Development of multiplex PCR-ligase detection reaction assay for detection of West Nile virus

S. Rondini, M. R. Pingle, S. Das, R. Tesh, M. S. Rundell, J. Hom, S. Stramer, K. Turner, S. N. Rossmann, R. Lanciotti, E. G. Spier, J. Muñoz-Jordán, D. Larone, O. E. Spitzer, F. Barany, L. M. Golightly

Research output: Contribution to journalArticle

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Abstract

We have developed a novel multiplex reverse transcription-PCR ligase detection reaction (RT-PCR/LDR) assay for the detection of West Nile virus (WNV) in both clinical and mosquito pool samples. The method relies on the amplification of three different genomic regions, one in the coding sequence of nonstructural protein NS2a and two in nonstructural protein NS5, to minimize the risk of detection failure due to genetic variation. The sensitivity of the PCR is complemented by the high specificity of the LDR step, and the detection of the LDR products can be achieved with capillary electrophoresis (CE) or a universal DNA microarray. We evaluated the limit of detection by both one-step and two-step multiplex RT-PCR/LDR/CE approaches, which reached, respectively, 0.005 and 0.017 PFU. The assay demonstrated 99% sensitivity when mosquito pool samples were tested and 100% sensitivity with clinical samples when the one-step approach was used. The broad strain coverage was confirmed by testing 34 WNV isolates belonging to lineages 1 and 2, and the high specificity of the assay was determined by testing other flaviviruses, as well as negative mosquito pool and clinical samples. In summary, the multiplex RT-PCR/LDR assay could represent a valuable complement to WNV serological diagnosis, especially in early symptomatic patients. In addition, the multiplexing capacity of the technique, which can be coupled to universal DNA microarray detection, makes it an amenable tool to develop a more comprehensive assay for viral pathogens.

Original languageEnglish (US)
Pages (from-to)2269-2279
Number of pages11
JournalJournal of Clinical Microbiology
Volume46
Issue number7
DOIs
StatePublished - Jul 2008

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West Nile virus
Multiplex Polymerase Chain Reaction
Ligases
Culicidae
Reverse Transcription
Polymerase Chain Reaction
Capillary Electrophoresis
Oligonucleotide Array Sequence Analysis
Flavivirus
Limit of Detection
Proteins

ASJC Scopus subject areas

  • Microbiology (medical)
  • Microbiology

Cite this

Rondini, S., Pingle, M. R., Das, S., Tesh, R., Rundell, M. S., Hom, J., ... Golightly, L. M. (2008). Development of multiplex PCR-ligase detection reaction assay for detection of West Nile virus. Journal of Clinical Microbiology, 46(7), 2269-2279. https://doi.org/10.1128/JCM.02335-07

Development of multiplex PCR-ligase detection reaction assay for detection of West Nile virus. / Rondini, S.; Pingle, M. R.; Das, S.; Tesh, R.; Rundell, M. S.; Hom, J.; Stramer, S.; Turner, K.; Rossmann, S. N.; Lanciotti, R.; Spier, E. G.; Muñoz-Jordán, J.; Larone, D.; Spitzer, O. E.; Barany, F.; Golightly, L. M.

In: Journal of Clinical Microbiology, Vol. 46, No. 7, 07.2008, p. 2269-2279.

Research output: Contribution to journalArticle

Rondini, S, Pingle, MR, Das, S, Tesh, R, Rundell, MS, Hom, J, Stramer, S, Turner, K, Rossmann, SN, Lanciotti, R, Spier, EG, Muñoz-Jordán, J, Larone, D, Spitzer, OE, Barany, F & Golightly, LM 2008, 'Development of multiplex PCR-ligase detection reaction assay for detection of West Nile virus', Journal of Clinical Microbiology, vol. 46, no. 7, pp. 2269-2279. https://doi.org/10.1128/JCM.02335-07
Rondini, S. ; Pingle, M. R. ; Das, S. ; Tesh, R. ; Rundell, M. S. ; Hom, J. ; Stramer, S. ; Turner, K. ; Rossmann, S. N. ; Lanciotti, R. ; Spier, E. G. ; Muñoz-Jordán, J. ; Larone, D. ; Spitzer, O. E. ; Barany, F. ; Golightly, L. M. / Development of multiplex PCR-ligase detection reaction assay for detection of West Nile virus. In: Journal of Clinical Microbiology. 2008 ; Vol. 46, No. 7. pp. 2269-2279.
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AU - Tesh, R.

AU - Rundell, M. S.

AU - Hom, J.

AU - Stramer, S.

AU - Turner, K.

AU - Rossmann, S. N.

AU - Lanciotti, R.

AU - Spier, E. G.

AU - Muñoz-Jordán, J.

AU - Larone, D.

AU - Spitzer, O. E.

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