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2021 年 1 月至 2023 年 7 月莱茵内卡尔/海德堡地区 SARS-CoV-2 的进化。

Evolution of SARS-CoV-2 in the Rhine-Neckar/Heidelberg Region 01/2021 - 07/2023.

机构信息

Heidelberg University, Medical Faculty Heidelberg, Department of Infectious Diseases, Virology, Heidelberg, Germany.

Heidelberg University, Medical Faculty Heidelberg, Department of Infectious Diseases, Virology, Heidelberg, Germany; Heidelberg University, Medical Faculty Heidelberg, Department of Infectious Diseases, Microbiology and Hygiene, Heidelberg, Germany.

出版信息

Infect Genet Evol. 2024 Apr;119:105577. doi: 10.1016/j.meegid.2024.105577. Epub 2024 Feb 23.

Abstract

In January 2021, the monitoring of circulating variants of SARS-CoV-2 was initiated in Germany under the Corona Surveillance Act, which was discontinued after July 2023. This initiative aimed to enhance pandemic containment, as specific amino acid changes, particularly in the spike protein, were associated with increased transmission and reduced vaccine efficacy. Our group conducted whole genome sequencing using the ARTIC protocol (currently V4) on Illumina's NextSeq 500 platform (and, starting in May 2023, on the MiSeq DX platform) for SARS-CoV-2 positive specimen from patients at Heidelberg University Hospital, associated hospitals, and the public health office in the Rhine-Neckar/Heidelberg region. In total, we sequenced 26,795 SARS-CoV-2-positive samples between January 2021 and July 2023. Valid sequences, meeting the requirements for upload to the German electronic sequencing data hub (DESH) operated by the Robert Koch Institute (RKI), were determined for 24,852 samples, and the lineage/clade could be identified for 25,912 samples. The year 2021 witnessed significant dynamics in the circulating variants in the Rhine-Neckar/Heidelberg region, including A.27.RN, followed by the emergence of B.1.1.7 (Alpha), subsequently displaced by B.1.617.2 (Delta), and the initial occurrences of B.1.1.529 (Omicron). By January 2022, B.1.1.529 had superseded B.1.617.2, dominating with over 90%. The years 2022 and 2023 were then characterized by the dominance of B.1.1.529 and its sublineages, particularly BA.5 and BA.2, and more recently, the emergence of recombinant variants like XBB.1.5. Since the global dominance of B.1.617.2, the identified variant distribution in our local study, apart from a time delay in the spread of new variants, can be considered largely representative of the global distribution. om a time delay in the spread of new variants, can be considered largely representative of the global distribution.

摘要

2021 年 1 月,根据《冠状病毒监测法》在德国启动了对 SARS-CoV-2 循环变异株的监测,该监测于 2023 年 7 月停止。这一举措旨在加强大流行的控制,因为特定的氨基酸变化,特别是在刺突蛋白中,与传播增加和疫苗效力降低有关。我们的小组使用 ARTIC 方案(目前为 V4)在 Illumina 的 NextSeq 500 平台(并从 2023 年 5 月开始在 MiSeq DX 平台)上对海德堡大学医院、附属医院和莱茵内卡尔/海德堡地区公共卫生办公室的 SARS-CoV-2 阳性患者标本进行全基因组测序。总共,我们在 2021 年 1 月至 2023 年 7 月期间对 26795 个 SARS-CoV-2 阳性样本进行了测序。符合德国罗伯特科赫研究所(RKI)运营的德国电子测序数据中心(DESH)上载要求的有效序列确定了 24852 个样本,并且可以确定 25912 个样本的谱系/分支。2021 年,莱茵内卡尔/海德堡地区的循环变异株出现了显著的动态变化,包括 A.27.RN,随后出现了 B.1.1.7(Alpha),随后被 B.1.617.2(Delta)取代,最初出现了 B.1.1.529(Omicron)。到 2022 年 1 月,B.1.1.529 已经取代了 B.1.617.2,占主导地位超过 90%。然后,2022 年和 2023 年的特点是 B.1.1.529 及其亚系,特别是 BA.5 和 BA.2 的主导地位,以及最近重组变体如 XBB.1.5 的出现。自 B.1.617.2 在全球占主导地位以来,除了新变体传播的时间延迟外,我们的本地研究中确定的变体分布可以被认为在很大程度上代表了全球分布。

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