Mushroom body input connections form independently of sensory activity in Drosophila melanogaster

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Molecular identification of Trichoderma species associated with Pleurotus ostreatus and natural substrates of the oyster mushroom

Green mold of Pleurotus ostreatus , caused by Trichoderma species, has recently resulted in crop losses worldwide. Therefore, there is an emerging need for rapid means of diagnosing the causal agents. A PCR assay was developed for rapid detection of Trichoderma pleurotum and Trichoderma pleuroticola , the two pathogens causing green mold of P. ostreatus . Three oligonucleotide primers were designed for identifying these species in a multiplex PCR assay based on DNA sequences within the fourth and fifth introns in the translation elongation factor 1α gene. The primers detected the presence of T. pleurotum and/or T. pleuroticola directly in the growing substrates of oyster mushrooms, without the need for isolating the pathogens. The assay was used to assess the presence of the two species in natural environments in which P. ostreatus can be found in Hungary, and demonstrated that T. pleuroticola was present in the growing substrates and on the surface of the basidiomes of wild oyster mushrooms. Other Trichoderma species detected in these substrates and habitats were Trichoderma harzianum, Trichoderma longibrachiatum and Trichoderma atroviride. Trichoderma pleurotum was not found in any of the samples from the forested areas tested in this study.     

Biology and life table parameters of the mushroom pest, Pediculaster fletchmanni （Acari： Siteroptidae）, at three constant temperatures

This paper is concerned with the bionomics and demography of Pediculaster fletchmanni Wicht （Acari： Siteroptidae） under controlled conditions （20 ± l, 22 ± 1 and 25 ± 1℃, 70% ± 5% relative humidity and a photoperiod of 16L ： 8D hours）. Glass Petri dishes inoculated with Trichoderma sp. mycelia were used as substrate and food source. The mean developmental time of the egg and the active larva did not differ significantly at the various constant temperatures, but these periods were significantly different for the quiescent larval stage. The preoviposition period ranged from 2.3 to 2.8 days, the ovipositional period increased with temperature increase, and all females died immediately after oviposition. The development of active larvae was the fastest of all life stages. The developmental threshold ranged between 5.25-14.22℃ the highest value being observed for the quiescent larval development. For immature development required 89.29 degree-days. Values of rm （intrinsic rate of increase） were 0.229, 0.398 and 0.386 for 20, 22 and 25℃ respectively. Finite rates of increase （λ） increased along with increasing temperature from 20-25℃ consequently the population doubling time （D） and mean generation time （T） showed significant differences with increasing temperature.     

Organotin in the Tagus estuary

The tri(n-butyl)tin (TBT) moiety has been shown to have complex ecotoxicological effects on estuarine populations. In the Tagus the massive die-off of the Portuguese oyster (Crassostrea angulata Lmk), has been attributed to the introduction and use of this contaminant by shipyards. This paper reviews previous work by others and reassesses our results obtained in water and sediments of the Tagus estuary, as a contribution to the understanding of tin geochemistry and organotin speciation in this estuary. Contrary to earlier results, the latest surveys show that in the open waters of the Tagus measurable concentrations of all the three butyltin species occur, exhibiting peak concentrations at two locations that indicate two previously undetected sources of TBT. TBT also presents a peak concentration in sediments near the Lisnave shipyards, as previously suggested. The latest surveys still detected methylated forms of tin, particularly monomethyltin (Me Sn³⁺), in Tagus sediments, with maximum concentrations in the vicinity of urban effluent discharges. The concentrations for TBT and its degradation products found in the Tagus are potentially harmful to the populations of gastropods and endemic bivalves.     

Alginate-entrapped Haslea ostrearia as inoculum for the greening of oysters

Entrapment in calcium alginate beads of the marine diatom, Haslea ostrearia, was successfully used for stock-culture managment and afterwards the sowing of ponds for the greening of oysters. After storage during almost 2 months, viable and cultivable cells were recovered from beads by dissolving alginate matrix but an original way lies in directly introducing beads in ponds and promoting natural cell leakage. © Rapid Science Ltd. 1998     

Promoting effect of wood vinegar compounds on fruit-body formation ofPleurotus ostreatus

The promoting effect of wood vinegar compounds on the fruiting ofPleurotus ostreatus (Japanese name, Hiratake) was investigated. Not only crude wood vinegar but its components, 3,5-dimethylphenol, 2-methoxyphenol, butanoic acid and 1-pentanol, had the ability to promote fruit-body formation on liquid medium. For use of these promoters industrially, a test for practical cultivation was carried out using a commercial sawdust medium. The addition of 100 µg/ml butanoic acid and 100 µg/ml 2-methoxyphenol into the sawdust medium after removal of the surface mycelial layer (kinkaki in Japanese) produced 29 and 23% higher yields of fruit-bodies than the control cultures (137.2 g/bottle), respectively. The addition of the crude wood vinegar as a medium component into sawdust substrates in the concentration range of 0.1–6% increased yields of fruit-bodies by 21–42% over the control.     

Identification of media supplements that improve the viability of primarily cell cultures ofCrassostrea gigas oysters

Media supplements have been investigated for their influence on the viability of primary cell cultures from the heart ofCrassostrea gigas oysters. Soluble factors of vertebrate origin were tested, belonging to five families of supplements that had proven to increase the viability of insect and mammal cell cultures. Using two-level complete factorial assays, factors and mutual interactions were screened within each family with a MTT reduction assay. Results pointed out the positive influence of hormones, growth factor, antioxidants and lipids on the mitochondrial metabolism of oyter's heart cells. Consequently, a new concentrated complex supplement was developed. At 10% (v/v) final concentration in modified Leibovitz L-15 medium, it increases by 30% the cellular viability of one-week old cultures as compared with non-supplemented medium, a similar improvement as the one obtained with 10% (v/v) fetal calf serum. Combined with fetal calf serum, this new supplement doubles the cellular viability of one-week old cultures and allows networks of cardiomuscular cells to be maintained functional over three monthsin vitro.Abbreviations MTT-3 (4,5-dimethylthiazol;-2-yl)2,5-diphenyl-tetrazolium bromide - FCS fetal calf serum     

The importance of runoff to DDT and PCB inputs to the Sado estuary and Ria Formosa

PCB congeners, DDT and metabolites were determined in suspended sediments and in the oysterCrassostrea angulata from the upper Sado estuary over two years (1987/88 and 1990) and from Ria Formosa during 1990. Levels of DDT concentrations in suspended sediments collected in both estuarine areas, either in 1988 or 1990, increased in winter. Otherwise, PCB concentrations varied in an erratic way. A DDT enrichment was also recorded inC. angulata in winter and an increase of only PCB concentration levels in oysters of the upper Sado estuary was registered at the same period. These results suggest that, in the absence of important direct sources of PCB and DDT, runoff appears to be the major source of those compounds in both the study areas. Levels of concentrations of these pollutants in oysters reflect either their increase in the environment or changes in particle dynamics in the two estuarine areas.     

Use of a Tetrazolium-based Cell Proliferation Assay to Measure Effects of In Vitro Conditions on Perkinsus marinus (Apicomplexa) Proliferation

ABSTRACT. Because the in vitro cell cycle of the apicomplexan oyster pathogen Perkinsus marinus generates cell populations heterogeneous for size and typified by aggregation, both turbidimetric and counting methods for determining population densities and proliferation rates are inaccurate or cumbersome. We show that a commercial, tetrazolium-based cell proliferation assay yields a soluble formazan chromophore upon intracellular reduction by P. marinus . at a rate proportional to cell population biovolume. Using this assay system, we have 1) defined selected culture system parameters which maximize P. marinus in vitro proliferation, 2) assessed selected chemosensitivities, and 3) standardized the assay system for quantification of densities and doubling times of populations propagated with our optimized system. Growth was supported by four tested base media and was maximized in 1:1 DME/Ham's F-12. Temperatures of 10–40° C permitted growth, which was maximized at 35° C. pH 6.0–8.5 permitted growth, which was maximized at 7.0–7.5. Osmolalities of 340–1,930 mOsm supported growth, which was maximized at 790 mOsm. Serum supplements from 1–10% (v/v) did not enhance log phase growth, but enhanced stationary phase metabolic activity in proportion to concentration. Our isolate (ATCC 50439) has a 13 h log phase doubling time when propagated under optimized conditions: 28° C, 800 mOsm, pH 7.0, 1:1 DME/Ham's F-12 medium, 5% (v/v) FBS. It is tolerant of antibacterial agents at concentrations commonly used in vertebrate tissue culture, but is inhibited by several antimycotics at similar concentrations.