Comprehensive genome analysis and comparisons of the swine pathogen, Chlamydia suis reveals unique ORFs and candidate host-specificity factors
ABSTRACT Chlamydia suis, a ubiquitous swine pathogen, has the potential for zoonotic transmission to humans and often encodes for resistance to the primary treatment antibiotic, tetracycline. Because of this emerging threat, comparative genomics for swine isolate R19 with inter- and intra-species ge...
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description | ABSTRACT
Chlamydia suis, a ubiquitous swine pathogen, has the potential for zoonotic transmission to humans and often encodes for resistance to the primary treatment antibiotic, tetracycline. Because of this emerging threat, comparative genomics for swine isolate R19 with inter- and intra-species genomes was performed. A 1.094 Mb genome was determined through de novo assembly of Illumina high throughput sequencing reads. Annotation and subsystem analyses were conducted, revealing 986 putative genes (Chls_###) that are predominantly orthologs to other known Chlamydia genes. Subsequent comparative genomics revealed a high level of genomic synteny and overall sequence identity with other Chlamydia while 92 unique C. suis open reading frames were annotated. Direct comparison of Chlamydia-specific gene families that included the plasticity zone, inclusion membrane proteins, polymorphic membrane proteins and the major outer membrane protein, demonstrated high gene content identity with C. trachomatis and C. muridarum. These comparisons also identified diverse components that potentially could contribute to host-specificity. This study constitutes the first genome-wide comparative analysis for C. suis, generating a fully annotated reference genome. These studies will enable focused efforts on factors that provide key species specificity and adaptation to cognate hosts that are attributed to chlamydial infections, including humans.
Pathogenomic comparison of fully sequenced and annotated Chlamydia suis revealed unique genetic elements that could encode virulence factors and proteins that contribute to host-specificity. |
doi_str_mv | 10.1093/femspd/ftaa035 |
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Chlamydia suis, a ubiquitous swine pathogen, has the potential for zoonotic transmission to humans and often encodes for resistance to the primary treatment antibiotic, tetracycline. Because of this emerging threat, comparative genomics for swine isolate R19 with inter- and intra-species genomes was performed. A 1.094 Mb genome was determined through de novo assembly of Illumina high throughput sequencing reads. Annotation and subsystem analyses were conducted, revealing 986 putative genes (Chls_###) that are predominantly orthologs to other known Chlamydia genes. Subsequent comparative genomics revealed a high level of genomic synteny and overall sequence identity with other Chlamydia while 92 unique C. suis open reading frames were annotated. Direct comparison of Chlamydia-specific gene families that included the plasticity zone, inclusion membrane proteins, polymorphic membrane proteins and the major outer membrane protein, demonstrated high gene content identity with C. trachomatis and C. muridarum. These comparisons also identified diverse components that potentially could contribute to host-specificity. This study constitutes the first genome-wide comparative analysis for C. suis, generating a fully annotated reference genome. These studies will enable focused efforts on factors that provide key species specificity and adaptation to cognate hosts that are attributed to chlamydial infections, including humans.
Pathogenomic comparison of fully sequenced and annotated Chlamydia suis revealed unique genetic elements that could encode virulence factors and proteins that contribute to host-specificity.</description><identifier>ISSN: 2049-632X</identifier><identifier>EISSN: 2049-632X</identifier><identifier>DOI: 10.1093/femspd/ftaa035</identifier><identifier>PMID: 32639528</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Annotations ; Antibiotics ; Care and treatment ; Chlamydia ; Chlamydia infections ; Chlamydia suis ; Comparative analysis ; Development and progression ; Diseases ; Gene families ; Genes ; Genetic aspects ; Genome-wide association studies ; Genomes ; Genomics ; Health aspects ; Host specificity ; Host-parasite relationships ; Major outer membrane protein ; Membrane proteins ; Membranes ; Methods ; Next-generation sequencing ; Open reading frames ; Pathogens ; Proteins ; Sexually transmitted diseases ; STD ; Subsystems ; Swine ; Synteny</subject><ispartof>Pathogens and Disease, 2021-03, Vol.79 (2), p.1</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of FEMS. 2021</rights><rights>The Author(s) 2020. Published by Oxford University Press on behalf of FEMS.</rights><rights>COPYRIGHT 2021 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c519t-f3e7d8478559e603a05db0ec25fb33a329431e1ba3573b4a1a26abb3eefda6ec3</citedby><cites>FETCH-LOGICAL-c519t-f3e7d8478559e603a05db0ec25fb33a329431e1ba3573b4a1a26abb3eefda6ec3</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/PMC7948067/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7948067/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,1598,27901,27902,53766,53768</link.rule.ids><linktorsrc>$$Uhttps://dx.doi.org/10.1093/femspd/ftaa035$$EView_record_in_Oxford_University_Press$$FView_record_in_$$GOxford_University_Press</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32639528$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dimond, Zoe E</creatorcontrib><creatorcontrib>Hefty, P Scott</creatorcontrib><title>Comprehensive genome analysis and comparisons of the swine pathogen, Chlamydia suis reveals unique ORFs and candidate host-specificity factors</title><title>Pathogens and Disease</title><addtitle>Pathog Dis</addtitle><description>ABSTRACT
Chlamydia suis, a ubiquitous swine pathogen, has the potential for zoonotic transmission to humans and often encodes for resistance to the primary treatment antibiotic, tetracycline. Because of this emerging threat, comparative genomics for swine isolate R19 with inter- and intra-species genomes was performed. A 1.094 Mb genome was determined through de novo assembly of Illumina high throughput sequencing reads. Annotation and subsystem analyses were conducted, revealing 986 putative genes (Chls_###) that are predominantly orthologs to other known Chlamydia genes. Subsequent comparative genomics revealed a high level of genomic synteny and overall sequence identity with other Chlamydia while 92 unique C. suis open reading frames were annotated. Direct comparison of Chlamydia-specific gene families that included the plasticity zone, inclusion membrane proteins, polymorphic membrane proteins and the major outer membrane protein, demonstrated high gene content identity with C. trachomatis and C. muridarum. These comparisons also identified diverse components that potentially could contribute to host-specificity. This study constitutes the first genome-wide comparative analysis for C. suis, generating a fully annotated reference genome. These studies will enable focused efforts on factors that provide key species specificity and adaptation to cognate hosts that are attributed to chlamydial infections, including humans.
Pathogenomic comparison of fully sequenced and annotated Chlamydia suis revealed unique genetic elements that could encode virulence factors and proteins that contribute to host-specificity.</description><subject>Annotations</subject><subject>Antibiotics</subject><subject>Care and treatment</subject><subject>Chlamydia</subject><subject>Chlamydia infections</subject><subject>Chlamydia suis</subject><subject>Comparative analysis</subject><subject>Development and progression</subject><subject>Diseases</subject><subject>Gene families</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genome-wide association studies</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>Host specificity</subject><subject>Host-parasite relationships</subject><subject>Major outer membrane protein</subject><subject>Membrane proteins</subject><subject>Membranes</subject><subject>Methods</subject><subject>Next-generation sequencing</subject><subject>Open reading frames</subject><subject>Pathogens</subject><subject>Proteins</subject><subject>Sexually transmitted diseases</subject><subject>STD</subject><subject>Subsystems</subject><subject>Swine</subject><subject>Synteny</subject><issn>2049-632X</issn><issn>2049-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqFkt1r1TAYxosobszdeikBbxTslo-mbW6EcXAqDAai4F14m745zWiTmrRHzj_h32zkHOf0xgSSl-T3PPngKYrnjF4wqsSlxSnN_aVdAKiQj4pTTitV1oJ_ffygPinOU7qjubWStU39tDgRvBZK8va0-LEJ0xxxQJ_cDskWfZiQgIdxn1zKRU9MJiC6FHwiwZJlQJK-O49khmUIWfGGbIYRpn3vgKQ1qyLuEMZEVu--rUhuP10fnfLgeliQDCEtZZrROOuMW_bEgllCTM-KJzYr8fw4nxVfrt993nwob27ff9xc3ZRGMrWUVmDTt1XTSqmwpgKo7DuKhkvbCQGCq0owZB0I2YiuAga8hq4TiLaHGo04K94efOe1m7A36JcIo56jmyDudQCn_97xbtDbsNONqlpaN9ng1dEghvzGtOjJJYPjCB7DmjSvOKtqxrnK6Mt_0LuwxvzDmZJMsIaJWmbq4kBtYUTtvA35XJN7j5MzwaN1ef2qVrRpOFXqj8DEkFJEe397RvWveOhDPPQxHlnw4uGb7_HfYcjA6wMQ1vl_Zj8Bac_Knw</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Dimond, Zoe E</creator><creator>Hefty, P Scott</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><scope>3V.</scope><scope>7T7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20210301</creationdate><title>Comprehensive genome analysis and comparisons of the swine pathogen, Chlamydia suis reveals unique ORFs and candidate host-specificity factors</title><author>Dimond, Zoe E ; Hefty, P Scott</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c519t-f3e7d8478559e603a05db0ec25fb33a329431e1ba3573b4a1a26abb3eefda6ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Annotations</topic><topic>Antibiotics</topic><topic>Care and treatment</topic><topic>Chlamydia</topic><topic>Chlamydia infections</topic><topic>Chlamydia suis</topic><topic>Comparative analysis</topic><topic>Development and progression</topic><topic>Diseases</topic><topic>Gene families</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genome-wide association studies</topic><topic>Genomes</topic><topic>Genomics</topic><topic>Health aspects</topic><topic>Host specificity</topic><topic>Host-parasite relationships</topic><topic>Major outer membrane protein</topic><topic>Membrane proteins</topic><topic>Membranes</topic><topic>Methods</topic><topic>Next-generation sequencing</topic><topic>Open reading frames</topic><topic>Pathogens</topic><topic>Proteins</topic><topic>Sexually transmitted diseases</topic><topic>STD</topic><topic>Subsystems</topic><topic>Swine</topic><topic>Synteny</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dimond, Zoe E</creatorcontrib><creatorcontrib>Hefty, P Scott</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>ProQuest Central (Corporate)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pathogens and Disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Dimond, Zoe E</au><au>Hefty, P Scott</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comprehensive genome analysis and comparisons of the swine pathogen, Chlamydia suis reveals unique ORFs and candidate host-specificity factors</atitle><jtitle>Pathogens and Disease</jtitle><addtitle>Pathog Dis</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>79</volume><issue>2</issue><spage>1</spage><pages>1-</pages><issn>2049-632X</issn><eissn>2049-632X</eissn><abstract>ABSTRACT
Chlamydia suis, a ubiquitous swine pathogen, has the potential for zoonotic transmission to humans and often encodes for resistance to the primary treatment antibiotic, tetracycline. Because of this emerging threat, comparative genomics for swine isolate R19 with inter- and intra-species genomes was performed. A 1.094 Mb genome was determined through de novo assembly of Illumina high throughput sequencing reads. Annotation and subsystem analyses were conducted, revealing 986 putative genes (Chls_###) that are predominantly orthologs to other known Chlamydia genes. Subsequent comparative genomics revealed a high level of genomic synteny and overall sequence identity with other Chlamydia while 92 unique C. suis open reading frames were annotated. Direct comparison of Chlamydia-specific gene families that included the plasticity zone, inclusion membrane proteins, polymorphic membrane proteins and the major outer membrane protein, demonstrated high gene content identity with C. trachomatis and C. muridarum. These comparisons also identified diverse components that potentially could contribute to host-specificity. This study constitutes the first genome-wide comparative analysis for C. suis, generating a fully annotated reference genome. These studies will enable focused efforts on factors that provide key species specificity and adaptation to cognate hosts that are attributed to chlamydial infections, including humans.
Pathogenomic comparison of fully sequenced and annotated Chlamydia suis revealed unique genetic elements that could encode virulence factors and proteins that contribute to host-specificity.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>32639528</pmid><doi>10.1093/femspd/ftaa035</doi><oa>free_for_read</oa></addata></record> |
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subjects | Annotations Antibiotics Care and treatment Chlamydia Chlamydia infections Chlamydia suis Comparative analysis Development and progression Diseases Gene families Genes Genetic aspects Genome-wide association studies Genomes Genomics Health aspects Host specificity Host-parasite relationships Major outer membrane protein Membrane proteins Membranes Methods Next-generation sequencing Open reading frames Pathogens Proteins Sexually transmitted diseases STD Subsystems Swine Synteny |
title | Comprehensive genome analysis and comparisons of the swine pathogen, Chlamydia suis reveals unique ORFs and candidate host-specificity factors |
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