• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肽基精氨酸脱亚氨酶(PPAD)T2变异等位基因增加对口腔微生物群组成及慢性牙周炎严重程度的影响。

Impact of increased peptidylarginine deiminase (PPAD) T2 variant allele on oral microbiota composition and severity of chronic periodontitis.

作者信息

Kaminska Marta, Dudzinska Noemie A M, Yucel-Lindberg Tülay, Söder Birgitta, Narayanan Aswathy, Potempa Jan, Mydel Piotr M

机构信息

Broegelmann Research Laboratory, Department of Clinical Science, Faculty of Medicine, University of Bergen, Bergen, Norway.

Division of Pediatric Dentistry, Department of Dental Medicine, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Oral Microbiol. 2025 Mar 20;17(1):2479903. doi: 10.1080/20002297.2025.2479903. eCollection 2025.

DOI:10.1080/20002297.2025.2479903
PMID:40123596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11926895/
Abstract

BACKGROUND

(Pg) is a keystone pathogen in periodontitis, encoding a unique peptidyl arginine deiminase (PPAD) linked to protein citrullination, a process associated with rheumatoid arthritis (RA). Recently, we identified a super-active PPAD variant (T2) in isolates. Here, we evaluated if the presence of the super-active T2 variant of PPAD affects the salivary microbiome, the severity of chronic periodontitis (CP), and subsequently CP's causative association with RA onset/progression.

PATIENTS/MATERIALS AND METHODS: We examined 56 CP patients and 36 healthy volunteers. and counts were measured RT-PCR, and PPAD variant was typed PCR. 16S rRNA from salivary DNA sequencing characterized microbiota composition, while CP severity was assessed through bleeding on probing (BoP), clinical attachment loss (CAL), and pocket depth (PD) parameters.

RESULTS

CP patients exhibited higher and counts, with 30.7% harbouring the PPAD-T2 variant, compared to only one healthy volunteer. Clinical CP parameters were unaffected by the PPAD variant. However, PPAD-T2 influenced oral microbiota composition, enriching certain genera.

CONCLUSION

While the PPAD variant did not affect CP severity, it influenced oral microbiota composition. Further research is needed to understand citrullination's role in oral microbiota and chronic inflammatory disease development.

摘要

背景

牙龈卟啉单胞菌(Pg)是牙周炎中的关键病原体,编码一种与蛋白质瓜氨酸化相关的独特肽基精氨酸脱氨酶(PPAD),该过程与类风湿性关节炎(RA)有关。最近,我们在分离株中鉴定出一种超活性PPAD变体(T2)。在此,我们评估了PPAD超活性T2变体的存在是否会影响唾液微生物群、慢性牙周炎(CP)的严重程度,以及随后CP与RA发病/进展的因果关系。

患者/材料与方法:我们检查了56名CP患者和36名健康志愿者。通过逆转录聚合酶链反应(RT-PCR)测量牙龈卟啉单胞菌和伴放线聚集杆菌数量,并通过聚合酶链反应(PCR)对PPAD变体进行分型。对唾液DNA测序得到的16S核糖体RNA进行分析,以确定微生物群组成,同时通过探诊出血(BoP)、临床附着丧失(CAL)和牙周袋深度(PD)参数评估CP严重程度。

结果

与仅一名健康志愿者相比,CP患者的牙龈卟啉单胞菌和伴放线聚集杆菌数量更高,30.7%的患者携带PPAD-T2变体。临床CP参数不受PPAD变体影响。然而,PPAD-T2影响口腔微生物群组成,使某些菌属富集。

结论

虽然PPAD变体不影响CP严重程度,但它影响口腔微生物群组成。需要进一步研究以了解瓜氨酸化在口腔微生物群和慢性炎症性疾病发展中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/f7b1171656a7/ZJOM_A_2479903_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/024fb3064f8f/ZJOM_A_2479903_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/fb78bc05ac6c/ZJOM_A_2479903_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/404d4be900af/ZJOM_A_2479903_F0003_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/b34895cb507f/ZJOM_A_2479903_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/98caf827b1da/ZJOM_A_2479903_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/00bd38c65060/ZJOM_A_2479903_F0007_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/f7b1171656a7/ZJOM_A_2479903_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/024fb3064f8f/ZJOM_A_2479903_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/fb78bc05ac6c/ZJOM_A_2479903_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/404d4be900af/ZJOM_A_2479903_F0003_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/b34895cb507f/ZJOM_A_2479903_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/98caf827b1da/ZJOM_A_2479903_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/00bd38c65060/ZJOM_A_2479903_F0007_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9350/11926895/f7b1171656a7/ZJOM_A_2479903_F0006_OC.jpg

相似文献

1
Impact of increased peptidylarginine deiminase (PPAD) T2 variant allele on oral microbiota composition and severity of chronic periodontitis.肽基精氨酸脱亚氨酶(PPAD)T2变异等位基因增加对口腔微生物群组成及慢性牙周炎严重程度的影响。
J Oral Microbiol. 2025 Mar 20;17(1):2479903. doi: 10.1080/20002297.2025.2479903. eCollection 2025.
2
Identification of a new genetic variant (G231N, E232T, N235D) of peptidylarginine deiminase from in advanced periodontitis.从晚期牙周炎中鉴定出一种新的肽基精氨酸脱亚氨酶基因变异(G231N、E232T、N235D)。
Front Immunol. 2024 Mar 21;15:1355357. doi: 10.3389/fimmu.2024.1355357. eCollection 2024.
3
Expression of anti-Porphyromonas gingivalis peptidylarginine deiminase immunoglobulin G and peptidylarginine deiminase-4 in patients with rheumatoid arthritis and periodontitis.抗牙龈卟啉单胞菌肽基精氨酸脱亚氨酶免疫球蛋白 G 和肽基精氨酸脱亚氨酶-4 在类风湿关节炎和牙周炎患者中的表达。
J Periodontal Res. 2016 Feb;51(1):103-11. doi: 10.1111/jre.12288. Epub 2015 Jun 11.
4
Defining the role of Porphyromonas gingivalis peptidylarginine deiminase (PPAD) in rheumatoid arthritis through the study of PPAD biology.通过研究牙龈卟啉单胞菌肽基精氨酸脱亚氨酶(PPAD)生物学特性来明确其在类风湿性关节炎中的作用。
Ann Rheum Dis. 2015 Nov;74(11):2054-61. doi: 10.1136/annrheumdis-2014-205385. Epub 2014 May 26.
5
Structure, function, and inhibition of a genomic/clinical variant of Porphyromonas gingivalis peptidylarginine deiminase.牙龈卟啉单胞菌蛋白精氨酸脱亚氨酶基因/临床变异体的结构、功能和抑制作用。
Protein Sci. 2019 Mar;28(3):478-486. doi: 10.1002/pro.3571. Epub 2019 Jan 30.
6
Inhibition of peptidyl arginine deiminase, a virulence factor, by antioxidant-rich : and evaluation.富含抗氧化剂的物质对作为毒力因子的肽基精氨酸脱亚氨酶的抑制作用及评估
Saudi J Biol Sci. 2022 Apr;29(4):2573-2581. doi: 10.1016/j.sjbs.2021.12.037. Epub 2021 Dec 17.
7
Peptidyl Arginine Deiminase (PPAD) in the Context of the Feed-Forward Loop of Inflammation in Periodontitis.肽基精氨酸脱亚氨酶(PPAD)在牙周炎炎症前馈环中的作用。
Int J Mol Sci. 2023 Aug 18;24(16):12922. doi: 10.3390/ijms241612922.
8
A Secreted Bacterial Peptidylarginine Deiminase Can Neutralize Human Innate Immune Defenses.一种分泌型细菌肽酰精氨酸脱亚氨酶能中和人体固有免疫防御。
mBio. 2018 Oct 30;9(5):e01704-18. doi: 10.1128/mBio.01704-18.
9
Conserved Citrullinating Exoenzymes in Porphyromonas Species.牙龈卟啉单胞菌属中保守的瓜氨酸化外切酶。
J Dent Res. 2018 May;97(5):556-562. doi: 10.1177/0022034517747575. Epub 2018 Jan 3.
10
Heightened immune response to autocitrullinated Porphyromonas gingivalis peptidylarginine deiminase: a potential mechanism for breaching immunologic tolerance in rheumatoid arthritis.对自身瓜氨酸化牙龈卟啉单胞菌肽基精氨酸脱亚氨酶的增强免疫反应:类风湿关节炎中打破免疫耐受的潜在机制。
Ann Rheum Dis. 2014 Jan;73(1):263-9. doi: 10.1136/annrheumdis-2012-202726. Epub 2013 Mar 5.

本文引用的文献

1
Identification of a new genetic variant (G231N, E232T, N235D) of peptidylarginine deiminase from in advanced periodontitis.从晚期牙周炎中鉴定出一种新的肽基精氨酸脱亚氨酶基因变异(G231N、E232T、N235D)。
Front Immunol. 2024 Mar 21;15:1355357. doi: 10.3389/fimmu.2024.1355357. eCollection 2024.
2
Saliva sampling method influences oral microbiome composition and taxa distribution associated with oral diseases.唾液采样方法会影响与口腔疾病相关的口腔微生物组组成和分类群分布。
PLoS One. 2024 Mar 28;19(3):e0301016. doi: 10.1371/journal.pone.0301016. eCollection 2024.
3
Effect of Hydrogen Sulfide on Essential Functions of Polymorphonuclear Leukocytes.
硫化氢对多形核白细胞基本功能的影响。
Toxins (Basel). 2023 Mar 4;15(3):198. doi: 10.3390/toxins15030198.
4
Oral mucosal breaks trigger anti-citrullinated bacterial and human protein antibody responses in rheumatoid arthritis.口腔黏膜破损可引发类风湿关节炎患者抗瓜氨酸化细菌和人体蛋白抗体应答。
Sci Transl Med. 2023 Feb 22;15(684):eabq8476. doi: 10.1126/scitranslmed.abq8476.
5
Anti-citrullinated Protein Antibody Generation, Pathogenesis, Clinical Application, and Prospects.抗瓜氨酸化蛋白抗体的产生、发病机制、临床应用及前景
Front Med (Lausanne). 2022 Jan 12;8:802934. doi: 10.3389/fmed.2021.802934. eCollection 2021.
6
Periodontal Disease: The Good, The Bad, and The Unknown.牙周病:好的、坏的和未知的。
Front Cell Infect Microbiol. 2021 Dec 7;11:766944. doi: 10.3389/fcimb.2021.766944. eCollection 2021.
7
Periodontal Inflammation and Systemic Diseases: An Overview.牙周炎与全身疾病:概述
Front Physiol. 2021 Oct 27;12:709438. doi: 10.3389/fphys.2021.709438. eCollection 2021.
8
Bacteria Are Associated With Parkinson's Disease.细菌与帕金森病有关。
Front Cell Infect Microbiol. 2021 May 3;11:652617. doi: 10.3389/fcimb.2021.652617. eCollection 2021.
9
Possible synergy effect of hydrogen sulfide and acetate produced by sulfate-reducing bacteria on inflammatory bowel disease development.硫酸盐还原菌产生的硫化氢和乙酸盐对炎症性肠病发展的可能协同作用。
J Adv Res. 2020 Mar 24;27:71-78. doi: 10.1016/j.jare.2020.03.007. eCollection 2021 Jan.
10
Current understanding of periodontal disease pathogenesis and targets for host-modulation therapy.牙周病发病机制的最新认识和宿主调控治疗的靶点。
Periodontol 2000. 2020 Oct;84(1):14-34. doi: 10.1111/prd.12331.