Compositions and methods for detection of BK virus

1. A method of detecting BK virus in a sample, the method comprising: (a) performing an amplifying step comprising contacting the sample with a set of primers to produce an amplification product, if a target nucleic acid of BK Virus is present in the sample; (b) performing a hybridization step comprising contacting the amplification product, if a target nucleic acid is present in the sample, with a probe; and (c) detecting the presence or absence of the amplification product, wherein the presence of the amplification product is indicative of the presence of BK virus in the sample, and wherein the absence of the amplification product is indicative of the absence of BK virus in the sample; wherein the set of primers consists of a first primer consisting of SEQ ID NO:4, and a second primer consisting of SEQ ID NO:5, and wherein the probe consists of SEQ ID NO:3 and optionally a label.

2. The method of claim 1 ,

wherein the hybridization step comprises contacting the amplification product with the probe, wherein the probe is labeled with a donor fluorescent moiety and a corresponding acceptor moiety;

wherein the detecting step comprises detecting the presence or absence of fluorescence resonance energy transfer (FRET) between the donor fluorescent moiety and the acceptor moiety of the probe; and

wherein the presence or absence of fluorescence is indicative of the presence of absence of BK Virus in the sample.

3. The method of claim 2 , wherein the amplification step comprises a polymerase enzyme having 5′ to 3′ nuclease activity.

4. The method of claim 2 , wherein the acceptor moiety is a quencher.

5. The method of claim 1 , wherein the sample is a biological sample.

6. The method of claim 5 , wherein the biological sample is blood, plasma, or urine.