Oral SARS-CoV-2 Infection and Risk for Long Covid.

IF 9 2区 医学 Q1 VIROLOGY
Joel Schwartz, Kristelle Capistrano, Heba Hussein, Avin Hafedi, Deepak Shukla, Afsar Naqvi
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引用次数: 0

Abstract

SARS-CoV-2 is an oral pathogen that infects and replicates in mucosal and salivary epithelial cells, contributing to oral post-acute sequelae COVID-19 (PASC) and other oral and non-oral pathologies. While pre-existing inflammatory oral diseases provides a conducive environment for the virus, acute infection and persistence of SARS-CoV-2 can also results in oral microbiome dysbiosis that further worsens poor oral mucosal health. Indeed, oral PASC includes periodontal diseases, dysgeusia, xerostomia, pharyngitis, oral keratoses, and pulpitis suggesting significant bacterial contributions to SARS-CoV-2 and oral tissue tropism. Dysbiotic microbiome-induced inflammation can promote viral entry via angiotensin-converting enzyme receptor-2 (ACE2), serine transmembrane TMPRSS2 and possibly other non-canonical pathways. Additionally, metabolites derived from a dysbiotic microbiome can alter the physiological and biochemical pathways related to the metabolism of lipids, carbohydrates, and amino acids. This may promote a pro-inflammatory microenvironment, leading to immune exhaustion, loss of tolerance, and susceptibility to a variety of oral pathogens, causing acute and later chronic inflammation. Microbial release of mimics of host metallopeptidases related to furin, ADAM17 (A disintegrin and metalloproteinase 17), and glycoprotein metabolites can further aid viral attachment to T cell immunoglobulin-like (TIMs), enhancing viral entry while simultaneously depressing oral mucosal immune resistance and clearance. Membrane reorganization characterised by neuroproteins, such as neuropilins, also functionally assists with SARS-CoV-2 entry and extends the pathogenesis of PASC from the oral cavity to the brain, gut, or other non-oral tissues. Thus, poor oral health, characterised by disrupted oral microbiomes can promote viral tropism, weaken antiviral resistance, and heightens susceptibility to SARS-CoV-2 infection. This immune dysfunction also increases the risk of additional viral infections, exacerbating oral conditions like periodontal and endodontic diseases. These persistent oral health issues can contribute to systemic inflammation, creating bidirectional effects between oral and non-oral tissues, potentially leading to Post-Acute Sequelae of COVID-19 (PASC).

口服SARS-CoV-2感染和长期感染风险。
SARS-CoV-2是一种口腔病原体,可在粘膜和唾液上皮细胞中感染和复制,导致口腔急性后后遗症COVID-19 (PASC)和其他口腔和非口腔病理。虽然先前存在的炎症性口腔疾病为病毒提供了有利的环境,但急性感染和SARS-CoV-2的持续存在也会导致口腔微生物群失调,从而进一步恶化口腔黏膜健康状况。事实上,口腔PASC包括牙周病、发音困难、口干症、咽炎、口腔角化病和牙髓炎,这表明细菌对SARS-CoV-2和口腔组织趋向性有重要作用。微生物组诱导的炎症可通过血管紧张素转换酶受体-2 (ACE2)、丝氨酸跨膜TMPRSS2和可能的其他非规范途径促进病毒进入。此外,来自益生菌群的代谢物可以改变与脂质、碳水化合物和氨基酸代谢相关的生理和生化途径。这可能会促进促炎微环境,导致免疫衰竭、耐受性丧失和对各种口腔病原体的易感性,从而引起急性和后来的慢性炎症。微生物释放与furin、ADAM17 (A disintegrin and metalloproteinase 17)和糖蛋白代谢产物相关的宿主金属肽酶模拟物,可进一步帮助病毒附着在T细胞免疫球蛋白样蛋白(TIMs)上,增强病毒进入,同时抑制口腔黏膜免疫抵抗和清除。以神经蛋白(如neuropilins)为特征的膜重组也在功能上协助SARS-CoV-2进入,并将PASC的发病机制从口腔扩展到大脑、肠道或其他非口腔组织。因此,以口腔微生物群被破坏为特征的口腔健康状况不佳可促进病毒趋向性,削弱抗病毒药物耐药性,并增加对SARS-CoV-2感染的易感性。这种免疫功能障碍也增加了其他病毒感染的风险,加剧了牙周和牙髓疾病等口腔疾病。这些持续的口腔健康问题可能导致全身性炎症,在口腔和非口腔组织之间产生双向影响,可能导致COVID-19急性后后遗症(PASC)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Reviews in Medical Virology
Reviews in Medical Virology 医学-病毒学
CiteScore
21.40
自引率
0.90%
发文量
88
期刊介绍: Reviews in Medical Virology aims to provide articles reviewing conceptual or technological advances in diverse areas of virology. The journal covers topics such as molecular biology, cell biology, replication, pathogenesis, immunology, immunization, epidemiology, diagnosis, treatment of viruses of medical importance, and COVID-19 research. The journal has an Impact Factor of 6.989 for the year 2020. The readership of the journal includes clinicians, virologists, medical microbiologists, molecular biologists, infectious disease specialists, and immunologists. Reviews in Medical Virology is indexed and abstracted in databases such as CABI, Abstracts in Anthropology, ProQuest, Embase, MEDLINE/PubMed, ProQuest Central K-494, SCOPUS, and Web of Science et,al.
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