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SARS-CoV-2 nasopharyngeal viral load in individuals infected with BA.2, compared to Alpha, Gamma, Delta and BA.1 variants: A single-center comparative analysis

Authors :
Ilaria Mastrorosa
Alessandro Cozzi-Lepri
Francesca Colavita
Eleonora Lalle
Valentina Mazzotta
Claudia Cimaglia
Jessica Paulicelli
Giulia Matusali
Lavinia Fabeni
Fabrizio Carletti
Silvia Rosati
Serena Vita
Giuseppina Giannico
Pierluca Piselli
Elisa Biliotti
Samir Al Moghazi
Silvia Mosti
Enrico Girardi
Emanuele Nicastri
Anna Rosa Garbuglia
Fabrizio Maggi
Francesco Vaia
Andrea Antinori
Source :
Journal of Clinical Virology. 157:105299
Publication Year :
2022
Publisher :
Elsevier BV, 2022.

Abstract

SARS-CoV-2 has evolved, leading to the emergence of new Variants Of Concern (VOCs) with significant impact on transmissibility. Although the transmission process is complex, higher nasopharyngeal viral load (NP-VL) can be considered as a proxy for greater transmissibility.The aim of this analysis was to compare NP-VL across a set of representative VOCs observed in mildly symptomatic patients.Observational single-center comparative analysis of patients with early mild-to-moderate COVID-19, enrolled within the early treatment access program of Lazzaro Spallanzani Institute (March 2021-March 2022). NP-VL before drug administration was estimated through RT-PCR, based on cycle threshold values (CTs); VOCs were identified by Sanger sequencing. VOCs' average treatment effect (ATE) was estimated on the CTs fitted in the log2 scale, controlling for potential confounders.A total of 707 patients were included. VOCs were: 10% Alpha, 3% Gamma, 34% Delta, 34% BA.1, 19% BA.2. Mean CTs for BA.1 and BA.2 were lower than Delta and BA.1, respectively. After adjusting for calendar time, age, immunodeficiency and vaccination, CTs for Gamma were lower than those seen for Alpha and higher than Delta, for Delta were similar to BA.1, for BA.2 were lower than Delta and BA.1.Our analysis shows higher NP-VL of BA.2 compared to previously circulating VOCs, even after controlling for factors potentially contributing to the amount of nasopharyngeal viral RNA, included vaccination, supporting the increased transmissibility of BA.2. Further studies are necessary to clarify this mechanism and to provide guidance for public health measures.

Details

ISSN :
13866532
Volume :
157
Database :
OpenAIRE
Journal :
Journal of Clinical Virology
Accession number :
edsair.doi.dedup.....b81217b55860eeb917288e71b94fa6a8
Full Text :
https://doi.org/10.1016/j.jcv.2022.105299