Journal Articles
- Roseovarius tibetensis sp. nov., a halophilic bacterium isolated from Lake LongmuCo on Tibetan Plateau
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Hui-bin Lu , Xiao-feng Xue , Dorji Phurbu , Peng Xing , Qing-long Wu
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J. Microbiol. 2018;56(11):783-789. Published online October 24, 2018
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DOI: https://doi.org/10.1007/s12275-018-8178-0
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Abstract
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Two Gram-stain negative halophilic strains, designated as
LM2T and LM4, were isolated from Lake LongmuCo on
Tibetan Plateau. These two strains were aerobic, catalaseand
oxidase- positive, nonmotile and rod-shaped organisms.
Phylogenetic analysis based on 16S rRNA gene sequences
indicated that LM2T and LM4 belong to the genus Roseovarius,
with Roseovarius tolerans EL-172T (97.3% and 97.4%
16S rRNA gene sequence similarity, respectively) and Roseovarius
azorensis SSW084T (95.5% and 95.6% 16S rRNA gene
sequence similarity, respectively) as their closest neighbors.
Q-10 was the sole respiratory quinone of these two strains.
The major fatty acids were C18:1 ω7c/C18:1 ω6c, C16:0, C19:0 cyclo
ω8c, and 11-methyl C18:1 ω7c. The polar lipids included
phosphatidylglycerol, diphosphatidylglycerol, phosphatidylethanolamine,
phosphatidylcholine, phospholipid of unknown
structure containing glucosamine, and unidentified
aminolipid. The DNA G + C content was between 64.2 and
64.5 mol%. DNA-DNA hybridization showed 96.7% relatedness
between LM2T and LM4, 24.9% relatedness between
LM2T and R. tolerans EL-172T, and 36.3% relatedness between
LM4 and R. tolerans EL-172T. Based on phylogenetic
analysis, DNA-DNA hybridization, a range of physiological
and biochemical characteristics, LM2T and LM4 belong to
the same species and were clearly distinguished from the type
strains of the genus Roseovarius. It was evident that LM2T
and LM4 could be classified as a novel species of the genus
Roseovarius, for which the name Roseovarius tibetensis sp. nov.
is proposed. The type strain is LM2T (= CGMCC 1.16230T =
KCTC 62028T).
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- Lithoautotrophic lifestyle of the widespread genusRoseovariusrevealed by physiological and genomic characterization ofRoseovarius autotrophicussp. nov
Galina Slobodkina, Nataliya Ratnikova, Alexander Merkel, Vadim Kevbrin, Alexandra Kuchierskaya, Alexander Slobodkin
FEMS Microbiology Ecology.2022;[Epub] CrossRef - Duganella rivus sp. nov., Duganella fentianensis sp. nov., Duganella qianjiadongensis sp. nov. and Massilia guangdongensis sp. nov., isolated from subtropical streams in China and reclassification of all species within genus Pseudoduganella
Hui-Bin Lu, Zhi-Peng Cai, Yong-Gang Yang, Mei-Ying Xu
Antonie van Leeuwenhoek.2020; 113(8): 1155. CrossRef - Massilia aquatica sp. nov., Isolated from a Subtropical Stream in China
Hui-Bin Lu, Tong-Chu Deng, Mei-Ying Xu
Current Microbiology.2020; 77(10): 3185. CrossRef -
Halomonas rituensis sp. nov. and Halomonas zhuhanensis sp. nov., isolated from natural salt marsh sediment on the Tibetan Plateau
Peixin Gao, Huibin Lu, Peng Xing, Qinglong L. Wu
International Journal of Systematic and Evolutionary Microbiology
.2020; 70(10): 5217. CrossRef -
Roseovarius spongiae sp. nov., a bacterium isolated from marine sponge
Lingping Zhuang, Lianzhong Luo
International Journal of Systematic and Evolutionary Microbiology
.2020; 70(1): 274. CrossRef - List of new names and new combinations previously effectively, but not validly, published
Aharon Oren, George M. Garrity
International Journal of Systematic and Evolutionary Microbiology.2019; 69(3): 597. CrossRef
- Microbial diversity in the rumen, reticulum, omasum, and abomasum of yak on a rapid fattening regime in an agro-pastoral transition zone
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Dan Xue , Huai Chen , Xiaolin Luo , Jiuqiang Guan , Yixin He , Xinquan Zhao
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J. Microbiol. 2018;56(10):734-743. Published online August 22, 2018
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DOI: https://doi.org/10.1007/s12275-018-8133-0
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Abstract
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The ruminant digestive system harbors a complex gut microbiome,
which is poorly understood in the case of the four
stomach compartments of yak. High-throughput sequencing
and quantitative PCR were used to analyse microbial communities
in the rumen, reticulum, omasum, and abomasum of
six domesticated yak. The diversity of prokaryotes was higher
in reticulum and omasum than in rumen and abomasum.
Bacteroidetes predominated in the four stomach compartments,
with abundance gradually decreasing in the trend
rumen > reticulum > omasum > abomasum. Microorganism
composition was different among the four compartments,
all of which contained high levels of bacteria, methanogens,
protozoa and anaerobic fungi. Some prokaryotic genera were
associated with volatile fatty acids and pH. This study provides
the first insights into the microorganism composition
of four stomach compartments in yak, and may provide a
foundation for future studies in this area.
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Microorganisms.2023; 11(9): 2219. CrossRef - “The Yak”—A remarkable animal living in a harsh environment: An overview of its feeding, growth, production performance, and contribution to food security
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Frontiers in Veterinary Science.2023;[Epub] CrossRef - Effects of Two Different Straw Pellets on Yak Growth Performance and Ruminal Microbiota during Cold Season
Xiangyan Wang, Bingang Shi, Zhi Zuo, Youpeng Qi, Shijie Zhao, Xueping Zhang, Lijuan Lan, Yu Shi, Xiu Liu, Shaobin Li, Jiqing Wang, Jiang Hu
Animals.2023; 13(3): 335. CrossRef - Isoacids supplementation improves growth performance and feed fiber digestibility associated with ruminal bacterial community in yaks
Fei Jiang, Yanhua Gao, Zhongli Peng, Xiulian Ma, Yinjie You, Zhibin Hu, Anxiang He, Yupeng Liao
Frontiers in Microbiology.2023;[Epub] CrossRef - Representativeness of Fecal Microbiota Is Limited to Cecum and Colon in Domestic Yak
Wen Qin, Pengfei Song, Jirong Li, Jiuxiang Xie, Shoudong Zhang
Sustainability.2022; 14(16): 10263. CrossRef - Dynamic changes in the yak rumen eukaryotic community and metabolome characteristics in response to feed type
Xiaojing Cui, Yue Liu, Hao Wu, Qingxiang Meng, Shujie Liu, Shatuo Chai, Lizhuang Hao, Zhenming Zhou
Frontiers in Veterinary Science.2022;[Epub] CrossRef - The Response of Ruminal Microbiota and Metabolites to Different Dietary Protein Levels in Tibetan Sheep on the Qinghai-Tibetan Plateau
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Frontiers in Veterinary Science.2022;[Epub] CrossRef - Yak Gut Microbiota: A Systematic Review and Meta-Analysis
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Frontiers in Microbiology.2022;[Epub] CrossRef - Effects of trace minerals supply from rumen sustained release boluses on milk yields and components, rumen fermentation and the rumen bacteria in lactating yaks (Bos grunniens)
Z.W. Zhao, Z.Y. Ma, H.C. Wang, C.F. Zhang
Animal Feed Science and Technology.2022; 283: 115184. CrossRef - Characterization of the bacterial microbiota across the different intestinal segments of the Qinghai semi-fine wool sheep on the Qinghai-Tibetan Plateau
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Animal Bioscience.2021; 34(12): 1921. CrossRef - Multi-Omics Analysis Reveals a Dependent Relationship Between Rumen Bacteria and Diet of Grass- and Grain-Fed Yaks
Chenchen Xu, Wenwen Liu, Baozhong Sun, Songshan Zhang, Shou Zhang, Yuanli Yang, Yuanhua Lei, Lan Chang, Peng Xie, Huayi Suo
Frontiers in Microbiology.2021;[Epub] CrossRef - Bacterial Community Characteristics in the Gastrointestinal Tract of Yak (Bos grunniens) Fully Grazed on Pasture of the Qinghai-Tibetan Plateau of China
Xueping Han, Hongjin Liu, Linyong Hu, Na Zhao, Shixiao Xu, Zhijia Lin, Yongwei Chen
Animals.2021; 11(8): 2243. CrossRef - Effects of rumen-protected methionine and lysine supplementation on milk yields and components, rumen fermentation, and the rumen microbiome in lactating yaks (Bos grunniens)
Z.W. Zhao, Z.Y. Ma, H.C. Wang, C.F. Zhang
Animal Feed Science and Technology.2021; 277: 114972. CrossRef - Response of sheep rumen fermentation and microbial communities to feed infected with the endophyte Epichloë gansuensis as evaluated with rumen-simulating technology
Yaling Ma, Hucheng Wang, Chunjie Li
Journal of Microbiology.2021; 59(8): 718. CrossRef - Brisket Disease Is Associated with Lower Volatile Fatty Acid Production and Altered Rumen Microbiome in Holstein Heifers
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Frontiers in Veterinary Science.2020;[Epub] CrossRef - Comparing the Bacterial Community in the Gastrointestinal Tracts Between Growth-Retarded and Normal Yaks on the Qinghai–Tibetan Plateau
Jian Ma, Yixiao Zhu, Zhisheng Wang, Xiong Yu, Rui Hu, Xueying Wang, Guang Cao, Huawei Zou, Ali Mujtaba Shah, Quanhui Peng, Bai Xue, Lizhi Wang, Suonan Zhao, Xiangying Kong
Frontiers in Microbiology.2020;[Epub] CrossRef - Bacterial communities in the solid, liquid, dorsal, and ventral epithelium fractions of yak (Bos grunniens) rumen
Qingmiao Ren, Huazhe Si, Xiaoting Yan, Chang Liu, Luming Ding, Ruijun Long, Zhipeng Li, Qiang Qiu
MicrobiologyOpen.2020;[Epub] CrossRef - Interactions Between Rumen Microbes, VFAs, and Host Genes Regulate Nutrient Absorption and Epithelial Barrier Function During Cold Season Nutritional Stress in Tibetan Sheep
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Frontiers in Microbiology.2020;[Epub] CrossRef - Yak rumen microbial diversity at different forage growth stages of an alpine meadow on the Qinghai-Tibet Plateau
Li Ma, Shixiao Xu, Hongjin Liu, Tianwei Xu, Linyong Hu, Na Zhao, Xueping Han, Xiaoling Zhang
PeerJ.2019; 7: e7645. CrossRef - Comparing the Microbial Community in Four Stomach of Dairy Cattle, Yellow Cattle and Three Yak Herds in Qinghai-Tibetan Plateau
Jinwei Xin, Zhixin Chai, Chengfu Zhang, Qiang Zhang, Yong Zhu, Hanwen Cao, Jincheng Zhong, Qiumei Ji
Frontiers in Microbiology.2019;[Epub] CrossRef - Dynamic Alterations in Yak Rumen Bacteria Community and Metabolome Characteristics in Response to Feed Type
Chang Liu, Hao Wu, Shujie Liu, Shatuo Chai, Qingxiang Meng, Zhenming Zhou
Frontiers in Microbiology.2019;[Epub] CrossRef
- Halomonas tibetensis sp. nov., isolated from saline lakes on Tibetan Plateau
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Hui-bin Lu , Peng Xing , Lei Zhai , Dorji Phurbu , Qian Tang , Qing-long Wu
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J. Microbiol. 2018;56(7):493-499. Published online June 14, 2018
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DOI: https://doi.org/10.1007/s12275-018-8076-5
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Abstract
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Strains pyc13T and ZGT13 were isolated from Lake Pengyan
and Lake Zigetang on Tibetan Plateau, respectively. Both
strains were Gram-negative, catalase- and oxidase-positive,
aerobic, rod-shaped, nonmotile, and nonflagellated bacteria.
Phylogenetic analysis based on 16S rRNA gene sequences
showed that strains pyc13T and ZGT13 belong to the genus
Halomonas, with Halomonas alkalicola 56-L4-10aEnT as
their closest neighbor, showing 97.4% 16S rRNA gene sequence
similarity. The predominant respiratory quinone of
both strains was Q-9, with Q-8 as a minor component. The
major fatty acids of both strains were C18:1 ω6c/C18:1 ω7c,
C16:1 ω6c/C16:1 ω7c, C16:0, and C12:0 3OH. The polar lipids of
both strains consisted of phosphatidylethanolamine, phosphatidylglycerol,
diphosphatidylglycerol, glycolipid, phospholipids
of unknown structure containing glucosamine,
and unidentified phospholipids. The DNA G + C content of
pyc13T and ZGT13 were 62.6 and 63.4 mol%, respectively.
The DNA-DNA hybridization values of strain pyc13T were
34, 41, 61, 35, and 35% with the reference strains H. alkalicola
56-L4-10aEnT, H. sediminicola CPS11T, H. mongoliensis
Z-7009T, H. ventosae Al12T, and H. fontilapidosi 5CRT, respectively.
Phenotypic, biochemical, genotypic, and DNA-DNA
hybridization data showed that strains pyc13T and ZGT13
represent a new species within the genus Halomonas, for
which the name H. tibetensis sp. nov. is proposed. The type
strain is pyc13T (= CGMCC 1.15949T = KCTC 52660T).
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Citations
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- The Bacterial Microbiota of Artisanal Cheeses from the Northern Caucasus
Tatiana V. Kochetkova, Ilya P. Grabarnik, Alexandra A. Klyukina, Kseniya S. Zayulina, Liliya A. Gavirova, Polina A. Shcherbakova, Gennady S. Kachmazov, Andrey I. Shestakov, Ilya V. Kublanov, Alexander G. Elcheninov
Fermentation.2023; 9(8): 719. CrossRef -
Halomonas profundi sp. nov., isolated from deep-sea sediment of the Mariana Trench
Fan Wang, Jin-Jian Wan, Xi-Ying Zhang, Yu Xin, Mei-Ling Sun, Peng Wang, Wei-Peng Zhang, Ji-Wei Tian, Yu-Zhong Zhang, Chun-Yang Li, Hui-Hui Fu
International Journal of Systematic and Evolutionary Microbiology
.2022;[Epub] CrossRef - Halomonas jincaotanensis sp. nov., isolated from the Pamir Plateau degrading polycyclic aromatic hydrocarbon
Xuying Bu, Zhanfeng Xia, Zhanwen Liu, Min Ren, Chuanxing Wan, Lili Zhang
Archives of Microbiology.2022;[Epub] CrossRef -
Halomonas rituensis sp. nov. and Halomonas zhuhanensis sp. nov., isolated from natural salt marsh sediment on the Tibetan Plateau
Peixin Gao, Huibin Lu, Peng Xing, Qinglong L. Wu
International Journal of Systematic and Evolutionary Microbiology
.2020; 70(10): 5217. CrossRef -
Halomonas montanilacus sp. nov., isolated from hypersaline Lake Pengyanco on the Tibetan Plateau
Huibin Lu, Peng Xing, Lei Zhai, Huabing Li, Qinglong Wu
International Journal of Systematic and Evolutionary Microbiology
.2020; 70(4): 2859. CrossRef - List of new names and new combinations previously effectively, but not validly, published
Aharon Oren, George M. Garrity
International Journal of Systematic and Evolutionary Microbiology.2018; 68(11): 3379. CrossRef
Research Support, Non-U.S. Gov't
- A Survey of the Geographic Distribution of Ophiocordyceps sinensis
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Yi Li , Xiao-Liang Wang , Lei Jiao , Yi Jiang , Hui Li , Si-Ping Jiang , Ngarong Lhosumtseiring , Shen-Zhan Fu , Cai-Hong Dong , Yu Zhan , Yi-Jian Yao
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J. Microbiol. 2011;49(6):913-919. Published online December 28, 2011
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DOI: https://doi.org/10.1007/s12275-011-1193-z
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Abstract
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Ophiocordyceps sinensis is one of the best known fungi in Traditional Chinese Medicine. Many efforts have been devoted to locating the production areas of this species resulting in various reports; however, its geographic distribution remains incompletely understood. Distribution of O. sinensis at the county level is clarified in this work based on both a literature search and fieldwork. More than 3600 publications related to O. sinensis were investigated, including scientific papers, books, and online information. Herbarium specimens of O. sinensis and field collections made by this research group during the years 2000-2010 were examined to verify the distribution sites. A total of 203 localities for O. sinensis have been found, of which 106 are considered as confirmed distribution sites, 65 as possible distribution sites, 29 as excluded distribution sites and three as suspicious distribution sites. The results show that O. sinensis is confined to the Tibetan Plateau and its surrounding regions, including Tibet, Gansu, Qinghai, Sichuan, and Yunnan provinces in China and in certain areas of the southern flank of the Himalayas, in the countries of Bhutan, India and Nepal, with 3,000 m as the lowest altitude for the distribution. The fungus is distributed from the southernmost site in Yulong Naxi Autonomous County in northwestern Yunnan Province to the northernmost site in the Qilian Mountains in Qilian County, Qinghai Province, and from the east edge of the Tibetan Plateau in Wudu County, Gansu Province to the westernmost site in Uttarakhand, India. The clarification of the geographic distribution of O. sinensis will lay the foundation for conservation and sustainable use of the species.
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Peter W. Heger, Ilka Meinert, Peter Nick, Peter Riedl, Michael Heinrich, Michael Straub
Pharmaceutical Biology.2025; 63(1): 82. CrossRef - Integrating 2D NMR-based metabolomics and in vitro assays to explore the potential viability of cultivated Ophiocordyceps sinensis as an alternative to the wild counterpart
Xiu Gu, Yanping Li, Yang Li, Xiaohui Duan, Youfan Hu, Jialuo Chen, Huan Du, Jing Bai, Chengyan He, Caihong Bai, Jinlin Guo, Jiahui Yang, Kaifeng Hu
Journal of Pharmaceutical and Biomedical Analysis.2025; 253: 116551. CrossRef - Comparative Metabolite Profiling Between Cordyceps sinensis and Other Cordyceps by Untargeted UHPLC-MS/MS
Jing Ma, Zhenjiang Chen, Kamran Malik, Chunjie Li
Biology.2025; 14(2): 118. CrossRef - Integrating divergent stakeholder perspectives for sustainable management of high-altitude ecosystems: insights from cordyceps harvesting in the Himalayas
Suraj Upadhaya, Beeju Poudyal, Chantal Tumpach
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Nadeem Salam, Harvinder Kaur Sidhu, Shaheeda Shaban, Zafar A. Reshi, Manzoor A. Shah
Journal of Asia-Pacific Biodiversity.2025; 18(1): 144. CrossRef - Molecular phylogenetics of the Ophiocordyceps sinensis-species complex lineage (Ascomycota, Hypocreales), with the discovery of new species and predictions of species distribution
Yongdong Dai, Siqi Chen, Yuanbing Wang, Yao Wang, Zhuliang Yang, Hong Yu
IMA Fungus.2024;[Epub] CrossRef - Ethnopharmacology and current conservational status of Cordyceps sinensis
Payas Arora, Nikita Bahuguna, Jigisha Anand, Prabhakar Semwal, Nishant Rai
Zeitschrift für Naturforschung C.2024;[Epub] CrossRef - Cordyceps: Alleviating ischemic cardiovascular and cerebrovascular injury - A comprehensive review
Yong Li, Liying He, Haoran Song, Xiuwen Bao, Shuqi Niu, Jing Bai, Junhao Ma, Run Yuan, Sijing Liu, Jinlin Guo
Journal of Ethnopharmacology.2024; 332: 118321. CrossRef - Effects of Drying Methods on Morphological Characteristics, Metabolite Content, and Antioxidant Capacity of Cordyceps sinensis
Mengjun Xiao, Tao Wang, Chuyu Tang, Min He, Yuling Li, Xiuzhang Li
Foods.2024; 13(11): 1639. CrossRef - Conservation of Endangered Cordyceps sinensis Through Artificial Cultivation Strategies of C. militaris, an Alternate
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Molecular Biotechnology.2024;[Epub] CrossRef - Quality Evaluation, health risk Assessment, and geographic origin tracing of Ophiocordyceps sinensis through mineral element analysis
Fen Wang, Junfeng Fan, Yabin An, Guoliang Meng, Bingyu Ji, Yi Li, Caihong Dong
Microchemical Journal.2024; 201: 110512. CrossRef - Tracing the geographical origin of endangered fungus Ophiocordyceps sinensis, especially from Nagqu, using UPLC-Q-TOF-MS
Fen Wang, Junfeng Fan, Yabin An, Guoliang Meng, Bingyu Ji, Yi Li, Caihong Dong
Food Chemistry.2024; 440: 138247. CrossRef - Knockdown of Thitarodes host genes influences dimorphic transition of Ophiocordyceps sinensis in the host hemolymph
Tanqi Sun, Yongling Jin, Zhongchen Rao, Wang Liyan, Rui Tang, Khalid Muhammad Zaryab, Mingyan Li, Zhenhao Li, Ying Wang, Jing Xu, Richou Han, Li Cao
Frontiers in Cellular and Infection Microbiology.2024;[Epub] CrossRef - Nutritional Profile Changes in an Insect–Fungus Complex of Antheraea pernyi Pupa Infected by Samsoniella hepiali
Shengchao Wang, Yun Meng, Dun Wang
Foods.2023; 12(14): 2796. CrossRef - Systematic analyses with genomic and metabolomic insights reveal a new species, Ophiocordyceps indica sp. nov. from treeline area of Indian Western Himalayan region
Aakriti Sharma, Ekjot Kaur, Robin Joshi, Pooja Kumari, Abhishek Khatri, Mohit Kumar Swarnkar, Dinesh Kumar, Vishal Acharya, Gireesh Nadda
Frontiers in Microbiology.2023;[Epub] CrossRef - Traceability Evaluation of Wild and Cultivated Cordyceps sinensis by Elemental Analysis and GasBench II Coupled to Stable Isotope Ratio Mass Spectrometry
Bo Ding, Yiwen Tao, Jianjun Xie, Guangfeng Zeng, Hongbo Huang
Food Analytical Methods.2023; 16(3): 515. CrossRef - Fractional extraction and structural characterization of glycogen particles from the whole cultivated caterpillar fungus Ophiocordyceps sinensis
Qing-Hua Liu, Yu-Dong Zhang, Zhang-Wen Ma, Zheng-Ming Qian, Zhi-Hong Jiang, Wei Zhang, Liang Wang
International Journal of Biological Macromolecules.2023; 229: 507. CrossRef - Systematic review of fungi, their diversity and role in ecosystem services from the Far Eastern Himalayan Landscape (FHL)
Wei Fang, Shiva Devkota, Karuppusamy Arunachalam, Khin Min Min Phyo, Bandana Shakya
Heliyon.2023; 9(1): e12756. CrossRef - Potential bioactivities via anticancer, antioxidant, and immunomodulatory properties of cultured mycelial enriched β-D-glucan polysaccharides from a novel fungus Ophiocordyceps sinensis OS8
Suwannachom Chatnarin, Mongkol Thirabunyanon
Frontiers in Immunology.2023;[Epub] CrossRef - Integrated metabolomics and transcriptomics reveal metabolites difference between wild and cultivated Ophiocordyceps sinensis
Jianshuang Zhang, Na Wang, Wanxuan Chen, Weiping Zhang, Haoshen Zhang, Hao Yu, Yin Yi
Food Research International.2023; 163: 112275. CrossRef - Uncovering caterpillar fungus (Ophiocordyceps sinensis) consumption patterns and linking them to conservation interventions
Jun He, Carsten Smith‐Hall, Wen Zhou, Weijia Zhou, Yunshang Wang, Ben Fan
Conservation Science and Practice.2022;[Epub] CrossRef - Understanding the sustainability of Chinese caterpillar fungus harvesting: the need for better data
Carsten Smith-Hall, Rune B. Bennike
Biodiversity and Conservation.2022; 31(2): 729. CrossRef - Medium optimization for high mycelial soluble protein content of Ophiocordyceps sinensis using response surface methodology
Chu-Yu Tang, Jie Wang, Xin Liu, Jian-Bo Chen, Jing Liang, Tao Wang, Wayne Roydon Simpson, Yu-Ling Li, Xiu-Zhang Li
Frontiers in Microbiology.2022;[Epub] CrossRef - Lipidomic profiling of wild cordyceps and its substituents by liquid chromatography-electrospray ionization-tandem mass spectrometry
Manting Lin, Shan Guo, Di Xie, Sheng Li, Hankun Hu
LWT.2022; 163: 113497. CrossRef - The potential role of medicinal mushrooms as prebiotics in aquaculture: A review
Kannan Mohan, Durairaj Karthick Rajan, Thirunavukkarasu Muralisankar, Abirami Ramu Ganesan, Kasi Marimuthu, Palanivel Sathishkumar
Reviews in Aquaculture.2022; 14(3): 1300. CrossRef - Glyceroglycolipids from the solid culture of Ophiocordyceps sinensis strain LY34 isolated from Tibet of China
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Mycology.2022; 13(3): 185. CrossRef -
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International Journal of Medicinal Mushrooms.2022; 24(11): 21. CrossRef - Microbial Diversity Analyses of Fertilized Thitarodes Eggs and Soil Provide New Clues About the Occurrence of Chinese Cordyceps
Yue-Hui Hong, Zhan-Hua Mai, Cheng-Ji Li, Qiu-Yi Zheng, Lian-Xian Guo
Current Microbiology.2022;[Epub] CrossRef - Novel formulation development from Ophiocordyceps sinensis (Berk.) for management of high-altitude maladies
Rakhee, Jigni Mishra, Renu Bala Yadav, D. K. Meena, Rajesh Arora, R. K. Sharma, Kshipra Misra
3 Biotech.2021;[Epub] CrossRef - Advances in research on chemical constituents and pharmacological effects of Paecilomyces hepiali
Akang Dan, Yujia Hu, Ruyan Chen, Xiangyang Lin, Yongqi Tian, Shaoyun Wang
Food Science and Human Wellness.2021; 10(4): 401. CrossRef - Typification of Sphaeria sinensis to precisely fix the application of the name of the economically important Chinese caterpillar fungus, Ophiocordyceps sinensis
Yi Li, Lan Jiang, David L. Hawksworth, Yong‐Hui Wang, Jiao‐Jiao Lu, Yi‐Jian Yao
TAXON.2021; 70(6): 1329. CrossRef - Potential range expansion and niche shift of the invasive Hyphantria cunea between native and invasive countries
Xinggang Tang, Yingdan Yuan, Xiaofei Liu, Jinchi Zhang
Ecological Entomology.2021; 46(4): 910. CrossRef - Structure and immunomodulatory activity of a water-soluble α-glucan from Hirsutella sinensis mycelia
Lin Rong, Guoqiang Li, Yuxia Zhang, Yuancan Xiao, Yajun Qiao, Mengmeng Yang, Lixin Wei, Hongtao Bi, Tingting Gao
International Journal of Biological Macromolecules.2021; 189: 857. CrossRef - Chinese caterpillar fungus (Ophiocordyceps sinensis) in China: Current distribution, trading, and futures under climate change and overexploitation
Yanqiang Wei, Liang Zhang, Jinniu Wang, Wenwen Wang, Naudiyal Niyati, Yanlong Guo, Xufeng Wang
Science of The Total Environment.2021; 755: 142548. CrossRef - Moderate warming will expand the suitable habitat of Ophiocordyceps sinensis and expand the area of O. sinensis with high adenosine content
Yanlong Guo, Zefang Zhao, Xin Li
Science of The Total Environment.2021; 787: 147605. CrossRef - The complete mitochondrial genome of Ophiocordyceps gracilis and its comparison with related species
Aifeire Abuduaini, Yuan-Bing Wang, Hui-Ying Zhou, Rui-Ping Kang, Ming-Liang Ding, Yu Jiang, Fei-Ya Suo, Luo-Dong Huang
IMA Fungus.2021;[Epub] CrossRef - Arsenic Content, Speciation, and Distribution in Wild Cordyceps sinensis
Yuancan Xiao, Cen Li, Wei Xu, Yuzhi Du, Ming Zhang, Hongxia Yang, Lixin Wei, Hongtao Bi, Adolfo Andrade-Cetto
Evidence-Based Complementary and Alternative Medicine.2021; 2021: 1. CrossRef - A simple and effective method to discern the true commercial Chinese cordyceps from counterfeits
Fu-Li Zhang, Xiao-Feng Yang, Dong Wang, Shao-Rong Lei, Ling-An Guo, Wen-Juan Liu, Jun Song
Scientific Reports.2020;[Epub] CrossRef - Analysis of Volatile Components in Different Ophiocordyceps sinensis and Insect Host Products
Xuehong Qiu, Li Cao, Richou Han
Molecules.2020; 25(7): 1603. CrossRef - Quorum Sensing Activity and Hyphal Growth by External Stimuli in the Entomopathogenic Fungus Ophiocordyceps sinensis
Guiqing Liu, Li Cao, Xuehong Qiu, Richou Han
Insects.2020; 11(4): 205. CrossRef - Genomic analyses reveal evolutionary and geologic context for the plateau fungus Ophiocordyceps sinensis
Jie Liu, Linong Guo, Zongwei Li, Zhe Zhou, Zhen Li, Qian Li, Xiaochen Bo, Shengqi Wang, Junli Wang, Shuangcheng Ma, Jian Zheng, Ying Yang
Chinese Medicine.2020;[Epub] CrossRef - Comparative metabolic profiling of Ophiocordyceps sinensis and its cultured mycelia using GC–MS
Jianshuang Zhang, Hao Yu, Shaosong Li, Xin Zhong, Haizhen Wang, Xin Liu
Food Research International.2020; 134: 109241. CrossRef - Uncovering fungal community composition in natural habitat of Ophiocordyceps sinensis using high-throughput sequencing and culture-dependent approaches
Chuan-Bo Zhang, Chao-Hui Ren, Yan-Li Wang, Qi-Qi Wang, Yun-Sheng Wang, Qing-Bei Weng
BMC Microbiology.2020;[Epub] CrossRef - Revealing mitogenome-wide DNA methylation and RNA editing of three Ascomycotina fungi using SMRT sequencing
Chaoxia Wang, Jianhua Feng, Yujiao Chen, Dongmei Li, Li Liu, Yuqian Wu, Shujun Zhang, Simiao Du, Yaozhou Zhang
Mitochondrion.2020; 51: 88. CrossRef - Microscopic Authentication of Commercial Herbal Products in the Globalized Market: Potential and Limitations
Mihael Cristin Ichim, Annette Häser, Peter Nick
Frontiers in Pharmacology.2020;[Epub] CrossRef - Vegetative development and host immune interaction of Ophiocordyceps sinensis within the hemocoel of the ghost moth larva, Thitarodes xiaojinensis
Miaomiao Li, Qian Meng, Huan Zhang, Ruoyao Ni, Guiling Zhou, Yanni Zhao, Peipei Wu, Ruihao Shu, Qilian Qin, Jihong Zhang
Journal of Invertebrate Pathology.2020; 170: 107331. CrossRef - Composition and predictive functional analysis of bacterial communities inhabiting Chinese Cordyceps insight into conserved core microbiome
Fei Xia, Xin Zhou, Yan Liu, Yuling Li, Xiaohui Bai, Xuanwei Zhou
BMC Microbiology.2019;[Epub] CrossRef - Characterization of Humic Substances in the Soils of Ophiocordyceps sinensis Habitats in the Sejila Mountain, Tibet: Implication for the Food Source of Thitarodes Larvae
Yan Li, Lian-Xian Guo, Qian-Zhi Zhou, Di Chen, Jin-Zhong Liu, Xiao-Ming Xu, Jiang-Hai Wang
Molecules.2019; 24(2): 246. CrossRef - Artificial Cultivation of the Chinese Cordyceps From Injected Ghost Moth Larvae
Guiqing Liu, Richou Han, Li Cao, Rebecca Schmidt-Jeffris
Environmental Entomology.2019; 48(5): 1088. CrossRef - Comparative study of the composition of cultivated, naturally grown Cordyceps sinensis, and stiff worms across different sampling years
Yujue Zhou, Min Wang, Hui Zhang, Zhuo Huang, Jun Ma, Branislav T. Šiler
PLOS ONE.2019; 14(12): e0225750. CrossRef - Complete mitochondrial genome of two Thitarodes species (Lepidoptera, Hepialidae), the host moths of Ophiocordyceps sinensis and phylogenetic implications
Min Zhang, Zhimei Gao, Jie Yin, Tingting Zhang, Xueyao Zhang, Dongwei Yuan, Tao Li, Yang Zhong, Enbo Ma, Zhumei Ren
International Journal of Biological Macromolecules.2019; 140: 794. CrossRef - Phylogeographic structures of the host insects of Ophiocordyceps sinensis
Yongdong Dai, Changkui Wu, Yuanbing Wang, Yao Wang, Luodong Huang, Xijun Dang, Xuanxue Mo, Pusheng Zeng, Zhuliang Yang, Darong Yang, Canming Zhang, Paul Lemetti, Hong Yu
Zoology.2019; 134: 27. CrossRef - High altitude organic gold: The production network for Ophiocordyceps sinensis from far-western Nepal
Mariève Pouliot, Dipesh Pyakurel, Carsten Smith-Hall
Journal of Ethnopharmacology.2018; 218: 59. CrossRef - Investigation on natural resources and species conservation of Ophiocordyceps sinensis, the famous medicinal fungus endemic to the Tibetan Plateau
Wenjing Wang, Ke Wang, Xiaoliang Wang, Ruiheng Yang, Yi Li, Yijian Yao
Protein & Cell.2018; 9(8): 671. CrossRef - Fungus-larva relation in the formation of Cordyceps sinensis as revealed by stable carbon isotope analysis
Lian-Xian Guo, Yue-Hui Hong, Qian-Zhi Zhou, Qing Zhu, Xiao-Ming Xu, Jiang-Hai Wang
Scientific Reports.2017;[Epub] CrossRef - SMRT Sequencing Revealed Mitogenome Characteristics and Mitogenome-Wide DNA Modification Pattern in Ophiocordyceps sinensis
Xincong Kang, Liqin Hu, Pengyuan Shen, Rui Li, Dongbo Liu
Frontiers in Microbiology.2017;[Epub] CrossRef - The mitochondrial genome of the lepidopteran host cadaver (Thitarodes sp.) of Ophiocordyceps sinensis and related phylogenetic analysis
Xincong Kang, Yongquan Hu, Jiang Hu, Liqin Hu, Feng Wang, Dongbo Liu
Gene.2017; 598: 32. CrossRef - Range shifts in response to climate change of Ophiocordyceps sinensis, a fungus endemic to the Tibetan Plateau
Yujing Yan, Yi Li, Wen-Jing Wang, Jin-Sheng He, Rui-Heng Yang, Hai-Jun Wu, Xiao-Liang Wang, Lei Jiao, Zhiyao Tang, Yi-Jian Yao
Biological Conservation.2017; 206: 143. CrossRef - Safety assessment of cultivated fruiting body of Ophiocordyceps sinensis evaluated through subacute toxicity in rats
Shin Yee Fung, Sook Shien Lee, Nget Hong Tan, Jayalakshmi Pailoor
Journal of Ethnopharmacology.2017; 206: 236. CrossRef - Detection of Ophiocordyceps sinensis and Its Common Adulterates Using Species-Specific Primers
Yang Liu, Xiao-yue Wang, Zi-tong Gao, Jian-ping Han, Li Xiang
Frontiers in Microbiology.2017;[Epub] CrossRef - Stable Carbon Isotope Composition of the Lipids in Natural Ophiocordyceps sinensis from Major Habitats in China and Its Substitutes
Lian-Xian Guo, Xiao-Ming Xu, Yue-Hui Hong, Yan Li, Jiang-Hai Wang
Molecules.2017; 22(9): 1567. CrossRef - Potential molecular mechanisms for fruiting body formation of Cordyceps illustrated in the case ofCordyceps sinensis
Kun Feng, Lan-ying Wang, Dong-jiang Liao, Xin-peng Lu, De-jun Hu, Xiao Liang, Jing Zhao, Zi-yao Mo, Shao-ping Li
Mycology.2017; 8(4): 231. CrossRef - Collecting Ophiocordyceps sinensis: an emerging livelihood strategy in the Garhwal, Indian Himalaya
Laura Caplins, Sarah J. Halvorson
Journal of Mountain Science.2017; 14(2): 390. CrossRef - Extraction, characterization and antioxidant activity of mycelial polysaccharides from Paecilomyces hepiali HN1
Zhongwei Wu, Mingxia Zhang, Minhao Xie, Zhuqing Dai, Xiaoqing Wang, Bing Hu, Hong Ye, Xiaoxiong Zeng
Carbohydrate Polymers.2016; 137: 541. CrossRef - Cordyceps collected from Bhutan, an appropriate alternative of Cordyceps sinensis
Ding-Tao Wu, Guang-Ping Lv, Jian Zheng, Qian Li, Shuang-Cheng Ma, Shao-Ping Li, Jing Zhao
Scientific Reports.2016;[Epub] CrossRef - Laboratory Rearing ofThitarodes armoricanusandThitarodes jianchuanensis(Lepidoptera: Hepialidae), Hosts of the Chinese Medicinal FungusOphiocordyceps sinensis(Hypocreales: Ophiocordycipitaceae)
Zui Tao, Li Cao, Yi Zhang, Yunshou Ye, Richou Han
Journal of Economic Entomology.2016; 109(1): 176. CrossRef - Morphological Observations and Fatty Acid Composition of Indoor-Cultivated Cordyceps sinensis at a High-Altitude Laboratory on Sejila Mountain, Tibet
Lian-Xian Guo, Xiao-Ming Xu, Fu-Rui Liang, Jian-Ping Yuan, Juan Peng, Chou-Fei Wu, Jiang-Hai Wang, Rita Grosch
PLOS ONE.2015; 10(5): e0126095. CrossRef - Metabolic characterization of natural and cultured Ophicordyceps sinensis from different origins by 1H NMR spectroscopy
Jianshuang Zhang, Xin Zhong, Shaosong Li, Guren Zhang, Xin Liu
Journal of Pharmaceutical and Biomedical Analysis.2015; 115: 395. CrossRef - Bacterial diversity in native habitats of the medicinal fungus Ophiocordyceps sinensis on Tibetan Plateau as determined using Illumina sequencing data
Rui-Heng Yang, Xiao-Liang Wang, Jin-He Su, Yi Li, Si-Ping Jiang, Fei Gu, Yi-Jian Yao
FEMS Microbiology Letters.2015;[Epub] CrossRef - Complete mitochondrial genome of the medicinal fungus Ophiocordyceps sinensis
Yi Li, Xiao-Di Hu, Rui-Heng Yang, Tom Hsiang, Ke Wang, De-Quan Liang, Fan Liang, De-Ming Cao, Fan Zhou, Ge Wen, Yi-Jian Yao
Scientific Reports.2015;[Epub] CrossRef - Quantitative assessment of the ecological impact of Chinese cordyceps collection in the typical production areas
Yanda Xu, Fen Li, Cui Xu, Shanghua Luo, Shijun Chao, Yang Guo, Chengcheng Liu, Linbo Zhang
Écoscience.2015; 22(2-4): 167. CrossRef - Impact of Climate Change on Potential Distribution of Chinese Caterpillar Fungus (Ophiocordyceps sinensis) in Nepal Himalaya
Uttam Babu Shrestha, Kamaljit S. Bawa, Helge Thorsten Lumbsch
PLoS ONE.2014; 9(9): e106405. CrossRef - Transcriptome analysis of the Ophiocordyceps sinensis fruiting body reveals putative genes involved in fruiting body development and cordycepin biosynthesis
Li Xiang, Ying Li, Yingjie Zhu, Hongmei Luo, Chunfang Li, Xiaolan Xu, Chao Sun, Jingyuan Song, Linchun Shi, Liu He, Wei Sun, Shilin Chen
Genomics.2014; 103(1): 154. CrossRef - Advances in research of the artificial cultivation ofOphiocordyceps sinensisin China
Xuan-Wei Zhou, Lin-Jun Li, En-Wei Tian
Critical Reviews in Biotechnology.2014; 34(3): 233. CrossRef - Detection of Ophiocordyceps sinensis in the roots of plants in alpine meadows by nested-touchdown polymerase chain reaction
Xin Zhong, Qing-yun Peng, Shao-Song Li, Hai Chen, Hong-Xia Sun, Gu-Ren Zhang, Xin Liu
Fungal Biology.2014; 118(4): 359. CrossRef - Chasing Chinese Caterpillar Fungus (Ophiocordyceps sinensis) Harvesters in the Himalayas: Harvesting Practice and Its Conservation Implications in Western Nepal
Uttam Babu Shrestha, Sujata Shrestha, Shivaraj Ghimire, Kamal Nepali, Bharat Babu Shrestha
Society & Natural Resources.2014; 27(12): 1242. CrossRef - Recent advances in Cordyceps sinensis polysaccharides: Mycelial fermentation, isolation, structure, and bioactivities: A review
Jing-Kun Yan, Wen-Qiang Wang, Jian-Yong Wu
Journal of Functional Foods.2014; 6: 33. CrossRef - Evaluation of nutritional and physical stress conditions during vegetative growth on conidial production and germination inOphiocordyceps sinensis
Shu-Yu Ren, Yi-Jian Yao
FEMS Microbiology Letters.2013; 346(1): 29. CrossRef - A real-time qPCR assay to quantify Ophiocordyceps sinensis biomass in Thitarodes larvae
Wei Lei, Shaosong Li, Qingyun Peng, Guren Zhang, Xin Liu
Journal of Microbiology.2013; 51(2): 229. CrossRef - DNA barcoding the commercial Chinese caterpillar fungus
Li Xiang, Jingyuan Song, Tianyi Xin, Yingjie Zhu, Linchun Shi, Xiaolan Xu, Xiaohui Pang, Hui Yao, Wenjia Li, Shilin Chen
FEMS Microbiology Letters.2013; : n/a. CrossRef - Detection ofOphiocordyceps sinensisin soil by quantitative real-time PCR
Qingyun Peng, Xin Zhong, Wei Lei, Guren Zhang, Xin Liu
Canadian Journal of Microbiology.2013; 59(3): 204. CrossRef - On the reliability of DNA sequences ofOphiocordyceps sinensisin public databases
Shu Zhang, Yong-Jie Zhang, Xing-Zhong Liu, Hong Zhang, Dian-Sheng Liu
Journal of Industrial Microbiology and Biotechnology.2013; 40(3-4): 365. CrossRef - A Systematic Review of the Mysterious Caterpillar Fungus Ophiocordyceps sinensis in DongChongXiaCao (冬蟲夏草 Dōng Chóng Xià Cǎo) and Related Bioactive Ingredients
Hui-Chen Lo, Chienyan Hsieh, Fang-Yi Lin, Tai-Hao Hsu
Journal of Traditional and Complementary Medicine.2013; 3(1): 16. CrossRef - Systematic analyses of Ophiocordyceps lanpingensis sp. nov., a new species of Ophiocordyceps in China
Zi-Hong Chen, Yong-Dong Dai, Hong Yu, Kun Yang, Zhong-Lin Yang, Feng Yuan, Wen-Bo Zeng
Microbiological Research.2013; 168(8): 525. CrossRef - Development of conventional and nested PCR assays for the detection of Ophiocordyceps sinensis
Guo‐Sheng Jin, Xiao‐Liang Wang, Yi Li, Wen‐Jing Wang, Rui‐Heng Yang, Shu‐Yu Ren, Yi‐Jian Yao
Journal of Basic Microbiology.2013; 53(4): 340. CrossRef