广泛性侵袭性牙周炎活性部位与疱疹病毒相关的微生物群评估。

Annali di stomatologia Pub Date : 2017-11-08 eCollection Date: 2017-04-01 DOI:10.11138/ads/2017.8.2.071
Claudio Passariello, Pierangelo Gigola, Luca Testarelli, Monica Puttini, Serena Schippa, Stefano Petti
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引用次数: 7

摘要

目的:本研究旨在探讨与广泛性侵袭性牙周炎(GAP)疾病进展和不同疱疹病毒合并感染相关的微生物模式。方法:从165例GAP患者的活性位点(AS)和非活性位点(n-AS)采集微生物标本,采用棋盘DNA-DNA杂交技术对40种细菌进行检测,采用PCR对单纯疱疹1型(HSV-1)、人巨细胞病毒(CMV)和eb病毒(EBV)进行检测。应用共因子分析和多元回归分析揭示了与三种病毒相关的特定微生物模式。结果:疱疹病毒检出率为37.6%。每一种病毒的检测都与AS牙龈下生物膜的特定模式有关。逻辑回归分析证实了几种病毒/细菌的关联:1)eb病毒与放线菌群聚集菌有关;ii)伴有放线菌、细小细孔菌、微细小单胞菌和核梭杆菌亚种的巨细胞病毒。polymorphum;iii) 1型单纯疱疹病毒伴牙龈卟啉单胞菌、连翘单宁菌、牙周梭菌和金黄色葡萄球菌。结论:微生物学数据表明疱疹病毒可能不仅仅是疾病进展的旁观者,牙龈下菌斑的特定模式与不同疱疹病毒的存在相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of microbiota associated with Herpesviruses in active sites of generalized aggressive periodontitis.

Evaluation of microbiota associated with Herpesviruses in active sites of generalized aggressive periodontitis.

Evaluation of microbiota associated with Herpesviruses in active sites of generalized aggressive periodontitis.

Aims: The present study aimed to investigate microbial patterns associated with disease progression and coinfection by different Herpesviruses in generalized aggressive periodontitis (GAP).

Methods: Microbiological samples were obtained from active (AS) and non-active (n-AS) sites in 165 subjects affected by GAP and were analyzed for 40 bacterial species by the Checkerboard DNA-DNA Hybridization technique and for Herpes simplex 1 (HSV-1), Human Cytomegalovirus (CMV), and Epstein Bar virus (EBV) by PCR.Common Factor Analysis and Multiple Regression Analysis were applied to disclose specific microbial patterns associated with the three viruses.

Results: Herpesviruses were detected in 37.6% of subjects. Detection of each of the searched viruses was associated with specific patterns of subgingival biofilm in AS. Logistic regression analyses evidenced several virus/bacteria associations: i) EBV with Aggregatibacter actinomycetemcomitans; ii) CMV with A. actinomycetemcomitans, Veillonella parvula, Parvimonas micra and Fusobacterium nucleatum subsp. polymorphum; iii) HSV-1 with Porphyromonas gingivalis, Tannerella forsythia, Fusobacterium periodonticum and Staphylococcus aureus.

Conclusions: Microbiological data suggest that Herpesviruses are probably not mere spectators of disease progression and that specific patterns of subgingival plaque are correlated with the presence of different Herpesviruses.

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