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First Report on Genome Analysis and Pathogenicity of Vibrio tubiashii FP17 from Farmed Ivory Shell (Babylonia areolata)
Ivory shell (Babylonia areolata) is a commercially important aquaculture species mainly found on the southeast coast of China. However, it has been greatly affected by vibriosis in recent years. In this study, FP17 (a potential pathogen) was isolated from a dying ivory shell with “acute death syndro...
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Published in: | Fishes 2022-12, Vol.7 (6), p.396 |
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description | Ivory shell (Babylonia areolata) is a commercially important aquaculture species mainly found on the southeast coast of China. However, it has been greatly affected by vibriosis in recent years. In this study, FP17 (a potential pathogen) was isolated from a dying ivory shell with “acute death syndrome” and confirmed as a pathogen via infectious experiment. Furthermore, phylogenetic analysis based on the average nucleotide identity (ANI) sequencing of the 16S rRNA gene and housekeeping genes (ftsz, gapA, gyrB, mreB, pyrH, rpoA, and topA) indicated that FP17 was identical to Vibrio tubiashii. Transmission electron microscopy showed that FP17 is curved and has a short rod shape, with a single flagellum. Besides, the calculated LD50 after the intramuscular injection of FP17 was 2.11 × 106 CFU/g at 14 d. The genome of the FP17 strain consists of two chromosomes and one plasmid with 5,261,336 bp and 45.08% GC content, including 4824 open reading frames (ORFs) and 150 non-coding RNAs (ncRNA). Genome mining revealed that 120 candidate gene clusters, including vibrioferrin and flagellum-related proteins, are responsible for virulence. Comparative genomic analysis showed that vibrioferrin genes, such as pvs and type Ⅵ secretion system protein genes (vas), are specific in V. tubiashii FP17 but not in the ATCC19109 strain. Furthermore, 92 antimicrobial resistance (AMR) genes, such as tufA, tet(35), crp, etc., were mapped within the genome as the potential candidate for virulence, consistent with antibiotic susceptibility assay. This is the first study to describe the complete genome sequence of V. tubiashii infecting ivory shell. The genetic characteristics, virulence factors, and antimicrobial resistance of the V. tubiashii strain FP17 were also explored. |
doi_str_mv | 10.3390/fishes7060396 |
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However, it has been greatly affected by vibriosis in recent years. In this study, FP17 (a potential pathogen) was isolated from a dying ivory shell with “acute death syndrome” and confirmed as a pathogen via infectious experiment. Furthermore, phylogenetic analysis based on the average nucleotide identity (ANI) sequencing of the 16S rRNA gene and housekeeping genes (ftsz, gapA, gyrB, mreB, pyrH, rpoA, and topA) indicated that FP17 was identical to Vibrio tubiashii. Transmission electron microscopy showed that FP17 is curved and has a short rod shape, with a single flagellum. Besides, the calculated LD50 after the intramuscular injection of FP17 was 2.11 × 106 CFU/g at 14 d. The genome of the FP17 strain consists of two chromosomes and one plasmid with 5,261,336 bp and 45.08% GC content, including 4824 open reading frames (ORFs) and 150 non-coding RNAs (ncRNA). Genome mining revealed that 120 candidate gene clusters, including vibrioferrin and flagellum-related proteins, are responsible for virulence. Comparative genomic analysis showed that vibrioferrin genes, such as pvs and type Ⅵ secretion system protein genes (vas), are specific in V. tubiashii FP17 but not in the ATCC19109 strain. Furthermore, 92 antimicrobial resistance (AMR) genes, such as tufA, tet(35), crp, etc., were mapped within the genome as the potential candidate for virulence, consistent with antibiotic susceptibility assay. This is the first study to describe the complete genome sequence of V. tubiashii infecting ivory shell. The genetic characteristics, virulence factors, and antimicrobial resistance of the V. tubiashii strain FP17 were also explored.</description><identifier>ISSN: 2410-3888</identifier><identifier>EISSN: 2410-3888</identifier><identifier>DOI: 10.3390/fishes7060396</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Analysis ; Antibiotics ; Antimicrobial agents ; Antimicrobial resistance ; Aquaculture ; Babylonia areolata ; Chromosomes ; Disease ; DNA-directed RNA polymerase ; Drug resistance ; Electron microscopy ; Epidemics ; Flagella ; Gene clusters ; Genes ; Genomes ; Genomic analysis ; Infections ; Mollusks ; Mortality ; Mortality causes ; Nucleotide sequence ; Nucleotides ; Open reading frames ; Pathogenesis ; Pathogenicity ; Pathogens ; Phylogenetics ; Phylogeny ; Plasmids ; Polyculture (aquaculture) ; Proteins ; rRNA 16S ; Salinity ; Secretion ; Toxicity tests ; Transmission electron microscopy ; Vibrio tubiashii ; Vibriosis ; Virulence ; Virulence factors ; whole genome sequencing</subject><ispartof>Fishes, 2022-12, Vol.7 (6), p.396</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-96b4d8345cc06def1d85385aa79d3a95c58b1c5f898c2fa26345401551d2c8043</citedby><cites>FETCH-LOGICAL-c370t-96b4d8345cc06def1d85385aa79d3a95c58b1c5f898c2fa26345401551d2c8043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2756686818/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2756686818?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25752,27923,27924,37011,44589,74997</link.rule.ids></links><search><creatorcontrib>Dai, Chen</creatorcontrib><creatorcontrib>Li, Xiaoxin</creatorcontrib><creatorcontrib>Luo, Dapeng</creatorcontrib><creatorcontrib>Liu, Qingming</creatorcontrib><creatorcontrib>Sun, Yun</creatorcontrib><creatorcontrib>Tu, Zhigang</creatorcontrib><creatorcontrib>Shen, Minghui</creatorcontrib><title>First Report on Genome Analysis and Pathogenicity of Vibrio tubiashii FP17 from Farmed Ivory Shell (Babylonia areolata)</title><title>Fishes</title><description>Ivory shell (Babylonia areolata) is a commercially important aquaculture species mainly found on the southeast coast of China. However, it has been greatly affected by vibriosis in recent years. In this study, FP17 (a potential pathogen) was isolated from a dying ivory shell with “acute death syndrome” and confirmed as a pathogen via infectious experiment. Furthermore, phylogenetic analysis based on the average nucleotide identity (ANI) sequencing of the 16S rRNA gene and housekeeping genes (ftsz, gapA, gyrB, mreB, pyrH, rpoA, and topA) indicated that FP17 was identical to Vibrio tubiashii. Transmission electron microscopy showed that FP17 is curved and has a short rod shape, with a single flagellum. Besides, the calculated LD50 after the intramuscular injection of FP17 was 2.11 × 106 CFU/g at 14 d. The genome of the FP17 strain consists of two chromosomes and one plasmid with 5,261,336 bp and 45.08% GC content, including 4824 open reading frames (ORFs) and 150 non-coding RNAs (ncRNA). Genome mining revealed that 120 candidate gene clusters, including vibrioferrin and flagellum-related proteins, are responsible for virulence. Comparative genomic analysis showed that vibrioferrin genes, such as pvs and type Ⅵ secretion system protein genes (vas), are specific in V. tubiashii FP17 but not in the ATCC19109 strain. Furthermore, 92 antimicrobial resistance (AMR) genes, such as tufA, tet(35), crp, etc., were mapped within the genome as the potential candidate for virulence, consistent with antibiotic susceptibility assay. This is the first study to describe the complete genome sequence of V. tubiashii infecting ivory shell. The genetic characteristics, virulence factors, and antimicrobial resistance of the V. tubiashii strain FP17 were also explored.</description><subject>Analysis</subject><subject>Antibiotics</subject><subject>Antimicrobial agents</subject><subject>Antimicrobial resistance</subject><subject>Aquaculture</subject><subject>Babylonia areolata</subject><subject>Chromosomes</subject><subject>Disease</subject><subject>DNA-directed RNA polymerase</subject><subject>Drug resistance</subject><subject>Electron microscopy</subject><subject>Epidemics</subject><subject>Flagella</subject><subject>Gene clusters</subject><subject>Genes</subject><subject>Genomes</subject><subject>Genomic analysis</subject><subject>Infections</subject><subject>Mollusks</subject><subject>Mortality</subject><subject>Mortality causes</subject><subject>Nucleotide sequence</subject><subject>Nucleotides</subject><subject>Open reading frames</subject><subject>Pathogenesis</subject><subject>Pathogenicity</subject><subject>Pathogens</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Plasmids</subject><subject>Polyculture (aquaculture)</subject><subject>Proteins</subject><subject>rRNA 16S</subject><subject>Salinity</subject><subject>Secretion</subject><subject>Toxicity tests</subject><subject>Transmission electron microscopy</subject><subject>Vibrio tubiashii</subject><subject>Vibriosis</subject><subject>Virulence</subject><subject>Virulence factors</subject><subject>whole genome sequencing</subject><issn>2410-3888</issn><issn>2410-3888</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpVkU1rGzEQhpfSQEOaY-6CXNLDttLqY0fHNNSpIZCQpLmKWX3EMuuVK8kt--_j1qUkp3kZHp6BeZvmjNHPnGv6JcSy8qWninKt3jXHnWC05QDw_lX-0JyWsqaUMq21BH3c_F7EXCq599uUK0kTufZT2nhyOeE4l1gITo7cYV2lZz9FG-tMUiBPccgxkbobIpZVjGRxx3oSctqQBeaNd2T5K-WZPKz8OJKLrzjMY5oiEsw-jVjx08fmKOBY_Om_edL8WHx7vPre3txeL68ub1rLe1pbrQbhgAtpLVXOB-ZAcpCIvXYctbQSBmZlAA22C9ipPSook5K5zgIV_KRZHrwu4dpsc9xgnk3CaP4uUn42mGu0oze8E70dqJQCeiEEHVhwLOgBggqsA7p3nR9c25x-7nypZp12ef-oYrpeKgUKGOyp9kDZnErJPvy_yqj5U5V5UxV_AYqhhi4</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Dai, Chen</creator><creator>Li, Xiaoxin</creator><creator>Luo, Dapeng</creator><creator>Liu, Qingming</creator><creator>Sun, Yun</creator><creator>Tu, Zhigang</creator><creator>Shen, Minghui</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>GNUQQ</scope><scope>H95</scope><scope>HCIFZ</scope><scope>L.G</scope><scope>LK8</scope><scope>M7P</scope><scope>PCBAR</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>DOA</scope></search><sort><creationdate>20221201</creationdate><title>First Report on Genome Analysis and Pathogenicity of Vibrio tubiashii FP17 from Farmed Ivory Shell (Babylonia areolata)</title><author>Dai, Chen ; Li, Xiaoxin ; Luo, Dapeng ; Liu, Qingming ; Sun, Yun ; Tu, Zhigang ; Shen, Minghui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c370t-96b4d8345cc06def1d85385aa79d3a95c58b1c5f898c2fa26345401551d2c8043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Analysis</topic><topic>Antibiotics</topic><topic>Antimicrobial agents</topic><topic>Antimicrobial resistance</topic><topic>Aquaculture</topic><topic>Babylonia areolata</topic><topic>Chromosomes</topic><topic>Disease</topic><topic>DNA-directed RNA polymerase</topic><topic>Drug resistance</topic><topic>Electron microscopy</topic><topic>Epidemics</topic><topic>Flagella</topic><topic>Gene clusters</topic><topic>Genes</topic><topic>Genomes</topic><topic>Genomic analysis</topic><topic>Infections</topic><topic>Mollusks</topic><topic>Mortality</topic><topic>Mortality causes</topic><topic>Nucleotide sequence</topic><topic>Nucleotides</topic><topic>Open reading frames</topic><topic>Pathogenesis</topic><topic>Pathogenicity</topic><topic>Pathogens</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>Plasmids</topic><topic>Polyculture (aquaculture)</topic><topic>Proteins</topic><topic>rRNA 16S</topic><topic>Salinity</topic><topic>Secretion</topic><topic>Toxicity tests</topic><topic>Transmission electron microscopy</topic><topic>Vibrio tubiashii</topic><topic>Vibriosis</topic><topic>Virulence</topic><topic>Virulence factors</topic><topic>whole genome sequencing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dai, Chen</creatorcontrib><creatorcontrib>Li, Xiaoxin</creatorcontrib><creatorcontrib>Luo, Dapeng</creatorcontrib><creatorcontrib>Liu, Qingming</creatorcontrib><creatorcontrib>Sun, Yun</creatorcontrib><creatorcontrib>Tu, Zhigang</creatorcontrib><creatorcontrib>Shen, Minghui</creatorcontrib><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>ProQuest Central Student</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>SciTech Premium Collection</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Earth, Atmospheric & Aquatic Science Database</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>DOAJ Directory of Open Access Journals</collection><jtitle>Fishes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dai, Chen</au><au>Li, Xiaoxin</au><au>Luo, Dapeng</au><au>Liu, Qingming</au><au>Sun, Yun</au><au>Tu, Zhigang</au><au>Shen, Minghui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>First Report on Genome Analysis and Pathogenicity of Vibrio tubiashii FP17 from Farmed Ivory Shell (Babylonia areolata)</atitle><jtitle>Fishes</jtitle><date>2022-12-01</date><risdate>2022</risdate><volume>7</volume><issue>6</issue><spage>396</spage><pages>396-</pages><issn>2410-3888</issn><eissn>2410-3888</eissn><abstract>Ivory shell (Babylonia areolata) is a commercially important aquaculture species mainly found on the southeast coast of China. However, it has been greatly affected by vibriosis in recent years. In this study, FP17 (a potential pathogen) was isolated from a dying ivory shell with “acute death syndrome” and confirmed as a pathogen via infectious experiment. Furthermore, phylogenetic analysis based on the average nucleotide identity (ANI) sequencing of the 16S rRNA gene and housekeeping genes (ftsz, gapA, gyrB, mreB, pyrH, rpoA, and topA) indicated that FP17 was identical to Vibrio tubiashii. Transmission electron microscopy showed that FP17 is curved and has a short rod shape, with a single flagellum. Besides, the calculated LD50 after the intramuscular injection of FP17 was 2.11 × 106 CFU/g at 14 d. The genome of the FP17 strain consists of two chromosomes and one plasmid with 5,261,336 bp and 45.08% GC content, including 4824 open reading frames (ORFs) and 150 non-coding RNAs (ncRNA). Genome mining revealed that 120 candidate gene clusters, including vibrioferrin and flagellum-related proteins, are responsible for virulence. Comparative genomic analysis showed that vibrioferrin genes, such as pvs and type Ⅵ secretion system protein genes (vas), are specific in V. tubiashii FP17 but not in the ATCC19109 strain. Furthermore, 92 antimicrobial resistance (AMR) genes, such as tufA, tet(35), crp, etc., were mapped within the genome as the potential candidate for virulence, consistent with antibiotic susceptibility assay. This is the first study to describe the complete genome sequence of V. tubiashii infecting ivory shell. The genetic characteristics, virulence factors, and antimicrobial resistance of the V. tubiashii strain FP17 were also explored.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/fishes7060396</doi><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Antibiotics Antimicrobial agents Antimicrobial resistance Aquaculture Babylonia areolata Chromosomes Disease DNA-directed RNA polymerase Drug resistance Electron microscopy Epidemics Flagella Gene clusters Genes Genomes Genomic analysis Infections Mollusks Mortality Mortality causes Nucleotide sequence Nucleotides Open reading frames Pathogenesis Pathogenicity Pathogens Phylogenetics Phylogeny Plasmids Polyculture (aquaculture) Proteins rRNA 16S Salinity Secretion Toxicity tests Transmission electron microscopy Vibrio tubiashii Vibriosis Virulence Virulence factors whole genome sequencing |
title | First Report on Genome Analysis and Pathogenicity of Vibrio tubiashii FP17 from Farmed Ivory Shell (Babylonia areolata) |
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