Your browser doesn't support javascript.
loading
SARS-CoV-2 Infection of Salivary Glands Compromises Oral Antifungal Innate Immunity and Predisposes to Oral Candidiasis.
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.
Afiliação
  • Alfaifi AA; Department of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland Baltimore, Maryland, United States of America.
  • Wang TW; Department of Restorative and Prosthetic Dental Sciences, College of Dentistry, King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.
  • Perez P; King Abdullah International Medical Research Center (KAIMRC), Riyadh, Saudi Arabia.
  • Sultan AS; Department of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland Baltimore, Maryland, United States of America.
  • Meiller TF; Salivary Disorders Unit, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Rock P; Department of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland Baltimore, Maryland, United States of America.
  • Kleiner DE; University of Maryland Greenebaum Cancer Center, University of Maryland Baltimore, Maryland, United States of America.
  • Chertow DS; Department of Oncology and Diagnostic Sciences, School of Dentistry, University of Maryland Baltimore, Maryland, United States of America.
  • Hewitt SM; University of Maryland Greenebaum Cancer Center, University of Maryland Baltimore, Maryland, United States of America.
  • Gasmi B; Department of Anesthesia, School of Medicine, University of Maryland Baltimore, Maryland, United States of America.
  • Stein S; Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Ramelli S; Critical Care Medicine Department, Clinical Center, National Institutes of Health, Bethesda, MD, USA.
  • Martin D; Laboratory of Virology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT, United States of America, USA.
  • Warner BM; Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Jabra-Rizk MA; Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
bioRxiv ; 2024 Jun 11.
Article em En | MEDLINE | ID: mdl-38798323
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 Candida albicans. 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 Candida colonization. Bulk RNA-sequencing of parotid salivary glands from COVID-19 autopsies demonstrated statistically significant decreased expression of histatin genes. In situ 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 Candida 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 C. albicans. 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 C. albicans in a heavily colonized subject. The importance of salivary histatin-5 in controlling the proliferation of C. albicans was demonstrated using an ex vivo assay where C. albicans 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.

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: BioRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos