Author:
Kim Ki Wook,Deveson Ira W.,Pang Chi Nam I.,Yeang Malinna,Naing Zin,Adikari Thiruni,Hammond Jillian M.,Stevanovski Igor,Beukers Alicia G.,Verich Andrey,Yin Simon,McFarlane David,Wilkins Marc R.,Stelzer-Braid Sacha,Bull Rowena A.,Craig Maria E.,van Hal Sebastiaan J.,Rawlinson William D.
Abstract
AbstractAccumulating 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.
Funder
JDRF International Postdoctoral Fellowship
UNSW ResTech Support Scheme
NCI Australasian Leadership Computing COVID-19 Grant
MRFF Investigator Grant
Cancer Institute NSW Early Career Fellowship
NSW State Government RAAP Scheme
UNSW COVID-19 Rapid Response Research Initiative
Publisher
Springer Science and Business Media LLC