Cytomegalovirus detected by qPCR in iris and ciliary body of immunocompetent corneal donors.


Journal

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
ISSN: 1873-5967
Titre abrégé: J Clin Virol
Pays: Netherlands
ID NLM: 9815671

Informations de publication

Date de publication:
Apr 2024
Historique:
received: 04 11 2023
revised: 25 12 2023
accepted: 30 12 2023
medline: 18 3 2024
pubmed: 15 1 2024
entrez: 14 1 2024
Statut: ppublish

Résumé

Cytomegalovirus (CMV) can cause a wide panel of ocular infections. The involvement of CMV as a cause of anterior uveitis in the immunocompetent patient is recent and remains poorly understood. To investigate the presence of CMV in anterior uveal tissues of immunocompetent corneal donors. We collected aqueous humor, iris, and ciliary body from both eyes of 25 donors died at the Limoges University Hospital between January 2020 and July 2021. CMV serology was determined for all patients from post-mortem blood sample. Ocular tissues were split in 2 fragments for qPCR and 2 for histological analysis. CMV genomes copies were quantified by Multiplex qPCR after DNA extraction. 16 of 25 patients (64%) displayed positive CMV serology, with a median age of 67 years. Viremia was positive in 3 of 16 (19%) CMV-positive patients. No CMV DNA copies were found from the aqueous humor samples. CMV DNA was detected in iris and ciliary body of 28 of 32 eyes of seropositive donors, and 5 of 18 eyes of seronegative donors. The median viral copy number [IQR] was 2.41 × 10 CMV DNA was found in iris and ciliary body of immunocompetent seropositive patients, but also, although less frequently, from seronegative donors. These results highlight mechanisms of infection, latency and reactivation of CMV in ocular tissues.

Sections du résumé

BACKGROUND BACKGROUND
Cytomegalovirus (CMV) can cause a wide panel of ocular infections. The involvement of CMV as a cause of anterior uveitis in the immunocompetent patient is recent and remains poorly understood.
OBJECTIVE OBJECTIVE
To investigate the presence of CMV in anterior uveal tissues of immunocompetent corneal donors.
STUDY DESIGN METHODS
We collected aqueous humor, iris, and ciliary body from both eyes of 25 donors died at the Limoges University Hospital between January 2020 and July 2021. CMV serology was determined for all patients from post-mortem blood sample. Ocular tissues were split in 2 fragments for qPCR and 2 for histological analysis. CMV genomes copies were quantified by Multiplex qPCR after DNA extraction.
RESULTS RESULTS
16 of 25 patients (64%) displayed positive CMV serology, with a median age of 67 years. Viremia was positive in 3 of 16 (19%) CMV-positive patients. No CMV DNA copies were found from the aqueous humor samples. CMV DNA was detected in iris and ciliary body of 28 of 32 eyes of seropositive donors, and 5 of 18 eyes of seronegative donors. The median viral copy number [IQR] was 2.41 × 10
CONCLUSION CONCLUSIONS
CMV DNA was found in iris and ciliary body of immunocompetent seropositive patients, but also, although less frequently, from seronegative donors. These results highlight mechanisms of infection, latency and reactivation of CMV in ocular tissues.

Identifiants

pubmed: 38219682
pii: S1386-6532(23)00259-7
doi: 10.1016/j.jcv.2023.105636
pii:
doi:

Substances chimiques

DNA, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105636

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Maxime Rocher (M)

Department of Ophthalmology, CHU Limoges, F-87000 Limoges, France; Univ. Limoges, INSERM, CHU Limoges, RESINFIT, U1092, F-87000 Limoges, France. Electronic address: maxime.rocher@unilim.fr.

Mathilde Duchesne (M)

Department of Pathology, CHU Limoges, F-87000 Limoges, France.

Déborah Andouard (D)

Univ. Limoges, INSERM, CHU Limoges, RESINFIT, U1092, F-87000 Limoges, France; National Reference Center for Herpesviruses, Department of Bacteriology-Virology-Hygiene, CHU Limoges, F-87000 Limoges, France.

Laurence Beral (L)

Department of Ophthalmology, CHU Pointe-à-Pitre, F-97120 Guadeloupe, France.

Marc Labriffe (M)

Department of Pharmacology, CHU Limoges, F-87000 Limoges, France.

Delphine Chainier (D)

CRBioLim, Department of Bacteriology-Virology-Hygiene, CHU Limoges, F-87000 Limoges, France.

Mélissa Gomes-Mayeras (M)

Univ. Limoges, INSERM, CHU Limoges, RESINFIT, U1092, F-87000 Limoges, France; National Reference Center for Herpesviruses, Department of Bacteriology-Virology-Hygiene, CHU Limoges, F-87000 Limoges, France.

Sébastien Hantz (S)

Univ. Limoges, INSERM, CHU Limoges, RESINFIT, U1092, F-87000 Limoges, France; National Reference Center for Herpesviruses, Department of Bacteriology-Virology-Hygiene, CHU Limoges, F-87000 Limoges, France.

Sophie Alain (S)

Univ. Limoges, INSERM, CHU Limoges, RESINFIT, U1092, F-87000 Limoges, France; National Reference Center for Herpesviruses, Department of Bacteriology-Virology-Hygiene, CHU Limoges, F-87000 Limoges, France; CRBioLim, Department of Bacteriology-Virology-Hygiene, CHU Limoges, F-87000 Limoges, France.

Pierre-Yves Robert (PY)

Department of Ophthalmology, CHU Limoges, F-87000 Limoges, France; Univ. Limoges, INSERM, CHU Limoges, RESINFIT, U1092, F-87000 Limoges, France.

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Classifications MeSH