Cargando…

Study of microbiocenosis of canine dental biofilms

Dental biofilm is a complex microbial community influenced by many exogenous and endogenous factors. Despite long-term studies, its bacterial composition is still not clearly understood. While most of the research on dental biofilms was conducted in humans, much less information is available from co...

Descripción completa

Detalles Bibliográficos
Autores principales: Kačírová, Jana, Maďari, Aladár, Mucha, Rastislav, Fecskeová, Lívia K., Mujakic, Izabela, Koblížek, Michal, Nemcová, Radomíra, Maďar, Marián
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492755/
https://www.ncbi.nlm.nih.gov/pubmed/34611253
http://dx.doi.org/10.1038/s41598-021-99342-5
_version_ 1784578987752685568
author Kačírová, Jana
Maďari, Aladár
Mucha, Rastislav
Fecskeová, Lívia K.
Mujakic, Izabela
Koblížek, Michal
Nemcová, Radomíra
Maďar, Marián
author_facet Kačírová, Jana
Maďari, Aladár
Mucha, Rastislav
Fecskeová, Lívia K.
Mujakic, Izabela
Koblížek, Michal
Nemcová, Radomíra
Maďar, Marián
author_sort Kačírová, Jana
collection PubMed
description Dental biofilm is a complex microbial community influenced by many exogenous and endogenous factors. Despite long-term studies, its bacterial composition is still not clearly understood. While most of the research on dental biofilms was conducted in humans, much less information is available from companion animals. In this study, we analyzed the composition of canine dental biofilms using both standard cultivation on solid media and amplicon sequencing, and compared the two approaches. The 16S rRNA gene sequences were used to define the bacterial community of canine dental biofilm with both, culture-dependent and culture-independent methods. After DNA extraction from each sample, the V3–V4 region of the 16S rRNA gene was amplified and sequenced via Illumina MiSeq platform. Isolated bacteria were identified using universal primers and Sanger sequencing. Representatives of 18 bacterial genera belonging to 5 phyla were isolated from solid media. Amplicon sequencing largely expanded this information identifying in total 284 operational taxonomic units belonging to 10 bacterial phyla. Amplicon sequencing revealed much higher diversity of bacteria in the canine dental biofilms, when compared to standard cultivation approach. In contrast, cultured representatives of several bacterial families were not identified by amplicon sequencing.
format Online
Article
Text
id pubmed-8492755
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-84927552021-10-07 Study of microbiocenosis of canine dental biofilms Kačírová, Jana Maďari, Aladár Mucha, Rastislav Fecskeová, Lívia K. Mujakic, Izabela Koblížek, Michal Nemcová, Radomíra Maďar, Marián Sci Rep Article Dental biofilm is a complex microbial community influenced by many exogenous and endogenous factors. Despite long-term studies, its bacterial composition is still not clearly understood. While most of the research on dental biofilms was conducted in humans, much less information is available from companion animals. In this study, we analyzed the composition of canine dental biofilms using both standard cultivation on solid media and amplicon sequencing, and compared the two approaches. The 16S rRNA gene sequences were used to define the bacterial community of canine dental biofilm with both, culture-dependent and culture-independent methods. After DNA extraction from each sample, the V3–V4 region of the 16S rRNA gene was amplified and sequenced via Illumina MiSeq platform. Isolated bacteria were identified using universal primers and Sanger sequencing. Representatives of 18 bacterial genera belonging to 5 phyla were isolated from solid media. Amplicon sequencing largely expanded this information identifying in total 284 operational taxonomic units belonging to 10 bacterial phyla. Amplicon sequencing revealed much higher diversity of bacteria in the canine dental biofilms, when compared to standard cultivation approach. In contrast, cultured representatives of several bacterial families were not identified by amplicon sequencing. Nature Publishing Group UK 2021-10-05 /pmc/articles/PMC8492755/ /pubmed/34611253 http://dx.doi.org/10.1038/s41598-021-99342-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kačírová, Jana
Maďari, Aladár
Mucha, Rastislav
Fecskeová, Lívia K.
Mujakic, Izabela
Koblížek, Michal
Nemcová, Radomíra
Maďar, Marián
Study of microbiocenosis of canine dental biofilms
title Study of microbiocenosis of canine dental biofilms
title_full Study of microbiocenosis of canine dental biofilms
title_fullStr Study of microbiocenosis of canine dental biofilms
title_full_unstemmed Study of microbiocenosis of canine dental biofilms
title_short Study of microbiocenosis of canine dental biofilms
title_sort study of microbiocenosis of canine dental biofilms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8492755/
https://www.ncbi.nlm.nih.gov/pubmed/34611253
http://dx.doi.org/10.1038/s41598-021-99342-5
work_keys_str_mv AT kacirovajana studyofmicrobiocenosisofcaninedentalbiofilms
AT madarialadar studyofmicrobiocenosisofcaninedentalbiofilms
AT mucharastislav studyofmicrobiocenosisofcaninedentalbiofilms
AT fecskeovaliviak studyofmicrobiocenosisofcaninedentalbiofilms
AT mujakicizabela studyofmicrobiocenosisofcaninedentalbiofilms
AT koblizekmichal studyofmicrobiocenosisofcaninedentalbiofilms
AT nemcovaradomira studyofmicrobiocenosisofcaninedentalbiofilms
AT madarmarian studyofmicrobiocenosisofcaninedentalbiofilms