Clinical Laboratory, Tokyo Medical and Dental University (TMDU) Hospital, Tokyo, Japan.
Infection Control and Prevention, Tokyo Medical and Dental University (TMDU) Hospital, Tokyo, Japan.
Immun Inflamm Dis. 2023 Feb;11(2):e783. doi: 10.1002/iid3.783.
Sublineage BA.5 of the SARS-CoV-2 Omicron variant rapidly spread and replaced BA.2 in July 2022 in Tokyo. A high viral load can be a possible cause of high transmissibility.
The copy numbers of SARS-CoV-2 in nasopharyngeal swab samples obtained from all patients visiting the hospital where this research was conducted were measured using reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Viral genotypes were determined using PCR-based melting curve analysis. Next, whole-genome sequencing was performed using approximately one fifth of the samples to verify the viral genotypes determined using PCR. Then, the copy numbers of the BA.1, BA.2, and BA.5 cases were compared. Contrary to expectations, the copy numbers of the BA.5 cases (median 4.7 × 10 copies/μL, n = 291) were significantly (p = .001) lower than those of BA.2 cases (median 1.1 × 10 copies/μL, n = 184). There was no significant difference (p = .44) between the BA.5 and BA.1 cases (median, 3.3 × 10 copies/μL; n = 215).
The results presented here suggest that the increased infectivity of BA.5 is not caused by higher viral loads, but presumably by other factors such as increased affinity to human cell receptors or immune escape due to its L452R mutation.
SARS-CoV-2 奥密克戎变异株的亚谱系 BA.5 于 2022 年 7 月在东京迅速传播并取代了 BA.2。高病毒载量可能是高传染性的一个原因。
使用逆转录定量聚合酶链反应(RT-qPCR)测量了从所有在本研究所在医院就诊的患者的鼻咽拭子样本中获得的 SARS-CoV-2 的拷贝数。使用基于 PCR 的熔解曲线分析确定病毒基因型。然后,使用大约五分之一的样本进行全基因组测序,以验证使用 PCR 确定的病毒基因型。然后,比较了 BA.1、BA.2 和 BA.5 病例的拷贝数。出乎意料的是,BA.5 病例的拷贝数(中位数 4.7×10 拷贝/μL,n=291)明显(p=0.001)低于 BA.2 病例(中位数 1.1×10 拷贝/μL,n=184)。BA.5 和 BA.1 病例之间没有显著差异(p=0.44)(中位数,3.3×10 拷贝/μL;n=215)。
这里呈现的结果表明,BA.5 的感染性增加不是由更高的病毒载量引起的,而是可能由于其他因素引起的,例如增加对人类细胞受体的亲和力或由于其 L452R 突变导致的免疫逃逸。