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Inoculum of arbuscular mycorrhizal fungi, with growing use in horticulture, is produced mainly in two technically different cultivation systems: in vivo culture in symbiosis with living host plants or in vitro culture in which the fungus life cycle develops in association with transformed roots. To evaluate the effectiveness and the infectivity of a defined isolate obtained by both production methods, a replicated comparative evaluation experiment was designed using different propagules of Rhizophagus irregularis produced in vivo on leek plants or in vitro in monoxenic culture on transformed carrot roots. The size of the spores obtained under both cultivation methods was first assessed and bulk inoculum, spores, sievings, and mycorrhizal root fragments were used to inoculate leek plantlets. Spores produced in vitro were significantly smaller than those produced in vivo. Although all mycorrhizal propagules used as a source of inoculum were able to colonize plants, in all cases, leek plants inoculated with propagules obtained in vivo achieved significantly higher mycorrhizal colonization rates than plants inoculated with in vitro inocula. Inoculation with in vivo bulk inoculum and in vivo mycorrhizal root fragments were the only treatments increasing plant growth. These results indicate that the production system of arbuscular mycorrhizal fungi itself can have implications in the stimulation of plant growth and in experimental results. [ABSTRACT FROM AUTHOR]

nthyllis cytisoides and Spartium junceum are two leguminous shrubs native of semiarid mediterranean areas, often used in revegetation strategies. Mycorrhization of both shrubs with Glomus intraradices BEG 72 enhanced both plants growth and water relations under drought stress. Root colonization achieved by Glomus mosseae was lower than the level achieved by G. intraradices in both plants studied, and the effects of the inoculation with G. mosseae BEG 116 were less positive than those observed for G. intraradices. Before the onset of the drought stress period the specific leaf weight (SLW) of S. junceum plants inoculated with G. mosseae was lower than the SLW of control and G. intraradices plants. At the end of the stress period, after 15 days of withholding water, the relative water content of S. junceum twigs was lower for G. mosseae inoculated plants and higher for G. intraradices inoculated plants, compared to control, non-inoculated plants. At the end of the recovery period, 15 days after the reestablishment of watering, there were no differences between inoculation treatments on the parameters related to the plants water status. Anthyllis cytisoides plants inoculated with G. intraradices had lower leaf osmotic potential, more leaves, and higher chlorophyll content (measured as SPAD values). Anthyllis cytisoides plants responded to drought defoliating, but defoliation was lower for the plants inoculated with G. intraradices. At the end of the drought, the leaf osmotic potential was lowest for G. intraradices plants as was the relative water content (RWC) whilst Glomus mosseae inoculated plants had the highest RWC, SLW and osmotic potential values. At the end of the recovery period, all plants recuperated the osmotic potential values measured at the pre-stress period. In our experiments, G. intraradices BEG 72 was found to be superior to G. mosseae BEG 116, this difference could be attributed to the origin of the fungus, native from a Mediterranean area, compared to G. mosseae (BEG116) isolated from the UK. [ABSTRACT FROM AUTHOR]

A study was conducted with the vine rootstock Richter 110 ( Vitis berlandieri Planch. x Vitis rupestris L.) in order to assess whether the colonisation by the arbuscular mycorrhizal fungus (AMF) Glomus intraradices (BEG 72) can delay the disease development in plants inoculated with the root-rot fungus Armillaria mellea (Vahl:Fr) Kummer, and to elucidate if the levels of polyamines (PAs) are modified in response to G. intraradices, A. mellea or by the dual infection. Four treatments were considered: control and G. intraradices-inoculated plants infected or not with A. mellea. Plant growth, mycorrhizal colonisation and disease development were monitored throughout the experiment. High performance liquid chromatography (HPLC) in combination with fluorescence spectrophotometry was used to separate and quantify free root and leaf polyamines. The slower development of pathogenic symptoms and the higher plant biomass of mycorrhizal plants inoculated with A. mellea indicate an increase of tolerance due to the AMF inoculation. The variations in free PA levels detected at the beginning of the pathogenic infection suggest that PAs may have a potential role in the signalling mechanisms of the tolerance of mycorrhizal plants against A. mellea. [ABSTRACT FROM AUTHOR]

Abstract: Psammophilic plants are characterized for their adaptability to the hard environmental conditions of the coastal sand dune habitats that limit the survival of most vegetation. Considering that mycorrhizal plants are known to be effective colonizers of degraded habitats, the influence of the arbuscular mycorrhizal (AM) symbiosis in plant growth was studied in fifteen psammophilic plant species: Lotus creticus, Dorycnium pentaphyllum, Otanthus maritimus, Thymbra capitata, Armeria maritima, Halimium halimifolium, Ononis natrix, Medicago marina, Genista umbellata, Crucinella maritima, Elymus farctus, Ammophila arenaria, Pancratium maritimum, Glaucium flavum and Limoniastrum monopetalum. Wild seeds were used in this study to compare the effect of plant inoculation with a consortium of native AM fungi isolated from a coastal sand dune and with the selected isolate Glomus intraradices BEG 72 versus non mycorrhizal plants. After six months growth, we found that eleven of the fifteen psammophilic species responded positively to AM fungi inoculation and both root and shoot development benefited considerably from the presence of the AM fungi. We can conclude that many of the psammophilic species produced after the germination of the wild seeds collected in their natural habitats show limited growth due in part to the lack of adequate AM fungal inoculum in the plants growing substrate. AM inoculation seems to be critical for their survival. [Copyright &y& Elsevier]