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Article: Potential utility of metagenomic sequencing for improving etiologic diagnosis of infective endocarditis

TitlePotential utility of metagenomic sequencing for improving etiologic diagnosis of infective endocarditis
Authors
KeywordsBartonella quintana
etiologic diagnosis
heart valve
Illumina MiSeq
infective endocarditis
Issue Date2019
PublisherFuture Medicine Ltd. The Journal's web site is located at http://www.futuremedicine.com/loi/fca
Citation
Future Cardiology, 2019, v. 15 n. 6, p. 411-424 How to Cite?
AbstractAim: To explore potential utility of metagenomic sequencing for improving etiologic diagnosis of infective endocarditis (IE) caused by fastidious bacteria. Materials & methods: Plasma and heart valves of two patients, who were diagnosed with IE caused by Bartonella quintana and Propionibacterium species, were sequenced by using Illumina MiSeq and Nanopore MinION. Results: For patient 1, B. quintana was detected in the plasma pool collected 4 days before valvular replacement surgery. For patient 2, Propionibacterium sp. oral taxon 193 was detected in the plasma sample collected on hospital day 1. Nearly complete bacterial genomes (>98%) were retrieved from resected heart valves of both patients, enabling detection of antibiotic resistance-associated features. Real-time sequencing of heart valves identified both pathogens within the first 16 min of sequencing runs. Conclusion: Metagenomic sequencing may be a helpful supplement to IE diagnostic workflow, especially when conventional tests fail to yield a diagnosis.
Persistent Identifierhttp://hdl.handle.net/10722/293164
ISSN
2020 SCImago Journal Rankings: 0.392
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChan, WS-
dc.contributor.authorAu, CH-
dc.contributor.authorLeung, HCM-
dc.contributor.authorHo, DN-
dc.contributor.authorLI, D-
dc.contributor.authorChan, TL-
dc.contributor.authorLam, TW-
dc.contributor.authorMa, ESK-
dc.contributor.authorTang, BSF-
dc.date.accessioned2020-11-23T08:12:44Z-
dc.date.available2020-11-23T08:12:44Z-
dc.date.issued2019-
dc.identifier.citationFuture Cardiology, 2019, v. 15 n. 6, p. 411-424-
dc.identifier.issn1479-6678-
dc.identifier.urihttp://hdl.handle.net/10722/293164-
dc.description.abstractAim: To explore potential utility of metagenomic sequencing for improving etiologic diagnosis of infective endocarditis (IE) caused by fastidious bacteria. Materials & methods: Plasma and heart valves of two patients, who were diagnosed with IE caused by Bartonella quintana and Propionibacterium species, were sequenced by using Illumina MiSeq and Nanopore MinION. Results: For patient 1, B. quintana was detected in the plasma pool collected 4 days before valvular replacement surgery. For patient 2, Propionibacterium sp. oral taxon 193 was detected in the plasma sample collected on hospital day 1. Nearly complete bacterial genomes (>98%) were retrieved from resected heart valves of both patients, enabling detection of antibiotic resistance-associated features. Real-time sequencing of heart valves identified both pathogens within the first 16 min of sequencing runs. Conclusion: Metagenomic sequencing may be a helpful supplement to IE diagnostic workflow, especially when conventional tests fail to yield a diagnosis.-
dc.languageeng-
dc.publisherFuture Medicine Ltd. The Journal's web site is located at http://www.futuremedicine.com/loi/fca-
dc.relation.ispartofFuture Cardiology-
dc.rightsPreprint The article has been submitted for publication to [the specified journal].-
dc.subjectBartonella quintana-
dc.subjectetiologic diagnosis-
dc.subjectheart valve-
dc.subjectIllumina MiSeq-
dc.subjectinfective endocarditis-
dc.titlePotential utility of metagenomic sequencing for improving etiologic diagnosis of infective endocarditis-
dc.typeArticle-
dc.identifier.emailLeung, HCM: cmleung3@hku.hk-
dc.identifier.emailLam, TW: twlam@cs.hku.hk-
dc.identifier.authorityLeung, HCM=rp00144-
dc.identifier.authorityChan, TL=rp00418-
dc.identifier.authorityLam, TW=rp00135-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.2217/fca-2018-0088-
dc.identifier.pmid31691592-
dc.identifier.scopuseid_2-s2.0-85074962865-
dc.identifier.hkuros318833-
dc.identifier.volume15-
dc.identifier.issue6-
dc.identifier.spage411-
dc.identifier.epage424-
dc.identifier.isiWOS:000501611600005-
dc.publisher.placeUnited Kingdom-

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