2005
DOI: 10.1016/j.jcv.2004.10.019
|View full text |Cite
|
Sign up to set email alerts
|

The design and application of DNA chips for early detection of SARS-CoV from clinical samples

Abstract: A blind-test of both peripheral blood and sputum specimens lead to the positive detection of SARS-CoV in 31 out of 34 patients. SARS-CoV was not found in peripheral blood or sputum specimens from three patients. Two of the 34 patients were only 3 days post-onset of symptoms and were subsequently confirmed to be SARS positive. Our results indicate that the gene chip-based molecular test is specific for SARS-CoV and allows early detection of patients with SARS with detection rate about 8% higher than the single … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
5
0

Year Published

2007
2007
2022
2022

Publication Types

Select...
8

Relationship

1
7

Authors

Journals

citations
Cited by 11 publications
(5 citation statements)
references
References 12 publications
0
5
0
Order By: Relevance
“…SARS-CoV and SARS-CoV-2 exhibit a very high genetic similarity; both include in their genome four main structural proteins: S, M, E, and N. The SARS-CoV-2 gene S has approximately 75% of the same nucleotide sequences as SARS-CoV, and both viruses bind to host cells using the human angiotensin-converting enzyme 2 receptors. 84,85 For SARS-CoV, several vaccines were tested in animal models, including recombinant S-protein-based vaccines, attenuated and whole inactivated vaccines, and vectored vaccines, but no vaccine was developed. 86 Studies from SARS-CoV have been a reference for the development of COVID-19 vaccines for which multiple strategies have been adopted, most of which target the S protein.…”
Section: Development Of Vaccine Against Sars and Covid-19mentioning
confidence: 99%
“…SARS-CoV and SARS-CoV-2 exhibit a very high genetic similarity; both include in their genome four main structural proteins: S, M, E, and N. The SARS-CoV-2 gene S has approximately 75% of the same nucleotide sequences as SARS-CoV, and both viruses bind to host cells using the human angiotensin-converting enzyme 2 receptors. 84,85 For SARS-CoV, several vaccines were tested in animal models, including recombinant S-protein-based vaccines, attenuated and whole inactivated vaccines, and vectored vaccines, but no vaccine was developed. 86 Studies from SARS-CoV have been a reference for the development of COVID-19 vaccines for which multiple strategies have been adopted, most of which target the S protein.…”
Section: Development Of Vaccine Against Sars and Covid-19mentioning
confidence: 99%
“…One of the crucial clinical questions asked about COVID-19 is whether this is a condition limited to the respiratory and gastrointestinal sites, or whether there is dissemination to other organs. In the 2003 SARS outbreak, there were two publications which found evidence of viral RNA in the blood, 77,78 and one publication demonstrating viral RNA in 33% of patients with MERS-CoV infection 79 ; however, there has been no published information on the other human coronaviruses. Although there has been interest in exploring the multi-organ tropism of this virus, 80 in view of the time frame of organs sampled from 20 to 81 days after infection correlation with damage due to direct virus interaction needs to be examined more closely.…”
Section: Dissemination and Transmission Viraemiamentioning
confidence: 99%
“…Wang and De Risi and colleagues developed a number of arrays for detection of known viral and emerging viral pathogens using hybridization to species-specific oligonucleotide probes [57,58,59] and using advanced bioinformatics analysis tools to reveal pathogen-specific signal patterns [60]. Similar methodologies have been used by these and other groups to identify meningitis-associated and emerging pathogens, including the severe acute respiratory syndrome (SARS) coronavirus [61,62,63,64]. Here we present development and validation of a meningitis diagnostic microarray; it’s reconfiguration onto the Alere Arraytube TM (Alere Technologies GmbH, Jena, Germany) platform and provide recommendations for its use in a diagnostic setting.…”
Section: Introductionmentioning
confidence: 99%