The implementation of a rapid sample preparation method for the detection of SARS-CoV-2 in a diagnostic laboratory in South Africa.
Gert J K MaraisMichelle NaidooNei-Yuan HsiaoZiyaad Valley-OmarHeidi SmutsDiana HardiePublished in: PloS one (2020)
The SARS-CoV-2 pandemic has resulted in shortages of both critical reagents for nucleic acid purification and highly trained staff as supply chains are strained by high demand, public health measures and frequent quarantining and isolation of staff. This created the need for alternate workflows with limited reliance on specialised reagents, equipment and staff. We present here the validation and implementation of such a workflow for preparing samples for downstream SARS-CoV-2 RT-PCR using liquid handling robots. The rapid sample preparation technique evaluated, which included sample centrifugation and heating prior to RT-PCR, showed a 97.37% (95% CI: 92.55-99.28%) positive percent agreement and 97.30% (95% CI: 90.67-99.52%) negative percent agreement compared to nucleic acid purification-based testing. This method was subsequently adopted as the primary sample preparation method in the Groote Schuur Hospital Virology Diagnostic Laboratory in Cape Town, South Africa.
Keyphrases
- sars cov
- south africa
- nucleic acid
- public health
- hiv positive
- respiratory syndrome coronavirus
- loop mediated isothermal amplification
- healthcare
- primary care
- molecularly imprinted
- real time pcr
- long term care
- quality improvement
- coronavirus disease
- emergency department
- hiv infected
- acute care
- resistance training
- hepatitis c virus
- simultaneous determination