Evaluation of an Optimal Epidemiological Typing Scheme for Legionella pneumophila with Whole-Genome Sequence Data Using Validation Guidelines
Sequence-based typing (SBT), analogous to multilocus sequence typing (MLST), is the current "gold standard" typing method for investigation of legionellosis outbreaks caused by Legionella pneumophila However, as common sequence types (STs) cause many infections, some investigations remain...
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description | Sequence-based typing (SBT), analogous to multilocus sequence typing (MLST), is the current "gold standard" typing method for investigation of legionellosis outbreaks caused by Legionella pneumophila However, as common sequence types (STs) cause many infections, some investigations remain unresolved. In this study, various whole-genome sequencing (WGS)-based methods were evaluated according to published guidelines, including (i) a single nucleotide polymorphism (SNP)-based method, (ii) extended MLST using different numbers of genes, (iii) determination of gene presence or absence, and (iv) a kmer-based method. L. pneumophila serogroup 1 isolates (n = 106) from the standard "typing panel," previously used by the European Society for Clinical Microbiology Study Group on Legionella Infections (ESGLI), were tested together with another 229 isolates. Over 98% of isolates were considered typeable using the SNP- and kmer-based methods. Percentages of isolates with complete extended MLST profiles ranged from 99.1% (50 genes) to 86.8% (1,455 genes), while only 41.5% produced a full profile with the gene presence/absence scheme. Replicates demonstrated that all methods offer 100% reproducibility. Indices of discrimination range from 0.972 (ribosomal MLST) to 0.999 (SNP based), and all values were higher than that achieved with SBT (0.940). Epidemiological concordance is generally inversely related to discriminatory power. We propose that an extended MLST scheme with ∼50 genes provides optimal epidemiological concordance while substantially improving the discrimination offered by SBT and can be used as part of a hierarchical typing scheme that should maintain backwards compatibility and increase discrimination where necessary. This analysis will be useful for the ESGLI to design a scheme that has the potential to become the new gold standard typing method for L. pneumophila. |
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A.</contributor><creatorcontrib>David, Sophia ; Mentasti, Massimo ; Tewolde, Rediat ; Aslett, Martin ; Harris, Simon R ; Afshar, Baharak ; Underwood, Anthony ; Fry, Norman K ; Parkhill, Julian ; Harrison, Timothy G ; Ledeboer, N. A.</creatorcontrib><description>Sequence-based typing (SBT), analogous to multilocus sequence typing (MLST), is the current "gold standard" typing method for investigation of legionellosis outbreaks caused by Legionella pneumophila However, as common sequence types (STs) cause many infections, some investigations remain unresolved. In this study, various whole-genome sequencing (WGS)-based methods were evaluated according to published guidelines, including (i) a single nucleotide polymorphism (SNP)-based method, (ii) extended MLST using different numbers of genes, (iii) determination of gene presence or absence, and (iv) a kmer-based method. L. pneumophila serogroup 1 isolates (n = 106) from the standard "typing panel," previously used by the European Society for Clinical Microbiology Study Group on Legionella Infections (ESGLI), were tested together with another 229 isolates. Over 98% of isolates were considered typeable using the SNP- and kmer-based methods. Percentages of isolates with complete extended MLST profiles ranged from 99.1% (50 genes) to 86.8% (1,455 genes), while only 41.5% produced a full profile with the gene presence/absence scheme. Replicates demonstrated that all methods offer 100% reproducibility. Indices of discrimination range from 0.972 (ribosomal MLST) to 0.999 (SNP based), and all values were higher than that achieved with SBT (0.940). Epidemiological concordance is generally inversely related to discriminatory power. We propose that an extended MLST scheme with ∼50 genes provides optimal epidemiological concordance while substantially improving the discrimination offered by SBT and can be used as part of a hierarchical typing scheme that should maintain backwards compatibility and increase discrimination where necessary. This analysis will be useful for the ESGLI to design a scheme that has the potential to become the new gold standard typing method for L. pneumophila.</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>DOI: 10.1128/JCM.00432-16</identifier><identifier>PMID: 27280420</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Bacteriology ; Genome, Bacterial ; Humans ; Legionella pneumophila ; Legionella pneumophila - classification ; Legionella pneumophila - genetics ; Molecular Epidemiology - methods ; Molecular Typing - methods ; Reproducibility of Results ; Sensitivity and Specificity ; Sequence Analysis, DNA</subject><ispartof>Journal of clinical microbiology, 2016-08, Vol.54 (8), p.2135-2148</ispartof><rights>Copyright © 2016 David et al.</rights><rights>Copyright © 2016 David et al. 2016 David et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-eea2748d65bfb6658925e5adeeea7d1cba68eb53a54cf2c5b51bfe1674cb03773</citedby><cites>FETCH-LOGICAL-c417t-eea2748d65bfb6658925e5adeeea7d1cba68eb53a54cf2c5b51bfe1674cb03773</cites><orcidid>0000-0003-4862-6507 ; 0000-0002-7069-5958</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963484/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963484/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,886,3189,27926,27927,53793,53795</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27280420$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Ledeboer, N. A.</contributor><creatorcontrib>David, Sophia</creatorcontrib><creatorcontrib>Mentasti, Massimo</creatorcontrib><creatorcontrib>Tewolde, Rediat</creatorcontrib><creatorcontrib>Aslett, Martin</creatorcontrib><creatorcontrib>Harris, Simon R</creatorcontrib><creatorcontrib>Afshar, Baharak</creatorcontrib><creatorcontrib>Underwood, Anthony</creatorcontrib><creatorcontrib>Fry, Norman K</creatorcontrib><creatorcontrib>Parkhill, Julian</creatorcontrib><creatorcontrib>Harrison, Timothy G</creatorcontrib><title>Evaluation of an Optimal Epidemiological Typing Scheme for Legionella pneumophila with Whole-Genome Sequence Data Using Validation Guidelines</title><title>Journal of clinical microbiology</title><addtitle>J Clin Microbiol</addtitle><description>Sequence-based typing (SBT), analogous to multilocus sequence typing (MLST), is the current "gold standard" typing method for investigation of legionellosis outbreaks caused by Legionella pneumophila However, as common sequence types (STs) cause many infections, some investigations remain unresolved. In this study, various whole-genome sequencing (WGS)-based methods were evaluated according to published guidelines, including (i) a single nucleotide polymorphism (SNP)-based method, (ii) extended MLST using different numbers of genes, (iii) determination of gene presence or absence, and (iv) a kmer-based method. L. pneumophila serogroup 1 isolates (n = 106) from the standard "typing panel," previously used by the European Society for Clinical Microbiology Study Group on Legionella Infections (ESGLI), were tested together with another 229 isolates. Over 98% of isolates were considered typeable using the SNP- and kmer-based methods. Percentages of isolates with complete extended MLST profiles ranged from 99.1% (50 genes) to 86.8% (1,455 genes), while only 41.5% produced a full profile with the gene presence/absence scheme. Replicates demonstrated that all methods offer 100% reproducibility. Indices of discrimination range from 0.972 (ribosomal MLST) to 0.999 (SNP based), and all values were higher than that achieved with SBT (0.940). Epidemiological concordance is generally inversely related to discriminatory power. We propose that an extended MLST scheme with ∼50 genes provides optimal epidemiological concordance while substantially improving the discrimination offered by SBT and can be used as part of a hierarchical typing scheme that should maintain backwards compatibility and increase discrimination where necessary. This analysis will be useful for the ESGLI to design a scheme that has the potential to become the new gold standard typing method for L. pneumophila.</description><subject>Bacteriology</subject><subject>Genome, Bacterial</subject><subject>Humans</subject><subject>Legionella pneumophila</subject><subject>Legionella pneumophila - classification</subject><subject>Legionella pneumophila - genetics</subject><subject>Molecular Epidemiology - methods</subject><subject>Molecular Typing - methods</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Sequence Analysis, DNA</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9v1DAQxS0Eokvhxhn5yIEU2_Gf5IKElmUBLeqhLXCzHGeyMXLsNE6K-iH4znjZUsGNk23Nz2_mzUPoOSVnlLLq9af15zNCeMkKKh-gFSV1VUhJvj1EK0JqUVBaqhP0JKXvhFDOhXiMTphiFeGMrNDPzY3xi5ldDDh22AR8Ps5uMB5vRtfC4KKPe2fz-_J2dGGPL2wPA-AuTngH-_wNvDd4DLAMcexdvv9wc4-_9tFDsYUQM3wB1wsEC_idmQ2-SgedL8a79th3u-RO3gVIT9GjzvgEz-7OU3T1fnO5_lDszrcf1293heVUzQWAYYpXrRRN10gpqpoJEKaFXFAttY2RFTSiNILbjlnRCNp0QKXitiGlUuUpenPUHZdmgNZCmCfj9Thl59OtjsbpfyvB9XofbzSvZckrngVe3glMMXtLsx5csodVBIhL0rSiNeWKc_YfKFFMSUnrjL46onaKKU3Q3U9EiT6ErXPY-nfYmsqMv_jbxT38J93yFywhqOc</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>David, Sophia</creator><creator>Mentasti, Massimo</creator><creator>Tewolde, Rediat</creator><creator>Aslett, Martin</creator><creator>Harris, Simon R</creator><creator>Afshar, Baharak</creator><creator>Underwood, Anthony</creator><creator>Fry, Norman K</creator><creator>Parkhill, Julian</creator><creator>Harrison, Timothy G</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>7X8</scope><scope>7QL</scope><scope>7TM</scope><scope>C1K</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4862-6507</orcidid><orcidid>https://orcid.org/0000-0002-7069-5958</orcidid></search><sort><creationdate>20160801</creationdate><title>Evaluation of an Optimal Epidemiological Typing Scheme for Legionella pneumophila with Whole-Genome Sequence Data Using Validation Guidelines</title><author>David, Sophia ; Mentasti, Massimo ; Tewolde, Rediat ; Aslett, Martin ; Harris, Simon R ; Afshar, Baharak ; Underwood, Anthony ; Fry, Norman K ; Parkhill, Julian ; Harrison, Timothy G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-eea2748d65bfb6658925e5adeeea7d1cba68eb53a54cf2c5b51bfe1674cb03773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Bacteriology</topic><topic>Genome, Bacterial</topic><topic>Humans</topic><topic>Legionella pneumophila</topic><topic>Legionella pneumophila - classification</topic><topic>Legionella pneumophila - genetics</topic><topic>Molecular Epidemiology - methods</topic><topic>Molecular Typing - methods</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Sequence Analysis, DNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>David, Sophia</creatorcontrib><creatorcontrib>Mentasti, Massimo</creatorcontrib><creatorcontrib>Tewolde, Rediat</creatorcontrib><creatorcontrib>Aslett, Martin</creatorcontrib><creatorcontrib>Harris, Simon R</creatorcontrib><creatorcontrib>Afshar, Baharak</creatorcontrib><creatorcontrib>Underwood, Anthony</creatorcontrib><creatorcontrib>Fry, Norman K</creatorcontrib><creatorcontrib>Parkhill, Julian</creatorcontrib><creatorcontrib>Harrison, Timothy G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>David, Sophia</au><au>Mentasti, Massimo</au><au>Tewolde, Rediat</au><au>Aslett, Martin</au><au>Harris, Simon R</au><au>Afshar, Baharak</au><au>Underwood, Anthony</au><au>Fry, Norman K</au><au>Parkhill, Julian</au><au>Harrison, Timothy G</au><au>Ledeboer, N. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of an Optimal Epidemiological Typing Scheme for Legionella pneumophila with Whole-Genome Sequence Data Using Validation Guidelines</atitle><jtitle>Journal of clinical microbiology</jtitle><addtitle>J Clin Microbiol</addtitle><date>2016-08-01</date><risdate>2016</risdate><volume>54</volume><issue>8</issue><spage>2135</spage><epage>2148</epage><pages>2135-2148</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><abstract>Sequence-based typing (SBT), analogous to multilocus sequence typing (MLST), is the current "gold standard" typing method for investigation of legionellosis outbreaks caused by Legionella pneumophila However, as common sequence types (STs) cause many infections, some investigations remain unresolved. 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Indices of discrimination range from 0.972 (ribosomal MLST) to 0.999 (SNP based), and all values were higher than that achieved with SBT (0.940). Epidemiological concordance is generally inversely related to discriminatory power. We propose that an extended MLST scheme with ∼50 genes provides optimal epidemiological concordance while substantially improving the discrimination offered by SBT and can be used as part of a hierarchical typing scheme that should maintain backwards compatibility and increase discrimination where necessary. This analysis will be useful for the ESGLI to design a scheme that has the potential to become the new gold standard typing method for L. pneumophila.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>27280420</pmid><doi>10.1128/JCM.00432-16</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-4862-6507</orcidid><orcidid>https://orcid.org/0000-0002-7069-5958</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bacteriology Genome, Bacterial Humans Legionella pneumophila Legionella pneumophila - classification Legionella pneumophila - genetics Molecular Epidemiology - methods Molecular Typing - methods Reproducibility of Results Sensitivity and Specificity Sequence Analysis, DNA |
title | Evaluation of an Optimal Epidemiological Typing Scheme for Legionella pneumophila with Whole-Genome Sequence Data Using Validation Guidelines |
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