Effect of Antibiotic Eye Drops on the Nasal Microbiome in Healthy Subjects-A Pilot Study.

antibiotic eye drops ciprofloxacin gentamicin nasal microbiome next-generation sequencing

Journal

Antibiotics (Basel, Switzerland)
ISSN: 2079-6382
Titre abrégé: Antibiotics (Basel)
Pays: Switzerland
ID NLM: 101637404

Informations de publication

Date de publication:
04 Mar 2023
Historique:
received: 07 01 2023
revised: 27 02 2023
accepted: 28 02 2023
medline: 30 3 2023
entrez: 29 3 2023
pubmed: 30 3 2023
Statut: epublish

Résumé

Antibiotic eye drops are frequently used in clinical practice. Due to the anatomical connection via the nasolacrimal duct, it seems possible that they have an influence on the nasal/pharyngeal microbiome. This was investigated by using two different commonly used antibiotic eye drops. 20 subjects were randomized to four groups of five subjects receiving eye drops containing gentamicin, ciprofloxacin, or, as controls, unpreserved povidone or benzalkonium chloride-preserved povidone. Nasal and pharyngeal swabs were performed before and after the instillation period. Swabs were analyzed by Illumina next-generation sequencing (NGS)-based 16S rRNA analysis. Bacterial culture was performed on solid media, and bacterial isolates were identified to the species level by MALDI-TOF MS. Species-dependent antimicrobial susceptibility testing was performed using single isolates and pools of isolates. Bacterial richness in the nose increased numerically from 163 ± 30 to 243 ± 100 OTUs (gentamicin) and from 114 ± 17 to 144 ± 45 OTUs (ciprofloxacin). Phylogenetic diversity index (pd) of different bacterial strains in the nasal microbiome increased from 12.4 ± 1.0 to 16.9 ± 5.6 pd (gentamicin) and from 10.2 ± 1.4 to 11.8 ± 3.1 pd (ciprofloxacin). Unpreserved povidone eye drops resulted in minimal changes in bacterial counts. Preservative-containing povidone eye drops resulted in no change. A minor increase (1-2-fold) in the minimal inhibitory concentration (MIC) was observed in single streptococcal isolates. Antibiotic eye drops could affect the nasal microbiome. After an instillation period of seven days, an increase in the diversity and richness of bacterial strains in the nasal microbiome was observed.

Sections du résumé

BACKGROUND BACKGROUND
Antibiotic eye drops are frequently used in clinical practice. Due to the anatomical connection via the nasolacrimal duct, it seems possible that they have an influence on the nasal/pharyngeal microbiome. This was investigated by using two different commonly used antibiotic eye drops.
METHODS METHODS
20 subjects were randomized to four groups of five subjects receiving eye drops containing gentamicin, ciprofloxacin, or, as controls, unpreserved povidone or benzalkonium chloride-preserved povidone. Nasal and pharyngeal swabs were performed before and after the instillation period. Swabs were analyzed by Illumina next-generation sequencing (NGS)-based 16S rRNA analysis. Bacterial culture was performed on solid media, and bacterial isolates were identified to the species level by MALDI-TOF MS. Species-dependent antimicrobial susceptibility testing was performed using single isolates and pools of isolates.
RESULTS RESULTS
Bacterial richness in the nose increased numerically from 163 ± 30 to 243 ± 100 OTUs (gentamicin) and from 114 ± 17 to 144 ± 45 OTUs (ciprofloxacin). Phylogenetic diversity index (pd) of different bacterial strains in the nasal microbiome increased from 12.4 ± 1.0 to 16.9 ± 5.6 pd (gentamicin) and from 10.2 ± 1.4 to 11.8 ± 3.1 pd (ciprofloxacin). Unpreserved povidone eye drops resulted in minimal changes in bacterial counts. Preservative-containing povidone eye drops resulted in no change. A minor increase (1-2-fold) in the minimal inhibitory concentration (MIC) was observed in single streptococcal isolates.
CONCLUSIONS CONCLUSIONS
Antibiotic eye drops could affect the nasal microbiome. After an instillation period of seven days, an increase in the diversity and richness of bacterial strains in the nasal microbiome was observed.

Identifiants

pubmed: 36978384
pii: antibiotics12030517
doi: 10.3390/antibiotics12030517
pmc: PMC10044076
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Clemens Nadvornik (C)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Martin Kallab (M)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Nikolaus Hommer (N)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Andreas Schlatter (A)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Theresa Stengel (T)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Gerhard Garhöfer (G)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Markus Zeitlinger (M)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Sabine Eberl (S)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Ingeborg Klymiuk (I)

Division of Cell Biology, Histology and Embryology, Gottfried Schatz Research Center, Medical University of Graz, 8036 Graz, Austria.

Slave Trajanoski (S)

Core Facility Computational Bioanalytics, Center for Medical Research, Medical University of Graz, 8036 Graz, Austria.

Marion Nehr (M)

Department of Clinical Microbiology, Clinical Institute of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Athanasios Makristathis (A)

Department of Clinical Microbiology, Clinical Institute of Laboratory Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Doreen Schmidl (D)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Alina Nussbaumer-Proell (A)

Department of Clinical Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Classifications MeSH