Evaluation of Aggregate Oral Fluid Sampling for Early Detection of African Swine Fever Virus Infection

  • Bonto Faburay
  • , Kathleen O’Hara
  • , Marta Remmenga
  • , Theophilus Odoom
  • , Sherry Johnson
  • , William Tasiame
  • , Matilda Ayim-Akonor
  • , Benita Anderson
  • , Kingsley Kwabena Amoako
  • , Diane Holder
  • , Wu Ping
  • , Michelle Zajac
  • , Vivian O’Donnell
  • , Lizhe Xu
  • , Robin Holland
  • , Corrie Brown
  • , Randall Levings
  • , Suelee Robbe-Austerman

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

African swine fever (ASF) needs to be controlled, and prevention of the spread of African swine fever virus (ASFV) is dependent on enhanced surveillance and early disease detection. Commercial swine operations, especially in North America, Europe, and Asia, are characterized by comparatively large numbers of pigs, and sampling individual pigs, which represents the main strategy for current ASF surveillance, can be both costly and labor intensive. A study performed in Ghana was designed to estimate the diagnostic sensitivity of pen-based aggregate oral fluid testing for ASFV in infected pigs in a pen of 30 animals and to evaluate its utility as a tool to support surveillance of ASF in the US. This study was performed in three phases: (i) virus (Ghana ASFV24) amplification in a target host species to generate the challenge inoculum; (ii) titration of the inoculum (10% spleen homogenate) in target host species to determine the minimum dose inducing acute ASF in pigs with survival up to 5–6 days post-inoculation (dpi); and (iii) the main study, involving 186 pigs, consisting of 6 replicates of 30 pigs per pen and one seeder pig inoculated with wildtype ASFV (highly virulent genotype II) per pen. Daily sampling of aggregate oral fluids, uncoagulated blood, oropharyngeal swabs, fecal and water nipple swabs, and recording of rectal temperatures and clinical observations was carried out. The seeder pigs were each inoculated intramuscularly with 0.5 mL of the 10% spleen homogenate, which induced the desired clinical course of ASF in the pigs, with survival of up to 6 dpi. ASFV DNA was detected in the seeder pigs as early as 1 dpi and 2 dpi in the blood and oropharyngeal swabs, respectively. Transmission of ASFV from the seeder pigs to the contact pig population was detected via positive amplification of ASFV DNA in aggregate oral fluid samples at 3 days post-contact (dpc) in 4 out of 6 pens, and in all 6 pens, at 4 dpc. Testing of oropharyngeal swabs and blood samples from individual pigs revealed a variable number of ASFV-positive pigs between 3 and 5 dpc, with detection of 100% positivity between 6 and 18 dpc, the study endpoint. These findings demonstrate the potential utility of aggregate oral fluid sampling for sensitive and early detection of ASFV incursion into naïve swine herds. It also demonstrates that testing of environmental samples from the premises could further enhance overall ASF early detection and surveillance strategies.

Original languageEnglish
Article number1089
JournalViruses
Volume17
Issue number8
DOIs
Publication statusPublished - Aug 2025

Keywords

  • African swine fever
  • African swine fever virus
  • aggregate oral fluid
  • blood
  • oropharyngeal swabs
  • surveillance

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