Статья

Strategies of RT-PCR-based assay design and surveillance of SARS-CoV-2 [СТРАТЕГИИ ДИЗАЙНА РТ-ПЦР-СИСТЕМ И ОРГАНИЗАЦИЯ МОНИТОРИНГА SARS-COV-2]

N. Kuznetsova, A. Pochtovyy, M. Nikiforova, V. Gushchin,
2021

High population density in the cities with bustling transportation systems and a thriving tourism industry can promote the global spread of a viral infection in a matter of days. The novel SARS-CoV-2 coronavirus has already infected over 2,000,000 people worldwide and caused upwards of 156,000 deaths. One of the factors driving the rapid unfolding of the pandemic is the absence of diagnostic tests for SARS-CoV-2 detection. Molecular techniques allow SARS-CoV-2 RNA to be quickly detected in clinical samples, aiding the differential diagnosis in severely ill patients and facilitating identification of asymptomatic carriers or presymptomatic individuals. Real-time PCR with fluorescent hybridization is the most available, highly sensitive and specific technique for SARS-CoV-2 RNA detection in biological samples. More RT-PCR assay kits are needed for mass screening, which will help to identify infected individuals and contain the current outbreak of COVID-19 in Russia. © 2020 Pirogov Russian National Research Medical University. All rights reserved.

Цитирование

Похожие публикации

Источник

Версии

  • 1. Version of Record от 2021-04-27

Метаданные

Об авторах
  • N. Kuznetsova
    Gamaleya Research Institute of Epidemiology and Microbiology, Moscow, Russian Federation
  • A. Pochtovyy
    Lomonosov Moscow State University, Moscow, Russian Federation
  • M. Nikiforova
  • V. Gushchin
Название журнала
  • Bulletin of Russian State Medical University
Выпуск
  • 2
Страницы
  • 19-22
Ключевые слова
  • ribosome RNA; RNA directed RNA polymerase; virus envelope protein; Article; coronavirus disease 2019; differential diagnosis; human; limit of detection; loop mediated isothermal amplification; mass screening; multiplex polymerase chain reaction; nanopore sequencing; nonhuman; nucleotide sequence; real time polymerase chain reaction; real time reverse transcription polymerase chain reaction; Severe acute respiratory syndrome coronavirus 2; virus detection; virus load; whole genome sequencing
Издатель
  • Pirogov Russian National Research Medical University
Тип документа
  • journal article
Тип лицензии Creative Commons
  • CC
Правовой статус документа
  • Свободная лицензия
Источник
  • scopus