Composition of subgingival microbiota associated with periodontitis and diagnosis of malignancy—a cross-sectional study
Periodontitis is one of the world’s most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and ti...
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Published in | Frontiers in microbiology Vol. 14; p. 1172340 |
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Abstract | Periodontitis is one of the world’s most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008–2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were
Actinobacteria
,
Proteobacteria
,
Firmicutes
,
Bacteroidetes
, and
Fusobacteria
. At the genus level,
Treponema
,
Fretibacterium
, and
Prevotella
were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients,
Corynebacterium
and
Streptococcus
were more abundant in the CSC group;
Prevotella
were more abundant in the DCL group; and
Rothia
,
Neisseria
, and
Capnocytophaga
were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera
Prevotella
,
Treponema
, and
Mycoplasma
. Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer. |
---|---|
AbstractList | Periodontitis is one of the world's most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008-2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were
,
,
,
, and
. At the genus level,
,
, and
were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients,
and
were more abundant in the CSC group;
were more abundant in the DCL group; and
,
, and
were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera
,
, and
. Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer. Periodontitis is one of the world’s most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008–2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were Actinobacteria, Proteobacteria, Firmicutes, Bacteroidetes, and Fusobacteria. At the genus level, Treponema, Fretibacterium, and Prevotella were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, Corynebacterium and Streptococcus were more abundant in the CSC group; Prevotella were more abundant in the DCL group; and Rothia, Neisseria, and Capnocytophaga were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera Prevotella, Treponema, and Mycoplasma. Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer. Periodontitis is one of the world’s most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008–2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were Actinobacteria , Proteobacteria , Firmicutes , Bacteroidetes , and Fusobacteria . At the genus level, Treponema , Fretibacterium , and Prevotella were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, Corynebacterium and Streptococcus were more abundant in the CSC group; Prevotella were more abundant in the DCL group; and Rothia , Neisseria , and Capnocytophaga were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera Prevotella , Treponema , and Mycoplasma . Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer. Periodontitis is one of the world's most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008-2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were Actinobacteria, Proteobacteria, Firmicutes, Bacteroidetes, and Fusobacteria. At the genus level, Treponema, Fretibacterium, and Prevotella were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, Corynebacterium and Streptococcus were more abundant in the CSC group; Prevotella were more abundant in the DCL group; and Rothia, Neisseria, and Capnocytophaga were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera Prevotella, Treponema, and Mycoplasma. Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer.Periodontitis is one of the world's most prevalent infectious conditions, affecting between 25 and 40% of the adult population. It is a consequence of the complex interactions between periodontal pathogens and their products, which trigger the host inflammatory response, chronic inflammation, and tissue destruction. Chronic systemic low-grade inflammation is involved in numerous diseases, and it is also known that long-lasting inflammation and chronic infections predispose one to cancer. Here, we characterized and compared the subgingival microbiota associated with periodontitis and diagnosis of malignancy in a longitudinal 10-year follow-up study. The study was conducted on 50 patients with periodontitis and 40 periodontally healthy individuals. The recorded clinical oral health parameters were periodontal attachment loss (AL), bleeding on probing (BOP), gingival index (GI), probing depth (PD), and plaque index (PI). Subgingival plaque was collected from each participant, from which DNA was extracted, and 16S rRNA gene amplicon sequencing performed. Cancer diagnoses data were collected between the years 2008-2018 from the Swedish Cancer Registry. The participants were categorized based on having cancer at the time of sample collection (CSC), having developed cancer later (DCL), and controls without any cancer. The most abundant phyla across all 90 samples were Actinobacteria, Proteobacteria, Firmicutes, Bacteroidetes, and Fusobacteria. At the genus level, Treponema, Fretibacterium, and Prevotella were significantly more abundant in samples of periodontitis patients compared to non-periodontitis individuals. With regard to samples of cancer patients, Corynebacterium and Streptococcus were more abundant in the CSC group; Prevotella were more abundant in the DCL group; and Rothia, Neisseria, and Capnocytophaga were more abundant in the control group. In the CSC group, we also found that the presence of periodontal inflammation, in terms of BOP, GI, and PLI, significantly correlated with species belonging to the genera Prevotella, Treponema, and Mycoplasma. Our results revealed that several subgingival genera were differentially enriched among the studied groups. These findings underscore the need for further research to fully understand the role that oral pathogens may play in the development of cancer. |
Author | Lundmark, Anna Hu, Yue O. O. Neogi, Ujjwal Yucel-Lindberg, Tülay Narayanan, Aswathy Meurman, Jukka Söder, Birgitta |
AuthorAffiliation | 3 Division of Periodontology, Department of Dental Medicine, Karolinska Institutet , Huddinge , Sweden 2 Division of Infectious Diseases, Department of Medicine Huddinge, Karolinska Institutet , Stockholm , Sweden 6 Department of Microbiology, Tumor and Cell Biology, Centre for Translational Microbiome Research, Karolinska Institutet , Stockholm , Sweden 1 Division of Clinical Microbiology, Department of Laboratory Medicine, ANA Futura, Karolinska Institutet , Stockholm , Sweden 8 The Systems Virology Lab, Division of Clinical Microbiology, Department of Laboratory Medicine, ANA Futura, Karolinska Institutet , Stockholm , Sweden 7 School of Environmental Science and Engineering, Hubei Polytechnic University , Huangshi , China 4 Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital , Helsinki , Finland 5 Division of Pediatric Dentistry, Department of Dental Medicine, Karolinska Institutet , Huddinge , Sweden |
AuthorAffiliation_xml | – name: 2 Division of Infectious Diseases, Department of Medicine Huddinge, Karolinska Institutet , Stockholm , Sweden – name: 4 Department of Oral and Maxillofacial Diseases, University of Helsinki and Helsinki University Hospital , Helsinki , Finland – name: 5 Division of Pediatric Dentistry, Department of Dental Medicine, Karolinska Institutet , Huddinge , Sweden – name: 1 Division of Clinical Microbiology, Department of Laboratory Medicine, ANA Futura, Karolinska Institutet , Stockholm , Sweden – name: 6 Department of Microbiology, Tumor and Cell Biology, Centre for Translational Microbiome Research, Karolinska Institutet , Stockholm , Sweden – name: 7 School of Environmental Science and Engineering, Hubei Polytechnic University , Huangshi , China – name: 3 Division of Periodontology, Department of Dental Medicine, Karolinska Institutet , Huddinge , Sweden – name: 8 The Systems Virology Lab, Division of Clinical Microbiology, Department of Laboratory Medicine, ANA Futura, Karolinska Institutet , Stockholm , Sweden |
Author_xml | – sequence: 1 givenname: Aswathy surname: Narayanan fullname: Narayanan, Aswathy – sequence: 2 givenname: Birgitta surname: Söder fullname: Söder, Birgitta – sequence: 3 givenname: Jukka surname: Meurman fullname: Meurman, Jukka – sequence: 4 givenname: Anna surname: Lundmark fullname: Lundmark, Anna – sequence: 5 givenname: Yue O. O. surname: Hu fullname: Hu, Yue O. O. – sequence: 6 givenname: Ujjwal surname: Neogi fullname: Neogi, Ujjwal – sequence: 7 givenname: Tülay surname: Yucel-Lindberg fullname: Yucel-Lindberg, Tülay |
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ContentType | Journal Article |
Copyright | Copyright © 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg. Copyright © 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg. 2023 Narayanan, Söder, Meurman, Lundmark, Hu, Neogi and Yucel-Lindberg |
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Keywords | supragingival plaque 16S rRNA gene sequencing cancer malignancy oral microbiota periodontitis |
Language | English |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Zhenting Xiang, University of Pennsylvania, United States; Peter Allan Jorth, Cedars-Sinai Medical Center, United States These authors have contributed equally to this work Edited by: Lihong Peng, Hunan University of Technology, China |
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Title | Composition of subgingival microbiota associated with periodontitis and diagnosis of malignancy—a cross-sectional study |
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