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A novel RdRp-based colorimetric RT-LAMP assay for rapid and sensitive detection of SARS-CoV-2 in clinical and sewage samples from Pakistan.
Haque, Muhammad Farhan Ul; Bukhari, Syeda Sadia; Ejaz, Rabia; Zaman, Faheem Uz; Sreejith, Kamalalayam Rajan; Rashid, Naeem; Umer, Muhammad; Shahzad, Naveed.
  • Haque MFU; School of Biological Sciences, University of the Punjab, Lahore, Pakistan.
  • Bukhari SS; School of Biological Sciences, University of the Punjab, Lahore, Pakistan.
  • Ejaz R; School of Biological Sciences, University of the Punjab, Lahore, Pakistan.
  • Zaman FU; School of Life Sciences, Forman Christian College University, Lahore, Pakistan.
  • Sreejith KR; Queensland Micro- and Nanotechnology Centre, Griffith University, Nathan Australia.
  • Rashid N; School of Biological Sciences, University of the Punjab, Lahore, Pakistan.
  • Umer M; Queensland Micro- and Nanotechnology Centre, Griffith University, Nathan Australia. Electronic address: m.umer@griffith.edu.au.
  • Shahzad N; School of Biological Sciences, University of the Punjab, Lahore, Pakistan. Electronic address: hnaveed.shahzad@gmail.com.
Virus Res ; 302: 198484, 2021 09.
Article in English | MEDLINE | ID: covidwho-1272769
ABSTRACT
Novel corona virus SARS-CoV-2, causing coronavirus disease 2019 (COVID-19), has become a global health challenge particularly for developing countries like Pakistan where overcrowded cities, inadequate sanitation, little health awareness and poor socioeconomic conditions exist. The SARS-CoV-2 has been known to spread primarily through direct contact and respiratory droplets. However, detection of SARS-CoV-2 in stool and sewage have raised the possibility of fecal-oral mode of transmission. Currently, quantitative reverse-transcriptase PCR (qRT-PCR) is the only method being used for SARS-CoV-2 detection, which requires expensive instrumentation, dedicated laboratory setup, highly skilled staff, and several hours to report results. Considering the high transmissibility and rapid spread, a robust, sensitive, specific and cheaper assay for rapid SARS-CoV-2 detection is highly needed. Herein, we report a novel colorimetric RT-LAMP assay for naked-eye detection of SARS-COV-2 in clinical as well as sewage samples. Our SARS-CoV-2 RdRp-based LAMP assay could successfully detect the virus RNA in 26/28 (93%) of RT-PCR positive COVID-19 clinical samples with 100% specificity (n = 7) within 20 min. We also tested the effect of various additives on the performance of LAMP assay and found that addition of 1 mg/ml bovine serum albumin (BSA) could increase the sensitivity of assay up to 101 copies of target sequence. Moreover, we also successfully applied this assay to detect SARS-CoV-2 in sewage waters collected from those areas of Lahore, a city of Punjab province of Pakistan, declared as virus hotspots by local government. Our optimized LAMP assay could provide a sensitive first tier strategy for SARS-CoV-2 screening and can potentially help diagnostic laboratories in better handling of high sample turnout during pandemic situation. By providing rapid naked-eye SARS-CoV-2 detection in sewage samples, this assay may support pandemic readiness and emergency response to any possible virus outbreaks in future.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Sewage / Nucleic Acid Amplification Techniques / Molecular Diagnostic Techniques / Pandemics / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Country/Region as subject: Asia Language: English Journal: Virus Res Journal subject: Virology Year: 2021 Document Type: Article Affiliation country: J.virusres.2021.198484

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Sewage / Nucleic Acid Amplification Techniques / Molecular Diagnostic Techniques / Pandemics / SARS-CoV-2 / COVID-19 Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Country/Region as subject: Asia Language: English Journal: Virus Res Journal subject: Virology Year: 2021 Document Type: Article Affiliation country: J.virusres.2021.198484