Cargando…
Curbside particulate matter and susceptibility to SARS–CoV-2 infection
BACKGROUND: Biologic plausibility for the association between exposure to particulate matter (PM) less than 10 μm in aerodynamic diameter (PM(10)) and coronavirus disease 2019 (COVID-19) morbidity in epidemiologic studies has not been determined. The upregulation of angiotensin-converting enzyme 2 (...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509961/ https://www.ncbi.nlm.nih.gov/pubmed/37781647 http://dx.doi.org/10.1016/j.jacig.2023.100141 |
_version_ | 1785107865939214336 |
---|---|
author | Miyashita, Lisa Foley, Gary Semple, Sean Gibbons, Joseph M. Pade, Corinna McKnight, Áine Grigg, Jonathan |
author_facet | Miyashita, Lisa Foley, Gary Semple, Sean Gibbons, Joseph M. Pade, Corinna McKnight, Áine Grigg, Jonathan |
author_sort | Miyashita, Lisa |
collection | PubMed |
description | BACKGROUND: Biologic plausibility for the association between exposure to particulate matter (PM) less than 10 μm in aerodynamic diameter (PM(10)) and coronavirus disease 2019 (COVID-19) morbidity in epidemiologic studies has not been determined. The upregulation of angiotensin-converting enzyme 2 (ACE2), the severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) entry receptor on host cells, by PM(10) is a putative mechanism. OBJECTIVE: We sought to assess the effect of PM(10) on SARS-CoV-2 infection of cells in vitro. METHODS: PM(10) from the curbside of London's Marylebone Road and from exhaust emissions was collected by cyclone. A549 cells, human primary nasal epithelial cells (HPNEpCs), SARS-CoV-2–susceptible Vero-E6 and Calu3 cells were cultured with PM(10). ACE2 expression (as determined by median fluorescent intensity) was assessed by flow cytometry, and ACE2 mRNA transcript level was assessed by PCR. The role of oxidative stress was determined by N-acetyl cysteine. The cytopathic effect of SARS-CoV-2 (percentage of infection enhancement) and expression of SARS-CoV-2 genes' open reading frame (ORF) 1ab, S protein, and N protein (focus-forming units/mL) were assessed in Vero-E6 cells. Data were analyzed by either the Mann-Whitney U test or Kruskal-Wallis test with the Dunn multiple comparisons test. RESULTS: Curbside PM(10) at concentrations of 10 μg/mL or more increased ACE2 expression in A549 cells (P = .0021). Both diesel PM(10) and curbside PM(10) in a concentration of 10 μg/mL increased ACE2 expression in HPNEpCs (P = .0022 and P = .0072, respectively). ACE2 expression simulated by curbside PM(10) was attenuated by N-acetyl cysteine in HPNEpCs (P = .0464). Curbside PM(10) increased ACE2 expression in Calu3 cells (P = .0256). In Vero-E6 cells, curbside PM(10) increased ACE2 expression (P = .0079), ACE2 transcript level (P = .0079), SARS-CoV-2 cytopathic effect (P = .0002), and expression of the SARS-CoV-2 genes' ORF1ab, S protein, and N protein (P = .0079). CONCLUSIONS: Curbside PM(10) increases susceptibility to SARS-COV-2 infection in vitro. |
format | Online Article Text |
id | pubmed-10509961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105099612023-09-29 Curbside particulate matter and susceptibility to SARS–CoV-2 infection Miyashita, Lisa Foley, Gary Semple, Sean Gibbons, Joseph M. Pade, Corinna McKnight, Áine Grigg, Jonathan J Allergy Clin Immunol Glob Original article BACKGROUND: Biologic plausibility for the association between exposure to particulate matter (PM) less than 10 μm in aerodynamic diameter (PM(10)) and coronavirus disease 2019 (COVID-19) morbidity in epidemiologic studies has not been determined. The upregulation of angiotensin-converting enzyme 2 (ACE2), the severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) entry receptor on host cells, by PM(10) is a putative mechanism. OBJECTIVE: We sought to assess the effect of PM(10) on SARS-CoV-2 infection of cells in vitro. METHODS: PM(10) from the curbside of London's Marylebone Road and from exhaust emissions was collected by cyclone. A549 cells, human primary nasal epithelial cells (HPNEpCs), SARS-CoV-2–susceptible Vero-E6 and Calu3 cells were cultured with PM(10). ACE2 expression (as determined by median fluorescent intensity) was assessed by flow cytometry, and ACE2 mRNA transcript level was assessed by PCR. The role of oxidative stress was determined by N-acetyl cysteine. The cytopathic effect of SARS-CoV-2 (percentage of infection enhancement) and expression of SARS-CoV-2 genes' open reading frame (ORF) 1ab, S protein, and N protein (focus-forming units/mL) were assessed in Vero-E6 cells. Data were analyzed by either the Mann-Whitney U test or Kruskal-Wallis test with the Dunn multiple comparisons test. RESULTS: Curbside PM(10) at concentrations of 10 μg/mL or more increased ACE2 expression in A549 cells (P = .0021). Both diesel PM(10) and curbside PM(10) in a concentration of 10 μg/mL increased ACE2 expression in HPNEpCs (P = .0022 and P = .0072, respectively). ACE2 expression simulated by curbside PM(10) was attenuated by N-acetyl cysteine in HPNEpCs (P = .0464). Curbside PM(10) increased ACE2 expression in Calu3 cells (P = .0256). In Vero-E6 cells, curbside PM(10) increased ACE2 expression (P = .0079), ACE2 transcript level (P = .0079), SARS-CoV-2 cytopathic effect (P = .0002), and expression of the SARS-CoV-2 genes' ORF1ab, S protein, and N protein (P = .0079). CONCLUSIONS: Curbside PM(10) increases susceptibility to SARS-COV-2 infection in vitro. Elsevier 2023-07-08 /pmc/articles/PMC10509961/ /pubmed/37781647 http://dx.doi.org/10.1016/j.jacig.2023.100141 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original article Miyashita, Lisa Foley, Gary Semple, Sean Gibbons, Joseph M. Pade, Corinna McKnight, Áine Grigg, Jonathan Curbside particulate matter and susceptibility to SARS–CoV-2 infection |
title | Curbside particulate matter and susceptibility to SARS–CoV-2 infection |
title_full | Curbside particulate matter and susceptibility to SARS–CoV-2 infection |
title_fullStr | Curbside particulate matter and susceptibility to SARS–CoV-2 infection |
title_full_unstemmed | Curbside particulate matter and susceptibility to SARS–CoV-2 infection |
title_short | Curbside particulate matter and susceptibility to SARS–CoV-2 infection |
title_sort | curbside particulate matter and susceptibility to sars–cov-2 infection |
topic | Original article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509961/ https://www.ncbi.nlm.nih.gov/pubmed/37781647 http://dx.doi.org/10.1016/j.jacig.2023.100141 |
work_keys_str_mv | AT miyashitalisa curbsideparticulatematterandsusceptibilitytosarscov2infection AT foleygary curbsideparticulatematterandsusceptibilitytosarscov2infection AT semplesean curbsideparticulatematterandsusceptibilitytosarscov2infection AT gibbonsjosephm curbsideparticulatematterandsusceptibilitytosarscov2infection AT padecorinna curbsideparticulatematterandsusceptibilitytosarscov2infection AT mcknightaine curbsideparticulatematterandsusceptibilitytosarscov2infection AT griggjonathan curbsideparticulatematterandsusceptibilitytosarscov2infection |