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免疫功能低下宿主中的 SARS-CoV-2:通过全基因组测序阐明恢复期血浆治疗和病毒进化。

SARS-CoV-2 in an immunocompromised host: convalescent plasma therapy and viral evolution elucidated by whole genome sequencing.

机构信息

Institute of Medical Microbiology, University of Zurich, Zurich, Switzerland.

Division of Clinical Bacteriology and Mycology, University Hospital Basel, Basel, Switzerland.

出版信息

BMJ Case Rep. 2023 Dec 9;16(12):e255255. doi: 10.1136/bcr-2023-255255.

Abstract

The evolution of SARS-CoV-2 within immunocompromised hosts who fail to clear the virus over many months has been proposed as a route to the development of Variants of Concern (VoCs). We present a case of an immunocompromised male patient with a prolonged SARS-CoV-2 infection. During hospitalisation, 7 weeks after first diagnosis, his condition worsened to require continuous ventilation support. Resolution of symptoms was observed after convalescent plasma therapy. Whole genome sequencing of the virus showed Pango lineage B.1.221. Between the first sample and the second from bronchoalveolar lavage fluid 7 weeks later, we identified eight mutations, including minor variants, which could be used to estimate the chronology of mutations. This suggests an elevated mutation rate, in-host accumulation of mutations and further evidence for sources of VoCs. Prolonged SARS-CoV-2 infections in immunocompromised hosts increase the likelihood of hospital stays and morbidity, and also pose an increased risk to global public health.

摘要

有人提出,在未能清除病毒长达数月的免疫功能低下宿主中,SARS-CoV-2 的进化可能是导致关注变种(VOC)出现的途径。我们报告了一例免疫功能低下的男性患者,他的 SARS-CoV-2 感染持续时间较长。在首次诊断后 7 周住院期间,他的病情恶化,需要持续通气支持。接受恢复期血浆治疗后症状缓解。对病毒进行全基因组测序显示,其属于 Pango 谱系 B.1.221。在首次样本和第二次支气管肺泡灌洗液样本之间相隔 7 周,我们发现了 8 个突变,包括次要变异,这些突变可用于估计突变的时间顺序。这表明突变率升高,在宿主内积累了突变,进一步证明了 VOC 的来源。免疫功能低下宿主中持续存在的 SARS-CoV-2 感染增加了住院和发病的可能性,也对全球公共卫生构成了更大的威胁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d89f/10728978/99d6aaf001cc/bcr-2023-255255f01.jpg

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