Detection of mycobacteria by multiplex nucleic acid amplification

• US 5,811,269 A
• Filed: 04/30/1996
• Issued: 09/22/1998
• Est. Priority Date: 04/30/1996
• Status: Expired due to Fees

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Wright, David J., Howard, Deborah R., Dey, Margaret S., Schram, James L., Nadeau, James G., Dean, Cheryl H.
• Primary Examiner(s): Horlick, Kenneth R.
• Assistant Examiner(s): Tung, Joyce
• Application Number:
  US08/640,378
• Time in Patent Office: 875 Days
• Field of Search: 536/22.1, 536/24.32, 435/91.2, 435/91.1
• US Class Current: 435/91.1
• CPC Class Codes: C12Q 1/689 for bacteria
• CPC Class Codes: C12Q 2600/16 Primer sets for multiplex assays

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.

Claims

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.

2. The oligonucleotide of claim 1 wherein the sequence required for the amplification reaction is a restriction endonuclease recognition site which is nicked by a restriction endonuclease during Strand Displacement Amplification.

3. The oligonucleotide of claim 1 selected from the group consisting 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;

19, SEQ ID NO;

20, SEQ ID NO;

21 and SEQ ID NO;

27.

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.

5. 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 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.

6. The method of claim 5 wherein:

a) the first amplification primer consists of SEQ ID NO;

1;

b) the first adapter primer consists of SEQ ID NO;

3, SEQ ID NO;

4, SEQ ID NO;

5 or SEQ ID NO;

27;

c) the second amplification primer consists of SEQ ID NO;

2, and;

d) the second adapter primer consists of SEQ ID NO;

6, SEQ ID NO;

7, SEQ ID NO;

23, SEQ ID NO;

24 or SEQ ID NO;

25.

7. The method o f claim 5 further comprising detecting the amplified first or second target.

8. The method of claim 7 where in the amplified first target is detected using SEQ ID NO:

13 and SEQ ID NO;

14.

9. The method of claim 7 wherein the amplified second target is detected using SEQ ID NO:

15 and SEQ ID NO;

16.

10. The method of claim 5 further comprising coamplifying an internal control sequence consisting of SEQ ID NO:

12, or SEQ ID NO;

12 in which thymine has been wholly or partially substituted with uridine, and detecting the amplified internal control sequence.

11. The method of claim 10 wherein the amplified internal control sequence is detected using SEQ ID NO:

1 7 and SEQ ID NO;

18.

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.

13. The method of claim 12 wherein:

a) the first amplification primer consists of SEQ ID NO;

1;

b) the first adapter primer consists of SEQ ID NO;

20;

c) the second amplification primer consists of SEQ ID NO;

19, and;

d) the second adapter primer consists of SEQ ID NO;

2 1.

14. The method of claim 12 further comprising detecting the amplified first or second target.

15. The method of claim 14 wherein the first amplified target is detected using SEQ ID NO:

22 and SEQ ID NO;

14.

16. The method of claim 14 wherein the second amplified target is detected using SEQ ID NO:

15 and SEQ ID NO;

16.

17. The method of claim 12 further comprising coamplifying an internal control sequence consisting of SEQ ID NO:

26, or SEQ ID NO;

26 in which thymine has been wholly or partially substituted with uridine, and detecting the amplified internal control sequence.

18. 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 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.

19. 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;

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.