| Literature DB >> 33594223 |
Ki Wook Kim1,2, Ira W Deveson3,4, Chi Nam I Pang5, Malinna Yeang2, Zin Naing2, Thiruni Adikari6,7, Jillian M Hammond3, Igor Stevanovski3, Alicia G Beukers8, Andrey Verich7, Simon Yin9, David McFarlane9, Marc R Wilkins5, Sacha Stelzer-Braid2,6, Rowena A Bull6,7, Maria E Craig1,2,10, Sebastiaan J van Hal8,11, William D Rawlinson12,13,14,15.
Abstract
Accumulating evidence supports the high prevalence of co-infections among Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) patients, and their potential to worsen the clinical outcome of COVID-19. However, there are few data on Southern Hemisphere populations, and most studies to date have investigated a narrow spectrum of viruses using targeted qRT-PCR. Here we assessed respiratory viral co-infections among SARS-CoV-2 patients in Australia, through respiratory virome characterization. Nasopharyngeal swabs of 92 SARS-CoV-2-positive cases were sequenced using pan-viral hybrid-capture and the Twist Respiratory Virus Panel. In total, 8% of cases were co-infected, with rhinovirus (6%) or influenzavirus (2%). Twist capture also achieved near-complete sequencing (> 90% coverage, > tenfold depth) of the SARS-CoV-2 genome in 95% of specimens with Ct < 30. Our results highlight the importance of assessing all pathogens in symptomatic patients, and the dual-functionality of Twist hybrid-capture, for SARS-CoV-2 whole-genome sequencing without amplicon generation and the simultaneous identification of viral co-infections with ease.Entities:
Year: 2021 PMID: 33594223 DOI: 10.1038/s41598-021-83642-x
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379