›› 2000, Vol. 18 ›› Issue (3): 9-158.

• 论著 • Previous Articles     Next Articles

RAPID SCREENING WITH A RECOMBINANT ANTIGEN (rK39) FOR DIAGNOSIS OF VISCERAL LEISHMANIASIS USING DIPSTICK *

QU Jing qi 1;GUAN Li ren 1;Imamu Shulidan 2;ZUO Xin ping 2;CHAI Jun jie 2;CHEN Sheng bang 3;Shinichiro Kawazu 4;Ken Katakura 5;Yoshigeru Matsumoto 6;S. G. Reed 7 K. P. Chang 8   

  1. 1 Institute of Parasit Diseases;Chinese Academy of Preventive Medicine,shanghai 200025;2 Institute for Endemic Disease Control and Research of Xinjing Urgur Autonomous Region,Urumqi,Xinjiang,China,Urumqi 830002;3Institute for Endemic Disease Control ,Langzhou,Gansu,China,Lanzhou 730002;4 national Institute of Animal Health,Tsukuba,Japan;5Jikei University School of Medicine,Tokyo,Japan;6Tokyo University,Japan;7 Infectious disease Reserch Institute,Seattle,USA;8Chicago Medical School,North Chicago,USA
  • Received:1900-01-01 Revised:1900-01-01 Online:2000-06-30 Published:2000-06-30

Abstract:  Objective] To evaluate the diagnostic value of the recombinant antigen of 39 amino acid repeats encoded by a kinesin like gene of Leishmania changasi (rK39) in serodiagnosis of visceral leishmaniasis (VL). [Methods] In Kashi, Xinjiang, 13 VL patients with splenomegaly and bone marrow aspirate culture positive were subjected to dipstick assay. A drop of whole blood or serum from patient was placed at the absorbing pad at the bottom of the dipstick. Flooding of the bottom protein with buffer allows serum proteins to migrate upwards, producing the positive band and Western blot analysis of rK39 subsequently performed with the sera collected. [Results] The end point titers of anti rK39 antibodies of these sera were determined by ELISA and found to fall within the range of 10 -2 to 10 -4 , which were consistent with the intensity of their reaction with rK39 in dipstick assay. The positive sera could also recognize the specific rK39 band as analyzed by Western blot analysis. [Conclusion] The rK39 dipstick assay is more rapid, specific, sensitive and less invasive than the conventional methods of diagnosis for VL in the areas of low endemicity.

Key words: Visceral leishmaniasis, recombinant antigen, dipstick.