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在猫感染新冠病毒的模型中,奥密克戎变种BA.1.1的致病性低于B.1 D614G和德尔塔变种。

The Omicron variant BA.1.1 presents a lower pathogenicity than B.1 D614G and Delta variants in a feline model of SARS-CoV-2 infection.

作者信息

Martins Mathias, do Nascimento Gabriela M, Nooruzzaman Mohammed, Yuan Fangfeng, Chen Chi, Caserta Leonardo C, Miller Andrew D, Whittaker Gary R, Fang Ying, Diel Diego G

机构信息

Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, United States of America.

Department of Pathobiology, College of Veterinary Medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.

出版信息

bioRxiv. 2022 Jun 16:2022.06.15.496220. doi: 10.1101/2022.06.15.496220.

DOI:10.1101/2022.06.15.496220
PMID:35734088
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9216722/
Abstract

UNLABELLED

Omicron (B.1.1.529) is the most recent SARS-CoV-2 variant of concern (VOC), which emerged in late 2021 and rapidly achieved global predominance in early 2022. In this study, we compared the infection dynamics, tissue tropism and pathogenesis and pathogenicity of SARS-CoV-2 D614G (B.1), Delta (B.1.617.2) and Omicron BA.1.1 sublineage (B.1.1.529) variants in a highly susceptible feline model of infection. While D614G- and Delta-inoculated cats became lethargic, and showed increased body temperatures between days 1 and 3 post-infection (pi), Omicron-inoculated cats remained subclinical and, similar to control animals, gained weight throughout the 14-day experimental period. Intranasal inoculation of cats with D614G- and the Delta variants resulted in high infectious virus shedding in nasal secretions (up to 6.3 log10 TCID .ml ), whereas strikingly lower level of viruses shedding (<3.1 log10 TCID .ml ) was observed in Omicron-inoculated animals. In addition, tissue distribution of the Omicron variant was markedly reduced in comparison to the D614G and Delta variants, as evidenced by viral RNA detection, immunofluorescence, and quantification of viral loads in tissues on days 3, 5, and 14 pi. Nasal turbinate, trachea, and lung were the main - but not the only - sites of replication for all three viral variants. However, only scarce virus staining and lower viral titers suggest lower levels of viral replication in tissues from Omicron-infected animals. Notably, while D614G- and Delta-inoculated cats had severe pneumonia, histologic examination of the lungs from Omicron-infected cats revealed mild to modest inflammation. Together, these results demonstrate that the Omicron variant BA.1.1 is less pathogenic than D614G and Delta variants in a highly susceptible feline model.

AUTHOR SUMMARY

The SARS-CoV-2 Omicron (B.1.1.529) variant of concern (VOC) emerged in South Africa late in 2021 and rapidly spread across the world causing a significant increase in the number of infections. Importantly, this variant was also associated with an increased risk of reinfections. However, the number of hospitalizations and deaths due to COVID-19 did not follow the same trends. These early observations, suggested effective protection conferred by immunizations and/or overall lower virulence of the highly mutated variant virus. In this study we present novel evidence demonstrating that the Omicron BA.1.1 variant of concern (VOC) presents a lower pathogenicity when compared to D614G- or Delta variants in cats. Clinical, virological and pathological evaluations revealed lower disease severity, viral replication and lung pathology in Omicron-infected cats when compared to D614G and Delta variant inoculated animals, confirming that Omicron BA.1.1 is less pathogenic in a highly susceptible feline model of infection.

摘要

未标注

奥密克戎(B.1.1.529)是最新出现的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变异株,于2021年末出现,并在2022年初迅速在全球占据主导地位。在本研究中,我们在高度易感的猫感染模型中比较了SARS-CoV-2 D614G(B.1)、德尔塔(B.1.617.2)和奥密克戎BA.1.1亚系(B.1.1.529)变异株的感染动态、组织嗜性、发病机制和致病性。接种D614G和德尔塔变异株的猫变得嗜睡,在感染后第1天至第3天体温升高,而接种奥密克戎变异株的猫仍无临床症状,并且与对照动物相似,在整个14天的实验期内体重增加。给猫鼻内接种D614G和德尔塔变异株后,鼻腔分泌物中出现高传染性病毒脱落(高达6.3 log10 TCID50/ml),而在接种奥密克戎变异株的动物中观察到病毒脱落水平显著降低(<3.1 log10 TCID50/ml)。此外,与D614G和德尔塔变异株相比,奥密克戎变异株的组织分布明显减少,这在感染后第3天、第5天和第14天通过病毒RNA检测、免疫荧光以及组织中病毒载量的定量得以证实。鼻甲、气管和肺是所有三种病毒变异株的主要复制部位,但并非唯一部位。然而,仅稀少的病毒染色和较低的病毒滴度表明奥密克戎感染动物组织中的病毒复制水平较低。值得注意的是,接种D614G和德尔塔变异株的猫患有严重肺炎,而对奥密克戎感染猫的肺组织学检查显示为轻度至中度炎症。总之,这些结果表明,在高度易感的猫模型中,奥密克戎BA.1.1变异株的致病性低于D614G和德尔塔变异株。

作者总结

SARS-CoV-2奥密克戎(B.1.1.529)变异株于2021年末在南非出现,并迅速在全球传播,导致感染数量显著增加。重要的是,该变异株还与再次感染风险增加有关。然而,因2019冠状病毒病(COVID-19)导致的住院和死亡人数并未呈现相同趋势。这些早期观察结果表明,免疫接种提供了有效的保护,和/或这种高度变异的病毒总体毒力较低。在本研究中,我们提供了新的证据,证明与猫体内的D614G或德尔塔变异株相比,奥密克戎BA.1.1变异株的致病性较低。临床、病毒学和病理学评估显示,与接种D614G和德尔塔变异株的动物相比,奥密克戎感染猫的疾病严重程度、病毒复制和肺部病理学表现较低,证实了奥密克戎BA.1.1在高度易感的猫感染模型中致病性较低。

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Inflammation. 2023 Feb;46(1):297-312. doi: 10.1007/s10753-022-01734-w. Epub 2022 Oct 10.
2
BA.2.12.1, BA.4 and BA.5 escape antibodies elicited by Omicron infection.BA.2.12.1、BA.4 和 BA.5 逃避奥密克戎感染诱导的抗体。
Nature. 2022 Aug;608(7923):593-602. doi: 10.1038/s41586-022-04980-y. Epub 2022 Jun 17.
3
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Viruses. 2022 Apr 28;14(5):919. doi: 10.3390/v14050919.
4
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Front Microbiol. 2022 May 4;13:840757. doi: 10.3389/fmicb.2022.840757. eCollection 2022.
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Nat Med. 2022 Jul;28(7):1491-1500. doi: 10.1038/s41591-022-01816-0. Epub 2022 Apr 8.