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dc.date.accessioned2016-08-08T11:36:34Z
dc.date.available2016-08-08T11:36:34Z
dc.date.created2016-07-17T20:43:07Z
dc.date.issued2016
dc.identifier.citationLangbach, Odd Kristoffersen, Anne Karin Abesha-Belay, Emnet Enersen, Morten Røkke, Ola Olsen, Ingar . Oral, intestinal, and skin bacteria in ventral hernia mesh implants.. Journal of Oral Microbiology. 2016, 8(31854)
dc.identifier.urihttp://hdl.handle.net/10852/51053
dc.description.abstractBackground: In ventral hernia surgery, mesh implants are used to reduce recurrence. Infection after mesh implantation can be a problem and rates around 6–10% have been reported. Bacterial colonization of mesh implants in patients without clinical signs of infection has not been thoroughly investigated. Molecular techniques have proven effective in demonstrating bacterial diversity in various environments and are able to identify bacteria on a gene-specific level. Objective: The purpose of this study was to detect bacterial biofilm in mesh implants, analyze its bacterial diversity, and look for possible resemblance with bacterial biofilm from the periodontal pocket. Methods: Thirty patients referred to our hospital for recurrence after former ventral hernia mesh repair, were examined for periodontitis in advance of new surgical hernia repair. Oral examination included periapical radiographs, periodontal probing, and subgingival plaque collection. A piece of mesh (1×1 cm) from the abdominal wall was harvested during the new surgical hernia repair and analyzed for bacteria by PCR and 16S rRNA gene sequencing. From patients with positive PCR mesh samples, subgingival plaque samples were analyzed with the same techniques. Results: A great variety of taxa were detected in 20 (66.7%) mesh samples, including typical oral commensals and periodontopathogens, enterics, and skin bacteria. Mesh and periodontal bacteria were further analyzed for similarity in 16S rRNA gene sequences. In 17 sequences, the level of resemblance between mesh and subgingival bacterial colonization was 98–100% suggesting, but not proving, a transfer of oral bacteria to the mesh. Conclusion: The results show great bacterial diversity on mesh implants from the anterior abdominal wall including oral commensals and periodontopathogens. Mesh can be reached by bacteria in several ways including hematogenous spread from an oral site. However, other sites such as gut and skin may also serve as sources for the mesh biofilm.en_US
dc.languageEN
dc.language.isoenen_US
dc.publisherCo-Action Publishing
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.titleOral, intestinal, and skin bacteria in ventral hernia mesh implantsen_US
dc.typeJournal articleen_US
dc.creator.authorLangbach, Odd
dc.creator.authorKristoffersen, Anne Karin
dc.creator.authorAbesha-Belay, Emnet
dc.creator.authorEnersen, Morten
dc.creator.authorRøkke, Ola
dc.creator.authorOlsen, Ingar
cristin.unitcode185,50,0,0
cristin.unitnameDet medisinske fakultet
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1368319
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal of Oral Microbiology&rft.volume=8&rft.spage=&rft.date=2016
dc.identifier.jtitleJournal of Oral Microbiology
dc.identifier.volume8
dc.identifier.doiorg/10.3402/jom.v8.31854
dc.identifier.urnURN:NBN:no-54533
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn2000-2297
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/51053/1/31854-206277-3-PB.pdf
dc.type.versionPublishedVersion
cristin.articleid31854


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