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 uBio  Web Results 71 - 80 of about 4227

Broader Terms:
   Haslea 
   Holophaga/Acidobacteria ensemble 
   Paralemanea 
   clinical samples 
   environmental samples 
   unclassified 
   uncultured 

More Specific:
   uncultured 
   uncultured ectomycorrhiza 
 
 


External Resources:



71.  Molecular Detection of Microorganisms Associated with Small Mammals and Their Ectoparasites in Mali.LinkIT
Diarra AZ, Kone AK, Doumbo Niare S, Laroche M, Diatta G, Atteynine SA, Coulibaly M, Sangare AK, Kouriba B, Djimde A, Dabo A, Sagara I, Davoust B, Ranque S, Thera MA, Raoult D, Doumbo OK, Parola P
The American journal of tropical medicine and hygiene, 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

72.  Vaginal Microbiota Is Stable throughout the Estrous Cycle in Arabian Maress.LinkIT
Barba M, Martínez-Boví R, Quereda JJ, Mocé ML, Plaza-Dávila M, Jiménez-Trigos E, Gómez-Martín Á, González-Torres P, Carbonetto B, García-Roselló E
Animals : an open access journal from MDPI, 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

73.  Bacterial communities of sponges from the wetland ecosystem of Little Rann of Kutch, India with particular reference to Planctomycetes.LinkIT
Kumar G, Radha V, Jagadeeshwari U, Sasikala C, Venkata Ramana C
3 Biotech, 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

74.  High-throughput cultivation based on dilution-to-extinction with catalase supplementation and a case study of cultivating acI bacteria from Lake Soyang.LinkIT
Kim S, Park MS, Song J, Kang I, Cho JC
Journal of microbiology (Seoul, Korea), 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

75.  UV-A Irradiation Increases Scytonemin Biosynthesis in Cyanobacteria Inhabiting Halites at Salar Grande, Atacama Desert.LinkIT
Orellana G, Gómez-Silva B, Urrutia M, Galetovi? A
Microorganisms, 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

76.  State of the Art in the Culture of the Human Microbiota: New Interests and Strategies.LinkIT
Tidjani Alou M, Naud S, Khelaifia S, Bonnet M, Lagier JC, Raoult D
Clinical microbiology reviews, 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

77.  Innovations to culturing the uncultured microbial majority.LinkIT
Lewis WH, Tahon G, Geesink P, Sousa DZ, Ettema TJG
Nature reviews. Microbiology, 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

78.  Seasonal Regime Shift in the Viral Communities of a Permafrost Thaw Lake.LinkIT
Girard C, Langlois V, Vigneron A, Vincent WF, Culley AI
Viruses, 2020
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=0

79.  Seasonal and Geographical Transitions in Eukaryotic Phytoplankton Community Structure in the Atlantic and Pacific Oceans.LinkIT
Choi CJ, Jimenez V, Needham DM, Poirier C, Bachy C, Alexander H, Wilken S, Chavez FP, Sudek S, Giovannoni SJ, Worden AZ
Frontiers in microbiology, 2020 Frontiers in microbiology Front Microbiol Seasonal and Geographical Transitions in Eukaryotic Phytoplankton Community Structure in the Atlantic and Pacific Oceans. 542372 10.3389/fmicb.2020.542372 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. Copyright © 2020 Choi, Jimenez, Needham, Poirier, Bachy, Alexander, Wilken, Chavez, Sudek, Giovannoni and Worden. Choi Chang Jae CJ Ocean EcoSystems Biology Unit, GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany. Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States. Jimenez Valeria V Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States. Needham David M DM Ocean EcoSystems Biology Unit, GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany. Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States. Poirier Camille C Ocean EcoSystems Biology Unit, GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany. Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States. Bachy Charles C Ocean EcoSystems Biology Unit, GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany. Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States. Alexander Harriet H Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States. Biology Department, Woods Hole Oceanographic Institution, Woods Hole, MA, United States. Wilken Susanne S Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States. Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, Amsterdam, Netherlands. Chavez Francisco P FP Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States. Sudek Sebastian S Monterey Bay Aquarium Research Institute, Moss Landing, CA, United States. Giovannoni Stephen J SJ Department of Microbiology, Oregon State University, Corvallis, OR, United States. Worden Alexandra Z AZ Ocean EcoSystems Biology Unit, GEOMAR Helmholtz Centre for Ocean Research Kiel, Kiel, Germany. 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This report is based on a colloquium, sponsored by the American Academy of Microbiology, convened September 2008 in Washington, DC. 2009
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