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Clinical Performance and Trends during the First Two Months of Monkeypox Virus PCR Testing at Two United States
Nicole A P Lieberman1, Patrick C Mathias1,2, Benjamin T Bradley3,4
1Department of Laboratory Medicine and Pathology, University of Washington School of Medicinegrid.471394.c, Seattle, Washington, USA.
Journal of Clinical Microbiology
|November 21, 2022
Summary
Testing for monkeypox virus (MPXV) expanded in the US. Analysis of 10,019 tests revealed high positivity in men and adults aged 30-49, with results supporting optimized specimen collection strategies.
Area of Science:
- Virology
- Epidemiology
- Public Health
Background:
- A human-to-human monkeypox virus (MPXV) outbreak emerged globally in 2022.
- US MPXV testing expanded from public health labs to clinical settings.
- Understanding testing characteristics is crucial for outbreak management.
Purpose of the Study:
- To analyze epidemiological features of MPXV testing.
- To evaluate specimen collection practices and cycle threshold (Ct) values.
- To inform optimal testing strategies during the MPXV outbreak.
Main Methods:
- Retrospective analysis of 10,019 MPXV PCR tests from two reference laboratories.
- Examination of demographic data, positivity rates, and Ct values.
- Comparison of results based on collection method and number of specimens.
Main Results:
- High positivity rates observed in men and individuals aged 30-49.
- Overall positivity rate remained elevated (~20%) but decreased over time.
- Significant differences in Ct values noted between laboratories and collection methods.
- High concordance (>95%) when multiple specimens were collected per individual.
- Individuals aged 50-59 showed distinct viral load distribution, possibly due to prior vaccinia vaccination.
Conclusions:
- Early US MPXV testing data highlights key demographic trends.
- Ct value variations suggest impact of specimen processing and collection.
- High concordance supports limiting the number of swabs per individual to optimize resource allocation.
- Further research into age-related viral load differences is warranted.

