TY - JOUR
T1 - Probe-lengthening amplification-assisted microchip electrophoresis for ultrasensitive bacteria screening
AU - Luo, Feifei
AU - Lu, Yuqi
AU - Li, Zhi
AU - Dai, Ge
AU - Chu, Zhaohui
AU - Zhang, Jingwen
AU - He, Pingang
AU - Wang, Qingjiang
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2020/12/15
Y1 - 2020/12/15
N2 - Probe-lengthening amplification (PLA) is a target-specific nucleic acid amplification method that realizes good selectivity by effectively avoiding nonspecific amplification. Here, we propose a probe-lengthening amplification-assisted microchip electrophoresis (MCE) strategy for sensitive analysis of 16S rRNA genes of five bacteria. In this assay, four specific short probes were designed for a target bacterium to recognize its bacterial 16S rRNA gene, integrated into longer DNA ligation duplexes using Ampligase, and subsequently separated and detected by MCE. Along with the rapid generation of ligation duplexes, this approach provides exponential amplification of nucleic acid signals that are useful for sensitive bacterial quantification. Through tactfully combining PLA and MCE, the detection sensitivity of bacterial genes was significantly improved, and a limit of detection (LOD) of 30 fM was realized for the artificial target DNA. This approach was also applied to detect actual bacterial genomic samples with excellent results, demonstrating the potential application of this methodology in infection diagnosis.
AB - Probe-lengthening amplification (PLA) is a target-specific nucleic acid amplification method that realizes good selectivity by effectively avoiding nonspecific amplification. Here, we propose a probe-lengthening amplification-assisted microchip electrophoresis (MCE) strategy for sensitive analysis of 16S rRNA genes of five bacteria. In this assay, four specific short probes were designed for a target bacterium to recognize its bacterial 16S rRNA gene, integrated into longer DNA ligation duplexes using Ampligase, and subsequently separated and detected by MCE. Along with the rapid generation of ligation duplexes, this approach provides exponential amplification of nucleic acid signals that are useful for sensitive bacterial quantification. Through tactfully combining PLA and MCE, the detection sensitivity of bacterial genes was significantly improved, and a limit of detection (LOD) of 30 fM was realized for the artificial target DNA. This approach was also applied to detect actual bacterial genomic samples with excellent results, demonstrating the potential application of this methodology in infection diagnosis.
KW - 16S rRNA gene
KW - Bacteria screening
KW - Microchip electrophoresis
KW - Probe-lengthening amplification
UR - https://www.scopus.com/pages/publications/85089816574
U2 - 10.1016/j.snb.2020.128784
DO - 10.1016/j.snb.2020.128784
M3 - 文章
AN - SCOPUS:85089816574
SN - 0925-4005
VL - 325
JO - Sensors and Actuators B: Chemical
JF - Sensors and Actuators B: Chemical
M1 - 128784
ER -