Value of Viral Nucleic Acid in Sputum and Feces and Specific IgM/IgG in Serum for the Diagnosis of Coronavirus Disease 2019.
Author(s): He Y, Luo J, Yang J, Song J, Wei L, Ma W
Publication: Front Cell Infect Microbiol, 2020, Vol. 10, Page 445
PubMed ID: 32850506 PubMed Review Paper? No
Purpose of Paper
This paper compared the detection of SARS-CoV-2, the virus that causes the novel 2019 coronavirus disease (COVID, COVID-19, COVID19), in matched nasal swab, oropharyngeal swab, feces, and sputum specimens using real-time qRT-PCR over the course of the patient’s hospitalization. SARS-CoV-2 IgM/IgG antibodies were detected in serum of patients using immunochromatography.
Conclusion of Paper
The detection rate of SARS-CoV-2 RNA by real-time qRT-PCR was highest in sputum specimens (19/20), followed by nasal swabs (14/20), fecal specimens (11/20), and then oropharyngeal swabs (10/20). SARS-CoV-2 was detectable in sputum a significantly longer average number of days compared to the other specimen types. SARS-CoV-2 IgG and IgM antibodies were detected in serum from all 20 patients.
Studies
-
Study Purpose
This study compared the detection of SARS-CoV-2 in matched nasal swab, oropharyngeal swab, feces, and sputum specimens using real-time qRT-PCR over the course of the patient’s hospitalization and detection of SARS-CoV-2 IgM/IgG antibodies in serum using immunochromatography. Specimens were collected from 20 hospitalized patients (median age=57.35 y; 14 males, 6 females) every day for a week and then every 2-3 days until patient discharge. Viral RNA was extracted from swab, sputum, and fecal specimens using a magnetic bead-based method (details for collection, processing, and storage not provided). The open reading frame (ORF1ab), nucleoprotein (N) gene regions of SARS-CoV-2 was detected by real-time qRT-PCR and specimens were determined positive if CT value was <40. Serum was separated from the blood specimen (tube type not specified) by centrifugation at 3,000 rpm for 15 min within 24 h after collection, inactivated at 56°C for 30 min, and stored at 4°C until analysis for SARS-CoV-2 IgM/IgG antibodies by immunochromatography.
Summary of Findings:
The detection rate of SARS-CoV-2 RNA was highest in sputum specimens (19/20), followed by nasal swabs (14/20), fecal specimens (11/20), and then oropharyngeal swabs (10/20). SARS-CoV-2 RNA was detected in sputum for a significantly longer average number of days compared to oropharyngeal swabs, nasal swabs, and feces (42.8 versus 32.0, 24.0, and 20.6 days, respectively; P<0.00017, P<0.00167, and P<0.00833, respectively). SARS-CoV-2 IgG and IgM antibodies were detected in serum of all 20 patients.
Biospecimens
- Cell - Nasal cavity
- Cell - Oral Cavity
- Bodily Fluid - Serum
- Bodily Fluid - Sputum
- Bodily Fluid - Feces
- Bodily Fluid - Blood
Preservative Types
- None (Fresh)
Diagnoses:
- Pneumonia/Respiratory Infection
Platform:
Analyte Technology Platform Protein Immunoaffinity chromatography RNA Real-time qRT-PCR Pre-analytical Factors:
Classification Pre-analytical Factor Value(s) Real-time qRT-PCR Specific Targeted nucleic acid ORF1ab/N gene regions of SARS-CoV-2
Biospecimen Acquisition Biospecimen location nasal swab
oropharyngeal swab
sputum
feces
serum