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Clinical and genomic features of Corynebacterium macginleyi-associated infectious keratitis

Infectious keratitis is a potentially sight threatening ophthalmological emergency. Contact lens wear is a common risk factor. Diagnostic advances such as MALDI-TOF MS provides new insights into the spectrum of corneal pathogens and on microbes previously considered as commensals. Corynebacterium ma...

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Autores principales: Sagerfors, Susanna, Poehlein, Anja, Afshar, Mastaneh, Lindblad, Birgitta Ejdervik, Brüggemann, Holger, Söderquist, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966771/
https://www.ncbi.nlm.nih.gov/pubmed/33727638
http://dx.doi.org/10.1038/s41598-021-85336-w
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author Sagerfors, Susanna
Poehlein, Anja
Afshar, Mastaneh
Lindblad, Birgitta Ejdervik
Brüggemann, Holger
Söderquist, Bo
author_facet Sagerfors, Susanna
Poehlein, Anja
Afshar, Mastaneh
Lindblad, Birgitta Ejdervik
Brüggemann, Holger
Söderquist, Bo
author_sort Sagerfors, Susanna
collection PubMed
description Infectious keratitis is a potentially sight threatening ophthalmological emergency. Contact lens wear is a common risk factor. Diagnostic advances such as MALDI-TOF MS provides new insights into the spectrum of corneal pathogens and on microbes previously considered as commensals. Corynebacterium macginleyi was described in 1995, and in 2018, the genomic features of three isolates were reported after whole-genome sequencing. Here we describe the clinical characteristics of patients with infectious keratitis (n = 29) presumably caused by Corynebacterium macginleyi, and analyze the genomic features of C. macginleyi (n = 22) isolated from the corneal ulcers of these patients. The disease course was uneventful apart from minor interventions such as corneal cross-linking and amniotic membrane transplant. Genome sequencing and comparison revealed a highly conserved core genome of C. macginleyi. Based on the analyses of single nucleotide polymorphisms, the population could be divided into two main clades that also differed in a few clade-specific genomic islands. Patients infected with an isolate belonging to the minor clade (n = 7) presented a more severe disease. Comparisons with other corynebacterial species clearly separated C. macginleyi. C. macginleyi may be considered a corneal pathogen; genomic analysis provided insights into its population structure and disease-causing potential.
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spelling pubmed-79667712021-03-19 Clinical and genomic features of Corynebacterium macginleyi-associated infectious keratitis Sagerfors, Susanna Poehlein, Anja Afshar, Mastaneh Lindblad, Birgitta Ejdervik Brüggemann, Holger Söderquist, Bo Sci Rep Article Infectious keratitis is a potentially sight threatening ophthalmological emergency. Contact lens wear is a common risk factor. Diagnostic advances such as MALDI-TOF MS provides new insights into the spectrum of corneal pathogens and on microbes previously considered as commensals. Corynebacterium macginleyi was described in 1995, and in 2018, the genomic features of three isolates were reported after whole-genome sequencing. Here we describe the clinical characteristics of patients with infectious keratitis (n = 29) presumably caused by Corynebacterium macginleyi, and analyze the genomic features of C. macginleyi (n = 22) isolated from the corneal ulcers of these patients. The disease course was uneventful apart from minor interventions such as corneal cross-linking and amniotic membrane transplant. Genome sequencing and comparison revealed a highly conserved core genome of C. macginleyi. Based on the analyses of single nucleotide polymorphisms, the population could be divided into two main clades that also differed in a few clade-specific genomic islands. Patients infected with an isolate belonging to the minor clade (n = 7) presented a more severe disease. Comparisons with other corynebacterial species clearly separated C. macginleyi. C. macginleyi may be considered a corneal pathogen; genomic analysis provided insights into its population structure and disease-causing potential. Nature Publishing Group UK 2021-03-16 /pmc/articles/PMC7966771/ /pubmed/33727638 http://dx.doi.org/10.1038/s41598-021-85336-w Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sagerfors, Susanna
Poehlein, Anja
Afshar, Mastaneh
Lindblad, Birgitta Ejdervik
Brüggemann, Holger
Söderquist, Bo
Clinical and genomic features of Corynebacterium macginleyi-associated infectious keratitis
title Clinical and genomic features of Corynebacterium macginleyi-associated infectious keratitis
title_full Clinical and genomic features of Corynebacterium macginleyi-associated infectious keratitis
title_fullStr Clinical and genomic features of Corynebacterium macginleyi-associated infectious keratitis
title_full_unstemmed Clinical and genomic features of Corynebacterium macginleyi-associated infectious keratitis
title_short Clinical and genomic features of Corynebacterium macginleyi-associated infectious keratitis
title_sort clinical and genomic features of corynebacterium macginleyi-associated infectious keratitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966771/
https://www.ncbi.nlm.nih.gov/pubmed/33727638
http://dx.doi.org/10.1038/s41598-021-85336-w
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