Some immunohistochemical experiments aiming at the electron-microscopic in situ identification of a dental plaque microorganism--Streptococcus mutans.

P Berthold, C H Berthold
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Abstract

The aim of the present investigation was to test a procedure useful for the electron-microscopic in situ identification of the presumptive cariogenic microorganism Streptococcus mutans (serotype d) growing in the human dental plaque. For this purpose, different parameters of an indirect immunohistochemical method were tested in three sets of experiments. In experiment set I, all serological and histochemical procedures were performed en bloc on specimens fixed only with glutaraldehyde before embedding in Vestopal W. Different marking substances, such as ferritin, alkaline phosphatase and horseradish peroxidase (HRP) were tested. The en bloc method using HRP-labelled antibodies was found useful for staining of in vitro-grown bacteria but failed when applied to dental plaque. In experiment set II, ultrathin sections of glutaraldehyde-fixed and glycol methacrylate-embedded in vitro-grown bacteria were section-stained. The bacteria became outlined with a highly electron-dense HRP reaction product which accumulated on top of the cell envelope. The same type of HRP reaction product was found on some bacteria in the 2-day-old dental plaque after section-staining. This system was further tested in a series of controls also using consecutive serial sections. In exp. set III, a number of different stationary and transient oral bacteria were immunohistochemically section-stained. A cross-reaction with bacteria belonging to S.salivarius was discovered and removed by absorbing the anti-S.mutans serotype d serum with S.salivarius (NCTC 8618).

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针对一种牙菌斑微生物变形链球菌的电镜原位鉴定的免疫组化实验。
本研究的目的是测试一种有用的程序,用于电子显微镜原位鉴定在人类牙菌斑中生长的假定的致龋微生物变形链球菌(血清型d)。为此,采用间接免疫组织化学方法对不同参数进行了三组实验。实验组1在Vestopal w包埋前,对仅用戊二醛固定的标本进行整体血清学和组织化学检查,检测不同标记物质,如铁蛋白、碱性磷酸酶和辣根过氧化物酶(HRP)。使用hrp标记抗体的整体方法被发现对体外培养的细菌染色有用,但不适用于牙菌斑。实验二采用戊二醛固定的超薄切片和甲基丙烯酸乙二醇酯包埋体外培养细菌的超薄切片进行切片染色。细菌被一种电子密度很高的HRP反应产物勾勒出来,这些产物积聚在细胞包膜的顶部。在2 d牙菌斑切片染色后,在部分细菌上发现了相同类型的HRP反应产物。该系统在一系列对照中进行了进一步的测试,也使用了连续的串行分段。在实验组III中,免疫组织化学切片染色了许多不同的固定和瞬时口腔细菌。发现了与唾液链球菌属细菌的交叉反应,并通过吸收抗s。用唾液链球菌(NCTC 8618)诱变血清d型血清。
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