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Microbial metabolic responses and CO2 emissions differentiated by soil water content variation in subarctic tundra soils
Dockyu Kim , Namyi Chae , Mincheol Kim , Sungjin Nam , Tai Kyoung Kim , Ki-Tea Park , Bang Yong Lee , Eungbin Kim , Hyoungseok Lee
J. Microbiol. 2022;60(12):1130-1138.   Published online November 24, 2022
DOI: https://doi.org/10.1007/s12275-022-2378-3
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  • 3 Web of Science
  • 3 Crossref
AbstractAbstract PDF
Recent rapid air temperature increases across the northernlatitude tundra have prolonged permafrost thawing and snow melting periods, resulting in increased soil temperature (Ts) and volumetric soil water content (SWC). Under prolonged soil warming at 8°C, Alaskan tundra soils were incubated in a microcosm system and examined for the SWC differential influence on the microbial decomposition activity of large molecular weight (MW) humic substances (HS). When one microcosm soil (AKC1-1) was incubated at a constant SWC of 41% for 90 days (T = 90) and then SWC was gradually decreased from 41% to 29% for another T = 90, the initial HS was partly depolymerized. In contrast, in AKC1-2 incubated at a gradually decreasing SWC from the initial 32% to 10% for T = 90 and then increasing to 27% for another T = 90, HS depolymerization was undetected. Overall, the microbial communities in AKC1-1 could maintain metabolic activity at sufficient and constant SWC during the initial T = 90 incubation. In contrast, AKC1-2 microbes may have been damaged by drought stress during the drying SWC regimen, possibly resulting in the loss of HS decomposition activity, which did not recover even after re-wetting to an optimal SWC range (20–40%). After T = 90, the CO2 production in both treatments was attributed to the increased decomposition of small-MW organic compounds (including aerobic HS-degradative products) within an optimal SWC range. We expect this study to provide new insights into the early effects of warming- and topography-induced SWC variations on the microbial contribution to CO2 emissions via HS decomposition in northern-latitude tundra soil.

Citations

Citations to this article as recorded by  
  • Unidirectional freeze–thaw redistributes water and amplifies soil microbial heterogeneity in a mecrocosm experiment
    Huimin Liu, Yaxian Hu, Yuan Song, Xianwen Li, Xiaorong Wei
    Geoderma.2025; 453: 117126.     CrossRef
  • Analysis of CO2 Emission from Urban Soils of the Kola Peninsula (European Arctic)
    M. V. Korneykova, V. I. Vasenev, N. V. Saltan, M. V. Slukovskaya, A. S. Soshina, M. S. Zavodskikh, Yu. L. Sotnikova, A. V. Dolgikh
    Eurasian Soil Science.2023; 56(11): 1653.     CrossRef
  • Analysis of CO2 Emission by Urban Soils under the Conditions of the Kola North
    M. V. Korneykova, V. I. Vasenev, N. V. Saltan, M. V. Slukovskaya, A. S. Soshina, M. S. Zavodskikh, Y. L. Sotnikova, A. V. Dolgikh
    Почвоведение.2023; (11): 1385.     CrossRef
Characterization of a Salmonella Enteritidis bacteriophage showing broad lytic activity against Gram-negative enteric bacteria
Shukho Kim , Sung-Hun Kim , Marzia Rahman , Jungmin Kim
J. Microbiol. 2018;56(12):917-925.   Published online October 25, 2018
DOI: https://doi.org/10.1007/s12275-018-8310-1
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  • 31 Crossref
AbstractAbstract PDF
In this study, we sought to isolate Salmonella Enteritidis-specific lytic bacteriophages (phages), and we found a lytic phage that could lyse not only S. Enteritidis but also other Gramnegative foodborne pathogens. This lytic phage, SS3e, could lyse almost all tested Salmonella enterica serovars as well as other enteric pathogenic bacteria including Escherichia coli, Shigella sonnei, Enterobacter cloacae, and Serratia marcescens. This SS3e phage has an icosahedral head and a long tail, indicating belong to the Siphoviridae. The genome was 40,793 base pairs, containing 58 theoretically determined open reading frames (ORFs). Among the 58 ORFs, ORF49, and ORF25 showed high sequence similarity with tail spike protein and lysozyme-like protein of Salmonella phage SE2, respectively, which are critical proteins recognizing and lysing host bacteria. Unlike SE2 phage whose host restricted to Salmonella enterica serovars Enteritidis and Gallinarum, SS3e showed broader host specificity against Gram-negative enteric bacteria; thus, it could be a promising candidate for the phage utilization against various Gram-negative bacterial infection including foodborne pathogens.

Citations

Citations to this article as recorded by  
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    Mengge Chen, Tong Yu, Xiangyu Cao, Jiaqi Pu, Deshu Wang, Hongkuan Deng
    Archives of Microbiology.2025;[Epub]     CrossRef
  • Two novel polyvalent phages: a promising approach for cross-order pathogen control in aquaculture
    Chengcheng Li, Yufei Yue, Rui Yin, Jiulong Zhao, Zengmeng Wang, Shailesh Nair, Yongyu Zhang
    Virology Journal.2025;[Epub]     CrossRef
  • Isolation and characterization of virulent bacteriophages and controlling Salmonella Enteritidis biofilms on chicken meat
    Xiaowen Sun, Fan Xue, Cong Cong, Bilal Murtaza, Chenxi Guo, Haochen Su, Xiaoyu Li, Lili Wang, Yongping Xu
    Microbial Pathogenesis.2025; 205: 107619.     CrossRef
  • Optimizing phage therapy for carbapenem-resistant Enterobacter cloacae bacteremia: insights into dose and timing
    Shi-Yong Fu, Xiu-Zhen Chen, Peng-Cheng Yi, Jie Gao, Wei-Xiao Wang, Shuang-Lin Gu, Jing-Han Gao, Du-Xian Liu, Han-Feng Xu, Yi Zeng, Chun-Mei Hu, Qin Zheng, Wei Chen, Pranita D. Tamma
    Antimicrobial Agents and Chemotherapy.2025;[Epub]     CrossRef
  • Therapeutic potential of novel phages with antibiotic combinations against ESBL-producing and carbapenem-resistant Escherichia Coli
    Md Shamsuzzaman, Shukho Kim, Jungmin Kim
    Journal of Global Antimicrobial Resistance.2025; 43: 86.     CrossRef
  • In vitro, genomic characterization and pre-clinical evaluation of a new thermostable lytic Obolenskvirus phage formulated as a hydrogel against carbapenem-resistant Acinetobacter baumannii
    Mahmoud M. Sherif, Neveen A. Abdelaziz, Mohammad Y. Alshahrani, Sarra E. Saleh, Khaled M. Aboshanab
    Scientific Reports.2025;[Epub]     CrossRef
  • Phage therapy as a promising solution for food safety: isolation and biological characterization of bacteriophage P2 for controlling Salmonella enterica infections
    Tran Khang Nam, Pham Thi Lanh, Man Hong Phuoc, Dong Van Quyen
    Academia Journal of Biology.2025; 47(2): 53.     CrossRef
  • Combating multidrug-resistant uropathogenic E. coli using lytic phages, enhancing antibiotic synergy and inhibiting biofilms
    Md Shamsuzzaman, Yoon-Jung Choi, Shukho Kim, Jungmin Kim
    International Microbiology.2025;[Epub]     CrossRef
  • Can natural preservatives serve as a new line of protective technology against bacterial pathogens in meat and meat products?
    Changyong Cheng, Lingli Jiang, Xiaoliang Li, Houhui Song, Weihuan Fang
    Food Quality and Safety.2024;[Epub]     CrossRef
  • Bacteriophage as a novel therapeutic approach for killing multidrug-resistant Escherichia coli ST131 clone
    Md Shamsuzzaman, Shukho Kim, Jungmin Kim
    Frontiers in Microbiology.2024;[Epub]     CrossRef
  • Characterization of two virulent Salmonella phages and transient application in egg, meat and lettuce safety
    XiaoWen Sun, Fan Xue, Cong Cong, Bilal Murtaza, LiLi Wang, XiaoYu Li, ShuYing Li, YongPing Xu
    Food Research International.2024; 190: 114607.     CrossRef
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    Shanshan Liu, Siew-Young Quek, Kang Huang
    Critical Reviews in Food Science and Nutrition.2024; 64(33): 12574.     CrossRef
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    Brenda Pei Chui Song, Angela Chiew Wen Ch'ng, Theam Soon Lim
    International Journal of Biological Macromolecules.2024; 256: 128455.     CrossRef
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    Rahim Azari, Mohammad Hashem Yousefi, Zohreh Taghipour, Jeroen Wagemans, Rob Lavigne, Saeid Hosseinzadeh, Seyed Mohammad Mazloomi, Marta Vallino, Sepideh Khalatbari-Limaki, Enayat Berizi
    International Journal of Food Microbiology.2023; 389: 110097.     CrossRef
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    Bin Yang, Yang Wang, Lu Gao, Sheng-qi Rao, Wen-yuan Zhou, Zhen-quan Yang, Xin-an Jiao, Benjamin Kumah Mintah, Mokhtar Dabbour
    Microbial Pathogenesis.2023; 174: 105948.     CrossRef
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    Fatih Ramazan İSTANBULLUGİL, Nuri TAŞ, Ulaş ACARÖZ, Damla ARSLAN-ACAROZ, Ömer ÇAKMAK, Sezen EVRENKAYA, Zeki GÜRLER
    Manas Journal of Agriculture Veterinary and Life Sciences.2023; 13(2): 210.     CrossRef
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    Daniel W. Bryan, Lauren K. Hudson, Jia Wang, Thomas G. Denes
    PHAGE.2023; 4(2): 90.     CrossRef
  • Newly Isolated Virulent Salmophages for Biocontrol of Multidrug-Resistant Salmonella in Ready-to-Eat Plant-Based Food
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    International Journal of Molecular Sciences.2023; 24(12): 10134.     CrossRef
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    Journal of Microbiology.2023; 61(12): 1063.     CrossRef
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    Frontiers in Cellular and Infection Microbiology.2023;[Epub]     CrossRef
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