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Reactivation of CMV and HSV-1 Among Severe COVID-19 Patients May be Triggered by Increased Level of Pulmonary Dioxin

PURPOSE: Reactivation of cytomegalovirus (CMV) infection was recently found to influence worse clinical outcome following SARS-CoV-2 infection (doi: 10.1186/s12979-020-00185-x). Other findings showed that CMV and herpes simplex virus 1 (HSV-1) reactivations are observed in patients with COVID-19 acu...

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Autores principales: Tsyrlov, I., Shur, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884754/
http://dx.doi.org/10.1016/j.ijid.2021.12.139
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author Tsyrlov, I.
Shur, I.
author_facet Tsyrlov, I.
Shur, I.
author_sort Tsyrlov, I.
collection PubMed
description PURPOSE: Reactivation of cytomegalovirus (CMV) infection was recently found to influence worse clinical outcome following SARS-CoV-2 infection (doi: 10.1186/s12979-020-00185-x). Other findings showed that CMV and herpes simplex virus 1 (HSV-1) reactivations are observed in patients with COVID-19 acute respiratory distress syndrome (ARDS) (HYPERLINK "https://doi.org/10.1186/s13054-020-03252-3" doi.org/10.1186/s13054-020-03252-3). Addressing occurrence of Herpesviridae reactivation in immunocompetent patients and still unspecified triggers of reactivation, we tested potent xenobiotic 2,3,7,8-tetrachrolodibenzo-p-dioxin (TCDD), which current body burden (DBB) ranges from 20 pg/g (TEQ in fat) in general population to 100 pg/g in older people. METHODS & MATERIALS: In silico quantitation of active dioxin response enhancers (DRE) in promoters of viral genes. Plaque assay of viral titer. Virus DNA hybridization assay. Clinico-epidemiological analysis. RESULTS: In silico analysis revealed in regulatory region of CMV IE genes from 5 to 10 DRE, and from 6 to 8 DRE in regulatory region of HSV-1 IE genes. We established that a picomolar TCDD can trigger up-regulation of CMV and HSV-1 genes via AhR:Arnt transcription factor in macrophage (doi.org/10.1016/j.ijid.2012.05.265) and glial human cell lines (doi.org/10.1016/j.jalz.2016.06.1268), respectively. In fact, viral reactivation may be triggered in COVID-19 ARDS patients by higher pulmonary TCDD concentrations, as lipid storm within lungs of severe COVID-19 patients has been recently reported (doi.org/10.1101/2020.12.04.20242115). Due to hydrophobic character (Log PO/W: 7.05), TCDD partitions into inflammatory lipids in lung tissue thus augmenting its local concentration. Population-based epidemiological data on SARS-CoV-2 first wave of pandemic showed that picomolar TCDD can reactivate CMV (measured by high CMV seropositivity), as cumulative mortality rate 4.5 times was revealed in Lombardi region of Italy where after Seveso industrial accident TCDD plasma level in pre-exposed subjects still is 15 times the level in rest of Italy (doi.org/10.3389/fpubh.2020.620416). Also, Arctic Native (AN) peoples have TCDD body burden 7 times that in general population, as they consume dioxin-contaminated fat in seafood, and their COVID-19 mortality is 2.2 times of that among non-AN Alaskans (doi: 10.15585/mmwr.mm6949a3). CONCLUSION: TCDD in picomolar range may trigger CMV expression in lung cells and commit virus to the lytic cycle, which can be applied to reactivation of Herpesviridae infection in immunocompetent patients with COVID-19 ARDS syndrome.
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spelling pubmed-88847542022-03-01 Reactivation of CMV and HSV-1 Among Severe COVID-19 Patients May be Triggered by Increased Level of Pulmonary Dioxin Tsyrlov, I. Shur, I. Int J Infect Dis Ps08.06 (189) PURPOSE: Reactivation of cytomegalovirus (CMV) infection was recently found to influence worse clinical outcome following SARS-CoV-2 infection (doi: 10.1186/s12979-020-00185-x). Other findings showed that CMV and herpes simplex virus 1 (HSV-1) reactivations are observed in patients with COVID-19 acute respiratory distress syndrome (ARDS) (HYPERLINK "https://doi.org/10.1186/s13054-020-03252-3" doi.org/10.1186/s13054-020-03252-3). Addressing occurrence of Herpesviridae reactivation in immunocompetent patients and still unspecified triggers of reactivation, we tested potent xenobiotic 2,3,7,8-tetrachrolodibenzo-p-dioxin (TCDD), which current body burden (DBB) ranges from 20 pg/g (TEQ in fat) in general population to 100 pg/g in older people. METHODS & MATERIALS: In silico quantitation of active dioxin response enhancers (DRE) in promoters of viral genes. Plaque assay of viral titer. Virus DNA hybridization assay. Clinico-epidemiological analysis. RESULTS: In silico analysis revealed in regulatory region of CMV IE genes from 5 to 10 DRE, and from 6 to 8 DRE in regulatory region of HSV-1 IE genes. We established that a picomolar TCDD can trigger up-regulation of CMV and HSV-1 genes via AhR:Arnt transcription factor in macrophage (doi.org/10.1016/j.ijid.2012.05.265) and glial human cell lines (doi.org/10.1016/j.jalz.2016.06.1268), respectively. In fact, viral reactivation may be triggered in COVID-19 ARDS patients by higher pulmonary TCDD concentrations, as lipid storm within lungs of severe COVID-19 patients has been recently reported (doi.org/10.1101/2020.12.04.20242115). Due to hydrophobic character (Log PO/W: 7.05), TCDD partitions into inflammatory lipids in lung tissue thus augmenting its local concentration. Population-based epidemiological data on SARS-CoV-2 first wave of pandemic showed that picomolar TCDD can reactivate CMV (measured by high CMV seropositivity), as cumulative mortality rate 4.5 times was revealed in Lombardi region of Italy where after Seveso industrial accident TCDD plasma level in pre-exposed subjects still is 15 times the level in rest of Italy (doi.org/10.3389/fpubh.2020.620416). Also, Arctic Native (AN) peoples have TCDD body burden 7 times that in general population, as they consume dioxin-contaminated fat in seafood, and their COVID-19 mortality is 2.2 times of that among non-AN Alaskans (doi: 10.15585/mmwr.mm6949a3). CONCLUSION: TCDD in picomolar range may trigger CMV expression in lung cells and commit virus to the lytic cycle, which can be applied to reactivation of Herpesviridae infection in immunocompetent patients with COVID-19 ARDS syndrome. Published by Elsevier Ltd. 2022-03 2022-02-28 /pmc/articles/PMC8884754/ http://dx.doi.org/10.1016/j.ijid.2021.12.139 Text en Copyright © 2021 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Ps08.06 (189)
Tsyrlov, I.
Shur, I.
Reactivation of CMV and HSV-1 Among Severe COVID-19 Patients May be Triggered by Increased Level of Pulmonary Dioxin
title Reactivation of CMV and HSV-1 Among Severe COVID-19 Patients May be Triggered by Increased Level of Pulmonary Dioxin
title_full Reactivation of CMV and HSV-1 Among Severe COVID-19 Patients May be Triggered by Increased Level of Pulmonary Dioxin
title_fullStr Reactivation of CMV and HSV-1 Among Severe COVID-19 Patients May be Triggered by Increased Level of Pulmonary Dioxin
title_full_unstemmed Reactivation of CMV and HSV-1 Among Severe COVID-19 Patients May be Triggered by Increased Level of Pulmonary Dioxin
title_short Reactivation of CMV and HSV-1 Among Severe COVID-19 Patients May be Triggered by Increased Level of Pulmonary Dioxin
title_sort reactivation of cmv and hsv-1 among severe covid-19 patients may be triggered by increased level of pulmonary dioxin
topic Ps08.06 (189)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8884754/
http://dx.doi.org/10.1016/j.ijid.2021.12.139
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