A symbiotic sugar transporter in the arbuscular mycorrhizal fungus Glomus sp.

Arbuscular mycorrhizal (AM) fungi live in mutualistic symbioses with plant roots, in which the fungus provides the plant with enhanced mineral uptake from the soil, principally phosphate, in exchange for carbon to support fungal growth (reviewed in Bonfante and Genre, 2010). Phosphate status is a critical parameter controlling the development of the symbiosis, as both high phosphate levels in the soil and inactivation of symbiotic plant phosphate transporters lead to reduced fungal growth within the root. Because of its role in plant nutrition and key role in the symbiosis, symbiotic phosphate transport has beenwell characterized. By contrast, carbon transport to the fungus is less well understood, and fungal transporters involved have not been identified to date. Now, Helber et al. (pages 3812– 3823) present a detailed characterization of a high-affinity monosaccharide transporter in the AM fungus Glomus sp DAOM 197198, which plays a major role in sugar uptake and growth and development of the fungal partner. A search of the first draft of the genome of Glomus sp DAOM 197198 (Martin et al., 2008) yielded three sequences with similarity to genes encoding monosaccharide transporters and one with similarity to a Suc transporter. One of these, named MST2, showed high expression during the in planta symbiotic phase of the fungal life cycle that was highly correlated with that of the the mycorrhiza-specific plant phosphate transporter gene PT4, which is used as an indicator of a functional AM association. In situ hybridization showed expression in arbuscules and in intercellular hyphae of the fungus colonizing the roots of Medicago truncatula. The authors investigated the biochemistry and substrate specifity of MST2 by heterologous expression in a monosaccharide transport-deficient strain of Saccharomyces cerevisiae. The protein was found to be a membrane-localized high-affinity transporter of Glc with a pH optimum at a likely apoplastic pH at the plant-fungal interface (pH 5). It was also capable of transporting Xyl, Man, and Fru, with affinity decreasing in that order, but was unable to transport the disaccharides Suc and maltose. Intriguingly, Xyl, but none of the other monosaccharides anaylzed, was found to induce MST2 expression of the extraradical mycelium (ERM), suggesting that xylose could be the trigger for MST2 expression in planta. Experiments with radiolabeled Xyl and Glc fed to ERM cultivated in carrot root culture showed that the ERM is capable of taking up both sugars. Uptake was blocked by the presence of a protonophore, suggesting it occurs by an active proton pumping mechanism. In addition, no radioactivity was found in plant root tissue in these assays, suggesting that sugar imported by the ERM is retained for fungal use. A tight connection between MST2 and AM symbiosis was confirmed by experiments showing that (1) a high concentration of phosphate in the medium led to rapid downregulation of MST2 in parallel with the decline in expression of the symbiotic phosphate transporter PT4, and (2) knockdown ofMST2 using RNA interference led to decreased mycorrhization in M. truncatula hairy root culture, as measured by a decreased number of arbuscules, abnormal arbuscule morphology, and several other parameters (see figure). This work demonstrates that the fungal sugar transporterMST2 is required for functional AM symbiosis and is likely the major transporter supplying the fungus with carbon from its plant host.