VPsero: Rapid Serotyping of Vibrio parahaemolyticus Using Serogroup-Specific Genes Based on Whole-Genome Sequencing Data

Vibrio parahaemolyticus has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products constitute a major nutritional source. It is a growing cause of diseases including gastroenteritis, wound infections, and septicemia. Serotyping a...

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Published inFrontiers in microbiology Vol. 12; p. 620224
Main Authors Bian, Shengzhe, Jia, Yangyang, Zhan, Qiuyao, Wong, Nai-Kei, Hu, Qinghua, Zhang, Wenwei, Zhang, Yongwei, Li, Liqiang
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 02.09.2021
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Abstract Vibrio parahaemolyticus has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products constitute a major nutritional source. It is a growing cause of diseases including gastroenteritis, wound infections, and septicemia. Serotyping assays use commercially available antisera to identify V. parahaemolyticus strains, but this approach is limited by high costs, complicated procedures, cross-immunoreactivity, and often subjective interpretation. By leveraging high-throughput sequencing technologies, we developed an in silico method based on comparison of gene clusters for lipopolysaccharide (LPSgc) and capsular polysaccharide (CPSgc) by firstly using the unique-gene strategy. The algorithm, VPsero, which exploits serogroup-specific genes as markers, covers 43 K and all 12 O serogroups in serotyping assays. VPsero is capable of predicting serotypes from assembled draft genomes, outputting LPSgc/CPSgc sequences, and recognizing possible novel serogroups or populations. Our tool displays high specificity and sensitivity in prediction toward V. parahaemolyticus strains, with an average sensitivity in serogroup prediction of 0.910 for O and 0.961 for K serogroups and a corresponding average specificity of 0.990 for O and 0.998 for K serogroups.
AbstractList has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products constitute a major nutritional source. It is a growing cause of diseases including gastroenteritis, wound infections, and septicemia. Serotyping assays use commercially available antisera to identify strains, but this approach is limited by high costs, complicated procedures, cross-immunoreactivity, and often subjective interpretation. By leveraging high-throughput sequencing technologies, we developed an method based on comparison of gene clusters for lipopolysaccharide (LPSgc) and capsular polysaccharide (CPSgc) by firstly using the unique-gene strategy. The algorithm, VPsero, which exploits serogroup-specific genes as markers, covers 43 K and all 12 O serogroups in serotyping assays. VPsero is capable of predicting serotypes from assembled draft genomes, outputting LPSgc/CPSgc sequences, and recognizing possible novel serogroups or populations. Our tool displays high specificity and sensitivity in prediction toward strains, with an average sensitivity in serogroup prediction of 0.910 for O and 0.961 for K serogroups and a corresponding average specificity of 0.990 for O and 0.998 for K serogroups.
Vibrio parahaemolyticus has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products constitute a major nutritional source. It is a growing cause of diseases including gastroenteritis, wound infections, and septicemia. Serotyping assays use commercially available antisera to identify V. parahaemolyticus strains, but this approach is limited by high costs, complicated procedures, cross-immunoreactivity, and often subjective interpretation. By leveraging high-throughput sequencing technologies, we developed an in silico method based on comparison of gene clusters for lipopolysaccharide (LPSgc) and capsular polysaccharide (CPSgc) by firstly using the unique-gene strategy. The algorithm, VPsero, which exploits serogroup-specific genes as markers, covers 43 K and all 12 O serogroups in serotyping assays. VPsero is capable of predicting serotypes from assembled draft genomes, outputting LPSgc/CPSgc sequences, and recognizing possible novel serogroups or populations. Our tool displays high specificity and sensitivity in prediction toward V. parahaemolyticus strains, with an average sensitivity in serogroup prediction of 0.910 for O and 0.961 for K serogroups and a corresponding average specificity of 0.990 for O and 0.998 for K serogroups.
Vibrio parahaemolyticus has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products constitute a major nutritional source. It is a growing cause of diseases including gastroenteritis, wound infections, and septicemia. Serotyping assays use commercially available antisera to identify V. parahaemolyticus strains, but this approach is limited by high costs, complicated procedures, cross-immunoreactivity, and often subjective interpretation. By leveraging high-throughput sequencing technologies, we developed an in silico method based on comparison of gene clusters for lipopolysaccharide (LPSgc) and capsular polysaccharide (CPSgc) by firstly using the unique-gene strategy. The algorithm, VPsero, which exploits serogroup-specific genes as markers, covers 43 K and all 12 O serogroups in serotyping assays. VPsero is capable of predicting serotypes from assembled draft genomes, outputting LPSgc/CPSgc sequences, and recognizing possible novel serogroups or populations. Our tool displays high specificity and sensitivity in prediction toward V. parahaemolyticus strains, with an average sensitivity in serogroup prediction of 0.910 for O and 0.961 for K serogroups and a corresponding average specificity of 0.990 for O and 0.998 for K serogroups.Vibrio parahaemolyticus has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products constitute a major nutritional source. It is a growing cause of diseases including gastroenteritis, wound infections, and septicemia. Serotyping assays use commercially available antisera to identify V. parahaemolyticus strains, but this approach is limited by high costs, complicated procedures, cross-immunoreactivity, and often subjective interpretation. By leveraging high-throughput sequencing technologies, we developed an in silico method based on comparison of gene clusters for lipopolysaccharide (LPSgc) and capsular polysaccharide (CPSgc) by firstly using the unique-gene strategy. The algorithm, VPsero, which exploits serogroup-specific genes as markers, covers 43 K and all 12 O serogroups in serotyping assays. VPsero is capable of predicting serotypes from assembled draft genomes, outputting LPSgc/CPSgc sequences, and recognizing possible novel serogroups or populations. Our tool displays high specificity and sensitivity in prediction toward V. parahaemolyticus strains, with an average sensitivity in serogroup prediction of 0.910 for O and 0.961 for K serogroups and a corresponding average specificity of 0.990 for O and 0.998 for K serogroups.
Vibrio parahaemolyticus has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products constitute a major nutritional source. It is a growing cause of diseases including gastroenteritis, wound infections, and septicemia. Serotyping assays use commercially available antisera to identify V. parahaemolyticus strains, but this approach is limited by high costs, complicated procedures, cross-immunoreactivity, and often subjective interpretation. By leveraging high-throughput sequencing technologies, we developed an in silico method based on comparison of gene clusters for lipopolysaccharide (LPSgc) and capsular polysaccharide (CPSgc) by firstly using the unique-gene strategy. The algorithm, VPsero, which exploits serogroup-specific genes as markers, covers 43 K and all 12 O serogroups in serotyping assays. VPsero is capable of predicting serotypes from assembled draft genomes, outputting LPSgc/CPSgc sequences, and recognizing possible novel serogroups or populations. Our tool displays high specificity and sensitivity in prediction toward V. parahaemolyticus strains, with an average sensitivity in serogroup prediction of 0.910 for O and 0.961 for K serogroups and a corresponding average specificity of 0.990 for O and 0.998 for K serogroups.
Author Wong, Nai-Kei
Zhan, Qiuyao
Zhang, Wenwei
Jia, Yangyang
Bian, Shengzhe
Li, Liqiang
Zhang, Yongwei
Hu, Qinghua
AuthorAffiliation 7 Shenzhen Center for Disease Control and Prevention , Shenzhen , China
3 School of Public Health (Shenzhen), Sun Yat-sen University , Guangzhou , China
6 Department of Pharmacology, Shantou University Medical College , Shantou , China
2 BGI Education Center, University of Chinese Academy of Sciences , Shenzhen , China
1 BGI-Shenzhen , Shenzhen , China
5 CAS Key Laboratory of Tropical Marine Bio-resources and Ecology, South China Sea Institute of Oceanology, Chinese Academy of Sciences , Guangzhou , China
4 Shenzhen Key Laboratory of Unknown Pathogen Identification , Shenzhen , China
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Cites_doi 10.1038/s41396-019-0461-5
10.1186/1471-2180-10-274
10.1099/mgen.0.000090
10.1128/JCM.00349-16
10.1128/JCM.00197-18
10.1016/j.tim.2018.08.004
10.1371/journal.pone.0147101
10.1128/JCM.00196-12
10.1128/JCM.00008-15
10.1093/femsre/fuw006
10.1016/j.tim.2018.06.006
10.1128/am.23.5.966-971.1972
10.1016/j.ijfoodmicro.2017.01.010
10.1371/journal.pgen.1007862
10.1016/b978-0-12-397169-2.00066-4
10.1038/s41396-020-0628-0
10.1371/journal.pntd.0002210
10.1099/mgen.0.000064
10.1186/s13059-019-1832-y
10.1093/bioinformatics/btu153
10.1128/jb.185.18.5431-5441.2003
10.1099/mgen.0.000339
10.1016/j.ijfoodmicro.2012.08.012
10.1099/mgen.0.000186
10.1128/JCM.00323-15
10.1016/j.ijfoodmicro.2019.108332
10.3389/fmicb.2020.546150
10.4103/sjmms.sjmms_30_17
10.1111/j.1348-0421.2008.00027.x
10.1099/mgen.0.000102
10.7717/peerj.2477
10.3389/fmicb.2021.635539
10.1128/CMR.00024-15
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Keywords genetic cluster
Vibrio parahaemolyticus
lipopolysaccharide (LPS)
capsular polysaccharide (CPS)
serotype
Language English
License Copyright © 2021 Bian, Jia, Zhan, Wong, Hu, Zhang, Zhang and Li.
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This article was submitted to Food Microbiology, a section of the journal Frontiers in Microbiology
Edited by: Antonio Valero, University of Córdoba, Spain
Reviewed by: Christopher John Grim, United States Food and Drug Administration, United States; Jeffrey Wayne Turner, Texas A&M University Corpus Christi, United States
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References Guo (B11) 2017; 245
Wyres (B33) 2020; 6
Bian (B2) 2020; 11
Zhou (B38) 2021
Epping (B7) 2018; 4
Kapatai (B17) 2016; 4
Pang (B23) 2019; 309
Rendueles (B24) 2018; 14
Chen (B4) 2010; 10
Emms (B6) 2019; 20
Shengzhe (B26) 2020
Geno (B9) 2015; 28
Szymanski (B28) 2015
Oliver (B22) 2015
Seemann (B25) 2014; 30
Twedt (B30) 1972; 23
Jones (B16) 2012; 50
van Tonder (B31) 2016; 2
Chen (B3) 2012; 159
de Filippis (B5) 2012
Zhang (B37) 2015; 53
Madden (B18) 2013
Yang (B35) 2019; 13
Thrane (B29) 2016; 54
Siddique (B27) 2021; 12
Wyres (B34) 2016; 2
Balloux (B1) 2018; 26
Holt (B13) 2020; 14
Mistou (B19) 2016; 40
Okura (B21) 2008; 52
Wick (B32) 2018; 56
Gavilan (B8) 2013; 7
Guvener (B12) 2003; 185
Yoshida (B36) 2016; 11
Joensen (B15) 2015; 53
Ghenem (B10) 2017; 5
Ingle (B14) 2016; 2
Mostowy (B20) 2018; 26
References_xml – volume: 13
  start-page: 2578
  year: 2019
  ident: B35
  article-title: Recent mixing of Vibrio parahaemolyticus populations.
  publication-title: ISME J.
  doi: 10.1038/s41396-019-0461-5
– year: 2012
  ident: B5
  publication-title: Molecular Typing in Bacterial Infections.
– volume: 10
  year: 2010
  ident: B4
  article-title: Genetic analysis of the capsule polysaccharide (K antigen) and exopolysaccharide genes in pandemic Vibrio parahaemolyticus O3:K6.
  publication-title: BMC Microbiol.
  doi: 10.1186/1471-2180-10-274
– volume: 2
  year: 2016
  ident: B31
  article-title: Putatively novel serotypes and the potential for reduced vaccine effectiveness: capsular locus diversity revealed among 5405 pneumococcal genomes.
  publication-title: Microb. Genom.
  doi: 10.1099/mgen.0.000090
– volume: 54
  start-page: 1782
  year: 2016
  ident: B29
  article-title: Application of whole-genome sequencing data for o-specific antigen analysis and in silico serotyping of Pseudomonas aeruginosa isolates.
  publication-title: J. Clin. Microbiol.
  doi: 10.1128/JCM.00349-16
– volume: 56
  year: 2018
  ident: B32
  article-title: Kaptive web: user-friendly capsule and lipopolysaccharide serotype prediction for Klebsiella genomes.
  publication-title: J. Clin. Microbiol.
  doi: 10.1128/JCM.00197-18
– volume: 26
  start-page: 1035
  year: 2018
  ident: B1
  article-title: From theory to practice: translating whole-genome sequencing (WGS) into the Clinic.
  publication-title: Trends Microbiol.
  doi: 10.1016/j.tim.2018.08.004
– start-page: 527
  year: 2015
  ident: B28
  article-title: Bacterial and Viral Infections
  publication-title: Essentials of Glycobiology
– volume: 11
  year: 2016
  ident: B36
  article-title: The Salmonella in silico typing resource (SISTR): an open web-accessible tool for rapidly typing and subtyping draft Salmonella genome assemblies.
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0147101
– volume: 50
  start-page: 2343
  year: 2012
  ident: B16
  article-title: Biochemical, serological, and virulence characterization of clinical and oyster Vibrio parahaemolyticus isolates.
  publication-title: J. Clin. Microbiol.
  doi: 10.1128/JCM.00196-12
– volume: 53
  start-page: 2410
  year: 2015
  ident: B15
  article-title: Rapid and easy in silico serotyping of Escherichia coli isolates by use of whole-genome sequencing data.
  publication-title: J. Clin. Microbiol.
  doi: 10.1128/JCM.00008-15
– volume: 40
  start-page: 464
  year: 2016
  ident: B19
  article-title: Bacterial glycobiology: rhamnose-containing cell wall polysaccharides in gram-positive bacteria.
  publication-title: FEMS Microbiol. Rev.
  doi: 10.1093/femsre/fuw006
– volume: 26
  start-page: 1008
  year: 2018
  ident: B20
  article-title: Diversity-generating machines: genetics of bacterial sugar-coating.
  publication-title: Trends Microbiol.
  doi: 10.1016/j.tim.2018.06.006
– volume: 23
  start-page: 966
  year: 1972
  ident: B30
  article-title: Antigenic relationships among strains of Vibrio parahaemolyticus.
  publication-title: Appl. Microbiol.
  doi: 10.1128/am.23.5.966-971.1972
– volume: 245
  start-page: 53
  year: 2017
  ident: B11
  article-title: Genetic and serological identification of three Vibrio parahaemolyticus strains as candidates for novel provisional O serotypes.
  publication-title: Int. J. Food Microbiol.
  doi: 10.1016/j.ijfoodmicro.2017.01.010
– volume: 14
  year: 2018
  ident: B24
  article-title: Genetic exchanges are more frequent in bacteria encoding capsules.
  publication-title: PLoS Genet.
  doi: 10.1371/journal.pgen.1007862
– year: 2013
  ident: B18
  article-title: The BLAST sequence analysis tool
  publication-title: The NCBI Handbook [Internet]
– start-page: 1169
  year: 2015
  ident: B22
  article-title: Vibrio parahaemolyticus and Vibrio vulnificus
  publication-title: Molecular Medical Microbiology
  doi: 10.1016/b978-0-12-397169-2.00066-4
– volume: 14
  start-page: 1713
  year: 2020
  ident: B13
  article-title: Diversity and evolution of surface polysaccharide synthesis loci in Enterobacteriales.
  publication-title: ISME J.
  doi: 10.1038/s41396-020-0628-0
– volume: 7
  year: 2013
  ident: B8
  article-title: Molecular epidemiology and genetic variation of pathogenic Vibrio parahaemolyticus in Peru.
  publication-title: PLoS negl. Trop. Dis.
  doi: 10.1371/journal.pntd.0002210
– volume: 2
  year: 2016
  ident: B14
  article-title: In silico serotyping of E. coli from short read data identifies limited novel O-loci but extensive diversity of O:H serotype combinations within and between pathogenic lineages.
  publication-title: Microb. Genom.
  doi: 10.1099/mgen.0.000064
– year: 2021
  ident: B38
  publication-title: EBEis–in Silico Serotype Prediction for Escherichia coli
– volume: 20
  year: 2019
  ident: B6
  article-title: OrthoFinder: phylogenetic orthology inference for comparative genomics.
  publication-title: Genome Biol.
  doi: 10.1186/s13059-019-1832-y
– volume: 30
  start-page: 2068
  year: 2014
  ident: B25
  article-title: Prokka: rapid prokaryotic genome annotation.
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btu153
– volume: 185
  start-page: 5431
  year: 2003
  ident: B12
  article-title: Multiple regulators control capsular polysaccharide production in Vibrio parahaemolyticus.
  publication-title: J. Bacteriol.
  doi: 10.1128/jb.185.18.5431-5441.2003
– volume: 6
  year: 2020
  ident: B33
  article-title: Identification of Acinetobacter baumannii loci for capsular polysaccharide (KL) and lipooligosaccharide outer core (OCL) synthesis in genome assemblies using curated reference databases compatible with Kaptive.
  publication-title: Microb. Genom.
  doi: 10.1099/mgen.0.000339
– volume: 159
  start-page: 122
  year: 2012
  ident: B3
  article-title: Development of O-serogroup specific PCR assay for detection and identification of Vibrio parahaemolyticus.
  publication-title: Int. J. Food Microbiol.
  doi: 10.1016/j.ijfoodmicro.2012.08.012
– volume: 4
  year: 2018
  ident: B7
  article-title: SeroBA: rapid high-throughput serotyping of Streptococcus pneumoniae from whole genome sequence data.
  publication-title: Microb. Genom.
  doi: 10.1099/mgen.0.000186
– volume: 53
  start-page: 1685
  year: 2015
  ident: B37
  article-title: Salmonella serotype determination utilizing high-throughput genome sequencing data.
  publication-title: J. Clin. Microbiol.
  doi: 10.1128/JCM.00323-15
– volume: 309
  year: 2019
  ident: B23
  article-title: Developing a novel molecular serotyping system based on capsular polysaccharide synthesis gene clusters of Vibrio parahaemolyticus.
  publication-title: Int. J. Food Microbiol.
  doi: 10.1016/j.ijfoodmicro.2019.108332
– year: 2020
  ident: B26
  publication-title: Genetic Structure, Function and Evolution of Capsule Biosynthesis Loci in Vibrio parahaemolyticus
– volume: 11
  year: 2020
  ident: B2
  article-title: Genetic structure, function, and evolution of capsule biosynthesis loci in Vibrio parahaemolyticus.
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2020.546150
– volume: 5
  start-page: 93
  year: 2017
  ident: B10
  article-title: Vibrio Parahaemolyticus: a review on distribution, pathogenesis, virulence determinants and epidemiology.
  publication-title: Saudi J. Med. Med. Sci.
  doi: 10.4103/sjmms.sjmms_30_17
– volume: 52
  start-page: 251
  year: 2008
  ident: B21
  article-title: Genetic analyses of the putative O and K antigen gene clusters of pandemic Vibrio parahaemolyticus.
  publication-title: Microbiol. Immunol.
  doi: 10.1111/j.1348-0421.2008.00027.x
– volume: 2
  year: 2016
  ident: B34
  article-title: Identification of Klebsiella capsule synthesis loci from whole genome data.
  publication-title: Microb. Genom.
  doi: 10.1099/mgen.0.000102
– volume: 4
  year: 2016
  ident: B17
  article-title: Whole genome sequencing of Streptococcus pneumoniae: development, evaluation and verification of targets for serogroup and serotype prediction using an automated pipeline.
  publication-title: PeerJ
  doi: 10.7717/peerj.2477
– volume: 12
  year: 2021
  ident: B27
  article-title: Characterization of pathogenic Vibrio parahaemolyticus isolated from fish aquaculture of the southwest coastal area of Bangladesh.
  publication-title: Front. Microbiol.
  doi: 10.3389/fmicb.2021.635539
– volume: 28
  start-page: 871
  year: 2015
  ident: B9
  article-title: Pneumococcal capsules and their types: past, present, and future.
  publication-title: Clin. Microbiol. Rev.
  doi: 10.1128/CMR.00024-15
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Snippet Vibrio parahaemolyticus has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products...
has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products constitute a major...
Vibrio parahaemolyticus has emerged as a significant enteropathogen in human and marine habitats worldwide, notably in regions where aquaculture products...
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StartPage 620224
SubjectTerms capsular polysaccharide (CPS)
genetic cluster
lipopolysaccharide (LPS)
Microbiology
serotype
Vibrio parahaemolyticus
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Title VPsero: Rapid Serotyping of Vibrio parahaemolyticus Using Serogroup-Specific Genes Based on Whole-Genome Sequencing Data
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