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Periodontitis may induce gut microbiota dysbiosis via salivary microbiota
The aim of this study was to identify whether periodontitis induces gut microbiota dysbiosis via invasion by salivary microbes. First, faecal and salivary samples were collected from periodontally healthy participants (PH group, n = 16) and patients with severe periodontitis (SP group, n = 21) and...
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Published in: | International journal of oral science 2022-06, Vol.14 (1), p.32-32, Article 32 |
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description | The aim of this study was to identify whether periodontitis induces gut microbiota dysbiosis via invasion by salivary microbes. First, faecal and salivary samples were collected from periodontally healthy participants (PH group,
n
= 16) and patients with severe periodontitis (SP group,
n
= 21) and analysed by 16S ribosomal RNA sequencing. Significant differences were observed in both the faecal and salivary microbiota between the PH and SP groups. Notably, more saliva-sourced microbes were observed in the faecal samples of the SP group. Then, the remaining salivary microbes were transplanted into C57BL6/J mice (the C-PH group and the C-SP group), and it was found that the composition of the gut microbiota of the C-SP group was significantly different from that of the C-PH group, with
Porphyromonadaceae
and
Fusobacterium
being significantly enriched in the C-SP group. In the colon, the C-SP group showed significantly reduced crypt depth and zonula occludens-1 expression. The mRNA expression levels of pro-inflammatory cytokines, chemokines and tight junction proteins were significantly higher in the C-SP group. To further investigate whether salivary bacteria could persist in the intestine, the salivary microbiota was stained with carboxyfluorescein diacetate succinimidyl ester and transplanted into mice. We found that salivary microbes from both the PH group and the SP group could persist in the gut for at least 24 h. Thus, our data demonstrate that periodontitis may induce gut microbiota dysbiosis through the influx of salivary microbes. |
doi_str_mv | 10.1038/s41368-022-00183-3 |
format | article |
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n
= 16) and patients with severe periodontitis (SP group,
n
= 21) and analysed by 16S ribosomal RNA sequencing. Significant differences were observed in both the faecal and salivary microbiota between the PH and SP groups. Notably, more saliva-sourced microbes were observed in the faecal samples of the SP group. Then, the remaining salivary microbes were transplanted into C57BL6/J mice (the C-PH group and the C-SP group), and it was found that the composition of the gut microbiota of the C-SP group was significantly different from that of the C-PH group, with
Porphyromonadaceae
and
Fusobacterium
being significantly enriched in the C-SP group. In the colon, the C-SP group showed significantly reduced crypt depth and zonula occludens-1 expression. The mRNA expression levels of pro-inflammatory cytokines, chemokines and tight junction proteins were significantly higher in the C-SP group. To further investigate whether salivary bacteria could persist in the intestine, the salivary microbiota was stained with carboxyfluorescein diacetate succinimidyl ester and transplanted into mice. We found that salivary microbes from both the PH group and the SP group could persist in the gut for at least 24 h. Thus, our data demonstrate that periodontitis may induce gut microbiota dysbiosis through the influx of salivary microbes.</description><identifier>ISSN: 1674-2818</identifier><identifier>EISSN: 2049-3169</identifier><identifier>DOI: 10.1038/s41368-022-00183-3</identifier><identifier>PMID: 35732628</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/326/41/2530 ; 692/699/255/1318 ; 692/699/3020/3029 ; Carboxyfluorescein diacetate ; Chemokines ; Cytokines ; Dentistry ; Digestive system ; Dysbacteriosis ; Feces ; Gastrointestinal tract ; Gene expression ; Gum disease ; Inflammation ; Intestinal microflora ; Medicine ; Microbiota ; Oral and Maxillofacial Surgery ; Orthopedics ; Periodontitis ; rRNA 16S ; Saliva ; Surgical Orthopedics ; Zonula occludens-1 protein</subject><ispartof>International journal of oral science, 2022-06, Vol.14 (1), p.32-32, Article 32</ispartof><rights>The Author(s) 2022</rights><rights>The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c583t-7d66c1ac2200db5ba6a6d4b194501fa9b13d0058c067e07b824b69bfb8bd73133</citedby><cites>FETCH-LOGICAL-c583t-7d66c1ac2200db5ba6a6d4b194501fa9b13d0058c067e07b824b69bfb8bd73133</cites><orcidid>0000-0002-6963-3530 ; 0000-0002-8398-2104</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2679466201/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2679466201?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids></links><search><creatorcontrib>Bao, Jun</creatorcontrib><creatorcontrib>Li, Lili</creatorcontrib><creatorcontrib>Zhang, Yangheng</creatorcontrib><creatorcontrib>Wang, Min</creatorcontrib><creatorcontrib>Chen, Faming</creatorcontrib><creatorcontrib>Ge, Shaohua</creatorcontrib><creatorcontrib>Chen, Bin</creatorcontrib><creatorcontrib>Yan, Fuhua</creatorcontrib><title>Periodontitis may induce gut microbiota dysbiosis via salivary microbiota</title><title>International journal of oral science</title><addtitle>Int J Oral Sci</addtitle><description>The aim of this study was to identify whether periodontitis induces gut microbiota dysbiosis via invasion by salivary microbes. First, faecal and salivary samples were collected from periodontally healthy participants (PH group,
n
= 16) and patients with severe periodontitis (SP group,
n
= 21) and analysed by 16S ribosomal RNA sequencing. Significant differences were observed in both the faecal and salivary microbiota between the PH and SP groups. Notably, more saliva-sourced microbes were observed in the faecal samples of the SP group. Then, the remaining salivary microbes were transplanted into C57BL6/J mice (the C-PH group and the C-SP group), and it was found that the composition of the gut microbiota of the C-SP group was significantly different from that of the C-PH group, with
Porphyromonadaceae
and
Fusobacterium
being significantly enriched in the C-SP group. In the colon, the C-SP group showed significantly reduced crypt depth and zonula occludens-1 expression. The mRNA expression levels of pro-inflammatory cytokines, chemokines and tight junction proteins were significantly higher in the C-SP group. To further investigate whether salivary bacteria could persist in the intestine, the salivary microbiota was stained with carboxyfluorescein diacetate succinimidyl ester and transplanted into mice. We found that salivary microbes from both the PH group and the SP group could persist in the gut for at least 24 h. Thus, our data demonstrate that periodontitis may induce gut microbiota dysbiosis through the influx of salivary microbes.</description><subject>631/326/41/2530</subject><subject>692/699/255/1318</subject><subject>692/699/3020/3029</subject><subject>Carboxyfluorescein diacetate</subject><subject>Chemokines</subject><subject>Cytokines</subject><subject>Dentistry</subject><subject>Digestive system</subject><subject>Dysbacteriosis</subject><subject>Feces</subject><subject>Gastrointestinal tract</subject><subject>Gene expression</subject><subject>Gum disease</subject><subject>Inflammation</subject><subject>Intestinal microflora</subject><subject>Medicine</subject><subject>Microbiota</subject><subject>Oral and Maxillofacial Surgery</subject><subject>Orthopedics</subject><subject>Periodontitis</subject><subject>rRNA 16S</subject><subject>Saliva</subject><subject>Surgical Orthopedics</subject><subject>Zonula occludens-1 protein</subject><issn>1674-2818</issn><issn>2049-3169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kUuLFDEURoMoTjv6B1wVuHFTevOoVLIRZPDRMKALXYebR7VpqitjUtXQ_95016COC1cJybmHy_cR8pLCGwpcvS2CcqlaYKwFoIq3_BHZMBC65VTqx2RDZS9apqi6Is9K2QNI1TH6lFzxrudMMrUh268hx-TTNMc5luaApyZOfnGh2S1zc4guJxvTjI0_lXoplTlGbAqO8Yj59BfxnDwZcCzhxf15Tb5__PDt5nN7--XT9ub9bes6xee291I6io4xAG87ixKlF5Zq0QEdUFvKPUCnHMg-QG8VE1ZqO1hlfc8p59dku3p9wr25y_FQ9zAJo7k8pLwzmOfoxmC4115QDQE7JpzgCCIIKQaJGoUHWl3vVtfdYg_BuzDNGccH0oc_U_xhduloNKO9FmfB63tBTj-XUGZziMWFccQppKUYJhUwrik7o6_-QfdpyVONqlJVJiW7bMRWqsZaSg7D72UomHPrZm3d1NbNpXVzjoSvQ6XC0y7kP-r_TP0CfPiuZQ</recordid><startdate>20220623</startdate><enddate>20220623</enddate><creator>Bao, Jun</creator><creator>Li, Lili</creator><creator>Zhang, Yangheng</creator><creator>Wang, Min</creator><creator>Chen, Faming</creator><creator>Ge, Shaohua</creator><creator>Chen, Bin</creator><creator>Yan, Fuhua</creator><general>Nature Publishing Group UK</general><general>Springer Nature B.V</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6963-3530</orcidid><orcidid>https://orcid.org/0000-0002-8398-2104</orcidid></search><sort><creationdate>20220623</creationdate><title>Periodontitis may induce gut microbiota dysbiosis via salivary microbiota</title><author>Bao, Jun ; 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First, faecal and salivary samples were collected from periodontally healthy participants (PH group,
n
= 16) and patients with severe periodontitis (SP group,
n
= 21) and analysed by 16S ribosomal RNA sequencing. Significant differences were observed in both the faecal and salivary microbiota between the PH and SP groups. Notably, more saliva-sourced microbes were observed in the faecal samples of the SP group. Then, the remaining salivary microbes were transplanted into C57BL6/J mice (the C-PH group and the C-SP group), and it was found that the composition of the gut microbiota of the C-SP group was significantly different from that of the C-PH group, with
Porphyromonadaceae
and
Fusobacterium
being significantly enriched in the C-SP group. In the colon, the C-SP group showed significantly reduced crypt depth and zonula occludens-1 expression. The mRNA expression levels of pro-inflammatory cytokines, chemokines and tight junction proteins were significantly higher in the C-SP group. To further investigate whether salivary bacteria could persist in the intestine, the salivary microbiota was stained with carboxyfluorescein diacetate succinimidyl ester and transplanted into mice. We found that salivary microbes from both the PH group and the SP group could persist in the gut for at least 24 h. Thus, our data demonstrate that periodontitis may induce gut microbiota dysbiosis through the influx of salivary microbes.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>35732628</pmid><doi>10.1038/s41368-022-00183-3</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-6963-3530</orcidid><orcidid>https://orcid.org/0000-0002-8398-2104</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/326/41/2530 692/699/255/1318 692/699/3020/3029 Carboxyfluorescein diacetate Chemokines Cytokines Dentistry Digestive system Dysbacteriosis Feces Gastrointestinal tract Gene expression Gum disease Inflammation Intestinal microflora Medicine Microbiota Oral and Maxillofacial Surgery Orthopedics Periodontitis rRNA 16S Saliva Surgical Orthopedics Zonula occludens-1 protein |
title | Periodontitis may induce gut microbiota dysbiosis via salivary microbiota |
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