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Development and validation of multiplex real-time PCR assays for rapid detection of cytomegalovirus, Epstein-Barr virus, and polyomavirus BK in whole blood from transplant candidates

  • The Catholic University of Korea
  • Genetree Research

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Transplant recipients are more susceptible to bacterial and viral infections. Cytomegalovirus (CMV), Epstein-Barr virus (EBV), and polyomavirus BK (BK) are risk factors for graft dysfunction. All three of them are latent viruses that can cause serious disease in immunocompromised patients. Mainly qualitative PCR tests are required for diagnosis and quantitative monitoring, which are used to follow the response to transplantation. We developed a multiplex real-time PCR (qPCR) method to detect these viruses during blood screenings of transplant recipients. We also validated analytical and clinical performance tests using the developed multiplex qPCR. The limit of detection (LOD) was 100, 125, and 183 copies/ml for CMV, EBV, and BK, respectively. These results had high linearity (R2 = 0.997) and reproducibility (CV range, 0.95–2.38%, 0.52–3.32%, and 0.31–2.45%, respectively). Among 183 samples, we detected 8 samples that were positive for CMV, while only 6 were positive for EBV, and 3 were positive for BK. Therefore, the viral infection prevalence in transplant candidates was 4.40% for CMV, 3.29% for EBV, and 1.64% for BK. This multiplex qPCR method should be used widely for diagnosing and monitoring latent viral infections in transplant recipients.

Original languageEnglish
Pages (from-to)593-599
Number of pages7
JournalJournal of Microbiology
Volume56
Issue number8
DOIs
StatePublished - 1 Aug 2018

Bibliographical note

Publisher Copyright:
© 2018, The Microbiological Society of Korea and Springer Nature B.V.

Keywords

  • Epstein-Barr virus
  • cytomegalovirus
  • multiplex qPCR
  • polyomavirus BK
  • transplant recipients

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