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严重急性呼吸综合征冠状病毒2感染唾液腺会损害口腔抗真菌固有免疫并易患口腔念珠菌病。

SARS-CoV-2 Infection of Salivary Glands Compromises Oral Antifungal Innate Immunity and Predisposes to Oral Candidiasis.

作者信息

Alfaifi Areej A, Wang Tristan W, Perez Paola, Sultan Ahmed S, Meiller Timothy F, Rock Peter, Kleiner David E, Chertow Daniel S, Hewitt Stephen M, Gasmi Billel, Stein Sydney, Ramelli Sabrina, Martin Daniel, Warner Blake M, Jabra-Rizk Mary Ann

机构信息

Department of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland Baltimore, Maryland, United States of America.

Department of Restorative and Prosthetic Dental Sciences, College of Dentistry, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.

出版信息

bioRxiv. 2024 Jun 11:2024.05.13.593942. doi: 10.1101/2024.05.13.593942.

Abstract

Saliva contains antimicrobial peptides considered integral components of host innate immunity, and crucial for protection against colonizing microbial species. Most notable is histatin-5 which is exclusively produced in salivary glands with uniquely potent antifungal activity against the opportunistic pathogen . Recently, SARS-CoV-2 was shown to replicate in salivary gland acinar cells eliciting local immune cell activation. In this study, we performed mechanistic and clinical studies to investigate the implications of SARS-CoV-2 infection on salivary histatin-5 production and colonization. Bulk RNA-sequencing of parotid salivary glands from COVID-19 autopsies demonstrated statistically significant decreased expression of histatin genes. hybridization, coupled with immunofluorescence for co-localization of SARS-CoV-2 spike and histatin in salivary gland cells, showed that histatin was absent or minimally present in acinar cells with replicating viruses. To investigate the clinical implications of these findings, salivary histatin-5 levels and oral burden in saliva samples from three independent cohorts of mild and severe COVID-19 patients and matched healthy controls were evaluated. Results revealed significantly reduced histatin-5 in SARS-CoV-2 infected subjects, concomitant with enhanced prevalence of . Analysis of prospectively recovered samples indicated that the decrease in histatin-5 is likely reversible in mild-moderate disease as concentrations tended to increase during the post-acute phase. Importantly, salivary cytokine profiling demonstrated correlations between activation of the Th17 inflammatory pathway, changes in histatin-5 concentrations, and subsequent clearance of in a heavily colonized subject. The importance of salivary histatin-5 in controlling the proliferation of was demonstrated using an assay where was able to proliferate in COVID-19 saliva with low histatin-5, but not with high histatin-5. Taken together, the findings from this study provide direct evidence implicating SARS-CoV-2 infection of salivary glands with compromised oral innate immunity, and potential predisposition to oral candidiasis.

摘要

唾液中含有抗菌肽,这些抗菌肽被认为是宿主固有免疫的重要组成部分,对于抵御定殖的微生物物种至关重要。最值得注意的是组蛋白-5,它仅在唾液腺中产生,对机会性病原体具有独特的强效抗真菌活性。最近,有研究表明严重急性呼吸综合征冠状病毒2(SARS-CoV-2)可在唾液腺腺泡细胞中复制,引发局部免疫细胞激活。在本研究中,我们进行了机制和临床研究,以调查SARS-CoV-2感染对唾液组蛋白-5产生和定殖的影响。对COVID-19尸检的腮腺进行批量RNA测序,结果显示组蛋白基因的表达在统计学上显著降低。原位杂交结合免疫荧光以确定SARS-CoV-2刺突蛋白与唾液腺细胞中组蛋白的共定位,结果表明在有复制病毒的腺泡细胞中,组蛋白不存在或含量极低。为了研究这些发现的临床意义,我们评估了来自三个独立队列的轻度和重度COVID-19患者以及匹配的健康对照的唾液样本中的唾液组蛋白-5水平和口腔念珠菌负荷。结果显示,SARS-CoV-2感染患者的组蛋白-5显著降低,同时念珠菌感染的患病率增加。对前瞻性收集的样本进行分析表明,在轻度至中度疾病中,组蛋白-5的降低可能是可逆的,因为在急性后期其浓度往往会升高。重要的是,唾液细胞因子分析表明,在一个念珠菌大量定殖的受试者中,Th17炎症途径的激活、组蛋白-5浓度的变化与随后念珠菌的清除之间存在相关性。使用一种实验证明了唾液组蛋白-5在控制念珠菌增殖方面的重要性,在该实验中,念珠菌能够在组蛋白-5含量低的COVID-19唾液中增殖,但在组蛋白-5含量高的唾液中则不能。综上所述,本研究结果提供了直接证据,表明SARS-CoV-2感染唾液腺会损害口腔固有免疫,并可能导致口腔念珠菌病易感性增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b22c/11181429/73ee428da48a/nihpp-2024.05.13.593942v2-f0001.jpg

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