29 results on '"Chang Jae Choi"'
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2. Bermudagrass Cultivars with Different Tolerance to Nematode Damage Are Characterized by Distinct Fungal but Similar Bacterial and Archaeal Microbiomes
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Chang Jae Choi, Jacqueline Valiente, Marco Schiavon, Braham Dhillon, William T. Crow, and Ulrich Stingl
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Microbiology (medical) ,Virology ,turfgrass ,bermudagrass ,microbiome ,mycobiome ,16S rRNA gene V4 and ITS2 amplicon sequencing ,Microbiology - Abstract
Turfgrass landscapes have expanded rapidly in recent decades and are a major vegetation type in urbanizing ecosystems. While turfgrass areas provide numerous ecosystem services in urban environments, ecological side effects from intensive management are raising concerns regarding their sustainability. One potentially promising approach to ameliorate the ecological impact and decrease the use of agricultural chemicals is to take advantage of naturally evolved turfgrass-associated microbes by harnessing beneficial services provided by microbiomes. Unfortunately, especially compared to agricultural crops, the microbiomes of turfgrasses are not well understood. Here, we analyzed microbial communities inhabiting the leaf and root endospheres as well as soil in two bermudagrass cultivars, ‘Latitude 36’ and ‘TifTuf’, which exhibit distinct tolerance to nematode damage, with the goal of identifying potential differences in the microbiomes that might explain their distinct phenotype. We used 16S rRNA gene V4 and ITS2 amplicon sequencing to characterize the microbiomes in combination with microbial cultivation efforts to identify potentially beneficial endophytic fungi and bacteria. Our results show that Latitude 36 and TifTuf showed markedly different fungal microbiomes, each harboring unique taxa from Ascomycota and Glomeromycota, respectively. In contrast, less difference was observed from bacterial and archaeal microbiomes, which were dominated by Bacteroidetes and Thaumarchaeota, respectively. The TifTuf microbiomes exhibited lower microbial diversity compared to Latitude 36. Many sequences could not be classified to a higher taxonomic resolution, indicating a relatively high abundance of hitherto undescribed microorganisms. Our results provide new insights into the structure and composition of turfgrass microbiomes but also raise important questions regarding the functional attributes of key taxa.
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- 2022
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3. A distinct lineage of giant viruses brings a rhodopsin photosystem to unicellular marine predators
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Chang Jae Choi, Keiichi Kojima, Nicholas A.T. Irwin, Alexandra Z. Worden, Edward F. DeLong, Sebastian Sudek, Patrick J. Keeling, Yuki Sudo, Elisabeth Hehenberger, Guy Leonard, Mikako Shirouzu, Charles Bachy, Susanne Wilken, Susumu Yoshizawa, Toshiaki Hosaka, Tomomi Kimura-Someya, Wataru Iwasaki, David M. Needham, Daniel K. Olson, Rex R. Malmstrom, Cheuk Man Yung, Daniel R. Mende, Yu Nakajima, Thomas A. Richards, Alyson E. Santoro, Rika Kurihara, Camille Poirier, and Freshwater and Marine Ecology (IBED, FNWI)
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Rhodopsin ,marine carbon cycle ,Oceans and Seas ,Genome, Viral ,Genome ,Viral Proteins ,viral evolution ,03 medical and health sciences ,MD Multidisciplinary ,Genetics ,Phycodnaviridae ,Seawater ,Giant Virus ,Mimiviridae ,Viral ,14. Life underwater ,Life Below Water ,Gene ,Ecosystem ,Phylogeny ,host-virus interactions ,030304 developmental biology ,0303 health sciences ,Multidisciplinary ,biology ,single-cell genomics ,030306 microbiology ,Neurosciences ,Eukaryota ,Biological Sciences ,biology.organism_classification ,Biological Evolution ,host–virus interactions ,Infectious Diseases ,PNAS Plus ,Evolutionary biology ,Metagenomics ,Giant Viruses ,Viral evolution ,biology.protein ,Protons ,Infection ,Environmental Sciences ,Bacteria - Abstract
Significance Although viruses are well-characterized regulators of eukaryotic algae, little is known about those infecting unicellular predators in oceans. We report the largest marine virus genome yet discovered, found in a wild predatory choanoflagellate sorted away from other Pacific microbes and pursued using integration of cultivation-independent and laboratory methods. The giant virus encodes nearly 900 proteins, many unlike known proteins, others related to cellular metabolism and organic matter degradation, and 3 type-1 rhodopsins. The viral rhodopsin that is most abundant in ocean metagenomes, and also present in an algal virus, pumps protons when illuminated, akin to cellular rhodopsins that generate a proton-motive force. Giant viruses likely provision multiple host species with photoheterotrophic capacities, including predatory unicellular relatives of animals., Giant viruses are remarkable for their large genomes, often rivaling those of small bacteria, and for having genes thought exclusive to cellular life. Most isolated to date infect nonmarine protists, leaving their strategies and prevalence in marine environments largely unknown. Using eukaryotic single-cell metagenomics in the Pacific, we discovered a Mimiviridae lineage of giant viruses, which infects choanoflagellates, widespread protistan predators related to metazoans. The ChoanoVirus genomes are the largest yet from pelagic ecosystems, with 442 of 862 predicted proteins lacking known homologs. They are enriched in enzymes for modifying organic compounds, including degradation of chitin, an abundant polysaccharide in oceans, and they encode 3 divergent type-1 rhodopsins (VirR) with distinct evolutionary histories from those that capture sunlight in cellular organisms. One (VirRDTS) is similar to the only other putative rhodopsin from a virus (PgV) with a known host (a marine alga). Unlike the algal virus, ChoanoViruses encode the entire pigment biosynthesis pathway and cleavage enzyme for producing the required chromophore, retinal. We demonstrate that the rhodopsin shared by ChoanoViruses and PgV binds retinal and pumps protons. Moreover, our 1.65-Å resolved VirRDTS crystal structure and mutational analyses exposed differences from previously characterized type-1 rhodopsins, all of which come from cellular organisms. Multiple VirR types are present in metagenomes from across surface oceans, where they are correlated with and nearly as abundant as a canonical marker gene from Mimiviridae. Our findings indicate that light-dependent energy transfer systems are likely common components of giant viruses of photosynthetic and phagotrophic unicellular marine eukaryotes.
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- 2019
4. Selective Uptake of Pelagic Microbial Community Members by Caribbean Reef Corals
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Kenneth D. Hoadley, Cheuk Man Yung, Chang Jae Choi, Camille Poirier, Alexandra Z. Worden, and Maria Hamilton
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0106 biological sciences ,Coral ,picoplankton ,01 natural sciences ,Applied Microbiology and Biotechnology ,Porites astreoides ,Microbial Ecology ,03 medical and health sciences ,bentho-pelagic coupling ,Animals ,Seawater ,14. Life underwater ,Reef ,030304 developmental biology ,0303 health sciences ,geography ,geography.geographical_feature_category ,Ecology ,biology ,Bacteria ,Coral Reefs ,010604 marine biology & hydrobiology ,Microbiota ,fungi ,Dinoflagellate ,technology, industry, and agriculture ,Eukaryota ,Coral reef ,biochemical phenomena, metabolism, and nutrition ,biology.organism_classification ,Synechococcus ,Anthozoa ,Microbial population biology ,Caribbean Region ,population characteristics ,Prochlorococcus ,coral heterotrophy ,Water Microbiology ,geographic locations ,Food Science ,Biotechnology - Abstract
We identify interactions between coral grazing behavior and the growth rates and cell abundances of pelagic microbial groups found surrounding a Caribbean reef. During incubation experiments with three reef corals, reductions in microbial cell abundance differed according to coral species and suggest specific coral or microbial mechanisms are at play., Coral reefs are possible sinks for microbes; however, the removal mechanisms at play are not well understood. Here, we characterize pelagic microbial groups at the CARMABI reef (Curaçao) and examine microbial consumption by three coral species: Madracis mirabilis, Porites astreoides, and Stephanocoenia intersepta. Flow cytometry analyses of water samples collected from a depth of 10 m identified 6 microbial groups: Prochlorococcus, three groups of Synechococcus, photosynthetic eukaryotes, and heterotrophic bacteria. Minimum growth rates (μ) for Prochlorococcus, all Synechococcus groups, and photosynthetic eukaryotes were 0.55, 0.29, and 0.45 μ day−1, respectively, and suggest relatively high rates of productivity despite low nutrient conditions on the reef. During a series of 5-h incubations with reef corals performed just after sunset or prior to sunrise, reductions in the abundance of photosynthetic picoeukaryotes, Prochlorococcus and Synechococcus cells, were observed. Of the three Synechococcus groups, one decreased significantly during incubations with each coral and the other two only with M. mirabilis. Removal of carbon from the water column is based on coral consumption rates of phytoplankton and averaged between 138 ng h−1 and 387 ng h−1, depending on the coral species. A lack of coral-dependent reduction in heterotrophic bacteria, differences in Synechococcus reductions, and diurnal variation in reductions of Synechococcus and Prochlorococcus, coinciding with peak cell division, point to selective feeding by corals. Our study indicates that bentho-pelagic coupling via selective grazing of microbial groups influences carbon flow and supports heterogeneity of microbial communities overlying coral reefs. IMPORTANCE We identify interactions between coral grazing behavior and the growth rates and cell abundances of pelagic microbial groups found surrounding a Caribbean reef. During incubation experiments with three reef corals, reductions in microbial cell abundance differed according to coral species and suggest specific coral or microbial mechanisms are at play. Peaks in removal rates of Prochlorococcus and Synechococcus cyanobacteria appear highest during postsunset incubations and coincide with microbial cell division. Grazing rates and effort vary across coral species and picoplankton groups, possibly influencing overall microbial composition and abundance over coral reefs. For reef corals, use of such a numerically abundant source of nutrition may be advantageous, especially under environmentally stressful conditions when symbioses with dinoflagellate algae break down.
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- 2021
5. Seasonality of the Microbial Community Composition in the North Atlantic
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Chang Jae Choi, Craig A. Carlson, Alexandra Z. Worden, Stephen J. Giovannoni, Luis M. Bolaños, and Nicholas Baetge
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phytoplankton community composition ,0106 biological sciences ,lcsh:QH1-199.5 ,Mesopelagic zone ,Ocean Engineering ,Subtropics ,lcsh:General. Including nature conservation, geographical distribution ,Aquatic Science ,Oceanography ,01 natural sciences ,Algal bloom ,North Atlantic subregions ,03 medical and health sciences ,Phytoplankton ,Marine ecosystem ,14. Life underwater ,North Atlantic Aerosols and Marine Ecosystems Study ,bacterioplankton community composition ,lcsh:Science ,030304 developmental biology ,Water Science and Technology ,0303 health sciences ,Global and Planetary Change ,Ecology ,010604 marine biology & hydrobiology ,Bacterioplankton ,amplicon sequence variants ,15. Life on land ,Spring bloom ,Plankton ,seasonal succession ,Geography ,13. Climate action ,lcsh:Q - Abstract
Planktonic communities constitute the basis of life in marine environments and have profound impacts in geochemical cycles. In the North Atlantic, seasonality drives annual transitions in the ecology of the water column. Phytoplankton bloom annually in spring as a result of these transitions, creating one of the major biological pulses in productivity on earth. The timing and geographical distribution of the spring bloom as well as the resulting biomass accumulation have largely been studied using the global capacity of satellite imaging. However, fine-scale variability in the taxonomic composition, spatial distribution, seasonal shifts, and ecological interactions with heterotrophic bacterioplankton has remained largely uncharacterized. The North Atlantic Aerosols and Marine Ecosystems Study (NAAMES) conducted four meridional transects to characterize plankton ecosystems in the context of the annual bloom cycle. Using 16S rRNA gene-based community profiles we analyzed the temporal and spatial variation in plankton communities. Seasonality in phytoplankton and bacterioplankton composition was apparent throughout the water column, with changes dependent on the hydrographic origin. From winter to spring in the subtropic and subpolar subregions, phytoplankton shifted from the predominance of cyanobacteria and picoeukaryotic green algae to diverse photosynthetic eukaryotes. By autumn, the subtropics were dominated by cyanobacteria, while a diverse array of eukaryotes dominated the subpolar subregions. Bacterioplankton were also strongly influenced by geographical subregions. SAR11, the most abundant bacteria in the surface ocean, displayed higher richness in the subtropics than the subpolar subregions. SAR11 subclades were differentially distributed between the two subregions. Subclades Ia.1 and Ia.3 co-occurred in the subpolar subregion, while Ia.1 dominated the subtropics. In the subtropical subregion during the winter, the relative abundance of SAR11 subclades “II” and 1c.1 were elevated in the upper mesopelagic. In the winter, SAR202 subclades generally prevalent in the bathypelagic were also dominant members in the upper mesopelagic zones. Co-varying network analysis confirmed the large-scale geographical organization of the plankton communities and provided insights into the vertical distribution of bacterioplankton. This study represents the most comprehensive survey of microbial profiles in the western North Atlantic to date, revealing stark seasonal differences in composition and richness delimited by the biogeographical distribution of the planktonic communities.
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- 2021
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6. Seasonal and Geographical Transitions in Eukaryotic Phytoplankton Community Structure in the Atlantic and Pacific Oceans
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Chang Jae Choi, Valeria Jimenez, David M. Needham, Camille Poirier, Charles Bachy, Harriet Alexander, Susanne Wilken, Francisco P. Chavez, Sebastian Sudek, Stephen J. Giovannoni, and Alexandra Z. Worden
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phytoplankton diversity ,single-cell genomics ,time-series ,lcsh:QR1-502 ,dictyochophytes ,chloroplast genome ,lcsh:Microbiology - Abstract
Much is known about how broad eukaryotic phytoplankton groups vary according to nutrient availability in marine ecosystems. However, genus- and species-level dynamics are generally unknown, although important given that adaptation and acclimation processes differentiate at these levels. We examined phytoplankton communities across seasonal cycles in the North Atlantic (BATS) and under different trophic conditions in the eastern North Pacific (ENP), using phylogenetic classification of plastid-encoded 16S rRNA amplicon sequence variants (ASVs) and other methodologies, including flow cytometric cell sorting. Prasinophytes dominated eukaryotic phytoplankton amplicons during the nutrient-rich deep-mixing winter period at BATS. During stratification (‘summer’) uncultured dictyochophytes formed ∼35 ± 10% of all surface plastid amplicons and dominated those from stramenopile algae, whereas diatoms showed only minor, ephemeral contributions over the entire year. Uncultured dictyochophytes also comprised a major fraction of plastid amplicons in the oligotrophic ENP. Phylogenetic reconstructions of near-full length 16S rRNA sequences established 11 uncultured Dictyochophyte Environmental Clades (DEC). DEC-I and DEC-VI dominated surface dictyochophytes under stratification at BATS and in the ENP, and DEC-IV was also important in the latter. Additionally, although less common at BATS, Florenciella-related clades (FC) were prominent at depth in the ENP. In both ecosystems, pelagophytes contributed notably at depth, with PEC-VIII (Pelagophyte Environmental Clade) and (cultured) Pelagomonas calceolata being most important. Q-PCR confirmed the near absence of P. calceolata at the surface of the same oligotrophic sites where it reached ∼1,500 18S rRNA gene copies ml–1 at the DCM. To further characterize phytoplankton present in our samples, we performed staining and at-sea single-cell sorting experiments. Sequencing results from these indicated several uncultured dictyochophyte clades are comprised of predatory mixotrophs. From an evolutionary perspective, these cells showed both conserved and unique features in the chloroplast genome. In ENP metatranscriptomes we observed high expression of multiple chloroplast genes as well as expression of a selfish element (group II intron) in the psaA gene. Comparative analyses across the Pacific and Atlantic sites support the conclusion that predatory dictyochophytes thrive under low nutrient conditions. The observations that several uncultured dictyochophyte lineages are seemingly capable of photosynthesis and predation, raises questions about potential shifts in phytoplankton trophic roles associated with seasonality and long-term ocean change.
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- 2020
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7. Small phytoplankton dominate western North Atlantic biomass
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Emmanuel Boss, Chang Jae Choi, Jason R. Graff, Nils Haëntjens, Robert T. O'Malley, Stephen J. Giovannoni, Françoise Morison, Toby K. Westberry, Alexandra Z. Worden, Peter Gaube, Lee Karp-Boss, Alison Chase, Michael J. Behrenfeld, Luis M. Bolaños, Susanne Menden-Deuer, Alice Della Penna, Oregon State University (OSU), University of Maine, Monterey Bay Aquarium Research Institute (MBARI), Monterey Bay Aquarium Research Institute, Helmholtz Centre for Ocean Research [Kiel] (GEOMAR), Department of Botany and Plant Pathology, Applied Physics Laboratory [Seattle] (APL-UW), University of Washington [Seattle], Laboratoire des Sciences de l'Environnement Marin (LEMAR) (LEMAR), Institut de Recherche pour le Développement (IRD)-Institut Français de Recherche pour l'Exploitation de la Mer (IFREMER)-Université de Brest (UBO)-Institut Universitaire Européen de la Mer (IUEM), Institut de Recherche pour le Développement (IRD)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Brest (UBO)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Brest (UBO)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), University of Rhode Island (URI), This research was supported by NASA NAAMES grant no. NNX15AE70G. We thank Mark Dasenko and Oregon State University CGRB for amplicon library preparation and sequencing. We thank Captains A. Lund and D. Bergeron and R/V Atlantis crew. We thank the NAAMES community for their input. This study has been conducted using E.U. Copernicus Marine Service Information (CMEMS) and the Group for High Resolution Sea Surface Temperature (GHRSST) Multi-scale Ultra-high Resolution (MUR) SST data (obtained from the NASA EOSDIS Physical Oceanography Distributed Active Archive Center (PO.DAAC) at the Jet Propulsion Laboratory, Pasadena, CA). Phylogenetic analyses were supported in part by GBMF3788 and NSF DEB-1639033 to AZW. A. DP is grateful for the support of the Applied Physics Laboratory Science and Engineering Enrichment Development (SEED) fellowship and of funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement No 749591. We thank Mimi Lyon-Edmondson, Faith Hoyle, Emma Jourdain, Emma Dullaert and Gretchen Spencer for assistance with the classification of IFCB images., and Institut de Recherche pour le Développement (IRD)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Brest (UBO)-Centre National de la Recherche Scientifique (CNRS)-Institut national des sciences de l'Univers (INSU - CNRS)-Université de Brest (UBO)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)
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Water microbiology ,Water mass ,lineages ,010504 meteorology & atmospheric sciences ,Cyanobacteria ,01 natural sciences ,Microbiology ,Article ,diversity ,03 medical and health sciences ,Algae ,Phytoplankton ,14. Life underwater ,Biomass ,nanoplankton ,Ecology, Evolution, Behavior and Systematics ,Microbial biooceanography ,030304 developmental biology ,0105 earth and related environmental sciences ,Diatoms ,0303 health sciences ,Biomass (ecology) ,biology ,variability ,ACL ,carbon ,time-series ,Community structure ,Spring bloom ,Plankton ,Biogeochemistry ,biology.organism_classification ,Annual cycle ,ocean ,Oceanography ,13. Climate action ,Seasons ,fluorescence ,Molecular ecology ,community structure ,[SDE.BE]Environmental Sciences/Biodiversity and Ecology ,export - Abstract
WOS:000522382500001; International audience; The North Atlantic phytoplankton spring bloom is the pinnacle in an annual cycle that is driven by physical, chemical, and biological seasonality. Despite its important contributions to the global carbon cycle, transitions in plankton community composition between the winter and spring have been scarcely examined in the North Atlantic. Phytoplankton composition in early winter was compared with latitudinal transects that captured the subsequent spring bloom climax. Amplicon sequence variants (ASVs), imaging flow cytometry, and flow-cytometry provided a synoptic view of phytoplankton diversity. Phytoplankton communities were not uniform across the sites studied, but rather mapped with apparent fidelity onto subpolar- and subtropical-influenced water masses of the North Atlantic. At most stations, cells \textless 20-mu m diameter were the main contributors to phytoplankton biomass. Winter phytoplankton communities were dominated by cyanobacteria and pico-phytoeukaryotes. These transitioned to more diverse and dynamic spring communities in which pico- and nano-phytoeukaryotes, including many prasinophyte algae, dominated. Diatoms, which are often assumed to be the dominant phytoplankton in blooms, were contributors but not the major component of biomass. We show that diverse, small phytoplankton taxa are unexpectedly common in the western North Atlantic and that regional influences play a large role in modulating community transitions during the seasonal progression of blooms.
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- 2020
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8. Viruses infecting a warm water picoeukaryote shed light on spatial co-occurrence dynamics of marine viruses and their hosts
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Simon Roux, Charmaine C. M. Yung, Danielle M. Jorgens, David M. Needham, Charles Bachy, Alexander J. Limardo, Alexandra Z. Worden, Matthew B. Sullivan, Maria Consuelo Gazitúa, and Chang Jae Choi
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Technology ,Zoology ,Bathycoccus prasinos ,Microbiology ,Article ,Bathycoccus ,03 medical and health sciences ,Marine bacteriophage ,Chlorophyta ,14. Life underwater ,Clade ,Ecology, Evolution, Behavior and Systematics ,Ecosystem ,Phylogeny ,Microbial biooceanography ,030304 developmental biology ,Infectivity ,0303 health sciences ,Picoeukaryote ,biology ,Ecotype ,030306 microbiology ,Host (biology) ,Water ,Biological Sciences ,biology.organism_classification ,Phylogenetics ,Infectious Diseases ,Viruses ,Infection ,Environmental Sciences - Abstract
The marine picoeukaryote Bathycoccus prasinos has been considered a cosmopolitan alga, although recent studies indicate two ecotypes exist, Clade BI (B. prasinos) and Clade BII. Viruses that infect Bathycoccus Clade BI are known (BpVs), but not that infect BII. We isolated three dsDNA prasinoviruses from the Sargasso Sea against Clade BII isolate RCC716. The BII-Vs do not infect BI, and two (BII-V2 and BII-V3) have larger genomes (~210 kb) than BI-Viruses and BII-V1. BII-Vs share ~90% of their proteins, and between 65% to 83% of their proteins with sequenced BpVs. Phylogenomic reconstructions and PolB analyses establish close-relatedness of BII-V2 and BII-V3, yet BII-V2 has 10-fold higher infectivity and induces greater mortality on host isolate RCC716. BII-V1 is more distant, has a shorter latent period, and infects both available BII isolates, RCC716 and RCC715, while BII-V2 and BII-V3 do not exhibit productive infection of the latter in our experiments. Global metagenome analyses show Clade BI and BII algal relative abundances correlate positively with their respective viruses. The distributions delineate BI/BpVs as occupying lower temperature mesotrophic and coastal systems, whereas BII/BII-Vs occupy warmer temperature, higher salinity ecosystems. Accordingly, with molecular diagnostic support, we name Clade BII Bathycoccus calidus sp. nov. and propose that molecular diversity within this new species likely connects to the differentiated host-virus dynamics observed in our time course experiments. Overall, the tightly linked biogeography of Bathycoccus host and virus clades observed herein supports species-level host specificity, with strain-level variations in infection parameters.
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- 2020
9. Classification and nomenclature of metacaspases and paracaspases: no more confusion with caspases
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Christiane Funk, Vanina E. Alvarez, Heinz D. Osiewacz, Juan José Cazzulo, Simon Stael, Boris Zhivotovsky, Chang Jae Choi, Frank Madeo, Jens Staal, Kailash C. Pandey, Lynn A. Megeney, Yigong Shi, Magali Casanova, Andrei Smertenko, Maurício F.M. Machado, Eric Lam, Renier A. L. van der Hoorn, Juergen Ruland, Ilana Berman-Frank, Panagiotis N. Moschou, Peter V. Bozhkov, Jeremy C. Mottram, Kay D. Bidle, Jerry Ståhlberg, Rudi Beyaert, Christopher M. Overall, Frédéric Bornancin, Kris Gevaert, Margot Thome, Assaf Vardi, Núria S. Coll, Patrick Gallois, Frank Van Breusegem, Thomas Nyström, Vishva M. Dixit, Marko Dolinar, Maria F. Suarez, Stephan Hailfinger, Nicolas Fasel, Emilio Gutierrez-Beltran, John A. Berges, Anna Linusson, Hannele Tuominen, Daniel Krappmann, Guy S. Salvesen, Marina Klemenčič, Elena A. Minina, Eugene V. Koonin, Canaan, Stephane, Swedish University of Agricultural Sciences (SLU), Universiteit Gent = Ghent University (UGENT), Universidad Nacional de San Martin (UNSAM), University of Wisconsin - Milwaukee, University of Haifa [Haifa], Rutgers, The State University of New Jersey [New Brunswick] (RU), Rutgers University System (Rutgers), Novartis Institutes for BioMedical Research (NIBR), Laboratoire d'ingénierie des systèmes macromoléculaires (LISM), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), University of Texas at Austin [Austin], Centre for Research in Agricultural Genomics (CRAG), Genentech, Inc., Genentech, Inc. [San Francisco], University of Ljubljana, Université de Lausanne = University of Lausanne (UNIL), Umeå University, Universidade de Mogi das Cruces = University of Mogi das Cruzes (UMC), Karl-Franzens-Universität Graz, University of Ottawa [Ottawa], Institute of Molecular Biology and Biotechnology (IMBB-FORTH), Foundation for Research and Technology - Hellas (FORTH), University of York [York, UK], University of Gothenburg (GU), Goethe-University Frankfurt am Main, University of British Columbia (UBC), National Institute of Malaria Research [New Dehli, Inde] (NIMR), Indian Council of Medical Research [New Dehli] (ICMR), Technische Universität Munchen - Université Technique de Munich [Munich, Allemagne] (TUM), Sanford Burnham Prebys Medical Discovery Institute, Westlake University [Zhejiang], Washington State University (WSU), Universidad de Málaga [Málaga] = University of Málaga [Málaga], University of Oxford, Weizmann Institute of Science [Rehovot, Israël], Lomonosov Moscow State University (MSU), Knut and Alice Wallenberg Foundation, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, Universiteit Gent = Ghent University [Belgium] (UGENT), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU), University of Lausanne (UNIL), Karl-Franzens-Universität [Graz, Autriche], University of Oxford [Oxford], University of Graz, and Technical University of Munich (TUM)
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Consensus ,METACASPASES ,Protein Conformation ,[SDV]Life Sciences [q-bio] ,Computational biology ,Article ,purl.org/becyt/ford/1 [https] ,Structure-Activity Relationship ,03 medical and health sciences ,0302 clinical medicine ,Terminology as Topic ,medicine ,Animals ,Humans ,CRYSTAL-STRUCTURE ,purl.org/becyt/ford/1.6 [https] ,SPECIFICITY ,Molecular Biology ,Nomenclature ,Caspase ,PARACASPASES ,ComputingMilieux_MISCELLANEOUS ,Plant Proteins ,030304 developmental biology ,Confusion ,0303 health sciences ,biology ,MALT1 ,Biology and Life Sciences ,Cell Biology ,3. Good health ,PROTEASES ,[SDV] Life Sciences [q-bio] ,KEY ,Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein ,Caspases ,biology.protein ,CLAN CD ,medicine.symptom ,030217 neurology & neurosurgery - Abstract
Metacaspases and paracaspases are proteases that were first identified as containing a caspase-like structural fold (Uren et al., 2000). Like caspases, metacaspases and paracaspases are multifunctional proteins regulating diverse biological phenomena, such as aging, immunity, proteostasis, and programmed cell death. The broad phylogenetic distribution of metacaspases and paracaspases across all kingdoms of life and large variation of their biochemical and structural features complicate classification and annotation of the rapidly growing number of identified homologs. Establishment of an adequate classification and unified nomenclature of metacaspases and paracaspases is especially important to avoid frequent confusion of these proteases with caspases—a tenacious misnomer that unfortunately does not appear to decline with time. This Letter represents a consensus opinion of researchers studying different aspects of caspases, metacaspases, and paracaspases in various organisms, ranging from microbes to plants and animals., This work was supported by the Knut and Alice Wallenberg Foundation.
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- 2020
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10. Contrasting Mixotrophic Lifestyles Reveal Different Ecological Niches in Two Closely Related Marine Protists
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Susanne Wilken, Chang Jae Choi, and Alexandra Z. Worden
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0106 biological sciences ,Oceans and Seas ,Plant Science ,Aquatic Science ,Biology ,010603 evolutionary biology ,01 natural sciences ,microbial food web ,Ochromonas ,mixotrophy ,chrysophytes ,Phytoplankton ,14. Life underwater ,Photosynthesis ,Life Style ,Ecosystem ,Ecological niche ,Facultative ,Microbial food web ,Obligate ,Ecology ,010604 marine biology & hydrobiology ,fungi ,Niche differentiation ,Eukaryota ,Regular Article ,Heterotrophic Processes ,15. Life on land ,13. Climate action ,phytoplankton ,phagotrophy ,Mixotroph ,Regular Articles - Abstract
Many marine microbial eukaryotes combine photosynthetic with phagotrophic nutrition, but incomplete understanding of such mixotrophic protists, their functional diversity, and underlying physiological mechanisms limits the assessment and modeling of their roles in present and future ocean ecosystems. We developed an experimental system to study responses of mixotrophic protists to availability of living prey and light, and used it to characterize contrasting physiological strategies in two stramenopiles in the genus Ochromonas. We show that oceanic isolate CCMP1393 is an obligate mixotroph, requiring both light and prey as complementary resources. Interdependence of photosynthesis and heterotrophy in CCMP1393 comprises a significant role of mitochondrial respiration in photosynthetic electron transport. In contrast, coastal isolate CCMP2951 is a facultative mixotroph that can substitute photosynthesis by phagotrophy and hence grow purely heterotrophically in darkness. In contrast to CCMP1393, CCMP2951 also exhibits a marked photoprotection response that integrates non-photochemical quenching and mitochondrial respiration as electron sink for photosynthetically produced reducing equivalents. Facultative mixotrophs similar to CCMP2951 might be well adapted to variable environments, while obligate mixotrophs similar to CCMP1393 appear capable of resource efficient growth in oligotrophic ocean environments. Thus, the responses of these phylogenetically close protists to the availability of different resources reveals niche differentiation that influences impacts in food webs and leads to opposing carbon cycle roles.
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- 2020
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11. Specialized proteomic responses and an ancient photoprotection mechanism sustain marine green algal growth during phosphate limitation
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Emily Nahas Reistetter, Charles Bachy, Chia-Lin Wei, Charles Ansong, Jian Guo, Alexandra Z. Worden, Stephen J. Callister, Ursula Goodenough, David S. Milner, Richard D. Smith, Lisa Sudek, Samuel O. Purvine, Thomas A. Richards, Valeria Jimenez, Denis Klimov, Richard O Dannebaum, Susanne Wilken, Govindarajan Kunde-Ramamoorthy, Virginia A. Elrod, Chang Jae Choi, and Freshwater and Marine Ecology (IBED, FNWI)
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0301 basic medicine ,Microbiology (medical) ,Immunology ,Cell Biology ,Biology ,Phosphate ,Photosynthesis ,biology.organism_classification ,Applied Microbiology and Biotechnology ,Microbiology ,Cell biology ,03 medical and health sciences ,chemistry.chemical_compound ,030104 developmental biology ,chemistry ,Algae ,Photoprotection ,Proteome ,Phytoplankton ,Genetics ,Photosystem ,Micromonas - Abstract
Marine algae perform approximately half of global carbon fixation, but their growth is often limited by the availability of phosphate or other nutrients. As oceans warm, the area of phosphate-limited surface waters is predicted to increase, resulting in ocean desertification. Understanding the responses of key eukaryotic phytoplankton to nutrient limitation is therefore critical. We used advanced photo-bioreactors to investigate how the widespread marine green alga Micromonas commoda grows under transitions from replete nutrients to chronic phosphate limitation and subsequent relief, analysing photosystem changes and broad cellular responses using proteomics, transcriptomics and biophysical measurements. We find that physiological and protein expression responses previously attributed to stress are critical to supporting stable exponential growth when phosphate is limiting. Unexpectedly, the abundance of most proteins involved in light harvesting does not change, but an ancient light-harvesting-related protein, LHCSR, is induced and dissipates damaging excess absorbed light as heat throughout phosphate limitation. Concurrently, a suite of uncharacterized proteins with narrow phylogenetic distributions increase multifold. Notably, of the proteins that exhibit significant changes, 70% are not differentially expressed at the mRNA transcript level, highlighting the importance of post-transcriptional processes in microbial eukaryotes. Nevertheless, transcript–protein pairs with concordant changes were identified that will enable more robust interpretation of eukaryotic phytoplankton responses in the field from metatranscriptomic studies. Our results show that P-limited Micromonas responds quickly to a fresh pulse of phosphate by rapidly increasing replication, and that the protein network associated with this ability is composed of both conserved and phylogenetically recent proteome systems that promote dynamic phosphate homeostasis. That an ancient mechanism for mitigating light stress is central to sustaining growth during extended phosphate limitation highlights the possibility of interactive effects arising from combined stressors under ocean change, which could reduce the efficacy of algal strategies for optimizing marine photosynthesis.
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- 2018
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12. The Lack of Knowledge on the Microbiome of Golf Turfgrasses Impedes the Development of Successful Microbial Products
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Uli Stingl, Chang Jae Choi, Braham Dhillon, and Marco Schiavon
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agricultural_sciences_agronomy ,turfgrasses ,microbiome ,microbial communities ,endophytes ,Agriculture ,biocontrol ,golf turf ,Agronomy and Crop Science - Abstract
Golf courses have a significant environmental impact. High water demands and the intensive use of agricultural chemicals have been a concern for decades and are therefore in the focus of efforts to make golf courses more environmentally sustainable. Products based on modifying or using plant-associated microbiota are one of the fastest growing sectors in agriculture, but their application on turfgrasses on golf courses is so far negligible. In this review, we summarize the limited knowledge on microbiomes of golf turf ecosystems and show that the lack of holistic studies addressing structure and function of golf turf microbiomes, including their responses to intense turf management procedures, is currently the main bottleneck for development and improvement of reliable, well-functioning microbial products. We further highlight the endosphere of turfgrasses, which is easily accessible for microbial cultivation through constant mowing, as the most stable and protected micro-environment. Many grass species do possess endophytic bacteria and fungi that have shown to improve the plants’ resistance towards microbial pathogens and insect pests, and several products using endophyte-enhanced grass varieties are commercially successful. We anticipated that this trend would tee-off on golf courses, too, once a more comprehensive understanding of golf turf microbiomes is available.
- Published
- 2021
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13. Insights into the loss factors of phytoplankton blooms: The role of cell mortality in the decline of two inshore Alexandrium blooms
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Deana L. Erdner, Chang Jae Choi, Taylor R. Sehein, Donald M. Anderson, and Michael L. Brosnahan
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0106 biological sciences ,congenital, hereditary, and neonatal diseases and abnormalities ,010504 meteorology & atmospheric sciences ,biology ,Ecology ,010604 marine biology & hydrobiology ,education ,fungi ,Cell ,nutritional and metabolic diseases ,Aquatic Science ,Plankton ,Oceanography ,biology.organism_classification ,01 natural sciences ,Algal bloom ,Article ,Cell loss ,medicine.anatomical_structure ,Alexandrium fundyense ,Phytoplankton ,medicine ,Eutrophication ,Bloom ,0105 earth and related environmental sciences - Abstract
While considerable effort has been devoted to understanding the factors regulating the development of phytoplankton blooms, the mechanisms leading to bloom decline and termination have received less attention. Grazing and sedimentation have been invoked as the main routes for the loss of phytoplankton biomass, and more recently, viral lysis, parasitism, and programmed cell death (PCD) have been recognized as additional removal factors. Despite the importance of bloom declines to phytoplankton dynamics, the incidence and significance of various loss factors in regulating phytoplankton populations have not been widely characterized in natural blooms. To understand mechanisms controlling bloom decline, we studied two independent, inshore blooms of Alexandrium fundyense, paying special attention to cell mortality as a loss pathway. We observed increases in the number of dead cells with PCD features after the peak of both blooms, demonstrating a role for cell mortality in their terminations. In both blooms, sexual cyst formation appears to have been the dominant process leading to bloom termination, as both blooms were dominated by small-sized gamete cells near their peaks. Cell death and parasitism became more significant as sources of cell loss several days after the onset of bloom decline. Our findings show two distinct phases of bloom decline, characterized by sexual fusion as the initial dominant cell removal processes followed by elimination of remaining cells by cell death and parasitism.
- Published
- 2017
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14. Specialized proteomic responses and an ancient photoprotection mechanism sustain marine green algal growth during phosphate limitation
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Jian, Guo, Susanne, Wilken, Valeria, Jimenez, Chang Jae, Choi, Charles, Ansong, Richard, Dannebaum, Lisa, Sudek, David S, Milner, Charles, Bachy, Emily Nahas, Reistetter, Virginia A, Elrod, Denis, Klimov, Samuel O, Purvine, Chia-Lin, Wei, Govindarajan, Kunde-Ramamoorthy, Thomas A, Richards, Ursula, Goodenough, Richard D, Smith, Stephen J, Callister, and Alexandra Z, Worden
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Proteomics ,Bioreactors ,Bacterial Proteins ,Chlorophyta ,Gene Expression Profiling ,Phytoplankton ,Gene Expression Regulation, Developmental ,Photosynthesis ,Phylogeny ,Phosphates - Abstract
Marine algae perform approximately half of global carbon fixation, but their growth is often limited by the availability of phosphate or other nutrients
- Published
- 2017
15. Quantitative biogeography of picoprasinophytes establishes ecotype distributions and significant contributions to marine phytoplankton
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Marguerite Blum, Alexandra Z. Worden, Sebastian Sudek, Ursula Goodenough, Matthew J. Church, Robyn Roth, Yoshimi M. Rii, Camille Poirier, Alexander J. Limardo, and Chang Jae Choi
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0106 biological sciences ,0301 basic medicine ,Chlorophyll ,Oceans and Seas ,Tropical Atlantic ,Environment ,Bathycoccus prasinos ,01 natural sciences ,Microbiology ,Bathycoccus ,Ostreococcus ,03 medical and health sciences ,Algae ,Chlorophyta ,Phytoplankton ,Seawater ,14. Life underwater ,Ecology, Evolution, Behavior and Systematics ,Phylogeny ,Ecotype ,Deep chlorophyll maximum ,biology ,Geography ,Ecology ,010604 marine biology & hydrobiology ,biology.organism_classification ,030104 developmental biology ,13. Climate action ,Upwelling ,Seasons - Abstract
Bathycoccus and Ostreococcus are broadly distributed marine picoprasinophyte algae. We enumerated small phytoplankton using flow cytometry and qPCR assays for phylogenetically distinct Bathycoccus clades BI and BII and Ostreococcus clades OI and OII. Among 259 photic-zone samples from transects and time-series, Ostreococcus maxima occurred in the North Pacific coastal upwelling for OI (36 713 ± 1485 copies ml−1) and the Kuroshio Front for OII (50 189 ± 561 copies ml−1) and the two overlapped only in frontal regions. The Bathycoccus overlapped more often with maxima along Line-P for BI (10 667 ± 1299 copies ml−1) and the tropical Atlantic for BII (4125 ± 339 copies ml−1). Only BII and OII were detected at warm oligotrophic sites, accounting for 34 ± 13 of 1589 ± 448 eukaryotic phytoplankton cells ml−1 (annual average) at Station ALOHA's deep chlorophyll maximum. Significant distributional and molecular differences lead us to propose that Bathycoccus clade BII represents a separate species which tolerates higher temperature oceanic conditions than Bathycoccus prasinos (BI). Morphological differences were not evident, but quick-freeze deep-etch electron microscopy provided insight into Bathycoccus scale formation. Our results highlight the importance of quantitative seasonal abundance data for inferring ecological distributions and demonstrate significant, differential picoprasinophyte contributions in mesotrophic and open-ocean waters. © 2017 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd.
- Published
- 2017
16. Newly discovered deep-branching marine plastid lineages are numerically rare but globally distributed
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Stephen J. Giovannoni, Gualtiero Spiro Jaeger, Chang Jae Choi, Camille Poirier, V.V.S.S. Sarma, Amala Mahadevan, Alexandra Z. Worden, Lisa Sudek, and Charles Bachy
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0301 basic medicine ,media_common.quotation_subject ,Climate Change ,Oceans and Seas ,030106 microbiology ,Photosynthesis ,Deep sea ,General Biochemistry, Genetics and Molecular Biology ,03 medical and health sciences ,Food chain ,Algae ,RNA, Ribosomal, 16S ,Phytoplankton ,Ecosystem ,14. Life underwater ,Plastids ,Plastid ,media_common ,Agricultural and Biological Sciences(all) ,biology ,Biochemistry, Genetics and Molecular Biology(all) ,Ecology ,fungi ,15. Life on land ,biology.organism_classification ,Biological Evolution ,Carbon ,030104 developmental biology ,Desertification ,13. Climate action ,General Agricultural and Biological Sciences - Abstract
Ocean surface warming is resulting in an expansion of stratified, low-nutrient environments, a process referred to as ocean desertification 1. A challenge for assessing the impact of these changes is the lack of robust baseline information on the biological communities that carry out marine photosynthesis. Phytoplankton perform half of global biological CO2 uptake, fuel marine food chains, and include diverse eukaryotic algae that have photosynthetic organelles (plastids) acquired through multiple evolutionary events 1–3. While amassing data from ocean ecosystems for the Baselines Initiative (6,177 near full-length 16S rRNA gene sequences and 9.4 million high-quality 16S V1-V2 amplicons) we identified two deep-branching plastid lineages based on 16S rRNA gene data. The two lineages have global distributions, but do not correspond to known phytoplankton. How the newly discovered phytoplankton lineages contribute to food chains and vertical carbon export to the deep sea remains unknown, but their prevalence in expanding, low nutrient surface waters suggests they will have a role in future oceans. © 2017 The Author(s)
- Published
- 2017
17. Cell death in algae: physiological processes and relationships with stress
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John A. Berges and Chang Jae Choi
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Programmed cell death ,Algae ,biology ,Apoptosis ,Phytoplankton ,Botany ,biology.organism_classification ,Cell biology - Published
- 2014
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18. Effects of intensity and seasonal timing of disturbances on a rocky intertidal benthic community on the southern coast of Korea
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Sangil Kim, Chang Jae Choi, Sang Rul Park, In-Soo Seo, Nam-Il Won, Sukgeun Jung, Hyuk Je Lee, and Yun Hee Kang
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Disturbance (geology) ,Algae ,biology ,Benthic zone ,Ecology ,fungi ,Intertidal zone ,Species diversity ,Species richness ,biology.organism_classification ,Algal bloom ,Bay ,Ecology, Evolution, Behavior and Systematics - Abstract
The effects of intensity and timing of disturbances on recovery of marine benthic organisms were investigated on a rocky intertidal shore in Gwangyang Bay, Korea. We hypothesized that the recovery pattern of the benthic community structure would be affected by disturbance intensity and season. Twenty-eight permanent plots were set up, with disturbance intensity (cleared plots and sterile plots) and seasonal disturbance (fall 1999 and spring 2000) incorporated into the experimental design. To monitor natural seasonal variation in benthic community abundances, we established seven permanent unmanipulated plots. Turf-forming algae were observed in the unmanipulated plots throughout the experimental period, whereas green algae and invertebrate presence varied with season. In the disturbance-intensity experiment, turf-forming and green algae were dominant in cleared plots. The highest coverage of sessile organisms was observed in sterile plots, which exhibited the highest species richness because of their relatively low macroalgal coverage. Seasonal effects of disturbance were an important factor in the recovery pattern of benthic organisms under high disturbance intensity. Coverage of green algae was higher in sterile spring plots than in sterile fall plots; this result was attributed to low spatial competition, as the disturbances occurred just before green algal blooms. On the other hand, the abundances of barnacles and bivalves were highest on sterile fall plots, as these organisms were suppressed by green algal blooms in other periods. These results indicate that the effects of disturbance intensity on benthic community recovery patterns can be influenced by season of disturbance.
- Published
- 2014
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19. Rapid effects of diverse toxic water pollutants on chlorophyll a fluorescence: Variable responses among freshwater microalgae
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Erica B. Young, John A. Berges, and Chang Jae Choi
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Chlorophyll ,Chlorophyll a ,Time Factors ,Environmental Engineering ,Photosystem II ,Fresh Water ,Biology ,Photosynthesis ,Fluorescence ,chemistry.chemical_compound ,Species Specificity ,Botany ,Microalgae ,Parathion methyl ,Atrazine ,Waste Management and Disposal ,Water Science and Technology ,Civil and Structural Engineering ,Chlorophyll A ,Ecological Modeling ,Terbuthylazine ,Pollution ,chemistry ,Environmental chemistry ,Carbofuran ,Water Pollutants, Chemical - Abstract
Chlorophyll a fluorescence of microalgae is a compelling indicator of toxicity of dissolved water contaminants, because it is easily measured and responds rapidly. While different chl a fluorescence parameters have been examined, most studies have focused on single species and/or a narrow range of toxins. We assessed the utility of one chl a fluorescence parameter, the maximum quantum yield of PSII (F(v)/F(m)), for detecting effects of nine environmental pollutants from a range of toxin classes on 5 commonly found freshwater algal species, as well as the USEPA model species, Pseudokirchneriella subcapitata. F(v)/F(m) declined rapidly over
- Published
- 2012
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20. Dentigerous Cysts Involving Maxillary Sinuses
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Sang Hag Lee, Tae Hoon Kim, Chang Jae Choi, Il Ho Park, Hak Chun Lee, Seung Hoon Lee, Hyuck Sung Kwon, and Heung Man Lee
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business.industry ,Medicine ,business - Published
- 2009
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21. Effect of dead phytoplankton cells on the apparent efficiency of photosystem II
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John A. Berges, Chang Jae Choi, Gill Malin, Daniel J. Franklin, and Claire Hughes
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Photoinhibition ,Ecology ,Photosystem II ,Productivity (ecology) ,Surface ocean ,Phytoplankton ,Botany ,Aquatic Science ,Biology ,Chlorophyll fluorescence ,Ecology, Evolution, Behavior and Systematics ,Primary productivity ,Photosystem - Abstract
Measurements of the efficiency of photosystem (PS) II have become widespread in bio- logical oceanography, and various forms are used to assess the 'health' of marine phytoplankton and to help estimate primary productivity. Absolute values of PS II efficiency depend to some extent on the measuring system, but changes in PS II efficiency are most commonly interpreted in terms of cel- lular acclimations to changing irradiance (including photoacclimation and photoinhibition) and nutri- ent availability (especially N and Fe). Recent measurements of phytoplankton viability in the surface ocean have revealed that in many regions phytoplankton assemblages may contain large proportions of dead cells. The effect of these dead cells on apparent PS II efficiency is largely unknown. By mix- ing live and dead cells and measuring PS II efficiency, we show that the presence of photosyntheti- cally non-functional (dead) cells has surprisingly little effect; in a number of species, mixtures in which 50% of the cells were dead had values of 0.5, similar to values often found in natural assem- blages. A simple model indicates that the non-linear nature of the fluorescence ratio is responsible for this unexpected result. We conclude that relatively high values of PS II efficiency cannot be used as evidence of low mortality. Our findings highlight the need for more information on the physiological status of both eukaryotic and prokaryotic microalgae in nature.
- Published
- 2009
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22. The Helicobacter Pylori Infection in Upper Aerodigetive Tract Mucosal Disease by Urea Breath Test(UBT)
- Author
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Jeong-Soo Woo, Hyung Jin Jun, Seung-Kuk Baek, Kwang-Yoon Jung, Chang Jae Choi, Sung Won Chae, Hyuck Sung Kwon, Jae Gu Cho, and Soon-Young Kwon
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Helicobacter pylori infection ,medicine.medical_specialty ,medicine.diagnostic_test ,business.industry ,Internal medicine ,Urea breath test ,Medicine ,Mucosal disease ,business ,Gastroenterology - Published
- 2008
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23. Dynamic Regulation of GacA in Type III Secretion, Pectinase Gene Expression, Pellicle Formation, and Pathogenicity of Dickeya dadantii (Erwinia chrysanthemi 3937)
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Amy O. Charkowski, Chang Jae Choi, Qiu Zhang, Xuan Yi, Ralph M. Reedy, Shihui Yang, Quan Peng, and Ching-Hong Yang
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Physiology ,Bacterial Toxins ,Microbiology ,Cell wall ,Magnoliopsida ,Bacterial Proteins ,Gene expression ,Gene Regulatory Networks ,Secretion ,RNA, Messenger ,Pectinase ,Plant Diseases ,Polysaccharide-Lyases ,chemistry.chemical_classification ,biology ,Dickeya chrysanthemi ,Gene Expression Regulation, Bacterial ,General Medicine ,Pathogenicity ,biology.organism_classification ,Dickeya dadantii ,Polygalacturonase ,Enzyme ,chemistry ,Genes, Bacterial ,Spectrophotometry ,Biofilms ,Erwinia chrysanthemi ,Mutation ,Agronomy and Crop Science - Abstract
Dickeya dadantii (Erwinia chrysanthemi 3937) secretes exoenzymes, including pectin-degrading enzymes, leading to the loss of structural integrity of plant cell walls. A type III secretion system (T3SS) is essential for full virulence of this bacterium within plant hosts. The GacS/GacA two-component signal transduction system participates in important biological roles in several gram-negative bacteria. In this study, a gacA deletion mutant (Ech137) of D. dadantii was constructed to investigate the effect of this mutation on pathogenesis and other phenotypes. Compared with wild-type D. dadantii, Ech137 had a delayed biofilm-pellicle formation. The production of pectate lyase (Pel), protease, and cellulase was diminished in Ech137 compared with the wild-type cells. Reduced transcription of two endo-Pel genes, pelD and pelL, was found in Ech137 using a green fluorescence protein-based fluorescence-activated cell sorter promoter activity assay. In addition, the transcription of T3SS genes dspE (an effector), hrpA (a structural protein of the T3SS pilus), and hrpN (a T3SS harpin) was reduced in Ech137. A lower amount of rsmB regulatory RNA was found in gacA mutant Ech137 compared with the wild-type bacterium by quantitative reverse-transcription polymerase chain reaction. Compared with wild-type D. dadantii, a lower amount of hrpL mRNA was observed in Ech137 at 12 h grown in medium. Although the role of RsmA, rsmB, and RsmC in D. dadantii is not clear, from the regulatory pathway revealed in E. carotovora, the lower expression of dspE, hrpA, and hrpN in Ech137 may be due to a posttranscriptional regulation of hrpL through the Gac-Rsm regulatory pathway. Consequently, the reduced exoenzyme production and Pel gene expression in the mutant may be partially due to the regulatory role of rsmB-RsmA on exoenzyme expression. Similar to in vitro results, a lower expression of T3SS and pectinase genes of Ech137 also was observed in bacterial cells inoculated into Saintpaulia ionantha leaves, perhaps accounting for the observed reduction in local maceration. Interestingly, compared with the wild-type D. dadantii, although a lower concentration of Ech137 was observed at day 3 and 4 postinoculation, there is no significant difference in bacterial concentration between the wild-type bacterium and Ech137 in the early stage of infection. Finally, the nearly abolished systemic invasion ability of Ech137 suggests that GacA of D. dadantii is essential for the pathogenicity and systemic movement of the bacterium in S. ionantha.
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- 2008
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24. Bilateral Lymphoepithelial Cysts of the Thyroid Gland
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Sung Woong Choi, Chang Jae Choi, Jeong Soo Woo, and Jae Gu Cho
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Pathology ,medicine.medical_specialty ,Endocrinology ,Text mining ,medicine.anatomical_structure ,business.industry ,Endocrinology, Diabetes and Metabolism ,Thyroid ,Medicine ,business - Published
- 2010
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25. New types of metacaspases in phytoplankton reveal diverse origins of cell death proteases
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Chang Jae Choi and John A. Berges
- Subjects
Cancer Research ,Proteases ,Programmed cell death ,Databases, Factual ,Immunology ,Apoptosis ,Evolution, Molecular ,Cellular and Molecular Neuroscience ,unicellular organism ,Transcription (biology) ,Phylogenetics ,evolution ,Plastid ,bacteria ,Gene ,Caspase ,Phylogeny ,Genetics ,biology ,fungi ,Cell Biology ,Sequence Analysis, DNA ,biology.organism_classification ,Protein Structure, Tertiary ,Caspases ,Phytoplankton ,metacaspase ,biology.protein ,Original Article ,Bacteria ,Peptide Hydrolases - Abstract
Metacaspases are evolutionarily distant homologs of caspases that are found outside the metazoan and are known to have key roles in programmed cell death (PCD). Two types of metacaspases (types I and II) have been defined in plants based on their domain structures; these have similarities to metazoan 'initiator' and 'executioner' caspases. However, we know little about metacaspases in unicellular organisms and even less about their roles in cell death. We identified a novel group of metacaspases in sequenced phytoplanktonic protists that show domain architectures distinct from either type I or II enzymes; we designate them as type III. Type III metacaspases exhibit a rearrangement of domain structures between N- and C-terminus. In addition, we found a group of metacaspase-like proteases in phytoplankton that show sequence homology with other metacaspases, but defy classification in conventional schemes. These metacaspase-like proteases exist in bacteria alongside a variant of type I metacaspases and we propose these bacterial metacaspases are the origins of eukaryotic metacaspases. Type II and III metacaspases were not detected in bacteria and they might be variants of bacterial type I metacaspases that evolved in plants and phytoplanktonic protists, respectively, during the establishment of plastids through the primary and secondary endosymbiotic events. A complete absence of metacaspases in protists that lost plastids, such as oomycetes and ciliates indicates the gene loss during the plastid-to-nucleus gene transfer. Taken together, our findings suggest endosymbiotic gene transfer (EGT) is a key mechanism resulting in the evolutionary diversity of cell death proteases.
- Published
- 2013
26. A head shake sensory organization test to improve the sensitivity of the sensory organization test in the elderly
- Author
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Soon Jae Hwang, Moo Kyun Park, Jae-Gu Cho, Chang Jae Choi, Hyun Woo Lim, and Sung Won Chae
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Adult ,Male ,medicine.medical_specialty ,Aging ,Sensory system ,Body Mass Index ,Young Adult ,Reference Values ,medicine ,Humans ,Young adult ,Postural Balance ,Aged ,Vestibular system ,Head shake ,business.industry ,Healthy population ,Healthy subjects ,Middle Aged ,Vestibular Function Tests ,Sensory Systems ,Test (assessment) ,Otorhinolaryngology ,Data Interpretation, Statistical ,Head Movements ,Sensation Disorders ,Physical therapy ,Female ,Neurology (clinical) ,business ,Body mass index - Abstract
Objective The head shake sensory organization test (HS-SOT) is an expansion of the sensory organization test (SOT), which evaluates impairment of the patient's ability to apply vestibular input while actively moving the head. HS-SOTs has been proposed to increase the sensitivity of SOTs. The purpose of this study was to investigate the value of HS-SOTs in a healthy population with respect to age and compare the sensitivity of HS-SOTs with that of SOTs in the elderly population. Methods One hundred two (n = 102) healthy subjects were divided into 3 age groups: the young adult group (between 20 and 39 yr), the adult group (between 40 and 59 yr), and the elderly group (between 60 and 79 yr). The subjects underwent SOTs and HS-SOTs. Results The equilibrium scores of HS-SOTs underwent more significant change than those of SOTs in the elderly group. The equilibrium score ratio SOT2/HS-SOT2 (HS-SOT during SOT condition 2) decreased by 4% more in the elderly group compared with that of the young adult group. The ratio of SOT5/HS-SOT5 decreased by 54% more in the elderly group compared with that of the young adult group. Conclusion In the elderly, equilibrium scores of HS-SOTs changed more than those of SOTs. In addition, SOT5/HS-SOT5 demonstrated more sensitive changes in the elderly than SOT2/HS-SOT2 did.
- Published
- 2011
27. Does the kyphotic change decrease the risk of fall?
- Author
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Hyun Woo Lim, Gi Jung Im, Moo Kyun Park, Sung Won Chae, Chang Jae Choi, and Jae-Gu Cho
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medicine.medical_specialty ,Dynamic posturography ,business.industry ,Posturography ,lcsh:R ,Kyphosis ,Poison control ,Motor control ,lcsh:Medicine ,medicine.disease ,lcsh:Otorhinolaryngology ,Gait ,lcsh:RF1-547 ,medicine.anatomical_structure ,Otorhinolaryngology ,medicine ,Physical therapy ,Surgery ,Original Article ,Ankle ,Latency (engineering) ,business ,Accidental falls ,Balance (ability) - Abstract
OBJECTIVES: Falls are a major problem in the elderly. Age-related degeneration of the human balance system increases the risk of falls. Kyphosis is a common condition of curvature of the upper spine in the elderly and its development occurs through degenerative change. However, relatively little is known about the effect of kyphotic changes on balance in the elderly. The aim of this study is to investigate the influence of kyphosis on the balance strategy through use of the motor control test (MCT) in computerized dynamic posturography. METHODS: Fifty healthy subjects who were not affected by other medical disorders that could affect gait or balance were enrolled in the study. By simulation of kyphotic condition through change of the angles of the line connecting the shoulder to the hip and the ankle axis by approximately 30°, the latency and amplitude of the MCT were measured in upright and kyphotic condition. RESULTS: In the kyphotic condition, latency was shortened in backward movement. In forward movement, latency was shortened only in large stimulation. The amplitude in forward movement was decreased in kyphotic condition. However, the change of amplitude was not significant in large intensity backward movement in the same condition. CONCLUSION: Kyphotic condition decreases the latency of MCT, especially in backward movement. These findings imply that kyphotic condition may serve as a protective factor against falls. Language: en
- Published
- 2010
28. The $Phaeodactylum$ genome reveals the evolutionary history of diatom genomes
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Yves Van de Peer, Michael R. Sussman, Frédéric Verret, Miyoshi Haruta, Angela Falciatore, John A. Berges, Leszek Rychlewski, Anusuya Willis, Richard E. Jorgensen, Michael Katinka, Jane Grimwood, Betina M. Porcel, Magali Siaut, Klaus Valentin, Pascal J. Lopez, Marc Heijde, Véronique Martin-Jézéquel, Jean-Louis Petit, Wim Vyverman, Edda Rayko, Klaas Vandepoele, Miroslav Oborník, Anthony Chiovitti, Alan Kuo, E. Virginia Armbrust, Matthew Robison, Alessandra De Martino, Nils Kröger, Susan Lucas, Colin Brownlee, Alison Taylor, Igor V. Grigoriev, Jonathan H. Badger, Kamel Jabbari, Jérome Fournet, Jeremy Schmutz, Uma Maheswari, Sacha Coesel, Michele S. Stanley, J. Chris Detter, Chang Jae Choi, Thomas Mock, Assaf Vardi, Markus Lommer, Aaron Kaplan, Yolaine Joubert, Florian Maumus, Katerina Jiroutova, Anton Montsant, Colleen A. Durkin, Cindy Martens, Bank Beszteri, Micaela S. Parker, Asaf Salamov, Linda K. Medlin, Karen M. McGinnis, Ansgar Gruber, Marie J. J. Huysman, Manuela Mangogna, Lucyan S. Wyrwicz, Jean-Paul Cadoret, Peter von Dassow, Daniel S. Rokhsar, Marie-Pierre Oudot-Le Secq, Carolyn A. Napoli, Beverley R. Green, Erica Lindquist, Peter G. Kroth, Chris Bowler, Andrew E. Allen, Tatiana A. Rynearson, Nicole Poulsen, Bethany D. Jenkins, Harris Shapiro, Robert Otillar, Jean Weissenbach, École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL), J. Craig Venter Institute, J. Craig Venter Institute [La Jolla, USA] (JCVI), Department of Energy / Joint Genome Institute (DOE), Los Alamos National Laboratory (LANL), DOE Joint Genome Institute [Walnut Creek], Center for Plant Systems Biology (PSB Center), Vlaams Instituut voor Biotechnologie [Ghent, Belgique] (VIB), Institut de biologie de l'Ecole Normale Supérieure (IBENS), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Alfred-Wegener-Institut, Helmholtz-Zentrum für Polar- und Meeresforschung (AWI), Biologie moléculaire des organismes photosynthétiques (UMR8186), Département de Biologie - ENS Paris, Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure - Paris (ENS-PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), Genoscope - Centre national de séquençage [Evry] (GENOSCOPE), Université Paris-Saclay-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Environnement, Bioénergie, Microalgues et Plantes (EBMP), Institut de Biosciences et Biotechnologies d'Aix-Marseille (ex-IBEB) (BIAM), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Marine Biological Association, Physiologie et biotechnologie des Algues (PBA), Biotechnologies et Ressources Marines (BRM), Institut Français de Recherche pour l'Exploitation de la Mer (IFREMER)-Institut Français de Recherche pour l'Exploitation de la Mer (IFREMER), Laboratory of Ecology and Evolution of Plankton, Stazione Zoologica Anton Dohrn (SZN), Génomique des Microorganismes (LGM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS), Marine Biogeochemistry, Leibniz-Institut für Meereswissenschaften (IFM-GEOMAR), Biology Institute, University of Arizona, School of Oceanography [Seattle], University of Washington [Seattle], Stanford School of Medicine [Stanford], Stanford Medicine, Stanford University-Stanford University, Station biologique de Roscoff [Roscoff] (SBR), European Project: 29849,DIATOMICS, Savelli, Bruno, Understanding Diatom Biology by Functional Genomics Approaches - DIATOMICS - 29849 - OLD, École normale supérieure - Paris (ENS Paris), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-École normale supérieure - Paris (ENS Paris), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Bioénergie et Microalgues (EBM), Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Institut Français de Recherche pour l'Exploitation de la Mer (IFREMER), Génomique des microorganismes, and Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure - Paris (ENS Paris)
- Subjects
0106 biological sciences ,Thalassiosira pseudonana ,Molecular Sequence Data ,01 natural sciences ,Genome ,Evolution, Molecular ,03 medical and health sciences ,DNA, Algal ,Phylogenetics ,[SDV.BID.EVO] Life Sciences [q-bio]/Biodiversity/Populations and Evolution [q-bio.PE] ,Gene family ,[SDV.BV]Life Sciences [q-bio]/Vegetal Biology ,[SDV.BV] Life Sciences [q-bio]/Vegetal Biology ,14. Life underwater ,Phaeodactylum tricornutum ,Gene ,030304 developmental biology ,Genetics ,Diatoms ,0303 health sciences ,Multidisciplinary ,biology ,Sequence Homology, Amino Acid ,Heterokont ,[SDV.BID.EVO]Life Sciences [q-bio]/Biodiversity/Populations and Evolution [q-bio.PE] ,fungi ,biology.organism_classification ,Protein Structure, Tertiary ,Diatom ,Genes, Bacterial ,Biologie ,010606 plant biology & botany ,Signal Transduction - Abstract
Diatoms are photosynthetic secondary endosymbionts found throughout marine and freshwater environments, and are believed to be responsible for around one-fifth of the primary productivity on Earth. The genome sequence of the marine centric diatom Thalassiosira pseudonana was recently reported, revealing a wealth of information about diatom biology. Here we report the complete genome sequence of the pennate diatom Phaeodactylum tricornutum and compare it with that of T. pseudonana to clarify evolutionary origins, functional significance and ubiquity of these features throughout diatoms. In spite of the fact that the pennate and centric lineages have only been diverging for 90 million years, their genome structures are dramatically different and a substantial fraction of genes (
- Published
- 2008
- Full Text
- View/download PDF
29. Inflammatory Myofibroblastic Tumor of the Nasal Cavity
- Author
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Jeong-Soo Woo, Jin Ho Jung, Chang Jae Choi, and Jae-Gu Cho
- Subjects
Nasal cavity ,Pathology ,medicine.medical_specialty ,Fatal outcome ,Lung ,business.industry ,macromolecular substances ,Malignant transformation ,medicine.anatomical_structure ,Otorhinolaryngology ,medicine ,Surgery ,Mesentery ,Head and neck ,business ,Myofibroblast ,Sinus (anatomy) - Abstract
Inflammatory myofibroblastic tumor is an uncommon tumor composed of myofibroblasts and various types of inflammatory infiltrates that rarely undergoes malignant transformation. It commonly involves the lung, liver, mesentery but rarely affects the head and neck region. Although inflammatory myofibroblastic tumor is generally considered a benign reactive inflammatory process, it may present clinically and radiologically as an invasive mass destructing the surrounding structures. Therefore, it should be considered as one of several differential diagnoses from malignant tumors. We present a case of inflammatory myofibroblastic tumor involving the nasal cavity, maxillary, ethmoid, and sphenoid sinus with a fatal outcome. Korean J Otorhinolaryngol-Head Neck Surg 2009;52:1005-8 Key WordsZZInflammatory myofibroblastic tumor·Nasal cavity·Steroids.
- Published
- 2009
- Full Text
- View/download PDF
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