Peiying Chen , Jing Yang , Yuanling Jin , Chujie Lu , Zhenzhen Feng , Fei Gao , Yuan Chen , Fuling Wang , Zhuo Shang , Wei Lin
{"title":"金糠蛋白对耐伊曲康唑烟曲霉的体外抑菌及抗菌活性研究","authors":"Peiying Chen , Jing Yang , Yuanling Jin , Chujie Lu , Zhenzhen Feng , Fei Gao , Yuan Chen , Fuling Wang , Zhuo Shang , Wei Lin","doi":"10.1016/j.mycmed.2023.101381","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Infections caused by azole-resistant <span><em>Aspergillus</em></span><span><span><span><span> are a rising public health threat with high mortality rates, high </span>treatment costs and limited available </span>antifungals, indicating an urgent need for new antifungals or strategies. Our aim was to investigate antifungal and antibiofilm activities of </span>auranofin, an FDA-approved anti-antirheumatic drug.</span></p></div><div><h3>Methods</h3><p><span><span><span>Fungal susceptibility testing for auranofin was carried out by the broth-based microdilution methods. Cell viability treated by auranofin was tested by </span>resazurin dye testing. The synergistic effect of auranofin and antifungal drugs was evaluated using checkboard assay. The inhibitory of biofilms were measured by </span>crystal violet<span><span><span> staining. Gene expression level analysis and </span>enzyme activity was investigated with qRT-PCR analysis and </span>DTNB assay. The key amino acid residues in the binding of auranofin with </span></span><em>A. fumigatus</em><span> thioredoxin reductase (</span><em>Af</em>TrxR) were indicated by structural analyses, site-directed mutagenesis, and microscale thermophoresis (MST) assays.</p></div><div><h3>Results</h3><p><span>Auranofin has fungicidal activity and </span><em>in vitro</em> antifungal spectrum including <span><em>Aspergillus flavus</em><span><span><em>, Aspergillus fumigatus, </em><em>Aspergillus terreus</em><em>, </em></span><em>Aspergillus niger</em><em>,</em></span></span><span> even itraconazole (ITC)-resistant </span><em>A. fumigatus</em>. Additionally, it has antibiofilm activities against ITC-resistant <em>A. fumigatus</em> by reducing the expression level of <em>SomA</em> and <em>MedA</em><span>. Moreover, we discovered a synergistic effect of auranofin and ITC or amphotericin B against ITC-resistant </span><em>A. fumigatus</em><span>. Auranofin downregulated the gene transcription of </span><em>Af</em>TrxR, and strongly inhibited the enzyme activity of <em>Af</em>TrxR through interacting with residues C145 and C148.</p></div><div><h3>Conclusions</h3><p>Auranofin has fungicidal and antibiofilm activities in <em>Aspergillus</em> spp. and is also a potentiator of ITC or amphotericin B <em>in vitro</em>.</p></div>","PeriodicalId":14824,"journal":{"name":"Journal de mycologie medicale","volume":null,"pages":null},"PeriodicalIF":2.2000,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In vitro antifungal and antibiofilm activities of auranofin against itraconazole-resistant Aspergillus fumigatus\",\"authors\":\"Peiying Chen , Jing Yang , Yuanling Jin , Chujie Lu , Zhenzhen Feng , Fei Gao , Yuan Chen , Fuling Wang , Zhuo Shang , Wei Lin\",\"doi\":\"10.1016/j.mycmed.2023.101381\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Infections caused by azole-resistant <span><em>Aspergillus</em></span><span><span><span><span> are a rising public health threat with high mortality rates, high </span>treatment costs and limited available </span>antifungals, indicating an urgent need for new antifungals or strategies. Our aim was to investigate antifungal and antibiofilm activities of </span>auranofin, an FDA-approved anti-antirheumatic drug.</span></p></div><div><h3>Methods</h3><p><span><span><span>Fungal susceptibility testing for auranofin was carried out by the broth-based microdilution methods. Cell viability treated by auranofin was tested by </span>resazurin dye testing. The synergistic effect of auranofin and antifungal drugs was evaluated using checkboard assay. The inhibitory of biofilms were measured by </span>crystal violet<span><span><span> staining. Gene expression level analysis and </span>enzyme activity was investigated with qRT-PCR analysis and </span>DTNB assay. The key amino acid residues in the binding of auranofin with </span></span><em>A. fumigatus</em><span> thioredoxin reductase (</span><em>Af</em>TrxR) were indicated by structural analyses, site-directed mutagenesis, and microscale thermophoresis (MST) assays.</p></div><div><h3>Results</h3><p><span>Auranofin has fungicidal activity and </span><em>in vitro</em> antifungal spectrum including <span><em>Aspergillus flavus</em><span><span><em>, Aspergillus fumigatus, </em><em>Aspergillus terreus</em><em>, </em></span><em>Aspergillus niger</em><em>,</em></span></span><span> even itraconazole (ITC)-resistant </span><em>A. fumigatus</em>. Additionally, it has antibiofilm activities against ITC-resistant <em>A. fumigatus</em> by reducing the expression level of <em>SomA</em> and <em>MedA</em><span>. Moreover, we discovered a synergistic effect of auranofin and ITC or amphotericin B against ITC-resistant </span><em>A. fumigatus</em><span>. Auranofin downregulated the gene transcription of </span><em>Af</em>TrxR, and strongly inhibited the enzyme activity of <em>Af</em>TrxR through interacting with residues C145 and C148.</p></div><div><h3>Conclusions</h3><p>Auranofin has fungicidal and antibiofilm activities in <em>Aspergillus</em> spp. and is also a potentiator of ITC or amphotericin B <em>in vitro</em>.</p></div>\",\"PeriodicalId\":14824,\"journal\":{\"name\":\"Journal de mycologie medicale\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2023-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal de mycologie medicale\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1156523323000252\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MYCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal de mycologie medicale","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1156523323000252","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MYCOLOGY","Score":null,"Total":0}
In vitro antifungal and antibiofilm activities of auranofin against itraconazole-resistant Aspergillus fumigatus
Background
Infections caused by azole-resistant Aspergillus are a rising public health threat with high mortality rates, high treatment costs and limited available antifungals, indicating an urgent need for new antifungals or strategies. Our aim was to investigate antifungal and antibiofilm activities of auranofin, an FDA-approved anti-antirheumatic drug.
Methods
Fungal susceptibility testing for auranofin was carried out by the broth-based microdilution methods. Cell viability treated by auranofin was tested by resazurin dye testing. The synergistic effect of auranofin and antifungal drugs was evaluated using checkboard assay. The inhibitory of biofilms were measured by crystal violet staining. Gene expression level analysis and enzyme activity was investigated with qRT-PCR analysis and DTNB assay. The key amino acid residues in the binding of auranofin with A. fumigatus thioredoxin reductase (AfTrxR) were indicated by structural analyses, site-directed mutagenesis, and microscale thermophoresis (MST) assays.
Results
Auranofin has fungicidal activity and in vitro antifungal spectrum including Aspergillus flavus, Aspergillus fumigatus, Aspergillus terreus, Aspergillus niger, even itraconazole (ITC)-resistant A. fumigatus. Additionally, it has antibiofilm activities against ITC-resistant A. fumigatus by reducing the expression level of SomA and MedA. Moreover, we discovered a synergistic effect of auranofin and ITC or amphotericin B against ITC-resistant A. fumigatus. Auranofin downregulated the gene transcription of AfTrxR, and strongly inhibited the enzyme activity of AfTrxR through interacting with residues C145 and C148.
Conclusions
Auranofin has fungicidal and antibiofilm activities in Aspergillus spp. and is also a potentiator of ITC or amphotericin B in vitro.
期刊介绍:
The Journal de Mycologie Medicale / Journal of Medical Mycology (JMM) publishes in English works dealing with human and animal mycology. The subjects treated are focused in particular on clinical, diagnostic, epidemiological, immunological, medical, pathological, preventive or therapeutic aspects of mycoses. Also covered are basic aspects linked primarily with morphology (electronic and photonic microscopy), physiology, biochemistry, cellular and molecular biology, immunochemistry, genetics, taxonomy or phylogeny of pathogenic or opportunistic fungi and actinomycetes in humans or animals. Studies of natural products showing inhibitory activity against pathogenic fungi cannot be considered without chemical characterization and identification of the compounds responsible for the inhibitory activity.
JMM publishes (guest) editorials, original articles, reviews (and minireviews), case reports, technical notes, letters to the editor and information. Only clinical cases with real originality (new species, new clinical present action, new geographical localization, etc.), and fully documented (identification methods, results, etc.), will be considered.
Under no circumstances does the journal guarantee publication before the editorial board makes its final decision.
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