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Core-Shell Beads as Microreactors for Phylogrouping of E. coli Strains.


ABSTRACT: Multiplex polymerase chain reaction (PCR) is an effective tool for simultaneous detection of target genes. Nevertheless, their use has been restricted due to the intrinsic interference between primer pairs. Performing several single PCRs in an array format instead of a multiplex PCR is a simple way to overcome this obstacle. However, there are still major technical challenges in designing a new generation of single PCR microreactors with a small sample volume, rapid thermal cycling, and no evaporation during amplification. We report a simple and robust core-shell bead array for a series of single amplifications. Four core-shell beads with a polymer coating and PCR mixture were synthesized using liquid marble formation and subsequent photo polymerization. Each bead can detect one target gene. We constructed a customised system for thermal cycling of these core-shell beads. Phylogrouping of the E. coli strains was carried out based on the fluorescent signal of the core-shell beads. This platform can be a promising alternative for multiplex nucleic acid analyses due to its simplicity and high throughput. The platform reported here also reduces the cycling time and avoids evaporation as well as contamination of the sample during the amplification process.

SUBMITTER: Gorgannezhad L 

PROVIDER: S-EPMC7464145 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Core-Shell Beads as Microreactors for Phylogrouping of <i>E. coli</i> Strains.

Gorgannezhad Lena L   Sreejith Kamalalayam Rajan KR   Christie Melody M   Jin Jing J   Ooi Chin Hong CH   Katouli Mohammad M   Stratton Helen H   Nguyen Nam-Trung NT  

Micromachines 20200807 8


Multiplex polymerase chain reaction (PCR) is an effective tool for simultaneous detection of target genes. Nevertheless, their use has been restricted due to the intrinsic interference between primer pairs. Performing several single PCRs in an array format instead of a multiplex PCR is a simple way to overcome this obstacle. However, there are still major technical challenges in designing a new generation of single PCR microreactors with a small sample volume, rapid thermal cycling, and no evapo  ...[more]

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