Detection of Antibodies Directed Towards Japanese Encephalitis Virus by PRNT

Serological detection of neutralizing antibodies directed towards Japanese encephalitis (JE) virus by Plaque Reduction Neutralization Test (PRNT).

Serology

Japanese Encephalitis virus (JE)

Arbovirus, Rabies, Rickettsia and Related Zoonotic Diseases

• Japanese encephalitis

Serum. Minimum volume of 250 µl required.

2 mL screw cap tubes.

Store samples refrigerated until shipped for testing. Ship samples on cold pack, or with wet or dry ice.

Shipping of specimens shall be done by a TDG certified individual in accordance with TDG regulations. For additional information regarding classification of specimens for the purposes of shipping, consult either Part 2 Appendix 3 of the TDG Regulations or section 3.6.2 of the IATA Dangerous Goods Regulations as applicable.

 

Suspected JEV infection. Submitted samples will first be analysed by the Viral Zoonoses Diagnostic Laboratory by JEV HI to determine if the patient has developed anti-JEV antibodies.  Samples that are reactive can be further analysed for the presence of neutralizing antibodies.  Samples that are HI non-reactive (negative) will not be tested by PRNT.

Completed Viral Zoonoses requisition including sender laboratory name, address and telephone number. Patient name and / or identifier (specimen reference number), date of birth, test(s) requested, collection date of specimen, date of on-set of symptoms, and clinical and travel history of patient.

This is not a routine test.  Please contact the Viral Zoonoses Diagnostic Laboratory before sending specimens.

This test is considered investigational as it has not been extensively validated or verified.

Testing is performed, in whole or in part, using a lab-developed test which has not been fully validated/verified due to a lack of well-characterized panel.

The detection of IgG antibodies in a single serum sample is indicative of past or present exposure to this virus. A 4 fold rise or greater in neutralizing antibody titre, or seroconversion in paired sera, is required to document a "confirmed case" of infection.

IgM can persist in serum for up to a year or more after arbovirus exposure.  Thus, detection of IgM by itself is not sufficient for confirmation of acute infection, but is consistent with an exposure at an undetermined time.

Isolation of an arbovirus or detection of nucleic acid by real-time RT-PCR in a clinical specimen provides clear evidence of infection associated with the current clinical illness.

 

14 calendar days after the completion of JE virus HI testing.

1. WHO. 2007. Guidelines for plaque reduction neutralization testing of human antibodies to dengue viruses

Pathogen Safety Data Sheets: Infectious Substances – Japanese encephalitis virus

For health professionals: Japanese encephalitis

Japanese encephalitis