This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Druce, J.
Right arrow Articles by Birch, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Druce, J.
Right arrow Articles by Birch, C.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, May 2002, p. 1728-1732, Vol. 40, No. 5
0095-1137/02/$04.00+0     DOI: 10.1128/JCM.40.5.1728-1732.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Utility of a Multiplex PCR Assay for Detecting Herpesvirus DNA in Clinical Samples

Julian Druce, Mike Catton, Doris Chibo, Kirsty Minerds, David Tyssen, Renata Kostecki, Bill Maskill, Wendy Leong-Shaw, Marie Gerrard, and Chris Birch*

Victorian Infectious Diseases Reference Laboratory (VIDRL), North Melbourne, Victoria, Australia

Received 31 October 2001/ Returned for modification 24 December 2001/ Accepted 23 February 2002

A multiplex PCR was designed to amplify herpes simplex virus types 1 and 2, cytomegalovirus, and varicella-zoster virus DNA present in a diverse range of clinical material. The susceptibility of these viruses to in vivo inhibition by at least one antiviral drug was an important consideration in their inclusion in the multiplex detection system. An aliquot of equine herpesvirus was introduced into each specimen prior to extraction and served as an indicator of potential inhibitors of the PCR and a detector of suboptimal PCR conditions. Compared to virus isolation and immunofluorescence-based antigen detection, the multiplex assay yielded higher detection rates for all viruses represented in the assay. The turnaround time for performance of the assay was markedly reduced compared to those for the other techniques used to identify these viruses. More than 21,000 tests have been performed using the assay. Overall, the multiplex PCR enabled the detection of substantially increased numbers of herpesviruses, in some cases in specimens or anatomical sites where previously they were rarely if ever identified using traditional detection methods.


* Corresponding author. Mailing address: VIDRL, 10 Wreckyn St., North Melbourne 3051, Victoria, Australia. Phone: (61 3) 93422626. Fax: (61 3) 93422666. Email: chris.birch{at}mh.org.au.


Journal of Clinical Microbiology, May 2002, p. 1728-1732, Vol. 40, No. 5
0095-1137/02/$04.00+0     DOI: 10.1128/JCM.40.5.1728-1732.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Sugita, S, Shimizu, N, Watanabe, K, Mizukami, M, Morio, T, Sugamoto, Y, Mochizuki, M (2008). Use of multiplex PCR and real-time PCR to detect human herpes virus genome in ocular fluids of patients with uveitis. Br J Ophthalmol 92: 928-932 [Abstract] [Full Text]  
  • Miller, C. S., Berger, J. R., Mootoor, Y., Avdiushko, S. A., Zhu, H., Kryscio, R. J. (2006). High prevalence of multiple human herpesviruses in saliva from human immunodeficiency virus-infected persons in the era of highly active antiretroviral therapy.. J. Clin. Microbiol. 44: 2409-2415 [Abstract] [Full Text]  
  • Espy, M. J., Uhl, J. R., Sloan, L. M., Buckwalter, S. P., Jones, M. F., Vetter, E. A., Yao, J. D. C., Wengenack, N. L., Rosenblatt, J. E., Cockerill, F. R. III, Smith, T. F. (2006). Real-Time PCR in Clinical Microbiology: Applications for Routine Laboratory Testing. Clin. Microbiol. Rev. 19: 165-256 [Abstract] [Full Text]  
  • Miller, C. S., Avdiushko, S. A., Kryscio, R. J., Danaher, R. J., Jacob, R. J. (2005). Effect of Prophylactic Valacyclovir on the Presence of Human Herpesvirus DNA in Saliva of Healthy Individuals after Dental Treatment. J. Clin. Microbiol. 43: 2173-2180 [Abstract] [Full Text]  
  • Alvarez-Lafuente, R, Fernandez-Gutierrez, B, Jover, J A, Judez, E, Loza, E, Clemente, D, Garcia-Asenjo, J A, Lamas, J R (2005). Human parvovirus B19, varicella zoster virus, and human herpes virus 6 in temporal artery biopsy specimens of patients with giant cell arteritis: analysis with quantitative real time polymerase chain reaction. Ann Rheum Dis 64: 780-782 [Abstract] [Full Text]  
  • Tran, T, Druce, J D, Catton, M C, Kelly, H, Birch, C J (2004). Changing epidemiology of genital herpes simplex virus infection in Melbourne, Australia, between 1980 and 2003. Sex. Transm. Infect. 80: 277-279 [Abstract] [Full Text]  
  • Birch, C J, Druce, J D, Catton, M C, MacGregor, L, Read, T (2003). Detection of varicella zoster virus in genital specimens using a multiplex polymerase chain reaction. Sex. Transm. Infect. 79: 298-300 [Abstract] [Full Text]