146 research outputs found

    Mycorrhizal colonization and its relationship with plant performance differs between exotic and native grassland plant species

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    Many grasslands have been transformed by exotic species with potentially novel ecological interactions. We hypothesized that exotic and native plant species differ, on average, in their percentage mycorrhizal colonization, and that mycorrhizal colonization is positively related to plant performance in the field. We compared colonization by arbuscular mycorrhizae (AM) fungi in perennial native and exotic species that were paired phylogenetically and by functional groups and grown under a common environment in field plots in Central Texas, USA. Roots were collected from plants in monoculture plots, stained, and percent colonization was assessed with a microscope. Aboveground biomass and dominance in mixture were used as measures of plant performance. Exotic species had significantly higher colonization of AM than native species, and this result was consistent across functional groups. Percent colonization was positively correlated with biomass and dominance in mixture across native species, but not across exotic species. Our results indicate that mycorrhizal dependence is a more important predictor of competitive balance among native than exotic plant species in the subhumid grasslands of the USA

    Microbial community structure and functions differ between native and novel (exotic-dominated) grassland ecosystems in an 8-year experiment

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    A Grasslands dominated by non-native (exotic) spe- cies have replaced purely native-dominated areas in many parts of the world forming ā€˜novelā€™ ecosystems. Altered precipitation patterns are predicted to exacerbate this trend. It is still poorly understood how soil microbial communities and their functions differ between high diversity native- and low diversity exotic-dominated sites and how altered precipitation will impact this difference. Methods We sampled 64 experimental grassland plots in central Texas with plant species mixtures of either all native or all exotic species; half with summer irrigation. We tested how native vs. exotic plant species mixtures and summer irrigation affected bacterial and fungal community composition and structure, the influence of niche vs. neutral processes for microbial phylotype co- occurrence (C-score analysis), and rates of phosphorus and nitrogen mineralization across an 8-year experiment. Results Native and exotic-dominated plots had sig- nificantly different fungal community composition and structure, but not diversity, throughout the length of the study, while changes in bacterial communities were limited to certain wet and cool years. Nitrogen and phosphorus mineralization rates were higher un- der native plant mixtures and correlated with the abundance of particular fungal species. Microbial communities were more structured in exotic than native grassland plots, especially for the fungal community. Conclusions The results indicate that conversion of native to exotic C4 dominated grasslands will more strongly impact fungal than bacterial community structure. Further- more, these impacts can alter ecosystem functioning be- lowground via changes in nitrogen and phosphorus cycling

    Soil depth and grassland origin cooperatively shape microbial community coā€occurrence and function

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    Many soils are deep, yet soil below 20 cm remains largely unexplored. Exotic plants can have shallower roots than native species, so their impact on microorganisms is anticipated to change with depth. Using environmental DNA and extracellular enzymatic activities, we studied fungal and bacterial community composition, diversity, function, and co-occurrence networks between native and exotic grasslands at soil depths up to 1 m. We hypothesized (1) the composition and network structure of both fungal and bacterial communities will change with increasing depth, and diversity and enzymatic function will decrease; (2) microbial enzymatic function and network connectedness will be lower in exotic grasslands; and (3) irrigation will alter microbial networks, increasing the overall connectedness. Microbial diversity decreased with depth, and community composition was distinctly different between shallow and deeper soil depths with higher numbers of unknown taxa in lower soil depths. Fungal communities differed between native and exotic plant communities. Microbial community networks were strongly shaped by biotic and abiotic factors concurrently and were the only microbial measurement affected by irrigation. In general, fungal communities were more connected in native plant communities than exotic, especially below 10 cm. Fungal networks were also more connected at lower soil depths albeit with fewer nodes. Bacterial communities demonstrated higher complexity, and greater connectedness and nodes, at lower soil depths for native plant communities. Exotic plant communitiesā€™ bacterial network connectedness altered at lower soil depths dependent on irrigation treatments. Microbial extracellular enzyme activity for carbon cycling enzymes significantly declined with soil depth, but enzymes associated with nitrogen and phosphorus cycling continued to have similar activities up to 1 m deep. Our results indicate that native and exotic grasslands have significantly different fungal communities in depths up to 1 m and that both fungal and bacterial networks are strongly shaped jointly by plant communities and abiotic factors. Soil depth is independently a major determinant of both fungal and bacterial community structures, functions, and co-occurrence networks and demonstrates further the importance of including soil itself when investigating plantā€“microbe interactions

    A first measurement of the interaction cross section of the tau neutrino

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    The DONuT experiment collected data in 1997 and published first results in 2000 based on four observed Ī½Ļ„\nu_\tau charged-current (CC) interactions. The final analysis of the data collected in the experiment is presented in this paper, based on 3.6Ɨ10173.6 \times 10^{17} protons on target using the 800 GeV Tevatron beam at Fermilab. The number of observed Ī½Ļ„\nu_\tau CC interactions is 9, from a total of 578 observed neutrino interactions. We calculated the energy-independent part of the tau-neutrino CC cross section (Ī½+Ī½Ė‰\nu + \bar \nu), relative to the well-known Ī½e\nu_e and Ī½Ī¼\nu_\mu cross sections. The ratio Ļƒ(Ī½Ļ„)\sigma(\nu_\tau)/Ļƒ(Ī½e,Ī¼)\sigma(\nu_{e,\mu}) was found to be 1.37Ā±0.35Ā±0.771.37\pm0.35\pm0.77. The Ī½Ļ„\nu_\tau CC cross section was found to be 0.72Ā±0.24Ā±0.36Ɨ10āˆ’380.72 \pm 0.24\pm0.36 \times 10^{-38} cm2GeVāˆ’1^{2}\rm{GeV}^{-1}. Both results are in agreement the Standard Model.Comment: 37 pages, 15 figure

    Non-Toxin-Producing Bacillus cereus Strains Belonging to the B. anthracis Clade Isolated from the International Space Station

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    ABSTRACT: In an ongoing Microbial Observatory investigation of the International Space Station (ISS), 11 Bacillus strains (2 from the Kibo Japanese experimental module, 4 from the U.S. segment, and 5 from the Russian module) were isolated and their whole genomes were sequenced. A comparative analysis of the 16S rRNA gene sequences of these isolates showed the highest similarity (>99%) to the Bacillus anthracis-B. cereus-B. thuringiensis group. The fatty acid composition, polar lipid profile, peptidoglycan type, and matrix-assisted laser desorption ionization-time of flight profiles were consistent with the B. cereus sensu lato group. The phenotypic traits such as motile rods, enterotoxin production, lack of capsule, and resistance to gamma phage/penicillin observed in ISS isolates were not characteristics of B. anthracis. Whole-genome sequence characterizations showed that ISS strains had the plcR non-B. anthracis ancestral "C" allele and lacked anthrax toxin-encoding plasmids pXO1 and pXO2, excluding their identification as B. anthracis. The genetic identities of all 11 ISS isolates characterized via gyrB analyses arbitrarily identified them as members of the B. cereus group, but traditional DNA-DNA hybridization (DDH) showed that the ISS isolates are similar to B. anthracis (88% to 90%) but distant from the B. cereus (42%) and B. thuringiensis (48%) type strains. The DDH results were supported by average nucleotide identity (>98.5%) and digital DDH (>86%) analyses. However, the collective phenotypic traits and genomic evidence were the reasons to exclude the ISS isolates from B. anthracis. Nevertheless, multilocus sequence typing and whole-genome single nucleotide polymorphism analyses placed these isolates in a clade that is distinct from previously described members of the B. cereus sensu lato group but closely related to B. anthracis. IMPORTANCE: The International Space Station Microbial Observatory (Microbial Tracking-1) study is generating a microbial census of the space station's surfaces and atmosphere by using advanced molecular microbial community analysis techniques supported by traditional culture-based methods and modern bioinformatic computational modeling. This approach will lead to long-term, multigenerational studies of microbial population dynamics in a closed environment and address key questions, including whether microgravity influences the evolution and genetic modification pathogenic (B. anthracis), food poisoning (B. cereus), and biotechnologically useful (B. thuringiensis) microorganisms; their presence in a closed system such as the ISS might be a concern for the health of crew members. A detailed characterization of these potential pathogens would lead to the development of suitable countermeasures that are needed for long-term future missions and a better understanding of microorganisms associated with space missions

    Structure of the ATP synthase catalytic complex (F(1)) from Escherichia coli in an autoinhibited conformation.

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    ATP synthase is a membrane-bound rotary motor enzyme that is critical for cellular energy metabolism in all kingdoms of life. Despite conservation of its basic structure and function, autoinhibition by one of its rotary stalk subunits occurs in bacteria and chloroplasts but not in mitochondria. The crystal structure of the ATP synthase catalytic complex (F(1)) from Escherichia coli described here reveals the structural basis for this inhibition. The C-terminal domain of subunit ɛ adopts a heretofore unknown, highly extended conformation that inserts deeply into the central cavity of the enzyme and engages both rotor and stator subunits in extensive contacts that are incompatible with functional rotation. As a result, the three catalytic subunits are stabilized in a set of conformations and rotational positions distinct from previous F(1) structures

    A Chaperonin Subunit with Unique Structures Is Essential for Folding of a Specific Substrate

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    Type I chaperonins are large, double-ring complexes present in bacteria (GroEL), mitochondria (Hsp60), and chloroplasts (Cpn60), which are involved in mediating the folding of newly synthesized, translocated, or stress-denatured proteins. In Escherichia coli, GroEL comprises 14 identical subunits and has been exquisitely optimized to fold its broad range of substrates. However, multiple Cpn60 subunits with different expression profiles have evolved in chloroplasts. Here, we show that, in Arabidopsis thaliana, the minor subunit Cpn60Ī²4 forms a heterooligomeric Cpn60 complex with Cpn60Ī±1 and Cpn60Ī²1ā€“Ī²3 and is specifically required for the folding of NdhH, a subunit of the chloroplast NADH dehydrogenase-like complex (NDH). Other Cpn60Ī² subunits cannot complement the function of Cpn60Ī²4. Furthermore, the unique C-terminus of Cpn60Ī²4 is required for the full activity of the unique Cpn60 complex containing Cpn60Ī²4 for folding of NdhH. Our findings suggest that this unusual kind of subunit enables the Cpn60 complex to assist the folding of some particular substrates, whereas other dominant Cpn60 subunits maintain a housekeeping chaperonin function by facilitating the folding of other obligate substrates

    Three-dimensional Numerical Modeling and Computational Fluid Dynamics Simulations to Analyze and Improve Oxygen Availability in the AMC Bioartificial Liver

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    A numerical model to investigate fluid flow and oxygen (O(2)) transport and consumption in the AMC-Bioartificial Liver (AMC-BAL) was developed and applied to two representative micro models of the AMC-BAL with two different gas capillary patterns, each combined with two proposed hepatocyte distributions. Parameter studies were performed on each configuration to gain insight in fluid flow, shear stress distribution and oxygen availability in the AMC-BAL. We assessed the function of the internal oxygenator, the effect of changes in hepatocyte oxygen consumption parameters in time and the effect of the change from an experimental to a clinical setting. In addition, different methodologies were studied to improve cellular oxygen availability, i.e. external oxygenation of culture medium, culture medium flow rate, culture gas oxygen content (pO(2)) and the number of oxygenation capillaries. Standard operating conditions did not adequately provide all hepatocytes in the AMC-BAL with sufficient oxygen to maintain O(2) consumption at minimally 90% of maximal uptake rate. Cellular oxygen availability was optimized by increasing the number of gas capillaries and pO(2) of the oxygenation gas by a factor two. Pressure drop over the AMC-BAL and maximal shear stresses were low and not considered to be harmful. This information can be used to increase cellular efficiency and may ultimately lead to a more productive AMC-BAL
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