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BA.2.12、BA.5.2和XBB.1与Delta变体在叙利亚仓鼠中的致病性比较

Comparative pathogenicity of BA.2.12, BA.5.2 and XBB.1 with the Delta variant in Syrian hamsters.

作者信息

Mohandas Sreelekshmy, Shete Anita, Kumar Abhimanyu, Wakchaure Kundan, Rai Vishal, Mote Chandrasekhar, Dighe Hitesh, Sarkale Prasad, Gawande Pranita, Yemul Jyoti, Suryawanshi Annasaheb, Joshi Yash, Yadav Pragya D

机构信息

Maximum Containment Facility, ICMR-National Institute of Virology, Pune, Maharashtra, India.

Department of Veterinary Pathology, Krantisinh Nana Patil College of Veterinary Science, Shirwal, Maharashtra, India.

出版信息

Front Microbiol. 2023 Jun 22;14:1183763. doi: 10.3389/fmicb.2023.1183763. eCollection 2023.

Abstract

Omicron variant is evolving into numerous sub variants with time and the information on the characteristics of these newly evolving variants are scant. Here we performed a pathogenicity evaluation of Omicron sub variants BA.2.12, BA.5.2 and XBB.1 against the Delta variant in 6-8-week-old Syrian hamster model. Body weight change, viral load in respiratory organs by real time RT-PCR/titration, cytokine mRNA quantification and histopathological evaluation of the lungs were performed. The intranasal infection of the BA.2.12, BA.5.2 and XBB.1 variants in hamster model resulted in body weight loss/reduced weight gain, inflammatory cytokine response and interstitial pneumonia with lesser severity compared to the Delta variant infection. Among the variants studied, BA.2.12 and XBB.1 showed lesser viral shedding through the upper respiratory tract, whereas the BA.5.2 showed comparable viral RNA shedding as that of the Delta variant. The study shows that the Omicron BA.2 sub variants may show difference in disease severity and transmissibility amongst each other whereas the overall disease severity of the Omicron sub variants studied were less compared to the Delta variant. The evolving Omicron sub variants and recombinants should be monitored for their properties.

摘要

随着时间的推移,奥密克戎变种正在演变成众多亚变种,而关于这些新出现变种特征的信息却很少。在此,我们在6-8周龄的叙利亚仓鼠模型中对奥密克戎亚变种BA.2.12、BA.5.2和XBB.1与德尔塔变种进行了致病性评估。我们进行了体重变化、通过实时RT-PCR/滴定法检测呼吸器官中的病毒载量、细胞因子mRNA定量以及肺部的组织病理学评估。在仓鼠模型中,BA.2.12、BA.5.2和XBB.1变种的鼻内感染导致体重减轻/体重增加减少、炎性细胞因子反应以及间质性肺炎,与德尔塔变种感染相比严重程度较低。在所研究的变种中,BA.2.12和XBB.1通过上呼吸道的病毒排出较少,而BA.5.2的病毒RNA排出与德尔塔变种相当。该研究表明,奥密克戎BA.2亚变种之间在疾病严重程度和传播性方面可能存在差异,而所研究的奥密克戎亚变种的总体疾病严重程度低于德尔塔变种。对于不断演变的奥密克戎亚变种和重组体,应监测它们的特性。

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