Abstract

We aimed to assess the duration of nasopharyngeal severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA persistence in adults self-confined at home after acute infection; and to identify the associations of SARS-CoV-2 persistence with respiratory virus co-detection and infection transmission. A cross-sectional intra-household study was conducted in metropolitan Barcelona (Spain) during the time period of April to June 2020. Every adult who was the first family member reported as SARS-CoV-2-positive by reverse transcription polymerase chain reaction (RT-PCR) as well as their household child contacts had nasopharyngeal swabs tested by a targeted SARS-CoV-2 RT-PCR and a multiplex viral respiratory panel after a 15 day minimum time lag. Four-hundred and four households (404 adults and 708 children) were enrolled. SARS-CoV-2 RNA was detected in 137 (33.9%) adults and 84 (11.9%) children. Rhinovirus/Enterovirus (RV/EV) was commonly found (83.3%) in co-infection with SARS-CoV-2 in adults. The mean duration of SARS-CoV-2 RNA presence in adults’ nasopharynx was 52 days (range 26–83 days). The persistence of SARS-CoV-2 was significantly associated with RV/EV co-infection (adjusted odds ratio (aOR) 9.31; 95% CI 2.57–33.80) and SARS-CoV-2 detection in child contacts (aOR 2.08; 95% CI 1.24–3.51). Prolonged nasopharyngeal SARS-CoV-2 RNA persistence beyond the acute infection phase was frequent in adults quarantined at home during the first epidemic wave; which was associated with RV/EV co-infection and could enhance intra-household infection transmission.

Highlights

  • The infectious coronavirus disease 2019 (COVID-19) caused by the new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has had devastating public health consequences globally since it first emerged in Wuhan, China in December 2019 [1]

  • Participant adults recovering or completely recovered from COVID-19 had tested positive for SARS-CoV-2 RNA detection in a nasopharyngeal swab at least 15 days before their household was visited for sample collection

  • All family members were tested by rapid immunochromatographic lateral flow assay (LFA) at the household visit, whereas only adults that gave their consent had venous blood extracted for subsequent enzyme-linked immunosorbent assay (ELISA) at the laboratory of the study site

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Summary

Introduction

The infectious coronavirus disease 2019 (COVID-19) caused by the new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has had devastating public health consequences globally since it first emerged in Wuhan, China in December 2019 [1]. Spain was one of the most strongly affected countries, with over 3.7 million cases and around 80,000 of deaths as of June 2021 [2]. SARS-CoV-2 RNA detection by reverse transcription polymerase chain reaction (RTPCR) is an accurate method that is widely used to diagnose and monitor COVID-19 [4]. Diverse case series studies have reported that SARS-CoV-2 RNA remains detectable in upper respiratory samples for between 11 and 20 days since symptom onset [5,6]. The impact of virus persistence on disease transmissibility remains incompletely understood [7]

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