Musiani M, Roda A, Zerbini M, Gentilomi G, Pasini P, Gallinella G, Venturoli S
Institute of Microbiology, University of Bologna, Italy.
J Clin Microbiol. 1996 May;34(5):1313-6. doi: 10.1128/jcm.34.5.1313-1316.1996.
A chemiluminescence in situ hybridization method was developed for the search of B19 parvovirus DNA in bone marrow cells, employing digoxigenin-labeled B19 DNA probes, immunoenzymatically detected with a highly sensitive 1,2-dioxetane phosphate as chemiluminescent substrate. The light emitted from the in situ-hybridized probe was analyzed and measured by a high-performance luminograph connected to an optical microscope and to a personal computer for the quantification of the photon fluxes from the single cells and for image analysis. The chemiluminescence in situ hybridization was applied to bone marrow cell smears of patients with aplastic crisis or hypoplastic anemia, who had been previously tested by in situ hybridization with colorimetric detection, dot blot hybridization, and nested PCR. The chemiluminescent assay provided an objective estimation of the data, proved specific, and showed an increased sensitivity in detecting B19 DNA compared with in situ hybridization with colorimetric detection.
开发了一种化学发光原位杂交方法,用于在骨髓细胞中检测B19细小病毒DNA,该方法采用地高辛配体标记的B19 DNA探针,以高灵敏度的1,2 - 二氧杂环丁烷磷酸酯作为化学发光底物进行免疫酶检测。通过连接到光学显微镜和个人计算机的高性能发光仪分析和测量原位杂交探针发出的光,以定量单细胞的光子通量并进行图像分析。将化学发光原位杂交应用于再生障碍危象或增生低下性贫血患者的骨髓细胞涂片,这些患者之前已通过比色检测原位杂交、斑点印迹杂交和巢式PCR进行过检测。化学发光检测提供了客观的数据评估,证明具有特异性,并且与比色检测原位杂交相比,在检测B19 DNA方面显示出更高的灵敏度。