Visual cues eliciting the feeding reaction of a planktivorous fish swimming in a current.
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The visual plankivorous feeding behaviour of the shiner perch (Cymatogaster aggregata) was investigated by means of a flow tank operated at various current speeds. Artemia salina was used as prey. In a second set of experiments, Artemia was darkened with black ink, to compare the visually mediated behaviour of C. aggregata while feeding on dark prey vs feeding on natural (i.e. semi-transparent) prey. The positions of the fish and its prey at the time of the feeding reaction of C. aggregata were measured in three dimensions. Prey were on average closer and more in line with the fish's axis when feeding reactions to darkened Artemia were considered, in comparison with natural Artemia. Three potential mechanisms triggering the feeding reaction of C. aggregata were explored: the prey may trigger a reaction in C. aggregata when it reaches a threshold (1) angular size, (2) angular velocity, or (3) rate of change of the angular size (i.e. loom) of the prey as it is carried passively by the current towards the fish. Our results show that angular velocity may trigger the fish's reaction when using semi-transparent prey, while loom may trigger the reaction to darkened prey. This suggests that feeding behaviour of planktivorous fish is flexible and can use different cues to trigger a motor reaction to prey with different visual characteristics. The feeding reaction appeared to occur at longer distances for semi-transparent rather than darkened Artemia. We suggest that semi-transparent Artemia were visible at greater distances because of their higher scattering (i.e. diffuse reflectance) that made them appear brighter when viewed against a dark background. (+info)
Aerobic heat shock activates trehalose synthesis in embryos of Artemia franciscana.
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Encysted embryos (cysts) of the brine shrimp, Artemia franciscana, contain large amounts of trehalose which they use as a major substrate for energy metabolism and biosynthesis for development under aerobic conditions at 25 degrees C. When cysts are placed at 42 degrees C (heat shock) these pathways stop, and the cysts re-synthesize the trehalose that was utilized during the previous incubation at 25 degrees C. Glycogen and glycerol, produced from trehalose at 25 degrees C, appear to be substrates for trehalose synthesis during heat shock. Anoxia prevents trehalose synthesis in cysts undergoing heat shock. These results are consistent with the view that trehalose may play a protective role in cells exposed to heat shock, and other environmental insults, in addition to being a storage form of energy and organic carbon for development. (+info)
Cell differentiation is a primary growth process in developing limbs of Artemia.
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The limb of the brine shrimp Artemia develops over a four-instar period when the protopod, endite, exopod, endopod, and epipod are defined and cell differentiation (change in cell shape) occurs. To understand the importance of cell differentiation in limb growth, development of the epidermis was studied in the first thoracopod of instar V-VIII larvae. Each region was established by instar V, and the larval epidermal cells developed into general epidermal (GEC), tendinal, setal, or transport cells by instar VI. Basal extensions of the GECs formed pillar structures. The epidermal cells decreased in height from 10 to 4 microm by instar VI. Increase in length and width resulted from both cell replication and expansion of the apical cell surface in differentiating cells. Growth occurred mainly by cell replication in instar V, whereas expansion of the cell surface in GEC and setae was the major growth process in instar VII. Increase in apical cell surface area occurred primarily by change in cell shape from columnar to squamous during instar V and by increase in total cell surface in subsequent instars. The results demonstrated that cell differentiation is a significant component of growth during limb development. (+info)
V-ATPase expression during development of Artemia franciscana embryos: potential role for proton gradients in anoxia signaling.
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Under anoxia, Artemia franciscana embryos downregulate metabolic processes and approach an ametabolic state. Entrance into this quiescent state is accompanied by a profound acidification of the intracellular space, and more than two decades of research now clearly demonstrates that this acidification is critical to metabolic downregulation in anoxic embryos. However, the proximal mechanisms responsible for the pH shift remain largely unidentified. Here, we report evidence demonstrating expression of the V-ATPase in encysted embryos and present an argument for its involvement in the intracellular acidification induced by anoxia. We identified a single B-subunit cDNA sharing the greatest degree of sequence similarity with ;generalist-type' homologues from mammals (brain-type) and invertebrates. Quantitative analysis of B-subunit mRNA demonstrates differential expression throughout early development, and western blot analyses confirm the expression of at least six V-ATPase subunits in both heavy membranes and microsomal vesicles. The critical need for proton pumping during the anoxia-tolerant stage of development is demonstrated by incubation with the V-ATPase inhibitor bafilomycin A1, which halts embryonic development. Importantly, net proton flux from V-ATPase-acidified compartments to the surrounding cytoplasm is likely under anoxia and may significantly contribute to the enigmatic acidification critical to quiescence. (+info)
V-ATPase inhibition prevents recovery from anoxia in Artemia franciscana embryos: quiescence signaling through dissipation of proton gradients.
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The metabolic downregulation critical for long-term survival of Artemia franciscana embryos under anoxia is mediated, in part, by a progressive intracellular acidification. However, very little is known about the mechanisms responsible for the pH transitions associated with exposure to, and recovery from, oxygen deprivation. In the present study, we demonstrate with 31P-NMR that incubation of intact embryos with the V-ATPase inhibitor bafilomycin A1 severely limits intracellular alkalinization during recovery from anoxia without affecting the restoration of cellular nucleotide triphosphate levels. Based on these data, it appears that oxidative phosphorylation and ATP resynthesis can only account for the first 0.3 pH unit alkalinization observed during aerobic recovery from the 1 pH unit acidification produced during 1 h of anoxia. The additional 0.7 pH unit increase requires proton pumping by the V-ATPase. Aerobic incubation with bafilomycin also suggests that V-ATPase inhibition alone is not enough to induce an acute dissipation of proton gradients under anoxia. In intact embryos, the dissipation of proton gradients and uncoupling of oxidative phosphorylation with carbonyl cyanide 3-chlorophenylhydrazone (CCCP) leads to an intracellular acidification similar to that seen after 1 h of anoxia. Subsequent exposure to anoxia, in the continued presence of CCCP, yields little additional acidification, suggesting that proton gradients are normally dissipated under anoxia. When combined with protons generated from net ATP hydrolysis, these data show that the dissipation of proton chemical gradients is sufficient to account for the reversible acidification associated with quiescence in these embryos. (+info)
Effects of bacteria on Artemia franciscana cultured in different gnotobiotic environments.
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The use of probiotics is receiving considerable attention as an alternative approach to control microbiota in aquaculture farms, especially in hatching facilities. However, application with consistent results is hampered by insufficient information on their modes of action. To investigate whether dead bacteria (allowing investigation of their nutritional effect) or live bacteria (allowing evaluation of their probiotic effect) have any beneficial effect towards Artemia franciscana and, subsequently, if live bacteria have probiotic effects beyond the effects observed with dead bacteria, a model system was employed using gnotobiotic Artemia as a test organism. Nauplii were cultured in the presence of 10 bacterial strains combined with four different major axenic live feeds (two strains of Saccharomyces cerevisiae and two strains of Dunaliella tertiolecta) differing in their nutritional values. In combination with poor- and medium-quality live feeds, dead bacteria exerted a strong effect on Artemia survival but a rather weak or no effect on individual length and constituted a maximum of only 5.9% of the total ash-free dry weight supplied. These effects were reduced or even disappeared when medium- to good-quality major feed sources were used, possibly due to improvements in the health status of Artemia. Some probiotic bacteria, such as GR 8 (Cytophaga spp.), improved (not always significantly) the performance of nauplii beyond the effect observed with dead bacteria, independently of the feed supplied. The present approach can be an excellent system to study the exact mode of action of bacteria, especially if combined with challenge tests or other types of analysis (e.g., transcriptome and proteonomic analysis). (+info)
Toxicity of some Fusarium section Sporotrichiella strains in relation to mycotoxin production.
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The relationship between the toxicities of crude extracts and purified toxins of Fusarium spp. belonging to the section Sporotrichiella has been assessed. Toxicity was determined on the basis of death of Artemia salina larvae and of viability and blastogenic response of bovine and human lymphocytes. Trichothecene-producing strains of Fusarium sporotrichioides and Fusarium poae were toxic to A. salina and to lymphocyte blastogenesis. A strain of Fusarium tricinctum, producing visoltricin and chlamydosporol, induced differentiated activity in different bioassays (toxicity to A. salina but only minor activity against lymphocyte blastogenesis). Other, non-toxin-producing strains of Fusarium chlamydosporum, F. poae, and F. tricinctum were not active in the tested biosystems. (+info)
Maternal effects on encystment in crosses between two geographic strains of Artemia franciscana.
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Maternal effects can have environmental or genetic causes. A method that can be used to demonstrate the genetic basis of a maternal effect is to look for grandfather effects in a backcross following reciprocal crosses. The absence of a grandfather effect would exclude a chromosomal basis for the maternal effect when the male sex is heterogametic (XX-XY sex determination system). However, in organisms in which the female is heterogametic (ZW-ZZ sex determination system), the absence of a grandfather effect does not rule out a chromosomal basis of the maternal effect, since the genes responsible for that effect can be located in the W chromosome, which is transmitted matrilineally. Conversely, the absence of a grandfather effect would point to a W-chromosome basis for the trait, provided that a maternal effect has been previously demonstrated. Distinguishing between W-located and autosome or Z-located maternal effects is important to understand the evolutionary dynamics of a trait. Here we report on a study of the chromosomal basis of maternal effects on two life-history traits related to encystment in the branchiopod crustacean Artemia franciscana, in which females are heterogametic. We performed crosses of two populations that differ in the number of cysts they produce. The proportion of encysted broods showed a maternal effect and was not affected by the grandfather's genotype, pointing to a W-chromosome basis. The average number of encysted offspring per brood showed a strong paternal effect and also a slight maternal effect. This trait also showed a grandfather effect, which suggests that the geographical variation has an autosomal or Z-chromosomal basis. (+info)