Methods for multiplexing amplification reactions

Patent metadata

Field	Value
Publication number	US-9206475-B2
Application number	US-201514589864-A
Country	US
Kind code	B2
Filing date	Jan 5, 2015
Priority date	Jun 6, 2000
Publication date	Dec 8, 2015
Grant date	Dec 8, 2015

Abstract

A two-step multiplex amplification reaction includes a first step which truncates the standard initial multiplex amplification round to “boost” the sample copy number by only a 100-1000 fold increase in the target. Following the first step the product is divided into optimized secondary single amplification reactions, each containing one of the primer sets that were used previously in the first or multiplexed booster step. The booster step can occur using an aqueous target nucleic acid or using a solid phase archived nucleic acid. In particular, nucleic acid sequences that uniquely identify E. Coli were identified using the multiplex amplification method.

First claim

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

1. A two-step method for amplifying multiple nucleic acid sequence targets contained in a sample comprising:
(a) performing a first round of multiplex amplification to form a plurality of first amplification products, comprising contacting the sample with a plurality of primer pairs specific to multiple nucleic acid sequence targets, wherein the first round of amplification is truncated prior to reaching a reaction plateau;
(b) dividing the plurality of first amplification products into at least two distinct aliquots; and,
(c) performing a second round of amplification with at least one of the at least two distinct aliquots, comprising contacting the plurality of first amplification products with a primer pair specific to one of the multiple nucleic acid sequence targets amplified with the plurality of primer pairs in (a) to form a plurality of second amplification products.

2. The method of claim 1 , wherein the plurality of first amplification products are diluted prior to being added to a reaction mixture used to perform the second round of amplification.

3. The method of claim 1 , wherein the first round of amplification or the second round of amplification or both the first round of amplification and the second round of amplification includes performing a polymerase chain reaction.

4. The method of claim 1 , wherein the first round of amplification or the second round of amplification or both the first round of amplification and the second round of amplification includes performing an isothermal amplification reaction.

5. The method of claim 1 , further comprising detecting at least one of the plurality of second amplification products.

6. The method of claim 1 , wherein the first round of amplification is truncated by exhaustion of at least one of the plurality of primer pairs prior to reaching an amplification reaction plateau attainable with a higher concentration of the at least one of the plurality of primer pairs.

7. The method of claim 1 , wherein the first round of amplification comprises about ten amplification cycles or less.

8. The method of claim 1 , wherein the first round of amplification is truncated by limiting to only a few logs of amplification.

9. The method of claim 1 , wherein the first round of amplification is truncated in early logarithmic phase.

10. The method of claim 1 , wherein the second round of amplification comprises performing singleplex amplification reactions in at least one of the at least two distinct aliquots.

11. The method of claim 1 , wherein the plurality of first amplification products are divided into over five distinct aliquots.

12. The method of claim 11 , wherein the second round of amplification comprises performing singleplex amplification reactions in each of the over five distinct aliquots.

13. The method of claim 1 , wherein the plurality of first amplification products are divided into between six and one hundred distinct aliquots.

14. The method of claim 13 , wherein the second round of amplification comprises performing singleplex amplification reactions in each of the between six and one hundred aliquots.

15. The method of claim 1 , wherein the second round of amplification comprises a detector probe.

16. The method of claim 1 , wherein the second round of amplification comprises a single dye homogeneous detection assay.

17. The method of claim 1 , wherein at least one primer pair in the second round of amplification is identical to a primer pair in the first round of amplification.

18. The method of claim 1 , wherein the plurality of first amplification products are divided into over five distinct aliquots, the second round of amplification comprises performing singleplex amplification reactions in each of the over five distinct aliquots, each singleplex amplification comprises a primer pair used in the first round of amplification, and wherein the method further comprises detecting at least one of the plurality of second amplification products.

19. The method of claim 18 , wherein the detecting is performed using a detector probe.

20. The method of claim 1 , wherein the plurality of first amplification products are divided into between six and one hundred distinct aliquots, the second round of amplification comprises performing singleplex amplification reactions in each of the between six and one hundred distinct aliquots, each singleplex amplification comprises a primer pair used in the first round of amplification, and wherein the method further comprises detecting at least one of the plurality of second amplification products.

Assignees

• Applied Biosystems Llc

Inventors

• Gerdes John C
• Best Elaine
• Marmaro Jeffrey M

Classifications

• C12Q1/6844

  Nucleic acid amplification reactions · CPC title

• C12Q1/686 Primary

  Polymerase chain reaction [PCR] · CPC title

• C12Q1/6806

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title

• C12Q2600/156

  Polymorphic or mutational markers · CPC title

• C12Q2600/16

  Primer sets for multiplex assays · CPC title