Microbial keratitis in Southern Malawi: a microbiological pilot study.


Journal

BMJ open ophthalmology
ISSN: 2397-3269
Titre abrégé: BMJ Open Ophthalmol
Pays: England
ID NLM: 101714806

Informations de publication

Date de publication:
22 Apr 2024
Historique:
received: 14 02 2024
accepted: 10 04 2024
medline: 24 4 2024
pubmed: 24 4 2024
entrez: 23 4 2024
Statut: epublish

Résumé

Microbial keratitis (MK) is a significant cause of blindness in sub-Saharan Africa. We investigated the feasibility of using a novel corneal impression membrane (CIM) for obtaining and processing samples by culture, PCR and whole-genome sequencing (WGS) in patients presenting with suspected MK in Malawi. Samples were collected from patients presenting with suspected MK using a 12 mm diameter polytetrafluoroethylene CIM disc. Samples were processed using culture and PCR for 71 eyes of 71 patients were included. The overall CIM isolation rate was 81.7% (58 positive samples from 71 participants). 69 (81.2%) of isolates were Gram-positive cocci. Coagulase-negative In a resource-poor setting, a CIM can be used to safely sample the cornea in patients presenting with suspected MK, enabling identification of causative microorganisms by culture and PCR. Although the microbiological spectrum found was limited to the dry season, these preliminary results could be used to guide empirical treatment.

Identifiants

pubmed: 38653537
pii: bmjophth-2024-001682
doi: 10.1136/bmjophth-2024-001682
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
RNA, Ribosomal, 16S 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: SBK is an editor of BMJ Open Ophthalmology. There are no other conflicts of interest

Auteurs

Tobi F Somerville (TF)

Department of Eye and Vision Sciences, University of Liverpool, Liverpool, UK tobi@liverpool.ac.uk.

Shaffi Mdala (S)

Queen Elizabeth Central Hospital, Blantyre, Southern Region, Malawi.
Ophthalmology Unit, Kamuzu University of Health Sciences, Blantyre, Southern Region, Malawi.

Thokozani Zungu (T)

Queen Elizabeth Central Hospital, Blantyre, Southern Region, Malawi.
Ophthalmology Unit, Kamuzu University of Health Sciences, Blantyre, Southern Region, Malawi.

Moira Gandiwa (M)

Ophthalmology Unit, Kamuzu University of Health Sciences, Blantyre, Southern Region, Malawi.
Kamuzu Central Hospital, Lilongwe, Central Region, Malawi.

Rose Herbert (R)

Department of Eye and Vision Sciences, University of Liverpool, Liverpool, UK.

Dean Everett (D)

Malawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
College of Medicine and Health Sciences, Infection Research Unit, Khalifa University, Abu Dhabi, UAE.

Caroline E Corless (CE)

Medical Microbiology, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Nicholas A V Beare (NAV)

University of Liverpool, Liverpool, UK.

Timothy Neal (T)

Department of Infection and Immunity, Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK.

Malcolm J Horsburgh (MJ)

Department of Infection Biology and Microbiomes, University of Liverpool, Liverpool, UK.

Alistair Darby (A)

Department of Infection Biology and Microbiomes, University of Liverpool, Liverpool, UK.

Stephen B Kaye (SB)

Department of Eye and Vision Sciences, University of Liverpool, Liverpool, UK.

Petros C Kayange (PC)

Queen Elizabeth Central Hospital, Blantyre, Southern Region, Malawi.
Ophthalmology Unit, Kamuzu University of Health Sciences, Blantyre, Southern Region, Malawi.

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Classifications MeSH