Simultaneous amplification of multiple targets

• US 5,422,252 A
• Filed: 06/04/1993
• Issued: 06/06/1995
• Est. Priority Date: 06/04/1993
• Status: Expired due to Term

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Little, Michael C., Nadeau, James G., Walker, George T.
• Primary Examiner(s): Parr, Margaret
• Assistant Examiner(s): MYERS, CARLA J
• Application Number:
  US08/073,197
• Time in Patent Office: 732 Days
• Field of Search: 435/6, 435/5, 435/91.2, 935/77, 935/78, 935/17
• US Class Current: 435/91.2
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 2525/131 incorporating a restriction site
• CPC Class Codes: C12Q 2525/155 incorporating/generating a new priming site
• CPC Class Codes: C12Q 2525/161 incorporating target specific and non-target specific sites
• CPC Class Codes: C12Q 2531/119 Strand displacement amplification [SDA]
• CPC Class Codes: C12Q 2537/143 Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
• CPC Class Codes: C12Q 2549/119 using nested primers
• CPC Class Codes: G11B 19/04 Arrangements for preventing, inhibiting, or warning against double recording on the same blank or against other recording or reproducing malfunctions
• CPC Class Codes: G11B 2005/0008 Magnetic conditionning of heads, e.g. biasing
• CPC Class Codes: G11B 5/09 Digital recording
• CPC Class Codes: G11B 5/1878 disposed immediately adjacent to the transducing gap, e.g. "Metal-In-Gap" structure
• CPC Class Codes: G11B 5/3113 for improving the magnetic domain structure or avoiding the formation or displacement of undesirable magnetic domains
• CPC Class Codes: G11B 5/455 Arrangements for functional testing of heads; Measuring arrangements for heads
• CPC Class Codes: G11B 5/465 Arrangements for demagnetisation of heads

Abstract

Methods for multiplex amplification of target nucleic acid sequences using a single pair of primers. Defined sequences are appended to the ends of multiple target sequences as part of the amplification reaction so that no steps in addition to amplification are required. The target sequences with the appended defined sequences need not be isolated prior to amplification. In one embodiment for coamplification of two target sequences, a sequence corresponding to a terminal segment of the first target sequence is appended to one end of the second target sequence and a sequence corresponding to a terminal segment of the second target sequence is appended to one end of the first target sequence. Amplification of the two targets then requires only a single pair of primers. Alternatively, a single defined sequence may be appended to the 5'"'"' and 3'"'"' ends of any number of selected targets. All such modified target sequences may then be amplified using a single pair of primers which hybridize to the defined end-sequences.

Claims

1. A method for simultaneously amplifying a first and a second target nucleic acid sequence by Strand Displacement Amplification (SDA) comprising:

a) hybridizing a first amplification primer to the 3'"'"' end of a first strand of the first target sequence, the first amplification primer comprising a 3'"'"' target binding sequence and a 5'"'"' recognition site for a restriction enzyme capable of nicking one strand of a double stranded hemimodified recognition site for the enzyme, extending the first amplification primer with polymerase to form a first extension product complementary to the first strand of the first target sequence, and displacing the first extension product;

b) hybridizing a first adapter primer to the first extension product at the 3'"'"' end of the complement of the first strand of the first target sequence, the 3'"'"' end of the first adapter primer comprising a target binding sequence which hybridizes to the first extension product and the 5'"'"' end of the first adapter primer comprising a sequence which is substantially identical to a 3'"'"' target binding sequence of a second amplification primer which hybridizes to a first strand of the second target sequence;

c) extending the first adapter primer with polymerase to form a second extension product and displacing the second extension product;

d) hybridizing the second amplification primer to the 3'"'"' end of the first strand of the second target sequence and a 5'"'"' recognition site for a restriction enzyme which nicks one strand of a double stranded hemimodified restriction enzyme recognition site, extending the second amplification primer with polymerase to form a third extension product complementary to the first strand of the second target sequence, and displacing the third extension product;

the first strand of the second target sequence, and displacing the third extension product;

e) hybridizing a second adapter primer to the third extension product at the 3'"'"' end of the complement of the first strand of the second target sequence, the 3'"'"' end of the second adapter primer comprising a target binding sequence which hybridizes to the third extension product and the 5'"'"' end of the second adapter primer comprising a sequence which is substantially identical to the target binding sequence of the first amplification primer;

f) extending the second adapter primer with polymerase to form a fourth extension product and displacing the fourth extension product, and;

g) simultaneously amplifying the second and fourth extension products in an SDA reaction using the first and second amplification primer.

2. The method according to claim 1 wherein the first, second, third and fourth extension products are displaced by extension of bumper primers.

3. The method according to claim 2 wherein the first and second amplification primers are present in approximately 10-fold excess over the first and second adapter primers.

4. The method according to claim 3 wherein the second and fourth extension products are amplified in an SDA reaction which employs a restriction enzyme selected from the group consisting of HincII, HindII, AvaI, NciI, and Fnu4HI for nicking the hemimodified restriction enzyme recognition site.

5. The method according to claim 4 wherein the IS6110 insertion element of Mycobacterium tuberculosis and the 16S ribosomal gene of Mycobacterium tuberculosis are simultaneously amplified.

6. The method of claim 1 wherein the first and second target sequences are double stranded, further comprising the steps of:

a) hybridizing the first adapter primer to the 3'"'"' end of a second strand of the first target sequence, extending the first adapter primer to form a fifth extension product complementary to the second strand of the first target sequence, and displacing the fifth extension product;

b) hybridizing the first amplification primer to the fifth extension product at the 3'"'"' end of the complement of the second strand of the first target sequence, extending the first amplification primer with polymerase to form a seventh extension product, and displacing the seventh extension product;

c) hybridizing the second adapter primer to the 3'"'"' end of a second strand of the second target sequence, extending the second adapter primer to form a sixth extension product complementary to the second strand of the second target sequence, and displacing the sixth extension product;

d) hybridizing the second amplification primer to the sixth extension product at the 3'"'"' end of the complement of the second strand of the second target sequence, extending the second amplification primer with polymerase to form an eighth extension product, and displacing the eighth extension product, and;

e) simultaneously amplifying the seventh and eight extension products in the SDA reaction using the first and second amplification primers.

7. A method for simultaneously amplifying a first and a second target nucleic acid sequence by Strand Displacement Amplification (SDA) comprising, in a reaction mix comprising adapter primers and amplification primers:

a) hybridizing a first adapter primer to the 3'"'"' end of the first target sequence, the 3'"'"' end of the adapter primer comprising a target binding sequence which hybridizes to the target sequence and the 5'"'"' end of the adapter primer comprising a first adapter sequence which is substantially identical to a 3'"'"' target binding sequence of a first amplification primer which hybridizes to a first strand of the second target sequence;

b) extending the first adapter primer with polymerase to produce a first extension product which is complementary to the first target sequence and displacing the first extension product;

c) hybridizing a second adapter primer to the 3'"'"' end of the first extension product at the 3'"'"' end of the complement of the first target sequence, the 3'"'"' end of the second adapter primer comprising a target binding sequence which hybridizes to the first extension product and the 5'"'"' end of the second adapter primer comprising a second adapter sequence which is substantially identical to a 3'"'"' target binding sequence of a second amplification primer which hybridizes to a second strand of the second target sequence;

d) extending the second adapter primer with polymerase to produce a second extension product, displacing the second extension product, and;

e) concurrently with production of the second extension product in the reaction mix, simultaneously amplifying the second extension product of the first target sequence and the second target sequence in an SDA reaction using the first and second amplification primers, the first and second amplification primers each further comprising a 5'"'"' recognition site for a restriction enzyme which nicks one strand of a hemimodified double stranded restriction enzyme recognition site.

8. The method according to claim 7 wherein the first and second adapter sequences are substantially identical and the second extension product of the first target sequence and the second target sequence are amplified using a single amplification primer.

9. The method according to claim 7 wherein the first and second extension products are displaced by extension of bumper primers.

10. The method according to claim 9 wherein the amplification primers first and second are present in approximately 10-fold excess over the first and second adapter primers.

11. The method according to claim 10 wherein the IS6110 insertion element of Mycobacterium tuberculosis and the 16S ribosomal gene of Mycobacterium tuberculosis are amplified.

12. The method according to claim 10 wherein the IS6110 insertion element of Mycobacterium tuberculosis and a target sequence from Mycobacterium avium are amplified.

13. The method according to claim 7 wherein the second extension product is amplified in an SDA reaction which employs a restriction enzyme selected from the group consisting of HincII, HindII, AvaI, NciI, and Fnu4HI for nicking the hemimodified restriction enzyme recognition site.

14. The method according to claim 7 further comprising the steps of:

a) hybridizing the second adapter primer to the 3'"'"' end of a second strand of the first target sequence, extending the second adapter primer to form a third extension product complementary to the second strand of the first target sequence, and displacing the third extension product;

b) hybridizing the first adapter primer to the third extension product at the 3'"'"' end of the complement of the first target sequence, extending the first adapter primer to form a fourth extension product, and displacing the fourth extension product, and;

c) concurrently with formation of the fourth extension product in the reaction mix, simultaneously amplifying the fourth extension product of the first target sequence and the second target sequence in the SDA reaction using the first and second amplification primers.

15. A method for simultaneously amplifying a first and a second target nucleic acid sequence in a primer extension amplification reaction comprising:

a) hybridizing a first amplification primer to the 3'"'"' end of the first target sequence, the first amplification primer comprising a 3'"'"' target binding sequence, extending the first amplification primer with polymerase to form a first extension product complementary to the first target sequence, and displacing the first extension product;

b) hybridizing a first adapter primer to the first extension product at the 3'"'"' end of the complement of the first target sequence, the 3'"'"' end of the first adapter primer comprising a target binding sequence which hybridizes to the first extension product and the 5'"'"' end of the first adapter primer being substantially identical to a 3'"'"' target binding sequence of a second amplification primer which hybridizes to the second target sequence;

c) extending the first adapter primer with polymerase to form a second extension product and displacing the second extension product;

d) hybridizing the 3'"'"' target binding sequence of the second amplification primer to the 3'"'"' end of the second target sequence, extending the second amplification primer with polymerase to form a third extension product complementary to the second target sequence, and displacing the third extension product;

e) hybridizing a second adapter primer to the third extension product at the 3'"'"' end of the complement of the second target sequence, the 3'"'"' end of the second adapter primer comprising a target binding sequence which hybridizes to the third extension product and the 5'"'"' end of the second adapter primer being substantially identical to the target binding sequence of the first amplification primer;

f) extending the second adapter primer with polymerase to form a fourth extension product and displacing the fourth extension product, and;

g) simultaneously amplifying the second and fourth extension products in a primer extension amplification reaction using the first and second amplification primers.

16. A method for simultaneously amplifying a first and second target nucleic acid sequence in a primer extension amplification reaction comprising, in a reaction mix comprising adapter primers and amplification primers:

a) hybridizing a first adapter primer to the 3'"'"' end of the first target sequence, the 3'"'"' end of the adapter primer comprising a target binding sequence which hybridizes to the target sequence and the 5'"'"' end of the adapter primer comprising a first adapter sequence which is substantially identical to a 3'"'"' target binding sequence of a first amplification primer which hybridizes to a first strand of the second target sequence;

b) extending the first adapter primer with polymerase to produce a first extension product which is complementary to the first target sequence and displacing the first extension product;

c) hybridizing a second adapter primer to the first extension product at the 3'"'"' end of the complement of the first target sequence, the 3'"'"' end of the second adapter primer comprising a target binding sequence which hybridizes to the first extension product and the 5'"'"' end of the second adapter primer comprising a second adapter sequence which is substantially identical to a 3'"'"' target binding sequence of a second amplification primer which hybridizes to a second strand of the second target sequence;

d) extending the second adapter primer with polymerase to produce a second extension product, displacing the second extension products, and;

e) concurrently with production of the second extension products in the reaction mix, simultaneously amplifying the second extension product of the first target and the second target sequence in a primer extension amplification reaction using the first and second target sequence in a primer extension amplification reaction using the first and second amplification primers.

17. The method according to any one of claims 7 or 16 further comprising appending adapter sequences to a third target nucleic acid sequence according to steps (a) through (d) and simultaneously amplifying the first, second and third target sequences using the first and second amplification primers.