Synergy America, Inc., Atlanta, Georgia, USA.
Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Microsc Res Tech. 2022 Jul;85(7):2740-2747. doi: 10.1002/jemt.24115. Epub 2022 Apr 4.
The identification of viral particles within a tissue specimen requires specific knowledge of viral ultrastructure and replication, as well as a thorough familiarity with normal subcellular organelles. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has underscored how challenging the task of identifying coronavirus by electron microscopy (EM) can be. Numerous articles have been published mischaracterizing common subcellular structures, including clathrin- or coatomer- coated vesicles, multivesicular bodies, and rough endoplasmic reticulum, as coronavirus particles in SARS-CoV-2 positive patient tissue specimens. To counter these misinterpretations, we describe the morphological features of coronaviruses that should be used to differentiate coronavirus particles from subcellular structures. Further, as many of the misidentifications of coronavirus particles have stemmed from attempts to attribute tissue damage to direct infection by SARS-CoV-2, we review articles describing ultrastructural changes observed in specimens from SARS-CoV-2-infected individuals that do not necessarily provide EM evidence of direct viral infection. Ultrastructural changes have been observed in respiratory, cardiac, kidney, and intestinal tissues, highlighting the widespread effects that SARS-CoV-2 infection may have on the body, whether through direct viral infection or mediated by SARS-CoV-2 infection-induced inflammatory and immune processes. HIGHLIGHTS: The identification of coronavirus particles in SARS-CoV-2 positive tissues continues to be a challenging task. This review provides examples of coronavirus ultrastructure to aid in the differentiation of the virus from common cellular structures.
鉴定组织标本中的病毒颗粒需要对病毒超微结构和复制有特定的了解,并且需要对正常亚细胞细胞器有透彻的了解。严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)大流行突显了通过电子显微镜(EM)鉴定冠状病毒的任务具有挑战性。许多文章错误地描述了常见的亚细胞结构,包括网格蛋白或衣壳蛋白包被小泡、多泡体和粗面内质网,将其误认为是 SARS-CoV-2 阳性患者组织标本中的冠状病毒颗粒。为了纠正这些误解,我们描述了冠状病毒的形态特征,这些特征可用于将冠状病毒颗粒与亚细胞结构区分开来。此外,由于许多冠状病毒颗粒的错误识别源于试图将组织损伤归因于 SARS-CoV-2 的直接感染,我们回顾了描述 SARS-CoV-2 感染个体标本中观察到的超微结构变化的文章,这些变化不一定提供直接病毒感染的 EM 证据。已经在呼吸道、心脏、肾脏和肠道组织中观察到超微结构变化,突出表明 SARS-CoV-2 感染可能对身体产生广泛影响,无论是通过直接病毒感染还是通过 SARS-CoV-2 感染诱导的炎症和免疫过程介导的。重点:鉴定 SARS-CoV-2 阳性组织中的冠状病毒颗粒仍然是一项具有挑战性的任务。本综述提供了冠状病毒超微结构的示例,以帮助将病毒与常见细胞结构区分开来。