Genetic Diversity of Clostridium sporogenes PA 3679 Isolates Obtained from Different Sources as Resolved by Pulsed-Field Gel Electrophoresis and High-Throughput Sequencing
Clostridium sporogenes PA 3679 is a nonpathogenic, nontoxic model organism for proteolytic Clostridium botulinum used in the validation of conventional thermal food processes due to its ability to produce highly heat-resistant endospores. Because of its public safety importance, the uncertain taxono...
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description | Clostridium sporogenes PA 3679 is a nonpathogenic, nontoxic model organism for proteolytic Clostridium botulinum used in the validation of conventional thermal food processes due to its ability to produce highly heat-resistant endospores. Because of its public safety importance, the uncertain taxonomic classification and genetic diversity of PA 3679 are concerns. Therefore, isolates of C. sporogenes PA 3679 were obtained from various sources and characterized using pulsed-field gel electrophoresis (PFGE) and whole-genome sequencing. The phylogenetic relatedness and genetic variability were assessed based on 16S rRNA gene sequencing and whole-genome single nucleotide polymorphism (SNP) analysis. All C. sporogenes PA 3679 isolates were categorized into two clades (clade I containing ATCC 7955 NCA3679 isolates 1961-2, 1990, and 2007 and clade II containing PA 3679 isolates NFL, UW, FDA, and Campbell and ATCC 7955 NCA3679 isolate 1961-4). The 16S maximum likelihood (ML) tree clustered both clades within proteolytic C. botulinum strains, with clade I forming a distinct cluster with other C. sporogenes non-PA 3679 strains. SNP analysis revealed that clade I isolates were more similar to the genomic reference PA 3679 (NCTC8594) genome (GenBank accession number AGAH00000000.1) than clade II isolates were. The genomic reference C. sporogenes PA 3679 (NCTC8594) genome and clade I C. sporogenes isolates were genetically distinct from those obtained from other sources (University of Wisconsin, National Food Laboratory, U.S. Food and Drug Administration, and Campbell's Soup Company). Thermal destruction studies revealed that clade I isolates were more sensitive to high temperature than clade II isolates were. Considering the widespread use of C. sporogenes PA 3679 and its genetic information in numerous studies, the accurate identification and genetic characterization of C. sporogenes PA 3679 are of critical importance. |
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W.</contributor><creatorcontrib>Schill, Kristin M ; Wang, Yun ; Butler, 3rd, Robert R ; Pombert, Jean-François ; Reddy, N Rukma ; Skinner, Guy E ; Larkin, John W ; Schaffner, D. W.</creatorcontrib><description>Clostridium sporogenes PA 3679 is a nonpathogenic, nontoxic model organism for proteolytic Clostridium botulinum used in the validation of conventional thermal food processes due to its ability to produce highly heat-resistant endospores. Because of its public safety importance, the uncertain taxonomic classification and genetic diversity of PA 3679 are concerns. Therefore, isolates of C. sporogenes PA 3679 were obtained from various sources and characterized using pulsed-field gel electrophoresis (PFGE) and whole-genome sequencing. The phylogenetic relatedness and genetic variability were assessed based on 16S rRNA gene sequencing and whole-genome single nucleotide polymorphism (SNP) analysis. All C. sporogenes PA 3679 isolates were categorized into two clades (clade I containing ATCC 7955 NCA3679 isolates 1961-2, 1990, and 2007 and clade II containing PA 3679 isolates NFL, UW, FDA, and Campbell and ATCC 7955 NCA3679 isolate 1961-4). The 16S maximum likelihood (ML) tree clustered both clades within proteolytic C. botulinum strains, with clade I forming a distinct cluster with other C. sporogenes non-PA 3679 strains. SNP analysis revealed that clade I isolates were more similar to the genomic reference PA 3679 (NCTC8594) genome (GenBank accession number AGAH00000000.1) than clade II isolates were. The genomic reference C. sporogenes PA 3679 (NCTC8594) genome and clade I C. sporogenes isolates were genetically distinct from those obtained from other sources (University of Wisconsin, National Food Laboratory, U.S. Food and Drug Administration, and Campbell's Soup Company). Thermal destruction studies revealed that clade I isolates were more sensitive to high temperature than clade II isolates were. Considering the widespread use of C. sporogenes PA 3679 and its genetic information in numerous studies, the accurate identification and genetic characterization of C. sporogenes PA 3679 are of critical importance.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AEM.02616-15</identifier><identifier>PMID: 26519392</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Clostridium - classification ; Clostridium - genetics ; Clostridium - isolation & purification ; Clostridium botulinum ; Clostridium botulinum - genetics ; Clostridium sporogenes ; DNA, Bacterial - genetics ; Electrophoresis, Gel, Pulsed-Field ; Food Microbiology ; Genetic diversity ; Genetic Variation ; Genomics ; Gram-positive bacteria ; High temperature physics ; High-Throughput Nucleotide Sequencing ; Maximum likelihood method ; Molecular Sequence Data ; Phylogenetics ; Phylogeny ; Polymorphism ; Polymorphism, Single Nucleotide ; RNA, Ribosomal, 16S ; Spores, Bacterial ; Spotlight ; United States</subject><ispartof>Applied and Environmental Microbiology, 2016-01, Vol.82 (1), p.384-393</ispartof><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright American Society for Microbiology Jan 2016</rights><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-a23c7d1e64c2e734961983f88f5c2a545d9e55bbaf1d618266e00bd313a44cb13</citedby><cites>FETCH-LOGICAL-c445t-a23c7d1e64c2e734961983f88f5c2a545d9e55bbaf1d618266e00bd313a44cb13</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/PMC4702626/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702626/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26519392$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Schaffner, D. W.</contributor><creatorcontrib>Schill, Kristin M</creatorcontrib><creatorcontrib>Wang, Yun</creatorcontrib><creatorcontrib>Butler, 3rd, Robert R</creatorcontrib><creatorcontrib>Pombert, Jean-François</creatorcontrib><creatorcontrib>Reddy, N Rukma</creatorcontrib><creatorcontrib>Skinner, Guy E</creatorcontrib><creatorcontrib>Larkin, John W</creatorcontrib><title>Genetic Diversity of Clostridium sporogenes PA 3679 Isolates Obtained from Different Sources as Resolved by Pulsed-Field Gel Electrophoresis and High-Throughput Sequencing</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Clostridium sporogenes PA 3679 is a nonpathogenic, nontoxic model organism for proteolytic Clostridium botulinum used in the validation of conventional thermal food processes due to its ability to produce highly heat-resistant endospores. Because of its public safety importance, the uncertain taxonomic classification and genetic diversity of PA 3679 are concerns. Therefore, isolates of C. sporogenes PA 3679 were obtained from various sources and characterized using pulsed-field gel electrophoresis (PFGE) and whole-genome sequencing. The phylogenetic relatedness and genetic variability were assessed based on 16S rRNA gene sequencing and whole-genome single nucleotide polymorphism (SNP) analysis. All C. sporogenes PA 3679 isolates were categorized into two clades (clade I containing ATCC 7955 NCA3679 isolates 1961-2, 1990, and 2007 and clade II containing PA 3679 isolates NFL, UW, FDA, and Campbell and ATCC 7955 NCA3679 isolate 1961-4). The 16S maximum likelihood (ML) tree clustered both clades within proteolytic C. botulinum strains, with clade I forming a distinct cluster with other C. sporogenes non-PA 3679 strains. SNP analysis revealed that clade I isolates were more similar to the genomic reference PA 3679 (NCTC8594) genome (GenBank accession number AGAH00000000.1) than clade II isolates were. The genomic reference C. sporogenes PA 3679 (NCTC8594) genome and clade I C. sporogenes isolates were genetically distinct from those obtained from other sources (University of Wisconsin, National Food Laboratory, U.S. Food and Drug Administration, and Campbell's Soup Company). Thermal destruction studies revealed that clade I isolates were more sensitive to high temperature than clade II isolates were. Considering the widespread use of C. sporogenes PA 3679 and its genetic information in numerous studies, the accurate identification and genetic characterization of C. sporogenes PA 3679 are of critical importance.</description><subject>Clostridium - classification</subject><subject>Clostridium - genetics</subject><subject>Clostridium - isolation & purification</subject><subject>Clostridium botulinum</subject><subject>Clostridium botulinum - genetics</subject><subject>Clostridium sporogenes</subject><subject>DNA, Bacterial - genetics</subject><subject>Electrophoresis, Gel, Pulsed-Field</subject><subject>Food Microbiology</subject><subject>Genetic diversity</subject><subject>Genetic Variation</subject><subject>Genomics</subject><subject>Gram-positive bacteria</subject><subject>High temperature physics</subject><subject>High-Throughput Nucleotide Sequencing</subject><subject>Maximum likelihood method</subject><subject>Molecular Sequence Data</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>RNA, Ribosomal, 16S</subject><subject>Spores, Bacterial</subject><subject>Spotlight</subject><subject>United States</subject><issn>0099-2240</issn><issn>1098-5336</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkktv1DAURi0EokNhxxpZYsOCFL-TbJBGw3RaqagVlLXlODeJqyRO7WSk-U38STy0VMDKku_R0X18CL2l5IxSVnxab7-eEaaoyqh8hlaUlEUmOVfP0YqQsswYE-QEvYrxjhAiiCpeohOmJC15yVbo5w5GmJ3FX9weQnTzAfsGb3of5-Bqtww4Tj74NlER36wxV3mJL6PvzZw-rqvZuBFq3AQ_JEXTQIBxxt_9Emyqm4i_QYL3CakO-GbpI9TZuYO-xjvo8bYHOwc_dT5AdIkfa3zh2i677YJf2m5akgvuFxitG9vX6EVjkuHN43uKfpxvbzcX2dX17nKzvsqsEHLODOM2rykoYRnkXJSKlgVviqKRlhkpZF2ClFVlGlorWjClgJCq5pQbIWxF-Sn6_OCdlmqA2qaJgun1FNxgwkF74_S_ldF1uvV7LfJ0CKaS4MOjIPjUfJz14KKFvjcj-CVqmsuCiYIKktD3_6F3aXdjGu9IcSnynByFHx8oG3yMAZqnZijRxxTolAL9OwWayoS_-3uAJ_jP2fkvWCOvwg</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Schill, Kristin M</creator><creator>Wang, Yun</creator><creator>Butler, 3rd, Robert R</creator><creator>Pombert, Jean-François</creator><creator>Reddy, N Rukma</creator><creator>Skinner, Guy E</creator><creator>Larkin, John W</creator><general>American Society for Microbiology</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>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>5PM</scope></search><sort><creationdate>20160101</creationdate><title>Genetic Diversity of Clostridium sporogenes PA 3679 Isolates Obtained from Different Sources as Resolved by Pulsed-Field Gel Electrophoresis and High-Throughput Sequencing</title><author>Schill, Kristin M ; 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W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic Diversity of Clostridium sporogenes PA 3679 Isolates Obtained from Different Sources as Resolved by Pulsed-Field Gel Electrophoresis and High-Throughput Sequencing</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>82</volume><issue>1</issue><spage>384</spage><epage>393</epage><pages>384-393</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><eissn>1098-6596</eissn><coden>AEMIDF</coden><abstract>Clostridium sporogenes PA 3679 is a nonpathogenic, nontoxic model organism for proteolytic Clostridium botulinum used in the validation of conventional thermal food processes due to its ability to produce highly heat-resistant endospores. Because of its public safety importance, the uncertain taxonomic classification and genetic diversity of PA 3679 are concerns. Therefore, isolates of C. sporogenes PA 3679 were obtained from various sources and characterized using pulsed-field gel electrophoresis (PFGE) and whole-genome sequencing. The phylogenetic relatedness and genetic variability were assessed based on 16S rRNA gene sequencing and whole-genome single nucleotide polymorphism (SNP) analysis. All C. sporogenes PA 3679 isolates were categorized into two clades (clade I containing ATCC 7955 NCA3679 isolates 1961-2, 1990, and 2007 and clade II containing PA 3679 isolates NFL, UW, FDA, and Campbell and ATCC 7955 NCA3679 isolate 1961-4). The 16S maximum likelihood (ML) tree clustered both clades within proteolytic C. botulinum strains, with clade I forming a distinct cluster with other C. sporogenes non-PA 3679 strains. SNP analysis revealed that clade I isolates were more similar to the genomic reference PA 3679 (NCTC8594) genome (GenBank accession number AGAH00000000.1) than clade II isolates were. The genomic reference C. sporogenes PA 3679 (NCTC8594) genome and clade I C. sporogenes isolates were genetically distinct from those obtained from other sources (University of Wisconsin, National Food Laboratory, U.S. Food and Drug Administration, and Campbell's Soup Company). Thermal destruction studies revealed that clade I isolates were more sensitive to high temperature than clade II isolates were. Considering the widespread use of C. sporogenes PA 3679 and its genetic information in numerous studies, the accurate identification and genetic characterization of C. sporogenes PA 3679 are of critical importance.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>26519392</pmid><doi>10.1128/AEM.02616-15</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Clostridium - classification Clostridium - genetics Clostridium - isolation & purification Clostridium botulinum Clostridium botulinum - genetics Clostridium sporogenes DNA, Bacterial - genetics Electrophoresis, Gel, Pulsed-Field Food Microbiology Genetic diversity Genetic Variation Genomics Gram-positive bacteria High temperature physics High-Throughput Nucleotide Sequencing Maximum likelihood method Molecular Sequence Data Phylogenetics Phylogeny Polymorphism Polymorphism, Single Nucleotide RNA, Ribosomal, 16S Spores, Bacterial Spotlight United States |
title | Genetic Diversity of Clostridium sporogenes PA 3679 Isolates Obtained from Different Sources as Resolved by Pulsed-Field Gel Electrophoresis and High-Throughput Sequencing |
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