Camille André, Cassandra L Schrank, Ana Victoria Cheng Jaramillo, Eleftherios Mylonakis, William M Wuest, Michael S Gilmore, Wooseong Kim, Paulo J M Bispo
{"title":"Antimicrobial activity of a new class of synthetic retinoid antibiotics and comparator agents against ocular staphylococci.","authors":"Camille André, Cassandra L Schrank, Ana Victoria Cheng Jaramillo, Eleftherios Mylonakis, William M Wuest, Michael S Gilmore, Wooseong Kim, Paulo J M Bispo","doi":"10.3389/frabi.2023.1101450","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Antimicrobial resistance is global pandemic that poses a major threat to vision health as ocular pathogens, especially staphylococcal species, are becoming increasingly resistant to first-line therapies. Here we evaluated the antimicrobial activity of a new class of synthetic retinoids in comparison to currently used antibiotics against clinically relevant ocular staphylococcal isolates.</p><p><strong>Methods: </strong>Antimicrobial susceptibility testing was performed by broth microdilution for 3 novel synthetic retinoids (CD1530, CD437, and a CD437 analogue) and 7 comparator antibiotics, against a collection of 216 clinical isolates.</p><p><strong>Results: </strong>CD437 MIC<sub>50</sub> and MIC<sub>90</sub> were 2 µg/mL for <i>Staphylococcus aureus</i>, and 1 µg/mL and 2 µg/mL respectively, for coagulase-negative staphylococci (CoNS). CD1530 (MIC<sub>50</sub> = 2 µg/mL for all species) also displayed good activity with an <i>in vitro</i> potency slightly lower (2-fold) for <i>S. aureus</i> (MIC<sub>90</sub> = 4 µg/mL) when compared to CD437. A CD437 analogue also demonstrated good <i>in vitro</i> activity (MIC<sub>50</sub> = 2 µg/mL for all species) and potency (MIC<sub>90</sub> = 2 µg/mL for MRSA and 4 µg/mL for MSSA and CoNS). <i>In vitro</i> potencies were similar or higher than that of comparator agents, and were not impacted by multidrug resistance phenotypes.</p><p><strong>Conclusion: </strong>Our results demonstrate that synthetic retinoids display potent <i>in vitro</i> activity against ocular staphylococcal species, including multidrug-resistant isolates.</p>","PeriodicalId":73065,"journal":{"name":"Frontiers in antibiotics","volume":" ","pages":"1101450"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11732056/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in antibiotics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/frabi.2023.1101450","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: Antimicrobial resistance is global pandemic that poses a major threat to vision health as ocular pathogens, especially staphylococcal species, are becoming increasingly resistant to first-line therapies. Here we evaluated the antimicrobial activity of a new class of synthetic retinoids in comparison to currently used antibiotics against clinically relevant ocular staphylococcal isolates.
Methods: Antimicrobial susceptibility testing was performed by broth microdilution for 3 novel synthetic retinoids (CD1530, CD437, and a CD437 analogue) and 7 comparator antibiotics, against a collection of 216 clinical isolates.
Results: CD437 MIC50 and MIC90 were 2 µg/mL for Staphylococcus aureus, and 1 µg/mL and 2 µg/mL respectively, for coagulase-negative staphylococci (CoNS). CD1530 (MIC50 = 2 µg/mL for all species) also displayed good activity with an in vitro potency slightly lower (2-fold) for S. aureus (MIC90 = 4 µg/mL) when compared to CD437. A CD437 analogue also demonstrated good in vitro activity (MIC50 = 2 µg/mL for all species) and potency (MIC90 = 2 µg/mL for MRSA and 4 µg/mL for MSSA and CoNS). In vitro potencies were similar or higher than that of comparator agents, and were not impacted by multidrug resistance phenotypes.
Conclusion: Our results demonstrate that synthetic retinoids display potent in vitro activity against ocular staphylococcal species, including multidrug-resistant isolates.