Journal article 618 views
A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter
Guillaume Méric,
Koji Yahara,
Leonardos Mageiros,
Ben Pascoe ,
Martin C. J Maiden,
Keith A Jolley,
Samuel K Sheppard
PLoS ONE, Volume: 9, Issue: 3, Start page: e92798
Swansea University Author: Ben Pascoe
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DOI (Published version): 10.1371/journal.pone.0092798
Abstract
The increasing availability of hundreds of whole bacterial genomes provides opportunities for enhanced understanding of the genes and alleles responsible for clinically important phenotypes and how they evolved. However, it is a significant challenge to develop easy-to-use and scalable methods for c...
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2014
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http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0092798 |
URI: | https://cronfa.swan.ac.uk/Record/cronfa16973 |
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<?xml version="1.0"?><rfc1807><datestamp>2014-03-28T00:56:08.3033927</datestamp><bib-version>v2</bib-version><id>16973</id><entry>2014-01-20</entry><title>A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter</title><swanseaauthors><author><sid>4660c0eb7e6bfd796cd749ae713ea558</sid><ORCID>0000-0001-6376-5121</ORCID><firstname>Ben</firstname><surname>Pascoe</surname><name>Ben Pascoe</name><active>true</active><ethesisStudent>false</ethesisStudent></author></swanseaauthors><date>2014-01-20</date><deptcode>PMSC</deptcode><abstract>The increasing availability of hundreds of whole bacterial genomes provides opportunities for enhanced understanding of the genes and alleles responsible for clinically important phenotypes and how they evolved. However, it is a significant challenge to develop easy-to-use and scalable methods for characterizing these large and complex data and relating it to disease epidemiology. Existing approaches typically focus on either homologous sequence variation in genes that are shared by all isolates, or non-homologous sequence variation - focusing on genes that are differentially present in the population. Here we present a comparative genomics approach that simultaneously approximates core and accessory genome variation in pathogen populations and apply it to pathogenic species in the genus Campylobacter. A total of 7 published Campylobacter jejuni and Campylobacter coli genomes were selected to represent diversity across these species, and a list of all loci that were present at least once was compiled. After filtering duplicates a 7-isolate reference pan-genome, of 3,933 loci, was defined. A core genome of 1,035 genes was ubiquitous in the sample accounting for 59% of the genes in each isolate (average genome size of 1.68 Mb). The accessory genome contained 2,792 genes. A Campylobacter population sample of 192 genomes was screened for the presence of reference pan-genome loci with gene presence defined as a BLAST match of ≥70% identity over ≥50% of the locus length - aligned using MUSCLE on a gene-by-gene basis. A total of 21 genes were present only in C. coli and 27 only in C. jejuni, providing information about functional differences associated with species and novel epidemiological markers for population genomic analyses. Homologs of these genes were found in several of the genomes used to define the pan-genome and, therefore, would not have been identified using a single reference strain approach.</abstract><type>Journal Article</type><journal>PLoS ONE</journal><volume>9</volume><journalNumber>3</journalNumber><paginationStart>e92798</paginationStart><publisher/><keywords>Campylobacter; coli; genomes; epidemiology; pathogenic bacteria</keywords><publishedDay>31</publishedDay><publishedMonth>12</publishedMonth><publishedYear>2014</publishedYear><publishedDate>2014-12-31</publishedDate><doi>10.1371/journal.pone.0092798</doi><url>http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0092798</url><notes/><college>COLLEGE NANME</college><department>Medicine</department><CollegeCode>COLLEGE CODE</CollegeCode><DepartmentCode>PMSC</DepartmentCode><institution>Swansea University</institution><apcterm/><lastEdited>2014-03-28T00:56:08.3033927</lastEdited><Created>2014-01-20T15:34:09.2718275</Created><path><level id="1">Faculty of Medicine, Health and Life Sciences</level><level id="2">Swansea University Medical School - Medicine</level></path><authors><author><firstname>Guillaume</firstname><surname>Méric</surname><order>1</order></author><author><firstname>Koji</firstname><surname>Yahara</surname><order>2</order></author><author><firstname>Leonardos</firstname><surname>Mageiros</surname><order>3</order></author><author><firstname>Ben</firstname><surname>Pascoe</surname><orcid>0000-0001-6376-5121</orcid><order>4</order></author><author><firstname>Martin C. J</firstname><surname>Maiden</surname><order>5</order></author><author><firstname>Keith A</firstname><surname>Jolley</surname><order>6</order></author><author><firstname>Samuel K</firstname><surname>Sheppard</surname><order>7</order></author></authors><documents/><OutputDurs/></rfc1807> |
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2014-03-28T00:56:08.3033927 v2 16973 2014-01-20 A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter 4660c0eb7e6bfd796cd749ae713ea558 0000-0001-6376-5121 Ben Pascoe Ben Pascoe true false 2014-01-20 PMSC The increasing availability of hundreds of whole bacterial genomes provides opportunities for enhanced understanding of the genes and alleles responsible for clinically important phenotypes and how they evolved. However, it is a significant challenge to develop easy-to-use and scalable methods for characterizing these large and complex data and relating it to disease epidemiology. Existing approaches typically focus on either homologous sequence variation in genes that are shared by all isolates, or non-homologous sequence variation - focusing on genes that are differentially present in the population. Here we present a comparative genomics approach that simultaneously approximates core and accessory genome variation in pathogen populations and apply it to pathogenic species in the genus Campylobacter. A total of 7 published Campylobacter jejuni and Campylobacter coli genomes were selected to represent diversity across these species, and a list of all loci that were present at least once was compiled. After filtering duplicates a 7-isolate reference pan-genome, of 3,933 loci, was defined. A core genome of 1,035 genes was ubiquitous in the sample accounting for 59% of the genes in each isolate (average genome size of 1.68 Mb). The accessory genome contained 2,792 genes. A Campylobacter population sample of 192 genomes was screened for the presence of reference pan-genome loci with gene presence defined as a BLAST match of ≥70% identity over ≥50% of the locus length - aligned using MUSCLE on a gene-by-gene basis. A total of 21 genes were present only in C. coli and 27 only in C. jejuni, providing information about functional differences associated with species and novel epidemiological markers for population genomic analyses. Homologs of these genes were found in several of the genomes used to define the pan-genome and, therefore, would not have been identified using a single reference strain approach. Journal Article PLoS ONE 9 3 e92798 Campylobacter; coli; genomes; epidemiology; pathogenic bacteria 31 12 2014 2014-12-31 10.1371/journal.pone.0092798 http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0092798 COLLEGE NANME Medicine COLLEGE CODE PMSC Swansea University 2014-03-28T00:56:08.3033927 2014-01-20T15:34:09.2718275 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Medicine Guillaume Méric 1 Koji Yahara 2 Leonardos Mageiros 3 Ben Pascoe 0000-0001-6376-5121 4 Martin C. J Maiden 5 Keith A Jolley 6 Samuel K Sheppard 7 |
title |
A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter |
spellingShingle |
A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter Ben Pascoe |
title_short |
A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter |
title_full |
A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter |
title_fullStr |
A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter |
title_full_unstemmed |
A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter |
title_sort |
A Reference Pan-Genome Approach to Comparative Bacterial Genomics: Identification of Novel Epidemiological Markers in Pathogenic Campylobacter |
author_id_str_mv |
4660c0eb7e6bfd796cd749ae713ea558 |
author_id_fullname_str_mv |
4660c0eb7e6bfd796cd749ae713ea558_***_Ben Pascoe |
author |
Ben Pascoe |
author2 |
Guillaume Méric Koji Yahara Leonardos Mageiros Ben Pascoe Martin C. J Maiden Keith A Jolley Samuel K Sheppard |
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2014 |
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Swansea University |
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10.1371/journal.pone.0092798 |
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Faculty of Medicine, Health and Life Sciences |
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url |
http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0092798 |
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description |
The increasing availability of hundreds of whole bacterial genomes provides opportunities for enhanced understanding of the genes and alleles responsible for clinically important phenotypes and how they evolved. However, it is a significant challenge to develop easy-to-use and scalable methods for characterizing these large and complex data and relating it to disease epidemiology. Existing approaches typically focus on either homologous sequence variation in genes that are shared by all isolates, or non-homologous sequence variation - focusing on genes that are differentially present in the population. Here we present a comparative genomics approach that simultaneously approximates core and accessory genome variation in pathogen populations and apply it to pathogenic species in the genus Campylobacter. A total of 7 published Campylobacter jejuni and Campylobacter coli genomes were selected to represent diversity across these species, and a list of all loci that were present at least once was compiled. After filtering duplicates a 7-isolate reference pan-genome, of 3,933 loci, was defined. A core genome of 1,035 genes was ubiquitous in the sample accounting for 59% of the genes in each isolate (average genome size of 1.68 Mb). The accessory genome contained 2,792 genes. A Campylobacter population sample of 192 genomes was screened for the presence of reference pan-genome loci with gene presence defined as a BLAST match of ≥70% identity over ≥50% of the locus length - aligned using MUSCLE on a gene-by-gene basis. A total of 21 genes were present only in C. coli and 27 only in C. jejuni, providing information about functional differences associated with species and novel epidemiological markers for population genomic analyses. Homologs of these genes were found in several of the genomes used to define the pan-genome and, therefore, would not have been identified using a single reference strain approach. |
published_date |
2014-12-31T03:19:29Z |
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11.036553 |