Methods for multiplexing amplification reactions

Patent metadata

Field	Value
Publication number	US-2017130259-A1
Application number	US-201615293387-A
Country	US
Kind code	A1
Filing date	Oct 14, 2016
Priority date	Jun 6, 2000
Publication date	May 11, 2017
Grant date	—

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

1 .- 18 . (canceled)

19 . A method for simultaneously amplifying multiple nucleic acid targets, comprising:
(a) contacting at least two primer pairs that target different nucleic acid sequences with multiple single stranded nucleic acid targets; (b) pre-amplifying said nucleic acid targets to about 100-1000 fold so that the reaction plateau is not reached; (c) dividing said pre-amplified targets into separate reaction chambers wherein the number of said chambers used is equal to the number of primer pairs; and (d) amplifying said pre-amplified targets; (e) detecting at least one target sequence in the divided pre-amplified sample.

20 . (canceled)

21 . (canceled)

22 . The method of claim 2019 , wherein the single stranded nucleic acid targets are DNA polynucleotides and the polymerase is a DNA polymerase.

23 . The method of claim 19 , wherein said targets are in an aqueous solution.

24 . The method of claim 19 , wherein said targets are irreversibly bound to a solid phase matrix.

25 . A two-step method for amplifying multiple nucleic acid sequence targets contained in a sample comprising:
(a) performing a first round of 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 each 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).

26 . The method of claim 25 , wherein the plurality of pairs include target specific primer pairs.

27 . The method of claim 26 , wherein at least one of the target specific primer pairs is complementary to human or bacterial gene targets.

28 . The method of claim 25 , wherein the plurality of first amplification products include nucleic acids from 100 base pairs to 1100 base pairs in length.

29 . The method of claim 25 , wherein the plurality of first amplification products contain nucleic acids having from 30% to 70% GC content.

30 . The method of claim 25 , wherein the first round of amplification includes performing a polymerase chain reaction.

31 . The method of claim 25 , wherein the first round of amplification includes performing an isothermal amplification reaction.

32 . The method of claim 25 , wherein the second round of amplification includes performing a polymerase chain reaction, strand displacement amplification or isothermal amplification.

33 . The method of claim 25 , further comprising (d) detecting at least one of the multiple nucleic acid sequence targets.

34 . The method of claim 25 , wherein at least one of the multiple nucleic acid sequence targets includes genomic DNA.

35 . The method of claim 25 , wherein at least one of the multiple nucleic acid sequence targets includes DNA or RNA extracted from tissue or culture samples.

36 . The method of claim 25 , wherein the first round of amplification is truncated by exhaustion of the plurality of primer pairs prior to reaching the amplification reaction plateau.

37 . The method of claim 25 , wherein the first round of amplification is truncated by limiting primer concentration of the plurality of primer pairs prior to reaching the amplification reaction plateau.

38 . The method of claim 25 , wherein the first round of amplification is truncated by limiting to only a few logs of amplification.

39 . The method of claim 25 , wherein the multiple nucleic acid sequence targets in (a) are amplified into early logarithmic phase.

40 . The method of claim 25 , wherein the second round of amplification comprises performing singleplex amplification reactions in each of the at least two distinct aliquots.

Assignees

• Applied Biosystems Llc

Inventors

• Gerdes John
• Best Elaine
• Marmaro Jeffrey M

Classifications

• C12Q1/6844

  Nucleic acid amplification reactions · 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

• C12Q1/686 Primary

  Polymerase chain reaction [PCR] · CPC title

• C12Q1/6827

  for detection of mutation or polymorphism · CPC title