Bacterial infection of interior tissues of legume root nodules is controlled at the epidermal cell layer and is closely coordinated with progressing organ development. Using spontaneous nodulating Lotus japonicus plant mutants to uncouple nodule organogenesis from infection, we have determined the role of 16 genes in these two developmental processes. We show that host-encoded mechanisms control three alternative entry processes operating in the epidermis, the root cortex and at the single cell level. Single cell infection did not involve the formation of trans-cellular infection threads and was independent of host Nod-factor receptors and bacterial Nod-factor signals. In contrast, Nod-factor perception was required for epidermal root hair infection threads, whereas primary signal transduction genes preceding the secondary Ca2+ oscillations have an indirect role. We provide support for the origin of rhizobial infection through direct intercellular epidermal invasion and subsequent evolution of crack entry and root hair invasions observed in most extant legumes.
Symbiosis between legumes and rhizobia is a non-pathogenic bacterial infection of a multicellular organism. Development of nitrogen-fixing root nodules is governed by a host genetic programme that synchronizes two processes running in parallel. Nodule primordia are formed from root cortical cells that re-initiate cell division, and simultaneously a bacterial infection process targets the developing primordia. This coordination has made separation of the molecular mechanisms underlying these two very different plant developmental processes difficult and has particularly limited the assignment of the specific role of plant genes governing bacterial infection. Adding further challenges to this analysis, microscopic investigation of a variety of wild and cultivated legume species has distinguished at least three different entry modes called infection thread invasion, crack entry and epidermal infection1.
At the cellular level, infection of model legumes Lotus japonicus (Lotus) and Medicago truncatula, as well as crops such as soybean, pea and clover, is initiated when bacteria are entrapped by a curled root hair2. Local cell wall hydrolysis and invagination of the plasma membrane then lead to formation of infection threads that traverse to the base of the root hair cell. These plant-derived tubular structures proceed into the root cortex, branch and ramify in the nodule primordium2. Finally, rhizobia colonizing infection threads are released into plant cells, in which, surrounded by a peribacteriod membrane, they reduce atmospheric dinitrogen to ammonium. Continued containment of invading bacteria within specialized plant membranes is the characteristic feature of this intracellular invasion process.
Loss-of-function mutants in Lotus and M. truncatula have shown that perception of the rhizobial lipochitin-oligosaccharide (Nod-factor)3,4 through Nod-factor receptors (NFR1 NFR5)5,6,7 is required to trigger the earliest physiological responses to Nod-factor signals, Ca2+ influx, membrane depolarization and Ca2+ oscillations (spiking)5,8, as well as for the initiation of nodule development5,6,7. Domain swaps and amino-acid substitutions have further suggested that the LysM domains of NFR1 and NFR5 receptors mediate the perception of bacterial Nod-factor and that recognition depends on Nod-factor structure9. The downstream signalling pathway is shared with mycorrhizal symbiosis and encompasses a leucine-rich repeat receptor kinase (SymRK)10,11, cation channels (Castor and Pollux)12,13,14, nucleoporins (Nup85 and Nup133)15,16, a calcium calmodulin-dependent protein kinase (CCaMK)17,18,19 and a nuclear localized coil–coil protein (Cyclops)20. SymRK, Castor, Pollux, Nup85 and Nup133 function upstream of Ca2+ spiking, whereas CCaMK and Cyclops were suggested to decode the Ca2+ oscillation signature17,18,19. The current understanding is that the Nod-factor perceived at the plasma membrane through NFR receptors, accompanied by activation of the SYMRK receptor, leads to transmission of a secondary signal releasing calcium spiking in the nucleoplasm21. In turn, this calcium oscillation signature is decoded by nuclear-localized CCaMK17,18,19. Similarly, the nuclear membrane localization of CASTOR and POLLUX potassium channel proteins suggests a role in the regulation of calcium channels and in the release of calcium from the nuclear envelope14. Several alternative functions were suggested for nucleoporins, including import of secondary signal(s), anchoring of potassium channel proteins, transport of the NSP2 proteins mentioned below and regulation of calcium fluxes15,16. Further downstream of the shared pathway, putative transcriptional regulators of the NIN22,23 GRAS (Nsp1, Nsp2)24,25,26,27 and ERF28,29 families are required for upregulation of nodule-expressed genes and initiation of nodulation30,31. Formation of nodule primordia involves dedifferentiation and reactivation of cortical root cells, and both gain-of-function and loss-of-function mutants have shown that cytokinin signalling through the cytokinin receptor (Lhk1)32,33 is important for reactivation of the cell cycle in cortical cells. The genetic requirement for infection thread development is less well described but both the Nap1 and Pir1 genes that encode proteins of the SCAR/WAVE complex activating actin rearrangement in root hairs34 and Cerberus, which encodes a putative E3 ubiquitin ligase35 are required for normal infection thread progression. Mutational perturbation of most of the genes mentioned above leads to simultaneous absence of, or severe impairment of, organ formation and infection thread development. This has made the dissection of direct and indirect roles of the affected proteins within the two processes virtually impossible. Circumventing this obstacle, in this study, we have taken advantage of the two Lotus gain-of-function alleles, snf1 and snf2, encoding a T265I calcium calmodulin-dependent kinase CCaMK17,36,37 and a L266F cytokinin receptor LHK132,33,36 respectively. These gain-of-function alleles uncouple organogenesis from infection and cause a development of empty spontaneous nodules in the absence of the bacterial symbiont, Mesorhizobium loti (M. loti), or bacterial Nod-factor signals. Using double, triple and quadruple mutants in the gain-of-function snf1 and snf2 genetic background, or transgenic roots, we have assigned genes and corresponding functions to separate paths or connecting cross-signalling functions in the complex molecular network controlling legume symbiosis. Altogether, the mechanistic role of 16 receptors and signal-transduction components previously characterized in a decade of gene discoveries was brought together in a synthesis defining a functional framework coordinating infection and organogenesis.
Genes required for organogenesis and indirectly for infection
We assumed that NFR1 and NFR5 receptors would be necessary for rhizobial infection of spontaneous nodule primordia and therefore we first investigated the effect of symrk, castor, pollux, nup133 and nup85 loss-of-function mutations on the formation and infection of spontaneous nodules. Analysis of SymRK gene function is presented in detail to illustrate the approach (Table 1; Supplementary Fig. S1 online). To distinguish the role of the SYMRK receptor in infection and organogenic processes more precisely, we determined the impact of two loss-of-function non-nodulating alleles (symrk-1 and symrk-3) caused by insertion of LORE retroelements10 in an snf1 genetic background, that is, in the presence of an autoactive CCaMK17. First, the effect on organogenesis was scored as the ability to form spontaneous nodules and, when no change in this capacity was observed, the effect on infection was subsequently scored as the frequency of pink functional nodules among the spontaneously formed non-functional white nodules. A set of snf1 and symrk single mutants and symrk snf1 double mutants were inoculated with M. loti on nitrogen-free agar slopes. As previously reported, snf1 mutants developed fully infected nitrogen-fixing pink nodules with a high frequency, resulting in green plants and plant growth, whereas symrk mutants did not develop any nodules or nodule primordia and plants were nitrogen starved, yellow and did not grow (Table 1a; Supplementary Fig. S1). Spontaneous nodule primordia developed in symrk snf1 double mutants. Unexpectedly, these spontaneous nodule primordia were also infected by M. loti, and nitrogen-fixing nodules, rescuing the non-nodulating and nitrogen-starved phenotype conferred by symrk mutations10, were established (Fig. 1a–c, Table 1a, Supplementary Fig. S1). The frequency of pink nodules in symrk-3 snf1 and symrk-1 snf1 double mutants was relatively high, ~20% compared with 69% in snf1 and 84% in wild type (Table 1a). This observation led us to determine whether the infections in symrk snf1 mutants took place through root hair infection threads, that is, whether SYMRK was dispensable for infection thread formation in the presence of autoactive snf1 CCaMK. Visualization of an M. loti strain constitutively expressing the β-galactosidase (lacZ) reporter gene showed invasion through root hair infection threads in symrk snf1 mutants (Figs. 1d–k and 2a–f). However, emergence was delayed and the number was reduced (five infection threads per wild-type root versus 0, and 55 versus 8, 1 and 2 weeks after inoculation, respectively). A closer inspection revealed infection threads in root hairs in close proximity to nodule primordia, and misguided infection thread growth associated with balloon-like swellings was not unusual (Figs. 1f and 2e–f). Light microscopy of thin sections of pink symrk snf1 nodules shows infected cells completely or partly occupying the inner root nodule tissue (Fig. 1g–i) and an average of 32 trans-cellular infection threads per section compared with 28 in wild type (Table 1a). Confirming the light microscopy results, electron microscopy micrographs visualized infection threads in nodules with infected cells (Fig. 1j,k). Containment of bacteria within infection threads without release as reported in SymRK/DMI2 RNA-mediated interference lines of Sesbania and Medicago38,39 was not observed, implying that signal transduction through the SYMRK receptor was dispensable for root hair infection thread formation and bacterial release in Lotus snf1 nodules.
Similar to symrk mutants, nucleoporin nup133 and nup85 mutants and potassium channel pollux and castor mutants show limited root hair responses to M. loti and lack the calcium-spiking characteristic for Nod-factor-induced signalling8,12,13,14,15,16. As previously reported, the inoculation of nup133 and nup85 mutants with M. loti resulted in a temperature-dependent non-functional and reduced infection phenotype15,16. In contrast, nup133 snf1 and nup85 snf1 double mutants were invaded through root hair infection threads and nitrogen-fixing nodules developed to rescue the ineffective nodulating phenotype of the single mutants at both the normal 21 °C growth conditions and the non-permissive 26 °C (Table 1a; Figs. 2g–l, 3 and 4; Supplementary Fig. S1). Infection threads were observed in root hairs in proximity to nodule primordia (Fig. 2g–j). Comparable infections of the non-nodulating castor and pollux mutants were observed using a dominant T265D version of CCaMK and transgenic roots generated by Agrobacterium rhizogenes-mediated transformation (Table 1a).
Genes required for infection but dispensable for organogenesis
nap1, pir1 and cerberus mutant plants have all previously been shown to develop nodule primordia with aberrant infection thread formation or progression34,35. To extend the infection thread observations, we transformed these mutants with the T265D construct of CCaMK. The phenotype of arrested infection threads and lack of infected nodules in the mutant plants transformed with T265D CCaMK confirmed that Nap1, Pir134 and Cerberus35 genes function in the infection thread pathway (Table 1b).
Gene functions required for both infection and organogenesis
Previous characterization of nin, nsp1 and nsp2 mutants suggests a function for these transcriptional regulators in both infection and organogenesis22,23,24,25,26,27. The lack of spontaneous nodules observed in nin-2 snf1 double mutants, as well as the unchanged phenotype of nsp1and nsp2 mutants, transformed with the T265D CCaMK construct confirmed their role in organogenesis. Microscopy of roots inoculated with the M. loti lacZ strain detected root hair deformations but no infection threads in nin-2 snf1 double mutants (Table 1c). The impaired infection and organogenesis phenotype were also unchanged in the nsp1 and nsp2 mutants transformed with the T265D variant of CCaMK (Table 1c).
Cross-talk between organogenesis and infection pathways
The availability of corresponding gain-of-function (snf1, snf2)17,32 and loss-of-function (ccamk, hit1)17,33 mutants of CCaMK and the Lhk1 cytokinin receptor genes enabled us to investigate the interdependence of organogenesis and root hair infection. Infection of reciprocal snf1 hit1 and ccamk-13 snf2 double mutants was analysed, together with symrk-3 snf1 and symrk-3 snf2 mutants. Inactivation of CCaMK in ccamk-13 snf2 resulted in an absence of infection of the spontaneously formed primordia caused by snf2 gain-of-function cytokinin receptor activity. In addition, inactivation of the SYMRK receptor in symrk-3 snf2 mutants resulted in a very low infection frequency of snf2-induced spontaneous nodules compared with the autoactive CCaMK-induced primordia in symrk-3 snf1 double mutants (Table 1d and a). Together, these results indicate a role for activated CCaMK in cross-signalling between the organogenic and root hair infection thread pathways and a role for SYMRK in the signalling leading to CCaMK activation. In the reciprocal combination of the loss-of-function cytokinin receptor, hit1, and the autoactive CCaMK in hit1 snf1 double mutants, an excessive infection thread formation comparable to the level observed in hit1 mutants was detected. As previously observed for hit1 mutants33, hit1 snf1 mutants show reduced nodulation, whereas organogenesis was absent in uninoculated plants (see Supplementary Table S1). The simplest conclusion from these two sets of experiments is that cross-signalling to the root hair infection pathway is CCaMK dependent and that cytokinin signalling mediated by the downstream-functioning snf2 gain-of-function cytokinin receptor was unable to activate the infection thread pathway effectively. See Supplementary Table S1 for the analysis documenting that CCaMK functions upstream of the LHK1 cytokinin receptor. We infer that cross-signalling through CCaMK seems to enhance the efficiency of nodule primordia infection and that cell division alone as in snf2 mutants is insufficient. CYCLOPS was recently suggested to function in the infection pathway and was shown to interact directly with CCaMK20,40. Our inspection of nodules on cyclops roots transformed with the T265D CCaMK construct confirms the absence of infection and infection threads in cyclops mutants (Table 1d), suggesting that CYCLOPS is important for CCaMK cross-signalling from the organogenic to the infection pathway. Previous experiments using a CaMV 35S promoter to drive T265D CCaMK expression resulted in organogenesis beyond the primordial stage, showing that CYCLOPS is dispensable for organogenesis20. In our experiments using the cognate CCaMK promoter, this is less obvious and a level of CYCLOPS-dependent back signalling from the infection pathway cannot be excluded.
Infection in the absence of NFR1 and NFR5 receptors
To determine the requirement for host Nod-factor perception in the intracellular root hair infection thread pathway, double, triple and quadruple mutants of Nfr1, Nfr5 and SymRK receptors unable to perceive the Nod-factor signal, and/or impaired in downstream signal transduction, were inoculated with M. loti. To our surprise, pink nodules developed in nfr1-1 snf1 and nfr5-2 snf1 double mutants, as well as in nfr1-1 nfr5-2 snf1, nfr1-1 nfr5-2 symrk-3 snf1 triple and quadruple mutant plants, although at 10- to 20-fold lower frequencies than in snf1 and wild-type plants (Figs. 4a, h–q and 5; Table 1e). Both normal pink nodules and pink sectored nodules were observed (Fig. 4b, c, and l–t). Most plants carrying these nodules displayed dark green leaves and grew, indicating nitrogen fixation in the nodules (Fig. 5a,b). Microscopy revealed that infected cells in sectored nodules were not distributed evenly (Fig. 4m, o and q) as seen in wild type and most but not all snf1 nodules (Fig. 4a,h,i). The invasion process was therefore followed using M. loti strains expressing enhanced green fluorescent protein (eGFP) or lacZ. Using fluorescence and light microscopy, we were unable to detect infection threads in root hairs of nfr1-1 snf1, nfr5-2 snf1, nfr1-1 nfr5-2 snf1 and nfr1-1 nfr5-2 symrk-3 snf1, but thin sections of nodules revealed trans-cellular infection threads in the central nodule tissue (Fig. 3a–c). Infection threads were also observed in electon microscopy micrographs (Fig. 3d–f). Thin sections of fully or partly infected nodules indicate that these were invaded through infection threads initiated by M. loti entering through cracks at the junctions of nodules and roots, followed by bacterial accumulation in intercellular pockets (Figs. 3g and 4r–t). In contrast to the corresponding snf1 double mutants, no infected pink nodules were observed in nfr1-1 snf2 and nfr5-2 snf2 mutants inoculated with M. loti (Table 1e).
Infection in the absence of Nod-factor signalling
To further investigate the role of the Nod-factor signal in this alternative intercellular entry process, a set of symrk-3 snf1, nfr1-1 snf1 and nfr1-1 nfr5-2 snf1, as well as a har1-3 snf1 hypernodulating mutant, which is impaired in the shoot regulation of nodule numbers by the HAR1 receptor kinase, were inoculated with M. loti nodC or nodA mutants unable to synthesize functional Nod-factors41. In symrk-3 snf1 mutants, no infected nodules were observed (Table 1e), but interestingly, infections were observed in nfr1-1 snf1, nfr1-1 nfr5-2 snf1 and snf1 har1 mutants even in the absence of Nod-factor and NFRs. Compared with wild-type and snf1 plants, infection frequencies were reduced 20- to 100-fold (Table 1e). Almost all of these pink nodules were sectored and showed irregular morphologies (Figs. 4d-g, 5c,d). Using fluorescence and light microscopy and M. loti strains expressing eGFP or lacZ, we were unable to detect infection threads in root hairs or trans-cellular infection threads. Inspection of thin sections of nodules of nfr1-1 snf1 and nfr1-1 nfr5-2 snf1 mutants inoculated with nodC or nodA mutants (Figs. 3h and 5e,f) indicates that infection of these nodule primordia occurs through intercellular epidermal entry and shows an anatomy in which only few cells, often only single cells, are infected (Fig. 5e–g). These infected cells seem enlarged compared with infected cells in wild-type nodules, suggesting size regulation in wild-type nodules. Infected cells that had recently divided were also observed (Fig. 5f–g). Extending the analysis using transmission electron microscopy (TEM), the absence of trans-cellular infection threads was confirmed. TEM micrographs, similar to fluorescence and light microscopy, only reveal intercellularly located bacteria and bacteria inside infected cells (Fig. 3i). Among all the sections obtained, two images show sub-cellular structures most likely representing the invasion mechanism operating at the single cell level (Fig. 3j–l). The thin section (Fig. 3j) shows an intracellular infection that seems to be connected to an adjacent intercellular pocket of bacteria. The TEM micrograph (Fig. 3k,l) shows a comparable infection structure. Here, an intercellular pocket of bacteria is located adjacent to an intracellular infection peg that seems to enlarge into a butterfly-shaped release structure containing numerous bacteria. We infer that these expanded intracellular infection pegs are induced by bacterial entry from the intercellular pocket and we propose to call this path for single-cell peg entry. In support of this interpretation, comparable short infection structures originating from intercellular bacteria were observed in lupinoid root nodules42,43.
The results presented here define the components of two parallel pathways facilitating infection thread formation and root nodule organogenesis, respectively (Fig. 6a). We have shown that the SYMRK receptor, the two nucleoporins (NUP133, NUP85) and the potassium channels (CASTOR and POLLUX) involved in signal transduction downstream of Nod-factor perception are dispensable for root hair infection thread development and invasion of nodule primordia in an snf1 genetic background. On the other hand, NFRs (NFR1 and NFR5) were required for root hair infection thread initiation, and NAP1 and PIR1 mediating actin rearrangement, together with the putative ubiquitin E3 ligase (CERBERUS), were required for infection thread progression. A simple explanation is an early branching of the NFR and Nod-factor-mediated signal transduction (Fig. 6a). NIN, NSP1 and NSP2 transcriptional regulators were required for both infection and organogenesis, supporting a role in both infection thread formation and cortical cell activation. Our results further indicate that calcium spiking by itself is dispensable for infection thread formation, as inactivation of SYMRK, nucleoporins (NUP133, NUP85) and potassium channels (CASTOR and POLLUX) results in an absence of calcium spiking8. At the same time, a presumed Ca2+ activation of CCaMK, as mimicked by the snf1 mutation, seems insufficient for root hair infection thread formation, as functional NFR1 and NFR5 receptors were required for root hair infection thread formation in snf1. Together this suggests that the NFR receptor-dependent Ca2+ influx observed in root hairs at high Nod-factor concentration or other, as yet undiscovered, NFR-dependent early responses may be a prerequisite for root hair infection thread formation. Supporting these interpretations, observation of morphological root hair responses in M. truncatula mutants, corresponding to our Lotus symrk, castor/pollux and ccamk mutants, also suggests a separate pathway leading to root hair curling44.
Absence of infection of cyclops primordia after expression of a T265D CCaMK from the CaMV 35S promoter20 and in our experiments from the CCaMK promoter, together with the reported protein–protein interaction between CCaMK and CYCLOPS, indicates a role for CYCLOPS in cross-signalling between organogenic and infection pathways20,40. The ineffective invasion in the snf2 mutant background supports this notion and indicates that component(s) responsible for cross-signalling from the organogenic pathway to the infection pathway depend on CCaMK activity while acting upstream of cytokinin responses. In accordance with this interpretation, the hit1snf1 double mutants inoculated with M. loti formed infection threads, whereas ccamk-13 snf2 mutants did not. We suggest that the delayed and the two- to threefold lower infection frequency observed in symrk, nup133, nup85, castor and pollux mutants within the snf1 background may result from a lack of synchronization between organogenesis and infection, leading to misguidance of infection threads as seen in hit1 mutants33. Alternatively, ineffective cross-signalling though autoactive CCaMK proteins may lead to a lower infection frequency. Similarly, lack of synchronization was suggested to explain the delayed nodulation in inoculation of Sesbania plant with a mixture of rhizobial mutant strains45.
Our results uncover unusual intercellular infection processes in the normally intracellularly root hair-infected Lotus plants (Fig. 6b). Intercellular infection and formation of trans-cellular infection threads within the root nodules occurred in the absence of functional NFR1 and NFR5 receptors, although at 10- to 20-fold lower frequencies than in snf1 and wild-type plants. Nevertheless, a comparison of infection thread formation induced by wild-type M. loti and nodC mutants shows that synthesis of the bacterial Nod-factor was required for the effective development of these trans-cellular nodule infection threads. The mechanism involved in such a cortical perception is unknown, but involvement of one or more of the 15 additional receptor kinases belonging to the Lotus NFR1 and NFR5 families is conceivable46. Six of these family members, Lys2, Lys3, Lys7, Lys12, Lys15 and Lys20, were expressed mainly in root and root nodules46 and are thus candidates for the cortical receptor or receptor components. Involvement of alternative epidermal or cortical NFRs is supported by observations in Sesbania, in which root hair infection was stringently dependent on an intact Nod-factor structure, whereas crack entry was less stringently controlled47,48 but still dependent on continuous Nod-factor synthesis for effective invasion49. Furthermore, the suggested cross-signalling through CCaMK and CYCLOPS interaction also seems to be required for nodule infection thread formation following the intercellular infection mode. Absence of intercellular infection in nfr1-1 snf2, nfr5-2 snf2, ccamk-13 snf2 and cyclops snf1 mutants concurs with this interpretation, as does the recent observation of impaired infection thread progression following RNA-mediated interference knockdown of CCaMK in Sesbania50.
Intercellular infection of single cells as observed in, for example, nfr1 nfr5 snf1 mutants inoculated with the bacterial nodC mutant may constitute the ground state of bacterial invasion mobilized during evolution of nodulation. This intercellular process was approximately 20- to 100-fold less effective than normal root hair invasion. Symbiosomes were observed in infected cells, indicating that endocytosis occurred in the absence of Nod-factor and NFR1 and NFR5 receptors. Endocytosis in the apparent absence of local Nod-factor synthesis in cortical infection threads was also observed in mixed inoculation of Sesbania49. In this context, the lack of infected nodules observed in symrk snf1 double mutant plants inoculated with nodC and nodA mutant strains is puzzling. This may suggest that the SYMRK receptor would be necessary for single cell infection in contrast to infection through infection threads. However, the low level of infection by nodC and nodA mutant strains observed on nfr1 nfr5 snf1 mutants cautions such a conclusion on the basis of negative results. Considering our positive results with nodC and nodA infection of nfr1 nfr5 snf1 mutants, we hypothesize that a capacity for direct intercellular infection may constitute an ancient invasion path that evolved at the emergence of the legume family or maybe at the emergence of the eurosid I clade containing all nodulating plants. Division of primary infected single cells would conceivably lead to the fully infected Nod-factor-independent nodulation observed in Aeschynomene-type nodules1,51. In a subsequent evolutionary step, the Nod-factor and cortical NFR-dependent crack entry and subsequent cortical infection thread propagation of invasion could have been established. The most highly evolved state envisaged is the root hair infection mode. This infection mode required Nod-factor, epidermal NFR1 and NFR5 receptors, and is predicted to also involve cortical NFRs with less stringency than NFR1 and NFR5 receptors. The ability of Sesbania to switch between a root hair infection mode requiring Nod-factor decorations and a crack entry mode less dependent on Nod-factor structure48 supports our interpretation, as does the infrequent and delayed infection of nodules in a root hairless mutant52 and rare events in flooded Lotus spp53. Overall, this model postulates an evolutionary process in which the advanced root hair infection bestowed a set of legume hosts with a tighter and more selective control of bacterial passage through the epidermis (Fig. 6b). Our observations also suggest that alternative invasion modes have been maintained during evolution and that they are not mutually exclusive. Presence of different infection modes in Sesbania, Chamaecrista1, and both a Nod-factor-dependent and a Nod-factor-independent mechanism for nodulation in Aeschynomene sensitiva51, is in accordance with these notions. On this basis, we propose that taking non-exclusive infection modes into account may contribute to resolving some of the difficulties in aligning nodule evolution and the legume phylogeny1. Further studies of the direct infection pathway(s) will not only impact biotechnological applications and improve our understanding of plant–microbe interactions but may be key to elucidate the evolution of symbiosis.
The L. japonicus mutants used in this study are all in an ecotype Gifu B-129 background54.
For details on M. loti strains, see Supplementary Table S2. The identity of bacteria in selected, infected nodules was confirmed by re-isolation of bacteria from surface-sterilized nodules, followed by genotyping by specific PCR. For primers, see Supplementary Table S3.
Double mutants and plant genotyping
Double, triple and quadruple mutants were obtained by crossing, followed by genotyping of offspring plants. Similarly, the genotypes of mutant plant lines in individual experiments were verified using allele-specific PCR and/or sequencing of PCR-amplified genomic fragments (for primers and conditions, see Supplementary Table S4). The non-nodulating mutants used to establish crack entry, single cell infection and cross-signalling mechanisms (summarized in Fig. 6a,b) carry stable mutations caused by insertion of LORE1 or LORE2 retrotransposons (symrk-1, symrk-3, nfr5-2), a deletion (ccamk-13) or a premature stop codon (nfr1-1). See Supplementary Table S4 for a full list of genotypes of the mutants used in this study.
The constitutively active T265D variant of the Lotus CCaMK gene driven by the native CCaMK promoter was constructed using overlap extension PCR for site-directed mutagenesis of the wild-type CCaMK construct17 and conventional cloning techniques. The construct complements the nodulation defect in Lotus ccamk mutants17 and causes spontaneous nodulation in the absence of rhizobia. Transgenic hairy roots carrying CCaMKT265D or control wild-type CCaMK genes were produced through A. rhizogenes transformation9.
Plant growth conditions
Seeds of wild type and mutants were surface sterilized for 20 min in a solution of 0.5−1.0% sodium hypochlorite and grown in a 16/8 h day/night regime of 21/16 °C for up to 7 weeks in square Petri dishes on solid 1/4 B&D slants without nitrate, or in Magenta containers (Sigma) on a substrate of Leca (Optiroc) and Vermiculite (3:1 mixture) supplemented with 75 ml of 1/4 B&D medium without nitrate. On plates, the plant roots were shielded from light by using a metal comb fitting the Petri dish and inserting the lower half of the Petri dish into a rack. Plants were grown with or without inoculation with M. loti strains (see below).
Red and white nodules/nodule primordia were counted and photographed using a Zeiss Discovery V8 stereomicroscope.
Infection thread analysis
To visualize infection threads, roots were inoculated with M. loti expressing lacZ or eGFP reporter genes. Each seedling was inoculated with 150−400 μl (OD600 ∼0.01 to 0.02) of M. loti expressing the relevant reporter gene and infection threads were visualized at selected time points after inoculation by staining for β-galactosidase activity8 After clearing in 30% lactic acid, the roots were mounted on glass slides in glycerol and observed with a bright field Zeiss Axioplan microscope with ×10, ×20 or ×40 objectives, equipped with DIC optics. For eGFP-expressing bacteria, intact roots were mounted on slides in deionized water and observed directly with a Zeiss fluorescence microscope with standard FITC filters. Images were taken with a Zeiss LSM 510 Meta confocal microscope, with excitation at 488 nm, and a BP 505−530 emission filter. Images were recorded with Axiovision software.
The number of infection threads was recorded either per root for short roots or per cm root for older, longer roots. Roots from at least two different plants were scored for each genotype and between 10 and 80 cm roots were inspected for each genotype. The number of infection threads in thin sections was counted in two representative sections of 10 different nodules for each plant genotype.
Nodules were prepared for light and TEM coupled with immunogold labelling with the rat monoclonal antibody MAC23642 and infection threads from all genotypes were labelled. Nodules that had been fixed in 2.5% glutaraldehyde in 0.1 M sodium cacodylate (pH 7.0) overnight at 4 °C were dehydrated in an ethanol series, and embedded in LR White acrylic resin (Agar Scientific). Semithin sections (1 μm) were taken for light microscopy and ultrathin (70 nm) sections were taken for TEM using a Leica UCT ultramicrotome. The semithin sections were collected on glass slides and stained with 0.1% toluidine blue, whereas the ultrathin sections were collected on pioloform-coated nickel grids and immunogold labelled with the MAC236 antibody. The sections were incubated for 2 h in MAC236 (diluted 1:10), followed by 30 min incubation in an anti-rat secondary antibody raised in rabbit (diluted 1:400) (Southern Biotechnology), and then for 1 h in 15 nm goat anti-rabbit gold (GE Healthcare) (diluted 1:100). The ultrathin sections were then stained with uranyl acetate for 10 min before being viewed and digitally photographed using a JEM 1400 transmission electron microscope (JEOL). Note that bacteria inside Lotus infection threads may seem crenellated53.
How to cite this article: Madsen L.H. et al. The molecular network governing nodule organogenesis and infection in the model legume Lotus japonicus. Nat. Commun. 1:10 doi: 10.1038/ncomms1009 (2010).
Copyright: © 2010 Madsen, L.H. et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permitsunrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
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The Danish National Research Foundation funded this study. We thank Nick Brewin for the MAC236 antibody, Krzysztof Szczyglowski for hit1 seeds and Masayoshi Kawaguchi for nup85 seeds.
The authors declare no competing financial interests.
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Madsen, L., Tirichine, L., Jurkiewicz, A. et al. The molecular network governing nodule organogenesis and infection in the model legume Lotus japonicus. Nat Commun 1, 10 (2010). https://doi.org/10.1038/ncomms1009
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