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Open AccessJournal ArticleDOI

Laboratory Diagnosis of SARS-CoV-2 Pneumonia.

TLDR
In this paper, the authors delineate the categories of testing measures developed to date, analyze the efficacy of collecting patient specimens from diverse regions of the respiratory tract, and present the up and coming technologies which have made pathogen identification easier and more accessible to the public.
Abstract
The emergence and rapid proliferation of Coronavirus Disease-2019, throughout the past year, has put an unprecedented strain on the global schema of health infrastructure and health economy. The time-sensitive agenda of identifying the virus in humans and delivering a vaccine to the public constituted an effort to flatten the statistical curve of viral spread as it grew exponentially. At the forefront of this effort was an exigency of developing rapid and accurate diagnostic strategies. These have emerged in various forms over the past year-each with strengths and weaknesses. To date, they fall into three categories: (1) those isolating and replicating viral RNA in patient samples from the respiratory tract (Nucleic Acid Amplification Tests; NAATs), (2) those detecting the presence of viral proteins (Rapid Antigen Tests; RATs) and serology-based exams identifying antibodies to the virus in whole blood and serum. The latter vary in their detection of immunoglobulins of known prevalence in early-stage and late-stage infection. With this review, we delineate the categories of testing measures developed to date, analyze the efficacy of collecting patient specimens from diverse regions of the respiratory tract, and present the up and coming technologies which have made pathogen identification easier and more accessible to the public.

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Citations
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Journal ArticleDOI

Probing the mutation independent interaction of DNA probes with SARS-CoV-2 variants through a combination of surface-enhanced Raman scattering and machine learning

TL;DR: In this article , a set of DNA probes targeting a specific segment of the nucleocapsid phosphoprotein (N) gene of SARS-CoV-2 with high binding efficiency was developed.
Journal ArticleDOI

A Novel Rapid Test to Detect Anti-SARS-CoV-2 N Protein IgG Based on Shear Horizontal Surface Acoustic Wave (SH-SAW)

TL;DR: In this article, a shear-horizontal surface acoustic wave (SH-SAW) biosensor was developed to detect the anti-SARS-CoV-2 nucleocapsid antibody.
Journal ArticleDOI

Laboratory Diagnosis for SARS-CoV-2 Infection

TL;DR: The optimal diagnostic test for SARS-CoV-2 infection should be selected based on a patient's clinical syndrome and presentation in relation to symptom onset as mentioned in this paper , and the optimal test should be chosen based on the patient's symptoms and presentation.
Journal ArticleDOI

Comparative analysis of chest radiography and lung ultrasound to predict intra-hospital prognosis of patients admitted for acute SARS-CoV-2 pneumonia (COVID-19)

TL;DR: In this paper , a comparison between the Schalekamp radiological lung scale and LUZ-score ultrasound scale was performed in stable COVID-19 patients, and the results showed that the LUZ scale failed to identify patients at higher risk at admission for the primary end-point.
Journal ArticleDOI

Peptide Binder with High-Affinity for the SARS-CoV-2 Spike Receptor-Binding Domain

TL;DR: The R1 peptide exhibited high-affinity for specific binding with the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein with a dissociation constant KD of (7.5 ± 1.9) × 10–10 M, which maintained high binding affinity with the RBD derived from Gamma, Lambda, Delta, and Omicron variants.
References
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Journal ArticleDOI

Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) by Mass Spectrometry.

TL;DR: Testing capacities have been upscaled, there is still a need for reliable high throughput test systems, specifically those that require alternative consumables, and MS is a fast, reliable and cost-effective alternative for the detection of SARS-CoV-2 from oral and nasopharyngeal swabs.
Journal ArticleDOI

Comparison of Two Commercial Platforms and a Laboratory-Developed Test for Detection of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) RNA.

TL;DR: In this paper, the performance of one laboratory developed test (LDT) and two commercial tests, cobas SARS-CoV-2 (Roche) and Amplidiag COVID-19 (Mobidiag), were evaluated for the detection of severe acute respiratory syndrome coronavirus 2 (SARS-coV)-2 RNA in respiratory specimens.
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Comparative evaluation of six immunoassays for the detection of antibodies against SARS-CoV-2.

TL;DR: The diagnostic performance of six immunoassays to detect antibodies against SARS-CoV-2 was compared, showing a specificity of 100 % and sensitivities over 97 % from 14 days after the onset of symptoms, as well as excellent levels of agreement.
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