首页> 美国卫生研究院文献>Journal of Bacteriology >Identification of Actinomyces israelii and Actinomyces naeslundii by Fluorescent-Antibody and Agar-Gel Diffusion Techniques
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Identification of Actinomyces israelii and Actinomyces naeslundii by Fluorescent-Antibody and Agar-Gel Diffusion Techniques

机译:荧光抗体和琼脂-凝胶扩散技术鉴定以色列放线菌和内生放线菌

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摘要

This study was an attempt to develop a fluorescent-antibody (FA) test to differentiate Actinomyces israelii and A. naeslundii as an aid in their laboratory identification. Two strains of A. israelii (X522 and A601) and two strains of A. naeslundii (X454 and X600), which had received intensive study by several investigators, were used for the immunization of rabbits. Working titers, based on tests with antigens prepared from the homologous strains and from well-established heterologous strains, were determined for each labeled antibody preparation. These conjugates and their normal serum control conjugates were used separately to stain 85 cultures of Actinomyes species and 23 strains of other species that might be confused with them. Acetone-precipitated soluble antigens from these same strains were tested with different antisera in the agar-gel diffusion test. Results showed that A. israelii (X522 and A601) and A. naeslundii (X454 and X600) labeled antiglobulins, when used at their working titers, stained most strains of their homologous species. Agar-gel diffusion results showed general agreement with those of the FA tests. The two tests appear to be equal in sensitivity, but the FA test is more specific, since several cross-reactions were noted with the agar-gel diffusion test whereas no cross-reactions were obtained with the FA reagents. Agar-gel and FA studies suggest that at least two serotypes of A. israelii may be associated with human disease. Although the majority of strains tested in this study appear to belong to a common serotype, “serotype 1,” two strains of an apparent second serotype, “serotype 2,” were encountered. FA staining of tissue impression smears from experimentally infected mice was successful when a counterstain, Evans Blue dye, was used.
机译:这项研究是尝试开发一种荧光抗体(FA)测试以区分以色列放线菌和内伊曲霉的方法,以帮助他们进行实验室鉴定。使用了几只研究人员进行深入研究的两株以色列曲霉(X522和A601)和两株纳氏芽孢杆菌(X454和X600)进行兔免疫。对于每种标记的抗体制剂,基于对由同源菌株和成熟的异源菌株制备的抗原的测试,确定了工作效价。这些结合物及其正常血清对照结合物分别用于对85种放线菌菌种和23种可能与它们混淆的菌株进行染色。在琼脂凝胶扩散试验中,用不同的抗血清测试了来自这些相同菌株的丙酮沉淀的可溶性抗原。结果显示,当按工作效价使用时,以色列A.(X522和A601)和naeslundii(X454和X600)标记的抗球蛋白会染色大多数其同源菌种。琼脂凝胶扩散结果表明与FA测试的结果基本一致。两种测试的灵敏度似乎相同,但FA测试更为特异性,因为在琼脂凝胶扩散测试中发现了几种交叉反应,而使用FA试剂则没有交叉反应。琼脂凝胶和FA研究表明,至少有两种血清型的以色列曲霉可能与人类疾病有关。尽管在这项研究中测试的大多数菌株似乎属于同一血清型,即“血清型1”,但遇到了两种明显的第二血清型“菌株2”的菌株。当使用复染剂Evans Blue染料时,来自实验感染小鼠的组织印象涂片的FA染色成功。

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