AAAR 32nd Annual Conference
September 30 - October 4, 2013
Oregon Convention Center
Portland, Oregon, USA
Abstract View
NanoPCR Detection of Bacterial Aerosols
Siyu Xu, MAOSHENG YAO, Peking University
Abstract Number: 16 Working Group: Bioaerosols: Characterization and Environmental Impact
Abstract Bioaerosol detection is of great importance in many fields, yet their low quantity in complex samples makes such an effort difficult. Here, we have investigated the use of nanoparticles (AgNPs, TiO2NPs and their combination) assisted PCR (nanoPCR) in enhancing the efficiency. Pure bacterial species E. coli and B. subtilis with serial dilutions were tested for obtaining optimal parameters such as nanoparticle concentration and the volume of the nanoparticle mixture. These optimal parameters were then applied to detecting indoor and outdoor bacterial aerosols collected using a liquid impinger. The PCR products were subsequently subjected to agarose gel electrophoresis and DNA stain.
The results showed that the enhancements varied with nanoparticle type, concentration level, and DNA template concentration. Data with E. coli and B. subtilis revealed that the optimal parameters were: 0.6 nM for TiO2NPs, 0.9 nM for AgNPs, 2 uL for the mixture, and diluted DNA templates. Our data also suggest that the mixture of AgNPs and TiO2NPs performed better compared to their individual ones especially for lower DNA levels when coupled with qPCR. BacLight DNA stain results showed that use of nanoparticles could form nanoparticle-DNA clusters, which led to concentrating local DNA and thus enhancing PCR detection. Our environmental bioaerosol monitoring data suggest that NanoPCR technique can be immediately applied to detecting 45 low quantity of airborne biological materials with up to 500 times enhancement. The developments in this work can further broaden qPCR applications in bioaerosol research fields.