发明名称 COMPOSITIONS AND METHODS OF DETECTING RESPIRATORY PATHOGENS USING NUCLEIC ACID PROBES AND SUBSETS OF BEADS
摘要 The present disclosure is instructional for a multiplex nucleic acid amplification assay to detect and identify multiple respiratory pathogens.
申请公布号 US2014309138(A1) 申请公布日期 2014.10.16
申请号 US201214349256 申请日期 2012.10.04
申请人 GENERA BIOSYSTEMS LIMITED 发明人 Poetter Karl Frederick;Vandegraaff Nick
分类号 C12Q1/70;C12Q1/68 主分类号 C12Q1/70
代理机构 代理人
主权项 1. A method of screening a sample for a multiplicity of respiratory pathogens to detect a particular pathogen, the method comprising: (a) isolating nucleic acid from the sample, which nucleic acid putatively comprises nucleic acid from one or more respiratory pathogens; (b) subjecting the nucleic acid to solid phase amplification with primer pairs comprising forward primers of SEQ ID NOs:1 to 16 or 33 or 35 and corresponding reverse primers of SEQ ID NOs:17 to 32 or 33 or 35, and wherein the oligonucleotide probes are selected from the group consisting of SEQ ID NOs:37 to 52 and 34 or 36 or with primer lairs and corresponding probes selected from 2 or more of the sequences listed in Table 8 SEQ ID NOs:74 to 126 or SEQ ID NOs:53 or 54) amplification; wherein an aqueous primer pair directs the amplification of a region of nucleic acid from a respiratory pathogen, the number of primer pairs being selected on the basis of the number of pathogens desired to be screened and wherein at least one member of the primer pair comprises a first optically detectable label that is incorporated into a resulting amplicon following amplification; wherein the amplicon is captured by hybridizing to an oligonucleotide probe that is complementary to a region of the amplicon and immobilized to a bead in a beadset, the beadset having subsets of beads, each subset being homogenous with respect to bead size and, optionally, intensity of a second optically detectable label, thereby creating a heterogeneous beadset based on size and/or second detectable label intensity and wherein the number of subsets corresponds to the number of respiratory pathogens to be screened; (c) determining to which of the beads an amplicon has bound on the basis of the intensity of the first detectable label and, where amplicons are bound to multiple subsets of beads, distinguishing between the multiple subsets of beads on the basis of bead size and, optionally, on the basis of second optically detectable label intensity; wherein binding of an amplicon to a particular subset of beads is indicative of the presence of a particular respiratory pathogen in the sample.
地址 Victoria AU