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Guowei Zhong 3 Articles
The C-22 sterol desaturase Erg5 is responsible for ergosterol biosynthesis and conidiation in Aspergillus fumigatus
Nanbiao Long , Guowei Zhong
J. Microbiol. 2022;60(6):620-626.   Published online April 18, 2022
DOI: https://doi.org/10.1007/s12275-022-1564-7
  • 1,147 View
  • 5 Download
  • 13 Web of Science
  • 13 Crossref
AbstractAbstract PDF
Aspergillus fumigatus is the most prevalent saprophytic fungi and can cause severe invasive aspergillosis in immunocompromised individuals. For infection of A. fumigatus, the small hydrophobic conidia have been shown to play a dominant role. In this study, we found that deletion of erg5, a C-22 sterol desaturase gene which function in the last two steps of ergosterol biosynthesis, was sufficient to block ergosterol biosynthesis and conidiation. The deletion phenotype was further verified by a conditional expression strain of erg5 using the inducible tet-on system. Strikingly, erg5 mutant displays increased susceptibility to antifungal azoles itraconazole. RNA sequencing analysis showed that erg5 deficiency resulted in changes in transcription mainly related to lipid, carbohydrate, and amino acid metabolism. Genes encoding ergosterol biosynthesis- related enzymes were found to be up-regulated in erg5 null mutants. However, genes involved in asexual development, including upstream regulators, melanin biosynthesis enzymes, heterotrimeric G proteins, and MAPK signaling, were down-regulated to various degrees. Furthermore, metabolomic study revealed that erg5 deficiency also resulted in altered lipid and amino acid metabolism, which was consistent with our transcriptomics analysis. Collectively, our study established a link between ergosterol biosynthesis and asexual development at the transcriptomics and metabolomics level in A. fumigatus.

Citations

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  • The blue light-responsive PdCYP61 gene modulates ergosterol biosynthesis, stress resistance, growth and pathogenicity in Penicillium digitatum
    Yulian Liu, Ziyan Qiu, Bingjie Wang, Shuqi Liu, Yujie Du, Chao-an Long
    Physiological and Molecular Plant Pathology.2027; 147: 103543.     CrossRef
  • Deciphering the role of ergosterol and sphingolipids in the antifungal mode of action of rhamnolipids on Sclerotiniaceae.
    Thomas Bergia, Sébastien Acket, Stéphanie Guénin, Laurent Gutierrez, Sonia Rippa
    Microbiological Research.2026; 308: 128490.     CrossRef
  • Morphological and molecular changes in Botrytis cinerea occurring after cold plasma treatment
    Jinling Miao, Shunjie Zhai, Weida Zhang, Minrui Guo, Jiankang Cao, Guogang Chen, Wanting Yang, Shaobo Cheng
    Postharvest Biology and Technology.2026; 240: 114420.     CrossRef
  • Ergosterol from Yeasts Promotes Helicobacter pylori Internalization into Candida albicans
    Javiera Contreras-Ormeño, Horliany Neira-König, Jessy Pavón-Pérez, Joaquín Olivares-Muñoz, Kimberly Sánchez-Alonzo, Apolinaria García-Cancino
    International Journal of Molecular Sciences.2026; 27(15): 6747.     CrossRef
  • The transcription factor CsAtf1 regulates CsErg5B to modulate conidial germination and fludioxonil sensitivity in Colletotrichum siamense
    Yuqing Lin, Kuaikuai Wang, Xiaoling Guan, Miao Song, Zhenyu Han, Wenbo Liu, Wei Wu, Yu Zhang, Weiguo Miao, Chunhua Lin
    Phytopathology Research.2026;[Epub]     CrossRef
  • Targeting fungal lipid synthesis for antifungal drug development and potentiation of contemporary antifungals
    Cecilia Gutierrez-Perez, Robert A. Cramer
    npj Antimicrobials and Resistance.2025;[Epub]     CrossRef
  • The analysis of transcriptomics reveals the function of TrPLD3 in the pathogenicity of Trichothecium roseum infecting apples
    Xiao Li, Qianqian Zhang, Qili Liu, Xiaobin Xu, Jinzhu Li, Dandan Zhu, Yuanyuan Zong, Huali Xue, Yang Bi
    Postharvest Biology and Technology.2025; 227: 113628.     CrossRef
  • Ergosterol synthase reduces ochratoxin A synthesis in Aspergillus carbonarius via oxidative stress pathway
    Saixue Yang, Yulan Ji, Gansukh Sunderiya, Wanxia Li, Yuchun Zhang, Xuan Wang, Dongyan Shao, Junling Shi, Xianqing Chen, Chunmei Jiang
    International Journal of Food Microbiology.2025; 443: 111395.     CrossRef
  • Exposure to Tebuconazole Drives Cross-Resistance to Clinical Triazoles in Aspergillus fumigatus
    Leandra Martins Meireles, Fabiano Silva Soares, Gonçalo Apolinário de Souza Filho, Rodrigo Scherer
    ACS Omega.2025; 10(42): 50407.     CrossRef
  • Quantitative proteomic analysis reveals Ga(III) polypyridyl catecholate complexes disrupt Aspergillus fumigatus mitochondrial function
    Magdalena Piatek, Brunella Grassiri, Lewis More O’Ferrall, Anna Maria Piras, Giovanna Batoni, Semih Esin, Christine O’Connor, Darren Griffith, Anne Marie Healy, Kevin Kavanagh
    JBIC Journal of Biological Inorganic Chemistry.2024; 29(7-8): 707.     CrossRef
  • Ergosterol Is Critical for Sporogenesis in Cryptococcus neoformans
    Amber R. Matha, Xiaofeng Xie, Xiaorong Lin
    Journal of Fungi.2024; 10(2): 106.     CrossRef
  • Erg4 Is Involved in Ergosterol Biosynthesis, Conidiation and Stress Response in Penicillium expansum
    Zhanhong Han, Yuanyuan Zong, Xuemei Zhang, Di Gong, Bin Wang, Dov Prusky, Edward Sionov, Huali Xue, Yang Bi
    Journal of Fungi.2023; 9(5): 568.     CrossRef
  • A chromosome-scale genome assembly of the grape powdery mildew pathogen Erysiphe necator reveals its genomic architecture and previously unknown features of its biology
    Alex Z. Zaccaron, Tara Neill, Jacob Corcoran, Walter F. Mahaffee, Ioannis Stergiopoulos, Gustavo H. Goldman
    mBio.2023;[Epub]     CrossRef
Deep convolutional neural network: a novel approach for the detection of Aspergillus fungi via stereomicroscopy
Haozhong Ma , Jinshan Yang , Xiaolu Chen , Xinyu Jiang , Yimin Su , Shanlei Qiao , Guowei Zhong
J. Microbiol. 2021;59(6):563-572.   Published online March 29, 2021
DOI: https://doi.org/10.1007/s12275-021-1013-z
  • 1,075 View
  • 4 Download
  • 17 Web of Science
  • 18 Crossref
AbstractAbstract PDF
Fungi of the genus Aspergillus are ubiquitously distributed in nature, and some cause invasive aspergillosis (IA) infections in immunosuppressed individuals and contamination in agricultural products. Because microscopic observation and molecular detection of Aspergillus species represent the most operator-dependent and time-intensive activities, automated and cost-effective approaches are needed. To address this challenge, a deep convolutional neural network (CNN) was used to investigate the ability to classify various Aspergillus species. Using a dissecting microscopy (DM)/stereomicroscopy platform, colonies on plates were scanned with a 35× objective, generating images of sufficient resolution for classification. A total of 8,995 original colony images from seven Aspergillus species cultured in enrichment medium were gathered and autocut to generate 17,142 image crops as training and test datasets containing the typical representative morphology of conidiophores or colonies of each strain. Encouragingly, the Xception model exhibited a classification accuracy of 99.8% on the training image set. After training, our CNN model achieved a classification accuracy of 99.7% on the test image set. Based on the Xception performance during training and testing, this classification algorithm was further applied to recognize and validate a new set of raw images of these strains, showing a detection accuracy of 98.2%. Thus, our study demonstrated a novel concept for an artificial-intelligence-based and cost-effective detection
method
ology for Aspergillus organisms, which also has the potential to improve the public’s understanding of the fungal kingdom.

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    Mycology.2026; 17(3): 677.     CrossRef
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    Decoding Infection and Transmission.2026; 4: 100089.     CrossRef
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    Bahareh Hasan Pour
    Mycoses.2025;[Epub]     CrossRef
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    Oscar J. Suarez, Daniel C. Ruiz-Ayala, Liliana Rojas Contreras, Manuel G. Forero, Jesús A. Medrano-Hermosillo, Abraham Efraim Rodriguez-Mata
    Agriculture.2025; 15(17): 1888.     CrossRef
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    Eliott Teston, Marc Sautour, Léa Boulnois, Nicolas Augey, Abdellah Dighab, Christophe Guillet, Dea Garcia-Hermoso, Fanny Lanternier, Marie-Elisabeth Bougnoux, Frédéric Dalle, Louise Basmaciyan, Mathieu Blot, Pierre-Emmanuel Charles, Jean-Pierre Quenot, Bi
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  • Attention-Guided Transfer Learning for Identification of Filamentous Fungi Encountered in the Clinical Laboratory
    Tsi-Shu Huang, Kevin Wang, Xiu-Yuan Ye, Chii-Shiang Chen, Fu-Chuen Chang, Paschalis Vergidis, Yang Zhang
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    Hang Pan, Lun Xie, Zhiliang Wang
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The putative polysaccharide synthase AfCps1 regulates Aspergillus fumigatus morphogenesis and conidia immune response in mouse bone marrow-derived macrophages
Sha Wang , Anjie Yuan , Liping Zeng , Sikai Hou , Meng Wang , Lei Li , Zhendong Cai , Guowei Zhong
J. Microbiol. 2021;59(1):64-75.   Published online November 17, 2020
DOI: https://doi.org/10.1007/s12275-021-0347-x
  • 946 View
  • 3 Download
  • 5 Web of Science
  • 4 Crossref
AbstractAbstract PDF
Aspergillus fumigatus is a well-known opportunistic pathogen that causes invasive aspergillosis (IA) infections with high mortality in immunosuppressed individuals. Morphogenesis, including hyphal growth, conidiation, and cell wall biosynthesis is crucial in A. fumigatus pathogenesis. Based on a previous random insertional mutagenesis library, we identified the putative polysaccharide synthase gene Afcps1 and its paralog Afcps2. Homologs of the cps gene are commonly found in the genomes of most fungal and some bacterial pathogens. Afcps1/cpsA is important in sporulation, cell wall composition, and virulence. However, the precise regulation patterns of cell wall integrity by Afcps1/cpsA and further effects on the immune response are poorly understood. Specifically, our in-depth study revealed that Afcps1 affects cell-wall stability, showing an increased resistance of ΔAfcps1 to the chitinmicrofibril destabilizing compound calcofluor white (CFW) and susceptibility of ΔAfcps1 to the β-(1,3)-glucan synthase inhibitor echinocandin caspofungin (CS). Additionally, deletion of Afcps2 had a normal sporulation phenotype but caused hypersensitivity to Na+ stress, CFW, and Congo red (CR). Specifically, quantitative analysis of cell wall composition using high-performance anion exchange chromatography- pulsed amperometric detector (HPAEC-PAD) analysis revealed that depletion of Afcps1 reduced cell wall glucan and chitin contents, which was consistent with the downregulation of expression of the corresponding biosynthesis genes. Moreover, an elevated immune response stimulated by conidia of the ΔAfcps1 mutant in marrow-derived macrophages (BMMs) during phagocytosis was observed. Thus, our study provided new insights into the function of polysaccharide synthase Cps1, which is necessary for the maintenance of cell wall stability and the adaptation of conidia to the immune response of macrophages in A. fumigatus.

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  • Computational Approaches for Discovering Virulence Factors in Coccidioides
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    Journal of Fungi.2025; 11(10): 754.     CrossRef
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  • Evidencing New Roles for the Glycosyl-Transferase Cps1 in the Phytopathogenic Fungus Botrytis cinerea
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