Host plant root exudates induce in M. loti a Ca2+ signal required for activation of nodulation genes Root exudates from the symbiotically compatible legume L. japonicus were collected from 3-week-old seedlings axenically grown in water and applied to M. loti cells. The dose used for Ca2+ measurements was in the range that induced significant expression of nodA, nodB, nodC genes in M. loti (Fig. 2A). This concentration was found to trigger a transient [Ca2+]i change characterized by a very rapid increase (1.38 ± 0.23 μM Ca2+) followed by a second sustained major Ca2+ peak (2.01 ± 0.24 μM) at about 10 min (Fig. 2B), with a slow decay within the considered time interval (30

min). The observed induction of transient [Ca2+]i changes in M. loti cells suggests a Ca2+-mediated perception Adriamycin chemical structure of signalling molecules contained

in host plant root exudates. Figure 2 Effect of plant root exudates and tetronic acid on [Ca 2+ ] i and nod gene expression in M. loti. A, Analysis of gene expression by semi-quantitative RT-PCR during control conditions (lane 1, white bars) and after 1 h treatment with L. japonicus root exudates (lane 2, black bars) or 1.5 mM tetronic acid (lane 2, striped bars). Relative transcript abundance was normalized against 16S rRNA. Data are the means ± SEM of three independent experiments. B, Monitoring of [Ca2+]i changes in M. loti cells challenged (arrow) with L. japonicus root exudates selleck screening library (black trace) or 1.5 mM tetronic acid (grey trace). Flavonoids are SC75741 components of root exudates that play a prominent role as inducers of structural nod

genes in rhizobia. Although flavonoids have been detected in L. japonicus seeds [26], those that specifically activate the expression of nod genes in M. loti have not yet been identified [27, 28]. The most common flavonoids, known as nod gene inducers in other rhizobia (10 μM naringenin, luteolin, daidzein, kaempferol, quercetin dehydrate) were not able to trigger transient Ca2+ for elevations in M. loti (data not shown). Tetronic acid, an aldonic acid previously reported to promote Nod factor biosynthesis in M. loti [29], was found to induce a detectable Ca2+ response (Fig. 2B). The kinetics of the Ca2+ trace was similar to that induced by crude root exudates, with a prompt Ca2+ spike (1.36 ± 0.16 μM Ca2+) and a subsequent flattened dome (maximal Ca2+ value of 1.29 ± 0.08 μM reached around 15 min after the elicitor application). Notably, this second phase of the Ca2+ transient induced by tetronic acid only partially accounted for the larger Ca2+ increase recorded with the whole L. japonicus root exudates (Fig. 2B). Likewise, the level of nod gene expression induced by tetronic acid was found to be lower (though significantly different from the control, P < 0.05) than that generated by total root exudates (Fig. 2A).