Respiratory syncytial virus (RSV) viral load detection assay
The invention concerns a method for the extraction of nucleic acids from biological samples e.g. tissue material or sputum derived from human or animal species and the quantitative detection thereafter of said nucleic acids e.g. in terms of viral load, more specifically RSV viral load detection.
1. A method for identifying, detecting or quantifying the presence of at least one target Respiratory Syncytial Virus (RSV) nucleic acid in a sample, comprising the following steps:
(a) providing two or more oligonucleotide components having the ability to anneal to the target RSV nucleic acid, wherein a first oligonucleotide component and a second oligonucleotide component are capable of forming a catalytically active multi-component nucleic acid enzyme (MNAzyme) once annealed to the target RSV nucleic acid;
(b) contacting said two or more oligonucleotide components with said sample wherein said sample permits the binding of said at least one target RSV nucleic acid to said two or more oligonucleotide components and formation of the MNAzyme;
(c) contacting the MNAzyme with a catalyzable nucleic acid reporter substrate that is separate from the at least one target RSV nucleic acid; and
(d) identifying, detecting or quantifying the presence of the target RSV nucleic acid by detecting catalysis of the nucleic acid reporter substrate.
2. The method according to claim 1 , wherein the viral load of RSV in said sample is determined by quantifying the catalytic products produced by the MNAzyme.
3. The method of claim 1 , wherein the catalytic activity of the MNAzyme comprises cleavage of a nucleic acid reporter substrate.
4. The method of claim 3 , wherein the nucleic acid reporter substrate is labeled.
5. The method of claim 4 , wherein detection of the label is enhanced following cleavage of the nucleic acid reporter substrate.
6. The method of claim 4 , wherein the label is a fluorophore.