Detection of North American West Nile Virus in Animal Tissue by a Reverse Transcription-Nested Polymerase Chain Reaction Assay
2001

Detecting West Nile Virus in Horses and Birds

Sample size: 128 publication Evidence: high

Author Information

Author(s): Donna J. Johnson, Eileen N. Ostlund, Douglas D. Pedersen, Beverly J. Schmitt

Primary Institution: Animal and Plant Health Inspection Service, U. S. Department of Agriculture, Ames, Iowa, USA

Hypothesis

The RT-nested PCR (RT-nPCR) procedure can accurately detect West Nile virus in equine and avian tissues.

Conclusion

The RT-nPCR method is a rapid and reliable way to detect West Nile virus in equine and avian tissues, proving to be significantly more sensitive than traditional methods.

Supporting Evidence

  • The RT-nPCR method was confirmed to be 1,000-fold more sensitive than cell culture for detecting the virus.
  • All RT-nPCR-positive brain samples were confirmed by virus isolation except three equine brain tissues.
  • Positive RT-nPCR results were obtained from tissues from some positive birds.

Takeaway

Scientists created a new test to find a virus in horses and birds that is usually hard to detect, and it works much better than older tests.

Methodology

The study used RT-nested PCR to detect West Nile virus in equine and avian tissues, comparing results with traditional virus isolation methods.

Potential Biases

The nested PCR procedure may lead to cross-contamination due to additional manipulation of reaction tubes.

Limitations

The study noted that equine blood-derived samples and CSF samples were not reliable for detecting the virus.

Participant Demographics

Equine samples included brain, blood, and cerebrospinal fluid from suspect WN virus-infected horses, and avian samples included brain tissues from various birds.

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