Effect of High Temperature Exposure and Laboratory Processing Techniques on the Diagnostic Performance of Dry Swabs for the Detection of African Swine Fever Virus

One of the key surveillance strategies for the early detection of an African swine fever (ASF) incursion into a country is the sampling of wild or feral pig populations. In Australia, the remote northern regions are considered a risk pathway for ASF incursion due to the combination of high numbers o...

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Main Authors: Leonard Izzard, David T. Williams, Peter A. Durr
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Viruses
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Online Access:https://www.mdpi.com/1999-4915/16/12/1812
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author Leonard Izzard
David T. Williams
Peter A. Durr
author_facet Leonard Izzard
David T. Williams
Peter A. Durr
author_sort Leonard Izzard
collection DOAJ
description One of the key surveillance strategies for the early detection of an African swine fever (ASF) incursion into a country is the sampling of wild or feral pig populations. In Australia, the remote northern regions are considered a risk pathway for ASF incursion due to the combination of high numbers of feral pigs and their close proximity to countries where ASF is present. These regions primarily consist of isolated arid rangelands with high average environmental temperatures. A specific objective of this study was to assess whether the exposure of swabs to the high temperatures that may be encountered in outback Australia, over an extended period, would reduce the diagnostic sensitivity (DSe) of real-time PCR (qPCR) to detect ASF virus (ASFV). We found that the extended heat exposure (up to 45 °C) of FLOQSwabs or GenoTube swabs, either prior to blood sampling or post sampling, showed no reduction in the DSe of the ASFV qPCR compared to swabs stored at room temperature (~21 °C). We also assessed an improved DNA extraction method for samples collected using GenoTube swabs to obtain DSe results comparable to FLOQSwabs. Taken together, these experiments demonstrate that dry swabs can provide the basis for an effective low-cost surveillance system for ASF in situations where extended exposure to high environmental temperatures is unavoidable.
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spelling doaj-art-8ebd7ae15bc14022a158cf2bee78bd532025-08-20T02:43:46ZengMDPI AGViruses1999-49152024-11-011612181210.3390/v16121812Effect of High Temperature Exposure and Laboratory Processing Techniques on the Diagnostic Performance of Dry Swabs for the Detection of African Swine Fever VirusLeonard Izzard0David T. Williams1Peter A. Durr2CSIRO, Australian Centre for Disease Preparedness (ACDP), Geelong, VIC 3220, AustraliaCSIRO, Australian Centre for Disease Preparedness (ACDP), Geelong, VIC 3220, AustraliaCSIRO, Australian Centre for Disease Preparedness (ACDP), Geelong, VIC 3220, AustraliaOne of the key surveillance strategies for the early detection of an African swine fever (ASF) incursion into a country is the sampling of wild or feral pig populations. In Australia, the remote northern regions are considered a risk pathway for ASF incursion due to the combination of high numbers of feral pigs and their close proximity to countries where ASF is present. These regions primarily consist of isolated arid rangelands with high average environmental temperatures. A specific objective of this study was to assess whether the exposure of swabs to the high temperatures that may be encountered in outback Australia, over an extended period, would reduce the diagnostic sensitivity (DSe) of real-time PCR (qPCR) to detect ASF virus (ASFV). We found that the extended heat exposure (up to 45 °C) of FLOQSwabs or GenoTube swabs, either prior to blood sampling or post sampling, showed no reduction in the DSe of the ASFV qPCR compared to swabs stored at room temperature (~21 °C). We also assessed an improved DNA extraction method for samples collected using GenoTube swabs to obtain DSe results comparable to FLOQSwabs. Taken together, these experiments demonstrate that dry swabs can provide the basis for an effective low-cost surveillance system for ASF in situations where extended exposure to high environmental temperatures is unavoidable.https://www.mdpi.com/1999-4915/16/12/1812ASFVswabsurveillanceheatDSe
spellingShingle Leonard Izzard
David T. Williams
Peter A. Durr
Effect of High Temperature Exposure and Laboratory Processing Techniques on the Diagnostic Performance of Dry Swabs for the Detection of African Swine Fever Virus
Viruses
ASFV
swab
surveillance
heat
DSe
title Effect of High Temperature Exposure and Laboratory Processing Techniques on the Diagnostic Performance of Dry Swabs for the Detection of African Swine Fever Virus
title_full Effect of High Temperature Exposure and Laboratory Processing Techniques on the Diagnostic Performance of Dry Swabs for the Detection of African Swine Fever Virus
title_fullStr Effect of High Temperature Exposure and Laboratory Processing Techniques on the Diagnostic Performance of Dry Swabs for the Detection of African Swine Fever Virus
title_full_unstemmed Effect of High Temperature Exposure and Laboratory Processing Techniques on the Diagnostic Performance of Dry Swabs for the Detection of African Swine Fever Virus
title_short Effect of High Temperature Exposure and Laboratory Processing Techniques on the Diagnostic Performance of Dry Swabs for the Detection of African Swine Fever Virus
title_sort effect of high temperature exposure and laboratory processing techniques on the diagnostic performance of dry swabs for the detection of african swine fever virus
topic ASFV
swab
surveillance
heat
DSe
url https://www.mdpi.com/1999-4915/16/12/1812
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