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Enzyme-linked Immunosorbent Assay to Detect Urinary Antibody Against Recombinant rKRP42 Antigen Made from Leishmania donovani for the Diagnosis of Visceral Leishmaniasis

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; 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; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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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; 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; 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; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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Ajijur RahmanDepartment 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; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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Atsuhide TakesueDepartment 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; 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; 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; Department of Parasitology, Kochi Medical School, Kochi University, Nankoku, Japan

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We recently reported the production of the recombinant kinesin-related protein of Leishmania donovani with a molecular weight of 42 kd (rKRP42) and the value of the antigen in serum-based ELISA for the diagnosis of visceral leishmaniasis (VL). In this study, the rKRP42 antigen was validated with ELISA using urine samples (rKRP42 urine ELISA). The urine-based ELISA showed 94% sensitivity (108 positives among 115 VL samples) and 99.6% specificity (239 negatives among 240 non-VL samples). The sensitivity and specificity are almost similar to our previous results by ELISA with acetone-treated L. donovani promastigote antigen and direct agglutination test, both methods being done by use of urine samples. A comparison of the rKRP42 urine ELISA with the commercially available urinary antigen detection kit (KAtex) using 108 VL samples showed much higher sensitivity of the ELISA (96.3%) than KAtex (55.6%). The use of the rKRP42 antigen with urine samples will facilitate epidemiologic studies.

Author Notes

Reprint requests: Mohammad Zahidul Islam, Department of Parasitology, Aichi Medical University School of Medicine, Nagakute, Aichi-ken 480-1195, Japan, E-mails: zahid@aichi-med-u.ac.jp and islammz@yahoo.com.
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