首页> 外文期刊>Journal of Zhejiang University. B >Association between infection of different strains of Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans in subgingival plaque and clinical parameters in chronic periodontitis
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Association between infection of different strains of Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans in subgingival plaque and clinical parameters in chronic periodontitis

机译:牙龈下斑块中不同菌株牙龈卟啉单胞菌和放线菌放线杆菌的感染与慢性牙周炎临床指标的关系

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Objective: The aim of this study was to investigate subgingival infection frequencies of Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans strains with genetic variation in Chinese chronic periodontitis (CP) patients and to evaluate its correlation with clinical parameters. Methods: Two multiplex polymerase chain reaction (PCR) assays were developed to detect the 16SrDNA, collagenase (prtC) and fimbria (fimA) genes of P. gingivalis and the 16SrDNA, leukotoxin (lktA) and fimbria-associated protein (fap) genes of A. actinomycetemcomitans in 60 sulcus samples from 30 periodontal healthy subjects and in 122 subgingival plaque samples from 61 patients with CP. The PCR products were further T-A cloned and sent for nucleotide sequence analysis. Results: The 16SrDNA,prtC and fimA genes of P. gingivalis were detected in 92.6%, 85.2% and 80.3% of the subgingival plaque samples respectively, while the 16SrDNA, lktA and fap genes of A. actinomycetemcomitans were in 84.4%, 75.4% and 50.0% respectively. Nucleotide sequence analysis showed 98.62%~100% homology of the PCR products in these genes with the reported sequences. P. gingivalis strains with prtC+/fimA+ and A. actinomycetemcomitans with lktA+ were predominant in deep pockets ( > 6 mm) or in sites with attachment loss ≥ 5 mm than in shallow pockets (3~4 mm) or in sites with attachment loss ≤ 2 mm (P < 0.05). P. gingivalis strains with prtC+/fimA+ also showed higher frequency in gingival index (GI)=3 than in GI=1 group (P < 0.05). Conclusion: Infection of P. gingivalis with prtC+/flmA+ and A. actinomycetemcomitans with lktA+ correlates with periodontal destruction of CP in Chinese. Nonetheless P. gingivalis fimA, prtC genes and A. actinomycetemcomitans IktA gene are closely associated with periodontal destruction, while A. actinomycetemcomitans fap gene is not.
机译:目的:研究中国慢性牙周炎(CP)患者具有遗传变异的牙龈卟啉单胞菌和放线杆菌放线杆菌菌株的龈下感染频率,并评估其与临床参数的相关性。方法:进行了两种多重聚合酶链反应(PCR)检测法,以检测牙龈卟啉单胞菌的16SrDNA,胶原酶(prtC)和菌毛(fimA)基因以及细菌的16SrDNA,白细胞毒素(lktA)和菌毛相关蛋白(fap)基因。来自30位牙周健康受试者的60个龈沟样本和61位CP患者的122个龈下菌斑样本中的放线菌。将PCR产物进一步T-A克隆并送去进行核苷酸序列分析。结果:牙龈卟啉单胞菌的16SrDNA,prtC和fimA基因分别在牙龈下菌斑样品中检出92.6%,85.2%和80.3%,而放线菌的16SrDNA,lktA和fap基因分别在84.4%,75.4%。和50.0%。核苷酸序列分析表明,这些基因的PCR产物与报道的序列具有98.62%〜100%的同源性。 prtC + / fimA +和lktA +的放线放线杆菌菌株在深袋(> 6 mm)或附着损失≥5 mm的部位比浅袋(3〜4 mm)或附着损失≤的部位更占优势。 2毫米(P <0.05)。 prtC + / fimA +的牙龈卟啉单胞菌菌株在牙龈指数(GI)= 3时也比GI = 1组更高(P <0.05)。结论:prtC + / flmA +感染牙龈卟啉单胞菌,lktA +感染放线放线杆菌,与中国牙周牙周炎的破坏有关。尽管如此,牙龈卟啉单胞菌fimA,prtC基因和A.放线放线杆菌IktA基因与牙周破坏密切相关,而A.放线放线杆菌fap基因却与牙周破坏密切相关。

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