Review
- Minireview] The molecular mechanism of azole resistance in Aspergillus fumigatus: from bedside to bench and back
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Xiaolei Wei , Yuanwei Zhang Zhang , Ling Lu
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J. Microbiol. 2015;53(2):91-99. Published online January 28, 2015
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DOI: https://doi.org/10.1007/s12275-015-5014-7
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Abstract
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The growing use of immunosuppressive therapies has resulted
in a dramatic increased incidence of invasive fungal
infections (IFIs) caused by Aspergillus fumigatus, a common
pathogen, and is also associated with a high mortality rate.
Azoles are the primary guideline-recommended therapy agents
for first-line treatment and prevention of IFIs. However,
increased azole usage in medicinal and agricultural settings
has caused azole-resistant isolates to repeatedly emerge in
the environment, resulting in a significant threat to human
health. In this review, we present and summarize current
research on the resistance mechanisms of azoles in A. fumigatus
as well as efficient susceptibility testing methods. Moreover,
we analyze and discuss the putative clinical (bedside)
indication of these findings from bench work.
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Citations
Citations to this article as recorded by

- Azole resistance in Aspergillus fumigatus- comprehensive review
Mthokozisi Dladla, Marieka Gyzenhout, Gert Marias, Soumya Ghosh
Archives of Microbiology.2024;[Epub] CrossRef -
Unveiling environmental transmission risks: comparative analysis of azole resistance in
Aspergillus fumigatus
clinical and environmental isolates from Yunnan, China
Jianchuan Gong, Jiarui Huang, Yongju Liu, Ying Zhang, Yuhong Gao, Gustavo H. Goldman
Microbiology Spectrum.2024;[Epub] CrossRef -
The mitochondrial protein Bcs1A regulates antifungal drug tolerance by affecting efflux pump expression in the filamentous pathogenic fungus
Aspergillus fumigatus
Guorong Yang, Weiwei Shi, Wenlin He, Jing Wu, Sutao Huang, Li Mo, Junjie Zhang, Huaxue Wang, Xiaogang Zhou, Gustavo H. Goldman
Microbiology Spectrum.2024;[Epub] CrossRef - The expression pattern, subcellular localization and function of three sterol 14α-demethylases in Aspergillus oryzae
Qi Jin, Ganghua Li, Kunhai Qin, Yitong Shang, Huanhuan Yan, Hongliang Liu, Bin Zeng, Zhihong Hu
Frontiers in Genetics.2023;[Epub] CrossRef - Mitochondrial Membrane-Associated Protein Mba1 Confers Antifungal Resistance by Affecting the Production of Reactive Oxygen Species in Aspergillus fumigatus
Guoxing Zhu, Shu Chen, Yuanwei Zhang, Ling Lu
Antimicrobial Agents and Chemotherapy.2023;[Epub] CrossRef - Drug-Resistant Aspergillus spp.: A Literature Review of Its Resistance Mechanisms and Its Prevalence in Europe
Maria Antonia De Francesco
Pathogens.2023; 12(11): 1305. CrossRef -
Deletion of
cox7c
Results in Pan-Azole Resistance in Aspergillus fumigatus
Mingcong Chen, Guowei Zhong, Sha Wang, Peiying Chen, Lei Li
Antimicrobial Agents and Chemotherapy.2022;[Epub] CrossRef - Cannabis and the Cancer Patient
Ilana M Braun, Donald I Abrams, Stacey E Blansky, Steven A Pergam
JNCI Monographs.2021; 2021(58): 68. CrossRef - Genome-Wide Association Analysis for Triazole Resistance in Aspergillus fumigatus
Yuying Fan, Yue Wang, Gregory A. Korfanty, Meagan Archer, Jianping Xu
Pathogens.2021; 10(6): 701. CrossRef - Analysis of the prochloraz‐Mn resistance risk and its molecular basis in Mycogone rosea from Agaricus bisporus
Yixin Du, Niuniu Shi, Hongchun Ruan, Jianqiang Miao, He Yan, Chunxi Shi, Furu Chen, Xili Liu
Pest Management Science.2021; 77(10): 4680. CrossRef -
Electron Donor Cytochrome
b
5
Is Required for Hyphal Tip Accumulation of Sterol-Rich Plasma Membrane Domains and Membrane Fluidity in Aspergillus fumigatus
Chi Zhang, Yiran Ren, Lu Gao, Huiyu Gu, Ling Lu, Rebecca E. Parales
Applied and Environmental Microbiology.2021;[Epub] CrossRef - Examining Signatures of Natural Selection in Antifungal Resistance Genes Across Aspergillus Fungi
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Frontiers in Fungal Biology.2021;[Epub] CrossRef - Uncovering New Mutations Conferring Azole Resistance in the Aspergillus fumigatus cyp51A Gene
Peiying Chen, Musang Liu, Qiuqiong Zeng, Zheng Zhang, Weida Liu, Hong Sang, Ling Lu
Frontiers in Microbiology.2020;[Epub] CrossRef - Synergistic Effect of Pyrvinium Pamoate and Azoles Against Aspergillus fumigatus in vitro and in vivo
Yi Sun, Lujuan Gao, Youwen Zhang, Ji Yang, Tongxiang Zeng
Frontiers in Microbiology.2020;[Epub] CrossRef - Recent trends in the epidemiology, diagnosis, treatment, and mechanisms of resistance in clinical Aspergillus species: A general review with a special focus on the Middle Eastern and North African region
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Frontiers in Genetics.2020;[Epub] CrossRef - Azole resistance mechanisms in Aspergillus: update and recent advances
Alba Pérez-Cantero, Loida López-Fernández, Josep Guarro, Javier Capilla
International Journal of Antimicrobial Agents.2020; 55(1): 105807. CrossRef - Calcium signaling pathway is involved in non-CYP51 azole resistance in Aspergillus fumigatus
Yeqi Li, Yuanwei Zhang, Ling Lu
Medical Mycology.2019; 57(Supplement): S233. CrossRef - Fungal cytochrome P450 protein Cyp51: What we can learn from its evolution, regulons and Cyp51-based azole resistance
Jinxing Song, Shizhu Zhang, Ling Lu
Fungal Biology Reviews.2018; 32(3): 131. CrossRef - Identification and Characterization of Key Charged Residues in the Cofilin Protein Involved in Azole Susceptibility, Apoptosis, and Virulence of Aspergillus fumigatus
Zhongyi Lu, Xiaodong Jia, Yong Chen, Xuelin Han, Fangyan Chen, Shuguang Tian, Xueting Su, Zongwei Li, Jingya Zhao, Xi Zhang, Mandong Hu, Liuyu Huang, Li Han
Antimicrobial Agents and Chemotherapy.2018;[Epub] CrossRef -
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Pair Reverse Regulates Azole Resistance by Conferring Extracellular Polysaccharide, Sphingolipid Pathway Intermediates, and Efflux Pumps to Biofilm
Nanbiao Long, Liping Zeng, Shanlei Qiao, Lei Li, Guowei Zhong
Antimicrobial Agents and Chemotherapy.2018;[Epub] CrossRef -
Screening and Characterization of a Non-
cyp51A
Mutation in an
Aspergillus fumigatus cox10
Strain Conferring Azole Resistance
Xiaolei Wei, Peiying Chen, Rongsui Gao, Yeqi Li, Anxue Zhang, Feifei Liu, Ling Lu
Antimicrobial Agents and Chemotherapy.2017;[Epub] CrossRef - A Putative Mitochondrial Iron Transporter MrsA in Aspergillus fumigatus Plays Important Roles in Azole-, Oxidative Stress Responses and Virulence
Nanbiao Long, Xiaoling Xu, Hui Qian, Shizhu Zhang, Ling Lu
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Fungal Genetics and Biology.2016; 86: 47. CrossRef - Triazole Susceptibilities in Thermotolerant Fungal Isolates from Outdoor Air in the Seoul Capital Area in South Korea
Seungeun Lee, Siyu Xu, Chemmeri Padasseri Bivila, Hyeyoung Lee, Myung Soo Park, Young Woon Lim, Naomichi Yamamoto, Kap-Hoon Han
PLOS ONE.2015; 10(9): e0138725. CrossRef
Research Support, Non-U.S. Gov'ts
- Molecular Screening of Streptomyces Isolates for Antifungal Activity and Family 19 Chitinase Enzymes
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Youssuf Gherbawy , Hesham Elhariry , Abdulla Altalhi , Bahig El-Deeb , Ghada Khiralla
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J. Microbiol. 2012;50(3):459-468. Published online June 30, 2012
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DOI: https://doi.org/10.1007/s12275-012-2095-4
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41
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33
Scopus
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Abstract
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Thirty soil-isolates of Streptomyces were analyzed to determine their antagonism against plant-pathogenic fungi including Fusarium oxysporum, Pythium aristosporum, Colletotrichum gossypii, and Rhizoctonia solani. Seven isolates showed antifungal activity against one or more strain of the tested fungi. Based on the 16S rDNA sequence analysis, these isolates were identified as Streptomyces tendae (YH3), S. griseus (YH8), S. variabilis (YH21), S. endus (YH24), S. violaceusniger (YH27A), S. endus (YH27B), and S. griseus (YH27C). The identity percentages ranged from 98 to 100%. Although some isolates belonged to the same species, there were many differences in their cultural and morphological characteristics. Six isolates out of seven showed chitinase activity according to a chitinolytic activity test and on colloidal chitin agar plates. Based on the conserved regions among the family 19 chitinase genes of Streptomyces sp. two primers were used for detection of the chitinase (chiC) gene in the six isolates. A DNA fragment of 1.4 kb was observed only for the isolates YH8, YH27A, and YH27C. In conclusion, six Streptomyces strains with potential chitinolytic activity were identified from the local environment in Taif City, Saudi Arabia. Of these isolates, three belong to family 19 chitinases. To our knowledge, this is the first reported presence of a chiC gene in S. violaceusniger YH27A.
- Endophytic Fungus Trichothecium roseum LZ93 Antagonizing Pathogenic Fungi In Vitro and Its Secondary Metabolites
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XiaoMei Zhang , GuoHong Li , Juan Ma , Ying Zeng , WeiGuang Ma , PeiJi Zhao
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J. Microbiol. 2010;48(6):784-790. Published online January 9, 2011
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DOI: https://doi.org/10.1007/s12275-010-0173-z
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34
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26
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Abstract
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The endophytic fungus Trichothecium roseum LZ93 from Maytenus hookeri was found to antagonize other pathogenic fungi in vitro. To identify which compound contributed substantially to the antagonism, we fermented the strain and purified its fermentation products. Eleven compounds were obtained, including two
trichothecenes, five rosenonolactones, two cardiotonic cyclodepsipeptides, and two sterols. Compound 11β-hydroxyrosenonolactone (1) was assigned according to 1D and 2D-NMR data for the first time. At the same time, the 1H and 13C-NMR assignments for 6β-hydroxyrosenonolactone (2) were revised. Of all of them, only
trichothecin (6) showed strong antifungal activity. Based on our observations of the antagonistic activity and the other experimental results, we suggest that the antifungal compound trichothecin was the main contributor to the antagonistic action of T. roseum LZ93.
- Diversity of Actinomycetes Antagonistic to Plant pathogenic Fungi in Cave and Sea-Mud Soils of Korea
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Kim, Beom Seok , Lee, Jung Yeop , Hwang, Byung Kook
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J. Microbiol. 1998;36(2):86-92.
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Abstract
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To isolate actinomycetes antagonistic to plant pathogenic fungi, soil samples were collected from caves and sea-shores in Korea. The 481 actinomycetes were isolated from the soil samples examined, representing more than 50% of total counts. Nocardioform actinomycetes were rare actinomycete genera. Saccharomonospora could be isolated only in 3 cave soil samples from Cheondong, Kosoo, and Nodong, but was not present in all the sea-mud soils examined. Dactylosporangium, Saccharomonospora, and Streptosporangium were very rare in both cave and sea-mud soils. The 311 of 481 actinomycete isolates inhibited the mycelial growth of at least one of the tested fungi. The isolation rates of antagonistic actinomycetes from cave soils ranged from 45.7% to 78%, and those of sea-mud soils were from 59.1% to 66.0%. The 96 of 136 Streptomyces isolates from cave soils, and 93 of 133 isolates from sea-mud soils showed antifungal activity. The proportion of antagonistic isolates of Nocardioform actinomycetes (13.6%) was lower than that of other genera. Among the actinomycetes from sea-mud soils, Dactylosporangium and Streptosporangium had highest proportions of actinomycete antagonists of 85.7% and 80%, respectively. The isolation rate of Nocardioform antagonist from sea-mud soils was 11.1% similar in the cabve soils. Streptomyces strains showed higher antifungal activities against plant pathogenic fungi than did other rare actinomycete antagonists.