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1.
PLoS One ; 16(3): e0248814, 2021.
Article in English | MEDLINE | ID: mdl-33739995

ABSTRACT

Ecological profiling of non-native species is essential to predict their dispersal and invasiveness potential across different areas of the world. Cassiopea is a monophyletic taxonomic group of scyphozoan mixotrophic jellyfish including C. andromeda, a recent colonizer of sheltered, shallow-water habitats of the Mediterranean Sea, such as harbors and other light-limited, eutrophic coastal habitats. To assess the ecophysiological plasticity of Cassiopea jellyfish and their potential to spread across the Mare Nostrum by secondary introductions, we investigated rapid photosynthetic responses of jellyfish to irradiance transitions-from reduced to increased irradiance conditions (as paradigm of transition from harbors to coastal, meso/oligotrophic habitats). Laboratory incubation experiments were carried out to compare oxygen fluxes and photobiological variables in Cassiopea sp. immature specimens pre-acclimated to low irradiance (PAR = 200 µmol photons m-2 s-1) and specimens rapidly exposed to higher irradiance levels (PAR = 500 µmol photons m-2 s-1). Comparable photosynthetic potential and high photosynthetic rates were measured at both irradiance values, as also shown by the rapid light curves. No significant differences were observed in terms of symbiont abundance between control and treated specimens. However, jellyfish kept at the low irradiance showed a higher content in chlorophyll a and c (0.76±0.51SD vs 0.46±0.13SD mg g-1 AFDW) and a higher Ci (amount of chlorophyll per cell) compared to jellyfish exposed to higher irradiance levels. The ratio between gross photosynthesis and respiration (P:R) was >1, indicating a significant input from the autotrophic metabolism. Cassiopea sp. specimens showed high photosynthetic performances, at both low and high irradiance, demonstrating high potential to adapt to sudden changes in light exposure. Such photosynthetic plasticity, combined with Cassiopea eurythermal tolerance and mixotrophic behavior, jointly suggest the upside-down jellyfish as a potentially successful invader in the scenario of a warming Mediterranean Sea.


Subject(s)
Introduced Species , Photosynthesis/physiology , Scyphozoa/physiology , Seawater , Analysis of Variance , Animals , Chlorophyll/analysis , Light , Mediterranean Sea , Organic Chemicals/analysis , Photosynthesis/radiation effects , Proteins/analysis , Scyphozoa/radiation effects , Symbiosis/physiology , Symbiosis/radiation effects
3.
Nat Commun ; 11(1): 1748, 2020 04 09.
Article in English | MEDLINE | ID: mdl-32273516

ABSTRACT

Corals have evolved as optimized photon augmentation systems, leading to space-efficient microalgal growth and outstanding photosynthetic quantum efficiencies. Light attenuation due to algal self-shading is a key limiting factor for the upscaling of microalgal cultivation. Coral-inspired light management systems could overcome this limitation and facilitate scalable bioenergy and bioproduct generation. Here, we develop 3D printed bionic corals capable of growing microalgae with high spatial cell densities of up to 109 cells mL-1. The hybrid photosynthetic biomaterials are produced with a 3D bioprinting platform which mimics morphological features of living coral tissue and the underlying skeleton with micron resolution, including their optical and mechanical properties. The programmable synthetic microenvironment thus allows for replicating both structural and functional traits of the coral-algal symbiosis. Our work defines a class of bionic materials that is capable of interacting with living organisms and can be exploited for applied coral reef research and photobioreactor design.


Subject(s)
Anthozoa/physiology , Bionics/methods , Coral Reefs , Microalgae/physiology , Animals , Anthozoa/radiation effects , Conservation of Natural Resources/methods , Ecosystem , Light , Microalgae/radiation effects , Photosynthesis/radiation effects , Printing, Three-Dimensional , Symbiosis/radiation effects
4.
Sci Rep ; 10(1): 2670, 2020 02 14.
Article in English | MEDLINE | ID: mdl-32060382

ABSTRACT

Ambrosia beetles (Coleoptera: Curculionidae: Scolytinae and Platypodinae) bore into tree xylem to complete their life cycle, feeding on symbiotic fungi. Ambrosia beetles are a threat to avocado where they have been found to vector a symbiotic fungus, Raffaelea lauricola, the causal agent of the laurel wilt disease. We assessed the repellency of methyl salicylate and verbenone to two putative laurel wilt vectors in avocado, Xyleborus volvulus (Fabricius) and Xyleborus bispinatus (Eichhoff), under laboratory conditions. Then, we tested the same two chemicals released from SPLAT flowable matrix with and without low-dose ethanol dispensers for manipulation of ambrosia beetle populations occurring in commercial avocado. The potential active space of repellents was assessed by quantifying beetle catch on traps placed 'close' (~5-10 cm) and 'far' (~1-1.5 m) away from repellent dispensers. Ambrosia beetles collected on traps associated with all in-field treatments were identified to species to assess beetle diversity and community variation. Xyleborus volvulus was not repelled by methyl salicylate (MeSA) or verbenone in laboratory assays, while X. bispinatus was repelled by MeSA but not verbenone. Ambrosia beetle trap catches were reduced in the field more when plots were treated with verbenone dispensers (SPLAT) co-deployed with low-dose ethanol dispensers than when treated with verbenone alone. Beetle diversity was highest on traps deployed with low-dose ethanol lures. The repellent treatments and ethanol lures significantly altered the species composition of beetles captured in experiment plots. Our results indicate that verbenone co-deployed with ethanol lures holds potential for manipulating ambrosia beetle vectors via push-pull management in avocado. This tactic could discourage immigration and/or population establishment of ambrosia beetles in commercial avocado and function as an additional tool for management programs of laurel wilt.


Subject(s)
Ophiostomatales/drug effects , Persea/microbiology , Plant Diseases/microbiology , Symbiosis/radiation effects , Animals , Bicyclic Monoterpenes/pharmacology , Coleoptera/microbiology , Coleoptera/pathogenicity , Insect Repellents/pharmacology , Insect Vectors/microbiology , Insect Vectors/pathogenicity , Ophiostomatales/pathogenicity , Persea/growth & development , Persea/parasitology , Plant Diseases/parasitology , Plant Diseases/prevention & control , Salicylates/pharmacology , Symbiosis/drug effects
5.
Photosynth Res ; 143(3): 287-299, 2020 Mar.
Article in English | MEDLINE | ID: mdl-31893333

ABSTRACT

Lichens are a symbiosis between a fungus and one or more photosynthetic microorganisms that enables the symbionts to thrive in places and conditions they could not compete independently. Exchanges of water and sugars between the symbionts are the established mechanisms that support lichen symbiosis. Herein, we present a new linkage between algal photosynthesis and fungal respiration in lichen Flavoparmelia caperata that extends the physiological nature of symbiotic co-dependent metabolisms, mutually boosting energy conversion rates in both symbionts. Measurements of electron transport by oximetry show that photosynthetic O2 is consumed internally by fungal respiration. At low light intensity, very low levels of O2 are released, while photosynthetic electron transport from water oxidation is normal as shown by intrinsic chlorophyll variable fluorescence yield (period-4 oscillations in flash-induced Fv/Fm). The rate of algal O2 production increases following consecutive series of illumination periods, at low and with limited saturation at high light intensities, in contrast to light saturation in free-living algae. We attribute this effect to arise from the availability of more CO2 produced by fungal respiration of photosynthetically generated sugars. We conclude that the lichen symbionts are metabolically coupled by energy conversion through exchange of terminal electron donors and acceptors used in both photosynthesis and fungal respiration. Algal sugars and O2 are consumed by the fungal symbiont, while fungal delivered CO2 is consumed by the alga.


Subject(s)
Carbon Dioxide/metabolism , Lichens/metabolism , Oxygen/metabolism , Photosynthesis , Symbiosis , Aerobiosis/radiation effects , Anaerobiosis/radiation effects , Cell Respiration/radiation effects , Chlorophyll/metabolism , Electrodes , Electron Transport/radiation effects , Fluorescence , Light , Oxidation-Reduction , Photosynthesis/radiation effects , Symbiosis/radiation effects , Time Factors , Water/metabolism
6.
Nat Commun ; 10(1): 5606, 2019 12 06.
Article in English | MEDLINE | ID: mdl-31811209

ABSTRACT

Feeding on unicellular photosynthetic organisms by unicellular eukaryotes is the base of the aquatic food chain and evolutionarily led to the establishment of photosynthetic endosymbionts/organelles. Photosynthesis generates reactive oxygen species and damages cells; thus, photosynthetic organisms possess several mechanisms to cope with the stress. Here, we demonstrate that photosynthetic prey also exposes unicellular amoebozoan and excavates predators to photosynthetic oxidative stress. Upon illumination, there is a commonality in transcriptomic changes among evolutionarily distant organisms feeding on photosynthetic prey. One of the genes commonly upregulated is a horizontally transferred homolog of algal and plant genes for chlorophyll degradation/detoxification. In addition, the predators reduce their phagocytic uptake while accelerating digestion of photosynthetic prey upon illumination, reducing the number of photosynthetic cells inside the predator cells, as this also occurs in facultative endosymbiotic associations upon certain stresses. Thus, some mechanisms in predators observed here probably have been necessary for evolution of endosymbiotic associations.


Subject(s)
Food Chain , Photosynthesis/physiology , Predatory Behavior/physiology , Symbiosis/physiology , Amoebozoa/physiology , Amoebozoa/radiation effects , Animals , Bacteria/metabolism , Bacterial Physiological Phenomena , Biological Evolution , Chlorophyll , Coculture Techniques , Eukaryota , Evolution, Molecular , Light/adverse effects , Naegleria/growth & development , Naegleria/physiology , Organelles/physiology , Oxidative Stress , Phagocytosis/physiology , Predatory Behavior/radiation effects , Protein Domains , Reactive Oxygen Species , Symbiosis/radiation effects , Transcriptome
7.
Nat Plants ; 4(9): 655-661, 2018 09.
Article in English | MEDLINE | ID: mdl-30127409

ABSTRACT

Nitrogen limits primary production in almost every biome on Earth1,2. Symbiotic nitrogen fixation, conducted by certain angiosperms and their endosymbiotic bacteria, is the largest potential natural source of new nitrogen into the biosphere3, influencing global primary production, carbon sequestration and element cycling. Because symbiotic nitrogen fixation represents an alternative to soil nitrogen uptake, much of the work on symbiotic nitrogen fixation regulation has focused on soil nitrogen availability4-8. However, because symbiotic nitrogen fixation is an energetically expensive process9, light availability to the plant may also regulate symbiotic nitrogen fixation rates10,11. Despite the importance of symbiotic nitrogen fixation to biosphere functioning, the environmental factors that most strongly regulate this process remain unresolved. Here we show that light regulates symbiotic nitrogen fixation more strongly than does soil nitrogen and that light mediates the response of symbiotic nitrogen fixation to soil nitrogen availability. In a shadehouse experiment, low light levels (comparable with forest understories) completely shut down symbiotic nitrogen fixation, whereas soil nitrogen levels that far exceeded plant demand did not fully downregulate symbiotic nitrogen fixation at high light. For in situ forest seedlings, light was a notable predictor of symbiotic nitrogen fixation activity, but soil-extractable nitrogen was not. Light as a primary regulator of symbiotic nitrogen fixation is a departure from decades of focus on soil nitrogen availability. This shift in our understanding of symbiotic nitrogen fixation regulation can resolve a long-standing biogeochemical paradox12, and it will improve our ability to predict how symbiotic nitrogen fixation will fuel the global forest carbon sink and respond to human alteration of the global nitrogen cycle.


Subject(s)
Nitrogen Fixation/radiation effects , Nitrogen/metabolism , Symbiosis/radiation effects , Fabaceae/growth & development , Fabaceae/metabolism , Fabaceae/physiology , Light , Rhizobiaceae/metabolism , Seedlings/growth & development , Soil , Trees/growth & development , Trees/metabolism , Trees/physiology , Tropical Climate
8.
Nat Commun ; 9(1): 1383, 2018 04 11.
Article in English | MEDLINE | ID: mdl-29643375

ABSTRACT

Understanding the mechanisms that promote cooperative behaviors of bacteria in their hosts is of great significance to clinical therapies. Environmental stress is generally believed to increase competition and reduce cooperation in bacteria. Here, we show that bacterial cooperation can in fact be maintained because of environmental stress. We show that Pseudomonas aeruginosa regulates the secretion of iron-scavenging siderophores in the presence of different environmental stresses, reserving this public good for private use in protection against reactive oxygen species when under stress. We term this strategy "conditional privatization". Using a combination of experimental evolution and theoretical modeling, we demonstrate that in the presence of environmental stress the conditional privatization strategy is resistant to invasion by non-producing cheaters. These findings show how the regulation of public goods secretion under stress affects the evolutionary stability of cooperation in a pathogenic population, which may assist in the rational development of novel therapies.


Subject(s)
Antibiosis/physiology , Iron/metabolism , Oligopeptides/biosynthesis , Pseudomonas aeruginosa/physiology , Siderophores/biosynthesis , Symbiosis/physiology , Anti-Bacterial Agents/pharmacology , Antibiosis/drug effects , Antibiosis/radiation effects , Biological Evolution , Colony Count, Microbial , Fluoresceins/chemistry , Fluorescent Dyes/chemistry , Oligopeptides/metabolism , Photons/adverse effects , Pseudomonas aeruginosa/drug effects , Pseudomonas aeruginosa/radiation effects , Siderophores/metabolism , Stress, Physiological , Symbiosis/drug effects , Symbiosis/radiation effects , Tobramycin/pharmacology
9.
Plant J ; 90(2): 221-234, 2017 Apr.
Article in English | MEDLINE | ID: mdl-28182317

ABSTRACT

Plastid evolution has been attributed to a single primary endosymbiotic event that occurred about 1.6 billion years ago (BYA) in which a cyanobacterium was engulfed and retained by a eukaryotic cell, although early steps in plastid integration are poorly understood. The photosynthetic amoeba Paulinella chromatophora represents a unique model for the study of plastid evolution because it contains cyanobacterium-derived photosynthetic organelles termed 'chromatophores' that originated relatively recently (0.09-0.14 BYA). The chromatophore genome is about a third the size of the genome of closely related cyanobacteria, but 10-fold larger than most plastid genomes. Several genes have been transferred from the chromatophore genome to the host nuclear genome through endosymbiotic gene transfer (EGT). Some EGT-derived proteins could be imported into chromatophores for function. Two photosynthesis-related genes (psaI and csos4A) are encoded by both the nuclear and chromatophore genomes, suggesting that EGT in Paulinella chromatophora is ongoing. Many EGT-derived genes encode proteins that function in photosynthesis and photoprotection, including an expanded family of high-light-inducible (ncHLI) proteins. Cyanobacterial hli genes are high-light induced and required for cell viability under excess light. We examined the impact of light on Paulinella chromatophora and found that this organism is light sensitive and lacks light-induced transcriptional regulation of chromatophore genes and most EGT-derived nuclear genes. However, several ncHLI genes have reestablished light-dependent regulation, which appears analogous to what is observed in cyanobacteria. We postulate that expansion of the ncHLI gene family and its regulation may reflect the light/oxidative stress experienced by Paulinella chromatophora as a consequence of the as yet incomplete integration of host and chromatophore metabolisms.


Subject(s)
Amoeba/cytology , Amoeba/metabolism , Chromatophores/metabolism , Light , Oxidative Stress/radiation effects , Photosynthesis/genetics , Photosynthesis/physiology , Plastids/metabolism , Symbiosis/radiation effects
10.
mBio ; 7(5)2016 10 04.
Article in English | MEDLINE | ID: mdl-27703075

ABSTRACT

Global warming impacts diverse organisms not only directly but also indirectly via other organisms with which they interact. Recently, the possibility that elevated temperatures resulting from global warming may substantially affect biodiversity through disrupting mutualistic/parasitic associations has been highlighted. Here we report an experimental demonstration that global warming can affect a pest insect via suppression of its obligate bacterial symbiont. The southern green stinkbug Nezara viridula depends on a specific gut bacterium for its normal growth and survival. When the insects were reared inside or outside a simulated warming incubator wherein temperature was controlled at 2.5°C higher than outside, the insects reared in the incubator exhibited severe fitness defects (i.e., retarded growth, reduced size, yellowish body color, etc.) and significant reduction of symbiont population, particularly in the midsummer season, whereas the insects reared outside did not. Rearing at 30°C or 32.5°C resulted in similar defective phenotypes of the insects, whereas no adult insects emerged at 35°C. Notably, experimental symbiont suppression by an antibiotic treatment also induced similar defective phenotypes of the insects, indicating that the host's defective phenotypes are attributable not to the heat stress itself but to the suppression of the symbiont population induced by elevated temperature. These results strongly suggest that high temperature in the midsummer season negatively affects the insects not directly but indirectly via the heat-vulnerable obligate bacterial symbiont, which highlights the practical relevance of mutualism collapse in this warming world. IMPORTANCE: Climate change is among the biggest environmental issues in the contemporary world, and its impact on the biodiversity and ecosystem is not only of scientific interest but also of practical concern for the general public. On the basis of our laboratory data obtained under strictly controlled environmental conditions and our simulated warming data obtained in seminatural settings (elevated 2.5°C above the normal temperature), we demonstrate here that Nezara viridula, the notorious stinkbug pest, suffers serious fitness defects in the summer season under the simulated warming conditions, wherein high temperature acts on the insect not directly but indirectly via suppression of its obligate gut bacterium. Our finding highlights that heat-susceptible symbionts can be the "Achilles' heel" of symbiont-dependent organisms under climate change conditions.


Subject(s)
Climate Change , Gastrointestinal Microbiome/radiation effects , Heteroptera/microbiology , Heteroptera/radiation effects , Symbiosis/radiation effects , Animals , Heteroptera/growth & development , Models, Theoretical , Temperature
11.
Mol Plant Microbe Interact ; 29(10): 786-796, 2016 10.
Article in English | MEDLINE | ID: mdl-27611874

ABSTRACT

In many legumes, roots that are exposed to light do not form nodules. Here, we report that blue light inhibits nodulation in Lotus japonicus roots inoculated with Mesorhizobium loti. Using RNA interference, we suppressed the expression of the phototropin and cryptochrome genes in L. japonicus hairy roots. Under blue light, plants transformed with an empty vector did not develop nodules, whereas plants exhibiting suppressed expression of cry1 and cry2 genes formed nodules. We also measured rhizobial growth to investigate whether the inhibition of nodulation could be caused by a reduced population of rhizobia in response to light. Although red light had no effect on rhizobial growth, blue light had a strong inhibitory effect. Rhizobial growth under blue light was partially restored in signature-tagged mutagenesis (STM) strains in which LOV-HK/PAS- and photolyase-related genes were disrupted. Moreover, when Ljcry1A and Ljcry2B-silenced plants were inoculated with the STM strains, nodulation was additively increased. Our data show that blue light receptors in both the host plant and the symbiont have a profound effect on nodule development. The exact mechanism by which these photomorphogenetic responses function in the symbiosis needs further study, but they are clearly involved in optimizing legume nodulation.


Subject(s)
Lotus/radiation effects , Mesorhizobium/radiation effects , Plant Root Nodulation/radiation effects , Symbiosis/radiation effects , Cryptochromes/genetics , Light , Lotus/genetics , Lotus/microbiology , Lotus/physiology , Mesorhizobium/physiology , Mutagenesis , Phototropins/genetics , Plant Proteins/genetics , Plant Roots/genetics , Plant Roots/microbiology , Plant Roots/physiology , Plant Roots/radiation effects , RNA Interference
12.
Sci Rep ; 6: 30930, 2016 08 09.
Article in English | MEDLINE | ID: mdl-27502580

ABSTRACT

Bleaching, the loss of algal symbionts, occurs in marine photosymbiotic organisms at water temperatures minimally exceeding average summer SST (sea surface temperatures). Pre-adaptation allows organisms to persist under warmer conditions, providing the tolerance can be carried to new habitats. Here we provide evidence for the existence of such adaptation in the benthic foraminifera Pararotalia calcariformata. This species occurs at a thermally polluted site in the Mediterranean, where water temperatures reach a maxima daily average of 36 °C during the summer. To test whether this occurrence represents a widespread adaptation, we conducted manipulative experiments exposing this species from an unpolluted site to elevated temperatures (20-42 °C). It was kept in co-culture with the more thermally sensitive foraminifera Amphistegina lobifera in two experiments (20-36 °C). Reduced photosynthetic activity in A. lobifera occurred at 32 °C whereas photochemical stress in P. calcariformata was first observed during exposure to 36 °C. Pararotalia calcariformata survived all treatment conditions and grew under 36 °C. The photosymbiosis in P. calcariformata is unusually thermally tolerant. These observations imply that marine eukaryote-eukaryote photosymbiosis can respond to elevated temperatures by drawing on a pool of naturally occurring pre-adaptations. It also provides a perspective on the massive occurrence of symbiont-bearing foraminifera in the early Cenozoic hothouse climate.


Subject(s)
Adaptation, Physiological/physiology , Foraminifera/physiology , Hot Temperature , Photochemistry , Symbiosis/physiology , Foraminifera/radiation effects , Mediterranean Region , Seawater , Symbiosis/radiation effects
13.
New Phytol ; 212(2): 472-84, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27321415

ABSTRACT

Coral bleaching is an important environmental phenomenon, whose mechanism has not yet been clarified. The involvement of reactive oxygen species (ROS) has been implicated, but direct evidence of what species are involved, their location and their mechanisms of production remains unknown. Histidine-mediated chemical trapping and singlet oxygen sensor green (SOSG) were used to detect intra- and extracellular singlet oxygen ((1) O2 ) in Symbiodinium cultures. Inhibition of the Calvin-Benson cycle by thermal stress or high light promotes intracellular (1) O2 formation. Histidine addition, which decreases the amount of intracellular (1) O2 , provides partial protection against photosystem II photoinactivation and chlorophyll (Chl) bleaching. (1) O2 production also occurs in cell-free medium of Symbiodinium cultures, an effect that is enhanced under heat and light stress and can be attributed to the excretion of (1) O2 -sensitizing metabolites from the cells. Confocal microscopy imaging using SOSG showed most extracellular (1) O2 around the cell surface, but it is also produced across the medium distant from the cells. We demonstrate, for the first time, both intra- and extracellular (1) O2 production in Symbiodinium cultures. Intracellular (1) O2 is associated with photosystem II photodamage and pigment bleaching, whereas extracellular (1) O2 has the potential to mediate the breakdown of symbiotic interaction between zooxanthellae and their animal host during coral bleaching.


Subject(s)
Anthozoa/physiology , Dinoflagellida/cytology , Dinoflagellida/radiation effects , Light , Photosynthesis/radiation effects , Singlet Oxygen/metabolism , Symbiosis/radiation effects , Animals , Dinoflagellida/drug effects , Extracellular Space/chemistry , Fluorescence , Histidine/pharmacology , Hot Temperature , Intracellular Space/chemistry , Photosynthesis/drug effects , Photosystem II Protein Complex/metabolism , Pigments, Biological/metabolism , Symbiosis/drug effects
14.
PLoS One ; 11(5): e0154116, 2016.
Article in English | MEDLINE | ID: mdl-27136455

ABSTRACT

Plant associations with root microbes represent some of the most important symbioses on earth. While often critically promoting plant fitness, nitrogen-fixing rhizobia and arbuscular mycorrhizal fungi (AMF) also demand significant carbohydrate allocation in exchange for key nutrients. Though plants may often compensate for carbon loss, constraints may arise under light limitation when plants cannot extensively increase photosynthesis. Under such conditions, costs for maintaining symbioses may outweigh benefits, turning mutualist microbes into parasites, resulting in reduced plant growth and reproduction. In natural systems plants commonly grow with different symbionts simultaneously which again may interact with each other. This might add complexity to the responses of such multipartite relationships. We experimented with lima bean (Phaseolus lunatus), which efficiently forms associations with both types of root symbionts. We applied full light and low-light to each of four treatments of microbial inoculation. After an incubation period of 14 weeks, we quantified vegetative aboveground and belowground biomass and number and viability of seeds to determine effects of combined inoculant and light treatment on plant fitness. Under light-limited conditions, vegetative and reproductive traits were inhibited in AMF and rhizobia inoculated lima bean plants relative to controls (un-colonized plants). Strikingly, reductions in seed production were most critical in combined treatments with rhizobia x AMF. Our findings suggest microbial root symbionts create additive costs resulting in decreased plant fitness under light-limited conditions.


Subject(s)
Light , Mycorrhizae/physiology , Phaseolus/microbiology , Rhizobium/physiology , Symbiosis/radiation effects , Phaseolus/metabolism , Phaseolus/radiation effects , Plant Roots/metabolism , Plant Roots/microbiology , Plant Roots/radiation effects , Root Nodules, Plant/metabolism , Root Nodules, Plant/microbiology , Root Nodules, Plant/radiation effects
15.
Cell Microbiol ; 18(11): 1642-1652, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27062511

ABSTRACT

Recent research has shown that the microbiota affects the biology of associated host epithelial tissues, including their circadian rhythms, although few data are available on how such influences shape the microarchitecture of the brush border. The squid-vibrio system exhibits two modifications of the brush border that supports the symbionts: effacement and repolarization. Together these occur on a daily rhythm in adult animals, at the dawn expulsion of symbionts into the environment, and symbiont colonization of the juvenile host induces an increase in microvillar density. Here we sought to define how these processes are related and the roles of both symbiont colonization and environmental cues. Ultrastructural analyses showed that the juvenile-organ brush borders also efface concomitantly with daily dawn-cued expulsion of symbionts. Manipulation of the environmental light cue and juvenile symbiotic state demonstrated that this behaviour requires the light cue, but not colonization. In contrast, symbionts were required for the observed increase in microvillar density that accompanies post dawn brush-border repolarization; this increase was induced solely by host exposure to phosphorylated lipid A of symbiont cells. These data demonstrate that a partnering of environmental and symbiont cues shapes the brush border and that microbe-associated molecular patterns play a role in the regulation of brush-border microarchitecture.


Subject(s)
Decapodiformes/physiology , Microvilli/microbiology , Vibrio/physiology , Animals , Circadian Rhythm , Decapodiformes/cytology , Decapodiformes/microbiology , Epithelial Cells/microbiology , Epithelial Cells/ultrastructure , Light , Microvilli/ultrastructure , Sense Organs/cytology , Sense Organs/microbiology , Symbiosis/radiation effects
16.
J Theor Biol ; 405: 82-93, 2016 09 21.
Article in English | MEDLINE | ID: mdl-26925812

ABSTRACT

Photosymbiosis is one of the most important evolutionary trajectories, resulting in the chloroplast and the subsequent development of all complex photosynthetic organisms. The ciliate Paramecium bursaria and the alga Chlorella have a well established and well studied light dependent endosymbiotic relationship. Despite its prominence, there remain many unanswered questions regarding the exact mechanisms of the photosymbiosis. Of particular interest is how a host maintains and manages its symbiont load in response to the allocation of nutrients between itself and its symbionts. Here we construct a detailed mathematical model, parameterised from the literature, that explicitly incorporates nutrient trading within a deterministic model of both partners. The model demonstrates how the symbiotic relationship can manifest as parasitism of the host by the symbionts, mutualism, wherein both partners benefit, or exploitation of the symbionts by the hosts. We show that the precise nature of the photosymbiosis is determined by both environmental conditions (how much light is available for photosynthesis) and the level of control a host has over its symbiont load. Our model provides a framework within which it is possible to pose detailed questions regarding the evolutionary behaviour of this important example of an established light dependent endosymbiosis; we focus on one question in particular, namely the evolution of host control, and show using an adaptive dynamics approach that a moderate level of host control may evolve provided the associated costs are not prohibitive.


Subject(s)
Chlorella/physiology , Paramecium/physiology , Photosynthesis/physiology , Symbiosis/physiology , Adaptation, Physiological/radiation effects , Chlorella/growth & development , Light , Paramecium/growth & development , Photosynthesis/radiation effects , Symbiosis/radiation effects
17.
Mycorrhiza ; 26(1): 47-56, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26003665

ABSTRACT

Seedlings of forest tree species are exposed to a number of abiotic (organ loss or damage, light shortage) and biotic (interspecific competition) stress factors, which may lead to an inhibition of growth and reproduction and, eventually, to plant death. Growth of the host and its mycorrhizal symbiont is often closely linked, and hence, host damage may negatively affect the symbiont. We designed a pot experiment to study the response of light-demanding Pinus sylvestris and shade-tolerant Fagus sylvatica seedlings to a set of abiotic and biotic stresses and subsequent effects on ectomycorrhizal (ECM) root tip colonization, seedling biomass, and leaf nitrogen content. The light regime had a more pronounced effect on ECM colonization than did juvenile damage. The interspecific competition resulted in higher ECM root tip abundance for Pinus, but this effect was insignificant in Fagus. Low light and interspecific competition resulted in lower seedling biomass compared to high light, and the effect of the latter was partially masked by high light. Leaf nitrogen responded differently in Fagus and Pinus when they grew in interspecific competition. Our results indicated that for both light-demanding (Pinus) and shade-tolerant (Fagus) species, the light environment was a major factor affecting seedling growth and ECM root tip abundance. The light conditions favorable for the growth of seedlings may to some extent compensate for the harmful effects of juvenile organ loss or damage and interspecific competition.


Subject(s)
Fagus/growth & development , Fagus/microbiology , Light , Mycorrhizae/physiology , Pinus sylvestris/growth & development , Pinus sylvestris/microbiology , Adaptation, Physiological/physiology , Biomass , Defoliants, Chemical , Fagus/physiology , Meristem/growth & development , Meristem/microbiology , Meristem/radiation effects , Mycorrhizae/growth & development , Mycorrhizae/radiation effects , Pinus sylvestris/radiation effects , Plant Leaves/chemistry , Plant Leaves/growth & development , Plant Leaves/microbiology , Plant Roots/microbiology , Seedlings/growth & development , Seedlings/physiology , Seedlings/radiation effects , Stress, Physiological/physiology , Symbiosis/radiation effects , Trees/growth & development , Trees/microbiology
18.
Article in English | MEDLINE | ID: mdl-26310104

ABSTRACT

Mass coral bleaching due to thermal stress represents a major threat to the integrity and functioning of coral reefs. Thermal thresholds vary, however, between corals, partly as a result of the specific type of endosymbiotic dinoflagellate (Symbiodinium sp.) they harbour. The production of reactive oxygen species (ROS) in corals under thermal and light stress has been recognised as one mechanism that can lead to cellular damage and the loss of their symbiont population (Oxidative Theory of Coral Bleaching). Here, we compared the response of symbiont and host enzymatic antioxidants in the coral species Acropora millepora and Montipora digitata at 28°C and 33°C. A. millepora at 33°C showed a decrease in photochemical efficiency of photosystem II (PSII) and increase in maximum midday excitation pressure on PSII, with subsequent bleaching (declining photosynthetic pigment and symbiont density). M. digitata exhibited no bleaching response and photochemical changes in its symbionts were minor. The symbiont antioxidant enzymes superoxide dismutase, ascorbate peroxidase, and catalase peroxidase showed no significant upregulation to elevated temperatures in either coral, while only catalase was significantly elevated in both coral hosts at 33°C. Increased host catalase activity in the susceptible coral after 5days at 33°C was independent of antioxidant responses in the symbiont and preceded significant declines in PSII photochemical efficiencies. This finding suggests a potential decoupling of host redox mechanisms from symbiont photophysiology and raises questions about the importance of symbiont-derived ROS in initiating coral bleaching.


Subject(s)
Anthozoa/physiology , Dinoflagellida/physiology , Oxidative Stress , Pigments, Biological/metabolism , Reactive Oxygen Species/metabolism , Stress, Physiological , Symbiosis , Animals , Anthozoa/growth & development , Anthozoa/parasitology , Anthozoa/radiation effects , Ascorbate Peroxidases/metabolism , Catalase/metabolism , Coral Reefs , Dinoflagellida/growth & development , Dinoflagellida/radiation effects , Hot Temperature/adverse effects , Pacific Ocean , Photobleaching/radiation effects , Photosystem II Protein Complex/metabolism , Protozoan Proteins/metabolism , Queensland , Species Specificity , Stress, Physiological/radiation effects , Sunlight/adverse effects , Superoxide Dismutase/metabolism , Symbiosis/radiation effects
19.
PLoS One ; 9(10): e110814, 2014.
Article in English | MEDLINE | ID: mdl-25360746

ABSTRACT

The light dependency of respiratory activity of two scleractinian corals was examined using O2 microsensors and CO2 exchange measurements. Light respiration increased strongly but asymptotically with elevated irradiance in both species. Light respiration in Pocillopora damicornis was higher than in Pavona decussata under low irradiance, indicating species-specific differences in light-dependent metabolic processes. Overall, the coral P. decussata exhibited higher CO2 uptake rates than P. damicornis over the experimental irradiance range. P. decussata also harboured twice as many algal symbionts and higher total protein biomass compared to P. damicornis, possibly resulting in self-shading of the symbionts and/or changes in host tissue specific light distribution. Differences in light respiration and CO2 availability could be due to host-specific characteristics that modulate the symbiont microenvironment, its photosynthesis, and hence the overall performance of the coral holobiont.


Subject(s)
Anthozoa/metabolism , Anthozoa/radiation effects , Light , Photosynthesis/radiation effects , Respiration/radiation effects , Animals , Anthozoa/physiology , Biological Transport/radiation effects , Carbon Dioxide/metabolism , Oxygen/metabolism , Symbiosis/radiation effects
20.
PLoS One ; 9(8): e105863, 2014.
Article in English | MEDLINE | ID: mdl-25170981

ABSTRACT

The morphological plasticity of scleractinian corals can be influenced by numerous factors in their natural environment. However, it is difficult to identify in situ the relative influence of a single biotic or abiotic factor, due to potential interactions between them. Light is considered as a major factor affecting coral skeleton morphology, due to their symbiotic relation with photosynthetic zooxanthellae. Nonetheless, most studies addressing the importance of light on coral morphological plasticity have focused on photosynthetically active radiation (PAR) intensity, with the effect of light spectra remaining largely unknown. The present study evaluated how different light spectra affect the skeleton macro- and microstructures in two coral species (Acropora formosa sensu Veron (2000) and Stylophora pistillata) maintained under controlled laboratory conditions. We tested the effect of three light treatments with the same PAR but with a distinct spectral emission: 1) T5 fluorescent lamps with blue emission; 2) Light Emitting Diodes (LED) with predominantly blue emission; and 3) Light Emitting Plasma (LEP) with full spectra emission. To exclude potential bias generated by genetic variability, the experiment was performed with clonal fragments for both species. After 6 months of experiment, it was possible to detect in coral fragments of both species exposed to different light spectra significant differences in morphometry (e.g., distance among corallites, corallite diameter, and theca thickness), as well as in the organization of their skeleton microstructure. The variability found in the skeleton macro- and microstructures of clonal organisms points to the potential pitfalls associated with the exclusive use of morphometry on coral taxonomy. Moreover, the identification of a single factor influencing the morphology of coral skeletons is relevant for coral aquaculture and can allow the optimization of reef restoration efforts.


Subject(s)
Anthozoa/radiation effects , Dinoflagellida/radiation effects , Light , Symbiosis/radiation effects , Animals , Anthozoa/classification , Anthozoa/ultrastructure , Dinoflagellida/physiology , Ecosystem , Microscopy, Electron, Scanning , Photosynthesis/radiation effects , Species Specificity
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