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本文引用的文献

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Polymerase chain reaction detection of 8 putative periodontal pathogens in subgingival plaque of gingivitis and advanced periodontitis lesions.聚合酶链反应检测牙龈炎和晚期牙周炎病变龈下菌斑中的8种假定牙周病原体。
Oral Microbiol Immunol. 1996 Aug;11(4):266-73. doi: 10.1111/j.1399-302x.1996.tb00180.x.
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Discrepancy between culture and DNA probe analysis for the detection of periodontal bacteria.用于检测牙周细菌的培养法与DNA探针分析法之间的差异。
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3
Multiplex PCR using conserved and species-specific 16S rRNA gene primers for simultaneous detection of Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis.使用保守的和物种特异性的16S rRNA基因引物进行多重PCR,以同时检测伴放线放线杆菌和牙龈卟啉单胞菌。
J Clin Microbiol. 1996 Nov;34(11):2674-8. doi: 10.1128/jcm.34.11.2674-2678.1996.
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Age and prevalence of Porphyromonas gingivalis in children.儿童牙龈卟啉单胞菌的年龄与患病率
J Clin Microbiol. 1996 Aug;34(8):2017-9. doi: 10.1128/jcm.34.8.2017-2019.1996.
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Periodontal status in the United States, 1988-1991: prevalence, extent, and demographic variation.1988 - 1991年美国的牙周状况:患病率、病变程度及人口统计学差异
J Dent Res. 1996 Feb;75 Spec No:672-83. doi: 10.1177/002203459607502S07.
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Simultaneous detection of Actinobacillus actinomycetemcomitans and Porphyromonas gingivalis by a rapid PCR method.通过快速聚合酶链反应方法同时检测伴放线放线杆菌和牙龈卟啉单胞菌
J Dent Res. 1995 Nov;74(11):1796-801. doi: 10.1177/00220345950740111301.
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Detection of Porphyromonas gingivalis associated with human periodontitis by DNA methods.用DNA方法检测与人类牙周炎相关的牙龈卟啉单胞菌。
Clin Infect Dis. 1993 Jun;16 Suppl 4:S317-8. doi: 10.1093/clinids/16.supplement_4.s317.
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Prevalence of periodontitis and suspected periodontal pathogens in families of adult periodontitis patients.成年牙周炎患者家族中牙周炎及疑似牙周病原体的患病率。
J Clin Periodontol. 1994 Feb;21(2):76-85. doi: 10.1111/j.1600-051x.1994.tb00283.x.
9
Comparison of three stool-processing methods for detection of Salmonella serogroups B, C2, and D by PCR.三种粪便处理方法用于通过聚合酶链反应检测沙门氏菌B、C2和D血清群的比较
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10
Alterations in sample preparation increase sensitivity of PCR assay for diagnosis of chancroid.样本制备的改进提高了用于诊断软下疳的聚合酶链反应检测的灵敏度。
J Clin Microbiol. 1995 Apr;33(4):1036-8. doi: 10.1128/jcm.33.4.1036-1038.1995.

通过一种简单的样本处理方法,采用聚合酶链反应(PCR)从唾液中检测牙龈卟啉单胞菌。

Detection of Porphyromonas gingivalis from saliva by PCR by using a simple sample-processing method.

作者信息

Mättö J, Saarela M, Alaluusua S, Oja V, Jousimies-Somer H, Asikainen S

机构信息

Research Laboratory, Institute of Dentistry, University of Helsinki, Finland.

出版信息

J Clin Microbiol. 1998 Jan;36(1):157-60. doi: 10.1128/JCM.36.1.157-160.1998.

DOI:10.1128/JCM.36.1.157-160.1998
PMID:9431940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC124827/
Abstract

Simple sample-processing methods for PCR detection of Porphyromonas gingivalis, a major pathogen causing adult periodontitis, from saliva were studied. The ability to detect P. gingivalis from 118 salivary samples by PCR after boiling and Chelex 100 processing was compared with bacterial culture. P. gingivalis was detected three times more often by PCR than by culture. Chelex 100 processing of saliva proved to be effective in preventing PCR inhibition and was applied to determine the occurrence of P. gingivalis in saliva samples from 263 Finnish subjects between 5 and 80 years of age. The occurrence of P. gingivalis increased with age, and it was detected by PCR in the saliva of 5.0% of subjects between 5 and 10 years of age, 13.8% of subjects between 11 and 20 years of age, 13.4% of subjects between 21 and 30 years of age, and 63.3% of subjects between 31 and 80 years of age. The results indicate that P. gingivalis is a rare finding in saliva from periodontally healthy children and young adults but a frequent one in saliva from adult periodontitis patients.

摘要

研究了用于从唾液中PCR检测牙龈卟啉单胞菌(一种导致成人牙周炎的主要病原体)的简单样本处理方法。将煮沸和Chelex 100处理后通过PCR从118份唾液样本中检测牙龈卟啉单胞菌的能力与细菌培养法进行了比较。通过PCR检测到牙龈卟啉单胞菌的频率是培养法的三倍。事实证明,Chelex 100处理唾液可有效防止PCR抑制,并用于确定263名年龄在5至80岁之间的芬兰受试者唾液样本中牙龈卟啉单胞菌的存在情况。牙龈卟啉单胞菌的存在情况随年龄增长而增加,在5至10岁的受试者中,5.0%的人唾液中通过PCR检测到该菌;在11至20岁的受试者中,13.8%的人检测到;在21至30岁的受试者中,13.4%的人检测到;在31至80岁的受试者中,63.3%的人检测到。结果表明,牙龈卟啉单胞菌在牙周健康的儿童和年轻人的唾液中很少见,但在成人牙周炎患者的唾液中很常见。