Validation of a direct multiplex real-time reverse transcription PCR assay for rapid detection of African swine fever virus using swine field samples in Vietnam

BMC Res Notes. 2024 Sep 2;17(1):240. doi: 10.1186/s13104-024-06898-2.

Abstract

Objective: This study validates a direct multiplex real-time reverse transcription polymerase chain reaction (rRT-PCR) assay which was previously established for enabling rapid and simultaneous detection of African swine fever (ASF) virus (ASFV) and classical swine fever virus. The assay eliminates the need for viral nucleic acid purification using a buffer system for crude extraction and an impurity-tolerant enzyme. However, the assay had not yet been validated using field samples of ASFV-infected pigs. Therefore, to address this gap, we tested 101 samples collected from pigs in Vietnam during 2018 and 2021 for validation.

Results: The rRT-PCR assay demonstrated a diagnostic sensitivity of 98.8% and a specificity of 100%. Remarkably, crude samples yielded results comparable to those of purified samples, indicating the feasibility of using crude samples without compromising accuracy in ASFV detection. Our findings emphasize the effectiveness of the rRT-PCR assay for the prompt and accurate diagnosis of both swine fever viruses, which is essential for effective disease prevention and control in swine populations.

Keywords: African swine fever; Crude samples; Multiplex real-time RT-PCR; Validation.

Publication types

  • Validation Study

MeSH terms

  • African Swine Fever Virus* / genetics
  • African Swine Fever Virus* / isolation & purification
  • African Swine Fever* / diagnosis
  • African Swine Fever* / virology
  • Animals
  • Multiplex Polymerase Chain Reaction / methods
  • Real-Time Polymerase Chain Reaction* / methods
  • Real-Time Polymerase Chain Reaction* / veterinary
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Reverse Transcriptase Polymerase Chain Reaction / standards
  • Sensitivity and Specificity*
  • Swine
  • Vietnam