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Viral infection and transmission in a large well-traced outbreak caused by the Delta SARS-CoV-2 variant

Baisheng Li, Aiping Deng, Kuibiao Li, Yao Hu, Zhencui Li, Qianling Xiong, Zhe Liu, Qianfang Guo, Lirong Zou, Huan Zhang, Meng Zhang, Fangzhu Ouyang, Juan Su, Wenzhe Su, Jing Xu, Huifang Lin, Jing Sun, Jingju Peng, Huiming Jiang, Pingping Zhou, Huanying Zhen, Jianpeng Xiao, Tao Liu, Rongfei Che, Hanri Zeng, Zhonghua Zheng, Yushi Huang, Jianxiang Yu, Lina Yi, Jie Wu, Jingdiao Chen, Haojie Zhong, Xiaoling Deng, Min Kang, Oliver G. Pybus, Matthew Hall, Katrina A. Lythgoe, Yan Li, Jun Yuan, Jianfeng He, Jing Lu
1Guangdong Provincial Center for Disease Control and Prevention, Guangzhou, Guangdong, China
2Guangdong Workstation for Emerging Infectious Disease Control and Prevention, Chinese Academy of Medical Sciences, Guangzhou, Guangdong, China
3Guangzhou Center for Disease Control and Prevention, Guangzhou, Guangdong, China
4Guangdong Provincial Institution of Public Health, Guangzhou, Guangdong, China
5Department of Zoology, University of Oxford, Oxford OX1 3SZ, UK
6Big Data Institute, Nuffield Department of Medicine, University of Oxford, Old Road Campus, Oxford OX3 7LF, UK
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We report the first local transmission of the Delta SARS-CoV-2 variant in mainland China. All 167 infections could be traced back to the first index case. The investigation on daily sequential PCR testing of the quarantined subjects indicated the viral load of the first positive test of Delta infections was ~1000 times higher than that of the 19A/19B strains infections back in the initial epidemic wave of 2020, suggesting the potential faster viral replication rate and more infectiousness of the Delta variant at the early stage of the infection. The 126 high-quality sequencing data and reliable epidemiological data indicated some minor intra-host single nucleotide variants (iSNVs) could be transmitted between hosts and finally fixed in the virus population during the outbreak. The minor iSNVs transmission between donor-recipient contribute at least 4 of 31 substitutions identified in the outbreak suggesting some iSNVs could quickly arise and reach fixation when the virus spread rapidly. Disease control measures, including the frequency of population testing, quarantine in pre-symptomatic phase and enhancing the genetic surveillance should be adjusted to account for the increasing prevalence of the Delta variant at global level.

During the global spread of SARS-CoV-2, the genetic variants of the viruses emerged, and some have been proved to be more transmissible or could escape from the host immunity, which posed an increased risk to global public health1–3. An emerging genetic lineage, B.1.617, has been dominant in the largest outbreak of COVID-19 in India since March 2021, gaining global attention. One sublineage, B.1.617.2, with spike protein mutations L452R, T478K and P681R, accounts for ~28% sequenced cases in Indian and rapidly replaced other lineages to become dominant in multiple regions and countries (https://outbreak.info/)4. The B.1.617.2 has been labeled as Variant of Concern (VOC), Delta (https://www.who.int/activities/tracking-SARS-CoV-2-variants). The virological profile of this VOC is needed to be urgently illustrated.
On May 21, 2021 the first local infection of the Delta variant in mainland China was identified. Similar to what has been done to the early epidemic in January 20205, strict interventions including population screen testing, activate contact tracing, and central quarantine/isolation have been carried out. However, in contrast to the restricted transmissions in 20205, a successive intergenerational transmission has been observed in the 2021 epidemic. Here, we investigated the epidemiological, genetic, and serological data from this well-traced outbreak to characterize the virological profile of the Delta SARS-CoV-2 variant and discuss how the intervention strategies need to be improved on the racing against this emerging variant.

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Publicado en el sitio 2021-08-12 14:53:21

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