Exploration of the ocular surface infection by SARS-CoV-2 and implications for corneal donation: An ex vivo study.
<h4>Background</h4>The risk of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) transmission through corneal graft is an ongoing debate and leads to strict restrictions in corneas procurement, leading to a major decrease in eye banking activity. The aims of this study are to...
| Main Authors: | , , , , , , , , , , , , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2022-03-01
|
| Series: | PLoS Medicine |
| Online Access: | https://journals.plos.org/plosmedicine/article/file?id=10.1371/journal.pmed.1003922&type=printable |
| _version_ | 1827770985484386304 |
|---|---|
| author | Corantin Maurin Zhiguo He Marielle Mentek Paul Verhoeven Sylvie Pillet Thomas Bourlet Françoise Rogues Jean Loup Pugniet Thierry Peyragrosse Marion Barallon Chantal Perrache Inès Aouimeur Sophie Acquart Sandrine Ninotta Marc Baud'huin Bertrand Vabres Sylvain Poinard Philippe Gain Gilles Thuret |
| author_facet | Corantin Maurin Zhiguo He Marielle Mentek Paul Verhoeven Sylvie Pillet Thomas Bourlet Françoise Rogues Jean Loup Pugniet Thierry Peyragrosse Marion Barallon Chantal Perrache Inès Aouimeur Sophie Acquart Sandrine Ninotta Marc Baud'huin Bertrand Vabres Sylvain Poinard Philippe Gain Gilles Thuret |
| author_sort | Corantin Maurin |
| collection | DOAJ |
| description | <h4>Background</h4>The risk of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) transmission through corneal graft is an ongoing debate and leads to strict restrictions in corneas procurement, leading to a major decrease in eye banking activity. The aims of this study are to specifically assess the capacity of human cornea to be infected by SARS-CoV-2 and promote its replication ex vivo, and to evaluate the real-life risk of corneal contamination by detecting SARS-CoV-2 RNA in corneas retrieved in donors diagnosed with Coronavirus Disease 2019 (COVID-19) and nonaffected donors.<h4>Methods and findings</h4>To assess the capacity of human cornea to be infected by SARS-CoV-2, the expression pattern of SARS-CoV-2 receptor angiotensin-converting enzyme 2 (ACE-2) and activators TMPRSS2 and Cathepsins B and L in ocular surface tissues from nonaffected donors was explored by immunohistochemistry (n = 10 corneas, 78 ± 11 years, 40% female) and qPCR (n = 5 corneas, 80 ± 12 years, 40% female). Additionally, 5 freshly excised corneas (80 ± 12 years, 40% female) were infected ex vivo with highly concentrated SARS-CoV-2 solution (106 median tissue culture infectious dose (TCID50)/mL). Viral RNA was extracted from tissues and culture media and quantified by reverse transcription quantitative PCR (RT-qPCR) (viral RNA copies) 30 minutes (H0) and 24 hours (H24) after infection. To assess the risk of corneal contamination by SARS-CoV-2, viral RNA was tested by RT-qPCR (Ct value) in both corneas and organ culture media from 14 donors diagnosed with COVID-19 (74 ± 10 years, 29% female) and 26 healthy donors (79 ± 13 years, 57% female), and in organ culture media only from 133 consecutive nonaffected donors from 2 eye banks (73 ± 13 years, 29% female). The expression of receptor and activators was variable among samples at both protein and mRNA level. Based on immunohistochemistry findings, ACE-2 was localized mainly in the most superficial epithelial cells of peripheral cornea, limbus, and conjunctiva, whereas TMPRSS2 was mostly expressed in all layers of bulbar conjunctiva. A significant increase in total and positive strands of IP4 RNA sequence (RdRp viral gene) was observed from 30 minutes to 24 hours postinfection in central cornea (1.1 × 108 [95% CI: 6.4 × 107 to 2.4 × 108] to 3.0 × 109 [1.4 × 109 to 5.3 × 109], p = 0.0039 and 2.2 × 107 [1.4 × 107 to 3.6 × 107] to 5.1 × 107 [2.9 × 107 to 7.5 × 107], p = 0.0117, respectively) and in corneoscleral rim (4.5 × 109 [2.7 × 109 to 9.6 × 109] to 3.9 × 1010 [2.6 × 1010 to 4.4 × 1010], p = 0.0039 and 3.1 × 108 [1.2 × 108 to 5.3 × 108] to 7.8 × 108 [3.9 × 108 to 9.9 × 108], p = 0.0391, respectively). Viral RNA copies in ex vivo corneas were highly variable from one donor to another. Finally, viral RNA was detected in 3 out of 28 corneas (11%) from donors diagnosed with COVID-19. All samples from the 159 nonaffected donors were negative for SARS-CoV-2 RNA. The main limitation of this study relates to the limited sample size, due to limited access to donors diagnosed with COVID-19 and concomitant decrease in the procurement corneas from nonaffected donors.<h4>Conclusions</h4>In this study, we observed the expression of SARS-CoV-2 receptors and activators at the human ocular surface and a variable increase in viral RNA copies 24 hours after experimental infection of freshly excised human corneas. We also found viral RNA only in a very limited percentage of donors with positive nasopharyngeal PCR. The low rate of positivity in donors diagnosed with COVID-19 calls into question the utility of donor selection algorithms.<h4>Trial registration</h4>Agence de la Biomédecine, PFS-20-011 https://www.agence-biomedecine.fr/. |
| first_indexed | 2024-03-11T12:47:15Z |
| format | Article |
| id | doaj.art-f43f0a092f724bd48c5e90e3ee569448 |
| institution | Directory Open Access Journal |
| issn | 1549-1277 1549-1676 |
| language | English |
| last_indexed | 2024-03-11T12:47:15Z |
| publishDate | 2022-03-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS Medicine |
| spelling | doaj.art-f43f0a092f724bd48c5e90e3ee5694482023-11-05T05:31:19ZengPublic Library of Science (PLoS)PLoS Medicine1549-12771549-16762022-03-01193e100392210.1371/journal.pmed.1003922Exploration of the ocular surface infection by SARS-CoV-2 and implications for corneal donation: An ex vivo study.Corantin MaurinZhiguo HeMarielle MentekPaul VerhoevenSylvie PilletThomas BourletFrançoise RoguesJean Loup PugnietThierry PeyragrosseMarion BarallonChantal PerracheInès AouimeurSophie AcquartSandrine NinottaMarc Baud'huinBertrand VabresSylvain PoinardPhilippe GainGilles Thuret<h4>Background</h4>The risk of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) transmission through corneal graft is an ongoing debate and leads to strict restrictions in corneas procurement, leading to a major decrease in eye banking activity. The aims of this study are to specifically assess the capacity of human cornea to be infected by SARS-CoV-2 and promote its replication ex vivo, and to evaluate the real-life risk of corneal contamination by detecting SARS-CoV-2 RNA in corneas retrieved in donors diagnosed with Coronavirus Disease 2019 (COVID-19) and nonaffected donors.<h4>Methods and findings</h4>To assess the capacity of human cornea to be infected by SARS-CoV-2, the expression pattern of SARS-CoV-2 receptor angiotensin-converting enzyme 2 (ACE-2) and activators TMPRSS2 and Cathepsins B and L in ocular surface tissues from nonaffected donors was explored by immunohistochemistry (n = 10 corneas, 78 ± 11 years, 40% female) and qPCR (n = 5 corneas, 80 ± 12 years, 40% female). Additionally, 5 freshly excised corneas (80 ± 12 years, 40% female) were infected ex vivo with highly concentrated SARS-CoV-2 solution (106 median tissue culture infectious dose (TCID50)/mL). Viral RNA was extracted from tissues and culture media and quantified by reverse transcription quantitative PCR (RT-qPCR) (viral RNA copies) 30 minutes (H0) and 24 hours (H24) after infection. To assess the risk of corneal contamination by SARS-CoV-2, viral RNA was tested by RT-qPCR (Ct value) in both corneas and organ culture media from 14 donors diagnosed with COVID-19 (74 ± 10 years, 29% female) and 26 healthy donors (79 ± 13 years, 57% female), and in organ culture media only from 133 consecutive nonaffected donors from 2 eye banks (73 ± 13 years, 29% female). The expression of receptor and activators was variable among samples at both protein and mRNA level. Based on immunohistochemistry findings, ACE-2 was localized mainly in the most superficial epithelial cells of peripheral cornea, limbus, and conjunctiva, whereas TMPRSS2 was mostly expressed in all layers of bulbar conjunctiva. A significant increase in total and positive strands of IP4 RNA sequence (RdRp viral gene) was observed from 30 minutes to 24 hours postinfection in central cornea (1.1 × 108 [95% CI: 6.4 × 107 to 2.4 × 108] to 3.0 × 109 [1.4 × 109 to 5.3 × 109], p = 0.0039 and 2.2 × 107 [1.4 × 107 to 3.6 × 107] to 5.1 × 107 [2.9 × 107 to 7.5 × 107], p = 0.0117, respectively) and in corneoscleral rim (4.5 × 109 [2.7 × 109 to 9.6 × 109] to 3.9 × 1010 [2.6 × 1010 to 4.4 × 1010], p = 0.0039 and 3.1 × 108 [1.2 × 108 to 5.3 × 108] to 7.8 × 108 [3.9 × 108 to 9.9 × 108], p = 0.0391, respectively). Viral RNA copies in ex vivo corneas were highly variable from one donor to another. Finally, viral RNA was detected in 3 out of 28 corneas (11%) from donors diagnosed with COVID-19. All samples from the 159 nonaffected donors were negative for SARS-CoV-2 RNA. The main limitation of this study relates to the limited sample size, due to limited access to donors diagnosed with COVID-19 and concomitant decrease in the procurement corneas from nonaffected donors.<h4>Conclusions</h4>In this study, we observed the expression of SARS-CoV-2 receptors and activators at the human ocular surface and a variable increase in viral RNA copies 24 hours after experimental infection of freshly excised human corneas. We also found viral RNA only in a very limited percentage of donors with positive nasopharyngeal PCR. The low rate of positivity in donors diagnosed with COVID-19 calls into question the utility of donor selection algorithms.<h4>Trial registration</h4>Agence de la Biomédecine, PFS-20-011 https://www.agence-biomedecine.fr/.https://journals.plos.org/plosmedicine/article/file?id=10.1371/journal.pmed.1003922&type=printable |
| spellingShingle | Corantin Maurin Zhiguo He Marielle Mentek Paul Verhoeven Sylvie Pillet Thomas Bourlet Françoise Rogues Jean Loup Pugniet Thierry Peyragrosse Marion Barallon Chantal Perrache Inès Aouimeur Sophie Acquart Sandrine Ninotta Marc Baud'huin Bertrand Vabres Sylvain Poinard Philippe Gain Gilles Thuret Exploration of the ocular surface infection by SARS-CoV-2 and implications for corneal donation: An ex vivo study. PLoS Medicine |
| title | Exploration of the ocular surface infection by SARS-CoV-2 and implications for corneal donation: An ex vivo study. |
| title_full | Exploration of the ocular surface infection by SARS-CoV-2 and implications for corneal donation: An ex vivo study. |
| title_fullStr | Exploration of the ocular surface infection by SARS-CoV-2 and implications for corneal donation: An ex vivo study. |
| title_full_unstemmed | Exploration of the ocular surface infection by SARS-CoV-2 and implications for corneal donation: An ex vivo study. |
| title_short | Exploration of the ocular surface infection by SARS-CoV-2 and implications for corneal donation: An ex vivo study. |
| title_sort | exploration of the ocular surface infection by sars cov 2 and implications for corneal donation an ex vivo study |
| url | https://journals.plos.org/plosmedicine/article/file?id=10.1371/journal.pmed.1003922&type=printable |
| work_keys_str_mv | AT corantinmaurin explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT zhiguohe explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT mariellementek explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT paulverhoeven explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT sylviepillet explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT thomasbourlet explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT francoiserogues explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT jeanlouppugniet explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT thierrypeyragrosse explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT marionbarallon explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT chantalperrache explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT inesaouimeur explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT sophieacquart explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT sandrineninotta explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT marcbaudhuin explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT bertrandvabres explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT sylvainpoinard explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT philippegain explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy AT gillesthuret explorationoftheocularsurfaceinfectionbysarscov2andimplicationsforcornealdonationanexvivostudy |