NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

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

  1. 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
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Pneumonia/Respiratory Infection
    Platform:
    AnalyteTechnology Platform
    Protein Immunoaffinity chromatography
    RNA Real-time qRT-PCR
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(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

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