Detection of mycobacteria by multiplex nucleic acid amplification
First Claim
1. An oligonucleotide consisting of a target binding sequence selected from the group consisting of the target binding sequences of SEQ ID NO:
- 1, SEQ ID NO;
2, SEQ ID NO;
3, SEQ ID NO;
4, SEQ ID NO;
5, SEQ ID NO;
6, SEQ ID NO;
7, SEQ ID NO;
23, SEQ ID NO;
24, SEQ ID NO;
25, SEQ ID NO;
20, SEQ ID NO;
21 and SEQ ID NO;
27 and, optionally, a sequence required for an amplification reaction or an adapter sequence.
1 Assignment
0 Petitions
Accused Products
Abstract
Primers and methods for adapter-mediated multiplex amplification of the IS6110 insertion element of the Mycobacterium tuberculosis (M.tb) complex and a 16S rDNA target common to essentially all mycobacteria are described. In certain embodiments, the primers are optimized for efficient multiplex amplification in thermophilic SDA. The multiplex Strand Displacement Amplification methods of the invention are capable, in a single amplification reaction, of simultaneously identifying M. tuberculosis and providing a screen for substantially all of the clinically relevant species of mycobacteria. Also disclosed are internal control sequences designed for coamplification with the two targets, allowing assessment of amplification efficiency and/or quantitation of the targets.
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Citations
19 Claims
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1. An oligonucleotide consisting of a target binding sequence selected from the group consisting of the target binding sequences of SEQ ID NO:
- 1, SEQ ID NO;
2, SEQ ID NO;
3, SEQ ID NO;
4, SEQ ID NO;
5, SEQ ID NO;
6, SEQ ID NO;
7, SEQ ID NO;
23, SEQ ID NO;
24, SEQ ID NO;
25, SEQ ID NO;
20, SEQ ID NO;
21 and SEQ ID NO;
27 and, optionally, a sequence required for an amplification reaction or an adapter sequence. - View Dependent Claims (2, 3)
- 1, SEQ ID NO;
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4. An oligonucleotide selected from the group consisting of SEQ ID NO:
- 12, SEQ ID NO;
13, SEQ ID NO;
22 and SEQ ID NO;
26.
- 12, SEQ ID NO;
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5. A method for simultaneously amplifying a first and a second target comprising:
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a) hybridizing a first amplification primer to the first target, the first amplification primer comprising the target binding sequence of SEQ ID NO;
1 and a recognition site for a restriction endonuclease which nicks one strand of a double-stranded hemimodified recognition site for the restriction endonuclease, extending the first amplification primer to produce a first extension product and displacing the first extension product;b) hybridizing to the first extension product a first adapter primer consisting of a target binding sequence selected from the group consisting of the target binding sequences of SEQ ID NO;
3, SEQ ID NO;
4, SEQ ID NO;
5 and SEQ ID NO;
27, and a first adapter sequence substantially identical to the target binding sequence of SEQ ID NO;
2, extending the first adapter primer to produce a second extension product and displacing the second extension product;c) hybridizing a second amplification primer to the second target, the second amplification primer comprising the target binding sequence of SEQ ID NO;
2 and the recognition site for the restriction endonuclease, extending the second amplification primer to produce a third extension product and displacing the third extension product;d) hybridizing to the third extension product a second adapter primer consisting of a target binding sequence selected from the group consisting of the target binding sequences of SEQ ID NO;
6, SEQ ID NO;
7, SEQ ID NO;
23, SEQ ID NO;
24 and SEQ ID NO;
25 and a second adapter sequence substantially identical to the target binding sequence of SEQ ID NO;
1, extending the second adapter primer to produce a fourth extension product, displacing the fourth extension product, and;e) si multaneously amplifying the second and fourth extension products using the first and second amplification primers. - View Dependent Claims (6, 7, 8, 9, 10, 11)
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12. A method for simultaneously amplifying a first and a second target comprising:
- a) hybridizing a first amplification primer to the first target, the first amplification primer comprising the target binding sequence of SEQ ID NO;
1 and a recognition site for a restriction endonuclease which nicks one strand of a double-stranded hemimodified recognition site for the restriction endonuclease, extending the first amplification primer to produce a first extension product and displacing the first extension product;b) hybridizing to the first extension product a first adapter primer consisting of a target binding sequence of SEQ ID NO;
20 and a first adapter sequence substantially identical to the target binding sequence of SEQ ID NO;
19, extending the first adapter primer to produce a second extension product and displacing the second extension product;c) hybridizing a second amplification primer to the second target, the second amplification primer comprising the target binding sequence of SEQ ID NO;
19 and the recognition site for the restriction endonuclease, extending the second amplification primer to produce a third extension product and displacing the third extension product;d) hybridizing to the third extension product a second adapter primer consisting of the target binding sequence of SEQ ID NO;
21 and a second adapter sequence substantially identical to the target binding sequence of SEQ ID NO;
1, extending the second adapter primer to produce a fourth extension product, displacing the fourth extension product, and;e) simultaneously amplifying the second and fourth extension products using the first and second amplification primers. - View Dependent Claims (13, 14, 15, 16, 17)
- a) hybridizing a first amplification primer to the first target, the first amplification primer comprising the target binding sequence of SEQ ID NO;
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18. A method for simultaneously amplifying a first and a second target comprising:
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a) hybridizing a first amplification primer to the first target, the first amplification primer comprising a target binding sequence selected from the group consisting of the target binding sequences of SEQ ID NO;
3, SEQ ID NO;
4, SEQ ID NO;
5 and SEQ ID NO;
27 and a recognition site for a restriction endonuclease which nicks one strand of a double-stranded hemimodified recognition site for the restriction endonuclease, extending the first amplification primer to produce a first extension product and displacing the first extension product;b) hybridizing to the first extension product a first adapter primer consisting of the target binding sequence of SEQ ID NO;
1, and a first adapter sequence substantially identical to the target binding sequence of SEQ ID NO;
2, extending the first adapter primer to produce a second extension product and displacing the second extension product;c) hybridizing a second amplification primer to the second target, the second amplification primer comprising a target binding sequence selected from the group consisting of the target binding sequences of SEQ ID NO;
6, SEQ ID NO;
7, SEQ ID NO;
23, SEQ ID NO;
24 and SEQ ID NO;
25 and the recognition site for the restriction endonuclease, extending the second amplification primer to produce a third extension product and displacing the third extension product;d) hybridizing to the third extension product a second adapter primer consisting of the target binding sequence of SEQ ID NO;
2 and a second adapter sequence substantially identical to the target binding sequence of SEQ ID NO;
1, extending the second adapter primer to produce a fourth extension product, displacing the fourth extension product, and;e) simultaneously amplifying the second and fourth extension products using the first and second amplification primers.
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19. A method for simultaneously amplifying a first and a second target comprising:
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a) hybridizing a first amplification primer to the first target, the first amplification primer comprising the target binding sequence of SEQ ID NO;
20 and a recognition site for a restriction endonuclease which nicks one strand of a double-stranded hemimodified recognition site for the restriction endonuclease, extending the first amplification primer to produce a first extension product and displacing the first extension product;b) hybridizing to the first extension product a first adapter primer consisting of a target binding sequence of SEQ ID NO;
1 and a first adapter sequence substantially identical to the target binding sequence of SEQ ID NO;
19, extending the first adapter primer to produce a second extension product and displacing the second extension product;c) hybridizing a second amplification primer to the second target, the second amplification primer comprising the target binding sequence of SEQ ID NO;
21 and the recognition site for the restriction endonuclease, extending the second amplification primer to produce a third extension product and displacing the third extension product;d) hybridizing to the third extension product a second adapter primer consisting of the target binding sequence of SEQ ID NO;
19 and a second adapter sequence substantially identical to the target binding sequence of SEQ ID NO;
1, extending the second adapter primer to produce a fourth extension product, displacing the fourth extension product, and;e) simultaneously amplifying the second and fourth extension products using the first and second amplification primers.
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Specification