Oligonucleotides, methods and kits for amplifying and detecting

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving virus or bacteriophage

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435 6, 435 912, 436501, 536 221, 536 231, 536 241, 536 243, 536 2431, 536 2432, 536 2433, 935 77, 935 78, C12Q 170

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058539816

ABSTRACT:
The present invention relates to two primers for amplifying a cytomegalovirus (CMV) nucleic acid suitable for a nucleic acid sequence-based amplification (NASBA) using a DNA-dependent RNA polymerase, a first primer containing a promoter sequence and a nucleic acid sequence consisting of at least fifteen continuous bases selected from the nucleic acid sequence of SEQ ID NO:1; a second primer containing a nucleic acid sequence consisting of at least fifteen continuous bases selected from the nucleic acid sequence of SEQ ID NO:2, NO:3 or NO:4; a detecting probe and/or a capturing probe containing a nucleic acid sequence consisting of at least continuous fifteen bases selected from the nucleic acid sequence(s) of SEQ ID NO:5, NO:6 and/or NO:7 wherein said sequence is modified if necessary; a reagent kit for detecting a CMV containing the above-mentioned primers and probes; and a nucleic acid sequence-based amplification (NASBA) using said primers. The advantages of the present invention are that CMV can be detected in an easy, rapid and specific manner with a high sensitivity.

REFERENCES:
patent: 5409818 (1995-04-01), Davey et al.
Kondo et al, "Human cytomegalovirus latent infection of granulocyte-macrophage progenitors", Proc. Natl. Acad. Sci. USA, vol. 91, pp. 11879-11883, Dec. 1994.
Sooknanan et al, "NASBA, A detection and amplification system uniquely suited for RNA", Biotechnology, vol. 13, pp. 563-564, Jun. 1995.
Vandamme et al, "Detection of HIV-1 RNA in plasma and serum samples using the NASBA amplification system compared to RNA-PCR", J. of Virol. Meth., vol. 52, pp. 121-132, 1995.

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