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Viral Load Kinetics of SARS-CoV-2 Infection in Saliva in Korean Patients: a Prospective Multi-center Comparative Study.

Identifieur interne : 000077 ( Main/Exploration ); précédent : 000076; suivant : 000078

Viral Load Kinetics of SARS-CoV-2 Infection in Saliva in Korean Patients: a Prospective Multi-center Comparative Study.

Auteurs : Seong Eun Kim [Corée du Sud] ; Ji Yeon Lee [Corée du Sud] ; Ahrang Lee [Corée du Sud] ; Soosung Kim [Corée du Sud] ; Kyung Hwa Park [Corée du Sud] ; Sook In Jung [Corée du Sud] ; Seung Ji Kang [Corée du Sud] ; Tae Hoon Oh [Corée du Sud] ; Uh Jin Kim [Corée du Sud] ; Seung Yeob Lee [Corée du Sud] ; Seung Jung Kee [Corée du Sud] ; Hee Chang Jang [Corée du Sud]

Source :

RBID : pubmed:32776725

Descripteurs français

English descriptors

Abstract

BACKGROUND

This study was performed to compare the viral load and kinetics of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in saliva with those in standard nasopharyngeal/oropharyngeal (NP/OP) swabs.

METHODS

Fifteen patients with SARS-CoV-2 infection from four hospitals were prospectively enrolled and matched samples of nasopharyngeal/oropharyngeal swabs and saliva were collected at Day 1 of admission and every other day till consequently negative for two times. Real-time reverse transcription polymerase chain reaction (rRT-PCR) was performed to detect the envelope (E) and RNA-dependent RNA polymerase (RdRP) genes.

RESULTS

The cycle threshold values of saliva were comparable to those of NP/OP swabs overall (

CONCLUSION

Saliva sample itself is not appropriate for initial diagnosis of coronavirus disease 2019 (COVID-19) to replace NP/OP swabs, especially for the person who does not produce sputum. COVID-19 cannot be excluded when the test using saliva is negative, and it is necessary to retest using NP/OP swabs.


DOI: 10.3346/jkms.2020.35.e287
PubMed: 32776725
PubMed Central: PMC7415999


Affiliations:


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Le document en format XML

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<p>
<b>BACKGROUND</b>
</p>
<p>This study was performed to compare the viral load and kinetics of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in saliva with those in standard nasopharyngeal/oropharyngeal (NP/OP) swabs.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>Fifteen patients with SARS-CoV-2 infection from four hospitals were prospectively enrolled and matched samples of nasopharyngeal/oropharyngeal swabs and saliva were collected at Day 1 of admission and every other day till consequently negative for two times. Real-time reverse transcription polymerase chain reaction (rRT-PCR) was performed to detect the envelope (E) and RNA-dependent RNA polymerase (RdRP) genes.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>The cycle threshold values of saliva were comparable to those of NP/OP swabs overall (</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSION</b>
</p>
<p>Saliva sample itself is not appropriate for initial diagnosis of coronavirus disease 2019 (COVID-19) to replace NP/OP swabs, especially for the person who does not produce sputum. COVID-19 cannot be excluded when the test using saliva is negative, and it is necessary to retest using NP/OP swabs.</p>
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<Title>Journal of Korean medical science</Title>
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<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">This study was performed to compare the viral load and kinetics of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in saliva with those in standard nasopharyngeal/oropharyngeal (NP/OP) swabs.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Fifteen patients with SARS-CoV-2 infection from four hospitals were prospectively enrolled and matched samples of nasopharyngeal/oropharyngeal swabs and saliva were collected at Day 1 of admission and every other day till consequently negative for two times. Real-time reverse transcription polymerase chain reaction (rRT-PCR) was performed to detect the envelope (E) and RNA-dependent RNA polymerase (RdRP) genes.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The cycle threshold values of saliva were comparable to those of NP/OP swabs overall (
<i>P</i>
= 0.720, Mann-Whitney U test). However, the overall sensitivity of rRT-PCR using saliva was 64% (34/53), which is lower than the 77% (41/53) using NP/OP swabs. The sensitivity of rRT-PCR using saliva was especially lower in early stage of symptom onset (1-5 days; 8/15; 53%) and in patients who did not have sputum (12/22; 55%).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Saliva sample itself is not appropriate for initial diagnosis of coronavirus disease 2019 (COVID-19) to replace NP/OP swabs, especially for the person who does not produce sputum. COVID-19 cannot be excluded when the test using saliva is negative, and it is necessary to retest using NP/OP swabs.</AbstractText>
<CopyrightInformation>© 2020 The Korean Academy of Medical Sciences.</CopyrightInformation>
</Abstract>
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<ForeName>Seong Eun</ForeName>
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<Affiliation>Department of Infectious Diseases, Chonnam National University Hospital, Gwangju, Korea.</Affiliation>
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<Affiliation>Department of Infectious Diseases, Keimyung University Dongsan Hospital, Daegu, Korea.</Affiliation>
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