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PRODUCTION OF RECOMBINANT KINESIN-RELATED PROTEIN OF LEISHMANIA DONOVANI AND ITS APPLICATION IN THE SERODIAGNOSIS OF VISCERAL LEISHMANIASIS

HIDEKAZU TAKAGIDepartment of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan; Department of Pharmacy, University of Rajshahi, Rajshahi, Bangladesh; Department of Medicine, Rajshahi Medical College, Rajshahi, Bangladesh; Encephalitis Surveillance in Bangladesh, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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MOHAMMAD ZAHIDUL ISLAMDepartment of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan; Department of Pharmacy, University of Rajshahi, Rajshahi, Bangladesh; Department of Medicine, Rajshahi Medical College, Rajshahi, Bangladesh; Encephalitis Surveillance in Bangladesh, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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MAKOTO ITOHDepartment of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan; Department of Pharmacy, University of Rajshahi, Rajshahi, Bangladesh; Department of Medicine, Rajshahi Medical College, Rajshahi, Bangladesh; Encephalitis Surveillance in Bangladesh, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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ANWAR UL ISLAMDepartment of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan; Department of Pharmacy, University of Rajshahi, Rajshahi, Bangladesh; Department of Medicine, Rajshahi Medical College, Rajshahi, Bangladesh; Encephalitis Surveillance in Bangladesh, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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A. R. M. SAIFUDDIN EKRAMDepartment of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan; Department of Pharmacy, University of Rajshahi, Rajshahi, Bangladesh; Department of Medicine, Rajshahi Medical College, Rajshahi, Bangladesh; Encephalitis Surveillance in Bangladesh, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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SULTANA MONIRA HUSSAINDepartment of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan; Department of Pharmacy, University of Rajshahi, Rajshahi, Bangladesh; Department of Medicine, Rajshahi Medical College, Rajshahi, Bangladesh; Encephalitis Surveillance in Bangladesh, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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YOSHIHISA HASHIGUCHIDepartment of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan; Department of Pharmacy, University of Rajshahi, Rajshahi, Bangladesh; Department of Medicine, Rajshahi Medical College, Rajshahi, Bangladesh; Encephalitis Surveillance in Bangladesh, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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EISAKU KIMURADepartment of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi, Japan; Department of Pharmacy, University of Rajshahi, Rajshahi, Bangladesh; Department of Medicine, Rajshahi Medical College, Rajshahi, Bangladesh; Encephalitis Surveillance in Bangladesh, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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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.

Author Notes

Reprint requests: Hidekazu Takagi, Department of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi-ken 480-1195, Japan, Telephone: 81-52-264-4811, Fax: 81-561-63-3645, E-mail: htakagi@aichi-med-u.ac.jp.
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