- Grimontia marina sp. nov., a Marine Bacterium Isolated from the Yellow Sea
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Ahyoung Choi , Kyung-Mi Kim , Ilnam Kang , Seok-Hyun Youn , Young-Sang Suh , Yoon Lee , Jang-Cheon Cho
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J. Microbiol. 2012;50(1):170-174. Published online February 27, 2012
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DOI: https://doi.org/10.1007/s12275-012-1615-6
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A novel species belonging to the genus Grimontia is described
in this study. A Gram-negative, chemoheterotrophic, obligately
aerobic, catalase- and oxidase-positive, motile by a
single polar flagellum, and rod-shaped bacterium, designated
IMCC5001T, was isolated from surface seawater of
the Yellow Sea. Strain IMCC5001T grew optimally at 30°C
in the presence of 3.5% NaCl. Phylogenetic analysis based
on 16S rRNA gene sequences showed that the isolate was
related most closely to Grimontia hollisae with a sequence
similarity of 95.8%, and formed a robust phyletic lineage
with Grimontia hollisae. Differential physiological characteristics
between the new strain and Grimontia hollisae
KCCM 41680T and chemotaxonomic characterization including
determination of DNA G+C content, fatty acid methyl
esters, quinone composition, and polar lipid profiles justified
the assignment of strain IMCC5001T to the genus Grimontia
as a novel species. In conclusion, strain IMCC5001T represents
a new species, for which the name Grimontia marina sp.
nov. is proposed, with the type strain IMCC5001T (=KCTC
22666T =NBRC 105794T).
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Enterovibrio paralichthyis sp. nov., isolated from the gut of an olive flounder Paralichthys olivaceus
Young-Ok Kim, In-Suk Park, Dong-Gyun Kim, Sooyeon Park, Sung Hoon Han, Jung-Hoon Yoon
International Journal of Systematic and Evolutionary Microbiology
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Bruno Gomez-Gil, Adrián González-Castillo, Mario J. Aguilar-Méndez, Alejandro López-Cortés, Jaime Gómez-Gutiérrez, Ana Roque, Elke Lang, Julissa Enciso-Ibarra Current Microbiology.2021; 78(10): 3782. CrossRef -
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.2021;[Epub] CrossRef - Heterologous expression of a cryptic gene cluster from Grimontia marina affords a novel tricyclic peptide grimoviridin
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Zhaobin Huang, Chunming Dong, Zongze Shao International Journal of Systematic and Evolutionary Microbiology.2016; 66(8): 3050. CrossRef - Grimontia celer sp. nov., from sea water
María J. Pujalte, Teresa Lucena, Lidia Rodrigo-Torres, Alexandra La Mura, María A. Ruvira, David R. Arahal International Journal of Systematic and Evolutionary Microbiology.2016; 66(8): 2906. CrossRef - Grimontia indica AK16T, sp. nov., Isolated from a Seawater Sample Reports the Presence of Pathogenic Genes Similar to Vibrio Genus
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International Journal of Systematic and Evolutionary Microbiology
.2013; 63(Pt_7): 2365. CrossRef - Notification of changes in taxonomic opinion previously published outside the IJSEM
International Journal of Systematic and Evolutionary Microbiology
.2013; 63(Pt_7): 2371. CrossRef
- Helicobacter pylori γ-Glutamyltranspeptidase Induces Cell Cycle Arrest at the G1-S Phase Transition
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Kyung-Mi Kim , Seung-Gyu Lee , Jung-Min Kim , Do-Su Kim , Jea-Young Song , Hyung-Lyun Kang , Woo-Kon Lee , Myung-Je Cho , Kwang-Ho Rhee , Hee-Shang Youn , Seung-Chul Baik
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J. Microbiol. 2010;48(3):372-377. Published online June 23, 2010
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DOI: https://doi.org/10.1007/s12275-010-9293-8
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909
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In our previous study, we showed that Helicobacter pylori γ-glutamyltranspeptidase (GGT) is associated with H. pylori-induced apoptosis through a mitochondrial pathway. To better understand the role of GGT in apoptosis, we examined the effect of GGT on cell cycle regulation in AGS cells. To determine the effect of recombinant GGT (rGGT) on cell cycle distribution and apoptosis, rGGT-treated and untreated AGS cells were analyzed in parallel by flow cytometry using propidium iodide (PI). We found that rGGT inhibited the growth of AGS cells in a time-dependent manner, and that the pre-exposure of cells to a caspase-3 inhibitor (z-DEVD-fmk) effectively blocked GGT-induced apoptosis. Cell cycle analysis showed G1 phase arrest and apoptosis in AGS cells following rGGT treatment. The rGGT-mediated G1 phase arrest was found to be associated with down-regulation of cyclin E, cyclin A, Cdk 4, and Cdk 6, and the up-regulation of the cyclindependent kinase (Cdk) inhibitors p27 and p21. Our results suggest that H. pylori GGT induces cell cycle arrest at the G1-S phase transition.
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- Mitochondrial Stress in Helicobacter pylori Infection and Associated Malignancies: A Review
Viola Varga, András Gelley, Eva Margittai, Buket Bagci, Edina Amalia Wappler-Guzzetta, Ibolya Czegle Antioxidants.2026; 15(3): 285. CrossRef - Influence of bacterial proteins on the host’s cell cycle
Francesca Benedetti, Camila Summers, Robert C. Gallo, Davide Zella Cell Cycle.2025; 24(21-24): 492. CrossRef - Implications of lncRNAs in Helicobacter pylori-associated gastrointestinal cancers: underlying mechanisms and future perspectives
Lei Zhang, Fei Yu, Yue Zhang, Peifeng Li Frontiers in Cellular and Infection Microbiology.2024;[Epub] CrossRef - Helicobacter pylori outer membrane vesicles and infected cell exosomes: new players in host immune modulation and pathogenesis
Xiuping Wang, Jianjun Wang, Lingxiang Mao, Yongliang Yao Frontiers in Immunology.2024;[Epub] CrossRef - Infiltration to infection: key virulence players of Helicobacter pylori pathogenicity
Arghyadeep Bhattacharjee, Om Saswat Sahoo, Ahana Sarkar, Saurabh Bhattacharya, Rukhsana Chowdhury, Samarjit Kar, Oindrilla Mukherjee Infection.2024; 52(2): 345. CrossRef - Utility of gamma‐glutamyl transpeptidase to lymphocyte count ratio in predicting prognosis of patients with oral cancer: A prospective cohort study in Southeastern China
Na Wang, Yulan Lin, Fa Chen, Fengqiong Liu, Jing Wang, Bingju Gao, Yu Qiu, Lisong Lin, Bin Shi, Baochang He Head & Neck.2023; 45(5): 1172. CrossRef - Helicobacter pylori and Its Role in Gastric Cancer
Victor E. Reyes Microorganisms.2023; 11(5): 1312. CrossRef - Helicobacter pylorivirulence factors: subversion of host immune system and development of various clinical outcomes
Roghayeh Mohammadzadeh, Shaho Menbari, Abbas Pishdadian, Hadi Farsiani Expert Reviews in Molecular Medicine.2023;[Epub] CrossRef - Both extracellular vesicles from helicobacter pylori-infected cells and helicobacter pylori outer membrane vesicles are involved in gastric/extragastric diseases
Chengyao Wang, Wenkun Li, Linlin Shao, Anni Zhou, Mengran Zhao, Peng Li, Zheng Zhang, Jing Wu European Journal of Medical Research.2023;[Epub] CrossRef - Helicobacter pylori-Induced Progranulin Promotes the Progression of the Gastric Epithelial Cell Cycle by Regulating CDK4
Zongjiao Ren, Jiayi Li, Xianhong Du, Wenjing Shi, Fulai Guan, Xiaochen Wang, Linjing Wang, Hongyan Wang Journal of Microbiology and Biotechnology.2022; 32(7): 844. CrossRef - Biomarker Characterization and Prediction of Virulence and Antibiotic Resistance from Helicobacter pylori Next Generation Sequencing Data
Joana S. Vital, Luís Tanoeiro, Ricardo Lopes-Oliveira, Filipa F. Vale Biomolecules.2022; 12(5): 691. CrossRef - Modern knowledge on pathogenesis, diagnosis and treatment of helicobacter infection
H. Yu. Kiselev, C. L. Gorlenko, Ya. A. El-Taravi, E. E. Porubayeva, E. V. Budanova Experimental and Clinical Gastroenterology.2021; (9): 15. CrossRef - Helicobacter pylori Virulence Factors—Mechanisms of Bacterial Pathogenicity in the Gastric Microenvironment
Jacek Baj, Alicja Forma, Monika Sitarz, Piero Portincasa, Gabriella Garruti, Danuta Krasowska, Ryszard Maciejewski Cells.2020; 10(1): 27. CrossRef - Helicobacter pylori Virulence Factors Exploiting Gastric Colonization and its Pathogenicity
Shamshul Ansari, Yoshio Yamaoka Toxins.2019; 11(11): 677. CrossRef - Identification of long noncoding RNA RP11-169F17.1 and RP11-669N7.2 as novel prognostic biomarkers of stomach adenocarcinoma based on integrated bioinformatics analysis
Jue Yang, Hui Song Epigenomics.2019; 11(11): 1307. CrossRef - A Novel Role for Helicobacter pylori Gamma-Glutamyltranspeptidase in Regulating Autophagy and Bacterial Internalization in Human Gastric Cells
Jimena Bravo, Paula Díaz, Alejandro H. Corvalán, Andrew F.G. Quest Cancers.2019; 11(6): 801. CrossRef - Pathogenesis and clinical management of Helicobacter pylori gastric infection
Breno Bittencourt de Brito, Filipe Antônio França da Silva, Aline Silva Soares, Vinícius Afonso Pereira, Maria Luísa Cordeiro Santos, Mariana Miranda Sampaio, Pedro Henrique Moreira Neves, Fabrício Freire de Melo World Journal of Gastroenterology.2019; 25(37): 5578. CrossRef - Comparison of enzymatic properties and small molecule inhibition of γ–glutamyltranspeptidases from pathogenic and commensal bacteria
Christian Bolz, Nina C. Bach, Hannelore Meyer, Gerhard Müller, Maciej Dawidowski, Grzegorz Popowicz, Stephan A. Sieber, Arne Skerra, Markus Gerhard Biological Chemistry.2017; 398(3): 341. CrossRef - Inhibition of Helicobacter pylori-induced inflammation in human gastric epithelial AGS cells by the fruits of Tribulus terrestris L. extracts
Hyun-A Lee, Ji-Hyun Yoo, Yungho Chung, Okjin Kim Journal of Biomedical Translational Research.2017; 18(3): 121. CrossRef - Heterogeneous Family of Cyclomodulins: Smart Weapons That Allow Bacteria to Hijack the Eukaryotic Cell Cycle and Promote Infections
Rachid A. El-Aouar Filho, Aurélie Nicolas, Thiago L. De Paula Castro, Martine Deplanche, Vasco A. De Carvalho Azevedo, Pierre L. Goossens, Frédéric Taieb, Gerard Lina, Yves Le Loir, Nadia Berkova Frontiers in Cellular and Infection Microbiology.2017;[Epub] CrossRef - Extended stability of cyclin D1 contributes to limited cell cycle arrest at G1-phase in BHK-21 cells with Japanese encephalitis virus persistent infection
Ji Young Kim, Soo Young Park, Hey Rhyoung Lyoo, Eung Seo Koo, Man Su Kim, Yong Seok Jeong Journal of Microbiology.2015; 53(1): 77. CrossRef - Helicobacter pylori-induced inflammation and epigenetic changes during gastric carcinogenesis
Manuel A Valenzuela World Journal of Gastroenterology.2015; 21(45): 12742. CrossRef - Helicobacter pylori γ-glutamyl transpeptidase-induced Ca2+ release via PLC–IP3 receptors in AGS cells
Eun-Hee Park, Jung-Min Kim, Kyung-Mi Kim, Dawon Kang, Young-Ah Cho, Jun-Young Choi, Jea-Young Song, Hyung-Lyun Kang, Woo-Kon Lee, Myung-Je Cho, Kwang-Ho Rhee, Ji-Hyun Seo, Hee-Shang Youn, Seung-Chul Baik Canadian Journal of Microbiology.2014; 60(12): 865. CrossRef - Role of Campylobacter jejuni gamma-glutamyl transpeptidase on epithelial cell apoptosis and lymphocyte proliferation
Pauline Floch, Vincent Pey, Michel Castroviejo, Jean William Dupuy, Marc Bonneu, Anaïs Hocès de la Guardia, Vincent Pitard, Francis Mégraud, Philippe Lehours Gut Pathogens.2014;[Epub] CrossRef - Crosstalk between Helicobacter pylori and Gastric Epithelial Cells Is Impaired by Docosahexaenoic Acid
Marta Correia, Valérie Michel, Hugo Osório, Meriem El Ghachi, Mathilde Bonis, Ivo G. Boneca, Hilde De Reuse, António A. Matos, Pascal Lenormand, Raquel Seruca, Ceu Figueiredo, Jose Carlos Machado, Eliette Touati, Georgina L. Hold PLoS ONE.2013; 8(4): e60657. CrossRef - The functional interplay of Helicobacter pylori factors with gastric epithelial cells induces a multi-step process in pathogenesis
Gernot Posselt, Steffen Backert, Silja Wessler Cell Communication and Signaling.2013;[Epub] CrossRef - Anthocyanins from black soybean inhibit Helicobacter pylori‐induced inflammation in human gastric epithelial AGS cells
Jung‐Min Kim, Kyung‐Mi Kim, En‐Hee Park, Ji‐Hyun Seo, Jae‐Young Song, Sung‐Chul Shin, Hyung‐Lyun Kang, Woo‐Kon Lee, Myung‐Je Cho, Kwang‐Ho Rhee, Hee‐Shang Youn, Seung‐Chul Baik Microbiology and Immunology.2013; 57(5): 366. CrossRef - Effect of Di(2-ethylhexyl)phthalate onHelicobacter pylori-Induced Apoptosis in AGS Cells
Chuang-Hao Lin, Chien-Yi Wu, Hwang-Shang Kou, Chiao-Yun Chen, Meng-Chuan Huang, Huang-Ming Hu, Meng-Chieh Wu, Chien-Yu Lu, Deng-Chyang Wu, Ming-Tsang Wu, Fu-Chen Kuo Gastroenterology Research and Practice.2013; 2013: 1. CrossRef - Lycopene inhibits Helicobacter pylori-induced ATM/ATR-dependent DNA damage response in gastric epithelial AGS cells
Sung Hee Jang, Joo Weon Lim, Tomohiro Morio, Hyeyoung Kim Free Radical Biology and Medicine.2012; 52(3): 607. CrossRef - Effects of Helicobacter pylori γ-Glutamyltranspeptidase on Apoptosis and Inflammation in Human Biliary Cells
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Steffen Backert, Marguerite Clyne Helicobacter.2011; 16(s1): 19. CrossRef - Purification and Characterization ofHelicobacter pyloriγ-Glutamyltranspeptidase
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György Miklós Buzás Orvosi Hetilap.2010; 151(49): 2003. CrossRef - Cell-Cycle Inhibition by Helicobacter pylori L-Asparaginase
Claudia Scotti, Patrizia Sommi, Maria Valentina Pasquetto, Donata Cappelletti, Simona Stivala, Paola Mignosi, Monica Savio, Laurent Roberto Chiarelli, Giovanna Valentini, Victor M. Bolanos-Garcia, Douglas Scott Merrell, Silvia Franchini, Maria Luisa Veron PLoS ONE.2010; 5(11): e13892. CrossRef
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