4.8 Article

A portable centrifugal genetic analyzer for multiplex detection of feline upper respiratory tract disease pathogens

Journal

BIOSENSORS & BIOELECTRONICS
Volume 193, Issue -, Pages -

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2021.113546

Keywords

Centrifugal microfluidics; Genetic analyzer; Loop-mediated isothermal amplification; Polymerase chain reaction; Point-of-care testing; Feline upper respiratory tract disease

Funding

  1. Engineering Research Center of Excellence Program of Korea Ministry of Science, ICT & Future Planning (MSIP) /National Research Foundation of Korea (NRF) [2021R1A5A6002853]
  2. National Research Foundation of Korea (NRF)
  3. Ministry of Science and ICT (MSIT) [2020R1A2C1003960]
  4. Korea Health Technology R&D Project/Korea Health Industry Devel-opment Institute (KHIDI) , Ministry of Health & Welfare of South Korea [HI20C0644]

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The portable genetic analyzer presented is equipped with an integrated centrifugal disc for analyzing major feline upper respiratory tract disease pathogens, with the capability of performing loop-mediated isothermal amplification (LAMP) or polymerase chain reaction (PCR) within 1.5 hours.
We present a portable genetic analyzer with an integrated centrifugal disc which is equipped with a glass-filter extraction column for purifying nucleic acid (NA) and multiple reaction chambers for analyzing major feline upper respiratory tract disease (FURTD) pathogens. We targeted four kinds of FURTD including Feline herpesvirus 1 (FHV), Mycoplasma felis (MPF), Bordetella bronchiseptica (BDB), and Chlamydophila felis (CDF). The portable genetic analyzer consists of a spinning motor, two pairs of Peltier heaters, two Minco heater, fluorescent optics, a touchscreen, and software for data analysis, so loop-mediated isothermal amplification (LAMP) or polymerase chain reaction (PCR) can be performed. The overall size of the genetic analyzer was 28 cm x 28 cm x 26 cm and the weight was 10 kg, which was deliverable for point-of-care testing (POCT). Owing to the sophisticated microchannel design and spinning program, the serial injection of the sample solution, the washing solution, and the elution solution was executed through a glass filter membrane for nucleic acid (NA) extraction, and then the cocktail with the purified genome was aliquoted into 9 reaction chambers for LAMP or PCR. The whole process for the LAMP reaction or the PCR was completed within 1.5 h. The fluorescence profiles by a scanning mode showed the matched results between the LAMP and the PCR.

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