- Metabolomic profiling reveals enrichment of cordycepin in senescence process of Cordyceps militaris fruit bodies
-
Junsang Oh , Deok-Hyo Yoon , Bhushan Shrestha , Hyung-Kyoon Choi , Gi-Ho Sung
-
J. Microbiol. 2019;57(1):54-63. Published online December 29, 2018
-
DOI: https://doi.org/10.1007/s12275-019-8486-z
-
-
1,262
View
-
3
Download
-
26
Web of Science
-
29
Crossref
-
Abstract
PDF
-
Cordyceps militaris is a species of Cordyceps that is classified
in the Cordycipitaceae family and is well known in East Asia
as a traditional medicinal mushroom. Its artificial fruit body
has been widely cultivated for commercial use in cosmetics,
functional food, and medicine. To explore the metabolites
associated with fruit body development, we conducted gas
chromatography mass spectrometry (GC-MS) analyses based
on developmental stage, which was divided into the growth
period (stage 1, stage 2, and stage 3) and aging period (stage
4). We detected 39 biochemical metabolites associated with
nucleotide, carbohydrate, and amino acid metabolism. Cordycepin,
one of the representative bioactive compounds in
C. militaris, was significantly enriched in stage 4 of aging period
and is associated with glucose accumulation. The accumulation
of cordycepin in stage 4 of aging period also seems
to be related to the glutamine and glutamic acid pathway. Our
results also showed enrichment of other bioactive compounds
such as mannitol and xylitol in stage 4 of aging period. Our
metabolomic profiling based on the developmental stages of
C. militaris is useful for exploring bioactive compounds (e.g.,
cordycepin, mannitol, GABA, and xylitol) that are enriched
in stage 4 of aging period and understanding the biosynthetic
mechanisms associated with cordycepin production. Through
optimization of fruit body cultivation by selecting stage 4 of
aging period as a harvesting time, our findings can be utilized
in food and medical applications of C. militaris in future.
-
Citations
Citations to this article as recorded by 
- Analysis of the Functional Components of Four “Sanghuang”‐Like Species Using UPLC‐ESI‐MS/MS‐Based Widely Targeted Metabolomics and TCMSP Database
Xiao-Ying Guo, Yue Qi, Xiao-Dan Yu, Ai-Guo Xu, Chun-Yang Zhi, Hong-Bo Guo, Charalampos Proestos Journal of Food Biochemistry.2026;[Epub] CrossRef - Integrative Network Pharmacology Study of Cordyceps militaris Compounds for Prostate Cancer Treatment
Sarah Cecilia Astrid Laihad, Trina Ekawati Tallei , Lydia Estelina Naomi Tendean , Grace Lendawati Amelia Turalaki, Sylvia Ritta Marunduh, Diana Shintawati Purwanto , Billy Johnson Kepel, Abdul Hawil Abas Heca Journal of Applied Sciences.2026; 4(1): 70. CrossRef - Application of Metabolomics in the Exploration of Bioactive Compounds and Drug Development from Medicinal Fungi
Yan Tong, Chuyu Tang, Bing Jia, Haoxu Tang, Jinxuan Yan, Yuling Li, Xiuzhang Li Metabolites.2026; 16(8): 576. CrossRef - Influence of Culture Conditions on Bioactive Compounds in Cordyceps militaris: A Comprehensive Review
Hye-Jin Park Foods.2025; 14(19): 3408. CrossRef - Light-Exposed Metabolic Responses of Cordyceps militaris through Transcriptome-Integrated Genome-Scale Modeling
Panyawarin Soommat, Nachon Raethong, Ratchaprapa Ruengsang, Roypim Thananusak, Teeraphan Laomettachit, Kobkul Laoteng, Treenut Saithong, Wanwipa Vongsangnak Biology.2024; 13(3): 139. CrossRef -
Core microbes in
Cordyceps militaris
sclerotia and their nitrogen metabolism-related ecological functions
Li Luo, Fei Dai, Zhongshun Xu, Jingqiang Guan, Gangxiang Fei, Jiaojiao Qu, Min Yao, Yuan Xue, Yeming Zhou, Xiao Zou, Christina A. Cuomo Microbiology Spectrum.2024;[Epub] CrossRef - Widely targeted metabolomics analysis of Sanghuangporus vaninii mycelia and fruiting bodies at different harvest stages
Yue Qi, Xiao-Ying Guo, Xin-Yue Xu, Jian-Xuan Hou, Shi-Lai Liu, Hong-Bo Guo, Ai-Guo Xu, Rui-Heng Yang, Xiao-Dan Yu Frontiers in Microbiology.2024;[Epub] CrossRef - Current Progress Regarding Cordyceps militaris, Its Metabolite Function, and Its Production
Yu-Chieh Chou, Ting-Hsuan Sung, Shi-Jing Hou, Darin Khumsupan, Shella Permatasari Santoso, Kuan-Chen Cheng, Shin-Ping Lin Applied Sciences.2024; 14(11): 4610. CrossRef -
Enhancement of Cordycepin Production through Liquid Static Fermentation of Caterpillar Medicinal Mushroom Cordyceps militaris (Ascomycetes)
Mahesh Borde, Shweta Kumawat, Sanjay K. Singh International Journal of Medicinal Mushrooms.2024; 26(11): 65. CrossRef - Genomic and Transcriptome Analysis Reveals the Biosynthesis Network of Cordycepin in Cordyceps militaris
Linshan Chai, Jianmei Li, Lingling Guo, Shuyu Zhang, Fei Chen, Wanqin Zhu, Yu Li Genes.2024; 15(5): 626. CrossRef - Future of Scarlet Caterpillar Club Fungus: A Review on Molecular Strategies for Cordycepin Enhancement
Rubi Kumari, Nayna Mukherjee, Aryan Sharma, Amitesh Chaman, Shankar Narayana Reddy, Shivika Sharma Biosciences Biotechnology Research Asia.2024; 21(3): 839. CrossRef - Transcriptome and metabolome profiling unveils the mechanisms of naphthalene acetic acid in promoting cordycepin synthesis in Cordyceps militaris
Xin Wang, Yin Li, Xiue Li, Lei Sun, Yetong Feng, Fangping Sa, Yupeng Ge, Shude Yang, Yu Liu, Weihuan Li, Xianhao Cheng Frontiers in Nutrition.2023;[Epub] CrossRef - Enhanced production of cordycepin under solid-state fermentation of Cordyceps militaris by using combinations of grains/substrates
Mahesh Borde, Sanjay K. Singh Brazilian Journal of Microbiology.2023; 54(4): 2765. CrossRef - Microbial synthesis of cordycepin, current systems and future perspectives
Xiyu Duan, Hui Yang, Chong Wang, Huhu Liu, Xiangyang Lu, Yun Tian Trends in Food Science & Technology.2023; 132: 162. CrossRef - Air Atmospheric Pressure Plasma Jet to Improve Fruiting Body Production and Enhance Bioactive Phytochemicals from Mutant Cordyceps militaris (White Cordyceps militaris)
Sujarinee Sangwanna, Weerasak Seelarat, Teerapap Panklai, Natthaphon Chaosuan, Ahkasit Subcharoen, Nuttapon Subcharoen, Nattapong Chanchula, Tanapak Inyod, Thanaphat Toemarrom, Atipong Bootchanont, Chakkaphan Wattanawikkam, Sorapong Pavasupree, Dheerawan Food and Bioprocess Technology.2023; 16(9): 1976. CrossRef - Dissecting Metabolic Regulation in Mycelial Growth and Fruiting Body Developmental Stages of Cordyceps militaris through Integrative Transcriptome Analysis
Roypim Thananusak, Kobkul Laoteng, Nachon Raethong, Mattheos Koffas, Wanwipa Vongsangnak Biotechnology and Bioprocess Engineering.2023; 28(3): 406. CrossRef - Functional genomics and systems biology of Cordyceps species for biotechnological applications
Nachon Raethong, Roypim Thananusak, Pattsarun Cheawchanlertfa, Pranesha Prabhakaran, Kittipong Rattanaporn, Kobkul Laoteng, Mattheos Koffas, Wanwipa Vongsangnak Current Opinion in Biotechnology.2023; 81: 102939. CrossRef - Effect of Cultivation Stages of Hericium erinaceus on the Contents of Major Components and α-Glucosidase Inhibitory Activity
Se Hwan Ryu, Beom Seok Kim, Ayman Turk, Sang Won Yeon, Solip Lee, Hak Hyun Lee, Sung Min Ko, Bang Yeon Hwang, Kyeong Lee Natural Product Sciences.2023; 29(3): 132. CrossRef - Enhanced Fruiting Body Production and Bioactive Phytochemicals from White Cordyceps militaris by Blending Cordyceps militaris and Using Cold Plasma Jet
Weerasak Seelarat, Sujarinee Sangwanna, Teerapap Panklai, Natthaphon Chaosuan, Atipong Bootchanont, Chakkaphan Wattanawikkam, Ahkasit Subcharoen, Nuttapon Subcharoen, Nattapong Chanchula, Dheerawan Boonyawan, Porramain Porjai Plasma Chemistry and Plasma Processing.2023; 43(1): 139. CrossRef - Cordycepin production by the potential fungal strains Cordyceps militaris BCC 2819 and Cordyceps cicadae BCC 19788 in submerged culture during batch and Fed-batch fermentation
Werapan Borworn, Nutaratat Pumin, Ariyaphuttarat Siriporn, Prathumpai Wai African Journal of Biotechnology.2022; 21(10): 483. CrossRef - Research Progress on Cordycepin Synthesis and Methods for Enhancement of Cordycepin Production in Cordyceps militaris
Li Wang, Huanhuan Yan, Bin Zeng, Zhihong Hu Bioengineering.2022; 9(2): 69. CrossRef - Application of Metabolomics in Fungal Research
Guangyao Li, Tongtong Jian, Xiaojin Liu, Qingtao Lv, Guoying Zhang, Jianya Ling Molecules.2022; 27(21): 7365. CrossRef - Cordycepin production by a novel endophytic fungus Irpex lacteus CHG05 isolated from Cordyceps hawkesii Gray
Ziying Liu, Guihua Leng, Jingbai Wen, Ganqi Deng, Jiayao Jiang Folia Microbiologica.2022; 67(6): 851. CrossRef - Heavy Metals, Halogenated Hydrocarbons, Phthalates, Glyphosate, Cordycepin, Alcohol, Drugs, and Herbs, Assessed for Liver Injury and Mechanistic Steps
Rolf Teschke, Tran Dang Xuan Frontiers in Bioscience-Landmark.2022;[Epub] CrossRef -
Effects on total phenolic and flavonoid content, antioxidant properties, and angiotensin I-converting enzyme inhibitory activity of beans by solid-state fermentation with
Cordyceps militaris
Weiwei Liu, Mengqian Dun, Xinyuan Liu, Guoying Zhang, Jianya Ling International Journal of Food Properties.2022; 25(1): 477. CrossRef - Effect of Spirulina biomass residue on yield and cordycepin and adenosine production of Cordyceps militaris culture
Siriluck Iamtham, Adisak Kaewkam, Sermsiri Chanprame, Wanida Pan-utai Bioresource Technology Reports.2022; 17: 100893. CrossRef - Enhancement of cordycepin production from Cordyceps militaris culture by epigenetic modification
Phongsakorn Kunhorm, Phongsakorn Chueaphromsri, Nipha Chaicharoenaudomrung, Parinya Noisa Biotechnology Letters.2022; 44(4): 581. CrossRef - Improved Cordycepin Production by Cordyceps militaris KYL05 Using Casein Hydrolysate in Submerged Conditions
Soo Kweon Lee, Ju Hun Lee, Hyeong Ryeol Kim, Youngsang Chun, Ja Hyun Lee, Hah Young Yoo, Chulhwan Park, Seung Wook Kim Biomolecules.2019; 9(9): 461. CrossRef - Cordyceps militaris polysaccharides exerted protective effects on diabetic nephropathy in mice via regulation of autophagy
Dan-Dan Chen, Rui Xu, Jiu-Yao Zhou, Jun-Qi Chen, Lin Wang, Xu-Sheng Liu, Chun-ling Liang, Bi-Hao Liu, Rui-Rui Lu, Jun-Biao Wu, Hua Lin Food & Function.2019; 10(8): 5102. CrossRef
- Species identity of Phellinus linteus (sanghuang) extensively used as a medicinal mushroom in Korea
-
Jae-Gu Han , Min-Woo Hyun , Chang Sun Kim , Jong Won Jo , Jae-Han Cho , Kang-Hyo Lee , Won-Sik Kong , Sang-Kuk Han , Junsang Oh , Gi-Ho Sung
-
J. Microbiol. 2016;54(4):290-295. Published online April 1, 2016
-
DOI: https://doi.org/10.1007/s12275-016-5520-2
-
-
1,376
View
-
2
Download
-
29
Crossref
-
Abstract
PDF
-
Sanghuang is a medicinal mushroom that has gained particular
attention in Korea. It has been extensively studied for
the past few decades as a natural immune booster and cancer
suppressor. Although the scientific name, Phellinus linteus,
has been commonly used to refer to the sanghuang mushroom,
the species identity of sanghuang has been called into question
due to the ambiguity of its circumscription and the inadequacy
of morphological distinctions within allied species. Because
the species concept of sanghuang has been elucidated by recent
molecular phylogenetic studies, it has become necessary
to clarify the taxonomic positions of sanghuang strains extensively
utilized in Korea. We conducted a phylogenetic analysis
of 74 strains belonging to the P. linteus-baumii complex based
on ITS nrDNA sequences. Parental stains of sanghuang varieties
formally registered in the Korea Seed & Variety Service,
including ASI 26046 (Corea sanghuang), 26114 (Boolro), and
26115 (HK 1-ho) were grouped with Sanghuangporus sanghuang
instead of P. linteus in the inferred phylogeny.
-
Citations
Citations to this article as recorded by 
- Host-associated differences in chemical composition and antioxidant activity of Phellinus igniarius
Peng Zhao, Fanjiao Zuo, Yan Feng, Na Zheng, Yameng Zhu, Ye Shang, Huizi Ouyang, Jun He Journal of Food Composition and Analysis.2026; 156: 109349. CrossRef - A conserved terpene cyclase gene in Sanghuangporus for abscisic acid-related sesquiterpenoid biosynthesis
Yoonhee Cho, Chang Wan Seo, Hyeonjae Cho, Yeongwoon Jin, Abel Severin Lupala, Sang Hee Shim, Young Woon Lim BMC Genomics.2025;[Epub] CrossRef - Medicinal Mushrooms: Bioactive Components, Pharmacological, Immunological and Toxicological Insights
Deepti Katiyar, Debaprasad Ghosh, Rajnandani Singh, Shreya Dixit, Samridhi Chopra, Sakshi Tripathi, Tanishk Saini ChemistrySelect.2025;[Epub] CrossRef -
The first complete mitochondrial genome of
Phellinus pomaceus
var.
prunastri
(Pers.) Pat. 1926 (Hymenochaetales: Hymenochaetaceae) and phylogenetic analysis
Wei Gao, Shuyi Chen, Qiang Li Mitochondrial DNA Part B.2024; 9(12): 1674. CrossRef - Preparation, characterization and cytotoxic activity of selenium nanoparticles stabilized with a heteropolysaccharide isolated from Sanghuangporus vaninii residue
Wenqi Chu, Peng Liu, Zhong Zhang, Di Wu, Wen Li, Wanchao Chen, Zhengpeng Li, Weike Wang, Yan Yang Carbohydrate Polymers.2024; 343: 122468. CrossRef - Comparative genomic analysis of Sanghuangporus sanghuang with other Hymenochaetaceae species
Xinyue Wang, Jiansheng Wei, Zhenwen Liu, Yi Wang, Xiaolong Yuan, Dong Wang, Junmei Niu, Yan Yang, Jing Zhou Brazilian Journal of Microbiology.2024; 55(1): 87. CrossRef - Research Progress of Bioactive Components in Sanghuangporus spp.
Jungu Lu, Manman Su, Xuan Zhou, Deming Li, Xinhui Niu, Yi Wang Molecules.2024; 29(6): 1195. CrossRef -
In vitro
and
in vivo
inhibitory effects of the Sanghuang mushroom extracts against
Candida albicans
Jiahui Du, Shuqing Jin, Ying Zhang, Wei Qiu, Yahui Dong, Yan Liu, Dengke Yin, Ye Yang, Weifang Xu Future Microbiology.2024; 19(11): 983. CrossRef - Sanghuangporus sanghuang extract extended the lifespan and healthspan of Caenorhabditis elegans via DAF-16/SIR-2.1
Zhenghan Dong, Yachao Wang, Cuiting Hao, Yuan Cheng, Xi Guo, Yanyu He, Yueyue Shi, Shuang Wang, Yunqi Li, Wei Shi Frontiers in Pharmacology.2023;[Epub] CrossRef - The mechanism of polysaccharide synthesis of Sanghuangporus sanghuang based on multi-omic analyses and feedback inhibition
Tingting Li, Qin Wang, Yan Yang, Dingka Song Carbohydrate Polymers.2023; 321: 121288. CrossRef - Current Status of ‘Sanghuang’ as a Group of Medicinal Mushrooms and Their Perspective in Industry Development
Li-Wei Zhou, Masoomeh Ghobad-Nejhad, Xue-Mei Tian, Yi-Fei Wang, Fang Wu Food Reviews International.2022; 38(4): 589. CrossRef - Pilot Study: Nutritional and Preclinical Safety Investigation of Fermented Hispidin-Enriched Sanghuangporus sanghuang Mycelia: A Promising Functional Food Material to Improve Sleep
I-Chen Li, Fang-Chia Chang, Ching-Chuan Kuo, Hsin-Tung Chu, Tsung-Ju Li, Chin-Chu Chen Frontiers in Nutrition.2022;[Epub] CrossRef - Hispolon alleviates oxidative damage by stimulating the Nrf2 signaling pathway in PC12 cells
Shoujiao Peng, Yanan Hou, Zihua Chen Archives of Biochemistry and Biophysics.2022; 727: 109303. CrossRef - The influence of monochromatic lights on flavonoid production by the fungus Sanghuangporus vaninii: Modeling of kinetic profiles and expression levels of important genes in flavonoid synthesis
Xiao-kui Ma, Hongyan Ma, Qi Chen, Yao Ma, Andrew J. Daugulis, Jian Liang, Peng Zheng Biochemical Engineering Journal.2021; 166: 107876. CrossRef - Cloning and characterization of a phosphomevalonate kinase gene from Sanghuangporus baumii
Shixin Wang, Zengcai Liu, Xutong Wang, Tingting Sun, Li Zou Biotechnology & Biotechnological Equipment.2021; 35(1): 934. CrossRef - Mushroom Inonotus sanghuang alleviates experimental pulmonary fibrosis: Implications for therapy of pulmonary fibrosis
Xing Su, Kun Liu, Yu Xie, Mengdi Zhang, Xiao Wu, Yijie Zhang, Junpeng Wang Biomedicine & Pharmacotherapy.2021; 133: 110919. CrossRef - A rapid analysis of antioxidants in Sanghuangporus baumii by online extraction-HPLC-ABTS
Qian-Hui Shen, Qi Huang, Ju-Ying Xie, Kun Wang, Zheng-Ming Qian, De-Qiang Li RSC Advances.2021; 11(41): 25646. CrossRef - Addressing widespread misidentifications of traditional medicinal mushrooms in Sanghuangporus (Basidiomycota) through ITS barcoding and designation of reference sequences
Shan Shen, Shi-Liang Liu, Ji-Hang Jiang, Li-Wei Zhou IMA Fungus.2021;[Epub] CrossRef - Anti-inflammatory effect of hispidin on LPS induced macrophage inflammation through MAPK and JAK1/STAT3 signaling pathways
Ying-Hao Han, Dong-Qin Chen, Mei-Hua Jin, Ying-Hua Jin, Jing Li, Gui-Nan Shen, Wei-Long Li, Yi-Xi Gong, Ying-Ying Mao, Dan-Ping Xie, Dong-Seok Lee, Li-Yun Yu, Sun-Uk Kim, Ji-Su Kim, Taeho Kwon, Yu-Dong Cui, Hu-Nan Sun Applied Biological Chemistry.2020;[Epub] CrossRef - Phellinus baumii enhances the immune response in cyclophosphamide-induced immunosuppressed mice
Jeong-Hyun Yoo, You-Suk Lee, SaeKwang Ku, Hae-Jeung Lee Nutrition Research.2020; 75: 15. CrossRef - Optimized production and safety evaluation of hispidin‐enriched Sanghuangporus sanghuang mycelia
I‐Chen Li, Chang Cheng Chen, Sen‐Je Sheu, I‐Hsuan Huang, Chin‐Chu Chen Food Science & Nutrition.2020; 8(4): 1864. CrossRef - Cyclofarnesane sesquiterpenoids from the fungus Sanghuangporus sp.
Oue-artorn Rajachan, Aphidech Sangdee, Kwanjai Kanokmedhakul, Sarawut Tontapha, Vittaya Amornkitbamrung, Somdej Kanokmedhakul Phytochemistry Letters.2020; 37: 17. CrossRef - Purification and characterization of a novel antioxidant Phelligridin LA produced by Inonotus baumii
Tianwen Wang, Hui Li, Chen Liang, Shiwei Sun, Ao Liu, Hu Zhu Journal of Chemical Technology & Biotechnology.2020; 95(9): 2483. CrossRef - Systematics is crucial for the traditional Chinese medicinal studies and industry of macrofungi
Li-Wei Zhou Fungal Biology Reviews.2020; 34(1): 10. CrossRef - Inonotus sanghuang Polyphenols Attenuate Inflammatory Response Via Modulating the Crosstalk Between Macrophages and Adipocytes
Mengdi Zhang, Yu Xie, Xing Su, Kun Liu, Yijie Zhang, Wuyan Pang, Junpeng Wang Frontiers in Immunology.2019;[Epub] CrossRef - Species Diversity, Phylogeny, Divergence Time, and Biogeography of the Genus Sanghuangporus (Basidiomycota)
Lin Zhu, Jie Song, Jun-Liang Zhou, Jing Si, Bao-Kai Cui Frontiers in Microbiology.2019;[Epub] CrossRef - Protective effect of a polyphenols-rich extract from Inonotus Sanghuang on bleomycin-induced acute lung injury in mice
Xing Su, Kun Liu, Yu Xie, Mengdi Zhang, Yong Wang, Min Zhao, Yilin Guo, Yijie Zhang, Junpeng Wang Life Sciences.2019; 230: 208. CrossRef - The Antitumor Potential of Extract of the Oak Bracket Medicinal Mushroom Inonotus baumii in SMMC-7721 Tumor Cells
Yue Yang, Pingya He, Ning Li Evidence-Based Complementary and Alternative Medicine.2019; 2019: 1. CrossRef - Evaluation of antioxidant, anti-inflammatory and anti-proliferative activities of ethanol extracts from different varieties of Sanghuang species
Wang-Ching Lin, Jeng-Shyan Deng, Shyh-Shyun Huang, Sheng-Hua Wu, Hui-Yi Lin, Guan-Jhong Huang RSC Advances.2017; 7(13): 7780. CrossRef
- Studies on seasonal dynamics of soil-higher fungal communities in Mongolian oak-dominant Gwangneung forest in Korea
-
Chang Sun Kim , Jong Woo Nam , Jong Won Jo , Sang-Yong Kim , Jae-Gu Han , Min Woo Hyun , Gi-Ho Sung , Sang-Kuk Han
-
J. Microbiol. 2016;54(1):14-22. Published online January 5, 2016
-
DOI: https://doi.org/10.1007/s12275-016-5521-1
-
-
921
View
-
0
Download
-
10
Crossref
-
Abstract
PDF
-
We surveyed macrofungi biweekly at defined plots from April
to December in 2014, in the Mongolian oak-dominant forest,
Gwangneung Forest, Pochen-si, Korea, and analyzed a soilhigher
fungal diversity during four seasons (represented by
April, August, October, and December). Based on morphological
observation of collected specimens, the collected macrofungi
were classified into 2 phyla 3 classes 7 orders, 14 families,
21 genera, and 33 species (36 specimens). DNA-based
community analyses indicated that soil-higher fungi were
classified into 2 phyla, 18 classes, 49 orders, 101 families, and
155 genera (83,360 sequence reads), defined herein as 155
genus-level operational taxonomic units (GOTUs). In the
present study, we evaluated and discussed the fungal diversity
in seasonal dynamics and soil layers based on collected
macrofungi and pyrosequencing data while considering environmental
parameters (pH, exchangeable K, T-P, NH4+, NO3-, OM, WR, TOC, and T-N). Moreover, principal components analysis (PCA) showed distinct clusters of the GOTU assemblage associated with the seasons.
-
Citations
Citations to this article as recorded by 
- Fire-Induced Changes in Soil Properties and Bacterial Communities in Rotational Shifting Cultivation Fields in Northern Thailand
Noppol Arunrat, Chakriya Sansupa, Sukanya Sereenonchai, Ryusuke Hatano, Rattan Lal Biology.2024; 13(6): 383. CrossRef - Diversity and species distribution of lichens in Gwangneung Forest
Jung Shin Park, En-Mi Sun, Jung-Jae Woo, Sang-Kuk Han, Soon-Ok Oh Journal of Asia-Pacific Biodiversity.2022; 15(4): 613. CrossRef - Statistical Evidence for Managing Forest Density in Consideration of Natural Volatile Organic Compounds
Yeji Choi, Geonwoo Kim, Sujin Park, Sangtae Lee, Soojin Kim, Eunsoo Kim Atmosphere.2021; 12(9): 1113. CrossRef - Immediate and legacy effects of snow exclusion on soil fungal diversity and community composition
Li Zhang, Yuzhi Ren, Kaijun Yang, Zhijie Li, Bo Tan, Yang Liu, Han Li, Chengming You, Sining Liu, Lixia Wang, Rui Yin, Jian Zhang, Zhenfeng Xu Forest Ecosystems.2021;[Epub] CrossRef - Comparison of Soil Higher Fungal Communities between Dead and Living Abies koreana in Mt. Halla, the Republic of Korea
Chang Sun Kim, Jong Won Jo, Hyen Lee, Young-Nam Kwag, Sung Eun Cho, Seung Hwan Oh Mycobiology.2020; 48(5): 364. CrossRef - Macrofungal diversity of urbanized areas in southern part of Korea
Sung Eun Cho, Young-Nam Kwag, Jong Won Jo, Sang-Kuk Han, Seung Hwan Oh, Chang Sun Kim Journal of Asia-Pacific Biodiversity.2020; 13(2): 189. CrossRef - Seasonal Change in Microbial Diversity and Its Relationship with Soil Chemical Properties in an Orchard
Xuhui Luo, Ming Kuang Wang, Guiping Hu, Boqi Weng, Varenyam Achal PLOS ONE.2019; 14(12): e0215556. CrossRef - One-time nitrogen fertilization shifts switchgrass soil microbiomes within a context of larger spatial and temporal variation
Huaihai Chen, Zamin K. Yang, Dan Yip, Reese H. Morris, Steven J. Lebreux, Melissa A. Cregger, Dawn M. Klingeman, Dafeng Hui, Robert L. Hettich, Steven W. Wilhelm, Gangsheng Wang, Frank E. Löffler, Christopher W. Schadt, Gabriel Moreno-Hagelsieb PLOS ONE.2019; 14(6): e0211310. CrossRef - Guild Patterns of Basidiomycetes Community Associated With Quercus mongolica in Mt. Jeombong, Republic of Korea
Seung-Yoon Oh, Hae Jin Cho, John A. Eimes, Sang-Kuk Han, Chang Sun Kim, Young Woon Lim Mycobiology.2018; 46(1): 13. CrossRef - Fungal communities in a Korean red pine stand, Gwangneung Forest, Korea
Chang Sun Kim, Sang-Kuk Han, Jong Woo Nam, Jong Won Jo, Young-Nam Kwag, Jae-Gu Han, Gi-Ho Sung, Young Woon Lim, Seunghwan Oh Journal of Asia-Pacific Biodiversity.2017; 10(4): 559. CrossRef
- Genipin as a novel chemical activator of EBV lytic cycle
-
Myoungki Son , Minjung Lee , Eunhyun Ryu , Aree Moon , Choon-Sik Jeong , Yong Woo Jung , Gyu Hwan Park , Gi-Ho Sung , Hyosun Cho , Hyojeung Kang
-
J. Microbiol. 2015;53(2):155-165. Published online January 28, 2015
-
DOI: https://doi.org/10.1007/s12275-015-4672-9
-
-
917
View
-
0
Download
-
29
Crossref
-
Abstract
PDF
-
Epstein-Barr virus (EBV) is a ubiquitous gammaherpesvirus
that causes acute infection and establishes life-long latency.
EBV causes several human cancers, including Burkitt's lymphoma,
nasopharyngeal and gastric carcinoma. Antiviral
agents can be categorized as virucides, antiviral chemotherapeutic
agents, and immunomodulators. Most antiviral agents
affect actively replicating viruses, but not their latent forms.
Novel antiviral agents must be active on both the replicating
and the latent forms of the virus. Gardenia jasminoides is an
evergreen flowering plant belonging to the Rubiaceae family
and is most commonly found growing wild in Vietnam,
Southern China, Taiwan, Japan, Myanmar, and India. Genipin
is an aglycone derived from an iridoid glycoside called geniposide,
which is present in large quantities in the fruit of
G. jasminoides. In this study, genipin was evaluated for its
role as an antitumor and antiviral agent that produces inhibitory
effects against EBV and EBV associated gastric carcinoma
(EBVaGC). In SNU719 cells, one of EBVaGCs, genipin
caused significant cytotoxicity (70 μM), induced methylation
on EBV C promoter and tumor suppressor gene
BCL7A, arrested cell-cycle progress (S phases), upregulated
EBV latent/lytic genes in a dose-dependent manner, stimulated
EBV progeny production, activated EBV F promoter
for EBV lytic activation, and suppressed EBV infection. These
results indicated that genipin could be a promising candidate
for antiviral and antitumor agents against EBV and
EBVaGC.
-
Citations
Citations to this article as recorded by 
- Research Progress of EB Virus-Associated Gastric Cancer
婷婷 宋 Advances in Clinical Medicine.2024; 14(08): 862. CrossRef - Genipin’s potential as an anti-cancer agent: from phytochemical origins to clinical prospects
Lapava Natallia, Aida Dama, Era Gorica, Karaliova Darya, Sheila I. Peña-Corona, Hernán Cortés, Antonello Santini, Dietrich Büsselberg, Gerardo Leyva-Gómez, Javad Sharifi-Rad Medical Oncology.2024;[Epub] CrossRef - Update of Natural Products and Their Derivatives Targeting Epstein–Barr Infection
Rosamaria Pennisi, Paola Trischitta, Marianna Costa, Assunta Venuti, Maria Pia Tamburello, Maria Teresa Sciortino Viruses.2024; 16(1): 124. CrossRef - Genipin-Crosslinking Effects on Biomatrix Development for Cutaneous Wound Healing: A Concise Review
Dewi Utami Nike, Nur Izzah Md Fadilah, Nusaibah Sallehuddin, Ahmad Yasser Hamdi Nor Azlan, Farrah Hani Imran, Manira Maarof, Mh Busra Fauzi Frontiers in Bioengineering and Biotechnology.2022;[Epub] CrossRef - Genipin, an Inhibitor of UCP2 as a Promising New Anticancer Agent: A Review of the Literature
Young Seok Cho International Journal of Molecular Sciences.2022; 23(10): 5637. CrossRef - Preparation, characterization, and in vitro release kinetics of doxorubicin-loaded magnetosomes
Shuang Zhang, Xinxin Fan, Guojing Zhang, Weidong Wang, Lei Yan Journal of Biomaterials Applications.2022; 36(8): 1469. CrossRef - An Integrated Analysis Reveals Geniposide Extracted From Gardenia jasminoides J.Ellis Regulates Calcium Signaling Pathway Essential for Influenza A Virus Replication
Lirun Zhou, Lei Bao, Yaxin Wang, Mengping Chen, Yingying Zhang, Zihan Geng, Ronghua Zhao, Jing Sun, Yanyan Bao, Yujing Shi, Rongmei Yao, Shanshan Guo, Xiaolan Cui Frontiers in Pharmacology.2021;[Epub] CrossRef - Synthesis of [3H] and [14C]genipin
Adele.E. Queen, David Hesk, David.M. Lindsay, William.J. Kerr, Kenneth Rehder, Tim Fennell, Wayne Mascarella, Desong Zhong, Scott Runyon Journal of Labelled Compounds and Radiopharmaceuticals.2020; 63(4): 196. CrossRef - Genipin inhibits rotavirus-induced diarrhea by suppressing viral replication and regulating inflammatory responses
Jong-Hwa Kim, Kiyoung Kim, Wonyong Kim Scientific Reports.2020;[Epub] CrossRef - Genipap (Genipa americana L.) juice intake biomarkers after medium-term consumption
Livia Dickson, Mathieu Tenon, Ljubica Svilar, Pascale Fança-Berthon, Jean-Charles Martin, Hervé Rogez, Fabrice Vaillant Food Research International.2020; 137: 109375. CrossRef - Evaluation on the antiviral activity of genipin against white spot syndrome virus in crayfish
Ai-Guo Huang, Xiao-Ping Tan, Shen-Ye Qu, Gao-Xue Wang, Bin Zhu Fish & Shellfish Immunology.2019; 93: 380. CrossRef - Comparative investigation on metabolite changes in ‘wu mi’ production by Vaccinium bracteatum Thunb. leaves based on multivariate data analysis using UPLC–QToF–MS
Mingcong Fan, Yihui Fan, Zhiming Rao, Yan Li, Haifeng Qian, Hui Zhang, Gangcheng Wu, Xiguang Qi, Li Wang Food Chemistry.2019; 286: 146. CrossRef - Selective oncolytic effect in Epstein-Barr virus (EBV)-associated gastric carcinoma through efficient lytic induction by Euphorbia extracts
Dong-eun Kim, Sunhee Jung, Hyung Won Ryu, Miri Choi, Mingu Kang, Hyunju Kang, Heung Joo Yuk, Hyejeong Jeong, Jiyeon Baek, Jae-Hyoung Song, Janghwan Kim, Hyojeung Kang, Sang-Bae Han, Sei-Ryang Oh, Sungchan Cho Journal of Functional Foods.2018; 42: 146. CrossRef - Curcuminoids as EBV Lytic Activators for Adjuvant Treatment in EBV-Positive Carcinomas
Octavia Ramayanti, Mitch Brinkkemper, Sandra Verkuijlen, Leni Ritmaleni, Mei Go, Jaap Middeldorp Cancers.2018; 10(4): 89. CrossRef - EBV transformation induces overexpression of hMSH2/3/6 on B lymphocytes and enhances γδT‐cell‐mediated cytotoxicity via TCR and NKG2D
Yu‐mei Dai, Hai‐ying Liu, Yun‐feng Liu, Yuan Zhang, Wei He Immunology.2018; 154(4): 673. CrossRef - Infection‐associated epigenetic alterations in gastric cancer: New insight in cancer therapy
Sadegh Fattahi, Mohadeseh Kosari‐Monfared, Elham Ghadami, Monireh Golpour, Parastoo Khodadadi, Mohammad Ghasemiyan, Haleh Akhavan‐Niaki Journal of Cellular Physiology.2018; 233(12): 9261. CrossRef - Plant-Derived Anticancer Agents: Lessons from the Pharmacology of Geniposide and Its Aglycone, Genipin
Solomon Habtemariam, Giovanni Lentini Biomedicines.2018; 6(2): 39. CrossRef - Main Human Urinary Metabolites after Genipap (Genipa americana L.) Juice Intake
Livia Dickson, Mathieu Tenon, Ljubica Svilar, Pascale Fança-Berthon, Raphael Lugan, Jean-Charles Martin, Fabrice Vaillant, Hervé Rogez Nutrients.2018; 10(9): 1155. CrossRef - Genipin: A natural blue pigment for food and health purposes
Iramaia Angélica Neri-Numa, Marina Gabriel Pessoa, Bruno Nicolau Paulino, Glaucia Maria Pastore Trends in Food Science & Technology.2017; 67: 271. CrossRef - Geniposide and geniposidic acid, modified forms of genipin, attenuate genipin-induced mitochondrial apoptosis without altering the anti-inflammatory ability in KGN cell line
Tao Zuo, Wenming Xu, Henli Li, Hang Song, Minghui Zhu Medicinal Chemistry Research.2017; 26(2): 499. CrossRef - Primary lymphocyte infection models for KSHV and its putative tumorigenesis mechanisms in B cell lymphomas
Sangmin Kang, Jinjong Myoung Journal of Microbiology.2017; 55(5): 319. CrossRef - Expression of toll‐like receptors in T lymphocytes stimulated with N‐(3‐oxododecanoyl)‐L‐homoserine lactone from Pseudomonas aeruginosa
Lei Bao, Jialin Yu, Haiying Zhong, Daochao Huang, Qi Lu APMIS.2017; 125(6): 553. CrossRef - Chemical Constituents from the Flowers of Wild Gardenia jasminoides J.Ellis
Hu Zhang, Ning Feng, Yan‐Tong Xu, Tian‐Xiang Li, Xiu‐Mei Gao, Yan Zhu, Yun Seon Song, Ya‐Nan Wang, Hong‐Hua Wu Chemistry & Biodiversity.2017;[Epub] CrossRef - The Suppressive Effects of Geniposide and Genipin on Helicobacter pylori Infections In Vitro and In Vivo
Chiung‐Hung Chang, Jin‐Bin Wu, Jai‐Sing Yang, Yen‐Ju Lai, Chiu‐Hsian Su, Chi‐Cheng Lu, Yuan‐Man Hsu Journal of Food Science.2017; 82(12): 3021. CrossRef - Antitumor Effects of Genipin: New and Emerging Insights from Recent Studies
Yu Su Shin, Miyeon Cho, Gyu Hwan Park, Hyosun Cho, Hyojeung Kang Journal of Bacteriology and Virology.2016; 46(2): 108. CrossRef - Iridoids are natural glycation inhibitors
Brett J. West, Shixin Deng, Akemi Uwaya, Fumiyuki Isami, Yumi Abe, Sho-ichi Yamagishi, C. Jarakae Jensen Glycoconjugate Journal.2016; 33(4): 671. CrossRef - Genipin Enhances Kaposi’s Sarcoma-Associated Herpesvirus Genome Maintenance
Miyeon Cho, Seok Won Jung, Soomin Lee, Kuwon Son, Gyu Hwan Park, Jong-Wha Jung, Yu Su Shin, Taegun Seo, Hyosun Cho, Hyojeung Kang, Shou-Jiang Gao PLOS ONE.2016; 11(10): e0163693. CrossRef - Anti-cancer effect of Cordyceps militaris in human colorectal carcinoma RKO cells via cell cycle arrest and mitochondrial apoptosis
Hwan Hee Lee, Seulki Lee, Kanghyo Lee, Yu Su Shin, Hyojeung Kang, Hyosun Cho DARU Journal of Pharmaceutical Sciences.2015;[Epub] CrossRef - Anti-tumor effect of Cordyceps militaris in HCV-infected human hepatocarcinoma 7.5 cells
Seulki Lee, Hwan Hee Lee, Jisung Kim, Joohee Jung, Aree Moon, Choon-Sik Jeong, Hyojeung Kang, Hyosun Cho Journal of Microbiology.2015; 53(7): 468. CrossRef
- Anti-influenza Effect of Cordyceps militaris through Immunomodulation in a DBA/2 Mouse Model
-
Hwan Hee Lee , Heejin Park , Gi-Ho Sung , Kanghyo Lee , Taeho Lee , Ilseob Lee , Man-seong Park , Yong Woo Jung , Yu Su Shin , Hyojeung Kang , Hyosun Cho
-
J. Microbiol. 2014;52(8):696-701. Published online July 18, 2014
-
DOI: https://doi.org/10.1007/s12275-014-4300-0
-
-
1,106
View
-
1
Download
-
27
Crossref
-
Abstract
PDF
-
The immune-modulatory as well as anti-influenza effects of Cordyceps extract were investigated using a DBA/2 mouse model. Three different concentrations of Cordyceps extract, red ginseng extract, or drinking water were orally administered
to mice for seven days, and then the mice were intranasally infected with 2009 pandemic influenza H1N1 virus. Body weight changes and survival rate were measured daily post-infection. Plasma IL-12, TNF-α, and the frequency of
natural killer (NK) cells were measured on day 4 post-infection. The DBA/2 strain was highly susceptible to H1N1 virus infection. We also found that Cordyceps extract had an antiinfluenza effect that was associated with stable body weight
and reduced mortality. The anti-viral effect of Cordyceps extract on influenza infection was mediated presumably by increased IL-12 expression and greater number of NK cells. However, high TNF-α expression after infection of H1N1
virus in mice not receiving treatment with Cordyceps extract suggested a two-sided effect of the extract on host immune regulation.
-
Citations
Citations to this article as recorded by 
- Quest for Anti-SARS-CoV-2 antiviral therapeutics: in-silico and in-vitro analysis of edible mushroom- Cordyceps militaris
Pradeep Gandhale, Rupesh Chikhale, Pukar Khanal, Vashkar Biswa, Raju Ali, Mohd Shahnawaz Khan, Nilambari Gurav, Muniappan Ayyanar, Sandeep Das, Shailendra Gurav Journal of Ayurveda and Integrative Medicine.2024; 15(3): 100979. CrossRef - Chitin Synthases in Cordyceps militaris: Genome-Wide Gene Identification, Evolutionary Insights, and Life Cycle Transcript Profiling
Shoumian Li, Huihui Ren, Jie Zhang, Shangpai Gao, Zixuan Chen, Guojie Li, Jinghua Tian, Junling Wang, Ming Li, Xiao Li, Caihong Dong Horticulturae.2024; 10(5): 494. CrossRef - Early Trends to Show the Efficacy of Cordyceps militaris in Mild to Moderate COVID Inflammation
Siddharth Dubhashi, Sagar Sinha, Sankalp Dwivedi, Jaishree Ghanekar, Sameer Kadam, Parineeta Samant, Vibha Datta, Sarman Singh, Irshad H Chaudry, Padma Gurmet, Harshawardhan Kelkar, Rakesh Mishra, Sagar Galwankar, Amit Agrawal Cureus.2023;[Epub] CrossRef - Chitinase Is Involved in the Fruiting Body Development of Medicinal Fungus Cordyceps militaris
Zi-Juan Zhang, Yuan-Yuan Yin, Yao Cui, Yue-Xuan Zhang, Bi-Yang Liu, You-Chu Ma, Yong-Nan Liu, Gao-Qiang Liu Life.2023; 13(3): 764. CrossRef - Boosting cordycepin production through plant-based oils for vegetarian consumption
Watcharin Yuttavanichakul, Nipaporn Kanthong, Nuntaporn Pungsungvorn Journal of Applied Research on Science and Technology (JARST).2023;[Epub] CrossRef - A Possible Synergistic Herbal Solution for COVID-19
Ephraim Shmaya Lansky Frontiers in Bioscience-Scholar.2022;[Epub] CrossRef - Un caso di COVID-19 curato con la micoterapia
Michel G. MALLARD Gazzetta Medica Italiana Archivio per le Scienze Mediche.2022;[Epub] CrossRef - Cordyceps militaris as a Bio Functional Food Source: Pharmacological Potential, Anti-Inflammatory Actions and Related Molecular Mechanisms
Abdul-Rehman Phull, Madiha Ahmed, Hye-Jin Park Microorganisms.2022; 10(2): 405. CrossRef - Medicinal Fungi with Antiviral Effect
Yu Zhang, Guoying Zhang, Jianya Ling Molecules.2022; 27(14): 4457. CrossRef - Antioxidant Activity of Mushroom Extracts/Polysaccharides—Their Antiviral Properties and Plausible AntiCOVID-19 Properties
Sechul Chun, Judy Gopal, Manikandan Muthu Antioxidants.2021; 10(12): 1899. CrossRef - Novel Fatty Acid in Cordyceps Suppresses
Influenza A (H1N1) Virus-Induced Proinflammatory Response
Through Regulating Innate Signaling Pathways
Run-Feng Li, Xiao-Bo Zhou, Hong-Xia Zhou, Zi-Feng Yang, Hai-Ming Jiang, Xiao Wu, Wen-Jia Li, Jian-Jian Qiu, Jia-Ning Mi, Ming Chen, Nan-Shan Zhong, Guo-Yuan Zhu, Zhi-Hong Jiang ACS Omega.2021; 6(2): 1505. CrossRef - Cysteine-Rich Hydrophobin Gene Family: Genome Wide Analysis, Phylogeny and Transcript Profiling in Cordyceps militaris
Xiao Li, Fen Wang, Yanyan Xu, Guijun Liu, Caihong Dong International Journal of Molecular Sciences.2021; 22(2): 643. CrossRef - Repurposing potential of Ayurvedic medicinal plants derived active principles against SARS-CoV-2 associated target proteins revealed by molecular docking, molecular dynamics and MM-PBSA studies
Akalesh Kumar Verma, Vikas Kumar, Sweta Singh, Bhabesh Ch. Goswami, Ihosvany Camps, Aishwarya Sekar, Sanghwa Yoon, Keun Woo Lee Biomedicine & Pharmacotherapy.2021; 137: 111356. CrossRef - A new nucleoside and two new pyrrole alkaloid derivatives from Cordyceps militaris
Yafu Xue, Leilei Wu, Yulian Ding, Xinming Cui, Zhuzhen Han, Hong Xu Natural Product Research.2020; 34(3): 341. CrossRef - CmVVD is involved in fruiting body development and carotenoid production and the transcriptional linkage among three blue‐light receptors in edible fungus Cordyceps militaris
Jiaojiao Zhang, Fen Wang, Ying Yang, Ying Wang, Caihong Dong Environmental Microbiology.2020; 22(1): 466. CrossRef - Effects of nanobubble water supplementation on biomass accumulation during mycelium cultivation of Cordyceps militaris and the antioxidant activities of extracted polysaccharides
Long Xiao, Shuang Sun, Kejuan Li, Zhongfang Lei, Kazuya Shimizu, Zhenya Zhang, Yasuhisa Adachi Bioresource Technology Reports.2020; 12: 100600. CrossRef - Analysis of reference genes stability and histidine kinase expression under cold stress in Cordyceps militaris
Yong-Nan Liu, Bi-Yang Liu, You-Chu Ma, Hai-Long Yang, Gao-Qiang Liu, Shwet Kamal PLOS ONE.2020; 15(8): e0236898. CrossRef - Trends in the Immunomodulatory Effects of Cordyceps militaris: Total Extracts, Polysaccharides and Cordycepin
Chun-Ting Lee, Keng-Shiang Huang, Jei-Fu Shaw, Jung-Ren Chen, Wen-Shuo Kuo, Gangxu Shen, Alexandru Mihai Grumezescu, Alina Maria Holban, Yi-Ting Wang, Jun-Sheng Wang, Yi-Ping Hsiang, Yu-Mei Lin, Hsiao-Han Hsu, Chih-Hui Yang Frontiers in Pharmacology.2020;[Epub] CrossRef - Effects ofCordyceps militarissupplementation on the immune response and upper respiratory infection in healthy adults: a randomized, double-blind, placebo-controlled study
Su Jin Jung, Ji Hyun Hwang, Mi Ra Oh, Soo Wan Chae Journal of Nutrition and Health.2019; 52(3): 258. CrossRef - Advance in Cordyceps militaris (Linn) Link polysaccharides: Isolation, structure, and bioactivities: A review
Jixian Zhang, Chaoting Wen, Yuqing Duan, Haihui Zhang, Haile Ma International Journal of Biological Macromolecules.2019; 132: 906. CrossRef - The blue-light receptor CmWC-1 mediates fruit body development and secondary metabolism in Cordyceps militaris
Tao Yang, Mingmin Guo, Huaijun Yang, Suping Guo, Caihong Dong Applied Microbiology and Biotechnology.2016; 100(2): 743. CrossRef - Cordyceps militaris (L.) Link: Chemical Bioactive Compounds and Pharmacological Activities
Do Hai Lan, Nguyen Thi Kim Thu, Pham Thi Lan, Pham Van Nha , Bui Thanh Tung Journal of Pharmacy and Nutrition Sciences .2016; 6(4): 153. CrossRef - Partial structural characterization, as well as immunomodulatory and anti-aging activities of CP2-c2-s2 polysaccharide from Cordyceps militaris
Xiaojuan Liu, Yicheng Huang, Yunjiao Chen, Yong Cao RSC Adv..2016; 6(106): 104094. CrossRef - Cultured Mycelium Cordyceps sinensis allevi¬ates CCl4-induced liver inflammation and fibrosis in mice by activating hepatic natural killer cells
Yuan Peng, Kai Huang, Li Shen, Yan-yan Tao, Cheng-hai Liu Acta Pharmacologica Sinica.2016; 37(2): 204. CrossRef - Cordyceps industry in China
Caihong Dong, Suping Guo, Wenfeng Wang, Xingzhong Liu Mycology.2015; 6(2): 121. CrossRef - Anti-cancer effect of Cordyceps militaris in human colorectal carcinoma RKO cells via cell cycle arrest and mitochondrial apoptosis
Hwan Hee Lee, Seulki Lee, Kanghyo Lee, Yu Su Shin, Hyojeung Kang, Hyosun Cho DARU Journal of Pharmaceutical Sciences.2015;[Epub] CrossRef - Anti-tumor effect of Cordyceps militaris in HCV-infected human hepatocarcinoma 7.5 cells
Seulki Lee, Hwan Hee Lee, Jisung Kim, Joohee Jung, Aree Moon, Choon-Sik Jeong, Hyojeung Kang, Hyosun Cho Journal of Microbiology.2015; 53(7): 468. CrossRef
- Bioactive Activities of Natural Products against Herpesvirus Infection
-
Myoungki Son , Minjung Lee , Gi-Ho Sung , Taeho Lee , Yu Su Shin , Hyosun Cho , Paul M. Lieberman , Hyojeung Kang
-
J. Microbiol. 2013;51(6):888-888.
-
DOI: https://doi.org/10.1007/s12275-013-0726-z
-
-
Abstract
PDF
-
In the article by Son et al. published in the Journal of Microbiology 2013; 51, 545-551.
- Acknowledgement should appear as shown below.
We gratefully acknowledge financial supports of Next Generation BioGreen 21 Program (Project No. PJ009508) and
Cooperative Research Program for Agriculture Science & Technology Development (Project No. PJ009241) from
Rural Development Administration, Republic of Korea.
- Co-corresponding author’s (Dr. Paul M. Lieberman) affiliation should appear as shown below.
6The Wistar Institute, Philadelphia, PA 19104, USA
- Two Novel Talaromyces Species Isolated from Medicinal Crops in Korea
-
Hyunkyu Sang , Tae-Jin An , Chang Sun Kim , Gyu-Sub Shin , Gi-Ho Sung , Seung Hun Yu
-
J. Microbiol. 2013;51(5):704-708. Published online October 31, 2013
-
DOI: https://doi.org/10.1007/s12275-013-3361-9
-
-
725
View
-
1
Download
-
21
Crossref
-
Abstract
PDF
-
Two novel biverticillate Talaromyces species, T. angelicus and T. cnidii, were collected from the medicinal crops Angelica gigas and Cnidium officinale, respectively, in Korea. Phylogenetic analyses with the nuclear ribosomal internal transcribed spacer (ITS) region and the β-tubulin gene as well as morphological analyses revealed that the two species differ from any known Talaromyces species. Talaromyces angelicus is related to T. flavovirens in the phylogeny of the ITS region, but the new species is grouped together with Penicillium liani and T. pinophilus in terms of its β-tubulin phylogeny, and its growth rate on Czapek yeast autolysate differs from that of T. flavovirens. Talaromyces cnidii is phylogenetically similar to T. siamensis, but exhibits differences in the morphologies of the colony margin, metulae, and conidia.
-
Citations
Citations to this article as recorded by 
- An Updated Taxonomy of Talaromyces (Trichocomaceae, Eurotiales): New Series and Species
Lu-Yao Peng, He Song, Yi-Fan Wang, Wen-Ying Zhuang, Xin-Cun Wang Journal of Fungi.2026; 12(7): 485. CrossRef - Modern taxonomy and approaches to the identification of the genus Talaromyces (Trichocomaceae, Eurotiales)
Е. А. Antonov, A. V. Aleksandrova, I. I. Antonova Микология и фитопатология.2024;[Epub] CrossRef - Talaromyces sedimenticola sp. nov., isolated from the Mariana Trench
Hongbo Zhou, Liting Xu, Wenxian Liu, Kaiwen Ta, Xincun Wang, Jianwei Guo, Wenxi Luo, Zhiyuan Peng, Qiaoni Huang, Yuguang Wang Antonie van Leeuwenhoek.2024;[Epub] CrossRef - New Fungal Strains from Peat Soil in Malaysia: Morphological and Molecular Characteristics
Efaq Ali Noman, Adel Ali Al-Gheethi, Baliks A. Talip, Radin Maya Saphira Radin Mohamed, Reyad Almoheer, Fairoz Ali Al-Wrafy, Najeeb Al-Shorgani, Hesham Ali El Enshasy Sustainability.2023; 15(7): 5902. CrossRef -
A New Species and Five New Records of
Talaromyces
(
Eurotiales
,
Aspergillaceae
) Belonging to Section
Talaromyces
in Korea
Thuong T. T. Nguyen, Hyang Burm Lee Mycobiology.2023; 51(5): 320. CrossRef - Fine Identification and Classification of a Novel Beneficial Talaromyces Fungal Species from Masson Pine Rhizosphere Soil
Xiao-Rui Sun, Ming-Ye Xu, Wei-Liang Kong, Fei Wu, Yu Zhang, Xing-Li Xie, De-Wei Li, Xiao-Qin Wu Journal of Fungi.2022; 8(2): 155. CrossRef - Isolation, Identification and Insecticidal Activity of the Secondary Metabolites of Talaromyces purpureogenus BS5
Ying Yue, Mingfang Jiang, Hanying Hu, Jinghui Wu, Haoran Sun, Hong Jin, Taiping Hou, Ke Tao Journal of Fungi.2022; 8(3): 288. CrossRef - New Species of Talaromyces (Fungi) Isolated from Soil in Southwestern China
Zhi-Kang Zhang, Xin-Cun Wang, Wen-Ying Zhuang, Xian-Hao Cheng, Peng Zhao Biology.2021; 10(8): 745. CrossRef - Six Newly Recorded Fungal Taxa from Freshwater Niche in Korea
Hyo Jin Lim, Thuong T. T Nguyen, Hyang Burm Lee Mycobiology.2021; 49(2): 105. CrossRef -
Four new species of
Talaromyces
section
Talaromyces
discovered in China
Shangzhu Wei, Xiuli Xu, Long Wang Mycologia.2021; 113(2): 492. CrossRef - Discovery and Extrolite Production of Three New Species of Talaromyces Belonging to Sections Helici and Purpurei from Freshwater in Korea
Thuong T. T. Nguyen, Jens Christian Frisvad, Paul M. Kirk, Hyo Jin Lim, Hyang Burm Lee Journal of Fungi.2021; 7(9): 722. CrossRef - New section and species in Talaromyces
Bing-Da Sun, Amanda J. Chen, Jos Houbraken, Jens C. Frisvad, Wen-Ping Wu, Hai-Lei Wei, Yu-Guang Zhou, Xian-Zhi Jiang, Robert A. Samson MycoKeys.2020; 68: 75. CrossRef - Mycoflora assessment, growth and toxigenic features of patulin‐producers in kiwifruit in China
Yuan Wang, Kewei Feng, Bin Liu, Zhiwei Zhang, Jianping Wei, Yahong Yuan, Tianli Yue Journal of the Science of Food and Agriculture.2018; 98(7): 2573. CrossRef - Three new species of Talaromyces sect. Talaromyces discovered from soil in China
Xian-Zhi Jiang, Zhong-Dong Yu, Yong-Ming Ruan, Long Wang Scientific Reports.2018;[Epub] CrossRef - Notes for genera: Ascomycota
Nalin N. Wijayawardene, Kevin D. Hyde, Kunhiraman C. Rajeshkumar, David L. Hawksworth, Hugo Madrid, Paul M. Kirk, Uwe Braun, Rajshree V. Singh, Pedro W. Crous, Martin Kukwa, Robert Lücking, Cletus P. Kurtzman, Andrey Yurkov, Danny Haelewaters, André Aptro Fungal Diversity.2017; 86(1): 1. CrossRef - NewTalaromycesspecies from indoor environments in China
A.J. Chen, B.D. Sun, J. Houbraken, J.C. Frisvad, N. Yilmaz, Y.G. Zhou, R.A. Samson Studies in Mycology.2016; 84(1): 119. CrossRef - Species List of Aspergillus, Penicillium and Talaromyces in Korea, Based on ‘One Fungus One Name’ System
The Korean Journal of Mycology.2016;[Epub] CrossRef - Cellulase and Xylanase Production by the Mexican Strain Talaromyces stollii LV186 and Its Application in the Saccharification of Pretreated Corn and Sorghum Stover
Montserrat Orencio-Trejo, Jessica Torres-Granados, Arelis Rangel-Lara, Esmeralda Beltrán-Guerrero, Santos García-Aguilar, Cessna Moss-Acosta, Humberto Valenzuela-Soto, Susana De la Torre-Zavala, Argel Gastelum-Arellanez, Alfredo Martinez, Axel Tiessen, Ed BioEnergy Research.2016; 9(4): 1034. CrossRef - Talaromyces neofusisporus and T. qii, two new species of section Talaromyces isolated from plant leaves in Tibet, China
Qi-Ming Wang, Yong-Hong Zhang, Bo Wang, Long Wang Scientific Reports.2016;[Epub] CrossRef - Five new Talaromyces species with ampulliform-like phialides and globose rough walled conidia resembling T. verruculosus
Cobus M. Visagie, Neriman Yilmaz, Jens C. Frisvad, Jos Houbraken, Keith A. Seifert, Robert A. Samson, Karin Jacobs Mycoscience.2015; 56(5): 486. CrossRef - Aspergillus, Penicillium and Talaromyces isolated from house dust samples collected around the world
C.M. Visagie, Y. Hirooka, J.B. Tanney, E. Whitfield, K. Mwange, M. Meijer, A.S. Amend, K.A. Seifert, R.A. Samson Studies in Mycology.2014; 78(1): 63. CrossRef
- Bioactive Activities of Natural Products against Herpesvirus Infection
-
Myoungki Son , Minjung Lee , Gi-Ho Sung , Taeho Lee , Yu Su Shin , Hyosun Cho , Paul M. Lieberman , Hyojeung Kang
-
J. Microbiol. 2013;51(5):545-551. Published online October 31, 2013
-
DOI: https://doi.org/10.1007/s12275-013-3450-9
-
-
969
View
-
0
Download
-
38
Crossref
-
Abstract
PDF
-
More than 90% of adults have been infected with at least one human herpesvirus, which establish long-term latent infection for the life of the host. While anti-viral drugs exist that limit herpesvirus replication, many of these are ineffective against latent infection. Moreover, drug-resistant strains of herpesvirus emerge following chemotherapeutic treatment. For example, resistance to acyclovir and related nucleoside analogues can occur when mutations arise in either HSV thymidine kinase or DNA polymerases. Thus, there exists an unmet medical need to develop new anti-herpesvirus agents with different mechanisms of action. In this Review, we discuss the promise of anti-herpetic substances derived from natural products including extracts and pure compounds from potential herbal medicines. One example is Glycyrrhizic acid isolated from licorice that shows promising antiviral activity towards human gammaherpesviruses. Secondly, we discuss anti-herpetic mechanisms utilized by several natural products in molecular level. While nucleoside analogues inhibit replicating herpesviruses in lytic replication, some natural products can disrupt the herpesvirus latent infection in the host cell. In addition, natural products can stimulate immune responses against herpesviral infection. These findings suggest that natural products could be one of the best choices for development of new treatments for latent herpesvirus infection, and may provide synergistic anti-viral activity when supplemented with nucleoside analogues. Therefore, it is important to identify which natural products are more efficacious anti-herpetic agents, and to understand the molecular mechanism in detail for further advance in the anti-viral therapies.
-
Citations
Citations to this article as recorded by 
- Lariciresinol: a potent natural compound with diverse therapeutic and health benefits
Ijaz Hussain, Azhar Rasul, Mudassir Hassan, Ravi Rawat, Yusuf Tutar Natural Product Research.2026; : 1. CrossRef - Nanocomplex hyaluronic acid/ganciclovir@ZIF-8 for ganciclovir efficient delivery and targeted anti-KSHV treatment
Fangling Li, Chengjing Liu, Wenyi Gu, Qianhe Xu, Dongmei Li, Dongdong Cao, Zhiyong Liu Cancer Nanotechnology.2025;[Epub] CrossRef - Macrophage‐Mediated Delivery of miR‐34a‐5p‐Nanoparticles for Pathogenic Inhibition of Kaposi's Sarcoma‐Associated Herpesvirus
Lixia Yao, Qing Zhang, Xingxing Gao, Fangling Li, Lei Zhang, Jinli Zhang, Wenyi Gu, Xiaohua Tan, Dongmei Li, Dongdong Cao, Yuanming Pan Journal of Medical Virology.2025;[Epub] CrossRef - Discovery of Phloroglucinol Derivatives as a New Type of Nonnucleoside Inhibitors with Anti-herpes Simplex Virus Type 1 Activity
Shu-Qin Wang, Qiao-Yun Song, Dong-Lin Zhong, Jie Jiao, Lei Zhang, Lu-Ming Deng, Zhi-Zhang Duan, Guan-Qiu Qin, Jian-Guo Song, Wei Tang, Wen-Cai Ye, Ying Wang, Li-Jun Hu Journal of Medicinal Chemistry.2025; 68(12): 12544. CrossRef - Identification of natural products targeting human herpesvirus DNA polymerase as antiviral lead
Hai-Yan Song, Shiyu Wu, Yuqi Li, Hong-Yan Lin, Xing-Xing Shi, Jiangqing Dong International Journal of Biological Macromolecules.2025; 323: 147095. CrossRef - Exploring phytobiotics in aquaculture: sources, mode of action, effects, administration, and its bioavailability in fish
Pandi Kalaiselvan, Kavitha Malarvizhi, Amit Ranjan Aquaculture International.2024; 32(5): 5737. CrossRef - Tilapia lake virus: understanding incidence, enhancing resistance, and exploring seaweed therapies
Sourabh Debbarma, Nitesh Kumar Yadav, Ng Chinglembi Devi, Bagthasingh Chrisolite, Yilbong Yirang, Dharmendra Kumar Meena, Soibam Khogen Singh, Naresh Kumar Mehta, Bhargavi Priyadarshini Mocherla Aquaculture International.2024; 32(7): 10313. CrossRef - Causality between herpes virus infections and allograft dysfunction after tissue and organ transplantation: a two-sample bidirectional Mendelian randomization study
Xiaojuan Qiu, Tianjiao Ma, Shishun Zhao, Zongyu Zheng Frontiers in Immunology.2024;[Epub] CrossRef - Association between human herpesviruses and multiple sclerosis: A systematic review and meta-analysis
Zohreh Khalesi, Vahid Tamrchi, Mohammad Hossein Razizadeh, Arash Letafati, Pouya Moradi, Arezoo Habibi, Negar Habibi, Jafar Heidari, Maryam Noori, Mahboubeh Nahid Samiei, Ziba Azarash, Mahdiyeh Hoseini, Hassan Saadati, Atefeh Bahavar, Maryam Farajzade, Se Microbial Pathogenesis.2023; 177: 106031. CrossRef - Delivery of miR-34a-5p by Folic Acid-Modified β-Cyclodextrin-Grafted Polyethylenimine Copolymer Nanocarriers to Resist KSHV
Fangling Li, Dongdong Cao, Wenyi Gu, Lin Cui, Zhongpeng Qiu, Zhiyong Liu, Dongmei Li, Xuhong Guo ACS Applied Nano Materials.2023; 6(12): 10826. CrossRef - Exploration of natural compounds against the human mpox virus DNA-dependent RNA polymerase in silico
Jameel M. Abduljalil, Abdo A. Elfiky, Alaa M. Elgohary Journal of Infection and Public Health.2023; 16(7): 996. CrossRef - Tackling the Future Pandemics: Broad-Spectrum Antiviral Agents (BSAAs) Based on A-Type Proanthocyanidins
Massimo E. Maffei, Cristiano Salata, Giorgio Gribaudo Molecules.2022; 27(23): 8353. CrossRef - The Role of the Natural Antioxidant Mechanism in Sperm Cells
Alicja Kowalczyk Reproductive Sciences.2022; 29(5): 1387. CrossRef - Viral infections in cultured fish and shrimps: current status and treatment methods
Haimanti Mondal, Natarajan Chandrasekaran, Amitava Mukherjee, John Thomas Aquaculture International.2022; 30(1): 227. CrossRef - Microalgal drugs: A promising therapeutic reserve for the future
Ankesh Ahirwar, Khushboo Kesharwani, Rahul Deka, Shreya Muthukumar, Mohd. Jahir Khan, Anshuman Rai, Vandana Vinayak, Sunita Varjani, Khashti Ballabh Joshi, Shruti Morjaria Journal of Biotechnology.2022; 349: 32. CrossRef - Palmitic Amide Triggers Virus Life Cycle via Enhancing Host Energy Metabolism
Xinyi Zhang, Jianjian Zhuang, Liquan Huang, Xiaobo Zhang Frontiers in Microbiology.2022;[Epub] CrossRef - 2-Methoxy-6-Acetyl-7-Methyljuglone: A Bioactive Phytochemical with Potential Pharmacological Activities
Atif Ali Khan Khalil, Asma Saleem Qazi, Abdul Nasir, Mi-Jeong Ahn, Muhammad Ajmal Shah, Muhammad Saad Ahmad, Wasim Sajjad, Tahir Ali, Muhammad Naeem, Fawad Ali Shah, Muhammad Tufail Ahmed Khan, Muhammad Romman, Shahfiq Ur Rehman, Adnan Haider, Raishma Anti-Cancer Agents in Medicinal Chemistry.2022; 22(4): 687. CrossRef - Natural Products and Their Derivatives against Human Herpesvirus Infection
Chattarin Ruchawapol, Man Yuan, Si-Min Wang, Wen-Wei Fu, Hong-Xi Xu Molecules.2021; 26(20): 6290. CrossRef - Antiviral activity of sulfated polysaccharides from Sargassum ilicifolium against fish Betanodavirus infection
Jyotsna, Parameswaran Vijayakumar, Tharmathass Stalin Dhas, Ravi Mani, Vasantharaja Raguraman Aquaculture International.2021; 29(3): 1049. CrossRef - Effects of Apigenin and Astragalus Polysaccharide on the Cryopreservation of Bull Semen
Hongtao Wang, Ping Lu, Chongshan Yuan, Jing Zhao, Hongyu Liu, Wenfa Lu, Jun Wang Animals.2021; 11(6): 1506. CrossRef - Viral UL8 Is Involved in the Antiviral Activity of Oleanolic Acid Against HSV-1 Infection
Tianhao Shan, Ju Ye, Jiaoyan Jia, Zhaoyang Wang, Yuzhou Jiang, Yiliang Wang, Yifei Wang, Kai Zheng, Zhe Ren Frontiers in Microbiology.2021;[Epub] CrossRef - Allicin and Glycyrrhizic Acid Display Antiviral Activity Against Latent and Lytic Kaposi Sarcoma-associated Herpesvirus
Yirui Xie, Ying Chen, Yongzheng Guo, Ying Huang, Biao Zhu Infectious Microbes and Diseases.2020; 2(1): 30. CrossRef - Anti-herpes simplex type-1 (HSV-1) activity from the roots of Jatropha multifida L
Ratchanaporn Chokchaisiri, Jaranwit Srijun, Waraluck Chaichompoo, Sarot Cheenpracha, Lucksagoon Ganranoo, Apichart Suksamrarn Medicinal Chemistry Research.2020; 29(2): 328. CrossRef - In Vitro Anti-HSV-1 Activity of Polyphenol-Rich Extracts and Pure Polyphenol Compounds Derived from Pistachios Kernels (Pistacia vera L.)
Maria Musarra-Pizzo, Rosamaria Pennisi, Ichrak Ben-Amor, Antonella Smeriglio, Giuseppina Mandalari, Maria Teresa Sciortino Plants.2020; 9(2): 267. CrossRef - Oleandrin: A bioactive phytochemical and potential cancer killer via multiple cellular signaling pathways
Nazia Kanwal, Azhar Rasul, Ghulam Hussain, Haseeb Anwar, Muhammad Ajmal Shah, Iqra Sarfraz, Ammara Riaz, Rabia Batool, Muhammad Shahbaz, Arif Hussain, Zeliha Selamoglu Food and Chemical Toxicology.2020; 143: 111570. CrossRef - A pilot study of oral tranexamic acid and Glycyrrhizin compound in the treatment of recalcitrant Riehl’s melanosis
Zhongyi Xu, Xiaoxue Xing, Chengfeng Zhang, Li Chen, Leihong Flora Xiang Journal of Cosmetic Dermatology.2019; 18(1): 286. CrossRef - Using glycyrrhizic acid to target sumoylation processes during Epstein-Barr virus latency
Gretchen L. Bentz, Angela J. Lowrey, Dustin C. Horne, Vy Nguyen, Austin R. Satterfield, Tabithia D. Ross, Abigail E. Harrod, Olga N. Uchakina, Robert J. McKallip, Luwen Zhang PLOS ONE.2019; 14(5): e0217578. CrossRef - The Antimicrobial and Antiviral Activity of Polyphenols from Almond (Prunus dulcis L.) Skin
Maria Musarra-Pizzo, Giovanna Ginestra, Antonella Smeriglio, Rosamaria Pennisi, Maria Teresa Sciortino, Giuseppina Mandalari Nutrients.2019; 11(10): 2355. CrossRef - Virucidal, antiviral and immunomodulatory activities of β-escin and Aesculus hippocastanum extract
Flavia M Michelini, Laura E Alché, Carlos A Bueno Journal of Pharmacy and Pharmacology.2018; 70(11): 1561. CrossRef - Perspective on Biotransformation and De Novo Biosynthesis of Licorice Constituents
Yujia Zhao, Bo Lv, Xudong Feng, Chun Li Journal of Agricultural and Food Chemistry.2017; 65(51): 11147. CrossRef - Fraxinus: A Plant with Versatile Pharmacological and Biological Activities
Iqra Sarfraz, Azhar Rasul, Farhat Jabeen, Tahira Younis, Muhammad Kashif Zahoor, Muhammad Arshad, Muhammad Ali, Rainer W. Bussmann Evidence-Based Complementary and Alternative Medicine.2017;[Epub] CrossRef - In vitro cytotoxicity and biological activities of Genipa americana (Rubiaceae) ethanolic extracts
Silva Campos Codignoto Paola, Batista de Araújo Shirley, Munhoz Bastos Natan, de Oliveira Fernandes Thais, Arielle Santana Barbosa Tamiris, Eduardo Dias Igidio Carlos, Faustino Fernando, Judite Bittencourt Fernandes Maria, Oliveira da Conceição Aline African Journal of Microbiology Research.2017; 11(9): 385. CrossRef - Apigenin inhibits African swine fever virus infection in vitro
Astghik Hakobyan, Erik Arabyan, Aida Avetisyan, Liana Abroyan, Lina Hakobyan, Hovakim Zakaryan Archives of Virology.2016; 161(12): 3445. CrossRef - Genipin Enhances Kaposi’s Sarcoma-Associated Herpesvirus Genome Maintenance
Miyeon Cho, Seok Won Jung, Soomin Lee, Kuwon Son, Gyu Hwan Park, Jong-Wha Jung, Yu Su Shin, Taegun Seo, Hyosun Cho, Hyojeung Kang, Shou-Jiang Gao PLOS ONE.2016; 11(10): e0163693. CrossRef - Genipin as a novel chemical activator of EBV lytic cycle
Myoungki Son, Minjung Lee, Eunhyun Ryu, Aree Moon, Choon-Sik Jeong, Yong Woo Jung, Gyu Hwan Park, Gi-Ho Sung, Hyosun Cho, Hyojeung Kang Journal of Microbiology.2015; 53(2): 155. CrossRef - Seaweed extracts as antimicrobial agents in aquaculture
Ioannis N Vatsos, Celine Rebours Journal of Applied Phycology.2015; 27(5): 2017. CrossRef - Bioactive natural products with anti-herpes simplex virus properties
Sherif T S Hassan, Radka Masarčíková, Kateřina Berchová Journal of Pharmacy and Pharmacology.2015; 67(10): 1325. CrossRef - A Novel Tricyclic Polyketide, Vanitaracin A, Specifically Inhibits the Entry of Hepatitis B and D Viruses by Targeting Sodium Taurocholate Cotransporting Polypeptide
Manabu Kaneko, Koichi Watashi, Shinji Kamisuki, Hiroki Matsunaga, Masashi Iwamoto, Fumihiro Kawai, Hirofumi Ohashi, Senko Tsukuda, Satomi Shimura, Ryosuke Suzuki, Hideki Aizaki, Masaya Sugiyama, Sam-Yong Park, Takayoshi Ito, Naoko Ohtani, Fumio Sugawara, Journal of Virology.2015; 89(23): 11945. CrossRef
- Penicillium daejeonium sp. nov., a New Species Isolated from a Grape and Schisandra Fruit in Korea
-
Hyunkyu Sang , Tae-Jin An , Chang Sun Kim , Young Phil Choi , Jian-Xin Deng , Narayan Chandra Paul , Gi-Ho Sung , Seung Hun Yu
-
J. Microbiol. 2013;51(4):536-539. Published online August 30, 2013
-
DOI: https://doi.org/10.1007/s12275-013-3291-6
-
-
728
View
-
2
Download
-
9
Crossref
-
Abstract
PDF
-
Two isolates of monoverticillate Penicillium species were collected from a grape and schisandra fruit in Korea. Multigene phylogenetic analyses with the nuclear ribosomal internal transcribed spacer (ITS) region and genes encoding β-tubulin (benA) and calmodulin (cmd), as well as morphological analyses revealed that the two isolates are members of the P. sclerotiorum complex in Penicillium subgenus Aspergilloides, but different from species of the P. sclerotiorum complex. The isolates are closely related to P. cainii, P. jacksonii, and P. viticola in terms of their multigene phylogeny, but their colony and conidiophore morphologies differ from those of closely related species. The name P. daejeonium is proposed for this unclassified new species belonging to the P. sclerotiorum complex in subgenus Aspergilloides.
-
Citations
Citations to this article as recorded by 
- Along the footpath of Penicillium discovery: Six new species from the Woodville Big Tree Forest Trail
Cobus M. Visagie, Neriman Yilmaz Mycologia.2023; 115(1): 87. CrossRef - Critical control point-based assessment and intervention of ochratoxin A risk in Angelicae Gigantis Radix production
Juil Kim, Tae Jin An, Yuseok Moon Frontiers in Microbiology.2022;[Epub] CrossRef - New Records of Four Species Belonging to Eurotiales from Soil and Freshwater in Korea
Monmi Pangging, Thuong T. T. Nguyen, Hyang Burm Lee Mycobiology.2019; 47(2): 154. CrossRef - Three Unrecorded Species Belonging toPenicilliumSectionSclerotiorafrom Marine Environments in Korea
Myung Soo Park, Dawoon Chung, Kyunghwa Baek, Young Woon Lim Mycobiology.2019; 47(2): 165. CrossRef - Selective antifungal activity of chitosan and sulfonated chitosan against postharvest fungus isolated from blueberry
Yuhong Liu, Zhimin Sun, Lili Xiu, Jianying Huang, Fengyan Zhou Journal of Food Biochemistry.2018; 42(6): e12658. CrossRef - A New record of four Penicillium species isolated from Agarum clathratum in Korea
Myung Soo Park, Seobihn Lee, Young Woon Lim Journal of Microbiology.2017; 55(4): 237. CrossRef - Phylogeny and morphological analyses of Penicillium section Sclerotiora (Fungi) lead to the discovery of five new species
Xin-Cun Wang, Kai Chen, Zhao-Qing Zeng, Wen-Ying Zhuang Scientific Reports.2017;[Epub] CrossRef - Species List of Aspergillus, Penicillium and Talaromyces in Korea, Based on ‘One Fungus One Name’ System
The Korean Journal of Mycology.2016;[Epub] CrossRef - Penicillium chroogomphum, a new species in Penicillium section Ramosa isolated from fruiting bodies of Chroogomphus rutilus in China
Chengbo Rong, Yuanwei Ma, Shouxian Wang, Yu Liu, Lanqing Wang, Kang Ma, Shijuan Dou, Yongli Yang, Feng Xu Mycoscience.2016; 57(1): 79. CrossRef
- Dysregulation of KSHV Replication by Extracts from Carthamus tinctorius L.
-
Han Lee , Hyosun Cho , Myoungki Son , Gi-Ho Sung , Taeho Lee , Sang-Won Lee , Yong Woo Jung , Yu Su Shin , Hyojeung Kang
-
J. Microbiol. 2013;51(4):490-498. Published online August 30, 2013
-
DOI: https://doi.org/10.1007/s12275-013-3282-7
-
-
698
View
-
0
Download
-
4
Crossref
-
Abstract
PDF
-
Carthamus tinctorius L. (CT) is traditionally used to reduce ailments from diseases of the musculoskeletal system and connective tissue and diseases of blood circulation and the cardiovascular system. Flower extracts from CT are known to have antibacterial activity, anti-inflammatory activity, and to inhibit tumor promotion in mouse skin carcinogenesis. In order to discover new antiviral agents from CT extracts, we tested whether CT extracts contain antiviral activity against gammaherpesvirus infection. This study demonstrated that treatment with CT extracts disrupted KSHV latency in the viral-infected host cells, iSLK-BAC16. n-Hexane and EtOH fractions of CT extracts critically affected at least two stages of the KHSV life-cycle by abnormally inducing KSHV lytic reactivation and by severely preventing KSHV virion release from the viral host cells. In addition to the effects on
KSHV itself, CT extract treatments induced cellular modifications by dysregulating cell-cycle and producing strong cytotoxicity. This study demonstrated for the first time that CT extracts have antiviral activities that could be applied to development of new anti-gammaherpesviral agents.
-
Citations
Citations to this article as recorded by 
- Carbon quantum dots reduced Ru nanoparticles loaded on the surface of MWCNTs for high-performance kaempferol sensing
Mengting Wang, Le Li, Yonghong Zhao, Gaixia Liu, Xiaoqian Zhang, Yanbing Chen, Chen Li, Zhengjiu Wang, Na Zhao, Shiguo Sun Microchemical Journal.2025; 215: 114478. CrossRef - Clinical efficacy and mechanistic insights of Xuebijing in hand, foot, and mouth disease: a meta-analysis with integrated pharmacological approaches
Jiaqi Li, Lei Wang, Ziqi Li, Yihan Sun, Meiyu Yu, Boying Xiao, Junyuan Lv, He Li, Jianming Wang, Hao Wen Annals of Medicine & Surgery.2025; 87(7): 4414. CrossRef - Carthami flos: a review of its ethnopharmacology, pharmacology and clinical applications
Yanhua Tu, Yingru Xue, Dandan Guo, Lianna Sun, Meili Guo Revista Brasileira de Farmacognosia.2015; 25(5): 553. CrossRef - Bioactive activities of natural products against herpesvirus infection
Myoungki Son, Minjung Lee, Gi-Ho Sung, Taeho Lee, Yu Su Shin, Hyosun Cho, Paul M. Lieberman, Hyojeung Kang Journal of Microbiology.2013; 51(5): 545. CrossRef
|