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通过对栀子提取物的β-葡萄糖苷酶依赖性绿色反应鉴定出致龋放线菌。

Cariogenic actinomyces identified with a beta-glucosidase-dependent green color reaction to Gardenia jasminoides extract.

作者信息

Chen L, Ma L, Park N H, Shi W

机构信息

School of Dentistry and Dental Research Institute, University of California, Los Angeles, California 90095, USA.

出版信息

J Clin Microbiol. 2001 Aug;39(8):3009-12. doi: 10.1128/JCM.39.8.3009-3012.2001.

DOI:10.1128/JCM.39.8.3009-3012.2001
PMID:11474036
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC88283/
Abstract

The oral bacteria Actinomyces naeslundii and Actinomyces viscosus are known to contribute to the initiation and progression of human dental caries, especially root caries. We report that both A. naeslundii and A. viscosus react with a component in the Gardenia jasminoides extract to produce a distinct green product. This green color reaction was found to be dependent on the bacterial beta-glucosidase. The reaction is specific for cariogenic actinomyces, and it can detect as few as 10(4) cells of A. naeslundii and A. viscosus per ml.

摘要

已知口腔细菌内氏放线菌和黏性放线菌会导致人类龋齿尤其是根龋的发生和发展。我们报告称,内氏放线菌和黏性放线菌均会与栀子提取物中的一种成分发生反应,生成一种独特的绿色产物。发现这种绿色显色反应依赖于细菌β-葡萄糖苷酶。该反应对致龋放线菌具有特异性,每毫升能检测到低至10⁴个内氏放线菌和黏性放线菌细胞。

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本文引用的文献

1
AEROBIC, GRAM-POSITIVE, FILAMENTOUS BACTERIA AS ETIOLOGIC AGENTS OF EXPERIMENTAL PERIODONTAL DISEASE IN HAMSTERS.需氧革兰氏阳性丝状菌作为仓鼠实验性牙周病的病原体
Arch Oral Biol. 1964 Jul-Aug;9:401-14. doi: 10.1016/0003-9969(64)90025-1.
2
Beta-glucosidase from Chalara paradoxa CH32: purification and properties.
J Agric Food Chem. 2000 Aug;48(8):3698-703. doi: 10.1021/jf0002591.
3
Development of multi-species consortia biofilms of oral bacteria as an enamel and root caries model system.作为牙釉质和根龋模型系统的口腔细菌多物种聚生体生物膜的开发。
Arch Oral Biol. 2000 Jan;45(1):27-40. doi: 10.1016/s0003-9969(99)00111-9.
4
The diversity and distribution of the predominant ribotypes of Actinomyces naeslundii genospecies 1 and 2 in samples from enamel and from healthy and carious root surfaces of teeth.内氏放线菌1型和2型优势核糖型在牙釉质以及牙齿健康和龋坏根面样本中的多样性与分布。
J Dent Res. 1999 Dec;78(12):1800-9. doi: 10.1177/00220345990780120601.
5
The isolation of Actinomyces naeslundii from sound root surfaces and root carious lesions.从健康牙根表面和根龋病变中分离出内氏放线菌。
Caries Res. 1998;32(2):100-6. doi: 10.1159/000016438.
6
Gaucher's disease: past, present and future.戈谢病:过去、现在与未来。
Baillieres Clin Haematol. 1997 Dec;10(4):621-34. doi: 10.1016/s0950-3536(97)80031-5.
7
Isolation and characterisation of an aryl-beta-D-glucoside uptake and utilisation system (abg) from the gram-positive ruminal Clostridium species C. longisporum.从革兰氏阳性瘤胃梭菌物种长孢梭菌中分离并鉴定一种芳基-β-D-葡萄糖苷摄取和利用系统(abg)。
Mol Gen Genet. 1998 Jan;257(2):213-8. doi: 10.1007/s004380050641.
8
Characterization of monoclonal antibodies for rapid identification of Actinomyces naeslundii in clinical samples.用于临床样本中内氏放线菌快速鉴定的单克隆抗体的特性分析
FEMS Microbiol Lett. 1997 May 15;150(2):255-62. doi: 10.1111/j.1574-6968.1997.tb10378.x.
9
Does assessment of microbial composition of plaque/saliva allow for diagnosis of disease activity of individuals?对菌斑/唾液的微生物组成进行评估能否诊断个体的疾病活动情况?
Community Dent Oral Epidemiol. 1997 Feb;25(1):76-81. doi: 10.1111/j.1600-0528.1997.tb00902.x.
10
Dental observations in Gaucher's disease: review of the literature and two case reports with 13- and 60-year follow-ups.戈谢病的口腔观察:文献综述及两例分别随访13年和60年的病例报告
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1996 Dec;82(6):650-9. doi: 10.1016/s1079-2104(96)80440-9.