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Antibiotic Susceptibility and Minimum Inhibitory Concentration for Stenotrophomonas maltophilia Ocular Infections

Stenotrophomonas maltophilia (S. maltophilia) is a Gram-negative, opportunistic pathogen that can lead to ocular infections, such as keratitis and endophthalmitis. The purpose of this study was to determine the antibiotic susceptibility and minimum inhibitory concentrations (MICs) of S. maltophilia...

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Autores principales: Ho, Margaret Ming-Chih, Sun, Ming-Hui, Wu, Wei-Chi, Lai, Chi-Chun, Yeh, Lung-Kun, Hwang, Yih-Shiou, Hsiao, Ching-Hsi, Chen, Kuan-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686969/
https://www.ncbi.nlm.nih.gov/pubmed/36358112
http://dx.doi.org/10.3390/antibiotics11111457
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author Ho, Margaret Ming-Chih
Sun, Ming-Hui
Wu, Wei-Chi
Lai, Chi-Chun
Yeh, Lung-Kun
Hwang, Yih-Shiou
Hsiao, Ching-Hsi
Chen, Kuan-Jen
author_facet Ho, Margaret Ming-Chih
Sun, Ming-Hui
Wu, Wei-Chi
Lai, Chi-Chun
Yeh, Lung-Kun
Hwang, Yih-Shiou
Hsiao, Ching-Hsi
Chen, Kuan-Jen
author_sort Ho, Margaret Ming-Chih
collection PubMed
description Stenotrophomonas maltophilia (S. maltophilia) is a Gram-negative, opportunistic pathogen that can lead to ocular infections, such as keratitis and endophthalmitis. The purpose of this study was to determine the antibiotic susceptibility and minimum inhibitory concentrations (MICs) of S. maltophilia isolates from ocular infections and to evaluate the differences in antibiotic MICs between keratitis and endophthalmitis isolates. The disc diffusion method revealed that S. maltophilia isolates exhibited 91% susceptibility to levofloxacin and moxifloxacin and 61% susceptibility to trimethoprim–sulfamethoxazole (TMP–SMX). The E-test indicated that S. maltophilia isolates exhibited 40%, 100%, 72%, 91%, 91%, and 93% susceptibility to ceftazidime, tigecycline, TMP–SMX, levofloxacin, gatifloxacin, and moxifloxacin, respectively. The MIC(90) values of amikacin, ceftazidime, cefuroxime, tigecycline, TMP–SMX, levofloxacin, gatifloxacin, and moxifloxacin were >256, >256, >256, 3, >32, 1, 2, and 0.75 µg/mL, respectively. The geometric mean MICs of ceftazidime, TMP–SMX, levofloxacin, gatifloxacin, and moxifloxacin were significantly lower for the keratitis isolates than for the endophthalmitis isolates (p = 0.0047, 0.003, 0.0029, 0.0003, and 0.0004, respectively). Fluoroquinolones showed higher susceptibility and lower MICs for the S. maltophilia isolates when compared with other antibiotics. Fluoroquinolones can be recommended for treating S. maltophilia ocular infections. Tigecycline and TMP–SMX could be alternative antibiotics for S. maltophilia ocular infections.
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spelling pubmed-96869692022-11-25 Antibiotic Susceptibility and Minimum Inhibitory Concentration for Stenotrophomonas maltophilia Ocular Infections Ho, Margaret Ming-Chih Sun, Ming-Hui Wu, Wei-Chi Lai, Chi-Chun Yeh, Lung-Kun Hwang, Yih-Shiou Hsiao, Ching-Hsi Chen, Kuan-Jen Antibiotics (Basel) Article Stenotrophomonas maltophilia (S. maltophilia) is a Gram-negative, opportunistic pathogen that can lead to ocular infections, such as keratitis and endophthalmitis. The purpose of this study was to determine the antibiotic susceptibility and minimum inhibitory concentrations (MICs) of S. maltophilia isolates from ocular infections and to evaluate the differences in antibiotic MICs between keratitis and endophthalmitis isolates. The disc diffusion method revealed that S. maltophilia isolates exhibited 91% susceptibility to levofloxacin and moxifloxacin and 61% susceptibility to trimethoprim–sulfamethoxazole (TMP–SMX). The E-test indicated that S. maltophilia isolates exhibited 40%, 100%, 72%, 91%, 91%, and 93% susceptibility to ceftazidime, tigecycline, TMP–SMX, levofloxacin, gatifloxacin, and moxifloxacin, respectively. The MIC(90) values of amikacin, ceftazidime, cefuroxime, tigecycline, TMP–SMX, levofloxacin, gatifloxacin, and moxifloxacin were >256, >256, >256, 3, >32, 1, 2, and 0.75 µg/mL, respectively. The geometric mean MICs of ceftazidime, TMP–SMX, levofloxacin, gatifloxacin, and moxifloxacin were significantly lower for the keratitis isolates than for the endophthalmitis isolates (p = 0.0047, 0.003, 0.0029, 0.0003, and 0.0004, respectively). Fluoroquinolones showed higher susceptibility and lower MICs for the S. maltophilia isolates when compared with other antibiotics. Fluoroquinolones can be recommended for treating S. maltophilia ocular infections. Tigecycline and TMP–SMX could be alternative antibiotics for S. maltophilia ocular infections. MDPI 2022-10-22 /pmc/articles/PMC9686969/ /pubmed/36358112 http://dx.doi.org/10.3390/antibiotics11111457 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ho, Margaret Ming-Chih
Sun, Ming-Hui
Wu, Wei-Chi
Lai, Chi-Chun
Yeh, Lung-Kun
Hwang, Yih-Shiou
Hsiao, Ching-Hsi
Chen, Kuan-Jen
Antibiotic Susceptibility and Minimum Inhibitory Concentration for Stenotrophomonas maltophilia Ocular Infections
title Antibiotic Susceptibility and Minimum Inhibitory Concentration for Stenotrophomonas maltophilia Ocular Infections
title_full Antibiotic Susceptibility and Minimum Inhibitory Concentration for Stenotrophomonas maltophilia Ocular Infections
title_fullStr Antibiotic Susceptibility and Minimum Inhibitory Concentration for Stenotrophomonas maltophilia Ocular Infections
title_full_unstemmed Antibiotic Susceptibility and Minimum Inhibitory Concentration for Stenotrophomonas maltophilia Ocular Infections
title_short Antibiotic Susceptibility and Minimum Inhibitory Concentration for Stenotrophomonas maltophilia Ocular Infections
title_sort antibiotic susceptibility and minimum inhibitory concentration for stenotrophomonas maltophilia ocular infections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9686969/
https://www.ncbi.nlm.nih.gov/pubmed/36358112
http://dx.doi.org/10.3390/antibiotics11111457
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