Gentilomi G, Zerbini M, Musiani M, Gallinella G, Gibellini D, Venturoli S, Re M C, Pileri S, Finelli C, La Placa M
Institute of Microbiology, University of Bologna, Italy.
Mol Cell Probes. 1993 Feb;7(1):19-24. doi: 10.1006/mcpr.1993.1003.
An in situ hybridization assay using a digoxigenin-labelled probe was developed to detect B19 DNA in bone marrow erythroid elements of immunodeficient patients with hypoplastic anaemia. A 700 bp Bam HI-Hin dIII fragment of B19 DNA was used to construct the probe by incorporating deoxyuridine triphosphate labelled with digoxigenin. The in situ hybridized B19 DNA probe was visualized by an immunoenzymatic reaction using antidigoxigenin Fab fragments labelled with alkaline phosphatase. Dark blue coloured inclusions at the enzyme site were detected in the nuclei of B19 infected erythroid cells at different stages of cell differentiation. Six out of the nine patients studied showed a positive reaction by in situ hybridization assay. The assay we developed proved highly specific and sensitive and it appears to be a suitable diagnostic test for investigating the possible role of B19 infection as a cause of haematopoietic disorders in immunocompromised hosts.
开发了一种使用地高辛素标记探针的原位杂交检测方法,以检测免疫缺陷性再生障碍性贫血患者骨髓红系细胞中的B19 DNA。通过掺入用地高辛素标记的三磷酸脱氧尿苷,使用B19 DNA的700 bp Bam HI-Hin dIII片段构建探针。使用碱性磷酸酶标记的抗地高辛素Fab片段通过免疫酶反应使原位杂交的B19 DNA探针可视化。在细胞分化不同阶段的B19感染红系细胞核中,在酶位点检测到深蓝色包涵体。所研究的9名患者中有6名通过原位杂交检测呈阳性反应。我们开发的检测方法被证明具有高度特异性和敏感性,似乎是一种合适的诊断测试,可用于研究B19感染作为免疫受损宿主造血障碍原因的可能作用。