MMWR Morb Mortal Wkly Rep. 2023 Feb 3;72(5):125-127. doi: 10.15585/mmwr.mm7205e2.
Monitoring emerging SARS-CoV-2 lineages and their epidemiologic characteristics helps to inform public health decisions regarding vaccine policy, the use of therapeutics, and health care capacity. When the SARS-CoV-2 Alpha variant emerged in late 2020, a spike gene (S-gene) deletion (Δ69-70) in the N-terminal region, which might compensate for immune escape mutations that impair infectivity (1), resulted in reduced or failed S-gene target amplification in certain multitarget reverse transcription-polymerase chain reaction (RT-PCR) assays, a pattern referred to as S-gene target failure (SGTF) (2). The predominant U.S. SARS-CoV-2 lineages have generally alternated between SGTF and S-gene target presence (SGTP), which alongside genomic sequencing, has facilitated early monitoring of emerging variants. During a period when Omicron BA.5-related sublineages (which exhibit SGTF) predominated, an XBB.1.5 sublineage with SGTP has rapidly expanded in the northeastern United States and other regions.
监测新出现的 SARS-CoV-2 谱系及其流行病学特征有助于为疫苗政策、治疗药物的使用以及医疗保健能力提供公共卫生决策依据。当 2020 年末出现 SARS-CoV-2 的 Alpha 变体时,其 N 端区域的刺突蛋白(S 蛋白)基因(S-gene)缺失(Δ69-70)可能补偿了削弱感染力的免疫逃逸突变(1),导致某些多靶点逆转录聚合酶链反应(RT-PCR)检测中 S 基因目标扩增减少或失败,这种模式被称为 S 基因目标失败(SGTF)(2)。美国主要的 SARS-CoV-2 谱系通常在 SGTF 和 S 基因目标存在(SGTP)之间交替,这与基因组测序一起,有助于早期监测新出现的变体。在 Omicron BA.5 相关亚谱系(表现出 SGTF)占主导地位的时期,具有 SGTP 的 XBB.1.5 亚谱系在美国东北部和其他地区迅速扩张。