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一种针对新 SARS-CoV-2 变异株的区域性公共卫生实验室早期检测和人群监测的应对预案。

A response playbook for early detection and population surveillance of new SARS-CoV-2 variants in a regional public health laboratory.

机构信息

Department of Internal Medicine, Regional Innovative Public Health Laboratory, Rush University Medical Center, Jelke 1259, 1750 W Harrison St, Chicago, IL, 60612, USA.

Chicago Department of Public Health, Chicago, IL, USA.

出版信息

BMC Public Health. 2024 Jan 2;24(1):59. doi: 10.1186/s12889-023-17536-0.

Abstract

BACKGROUND

Timely genomic surveillance is required to inform public health responses to new SARS-CoV-2 variants. However, the processes involved in local genomic surveillance introduce inherent time constraints. The Regional Innovative Public Health Laboratory in Chicago developed and employed a genomic surveillance response playbook for the early detection and surveillance of emerging SARS-CoV-2 variants.

METHODS

The playbook outlines modifications to sampling strategies, laboratory workflows, and communication processes based on the emerging variant's predicted viral characteristics, observed public health impact in other jurisdictions and local community risk level. The playbook outlines procedures for implementing and reporting enhanced and accelerated genomic surveillance, including supplementing whole genome sequencing (WGS) with variant screening by quantitative PCR (qPCR).

RESULTS

The ability of the playbook to improve the response to an emerging variant was tested for SARS-CoV-2 Omicron BA.1. Increased submission of clinical remnant samples from local hospital laboratories enabled detection of a new variant at an average of 1.4% prevalence with 95% confidence rather than 3.5% at baseline. Genotyping qPCR concurred with WGS lineage assignments in 99.9% of 1541 samples with results by both methods, and was more sensitive, providing lineage results in 90.4% of 1833 samples rather than 85.1% for WGS, while significantly reducing the time to lineage result.

CONCLUSIONS

The genomic surveillance response playbook provides a structured, stepwise, and data-driven approach to responding to emerging SARS-CoV-2 variants. These pre-defined processes can serve as a template for other genomic surveillance programs to streamline workflows and expedite the detection and public health response to emerging variants. Based on the processes piloted during the Omicron BA.1 response, this method has been applied to subsequent Omicron subvariants and can be readily applied to future SARS-CoV-2 emerging variants and other public health surveillance activities.

摘要

背景

及时的基因组监测对于指导针对新出现的 SARS-CoV-2 变体的公共卫生应对措施至关重要。然而,本地基因组监测所涉及的过程存在固有时间限制。芝加哥地区创新公共卫生实验室开发并采用了一份基因组监测应对手册,用于早期检测和监测新出现的 SARS-CoV-2 变体。

方法

该手册根据新兴变体的预测病毒特征、其他司法管辖区的观察到的公共卫生影响以及当地社区的风险水平,概述了采样策略、实验室工作流程和沟通流程的修改。该手册概述了实施和报告增强和加速基因组监测的程序,包括通过定量 PCR(qPCR)进行变体筛选来补充全基因组测序(WGS)。

结果

该手册提高了对新出现变体的应对能力,通过增加来自当地医院实验室的临床剩余样本的提交,以 95%的置信度在平均 1.4%的流行率下检测到了新变体,而基线时的流行率为 3.5%。在两种方法都获得结果的 1541 个样本中,基因分型 qPCR 与 WGS 谱系分配的一致性为 99.9%,而 WGS 的敏感性为 85.1%,在 1833 个样本中提供了谱系结果,90.4%,同时显著缩短了谱系结果的时间。

结论

基因组监测应对手册为应对新出现的 SARS-CoV-2 变体提供了一种结构化、逐步和数据驱动的方法。这些预先定义的流程可以作为其他基因组监测计划的模板,以简化工作流程并加快对新出现变体的检测和公共卫生应对。基于在 Omicron BA.1 应对期间试点的流程,该方法已应用于随后的 Omicron 亚变体,并且可以轻松应用于未来的 SARS-CoV-2 新出现变体和其他公共卫生监测活动。

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