Regulation Of Symbiosis Research Articles

Construction of highly-effective symbiotic bacteria: Evolutionary models and genetic approaches

Using the example of N2-fixing legume-rhizobial symbiosis, we demonstrated that the origin and evolution of bacteria symbiotic for plants involve the following: 1) the formation of novel sym gene systems based on reorganizations of the bacterial genomes and on the gene transfer from the distant organisms; 2) the loss of genes encoding for functions that are required for autonomous performance but interfere with symbiotic functions (negative regulators of symbiosis). Therefore, the construction of effective rhizobia strains should involve improvement of sym genes activities (for instance, nif, fix, and dct genes, encoding for nitrogenase synthesis or for the energy supply of N2 fixation), as well as the inactivation of negative regulators of symbiosis identified in our lab (eff genes encoding for the transport of sugars, and the production of polysaccharides, and storage compounds, as well as for oxidative-reductive processes).

MtROP8 is involved in root hair development and the establishment of symbiotic interaction between Medicago truncatula and Sinorhizobium meliloti

Emerging evidence has demonstrated that ROP GTPases play important roles in symbiosis, but the molecular mechanisms on their regulation in symbiosis are largely unknown. In this study, we showed that MtROP8 is involved in the symbiotic interaction between Medicago truncatula and Sinorhizobium meliloti. Expression analyses showed that MtROP8 was down-regulated in the early infected roots, but significantly up-regulated in nodules compared to the roots. Phenotypic analysis of RNA interference (RNAi)-mediated silencing of MtROP8 revealed that knock-down of MtROP8 expression resulted in various developmental defects of root hairs, including branched hairs, short bulbous root hairs, and even root hairs with apparent swollen bases, which were caused by the modification of the distribution and the levels of reactive oxygen species (ROS). Moreover, infection events were increased in transgenic roots harboring the MtROP8 RNAi construct in response to S. meliloti inoculation, concomitant with enhanced nodulation. These results indicate that MtROP8 participates in root hair development and the establishment of the symbiotic interaction by regulating ROS production and distribution.

Hydrogen Peroxide and Nitric Oxide: Key Regulators of the Legume—Rhizobiumand Mycorrhizal Symbioses

During the Legume-Rhizobium symbiosis, hydrogen peroxide (H(2)O(2)) and nitric oxide (NO) appear to play an important signaling role in the establishment and the functioning of this interaction. Modifications of the levels of these reactive species in both partners impair either the development of the nodules (new root organs formed on the interaction) or their N(2)-fixing activity. NADPH oxidases (Noxs) have been recently described as major sources of H(2)O(2) production, via superoxide anion dismutation, during symbiosis. Nitrate reductases (NR) and electron transfer chains from both partners were found to significantly contribute to NO production in N(2)-fixing nodules. Both S-sulfenylated and S-nitrosylated proteins have been detected during early interaction and in functioning nodules, linking reactive oxygen species (ROS)/NO production to redox-based protein regulation. NO was also found to play a metabolic role in nodule energy metabolism. H(2)O(2) may control the infection process and the subsequent bacterial differentiation into the symbiotic form. NO is required for an optimal establishment of symbiosis and appears to be a key player in nodule senescence. A challenging question is to define more precisely when and where reactive species are generated and to develop adapted tools to detect their production in vivo. To investigate the role of Noxs and NRs in the production of H(2)O(2) and NO, respectively, the use of mutants under the control of organ-specific promoters will be of crucial interest. The balance between ROS and NO production appears to be a key point to understand the redox regulation of symbiosis.

Legumes regulate Rhizobium bacteroid development and persistence by the supply of branched-chain amino acids.

One of the largest contributions to biologically available nitrogen comes from the reduction of N(2) to ammonia by rhizobia in symbiosis with legumes. Plants supply dicarboxylic acids as a carbon source to bacteroids, and in return they receive ammonia. However, metabolic exchange must be more complex, because effective N(2) fixation by Rhizobium leguminosarum bv viciae bacteroids requires either one of two broad-specificity amino acid ABC transporters (Aap and Bra). It was proposed that amino acids cycle between plant and bacteroids, but the model was unconstrained because of the broad solute specificity of Aap and Bra. Here, we constrain the specificity of Bra and ectopically express heterologous transporters to demonstrate that branched-chain amino acid (LIV) transport is essential for effective N(2) fixation. This dependence of bacteroids on the plant for LIV is not due to their known down-regulation of glutamate synthesis, because ectopic expression of glutamate dehydrogenase did not rescue effective N(2) fixation. Instead, the effect is specific to LIV and is accompanied by a major reduction in transcription and activity of LIV biosynthetic enzymes. Bacteroids become symbiotic auxotrophs for LIV and depend on the plant for their supply. Bacteroids with aap bra null mutations are reduced in number, smaller, and have a lower DNA content than wild type. Plants control LIV supply to bacteroids, regulating their development and persistence. This makes it a critical control point for regulation of symbiosis.

ROLE OF SIGNAL EXCHANGE IN CONTROL OF RHIZOBIUM - LEGUME SYMBIOSIS SPECIFICITY

The signal molecules produced by legume plants and soil bacteria rhizobia and involved in early steps of symbiosis regulation were identified through the evaluation of molecular mechanisms of plant-rhizobia communication. The molecular dialog between plants and rhizobia is initiated by plant flavanoids inducing the synthesis and secretion of lipochitooligosaccharide molecules Nod factors by rhizobial bacteria. Nod factors are N-acetylglucosamine oligomers, modified by fatty acid and certain chemical groups. Nod factors trigger a set of plant reactions resulting in a formation of root nodules - nitrogen fixing symbiotic organs. Fine chemical structure of signal molecules determines host specificity of the symbiosis. Nod factors are active in low concentrations and possess mitogenic and morphogenic activity, therefore they are recognized as the new class of growth regulators. In this paper the modern data about study of Nod factor perception mechanisms and signal transduction pathway in legume plants are presented and considered with perspective for future application of these knowledge for practical increasing of symbiosis efficiency from plant side. This work was supported by RFBR 07-08-00700a (Russian Foundation of Basic Research), CRDF RUXO-012-ST-06 (BP2M12) and HIII-5399. 2008. 4, RFBR-NWO (06-04-89000-НВОЦ-а) grants.

Symbiosis regulation in a facultatively symbiotic temperate coral: zooxanthellae division and expulsion

Zooxanthellae mitotic index (MI) and expulsion rates were measured in the facultatively symbiotic scleractinian Astrangia poculata during winter and summer off the southern New England coast, USA. While MI was significantly higher in summer than in winter, mean expulsion rates were comparable between seasons. Corals therefore appear to allow increases in symbiont density when symbiosis is advantageous during the warm season, followed by a net reduction during the cold season when zooxanthellae may draw resources from the coral. Given previous reports that photosynthesis in A. poculata symbionts does not occur below approximately 6°C, considerable zooxanthellae division at 3°C and in darkness suggests that zooxanthellae are heterotrophic at low seasonal temperatures. Finally, examination of expulsion as a function of zooxanthellae density revealed that corals with very low zooxanthellae densities export a significantly greater proportion of their symbionts, apparently allowing them to persist in a stable azooxanthellate state.

The Actinorhizal Symbiosis.

The term "actinorhiza" refers both to the filamentous bacteria Frankia, an actinomycete, and to the root location of nitrogen-fixing nodules. Actinorhizal plants are classified into four subclasses, eight families, and 25 genera comprising more than 220 species. Although ontogenically related to lateral roots, actinorhizal nodules are characterized by differentially expressed genes, supporting the idea of the uniqueness of this new organ. Two pathways for root infection have been described for compatible Frankia interactions: root hair infection or intercellular penetration. Molecular phylogeny groupings of host plants correlate with morphologic and anatomic features of actinorhizal nodules. Four clades of actinorhizal plants have been defined, whereas Frankia bacteria are classified into three major phylogenetic groups. Although the phylogenies of the symbionts are not fully congruent, a close relationship exists between plant and bacterial groups. A model for actinorhizal specificity is proposed that includes different levels or degrees of specificity of host-symbiont interactions, from fully compatible to incompatible. Intermediate, compatible, but delayed or limited interactions are also discussed. Actinorhizal plants undergo feedback regulation of symbiosis involving at least two different and consecutive signals that lead to a mechanism controlling root nodulation. These signals mediate the opening or closing of the window of susceptibility for infection and inhibit infection and nodule development in the growing root, independently of infection mechanism. The requirement for at least two molecular recognition steps in the development of actinorhizal symbioses is discussed.