Camille André, Cassandra L Schrank, Ana Victoria Cheng Jaramillo, Eleftherios Mylonakis, William M Wuest, Michael S Gilmore, Wooseong Kim, Paulo J M Bispo
{"title":"一类新的合成类维甲酸抗生素及其比较剂对眼部葡萄球菌的抑菌活性","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":"{\"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}","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}
Antimicrobial activity of a new class of synthetic retinoid antibiotics and comparator agents against ocular staphylococci.
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.