Zhang Qing, Feng Zhaomin, Hao Yiwei, Wei Lirong, Wang Aibin, Han Zhixing, Tian Meimei, Sun Sheng, Li Xin'gang, Xue Tianjiao, Kong Xiangjing, Li Baoliang, Kou Cheng, Wang Quanyi, Huo Da, Wang Linghang
Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Beijing Center for Disease Prevention and Control, Beijing, China.
China CDC Wkly. 2023 Feb 24;5(8):180-183. doi: 10.46234/ccdcw2023.030.
In November 2021, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant was identified as the variant of concern and has since spread globally, replacing other cocirculating variants. To better understand the dynamic changes in viral load over time and the natural history of the virus infection, we analyzed the expression of the open reading frames 1ab (ORF1ab) and nucleocapsid (N) genes in patients infected with Omicron.
We included patients initially admitted to the hospital for SARS-CoV-2 infection between November 5 and December 25, 2022. We collected daily oropharyngeal swabs for quantitative reverse transcriptase-polymerase chain reaction tests using commercial kits. We depicted the cycle threshold (Ct) values for amplification of ORF1ab and N genes from individual patients in age-specific groups in a time series.
A total of 480 inpatients were included in the study, with a median age of 59 years (interquartile range, 42 to 78; range, 16 to 106). In the <45-year-old age group, the Ct values for ORF1ab and N gene amplification remained below 35 for 9.0 and 11.5 days, respectively. In the ≥80-year-old age group, the Ct values for ORF1ab and N genes stayed below 35 for 11.5 and 15.0 days, respectively, which was the longest among all age groups. The Ct values for N gene amplification took longer to rise above 35 than those for ORF1ab gene amplification.
The time to test negative varied among different age groups, with viral nucleic acid shedding taking longer in older age groups compared to younger age groups. As a result, the time to resolution of Omicron infection increased with increasing age.
2021年11月,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎变异株被确定为值得关注的变异株,此后在全球范围内传播,取代了其他共同流行的变异株。为了更好地了解病毒载量随时间的动态变化以及病毒感染的自然史,我们分析了感染奥密克戎的患者中开放阅读框1ab(ORF1ab)和核衣壳(N)基因的表达。
我们纳入了2022年11月5日至12月25日期间因SARS-CoV-2感染首次入院的患者。我们使用商用试剂盒收集每日口咽拭子进行定量逆转录-聚合酶链反应检测。我们按时间序列描绘了各年龄组个体患者ORF1ab和N基因扩增的循环阈值(Ct)值。
本研究共纳入480例住院患者,中位年龄为59岁(四分位间距,42至78岁;范围,16至106岁)。在<45岁年龄组中,ORF1ab和N基因扩增的Ct值分别在9.0天和11.5天内保持低于35。在≥80岁年龄组中,ORF1ab和N基因的Ct值分别在11.5天和15.0天内保持低于35,这在所有年龄组中是最长的。N基因扩增的Ct值升至35以上的时间比ORF1ab基因扩增的Ct值更长。
不同年龄组检测转阴的时间不同,老年组病毒核酸脱落时间比年轻组更长。因此,奥密克戎感染的恢复时间随年龄增长而增加。