Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Department of Biomedical Sciences, BK21 Graduate Program, Korea University College of Medicine, Seoul, Republic of Korea.
J Med Virol. 2023 Jan;95(1):e28369. doi: 10.1002/jmv.28369.
There are limited data comparing the transmission rates and kinetics of viable virus shedding of the Omicron variant to those of the Delta variant. We compared these rates in hospitalized patients infected with Delta and Omicron variants. We prospectively enrolled adult patients with COVID-19 admitted to a tertiary care hospital in South Korea between September 2021 and May 2022. Secondary attack rates were calculated by epidemiologic investigation, and daily saliva samples were collected to evaluate viral shedding kinetics. Genomic and subgenomic SARS-CoV-2 RNA was measured by PCR, and virus culture was performed from daily saliva samples. A total of 88 patients with COVID-19 who agreed to daily sampling and were interviewed, were included. Of the 88 patients, 48 (59%) were infected with Delta, and 34 (41%) with Omicron; a further 5 patients gave undetectable or inconclusive RNA PCR results and 1 was suspected of being coinfected with both variants. Omicron group had a higher secondary attack rate (31% [38/124] vs. 7% [34/456], p < 0.001). Survival analysis revealed that shorter viable virus shedding period was observed in Omicron variant compared with Delta variant (median 4, IQR [1-7], vs. 8.5 days, IQR [5-12 days], p < 0.001). Multivariable analysis revealed that moderate-to-critical disease severity (HR: 1.96), and immunocompromised status (HR: 2.17) were independent predictors of prolonged viral shedding, whereas completion of initial vaccine series or first booster-vaccinated status (HR: 0.49), and Omicron infection (HR: 0.44) were independently associated with shorter viable virus shedding. Patients with Omicron infections had higher transmission rates but shorter periods of transmissible virus shedding than those with Delta infections.
关于奥密克戎变异株活病毒脱落的传播率和动力学与德尔塔变异株相比的数据有限。我们比较了住院感染德尔塔和奥密克戎变异株的患者的这些比率。我们前瞻性地招募了 2021 年 9 月至 2022 年 5 月期间在韩国一家三级保健医院因 COVID-19 住院的成年患者。通过流行病学调查计算二次攻击率,并采集每日唾液样本评估病毒脱落动力学。通过 PCR 测量全基因组和亚基因组 SARS-CoV-2 RNA,从每日唾液样本中进行病毒培养。共纳入 88 例同意每日采样和接受访谈的 COVID-19 患者。88 例患者中,48 例(59%)感染德尔塔,34 例(41%)感染奥密克戎;另有 5 例 RNA PCR 结果不可检测或不确定,1 例疑似同时感染两种变异株。奥密克戎组的二次攻击率较高(31%[38/124] vs. 7%[34/456],p<0.001)。生存分析显示,与德尔塔变异株相比,奥密克戎变异株的活病毒脱落期更短(中位数 4 天,IQR[1-7] vs. 8.5 天,IQR[5-12 天],p<0.001)。多变量分析显示,中度至重症疾病严重程度(HR:1.96)和免疫功能低下状态(HR:2.17)是病毒脱落延长的独立预测因素,而初始疫苗系列完成或首次加强疫苗接种状态(HR:0.49)和奥密克戎感染(HR:0.44)与较短的活病毒脱落独立相关。奥密克戎感染患者的传播率较高,但具有传染性的病毒脱落期比德尔塔感染患者短。