• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Physiological Responses of Aspergillus niger Challenged with Itraconazole.黑曲霉在受到伊曲康唑挑战时的生理反应。
Antimicrob Agents Chemother. 2021 May 18;65(6). doi: 10.1128/AAC.02549-20.
2
Erg4A and Erg4B Are Required for Conidiation and Azole Resistance via Regulation of Ergosterol Biosynthesis in Aspergillus fumigatus.烟曲霉中麦角甾醇生物合成的调控需要Erg4A和Erg4B来实现分生孢子形成和唑类抗性。
Appl Environ Microbiol. 2017 Feb 1;83(4). doi: 10.1128/AEM.02924-16. Print 2017 Feb 15.
3
Phenotypic plasticity and the evolution of azole resistance in Aspergillus fumigatus; an expression profile of clinical isolates upon exposure to itraconazole.烟曲霉表型可塑性与唑类耐药性的进化;临床分离株在接触伊曲康唑时的表达谱。
BMC Genomics. 2019 Jan 9;20(1):28. doi: 10.1186/s12864-018-5255-z.
4
Fungal Zn(II)Cys Transcription Factor ADS-1 Regulates Drug Efflux and Ergosterol Metabolism under Antifungal Azole Stress.真菌 Zn(II)Cys 转录因子 ADS-1 在抗真菌唑类药物应激下调控药物外排和麦角固醇代谢。
Antimicrob Agents Chemother. 2021 Jan 20;65(2). doi: 10.1128/AAC.01316-20.
5
Drug Sensitivity and Resistance Mechanism in Aspergillus Section Strains from Japan.日本曲霉属菌株的药物敏感性及耐药机制
Antimicrob Agents Chemother. 2017 Jul 25;61(8). doi: 10.1128/AAC.02583-16. Print 2017 Aug.
6
Triazole Susceptibilities in Thermotolerant Fungal Isolates from Outdoor Air in the Seoul Capital Area in South Korea.韩国首尔首都地区室外空气中耐热真菌分离株对三唑类药物的敏感性
PLoS One. 2015 Sep 25;10(9):e0138725. doi: 10.1371/journal.pone.0138725. eCollection 2015.
7
Susceptibility Testing of Common and Uncommon Aspergillus Species against Posaconazole and Other Mold-Active Antifungal Azoles Using the Sensititre Method.使用Sensititre法对常见和罕见曲霉菌种进行泊沙康唑及其他抗霉菌活性唑类药物的药敏试验。
Antimicrob Agents Chemother. 2017 May 24;61(6). doi: 10.1128/AAC.00168-17. Print 2017 Jun.
8
The Aspergillus fumigatus Damage Resistance Protein Family Coordinately Regulates Ergosterol Biosynthesis and Azole Susceptibility.烟曲霉抗损伤蛋白家族协同调节麦角固醇生物合成及唑类药物敏感性。
mBio. 2016 Feb 23;7(1):e01919-15. doi: 10.1128/mBio.01919-15.
9
Activity of Isavuconazole and Other Azoles against Candida Clinical Isolates and Yeast Model Systems with Known Azole Resistance Mechanisms.艾沙康唑及其他唑类药物对念珠菌临床分离株和具有已知唑类耐药机制的酵母模型系统的活性。
Antimicrob Agents Chemother. 2015 Oct 19;60(1):229-38. doi: 10.1128/AAC.02157-15. Print 2016 Jan.
10
Transcription factor ADS-4 regulates adaptive responses and resistance to antifungal azole stress.转录因子ADS-4调节适应性反应及对抗真菌唑类应激的抗性。
Antimicrob Agents Chemother. 2015 Sep;59(9):5396-404. doi: 10.1128/AAC.00542-15. Epub 2015 Jun 22.

引用本文的文献

1
Identification of protein-degraders in an anaerobic digester by protein stable isotope probing and metagenomics.通过蛋白质稳定同位素示踪和宏基因组学鉴定厌氧消化器中的蛋白质降解剂。
Appl Microbiol Biotechnol. 2025 Apr 10;109(1):87. doi: 10.1007/s00253-025-13483-5.
2
cyp51A mutations, protein modeling, and efflux pump gene expression reveals multifactorial complexity towards understanding Aspergillus section Nigri azole resistance mechanism.环细胞色素 P45051A 突变、蛋白质建模和外排泵基因表达揭示了理解黑曲霉属唑类耐药机制的多因素复杂性。
Sci Rep. 2024 Mar 14;14(1):6156. doi: 10.1038/s41598-024-55237-9.
3
Energetically exploiting lignocellulose-rich residues in anaerobic digestion technologies: from bioreactors to proteogenomics.大力开发厌氧消化技术中富含木质纤维素的残留物:从生物反应器到蛋白质基因组学
Biotechnol Biofuels Bioprod. 2023 Nov 28;16(1):183. doi: 10.1186/s13068-023-02432-x.
4
Antagonism of the Azoles to Olorofim and Cross-Resistance Are Governed by Linked Transcriptional Networks in Aspergillus fumigatus.唑类药物对奥利万星的拮抗作用和交叉耐药性由烟曲霉中的连锁转录网络调控。
mBio. 2022 Dec 20;13(6):e0221522. doi: 10.1128/mbio.02215-22. Epub 2022 Oct 26.
5
Induced Cell Cycle Arrest in Triple-Negative Breast Cancer by Combined Treatment of Itraconazole and Rapamycin.伊曲康唑与雷帕霉素联合治疗诱导三阴性乳腺癌细胞周期停滞
Front Pharmacol. 2022 Apr 19;13:873131. doi: 10.3389/fphar.2022.873131. eCollection 2022.

本文引用的文献

1
How to interpret MICs of antifungal compounds according to the revised clinical breakpoints v. 10.0 European committee on antimicrobial susceptibility testing (EUCAST).如何根据修订后的临床折点 v.10.0 欧洲抗菌药物敏感性试验委员会 (EUCAST) 来解释抗真菌化合物的 MIC 值。
Clin Microbiol Infect. 2020 Nov;26(11):1464-1472. doi: 10.1016/j.cmi.2020.06.007. Epub 2020 Jun 17.
2
Strong variance in the inflammatory and cytotoxic potentials of Penicillium and Aspergillus species from cleaning workers' exposure in nursing homes.养老院清洁工暴露于青霉属和曲霉属中各物种的炎症和细胞毒性潜能存在很大差异。
Sci Total Environ. 2020 Jul 1;724:138231. doi: 10.1016/j.scitotenv.2020.138231. Epub 2020 Mar 26.
3
Impact of polyethylene on salivary glands proteome in Galleria melonella.聚乙稀对金瓜幼虫唾液腺蛋白质组的影响。
Comp Biochem Physiol Part D Genomics Proteomics. 2020 Jun;34:100678. doi: 10.1016/j.cbd.2020.100678. Epub 2020 Feb 24.
4
Towards a risk evaluation of workers' exposure to handborne and airborne microbial species as exemplified with waste collection workers.针对劳动者手部和空气中微生物暴露风险的评估——以废物收集工为例。
Environ Res. 2020 Apr;183:109177. doi: 10.1016/j.envres.2020.109177. Epub 2020 Jan 23.
5
Identification of emulsifier potato peptides by bioinformatics: application to omega-3 delivery emulsions and release from potato industry side streams.通过生物信息学鉴定乳化剂马铃薯肽:在 omega-3 传递乳液中的应用和从马铃薯工业副产物中的释放。
Sci Rep. 2020 Jan 20;10(1):690. doi: 10.1038/s41598-019-57229-6.
6
Resistance mechanism and proteins in species against antifungal agents.物种中对抗真菌剂的抗性机制和蛋白质。
Mycology. 2019 Feb 6;10(3):151-165. doi: 10.1080/21501203.2019.1574927. eCollection 2019.
7
Ctt1 catalase activity potentiates antifungal azoles in the emerging opportunistic pathogen Saccharomyces cerevisiae.Ctt1 过氧化氢酶活性增强了新兴机会性病原体酿酒酵母中的抗真菌唑类药物。
Sci Rep. 2019 Jun 24;9(1):9185. doi: 10.1038/s41598-019-45070-w.
8
AtrR Is an Essential Determinant of Azole Resistance in Aspergillus fumigatus.AtrR 是烟曲霉唑类耐药性的一个必需决定因素。
mBio. 2019 Mar 12;10(2):e02563-18. doi: 10.1128/mBio.02563-18.
9
Emerging threat of triazole-resistant Aspergillus fumigatus.三唑耐药烟曲霉的出现威胁。
J Antimicrob Chemother. 2019 Apr 1;74(4):835-842. doi: 10.1093/jac/dky517.
10
The PRIDE database and related tools and resources in 2019: improving support for quantification data.PRIDE 数据库及相关工具和资源在 2019 年的进展:提高定量数据支持。
Nucleic Acids Res. 2019 Jan 8;47(D1):D442-D450. doi: 10.1093/nar/gky1106.

黑曲霉在受到伊曲康唑挑战时的生理反应。

Physiological Responses of Aspergillus niger Challenged with Itraconazole.

机构信息

Department of Chemistry and Bioscience, Aalborg University, Aalborg East, Denmark.

The National Research Centre for the Working Environment, Copenhagen East, Denmark.

出版信息

Antimicrob Agents Chemother. 2021 May 18;65(6). doi: 10.1128/AAC.02549-20.

DOI:10.1128/AAC.02549-20
PMID:33820768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8316071/
Abstract

is an opportunistic pathogen commonly found in a variety of indoor and outdoor environments. An environmental isolate of from a pig farm was resistant to itraconazole, and in-depth investigations were conducted to better understand cellular responses that occur during growth when this pathogen is exposed to an antifungal. Using a combination of cultivation techniques, antibiotic stress testing, and label-free proteomics, this study investigated the physiological and metabolic responses of to sublethal levels of antifungal stress. Challenging with itraconazole inhibited growth, and the MIC was estimated to be > 16 mg · liter Through the proteome analysis, 1,305 unique proteins were identified. During growth with 2 and 8 mg · liter itraconazole, a total of 91 and 50 proteins, respectively, were significantly differentially expressed. When challenged with itraconazole, exhibited decreased expression of peroxidative enzymes, increased expression of an ATP-binding cassette (ABC) transporter most likely involved as an azole efflux pump, and inhibited ergosterol synthesis; however, several ergosterol biosynthesis proteins increased in abundance. Furthermore, reduced expression of proteins involved in the production of ATP and reducing power from both the tricarboxylic acid (TCA) and glyoxylate cycles was observed. The mode of action of triazoles in therefore appears more complex than previously anticipated, and these observations may help highlight future targets for antifungal treatment.

摘要

是一种机会性病原体,常见于各种室内和室外环境中。从一个养猪场分离得到的一株 对伊曲康唑具有耐药性,因此进行了深入的研究,以更好地了解该病原体在暴露于抗真菌剂时生长过程中发生的细胞反应。本研究采用培养技术、抗生素应激测试和无标记蛋白质组学相结合的方法,研究了 对亚致死水平抗真菌应激的生理和代谢反应。用伊曲康唑挑战 ,抑制其生长,MIC 估计>16 毫克/升。通过蛋白质组分析,鉴定出 1305 种独特的蛋白质。在含有 2 和 8 毫克/升伊曲康唑的条件下生长时,分别有 91 和 50 种蛋白质的表达水平显著差异。当受到伊曲康唑的挑战时, 表现出过氧化物酶表达减少,可能作为唑类外排泵的 ABC 转运蛋白表达增加,以及抑制麦角固醇合成;然而,几种麦角固醇生物合成蛋白的丰度增加。此外,还观察到来自三羧酸 (TCA) 和乙醛酸循环的 ATP 和还原力产生的蛋白质的表达减少。因此,三唑类药物在 中的作用模式似乎比预期的更为复杂,这些观察结果可能有助于突出未来抗真菌治疗的靶点。