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简短报告:杜氏利什曼原虫重组驱动蛋白相关蛋白的制备及其在内脏利什曼病血清诊断中的应用

Short report: production of recombinant kinesin-related protein of Leishmania donovani and its application in the serodiagnosis of visceral leishmaniasis.

作者信息

Takagi Hidekazu, Islam Mohammad Zahidul, Itoh Makoto, Islam Anwar Ul, Saifuddin Ekram A R M, Hussain Sultana Monira, Hashiguchi Yoshihisa, Kimura Eisaku

机构信息

Department of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan.

出版信息

Am J Trop Med Hyg. 2007 May;76(5):902-5.

Abstract

To detect IgG antibody in the serodiagnosis of visceral leishmaniasis (VL), a recombinant antigen rK39, which is part of a Leishmania chagasi kinesin-related protein, has been used successfully and showed high sensitivity and specificity. We report production of a recombinant protein rKRP42, which is part of an L. donovani kinesin-related protein and a homolog of rK39, and its application in an enzyme-linked immunosorbent assay (ELISA) for the diagnosis of VL. When rKRP42 and rK39 were compared, amino acid sequence analysis showed 89.3% identity and 98.7% homology, with rKRP42 having 39 more amino acids than rK39. The ELISA using rKRP42 showed a sensitivity of 94.6% (70 positive samples among 74 from VL patients) and a specificity of 99.3% (148 negative samples among 149 samples from Japanese controls), whereas the sensitivity of the commercial rK39 dipstick test was 93.2% (69 positive samples among 74 from patients with VL). The rKRP42 is a promising new antigen in developing immunodiagnostic methods for VL.

摘要

为了在内脏利什曼病(VL)的血清学诊断中检测IgG抗体,一种重组抗原rK39已成功应用,它是恰加斯利什曼原虫一种驱动蛋白相关蛋白的一部分,具有高敏感性和特异性。我们报道了一种重组蛋白rKRP42的制备,它是杜氏利什曼原虫驱动蛋白相关蛋白的一部分,是rK39的同源物,并将其应用于酶联免疫吸附测定(ELISA)诊断VL。当比较rKRP42和rK39时,氨基酸序列分析显示二者具有89.3%的同一性和98.7%的同源性,rKRP42比rK39多39个氨基酸。使用rKRP42的ELISA显示敏感性为94.6%(74例VL患者样本中有70例阳性),特异性为99.3%(149例日本对照样本中有148例阴性),而商用rK39试纸条检测的敏感性为93.2%(74例VL患者样本中有69例阳性)。rKRP42是开发VL免疫诊断方法中一种有前景的新抗原。

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