Hostname: page-component-8448b6f56d-cfpbc Total loading time: 0 Render date: 2024-04-23T11:03:34.918Z Has data issue: false hasContentIssue false

Serodiagnosis of Japanese encephalitis among Nepalese patients by the particle agglutination assay

Published online by Cambridge University Press:  07 October 2003

B. PANDEY
Affiliation:
Department of Molecular Epidemiology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan Sukra Raj Tropical and Infectious Disease Hospital, Teku, Kathmandu, Nepal
A. YAMAMOTO
Affiliation:
New Ceramics Department, Asahi Optical Co. Ltd., Tokyo, Japan Department of Virology 1, National Institute of Infectious Diseases, Tokyo, Japan
K. MORITA
Affiliation:
Department of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan
Y. KUROSAWA
Affiliation:
New Ceramics Department, Asahi Optical Co. Ltd., Tokyo, Japan
S. RAI
Affiliation:
Department of Microbiology, Nepal Medical College, Kathmandu, Nepal
S. ADHIKARI
Affiliation:
Department of Microbiology, Tribhuban University, Kathmandu, Nepal
P. KANDEL
Affiliation:
Department of Microbiology, Tribhuban University, Kathmandu, Nepal
I. KURANE
Affiliation:
Department of Virology 1, National Institute of Infectious Diseases, Tokyo, Japan
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Japanese encephalitis (JE) is a serious health problem in the southwestern region of Nepal. Serological diagnostic kits for routine diagnostic use in this region have not been available. This study was performed to examine if the particle agglutination (PA) assay for Japanese encephalitis virus (JEV) IgM could be applicable to the samples collected in Nepal and also to evaluate the accuracy of clinical diagnosis of JE. One hundred and ninety-three blood samples were collected from the patients clinically diagnosed with JE or other infectious diseases in the JE-endemic, southwestern region of Nepal, in 2000. The PA assay was performed on these 193 serum samples and the results were compared with those by IgM-capture ELISA. Eighty-six samples were IgM-positive by the PA assay, and 71 of 86 were also positive by IgM-capture ELISA (sensitivity, 99%; specificity, 88%; positive predictive value, 0·82; negative predictive value, 0·99). These results suggest that the PA assay is a simple, reliable and useful diagnostic test to support clinical diagnosis in rural hospitals of Asia including Nepal.

Type
Research Article
Copyright
2003 Cambridge University Press