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Flavobacterium zhairuonensis sp. nov., a gliding bacterium isolated from marine sediment of the East China Sea
Sanjit Chandra Debnath , Ahmed Mohammed Abdo Miyah , Can Chen , Huan Sheng , Xue-Wei Xu , Yue-Hong Wu , Dao-Qiong Zheng , Jin-Zhong Xu , Ya-Nan Di , Pin-Mei Wang , Li Shen
J. Microbiol. 2019;57(12):1065-1072.   Published online September 27, 2019
DOI: https://doi.org/10.1007/s12275-019-9194-4
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AbstractAbstract
A yellow pigmented, Gram-stain-negative, aerobic bacterium designated A5.7T was studied to evaluate the taxonomic position following the modern polyphasic approach. The strain was isolated from sediments near Zhairuo Island, which is situated in the East China Sea. Cells were non-spore forming rods without flagella but showed motility by gliding. Growth was observed at 15–35°C (optimum 28°C), pH 6.0–9.0 (optimum pH 6.5) and 0–2% (w/v) NaCl (optimum 0–0.5%) in LB broth. The major respiratory quinone of A5.7T was menaquinone 6. The major polar lipid of A5.7T was phosphatidylethanolamine and the predominant fatty acids (> 5%) were iso-C15:0, iso-C17:0 3-OH, C15:1 ω6c, iso-C15:0 3-OH, iso-C15:1 G, summed feature 3 (C16:1 ω7c and/or C16:1 ω6c) and summed feature 9 (iso-C17:1 ω9c and/or C16:0 10-methyl). Phylogenetic analysis based on 16S rRNA gene sequences showed that the isolate belongs to the genus Flavobacterium and shares the highest sequence similarities with Flavobacterium sharifuzzamanii A7.6T (98.5%), Flavobacterium tistrianum GB 56.1T (98.3%), Flavobacterium nitrogenifigens NXU-44T (97.8%), Flavobacterium anhuiense D3T (97.6%), Flavobacterium ginsenosidimutans THG 01T (97.6%), and Flavobacterium foetidum CJ42T (97.6%). Digital DNA-DNA hybridization and average nucleotide identity values between the strain and its closest phylogenetic neighbors showed the ranges from 19.6 to 34.1% and 73.7 to 87.9%, respectively. Therefore, based on polyphasic characteristics, strain A5.7T represents a novel species of the genus Flavobacterium for which the name Flavobacterium zhairuonensis sp. nov. is proposed. The type strain is A5.7T (= KCTC 62406T = MCCC 1K03494T).

Citations

Citations to this article as recorded by  
  • Three novel species of the genus Flavobacterium, Flavobacterium odoriferum sp. nov., Flavobacterium fragile sp. nov. and Flavobacterium luminosum sp. nov., isolated from activated sludge
    Qi Ran, Xinran Du, Lin Han, Jingjing Wang, Yue-zhong Li
    International Journal of Systematic and Evolutionary Microbiology .2024;[Epub]     CrossRef
  • Ten Novel Species Belonging to the Genus Flavobacterium, Isolated from Freshwater Environments: F. praedii sp. nov., F. marginilacus sp. nov., F. aestivum sp. nov., F. flavigenum sp. nov., F. luteolum sp. nov., F. gelatinilyticum sp. nov., F. aquiphilum s
    Hyunyoung Jo, Miri S. Park, Yeonjung Lim, Ilnam Kang, Jang-Cheon Cho
    Journal of Microbiology.2023; 61(5): 495.     CrossRef
  • Description of Flavobacterium cyclinae sp. nov. and Flavobacterium channae sp. nov., isolated from the intestines of Cyclina sinensis (Corb shell) and Channa argus (Northern snakehead)
    Seomin Kang, Jae-Yun Lee, Jeong Eun Han, Yun-Seok Jeong, Do-Hun Gim, Jin-Woo Bae
    Journal of Microbiology.2022; 60(9): 890.     CrossRef
  • Flavobacterium litorale sp. nov., isolated from red alga
    Neak Muhammad, Ho Le Han, Yong-Jae Lee, Jaeho Ko, Tra T. H. Nguyen, Song-Gun Kim
    International Journal of Systematic and Evolutionary Microbiology .2022;[Epub]     CrossRef
  • Flavobacterium salilacus sp. nov., isolated from surface water of a hypersaline lake, and descriptions of Flavobacterium salilacus subsp. altitudinum subsp. nov. and Flavobacterium salilacus subsp. salilacus subsp. nov.
    Sanjit Chandra Debnath, Can Chen, Ishrat Khan, Wen-Jie Wang, Dao-Qiong Zheng, Jin-Zhong Xu, Pin-Mei Wang
    International Journal of Systematic and Evolutionary Microbiology .2020; 70(7): 4250.     CrossRef
  • List of new names and new combinations previously effectively, but not validly, published
    Aharon Oren, George Garrity
    International Journal of Systematic and Evolutionary Microbiology .2020; 70(3): 1443.     CrossRef
  • Flavobacterium phycosphaerae sp. nov. isolated from the phycosphere of Microcystis aeruginosa
    Minkyung Kim, Byoung-Hee Lee, Ki-Eun Lee, Woojun Park
    International Journal of Systematic and Evolutionary Microbiology .2019;[Epub]     CrossRef
Trichoderma biodiversity in major ecological systems of China
Kai Dou , Jinxin Gao , Chulong Zhang , Hetong Yang , Xiliang Jiang , Jishun Li , Yaqian Li , Wei Wang , Hongquan Xian , Shigui Li , Yan Liu , Jindong Hu , Jie Chen
J. Microbiol. 2019;57(8):668-675.   Published online May 23, 2019
DOI: https://doi.org/10.1007/s12275-019-8357-7
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  • 28 Web of Science
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AbstractAbstract
An investigation of Trichoderma biodiversity involving a large-scale environmental gradient was conducted to understand the Trichoderma distribution in China. A total of 3,999 isolates were isolated from forestry, grassland, wetland and agriculture ecosystems, and 50 species were identified based on morphological characteristics and sequence analysis of genetic markers. Trichoderma harzianum showed the largest proportion of isolates and the most extensive distribution. Hypocrea semiorbis, T. epimyces, T. konilangbra, T. piluliferum, T. pleurotum, T. pubescens, T. strictipilis, T. hunua, T. oblongisporum and an unidentified species, Trichoderma sp. MA 3642, were first reported in China. Most Trichoderma species were distributed in Jilin and Heilongjiang Provinces in northeast China and the fewest were distributed in Qinghai Province. Based on the division of ecological and geographic factors, forestry ecosystems and low-altitude regions have the greatest species biodiversity of Trichoderma.

Citations

Citations to this article as recorded by  
  • Eleven new species of Trichoderma (Hypocreaceae, Hypocreales) from China
    Rui Zhao, Ke-Yu Chen, Li-Juan Mao, Chu-Long Zhang
    Mycology.2025; 16(1): 180.     CrossRef
  • The Distribution Characteristics of Trichoderma in Turf and Its Inhibitory Effect on Rhizoctonia solani
    Qichen Niu, Lu Gan, Shuxia Yin, Ning Zhang, Xin Suo, Guanfang Jin, Ruoyi Tang, Man Liu
    Agronomy.2025; 15(3): 733.     CrossRef
  • Genomic Characterization and Establishment of a Genetic Manipulation System for Trichoderma sp. (Harzianum Clade) LZ117
    Jie Yang, Cristopher Reyes Loaiciga, Hou-Ru Yue, Ya-Jing Hou, Jun Li, Cheng-Xi Li, Jing Li, Yue Zou, Shuai Zhao, Feng-Li Zhang, Xin-Qing Zhao
    Journal of Fungi.2024; 10(10): 697.     CrossRef
  • Trichoderma Diversity in Mexico: A Systematic Review and Meta-Analysis
    Hector Osvaldo Ahedo-Quero, Teodulfo Aquino-Bolaños, Yolanda Donají Ortiz-Hernández, Edgar García-Sánchez
    Diversity.2024; 16(1): 68.     CrossRef
  • Screening of the Biocontrol Efficacy of Potent Trichoderma Strains against Fusarium oxysporum f.sp. ciceri and Scelrotium rolfsii Causing Wilt and Collar Rot in Chickpea
    Ranjna Kumari, Vipul Kumar, Ananta Prasad Arukha, Muhammad Fazle Rabbee, Fuad Ameen, Bhupendra Koul
    Microorganisms.2024; 12(7): 1280.     CrossRef
  • First report of Trichoderma guizhouense isolated from soil in Türkiye
    Yunus Korkom, Ayhan Yıldız
    Journal of Plant Diseases and Protection.2024; 131(2): 619.     CrossRef
  • Biocontrol mechanisms of poplar leaf blight due to Nigrospora oryzae
    Jing Han, Zhantong Lu, Huifang Zhang, Shida Ji, Bin Liu, Ning Kong, Yongfeng Yang, Baoyue Xing, Zhihua Liu
    Physiologia Plantarum.2024;[Epub]     CrossRef
  • Genetic diversity and antagonistic properties of Trichoderma strains from the crop rhizospheres in southern Rajasthan, India
    Prashant P. Jambhulkar, Bhumica Singh, M. Raja, Adnan Ismaiel, Dilip K. Lakshman, Maharishi Tomar, Pratibha Sharma
    Scientific Reports.2024;[Epub]     CrossRef
  • Phosphate-solubilising bacteria promote horticultural plant growth through phosphate solubilisation and phytohormone regulation
    Yu Zhao, Sicen Liu, Bing He, Min Sun, Jishou Li, Rong Peng, Liangliang Sun, Xiaopeng Wang, Youpeng Cai, Hehe Wang, Xueqing Geng
    New Zealand Journal of Crop and Horticultural Science.2024; 52(2): 125.     CrossRef
  • First Report of Enterobacter cloacae Causing Stem, Leaf, and Fruit Rot on Tomato in China
    Yazhong Jin, Xingbiao Wu, Rina Sa, Hanchi Dong, Yanan Xiong, Shuping He, Chunxia Li, Xueqing Geng
    Plant Disease.2023; 107(6): 1936.     CrossRef
  • Structure and ecological function of the soil microbiome associated with ‘Sanghuang’ mushrooms suffering from fungal diseases
    Weifang Xu, Tao Sun, Jiahui Du, Shuqing Jin, Ying Zhang, Guofa Bai, Wanyu Li, Dengke Yin
    BMC Microbiology.2023;[Epub]     CrossRef
  • Beneficial and biocontrol effects of Trichoderma atroviride, a dominant species in white birch rhizosphere soil
    Kuo Liu, Yu-Zhou Zhang, Hua-Ying Du, Zhi-Ying Wang, Pei-Wen Gu, Zhi-Hua Liu, Ze-Yang Yu
    Frontiers in Microbiology.2023;[Epub]     CrossRef
  • Three new species of Trichoderma (Hypocreales, Hypocreaceae) from soils in China
    Rui Zhao, Li-Juan Mao, Chu-Long Zhang
    MycoKeys.2023; 97: 21.     CrossRef
  • Combination of Aspergillus niger MJ1 with Pseudomonas stutzeri DSM4166 or mutant Pseudomonas fluorescens CHA0-nif improved crop quality, soil properties, and microbial communities in barrier soil
    Haiping Ni, Yuxia Wu, Rui Zong, Shiai Ren, Deng Pan, Lei Yu, Jianwei Li, Zhuling Qu, Qiyao Wang, Gengxing Zhao, Jianzhong Zhao, Lumin Liu, Tao Li, Youming Zhang, Qiang Tu
    Frontiers in Microbiology.2023;[Epub]     CrossRef
  • Journey of Trichoderma from Pilot Scale to Mass Production: A Review
    Vipul Kumar, Bhupendra Koul, Pooja Taak, Dhananjay Yadav, Minseok Song
    Agriculture.2023; 13(10): 2022.     CrossRef
  • Trichoderma hamatum and Its Benefits
    Rathna Silviya Lodi, Chune Peng, Xiaodan Dong, Peng Deng, Lizeng Peng
    Journal of Fungi.2023; 9(10): 994.     CrossRef
  • Biocontrol Potential of Trichoderma harzianum and Zinc Nanoparticles to Mitigate Gray Mold Disease of Tomato
    Muhammad Imran, Kamal A. M. Abo-Elyousr, Mohamed E. El-Sharnouby, Esmat F. Ali, Nashwa M. A. Sallam, Hadeel M. M. Khalil Bagy, Ismail R. Abdel-Rahim
    Gesunde Pflanzen.2023; 75(1): 151.     CrossRef
  • Screening and biocontrol evaluation of indigenous native Trichoderma spp. against early blight disease and their field assessment to alleviate natural infection
    Muhammad Imran, Kamal A. M. Abo-Elyousr, Magdi A. Mousa, Maged M. Saad
    Egyptian Journal of Biological Pest Control.2022;[Epub]     CrossRef
  • Trichoderma: Advent of Versatile Biocontrol Agent, Its Secrets and Insights into Mechanism of Biocontrol Potential
    Nazia Manzar, Abhijeet Shankar Kashyap, Ravi Shankar Goutam, Mahendra Vikram Singh Rajawat, Pawan Kumar Sharma, Sushil Kumar Sharma, Harsh Vardhan Singh
    Sustainability.2022; 14(19): 12786.     CrossRef
  • A novel salt-tolerant strain Trichoderma atroviride HN082102.1 isolated from marine habitat alleviates salt stress and diminishes cucumber root rot caused by Fusarium oxysporum
    Chongyuan Zhang, Weiwei Wang, Yihui Hu, Zhongpin Peng, Sen Ren, Ming Xue, Zhen Liu, Jumei Hou, Mengyu Xing, Tong Liu
    BMC Microbiology.2022;[Epub]     CrossRef
  • Trichogenic Silver-Based Nanoparticles for Suppression of Fungi Involved in Damping-Off of Cotton Seedlings
    Shimaa A. Zaki, Salama A. Ouf, Kamel A. Abd-Elsalam, Amal A. Asran, Mohamed M. Hassan, Anu Kalia, Fawziah M. Albarakaty
    Microorganisms.2022; 10(2): 344.     CrossRef
  • Diversity and effects of competitive Trichoderma species in Ganoderma lucidum–cultivated soils
    Yongjun Wang, Linzhou Zeng, Jiayi Wu, Hong Jiang, Li Mei
    Frontiers in Microbiology.2022;[Epub]     CrossRef
  • Biocontrol and growth-promoting effect of Trichoderma asperellum TaspHu1 isolate from Juglans mandshurica rhizosphere soil
    Zeyang Yu, Zhiying Wang, Yuzhou Zhang, Yucheng Wang, Zhihua Liu
    Microbiological Research.2021; 242: 126596.     CrossRef
  • Trichoderma harzianum-Mediated ZnO Nanoparticles: A Green Tool for Controlling Soil-Borne Pathogens in Cotton
    Shimaa A. Zaki, Salama A. Ouf, Fawziah M. Albarakaty, Marian M. Habeb, Aly A. Aly, Kamel A. Abd-Elsalam
    Journal of Fungi.2021; 7(11): 952.     CrossRef
  • How Do Trichoderma Genus Fungi Win a Nutritional Competition Battle against Soft Fruit Pathogens? A Report on Niche Overlap Nutritional Potentiates
    Karolina Oszust, Justyna Cybulska, Magdalena Frąc
    International Journal of Molecular Sciences.2020; 21(12): 4235.     CrossRef
  • Isolation of Trichoderma in the rhizosphere soil of Syringa oblata from Harbin and their biocontrol and growth promotion function
    Bin Liu, Shida Ji, Huifang Zhang, Yucheng Wang, Zhihua Liu
    Microbiological Research.2020; 235: 126445.     CrossRef
Research Support, Non-U.S. Gov'ts
Bacterial Diversity in the Mountains of South-West China: Climate Dominates Over Soil Parameters
Dharmesh Singh , Lingling Shi , Jonathan M. Adams
J. Microbiol. 2013;51(4):439-447.   Published online August 30, 2013
DOI: https://doi.org/10.1007/s12275-013-2446-9
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AbstractAbstract
Certain patterns in soil bacterial diversity and community composition have become evident from metagenomics studies on a range of scales, from various parts of the world. For example, soil pH has generally been seen as dominating variation in bacterial diversity, above all other soil and climate parameters. It is important however to test the generality of these relationships by studying previously unsampled areas. We compared soil bacterial diversity and community composition under a wide range of climatic and edaphic conditions in mountainous Yunnan Province, SW China. Soil samples were taken from a range of primary forest types and altitudes, reflecting the great variation of forest environments in this region. From each soil sample, DNA was extracted and pyrosequenced for bacterial 16S rRNA gene identification. In contrast to other recent studies from other parts of the world, pH was a weaker predictor of bacterial community composition and diversity than exchangeable Ca2+ concentration, and also the more poorly defined >environmental parameter of elevation. Samples from within each forest type clustered strongly, showing the distinctive pattern of their microbial communities on a regional scale. It is clear that on a regional scale in a very heterogeneous environment, additional factors beyond pH can emerge as more important in determining bacterial diversity.
Highland Macrolichen Flora of Northwestern Yunnan, China
Jae-Seoun Hur , Li-Song Wang , Soon-Ok Oh , Gyoung Hee Kim , Kwang-Mi Lim , Jae-Sung Jung , Young Jin Koh
J. Microbiol. 2005;43(3):228-236.
DOI: https://doi.org/2222 [pii]
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AbstractAbstract
Fifty-six species in 36 genera of macrolichens are reported from the Zhongdian area, northwest Yunnan, China during the lichenological expedition for highland macrolichen survey in June, 2004. More than 60% of these species have not been reported in South Korea. All of the 182 collected specimens are deposited in the Korean Lichen Research Institute (KoLRI) at Sunchon National University in Korea, and some of them are duplicated in the lichen herbarium, Crytogamic Herbarium, Kunming Institute of Botany, Academia Sinica (KUN-L) in China. This is the first report on the macrolichen flora in the visited areas.
High Prevalence of the China 1 Strain of Epstein-Barr Virus in Korea as Determined by Sequence Polymorphisms in the Carboxy-Terminal Tail of LMP1
Sung-Gyu Cho , Won-Keun Lee
J. Microbiol. 2003;41(2):129-136.
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AbstractAbstract
The Epstein-Barr virus (EBV)-encoded latent membrane protein 1 (LMP1) exhibits considerable sequence heterogeneity among EBV isolates. Seven distinct EBV strains have been defined based on sequence polymorphisms in the LMP1 gene, which are designated China 1, China 2, China 3, Alaskan, Mediterranean, NC, and the B95-8 strains. In this study, we analyzed a 30-bp deletion and sequence variations in the carboxy-terminal region of the LMP1 gene in 12 EBV isolates from spontaneous lymphoblastoid cell lines derived from individuals with non-EBV associated cancers in Korea. Eleven of the 12 isolates showed a 30-bp deletion spanning LMP1 amino acids 342 to 353, suggesting a high prevalence of the LMP1 30-bp deletion variant among EBV isolates in Korea. In addition, all 12 isolates had a 15-bp common deletion in the 33-bp repeat region and multiple base-pair changes relative to the prototype B95-8 EBV strain along with variations in the number of the 33-bp repeats. The bp changes at positions 168746, 168694, 168687, 168395, 168357, 168355, 168631, 168320, 168308, 168295, and 168225 were highly conserved among the isolates. Comparative analysis of sequence change patterns in the LMP1 carboxy-terminal coding region identified nine 30-bp deletion variants as China 1, two deletion variants as a possible interstrain between the Alaskan and China 1 strains, and a single undeleted variant as a possible variant of the Alaskan strain. These results suggest the predominance of the China 1 EBV strain in the Korean population.

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