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Culturomic and quantitative real- time- polymerase chain reaction analyses for early contamination of abutments with different surfaces: A randomized clinical trial

dc.contributor.authorCanullo, Luigi
dc.contributor.authorMasucci, Luca
dc.contributor.authorQuaranta, Gianluca
dc.contributor.authorPatini, Romeo
dc.contributor.authorCaponio, Vito Carlo Alberto
dc.contributor.authorPesce, Paolo
dc.contributor.authorRavidà, Andrea
dc.contributor.authorPenarrocha‐oltra, David
dc.contributor.authorPenarrocha‐diago, Miguel
dc.date.accessioned2021-09-08T14:33:51Z
dc.date.available2022-09-08 10:33:50en
dc.date.available2021-09-08T14:33:51Z
dc.date.issued2021-08
dc.identifier.citationCanullo, Luigi; Masucci, Luca; Quaranta, Gianluca; Patini, Romeo; Caponio, Vito Carlo Alberto; Pesce, Paolo; Ravidà, Andrea ; Penarrocha‐oltra, David ; Penarrocha‐diago, Miguel (2021). "Culturomic and quantitative real- time- polymerase chain reaction analyses for early contamination of abutments with different surfaces: A randomized clinical trial." Clinical Implant Dentistry and Related Research 23(4): 568-578.
dc.identifier.issn1523-0899
dc.identifier.issn1708-8208
dc.identifier.urihttps://hdl.handle.net/2027.42/169240
dc.description.abstractBackgroundRough and/or plasma- activated abutments seem to be able to increase soft tissue adhesion and stability; however, limited evidence is available about bacterial contamination differences.PurposeThe aim was to investigate the oral microbiota on four dental abutments with different surfaces by quantitative real- time polymerase chain reaction (qRT- PCR) and culturomic approach.MethodsForty patients needing a single implant rehabilitation were involved in the study. Forty healing abutments, especially designed for the study, were divided into four groups according to the surface topography (1. machined [MAC], 2. machined plasma of argon treated [plasmaMAC], 3. ultrathin threaded microsurface [UTM], 4. UTM plasma of argon treated [Plasma UTM]). Random assignment was performed according to predefined randomization tables. All patients underwent surgical intervention for implant and contextual healing abutment positioning. After 2 months of healing, a sterile cotton swab was used for microbiological sampling for culturomics, while sterile paper points inserted into the sulcus were used for qRT- PCR.ResultsAt the end of the study, 36 patients completed all procedures and a total of 36 abutments (9 per group) were analyzed. qRT- PCR retrieved data for 23 bacterial species whereas culturomics revealed the presence of 74 different bacteria, most of them not routinely included into oral cavity microbiological kits of analysis or never found before in the oral microenvironment. No statistically significant differences emerged analyzing the four different surfaces (p =- 0.053). On the contrary, higher total and specific bacterial counts were detected in the plasma- treated surfaces compared to the untreated ones (p =- 0.021).ConclusionsAbutments with different topographies and surface treatments resulted contaminated by similar oral bacterial flora. Abutments with moderately rough surface were not associated with a greater bacterial adhesion compared to machined ones. Conversely, more bacteria were found around plasma- treated abutments. Furthermore, data reported suggested to include new species not previously sought in the routine analyses of the oral bacterial microflora.
dc.publisherJohn Wiley & Sons, Inc.
dc.subject.otherdental abutments
dc.subject.otherdental implants
dc.subject.otheroral microbiota
dc.subject.otherRCT
dc.subject.othersurface properties
dc.titleCulturomic and quantitative real- time- polymerase chain reaction analyses for early contamination of abutments with different surfaces: A randomized clinical trial
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelDentistry
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/169240/1/cid13028_am.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/169240/2/cid13028.pdf
dc.identifier.doi10.1111/cid.13028
dc.identifier.sourceClinical Implant Dentistry and Related Research
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dc.working.doiNOen
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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