- Interferon-mediated antiviral activities of Angelica tenuissima Nakai and its active components
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Prasanna Weeratunga , Md Bashir Uddin , Myun Soo Kim , Byeong-Hoon Lee , Tae-Hwan Kim , Ji-Eun Yoon , Jin Yeul Ma , Hongik Kim , Jong-Soo Lee
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J. Microbiol. 2018;56(9):690-690.
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DOI: https://doi.org/10.1007/s12275-018-0579-6
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Abstract
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The above article by Weeratunga et al. has been retracted from Journal of Microbiology at the request of the corresponding
author. The authors found that they were unable to reproduce Figure 1, Figure 3(A), Figure 4(A) and Figure 7(D) presented in
this paper. All of the authors agreed to this retraction. The authors regret any inconvenience that this may cause and apologize
sincerely to the readers, reviewers, and editors of Journal of Microbiology.
- Dense Granule Protein-7 (GRA-7) of Toxoplasma gondii inhibits viral replication in vitro and in vivo
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Prasanna Weeratunga , Thilina U. B. Herath , Tae-Hwan Kim , Hyun-Cheol Lee , Jae-Hoon Kim , Byeong-Hoon Lee , Eun-Seo Lee , Kiramage Chathuranga , W. A. Gayan Chathuranga , Chul-Su Yang , Jin Yeul Ma , Jong-Soo Lee
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J. Microbiol. 2017;55(11):909-917. Published online October 27, 2017
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DOI: https://doi.org/10.1007/s12275-017-7392-5
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1,106
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10
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17
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Abstract
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Dense granule protein-7 (GRA-7) is an excretory protein of
Toxoplasma gondii. It is a potential serodiagnostic marker
and vaccine candidate for toxoplasmosis. Previous reports
demonstrated that GRA-7 induces innate immune responses
in macrophages by interacting with TRAF6 via the MyD88-
dependent pathway. In the present study, we evaluated the
antiviral activity and induction of an antiviral state by GRA-7
both in vitro and in vivo. It was observed that GRA-7 markedly
reduced the replication of vesicular stomatitis virus (VSVGFP),
influenza A virus (PR8-GFP), coxsackievirus (H3-
GFP), herpes simplex virus (HSV-GFP), and adenovirus-GFP
in epithelial (HEK293T/HeLa) and immune (RAW264.7)
cells. These antiviral activities of GRA-7 were attributed to
the induction of type I interferon (IFN) signaling, resulting
in the secretion of IFNs and pro-inflammatory cytokines.
Additionally, in BALB/c mice, intranasal administration of
GRA-7 prevented lethal infection by influenza A virus (H1N1)
and exhibited prophylactic effects against respiratory syncytial
virus (RSV-GFP). Collectively, these results suggested
that GRA-7 exhibits immunostimulatory and broad spectrum
antiviral activities via type I IFN signaling. Thus, GRA-7 can
be potentially used as a vaccine adjuvant or as a candidate
drug with prophylactic potential against viruses.
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Citations
Citations to this article as recorded by 
- Global research landscape and trends in Toxoplasma gondii from 2003 to 2022: A bibliometric analysis
Shi-Jie Fan, Ming Pan, Chen-Yang Xia, Pin Yang, Si-Yang Huang Veterinary Parasitology.2025; 335: 110438. CrossRef - Study of dense granule proteins in Eimeria spp. identifies a limited repertoire with potential as vaccine candidates
Gonzalo Sanchez-Arsuaga, Damer P. Blake, Fiona M. Tomley, Virginia Marugan-Hernandez Frontiers in Immunology.2025;[Epub] CrossRef - Effect of SARS-CoV-2 and Toxoplasma gondii co-infection on IFN-γ and TNF-α expression and its impact on disease severity
Magda S.A. Abdeltawab, Mohamed Fateen, Shimaa Saad El-Din, Riem M. Elmessiery, Osama Mohammady Mohamed, Khaled Marzouk Sadek, Engy Medhat, Alshaimaa M.R. Hamed Cytokine.2024; 177: 156545. CrossRef - Impact of latent toxoplasmosis on pneumonic and non-pneumonic COVID-19 patients with estimation of relevant oxidative stress biomarkers
Doaa A. Hamdy, Ragaey A. Eid, Heba Abdel-Tawab, Mohamed A. El-Badry, Abdelrahman M. Abdallah, Wegdan M. Abd El Wahab Folia Parasitologica.2024;[Epub] CrossRef - IFNs in host defence and parasite immune evasion during Toxoplasma gondii infections
Carsten G. K. Lüder Frontiers in Immunology.2024;[Epub] CrossRef - Current vaccine candidate of toxoplasmosis
Eden WOLDEGERIMA, Fasika GETACHEW, Meseret MISGANAW, Yohannes MESFIN, Debaka BELETE, Tekeba SISAY, Nega BERHANE Journal of Life Science and Biomedicine.2024; : 54. CrossRef - Prevalence of Toxoplasma gondii infection in COVID-19 patients: A systematic review and meta-analysis
Mahdi Fakhar, Khadijeh Najafi Ghobadi, Nastaran Barati, Salman Zafari, Seyed Ali Hosseini, Eissa Soleymani, Seyedmousa Motavallihaghi Microbial Pathogenesis.2024; 197: 107064. CrossRef - Clinical and Immunological Impacts of Latent Toxoplasmosis on COVID-19 Patients
Samar Habib, Eman Hamza, Randa El-Gamal, Nessma A Nosser, Wafaa A Aboukamar, Sherehan Abdelsalam, Ali Sobh, Mohamed Elegezy, Mohamed Elbayoumy, Waleed Eldars, Khaled Elmasry, Marwa H Elnagdy Cureus.2023;[Epub] CrossRef - Association between breakthrough infection with COVID-19 and Toxoplasma gondii: a cross-sectional study
Marwa A. Gouda, Hind S. AboShabaan, Ahmed S. Abdelgawad, Aliaa Sabry Abdel Wahed, Khaled A. Abd El-Razik, Yara Elsaadawy, Ayman. A. Abdel-Wahab, Yousry Hawash Scientific Reports.2023;[Epub] CrossRef - Toxoplasmosis and symptoms severity in patients with COVID-19 in referral centers in Northern Iran
Ali Geraili, Alireza Badirzadeh, Maryam Sadeghi, Seyed Mahmoud Mousavi, Parisa Mousavi, Zabihollah Shahmoradi, Sayed-Mohsen Hosseini, Seyed Hossein Hejazi, Raheleh Rafiei-Sefiddashti Journal of Parasitic Diseases.2023; 47(1): 185. CrossRef - Synergistic effect of GRA7 and profilin proteins in vaccination against chronic Toxoplasma gondii infection
Nadia Arcon, Mariano S. Picchio, Ignacio M. Fenoy, Rosalía E. Moretta, Ariadna S. Soto, Matías D. Perrone Sibilia, Vanesa R. Sánchez, Cecilia A. Prato, María Virginia Tribulatti, Alejandra Goldman, Valentina Martin Vaccine.2021; 39(6): 933. CrossRef - GRA8 DNA vaccine formulations protect against chronic toxoplasmosis
Muhammet Karakavuk, Hüseyin Can, Aytül Gül, Aysu Değirmenci Döşkaya, Sedef Erkunt Alak, Cemal Ün, Adnan Yüksel Gürüz, Mert Döşkaya Microbial Pathogenesis.2021; 158: 105016. CrossRef - Role of interferon gamma in SARS-CoV-2-positive patients with parasitic infections
Enas Fakhry Abdel-Hamed, Mohamed N. Ibrahim, Nahed E. Mostafa, Howayda S. F. Moawad, Nahla E. Elgammal, Ehab M. Darwiesh, Dina S. El-rafey, Nissreen E. ElBadawy, Emad Ali Al-Khoufi, Salwa I. Hindawi Gut Pathogens.2021;[Epub] CrossRef - The role of polyspecific T-cell exhaustion in severe outcomes for COVID-19 patients having latent pathogen infections such as Toxoplasma gondii
Kevin Roe Microbial Pathogenesis.2021; 161: 105299. CrossRef -
Preparation of colloidal gold immunochromatographic test strips for the diagnosis of
Toxoplasma gondii
Yuanxi Shen, Zhaozhe Wang, Jiajing Li, Rui Xu, Rongyi Ji, Jiaojiao Lin, Chuangang Zhu Food and Agricultural Immunology.2020; 31(1): 630. CrossRef - A negative covariation between toxoplasmosis and CoVID-19 with alternative interpretations
Łukasz Jankowiak, Lajos Rozsa, Piotr Tryjanowski, Anders Pape Møller Scientific Reports.2020;[Epub] CrossRef - Characterization of a novel secretory spherical body protein in Babesia orientalis and Babesia orientalis-infected erythrocytes
Jiaying Guo, Muxiao Li, Yali Sun, Long Yu, Pei He, Zheng Nie, Xueyan Zhan, Yangnan Zhao, Xiaoying Luo, Sen Wang, Siqi Aoyang, Qin Liu, Cuiqin Huang, Lan He, Junlong Zhao Parasites & Vectors.2018;[Epub] CrossRef
- Coptidis Rhizoma extract inhibits replication of respiratory syncytial virus in vitro and in vivo by inducing antiviral state
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Byeong-Hoon Lee , Kiramage Chathuranga , Md Bashir Uddin , Prasanna Weeratunga , Myun Soo Kim , Won-Kyung Cho , Hong Ik Kim , Jin Yeul Ma , Jong-Soo Lee
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J. Microbiol. 2017;55(6):488-498. Published online May 28, 2017
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DOI: https://doi.org/10.1007/s12275-017-7088-x
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1,164
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27
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Abstract
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Coptidis Rhizoma is derived from the dried rhizome of Ranun-culaceous plants and is a commonly used traditional Chinese medicine. Although Coptidis Rhizoma is commonly used for its many therapeutic effects, antiviral activity against respi-ratory syncytial virus (RSV) has not been reported in detail. In this study, we evaluated the antiviral activities of Coptidis Rhizoma extract (CRE) against RSV in human respiratory tract cell line (HEp2) and BALB/c mice. An effective dose of CRE significantly reduces the replication of RSV in HEp2 cells and reduces the RSV-induced cell death. This antiviral activity against RSV was through the induction of type I inter-feron-related signaling and the antiviral state in HEp2 cells. More importantly, oral administration of CRE exhibited prophylactic effects in BALB/c mice against RSV. In HPLC analysis, we found the presence of several compounds in the aqueous fraction and among them; we confirmed that pal-matine was related to the antiviral properties and immune- modulation effect. Taken together, an extract of Coptidis Rhi-zoma and its components play roles as immunomodulators and could be a potential source as promising natural antivirals that can confer protection to RSV. These outcomes should encourage further allied studies in other natural products.
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- Interferon-mediated antiviral activities of Angelica tenuissima Nakai and its active components
-
Prasanna Weeratunga , Md Bashir Uddin , Myun Soo Kim , Byeong-Hoon Lee , Tae-Hwan Kim , Ji-Eun Yoon , Jin Yeul Ma , Hongik Kim , Jong-Soo Lee
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J. Microbiol. 2016;54(1):57-70. Published online January 5, 2016
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DOI: https://doi.org/10.1007/s12275-016-5555-4
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1,008
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0
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5
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Abstract
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Angelica tenuissima Nakai is a widely used commodity in
traditional medicine. Nevertheless, no study has been conducted
on the antiviral and immune-modulatory properties
of an aqueous extract of Angelica tenuissima Nakai. In the
present study, we evaluated the antiviral activities and the
mechanism of action of an aqueous extract of Angelica tenuissima
Nakai both in vitro and in vivo. In vitro, an effective
dose of Angelica tenuissima Nakai markedly inhibited the
replication of Influenza A virus (PR8), Vesicular stomatitis
virus (VSV), Herpes simplex virus (HSV), Coxsackie virus,
and Enterovirus (EV-71) on epithelial (HEK293T/HeLa) and
immune (RAW264.7) cells. Such inhibition can be described
by the induction of the antiviral state in cells by antiviral, IFNrelated
gene induction and secretion of IFNs and pro-inflammatory
cytokines. In vivo, Angelica tenuissima Nakai
treated BALB/c mice displayed higher survivability and lower
lung viral titers when challenged with lethal doses of highly
pathogenic influenza A subtypes (H1N1, H5N2, H7N3, and
H9N2). We also found that Angelica tenuissima Nakai can
induce the secretion of IL-6, IFN-λ, and local IgA in bronchoalveolar
lavage fluid (BALF) of Angelica tenuissima Nakai
treated mice, which correlating with the observed prophylactic
effects. In HPLC analysis, we found the presence of several
compounds in the aqueous fraction and among them; we
evaluated antiviral properties of ferulic acid. Therefore, an
extract of Angelica tenuissima Nakai and its components,
including ferulic acid, play roles as immunomodulators and
may be potential candidates for novel anti-viral/anti-influenza
agents.
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- The stimulatory effect of Angelica tenuissima Nakai in osteoblastic/odontoblastic differentiation of human periodontal ligament stem cells
Won-Jong Park, Youn Ho Han Korean Journal of Dental Materials.2022; 49(4): 187. CrossRef - Fermented Angelicae tenussimae with Aspergillus oryzae Improves Skin Barrier Properties, Moisturizing, and Anti-Inflammatory Responses
Chang-Woo Ha, Eun-Hwa Sohn, Sung-Hyeok Kim, Sohee Jang, Myung-Rye Park, Youn-Kyu Kim, In-Young Bae International Journal of Molecular Sciences.2022; 23(20): 12072. CrossRef - Extract of Polygala tenuifolia, Angelica tenuissima, and Dimocarpus longan Reduces Behavioral Defect and Enhances Autophagy in Experimental Models of Parkinson’s Disease
Huan Li, Joonki Kim, Huynh Nguyen Khanh Tran, Chang Hwan Lee, Jonghyun Hur, Min Cheol Kim, Hyun Ok Yang NeuroMolecular Medicine.2021; 23(3): 428. CrossRef - Chemical Constituents of the Root of Angelica tenuissima and their Anti-allergic Inflammatory Activity
Hyun Gyu Choi, In-Gyu Je, Geum Jin Kim, Joo-Won Nam, Sang Hee Shim, Sang-Hyun Kim, Hyukjae Choi Natural Product Communications.2017;[Epub] CrossRef - Inhibitory effects of bee venom and its components against viruses in vitro and in vivo
Md Bashir Uddin, Byeong-Hoon Lee, Chamilani Nikapitiya, Jae-Hoon Kim, Tae-Hwan Kim, Hyun-Cheol Lee, Choul Goo Kim, Jong-Soo Lee, Chul-Joong Kim Journal of Microbiology.2016; 54(12): 853. CrossRef
- Bacillus manliponensis sp. nov., a New Member of the Bacillus cereus Group Isolated from Foreshore Tidal Flat Sediment
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Min Young Jung , Joong-Su Kim , Woon Kee Paek , Jeongheui Lim , Hansoo Lee , Pyoung Il Kim , Jin Yeul Ma , Wonyong Kim , Young-Hyo Chang
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J. Microbiol. 2011;49(6):1027-1032. Published online December 28, 2011
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DOI: https://doi.org/10.1007/s12275-011-1049-6
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844
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Abstract
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A Gram-positive, endospore-forming, new Bacillus species, strain BL4-6T, was isolated from tidal flat sediment of the Yellow Sea. Strain BL4-6T is a straight rod, with motility by peritrichate flagella. The cell wall contains meso-diaminopimelic acid, and the major respiratory quinone is menaquinone-7. The major fatty acids are iso-C15:0 and summed feature 3 (containing C16:1 ω7c/ iso-C15:0 2OH, and/or iso-C15:0 2OH/C16:1 ω7c). Cells are catalase-positive and oxidase-negative. The G+C content of the genomic DNA is 38.0 mol%. Based on a comparative 16S rRNA gene sequence analysis, the isolate belongs to the genus Bacillus, forms a clade with the Bacillus cereus group, and is closely related to Bacillus mycoides (98.5%), Bacillus cereus (98.5%), Bacillus anthracis (98.4%), Bacillus thuringiensis (98.4%), Bacillus weihenstephanensis (98.1%), and Bacillus pseudomycoides (97.5%). The isolate showed less than 85% similarity of the gyrA gene sequence and below 95% similarity of the rpoB gene sequence to the members of this group. DNA-DNA relatedness between strain BL4-6T and B. cereus group was found to be in a range of 22.8-42.3%, and thus BL4-6T represents a unique species. On the basis of these studies, strain BL4-6T (=KCTC 13319T =JCM 15802T) is proposed to represent the type strain of a novel species, Bacillus manliponensis sp. nov.
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Laura M. Carroll, Rian Pierneef, Aletta Mathole, Abimbola Atanda, Itumeleng Matle, Xianqin Yang Microbiology Spectrum.2022;[Epub] CrossRef - Regulation of Enterotoxins Associated with Bacillus cereus Sensu Lato Toxicoinfection
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Zahirotul Hikmah Hassan International Food Research Journal.2022; 29(3): 496. CrossRef - Bacillus cereus food intoxication and toxicoinfection
Jelena Jovanovic, Vincent F. M. Ornelis, Annemieke Madder, Andreja Rajkovic Comprehensive Reviews in Food Science and Food Safety.2021; 20(4): 3719. CrossRef - The Possible Transmission and Potential Enterotoxicity of Bacillus cereus on Lettuce Farms in Five Chinese Provinces
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N. Nursyirwani, J. Samiaji, A. Tanjung, I. Effendi, K. M. Claudia IOP Conference Series: Earth and Environmental Science.2021; 695(1): 012044. CrossRef - The Food Poisoning Toxins of Bacillus cereus
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Aharon Oren, George M. Garrity
International Journal of Systematic and Evolutionary Microbiology
.2021;[Epub] CrossRef - Bacillus cytotoxicus Genomics: Chromosomal Diversity and Plasmidome Versatility
Nancy Fayad, Klèma Marcel Koné, Annika Gillis, Jacques Mahillon Frontiers in Microbiology.2021;[Epub] CrossRef - Potential Enterotoxicity of Phylogenetically Diverse Bacillus cereus Sensu Lato Soil Isolates from Different Geographical Locations
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Audrey Leprince, Manon Nuytten, Annika Gillis, Jacques Mahillon Viruses.2020; 12(9): 1052. CrossRef - You Can’t B. cereus – A Review of Bacillus cereus Strains That Cause Anthrax-Like Disease
Victoria M. Baldwin Frontiers in Microbiology.2020;[Epub] CrossRef - The Bacillus cereus Food Infection as Multifactorial Process
Nadja Jessberger, Richard Dietrich, Per Einar Granum, Erwin Märtlbauer Toxins.2020; 12(11): 701. CrossRef - Proposal of a Taxonomic Nomenclature for the Bacillus cereus Group Which Reconciles Genomic Definitions of Bacterial Species with Clinical and Industrial Phenotypes
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Laura M. Carroll, Rachel A. Cheng, Jasna Kovac Frontiers in Microbiology.2020;[Epub] CrossRef - Chromate tolerance and removal of bacterial strains isolated from uncontaminated and chromium-polluted environments
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Marc J. A. Stevens, Taurai Tasara, Jochen Klumpp, Roger Stephan, Monika Ehling-Schulz, Sophia Johler Scientific Reports.2019;[Epub] CrossRef - Typing and evaluating heat resistance of Bacillus cereus sensu stricto isolated from the processing environment of powdered infant formula
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Nancy Fayad, Mireille Kallassy Awad, Jacques Mahillon BMC Genomics.2019;[Epub] CrossRef - Quality control of batches of bacteriological examination kits «Selective differential-diagnostic medium for recovery of Bacillus anthracis and closely related bacilli of Bacillus cereus group»
A G Ryazanova, L Yu Aksenova, A A Zuenco, T M Gridina, N P Buravtseva, E I Eremenko Bulletin of the Russian Military Medical Academy.2018; 20(3): 144. CrossRef - Genes under positive selection in the core genome of pathogenic Bacillus cereus group members
Jean-Philippe Rasigade, Florian Hollandt, Thierry Wirth Infection, Genetics and Evolution.2018; 65: 55. CrossRef - Bacillus cereus group: genetic aspects related to food safety and dairy processing
Gabriel Augusto Marques Rossi, Carlos Eduardo Gamero Aguilar, Higor Oliveira Silva, Ana Maria Centola Vidal Arquivos do Instituto Biológico.2018;[Epub] CrossRef - Phylogenetic and toxinogenic characteristics of Bacillus cereus group members isolated from spices and herbs
Hendrik Frentzel, Britta Kraushaar, Gladys Krause, Dorina Bodi, Heidi Wichmann-Schauer, Bernd Appel, Anneluise Mader Food Control.2018; 83: 90. CrossRef - Pan-genome and phylogeny of Bacillus cereus sensu lato
Adam L. Bazinet BMC Evolutionary Biology.2017;[Epub] CrossRef - Spores and vegetative cells of phenotypically and genetically diverse Bacillus cereus sensu lato are common bacteria in fresh water of northeastern Poland
Marek Bartoszewicz, Urszula Czyżewska Canadian Journal of Microbiology.2017; 63(12): 939. CrossRef - Ribosomal background of the Bacillus cereus group thermotypes
Krzysztof Fiedoruk, Justyna M. Drewnowska, Tamara Daniluk, Katarzyna Leszczynska, Piotr Iwaniuk, Izabela Swiecicka Scientific Reports.2017;[Epub] CrossRef - Taxonomy, virulence and life cycles of Bacillus cereus sensu lato
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Helen Glenwright, Susanne Pohl, Ferran Navarro, Elisenda Miro, Guillermo Jiménez, Anicet R. Blanch, Colin R. Harwood Frontiers in Microbiology.2017;[Epub] CrossRef - Complete Genome sequence of the nematicidal Bacillus thuringiensis MYBT18246
Jacqueline Hollensteiner, Anja Poehlein, Cathrin Spröer, Boyke Bunk, Anna E. Sheppard, Philip Rosentstiel, Hinrich Schulenburg, Heiko Liesegang Standards in Genomic Sciences.2017;[Epub] CrossRef -
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Rachel A. Miller, Sarah M. Beno, David J. Kent, Laura M. Carroll, Nicole H. Martin, Kathryn J. Boor, Jasna Kovac
International Journal of Systematic and Evolutionary Microbiology
.2016; 66(11): 4744. CrossRef - Chromosome-Directed PCR-Based Detection and Quantification of Bacillus cereus Group Members with Focus on B. thuringiensis Serovar israelensis Active against Nematoceran Larvae
Salome Schneider, Niels B. Hendriksen, Petter Melin, Jan O. Lundström, Ingvar Sundh, J. L. Schottel Applied and Environmental Microbiology.2015; 81(15): 4894. CrossRef - Genomic insights into the taxonomic status of the Bacillus cereus group
Yang Liu, Qiliang Lai, Markus Göker, Jan P. Meier-Kolthoff, Meng Wang, Yamin Sun, Lei Wang, Zongze Shao Scientific Reports.2015;[Epub] CrossRef - Bacillus bingmayongensis sp. nov., isolated from the pit soil of Emperor Qin’s Terra-cotta warriors in China
Bo Liu, Guo-Hong Liu, Gui-Ping Hu, Sengonca Cetin, Nai-Quan Lin, Jian-Yang Tang, Wei-Qi Tang, Ying-Zhi Lin Antonie van Leeuwenhoek.2014; 105(3): 501. CrossRef - Polyester production by halophilic and halotolerant bacterial strains obtained from mangrove soil samples located in Northern Vietnam
Doan Van‐Thuoc, Tran Huu‐Phong, Nguyen Thi‐Binh, Nguyen Thi‐Tho, Duong Minh‐Lam, Jorge Quillaguamán MicrobiologyOpen.2012; 1(4): 395. CrossRef - Genome Sequence of the Aerobic Bacterium Bacillus sp. Strain FJAT-13831
Guohong Liu, Bo Liu, Naiquan Lin, Weiqi Tang, Jianyang Tang, Yingzhi Lin Journal of Bacteriology.2012; 194(23): 6633. CrossRef
- Genome Sequence Analysis of H5N1 Influenza A Virus Isolated from a Vietnamese in 2007
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Dieu Linh Tran , Kangmo Kim , Jae Yoo Choi , Hyun Dong Paik , Si-Woo Choi , Jin Yeul Ma , Sung-Soon Kim , Sung Joon Ahn , Young Bong Kim
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J. Microbiol. 2011;49(2):274-279. Published online May 3, 2011
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DOI: https://doi.org/10.1007/s12275-011-0311-2
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Highly pathogenic H5N1 avian influenza A virus (AIV) crossed the species barrier and caused a number of deaths in humans in Vietnam and 14 other countries. Since the last report of human H5N1 infection in November 2005, the first documented H5N1 human infection was reported in June 2007 in Vietnam and was followed by 7 more cases, including 5 fatalities. In this study, we isolated and analyzed the full length of the H5N1 genome from a sample from the first patient in 2007. Phylogenetic analysis of eight genomic segments of the H5N1 virus strain (A/Vietnam/HN/2007, VNH07) revealed that this strain appears to be of genotype V and contains the HA gene, which is classified into clade 2.3.4. The deduced amino acid sequence of the HA protein has a typical affinity sequence for α2,3 linkage (SAα2,3-Gal) receptors
and typical multibasic cleavage sequences. Compared with other H5N1 isolates, VNH07 showed that the possible reassortments for the NA and NP segments occurred between A/goose/Guangxi/3017/2005-like isolates (2.3.2) and A/human/Zhejiang/16/2006-like isolates (2.3.4).
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- Rethinking Approaches to Improve the Utilization of Nucleic Acid Amplification Tests for Detection and Characterization of Influenza A in Diagnostic and Reference Laboratories
Kanti Pabbaraju, Sallene Wong, Steven J Drews Future Microbiology.2011; 6(12): 1443. CrossRef
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