Key result
PenCheck lateral flow assay detects African swine fever virus at PCR values below 23 Ct.
Why the study?
Rapid and inexpensive detection tools for African swine fever virus are needed for field samples in remote areas with limited laboratory access during outbreaks or surveillance.
Observational
May aid rapid ASFV screening at high loads; leaves open validation versus PCR across infection stages.
Antibody-based lateral flow assay (LFA) is a quick and inexpensive tool used to detect pathogens in field samples, especially in hard-to-reach remote areas that may have limited access to central laboratories during an outbreak or surveillance. In this study, we investigated the ability of a commercially available LFA, PenCheck®, to detect African swine fever virus (ASFV) in clinical samples derived from pigs infected with highly virulent ASFV strains. The assay was specific and positively identified the majority of pigs showing high fever during the early stages (between 3 and 5 days) of infection. PenCheck® LFA also detected ASFV in serum and tissue samples collected from pigs that succumbed to experimental ASFV infection and whole blood, plasma, and tissue samples from the field. The limit of detection of the assay was ASFV titer 107.80 TCID50/mL, corresponding to ASFV real-time PCR values below 23 Ct. Although the sensitivity of the assay is less than that of the laboratory-based real-time PCR assays, the results obtained with the PenCheck® LFA in this study suggest that it can be used as a herd-level, field-deployable, and easy-to-use diagnostic tool to identify ASF-affected farms when access to portable molecular assays or central laboratories is not possible.
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Onyilagha et al. (2022) conducted an observational in African swine fever virus (ASFV) infection. PenCheck® lateral flow assay vs. Laboratory-based real-time PCR assays was evaluated on Limit of detection of ASFV. The PenCheck® lateral flow assay detected African swine fever virus in clinical samples with a limit of detection of 10^7.80 TCID50/mL, corresponding to real-time PCR values below 23 Ct.
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