoABCD-1 was less expressed under co-culture conditions than under the AAB culture conditions, whereas the converse was true for cyoABCD-2. Asaia bogorensis shared pathogenesis-related genes with another pathogenic AAB, Granulibacter bethesdensis, including a gene coding pathogen-specific large bacterial adhesin and additional genes for the inhibition of oxidation and antibiotic resistance. Expression alteration of the respiratory chain and unique hypothetical genes may be key traits that enable the bacterium to survive under the co-culture conditions. |
doi_str_mv | 10.1093/dnares/dsv018 |
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Here, we determined the complete genomic sequence of the As. bogorensis type strain NBRC 16594, and conducted comparative analyses of gene expression under different conditions of co-culture with mammalian cells and standard AAB culture. The genome of As. bogorensis contained 2,758 protein-coding genes within a circular chromosome of 3,198,265 bp. There were two complete operons encoding cytochrome bo3-type ubiquinol terminal oxidases: cyoABCD-1 and cyoABCD-2. The cyoABCD-1 operon was phylogenetically common to AAB genomes, whereas the cyoABCD-2 operon belonged to a lineage distinctive from the cyoABCD-1 operon. Interestingly, cyoABCD-1 was less expressed under co-culture conditions than under the AAB culture conditions, whereas the converse was true for cyoABCD-2. Asaia bogorensis shared pathogenesis-related genes with another pathogenic AAB, Granulibacter bethesdensis, including a gene coding pathogen-specific large bacterial adhesin and additional genes for the inhibition of oxidation and antibiotic resistance. Expression alteration of the respiratory chain and unique hypothetical genes may be key traits that enable the bacterium to survive under the co-culture conditions.</description><identifier>ISSN: 1340-2838</identifier><identifier>EISSN: 1756-1663</identifier><identifier>DOI: 10.1093/dnares/dsv018</identifier><identifier>PMID: 26358298</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Acetobacteraceae - classification ; Acetobacteraceae - genetics ; Acetobacteraceae - pathogenicity ; Adhesins, Bacterial - genetics ; Amino Acid Sequence ; Animals ; Coculture Techniques ; Drug Resistance, Bacterial - genetics ; Gene Expression Profiling ; Genome, Bacterial ; Humans ; Mice ; Molecular Sequence Data ; Operon ; Opportunistic Infections - microbiology ; Oxidoreductases - biosynthesis</subject><ispartof>DNA research, 2015-10, Vol.22 (5), p.357-366</ispartof><rights>The Author 2015. Published by Oxford University Press on behalf of Kazusa DNA Research Institute.</rights><rights>The Author 2015. Published by Oxford University Press on behalf of Kazusa DNA Research Institute. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c348t-d671b243237e207844a010d32bd11c77034472e5a28321626bf97bdf4245e4a33</citedby><cites>FETCH-LOGICAL-c348t-d671b243237e207844a010d32bd11c77034472e5a28321626bf97bdf4245e4a33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596401/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596401/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26358298$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kawai, Mikihiko</creatorcontrib><creatorcontrib>Higashiura, Norie</creatorcontrib><creatorcontrib>Hayasaki, Kimie</creatorcontrib><creatorcontrib>Okamoto, Naruhei</creatorcontrib><creatorcontrib>Takami, Akiko</creatorcontrib><creatorcontrib>Hirakawa, Hideki</creatorcontrib><creatorcontrib>Matsushita, Kazunobu</creatorcontrib><creatorcontrib>Azuma, Yoshinao</creatorcontrib><title>Complete genome and gene expression analyses of Asaia bogorensis reveal unique responses to culture with mammalian cells as a potential opportunistic human pathogen</title><title>DNA research</title><addtitle>DNA Res</addtitle><description>Asaia bogorensis, a member of acetic acid bacteria (AAB), is an aerobic bacterium isolated from flowers and fruits, as well as an opportunistic pathogen that causes human peritonitis and bacteraemia. Here, we determined the complete genomic sequence of the As. bogorensis type strain NBRC 16594, and conducted comparative analyses of gene expression under different conditions of co-culture with mammalian cells and standard AAB culture. The genome of As. bogorensis contained 2,758 protein-coding genes within a circular chromosome of 3,198,265 bp. There were two complete operons encoding cytochrome bo3-type ubiquinol terminal oxidases: cyoABCD-1 and cyoABCD-2. The cyoABCD-1 operon was phylogenetically common to AAB genomes, whereas the cyoABCD-2 operon belonged to a lineage distinctive from the cyoABCD-1 operon. Interestingly, cyoABCD-1 was less expressed under co-culture conditions than under the AAB culture conditions, whereas the converse was true for cyoABCD-2. Asaia bogorensis shared pathogenesis-related genes with another pathogenic AAB, Granulibacter bethesdensis, including a gene coding pathogen-specific large bacterial adhesin and additional genes for the inhibition of oxidation and antibiotic resistance. Expression alteration of the respiratory chain and unique hypothetical genes may be key traits that enable the bacterium to survive under the co-culture conditions.</description><subject>Acetobacteraceae - classification</subject><subject>Acetobacteraceae - genetics</subject><subject>Acetobacteraceae - pathogenicity</subject><subject>Adhesins, Bacterial - genetics</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Coculture Techniques</subject><subject>Drug Resistance, Bacterial - genetics</subject><subject>Gene Expression Profiling</subject><subject>Genome, Bacterial</subject><subject>Humans</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Operon</subject><subject>Opportunistic Infections - microbiology</subject><subject>Oxidoreductases - biosynthesis</subject><issn>1340-2838</issn><issn>1756-1663</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU9v1DAQxSMEoqXlyBX5yCXU_xJnL0jVqrRIlbjQszVJJrtGjh08zkK_Dx8Ur7ZUIFny2P75-XleVb0T_KPgG3U1BkhIVyMduOheVOfCNG0t2la9LLXSvJad6s6qN0TfOdeiUeZ1dSZb1XRy051Xv7dxXjxmZDsMcUYGYTyWyPDXUoTJxVD2wD8SEosTuyZwwPq4iwkDOWIJDwiercH9WLGsaInhyObIhtXnNSH76fKezTDP4B0ENqD3xKAMtsSMIbtyPy5LTLmoUHYD269zARfI-1jMXFavJvCEb5_mi-rh88237V19__X2y_b6vh6U7nI9tkb0UiupDEpuOq2BCz4q2Y9CDMZwpbWR2EBpiRStbPtpY_px0lI3qEGpi-rTSXdZ-xnHoVhL4O2S3Azp0UZw9v-T4PZ2Fw9WN5tWc1EEPjwJpFi6QdnOjo7fhYBxJSuMLJl0ipuC1id0SJEo4fT8jOD2mKw9JWtPyRb-_b_enum_Uao_QMWmaQ</recordid><startdate>20151001</startdate><enddate>20151001</enddate><creator>Kawai, Mikihiko</creator><creator>Higashiura, Norie</creator><creator>Hayasaki, Kimie</creator><creator>Okamoto, Naruhei</creator><creator>Takami, Akiko</creator><creator>Hirakawa, Hideki</creator><creator>Matsushita, Kazunobu</creator><creator>Azuma, Yoshinao</creator><general>Oxford University Press</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151001</creationdate><title>Complete genome and gene expression analyses of Asaia bogorensis reveal unique responses to culture with mammalian cells as a potential opportunistic human pathogen</title><author>Kawai, Mikihiko ; Higashiura, Norie ; Hayasaki, Kimie ; Okamoto, Naruhei ; Takami, Akiko ; Hirakawa, Hideki ; Matsushita, Kazunobu ; Azuma, Yoshinao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-d671b243237e207844a010d32bd11c77034472e5a28321626bf97bdf4245e4a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acetobacteraceae - classification</topic><topic>Acetobacteraceae - genetics</topic><topic>Acetobacteraceae - pathogenicity</topic><topic>Adhesins, Bacterial - genetics</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Coculture Techniques</topic><topic>Drug Resistance, Bacterial - genetics</topic><topic>Gene Expression Profiling</topic><topic>Genome, Bacterial</topic><topic>Humans</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Operon</topic><topic>Opportunistic Infections - microbiology</topic><topic>Oxidoreductases - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawai, Mikihiko</creatorcontrib><creatorcontrib>Higashiura, Norie</creatorcontrib><creatorcontrib>Hayasaki, Kimie</creatorcontrib><creatorcontrib>Okamoto, Naruhei</creatorcontrib><creatorcontrib>Takami, Akiko</creatorcontrib><creatorcontrib>Hirakawa, Hideki</creatorcontrib><creatorcontrib>Matsushita, Kazunobu</creatorcontrib><creatorcontrib>Azuma, Yoshinao</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>DNA research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawai, Mikihiko</au><au>Higashiura, Norie</au><au>Hayasaki, Kimie</au><au>Okamoto, Naruhei</au><au>Takami, Akiko</au><au>Hirakawa, Hideki</au><au>Matsushita, Kazunobu</au><au>Azuma, Yoshinao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complete genome and gene expression analyses of Asaia bogorensis reveal unique responses to culture with mammalian cells as a potential opportunistic human pathogen</atitle><jtitle>DNA research</jtitle><addtitle>DNA Res</addtitle><date>2015-10-01</date><risdate>2015</risdate><volume>22</volume><issue>5</issue><spage>357</spage><epage>366</epage><pages>357-366</pages><issn>1340-2838</issn><eissn>1756-1663</eissn><abstract>Asaia bogorensis, a member of acetic acid bacteria (AAB), is an aerobic bacterium isolated from flowers and fruits, as well as an opportunistic pathogen that causes human peritonitis and bacteraemia. Here, we determined the complete genomic sequence of the As. bogorensis type strain NBRC 16594, and conducted comparative analyses of gene expression under different conditions of co-culture with mammalian cells and standard AAB culture. The genome of As. bogorensis contained 2,758 protein-coding genes within a circular chromosome of 3,198,265 bp. There were two complete operons encoding cytochrome bo3-type ubiquinol terminal oxidases: cyoABCD-1 and cyoABCD-2. The cyoABCD-1 operon was phylogenetically common to AAB genomes, whereas the cyoABCD-2 operon belonged to a lineage distinctive from the cyoABCD-1 operon. Interestingly, cyoABCD-1 was less expressed under co-culture conditions than under the AAB culture conditions, whereas the converse was true for cyoABCD-2. Asaia bogorensis shared pathogenesis-related genes with another pathogenic AAB, Granulibacter bethesdensis, including a gene coding pathogen-specific large bacterial adhesin and additional genes for the inhibition of oxidation and antibiotic resistance. Expression alteration of the respiratory chain and unique hypothetical genes may be key traits that enable the bacterium to survive under the co-culture conditions.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>26358298</pmid><doi>10.1093/dnares/dsv018</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetobacteraceae - classification Acetobacteraceae - genetics Acetobacteraceae - pathogenicity Adhesins, Bacterial - genetics Amino Acid Sequence Animals Coculture Techniques Drug Resistance, Bacterial - genetics Gene Expression Profiling Genome, Bacterial Humans Mice Molecular Sequence Data Operon Opportunistic Infections - microbiology Oxidoreductases - biosynthesis |
title | Complete genome and gene expression analyses of Asaia bogorensis reveal unique responses to culture with mammalian cells as a potential opportunistic human pathogen |
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