Final Report Nucleic Acid System - Hybrid PCR and Multiplex Assay Project Phase 2

Koopman, R P ; Langlois, R G ; Nasarabadi, S ; Benett, W J ; Colston, B W ; Johnson, D C ; Brown, S B ; Stratton, P L ; Milanovich, F P

Lawrence Livermore National Laboratory

关键词: Pathogens;    Functionals;    Biological Warfare;    Nucleic Acids;    Cell Flow Systems;   

DOI  :  10.2172/15002758
RP-ID  :  UCRL-ID-148188
RP-ID  :  W-7405-ENG-48
RP-ID  :  15002758

美国|英语

来源: UNT Digital Library

【 摘 要 】

This report covers phase 2 (year 2) of the Nucleic Acid System--Hybrid PCR and Multiplex Assay project. The objective of the project is to reduce to practice the detection and identification of biological warfare pathogens by the nucleic acid recognition technique of PCR (polymerase chain reaction) in a multiplex mode using flow cytometry. The Hybrid instrument consists of a flow-through PCR module capable of handling a multiplexed PCR assay, a hybridizing module capable of hybridizing multiplexed PCR amplicons and beads, and a flow cytometer module for bead-based identification, all controlled by a single computer. Multiplex immunoassay using bead-based Luminex flow cytometry is available, allowing rapid screening for many agents. PCR is highly specific and complements and verifies immunoassay. It can also be multiplexed and detection provided using the bead-based Luminex flow cytometer. This approach allows full access to the speed and 100-fold multiplex capability of flow cytometry for rapid screening as well as the accuracy and specificity of PCR. This project has two principal activities: (1) Design, build and test a prototype hybrid PCR/flow cytometer with the basic capabilities for rapid, broad spectrum detection and identification, and (2) Develop and evaluate multiplex flow analysis assay protocols and reagents for the simultaneous detection of PCR products. This project requires not only building operationally functional instrumentation but also developing the chemical assays for detection of priority pathogens. This involves development and evaluation of multiplex flow analysis assay protocols and reagents for the simultaneous detection of PCR products.