Anti-WNV IgG

Useful For

 

Presumptive diagnosis of West Nile virus infection

 

Reflex Tests

 

Reporting Name

Available Separately

Always Performed

WNV Antibody IgG YES YES
WNV Antibody IgM YES YES
Plaque Reduction Neutralization Test (PRNT) NO NO

 

Testing Algorithm

 

WNV IgG and /or IgM reactive specimens will be confirmed by Plaque Reduction Neutralization Test (PRNT).

 

Indications for Testing

 

Aid in the differential diagnosis of meningoencephalitis presenting during mosquito season (in Newfoundland & Labrador mosquito season is typically June through December), otherwise in returning travelers from endemic countries.

 

This assay is not intended as a screening tool and should only be interpreted in the context of clinically established meningoencephalitis.

 

Special Instructions and Forms

 

Completion of relevant patient/travel history on laboratory requisition is mandatory for testing to proceed.

 

Clinical Information

 

Most people who are infected with WNV will not have any type of illness. It is estimated that about 20% of those who become infected will develop West Nile fever with mild symptoms, including fever, headache, myalgia, and occasionally a skin rash on the trunk of the body. About 1 of 150 WNV infections (<1%) result in meningitis or encephalitis. Case fatality rates among patients hospitalized during recent outbreaks have ranged from 4% to 14%. Advanced age is the most important risk factor for death, and patients older than 70 years of age are at particularly high risk.

 

Laboratory diagnosis is best achieved by demonstration of specific IgG and IgM class antibodies in serum specimens. PCR can detect WNV RNA in specimens from patients with WNV infection when specific antibodies to the virus are not present. However, the likelihood of detection is relatively low as the sensitivity of PCR detection is approximately 55% in cerebrospinal fluid and approximately 10% in blood, from patients with known WNV infection.

 

West Nile virus (WNV) is a mosquito-borne flavivirus (single-stranded RNA) that primarily infects birds but occasionally infects horses and humans. WNV was first isolated in 1937 from an infected person in the West Nile district of Uganda. Until the viral infection was recognized in 1999 in birds in New York City, WNV was found only in the Eastern Hemisphere, with wide distribution in Africa, Asia, the Middle East, and Europe. In 2002, a total of 3,389 human cases of WNV infection were reported from 37 states (794 cases in Illinois); 2,354 (69%) presented with meningoencephalitis, 704 (21%) had West Nile fever, and 331 (10%) had an unspecified illness. Overall, the WNV epidemic in the United States was the largest arboviral meningoencephalitis outbreak documented in the Western hemisphere. In addition, 33 cases of probable WNV infection occurred among persons who had received blood components in the month before illness onset.

 

Reference Values

 

Non-reactive

 

Interpretation

 

Anti-WNV IgG

 

REACTIVE: Presence of specific IgG class antibodies in a serum specimen indicates past or current infection or exposure to WNV or another flavivirus. Antigenic cross-reactivity with cytomegalovirus (CMV), enterovirus (in children) and/or bunyaviruses can occur. Due to flavivirus cross-reactivity persons previously infected with or vaccinated against other flaviviruses (Japanese encephalitis virus, dengue virus, yellow fever virus) may yield REACTIVE results, interpret with caution.

 

NON-REACTIVE: Absence of IgG class antibodies is presumptive evidence that the patient was not infected with West Nile Virus or another flavivirus. Specimens drawn early in the disease progression may be negative for IgG-specific antibodies to WNV. If WNV infection is suspected, a second specimen drawn approximately 7 – 14 days later should be tested. By week 3 postinfection, virtually all infected persons should have developed IgG antibodies to WNV. If acute-phase infection is suspected, serum specimens drawn within approximately 7 days postinfection should be compared with a specimen drawn approximately 14 to 21 days after infection to demonstrate rising IgG antibody levels between the 2 serum specimens (notify laboratory).

 

INDETERMINATE: The specimen tested near the cut-off. A follow-up specimen 2 – 3 weeks later should be submitted.

 

Clinical Reference

 

Focus Diagnostics. 2004. West Nile Virus IgG DxSelect™, Enzyme-linked Immunosorbent Assay (ELISA): package insert. Focus Diagnostics, Cypress, CA.

 

Lanciotti, R. S., and Tsai, T. F. 2007. Arboviruses, p. 1486-1500. In Murray, P. R., Baron, E. J., Jorgensen, J. H., Landry, M. L., and Pfaller, M. A. Manual of Clinical Microbiology, 9th ed., vol. 2. ASM Press, American Society for Microbiology, Washington, DC.

 

Vaughn, D. W., Barrett, A., and Solomon, T. 2010. Flaviviruses (Yellow Fever, Dengue, Dengue Hemorrhagic Fever, Japanese Encephalitis, West Nile Encephalitis, St. Louis Encephalitis, Tick-Borne Encephalitis), p. 2133-2156. In Mandell, D., Bennett, J. E., and Dolin, R. Principles and practice of infectious diseases, 7th ed., vol. 2. Churchill Livingstone, Elsevier, Philadelphia, PA.

 

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