PROBE DETECTION OF LOOP-MEDIATED AMPLIFICATION PRODUCTS
Disclosed herein are methods and compositions for detecting amplicon generated using loop-mediated amplification (LAMP). In particular, the invention relates to compositions comprising molecular beacons and/or LAMP primers and methods for generating and detecting LAMP amplicons. In particular, molecular beacons that bind to novel regions of a LAMP amplicon, and methods of using these probes, are provided.
1 . A composition comprising a LAMP primer set and an oligonucleotide probe comprising a detectable label,
wherein said LAMP primer set, when used in a LAMP amplification reaction in the presence of a target nucleic acid, generates an amplicon comprising a first region or a second region, wherein the first region comprises a B1 region and an F1c region and extends from the 5′ end of the B1 region to the 3′ end of the F1c region, and wherein the second region comprises an F1 region and a B1c region and extends from the 5′ end of the F1 region to the 3′ end of the B1c region, and wherein the amplicon further comprises a probe target sequence; and
wherein the oligonucleotide probe binds specifically to said amplicon at the probe target sequence, wherein the probe target sequence overlaps with the first region or the second region.
2 . The composition of claim 1 , wherein the target nucleic acid comprises a B2 and a B1 region in this order from a 5′ terminal side, and an F2c and an F1c region in this order from a 3′ terminal side.
3 . The composition of claim 2 , wherein the LAMP primer set comprises:
a forward inner primer comprising an F1c region and an F2 region, wherein said F1c region of the forward inner primer comprises a sequence substantially identical to the F1c region of said target nucleic acid and wherein said F2 region of the forward inner primer comprises a sequence substantially complementary to the F2c region of the target nucleic acid; and
a backward inner primer comprising a B1c region and a B2 region, wherein said B1c region of the backward inner primer comprises a sequence substantially complementary to a B1 region of the target nucleic acid and wherein said B2 region of the backward inner primer comprises a sequence substantially identical to the B2 region of the target nucleic acid sequence.
4 . The composition of claim 3 , wherein said target nucleic acid further comprises an F3c region 3′ of said F2c region and a B3 region 5′ of said B2 region, and wherein said LAMP primer set further comprises a forward outer primer and a backward outer primer, wherein said forward outer primer comprises a sequence substantially complementary to the F3c region of the target nucleic acid and wherein said backward outer primer comprises a sequence substantially identical to the B3 region of the target nucleic acid.
5 . The composition of claim 3 , wherein said LAMP primer set further comprises a loop forward primer and a loop backward primer, wherein said loop forward primer comprises a sequence substantially identical to a sequence between said F1c and said F2c region of said target nucleic acid, and wherein said loop backward primer comprises a sequence substantially complementary to a sequence between said B1 and said B2 region of said target nucleic acid.
6 . The composition of claim 1 , wherein the oligonucleotide probe comprises a sequence substantially complementary to the probe target sequence.
7 . The composition of claim 1 , wherein the probe target sequence overlaps the first region or the second region of the amplicon by at least 3 nucleotides.
8 . The composition of claim 7 , wherein the probe target sequence overlaps the first region or the second region of the amplicon by at least 7 nucleotides.
9 . The composition of claim 8 , wherein the probe target sequence overlaps the first region or the second region of the amplicon by at least 10 nucleotides.
10 . The composition of claim 9 , wherein the probe target sequence is located completely within the first region or the second region of the amplicon.
11 . The composition of claim 1 , wherein the probe target sequence overlaps with at least 3 nucleotides, at least 7 nucleotides, at least 10 nucleotides, or all of the F1 region, the F1c region, the B1 region, or the B1c region of the amplicon.
12 . (canceled)
13 . (canceled)
14 . The composition of claim 1 , wherein said detectable label is a fluorophore.
15 . The composition of claim 1 , wherein said oligonucleotide probe further comprises a quencher.
16 . The composition of claim 15 , wherein said quencher is covalently bound to a terminus of the oligonucleotide probe.
17 .- 20 . (canceled)
21 . A method of detecting the presence or absence of a target nucleic acid in a test sample, the method comprising:
mixing the test sample with a reaction mixture comprising a strand displacement DNA polymerase and a LAMP primer set;
exposing said test sample to loop-mediated amplification reaction conditions to generate an amplicon from the target nucleic acid, if present in said test sample, wherein the amplicon comprises a probe target sequence;
contacting the test sample with an oligonucleotide probe comprising a detectable label, wherein the oligonucleotide probe binds specifically to the amplicon at the probe target sequence, if present, wherein the probe target sequence overlaps with a first region or a second region, wherein the first region comprises a B1 region and an F1c region and extends from the 5′ end of the B1 region to the 3′ end of the F1c region, and wherein the second region comprises an F1 region and a B1c region and extends from the 5′ end of the F1 region to the 3′ end of the B1c region; and
detecting the presence or absence of a signal from the detectable label, wherein the presence of said signal is indicative of the presence of the target nucleic acid in the test sample.
22 . The method of claim 21 , wherein said loop-mediated amplification reaction is performed at a temperature of between about 60° C. and about 67° C.
23 . The method of claim 22 , wherein said loop-mediated amplification reaction is performed for less than 30 minutes.
24 . The method of claim 23 , wherein said loop-mediated amplification reaction is performed for less than 15 minutes.
25 . (canceled)
26 . (canceled)
27 . The method claim 21 , wherein said reaction mixture further comprises a reverse transcriptase.
28 . A method of detecting the presence or absence of a target nucleic acid in a test sample, the method comprising:
providing a test sample suspected of comprising a target nucleic acid, wherein said test sample comprises the composition of claim 1 and a strand displacement DNA polymerase;
exposing said test sample to conditions sufficient to generate an amplicon from the target nucleic acid, if present in said test sample, via a loop-mediated amplification reaction; and
detecting the presence or absence of a signal from the detectable label, wherein the presence of said signal is indicative of the presence of the target nucleic acid in the test sample.
29 . (canceled)