Detectable 2019-nCoV viral RNA in blood is a strong indicator for the further clinical severity.
Identifieur interne : 000A10 ( PubMed/Corpus ); précédent : 000A09; suivant : 000A11Detectable 2019-nCoV viral RNA in blood is a strong indicator for the further clinical severity.
Auteurs : Weilie Chen ; Yun Lan ; Xiaozhen Yuan ; Xilong Deng ; Yueping Li ; Xiaoli Cai ; Liya Li ; Ruiying He ; Yizhou Tan ; Xizi Deng ; Ming Gao ; Guofang Tang ; Lingzhai Zhao ; Jinlin Wang ; Qinghong Fan ; Chunyan Wen ; Yuwei Tong ; Yangbo Tang ; Fengyu Hu ; Feng Li ; Xiaoping TangSource :
- Emerging microbes & infections [ 2222-1751 ] ; 2020.
English descriptors
- KwdEn :
- MESH :
- chemical , blood : RNA, Viral.
- genetics : Betacoronavirus, RNA, Viral.
- isolation & purification : Betacoronavirus.
- virology : Coronavirus Infections, Pneumonia, Viral.
- Humans, Real-Time Polymerase Chain Reaction, Retrospective Studies, Severity of Illness Index.
Abstract
The novel coronavirus (2019-nCoV) infection caused pneumonia. we retrospectively analyzed the virus presence in the pharyngeal swab, blood, and the anal swab detected by real-time PCR in the clinical lab. Unexpectedly, the 2109-nCoV RNA was readily detected in the blood (6 of 57 patients) and the anal swabs (11 of 28 patients). Importantly, all of the 6 patients with detectable viral RNA in the blood cohort progressed to severe symptom stage, indicating a strong correlation of serum viral RNA with the disease severity (p-value = 0.0001). Meanwhile, 8 of the 11 patients with annal swab virus-positive was in severe clinical stage. However, the concentration of viral RNA in the anal swab (Ct value = 24 + 39) was higher than in the blood (Ct value = 34 + 39) from patient 2, suggesting that the virus might replicate in the digestive tract. Altogether, our results confirmed the presence of virus RNA in extra-pulmonary sites.
DOI: 10.1080/22221751.2020.1732837
PubMed: 32102625
Links to Exploration step
pubmed:32102625Le document en format XML
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<front><div type="abstract" xml:lang="en">The novel coronavirus (2019-nCoV) infection caused pneumonia. we retrospectively analyzed the virus presence in the pharyngeal swab, blood, and the anal swab detected by real-time PCR in the clinical lab. Unexpectedly, the 2109-nCoV RNA was readily detected in the blood (6 of 57 patients) and the anal swabs (11 of 28 patients). Importantly, all of the 6 patients with detectable viral RNA in the blood cohort progressed to severe symptom stage, indicating a strong correlation of serum viral RNA with the disease severity (<i>p</i>
-value = 0.0001). Meanwhile, 8 of the 11 patients with annal swab virus-positive was in severe clinical stage. However, the concentration of viral RNA in the anal swab (Ct value = 24 + 39) was higher than in the blood (Ct value = 34 + 39) from patient 2, suggesting that the virus might replicate in the digestive tract. Altogether, our results confirmed the presence of virus RNA in extra-pulmonary sites.</div>
</front>
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<Abstract><AbstractText>The novel coronavirus (2019-nCoV) infection caused pneumonia. we retrospectively analyzed the virus presence in the pharyngeal swab, blood, and the anal swab detected by real-time PCR in the clinical lab. Unexpectedly, the 2109-nCoV RNA was readily detected in the blood (6 of 57 patients) and the anal swabs (11 of 28 patients). Importantly, all of the 6 patients with detectable viral RNA in the blood cohort progressed to severe symptom stage, indicating a strong correlation of serum viral RNA with the disease severity (<i>p</i>
-value = 0.0001). Meanwhile, 8 of the 11 patients with annal swab virus-positive was in severe clinical stage. However, the concentration of viral RNA in the anal swab (Ct value = 24 + 39) was higher than in the blood (Ct value = 34 + 39) from patient 2, suggesting that the virus might replicate in the digestive tract. Altogether, our results confirmed the presence of virus RNA in extra-pulmonary sites.</AbstractText>
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<Author ValidYN="Y"><LastName>Zhao</LastName>
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<Author ValidYN="Y"><LastName>Hu</LastName>
<ForeName>Fengyu</ForeName>
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<Author ValidYN="Y"><LastName>Li</LastName>
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<Author ValidYN="Y"><LastName>Tang</LastName>
<ForeName>Xiaoping</ForeName>
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