Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Dec;27(12):1858.e1-1858.e7.
doi: 10.1016/j.cmi.2021.08.001. Epub 2021 Aug 9.

Upper respiratory tract SARS-CoV-2 RNA loads in symptomatic and asymptomatic children and adults

Affiliations

Upper respiratory tract SARS-CoV-2 RNA loads in symptomatic and asymptomatic children and adults

Rosa Costa et al. Clin Microbiol Infect. 2021 Dec.

Abstract

Objectives: Studies comparing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA load in the upper respiratory tract (URT) between children and adults-who either presented with coronavirus disease 2019 (COVID-19) or were asymptomatic-have yielded inconsistent results. Here, we conducted a retrospective, single-centre study to address this issue.

Patients and methods: Included were 1184 consecutive subjects (256 children and 928 adults) testing positive for SARS-CoV-2 RNA in nasopharyngeal exudates (NPs); of these, 424 (121 children and 303 adults) had COVID-19 and 760 (135 children and 625 adults) were asymptomatic close contacts of COVID-19 patients. SARS-CoV-2 RNA testing was carried out using the TaqPath COVID-19 Combo Kit (Thermo Fisher Scientific, MS, USA). The AMPLIRUN® TOTAL SARS-CoV-2 RNA Control (Vircell SA, Granada, Spain) was used for estimating SARS-CoV-2 RNA loads (in copies/mL). SARS-CoV-2 RNA loads at the time of laboratory diagnosis (single specimen/patient) were used for comparison purposes.

Results: Median initial SARS-CoV-2 RNA load was lower (p 0.094) in children (6.98 log10 copies/mL, range 3.0-11.7) than in adults (7.14 log10 copies/mL, range 2.2-13.4) with COVID-19. As for asymptomatic individuals, median SARS-CoV-2 RNA load was comparable (p 0.97) in children (6.20 log10 copies/mL, range 1.8-11.6) and adults (6.48 log10 copies/mL, range 1.9-11.8). Children with COVID-19 symptoms displayed SARS-CoV-2 RNA loads (6.98 log10 copies/mL, range 3.0-11.7) comparable to those of their asymptomatic counterparts (6.20 log10 copies/mL, range 1.8-11.6) (p 0.61). Meanwhile in adults, median SARS-CoV-2 RNA load was significantly higher in symptomatic (7.14 log10 copies/mL, range 2.2-13.4) than in asymptomatic subjects (6.48 log10 copies/mL, range 1.9-11.8) (p < 0.001). Overall, the observed URT SARS-CoV-2 RNA clearance rate was faster in children than in adults.

Conclusions: Based on viral load data at the time of diagnosis, our results suggest that SARS-CoV-2-infected children, with or without COVID-19, may display NP viral loads of comparable magnitude to those found in their adult counterparts. However, children may have shorter viral shedding than adults.

Keywords: Adults; COVID-19; Children; SARS-CoV-2 RNA; Upper respiratory tract; Viral load.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Overall initial severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA loads in nasopharyngeal specimens from children and adults with coronavirus disease 2019 (COVID-19). Medians are indicated by midlines; the top and bottom edges of boxes represent the interquartile range (IQR). Whiskers indicate the upper and lower values. The number of patients in each group as well as p values for comparisons between groups (median SARS-CoV-2 RNA levels) are shown.
Fig. 2
Fig. 2
Initial severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA loads in nasopharyngeal specimens from children and adults with coronavirus disease 2019 (COVID-19) according to the time of sampling after symptom onset. Medians are indicated by midlines; the top and bottom edges of boxes represent the interquartile range (IQR). Whiskers indicate the upper and lower values. The number of patients in each group as well as p values for comparisons between groups (median SARS-CoV-2 RNA levels) are shown.
Fig. 3
Fig. 3
Correlation between initial severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA load in nasopharyngeal specimens from (A) adults and (B) children with coronavirus disease 2019 (COVID-19), and from (C) asymptomatic adults and (D) children and age of participants.
Fig. 4
Fig. 4
Overall initial severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA loads in nasopharyngeal specimens from asymptomatic children and adults with coronavirus disease 2019 (COVID-19). Medians are indicated by midlines; the top and bottom edges of boxes represent the interquartile range (IQR). Whiskers indicate the upper and lower values. The number of patients in each group as well as p values for comparisons between groups (median SARS-CoV-2 RNA levels) are shown.
Fig. 5
Fig. 5
Comparison of initial severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA loads in nasopharyngeal specimens from (A) children and (B) adults either asymptomatic or presenting with coronavirus disease 2019 (COVID-19). Medians are indicated by midlines; the top and bottom edges of boxes represent the interquartile range (IQR). Whiskers indicate the upper and lower values. The number of patients in each group as well as p values for comparisons between groups (median SARS-CoV-2 RNA levels) are shown.
figs1
figs1
figs2
figs2
figs3
figs3

References

    1. Viner R.M., Mytton O.T., Bonell C., Melendez-Torres G.J., Ward J., Hudson L., et al. Susceptibility to SARS-CoV-2 infection among children and adolescents compared with adults: a systematic review and meta-analysis. JAMA Pediatr. 2021;175:143–156. - PMC - PubMed
    1. Wölfel R., Corman V.M., Guggemos W., Seilmaier M., Zange S., Müller M.A. Virological assessment of hospitalized patients with COVID-2019. Nature. 2020;581:465–469. - PubMed
    1. Huang C.G., Lee K.M., Hsiao M.J., Yang S.L., Huang P.N., Gong Y.N. Culture-based virus isolation to evaluate potential infectivity of clinical specimens tested for COVID-19. J Clin Microbiol. 2020;58 - PMC - PubMed
    1. Bullard J., Dust K., Funk D., Strong J.E., Alexander D., Garnett L. Predicting infectious severe acute respiratory syndrome coronavirus 2 from diagnostic samples. Clin Infect Dis. 2020:ciaa638. - PMC - PubMed
    1. L’Huillier A.G., Torriani G., Pigny F., Kaiser L., Eckerle I. Culture-competent SARS-CoV-2 in nasopharynx of symptomatic neonates, children, and adolescents. Emerg Infect Dis. 2020;26:26. - PMC - PubMed