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Anyplex rv16

Manufactured by Seegene

The Anyplex RV16 is a molecular diagnostic instrument developed by Seegene. It is designed for the simultaneous detection and identification of 16 common respiratory viruses. The device utilizes real-time PCR technology to provide accurate and efficient analysis of respiratory samples.

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2 protocols using anyplex rv16

1

Coronavirus Respiratory Infection Surveillance

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This was a series of prospective cases between January 2013 and February 2014, which included all patients with acute respiratory infections caused by coronavirus in a population over 18 years of age. Throat swabs were taken and assessed for the presence of the coronaviruses OC43, NL63 and 229E. These swabs were used as the only respiratory sample to avoid potential difficulties in the interpretation of the results based on the sample type. The throat swabs were sent to the laboratory in a viral transport medium (MTV, Vircell, Granada, Spain). Only one sample per patient was considered. The samples were processed to detect the various respiratory viruses using a real-time genomic amplification technique (commercial real-time reverse transcription polymerase chain reaction kit), which provides simultaneous and differential detection of 16 different respiratory viruses (Anyplex RV16, Seegene, South Korea). Blood cultures were performed for patients with suspected pneumonia, and serological determinations for Mycoplasma pneumoniae and Chlamydia pneumoniae were conducted. The medical records and epidemiological data of the patients with coronavirus were reviewed. The statistical analysis was performed using the chi-squared test and Student's t-test for paired data. Values of p < .05 were considered significant.
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2

Molecular Detection of EV-D68 and Respiratory Viruses

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RNA was extracted from 200 μl of nasopharyngeal swab or clarified stool suspensions (pre-treated to chloroform) using a QIAmp Viral RNA Mini Kit (QIAGEN, Hilden, Germany) according to the manufacturer’s specifications. RNAs were eluted with 60 μl nuclease-free water and stored at −80 °C until use.
All specimens from ILI and AFP patients collected from June to September 2016 were screened for EV-D68 by rRT-PCR as previously described41 (link). The AgPath-ID TM one-step quantitative RT-PCR kit (Thermo Fisher Scientific, USA) was used according to the manufacturer’s instructions. Respiratory specimens were tested for respiratory viruses using the Anyplex RV16 (Seegene). Fecal specimens were inoculated onto RD cells after chloroform treatment for EV isolation according to the procedures described in the laboratory manual for the WHO Global Polio Laboratory Network40 .
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