Spore development and nuclear inheritance in arbuscular mycorrhizal fungi
© Marleau et al; licensee BioMed Central Ltd. 2011
Received: 20 August 2010
Accepted: 24 February 2011
Published: 24 February 2011
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© Marleau et al; licensee BioMed Central Ltd. 2011
Received: 20 August 2010
Accepted: 24 February 2011
Published: 24 February 2011
A conventional tenet of classical genetics is that progeny inherit half their genome from each parent in sexual reproduction instead of the complete genome transferred to each daughter during asexual reproduction. The transmission of hereditary characteristics from parents to their offspring is therefore predictable, although several exceptions are known. Heredity in microorganisms, however, can be very complex, and even unknown as is the case for coenocytic organisms such as Arbuscular Mycorrhizal Fungi (AMF). This group of fungi are plant-root symbionts, ubiquitous in most ecosystems, which reproduce asexually via multinucleate spores for which sexuality has not yet been observed.
We examined the number of nuclei per spore of four AMF taxa using high Z-resolution live confocal microscopy and found that the number of nuclei was correlated with spore diameter. We show that AMF have the ability, through the establishment of new symbioses, to pass hundreds of nuclei to subsequent generations of multinucleated spores. More importantly, we observed surprising heterogeneity in the number of nuclei among sister spores and show that massive nuclear migration and mitosis are the mechanisms by which AMF spores are formed. We followed spore development of Glomus irregulare from hyphal swelling to spore maturity and found that the spores reached mature size within 30 to 60 days, and that the number of nuclei per spores increased over time.
We conclude that the spores used for dispersal of AMF contain nuclei with two origins, those that migrate into the spore and those that arise by mitosis in the spore. Therefore, these spores do not represent a stage in the life cycle with a single nucleus, raising the possibility that AMF, unlike all other known eukaryotic organisms, lack the genetic bottleneck of a single-nucleus stage.
The Arbuscular Mycorrhizal Fungi (AMF) are a group of root-inhabiting, symbiotic organisms that are widely distributed geographically and are among the most common soil fungi. AMF form symbioses with the roots of approximately 80% of all vascular plant species . These fungi offer a wide variety of host benefits, the most well-known being an increase of mineral uptake, particularly of phosphorus , a better drought tolerance through increased water uptake [3, 4] and a higher resistance to root pathogens . Mycorrhizal plants also experience improved nodule function in the case of legumes  and better soil structure, due to the ability of the fungi to bind soil particles and decrease soil erosion .
AMF have existed unchanged morphologically for at least 460 million years, despite lacking sexual reproduction . AMF are coenocytic organisms that have evolved to be multigenomic, possessing a large amount of genetic variation for ribosomal DNA [8–12], non-coding regions  and also for protein-coding genes [12, 14, 15] not only between individuals, but among nuclei within an individual (one 'individual' refers here to a single spore). Reproduction occurs by asexual spores that contain hundreds or even thousands of nuclei [16, 17], and these spores are the only form under which species can be identified morphologically, although AMF can be also identified using molecular markers. The ability of spores to germinate is a prerequisite for the establishment of mycorrhizal symbiosis for many AMF taxa. However, while the developmental process leading to the accumulation of nuclei within spores has been recently reported to occur by the transport of numerous nuclei into the developing spore in the AMF Glomus etunicatum , whether or not mitosis happens within spores is not known. Fungal mitosis has been accurately described and illustrated mainly in ascomycetes and basidiomycetes and is usually intranuclear (reviewed in Aist and Morris, 1999 ) because the nuclear envelope remains intact, often until anaphase B. Coenocytic fungi such as zygomycetes have also an intranuclear mitosis. However, the coexistence of numerous nuclei within a common cytoplasm and mitosis phases that are not easily distinguishable causes many difficulties in studying mitosis in coenocytic fungi, although exceptions have been reported in Basidiobolus ranarum . To test whether mitosis is involved during sporulation in AMF, we used mitosis inhibitors. Many mitosis inhibitors have been successfully tested on AMF. For example, Aphidicolin, which is a specific DNA polymerase α inhibitor that blocks the cell cycle at early S phase, was used to study nuclear division in AMF during in vitro development . Carbendazim, which prevents microtubule formation and inhibits mitosis in fungal cells, was also used to investigate phosphorus transport and succinate dehydrogenase activity in three AMF . We chose the use of aphidicolin in our experiment because it has been shown to inhibit efficiently mitosis in AMF without any effect on spore germination .
To investigate the mechanisms of AMF spore formation in other taxa, and by extension, the amount of genetic material inherited by AMF offspring, we first counted the number of nuclei in live spores belonging to four different AMF taxa. All these taxa were grown in in vitro culture with Agrobacterium rhizogenes T-DNA transformed-carrot roots and were examined using confocal microscopy with a high z-resolution for three-dimensional (3D) reconstructions, which allows a direct counting of nuclei and visualization of their 3D architecture. We addressed five specific questions: 1) what is the correlation between spore diameter and the number of nuclei per spore? 2) Is there any heterogeneity in the number of nuclei among spores of similar diameter? 3) What is the mechanism of spore formation in the AMF G. irregulare ? 4) What is the minimum number of nuclei required to make up a viable spore that can germinate and establish a functional symbiosis in G. irregulare ? 5) Do the extraradical phases of AMF lack a single nuclear stage? These questions are of fundamental importance to our comprehension of AMF reproduction by sporulation, and their answers will bring a new level of knowledge to AMF genetics and evolution. Insight into AMF genetics is the cornerstone on which understanding the role of mycorrhizal symbiosis in nature will be based.
We used two independent, but complementary, imaging experiments to examine the nuclear inheritance process. In a two-compartmented in vitro system , G. irregulare was grown on transformed carrot roots that were restricted to one compartment (proximal). Only the fungus was permitted to grow on to the second compartment (distal) containing the same media lacking the sugar and complemented with aphidicolin . The formation of spores over time was monitored in the distal compartment. We found that while aphidicolin did not inhibit spore formation or hyphal growth, the number of newly produced spores was reduced by 14-fold in comparison to the control (Additional File 4). We then examined the number of nuclei per spore and the diameter of spores that were produced in the distal compartment for both aphidicolin and control treatments. The aphidicolin had no significant effect on the spore diameter (W = 782, p = 0.753), but reduced the number of nuclei per spore by 54.86% (W = 1207.5, p = 0.00001) (Additional File 5). On average, nuclear number per spore was 55.23 ± 40.31 SE, (n = 22) and 168.30 ± 90.66 SE, (n = 165) for aphidicolin and control treatments, respectively.
A, Spore volume increase of in vitro differentiated spores of G. irregulare over time (n = 25); B, Percent spore viability and percent spore germination of in vitro differentiated spores of G. irregulare over time (n = 25, for each selected age category)
Age of spores
Mean spore diameter/radius (μm)
Spore volume (mm3)
Number of nuclei in the different architectural structures forming the extraradical mycelium of G. diaphanum (n = 21 spores, 20 RH and 22 FB)
Diameter × length2 (μm)
Nb of nuclei
6.9 × 157.3
3.3 × 131.0
The number of nuclei in spores has been previously estimated by several methods with widely divergent results . For example, using a model in which nuclei occur as a single layer around the periphery of the cytoplasm , the number of nuclei in Gigaspora margarita spores was estimated at about 20,000, while a different method based on digital image measurements estimated the number of nuclei per spore to be about 2,000 . Here we used confocal microscopy with a high z-resolution for three-dimensional (3D) reconstructions, which allow a direct counting of nuclei and visualization of their 3D architecture in live spores. As far as we know, this is a novel rapid and high-accuracy method for determining the number of nuclei per spores in AMF. Recently, Jany and Pawlowska  have reconstructed 3D images of the AMF G. etunicatum using deconvolution, a computational based-method used to reduce out-of-focus fluorescence in 3D microscope images.
We found a surprisingly high heterogeneity in the number of nuclei per spore of different diameter classes. The number of nuclei in G. irregulare spores varied by about 5-fold in the diameter class 94-103 μm. Clearly, the spores of the AMF used here do not have a constant number of nuclei.
We used two independent but complementary imaging experiments based on aphidicolin treatment and time-lapse live cellular imaging to examine the nuclear inheritance process in G. irregulare and G. diaphanum. We used G. irregulare in aphidicolin treatment because it is fast growing under in vitro culture. However, G. diaphanum was chosen for time-lapse experiments because its spores contained the higher number of nuclei. When tested on AMF spores, aphidicolin does not inhibit spore germination of the AMF G. margarita, but rapidly reduces the rate of hyphal growth and arrests growth after four days, owing to efficient inhibition of DNA synthesis . We tested aphidicolin on yeast cells and found that no mitosis occurred in samples grown in media complemented with aphidicolin whereas optical density (DO) increased over time in samples without aphidicolin (data not shown). When spore formation was monitored over time in the distal compartment, we found that the aphidicolin did not inhibit the spore formation or the hyphal growth, but the number of newly produced spores was dramatically reduced. Aphidicolin had no significant effect on the spore diameter (F 1.88 = 0.02, P = 0.90), but reduced the number of nuclei per spore by approximately three-fold (F 1.88 = 15.18, P ≤ 0.0002). Since the nuclei observed in the spores differentiated in the distal compartment (containing aphidicolin) could not have been produced by mitosis in the newly formed spores, they must have migrated from the proximal compartment, through hyphae, into the developing spore. Considering that the average nuclear number per spore treated with aphidicolin was approximately three times less than that of the control, at least one mitotic cycle must occur that during spore development, allowing a duplication of the migrated nuclei. To confirm this nuclear migration, we made direct observations of individual nuclei in live cells in real time. Time-lapse series taken with a confocal microscope of the AMF G. diaphanum spores clearly show nuclear migration from the hypha into the developing spores. In total, we observed 534 live AMF spores of four taxa, all of which showed continuous connections between hyphal and spore cytoplasm without any apparent septa (Additional File 8). These results support the hypothesis that AMF spores are formed by a massive nuclear migration and are in agreement with results reported using G. etunicatum . Interestingly, these nuclei could potentially carry different genomes, as there is considerable evidence suggesting that AMF contain populations of genetically different nucleotypes coexisting in a common cytoplasm [12, 14, 15, 25–28]. In addition, genetic exchange has only recently been demonstrated to occur among AMF isolates that are genetically distinct . There is as well recent evidence showing that genetic exchange and segregation in AMF significantly affects the plant response .
Taken together, our results clearly show that AMF spores accumulate up to thousands of nuclei by nuclear migration and mitosis. However, one potential consequence of this mechanism is the loss of the genetic diversity by drift-driven processes. During sporulation, the evolutionary process of change in the nucleotype frequencies (or genome frequencies) of a nuclear population from one generation to the next is due to the phenomenon of probability, in which pure chance events determine which nuclei within the overall nuclear population will be carried forward while others disappear. Two strategies could be envisaged to counter a potential loss of genetic diversity in AMF, either a selective sampling of certain nucleotypes from the overall population, or random selection coupled with a mechanism to ensure that spores contain adequate numbers of nuclei. Although previous models have demonstrated that hyphal fusion and nuclear exchange is an important mechanism for the maintenance of high nuclear diversity , this has been also reported to occur between genetically different isolate of the AMF G. intraradices . Recombination has been reported to occur in AMF  but at low frequency and thus is likely to contribute significantly in maintaining the unusual high genetic diversity observed frequently within AMF isolates [12, 28]. It has been reported that recombination repair of double-strand DNA breaks in mitotic cells is associated with a 100-fold higher mutation rate in Saccharomyces cerevisiae . In addition, S. paradoxus has a low frequency of recombination rate but maintains a completely outbreeding population structure .
We also wished to estimate the minimum number of nuclei to make up a viable spore (i.e., able to germinate). To address this issue, we followed spore formation of the AMF G. irregulare over time for 120 days using optical microscopy. We examined the number of nuclei in mature spores that failed to germinate and observed that some had the same number of nuclei as others that were able to germinate. However, while this runs counter to the idea that spore germination requires a minimum number of nuclei, it is possible that this minimum number may vary due to other factors such as spore maturity or dormancy. Interestingly, G. etunicatum spores reached their mature size within 2-3 days , while G. irregulare isolate DAOM-197198 spores took 30 to 60 days to reach their mature size (Figure 5 and Additional Files 9 and 10). This is surprising because G. irregulare is a very fast growing AMF and therefore used as commercial inoculant sold worldwide while the G. etunicatum isolate NPI used in our laboratory has an extremely slow growth rate.
We examined various stages of the extraradical phases of G. irregulare including the symbiotic phase (running hyphae, branching hyphae and developing spores) and the resting phase (mature spores) and did not observe any structure with a single nucleus (Table 2). Although our observations were based on in vitro laboratory cultures, a single cell with a single nucleus has also never been found in nature, even though AMF are well studied in natural ecosystems. Our results provide no support for sexual reproduction or a single-nucleus stage in the life cycle of AMF, which suggests that asexual reproduction dominates in these fungi. However, demonstrations of hyphal fusion between individuals  and reports of recombination [13, 31, 35] indicate that genetic exchange and recombination also contribute to the population structure of these fungi. It has been hypothesized that auxiliary cells in Gigaspora species might represent vestiges of relict reproductive structures  but without evidence of karyogamy. Tommerup [37, 38] has reported the formation of what was interpreted as zygospores in Gigaspora decipiens in 0.24% of hyphal contacts in a monosporal-grown mycelium, while all other contacts resulted in vegetative growth with or without anastomosis formation. Except for this case, to our knowledge gametangial formation has never been reported elsewhere despite many descriptions of the extramatrical mycelia architecture [39–42] and an extensive literature on intraradical colonization [43, 44].
We reported that AMF spores contain a high heterogeneity in the number of nuclei among sister spores and showed that massive nuclear migration and mitosis are the mechanisms contributing to the sporulation in AMF. The high levels of genetic variation within individuals combined with the large number of nuclei in AMF spores may thus be the evolutionary strategy adapted by AMF in order to reconcile their multigenomic organization with the need to remain adaptable to diverse micro-environmental changes. The finding that mitosis occurs in spore formation in AMF brings a new level of understanding of reproduction and nuclear inheritance processes in this major eukaryotic symbiosis.
The four AMF species, Glomus irregulare (isolate DAOM-197198, previously known as G. intraradices ), G. cerebriforme (DAOM-227022), G. aggregatum (strain 2101-sp) and G. diaphanum (DAOM-229456) used in our studies, were obtained from the Glomeromycota In vitro Collection (GINCO). These strains were co-cultured with Ri T-DNA-transformed carrot roots (Daucus carota L.). AMF strains and transformed carrot roots were cultured and maintained on a minimal (M) medium  solidified with 0.4 w/v Gellan gum at 25°C.
Arbuscular mycorrhizal fungal spores were freshly collected from plates by dissolving the Gellan gum in citrate solution , washed with sterile water and immediately stained with 2% (v/v) of SytoGreen 13 live fluorescent dye (Invitrogen, Canada), for 30 min at room temperature and in darkness. Stained spores were mounted in an 80% glycerol solution and visualized using a Zeiss LSM 5 DUO confocal microscope equipped with Piezo (xy) stage. Specimens were imaged with an objective LCI Plan-Neofluotar 63× (NA 1.3) in water and glycerine immersion and using an argon laser at 488 nm. For each specimen, z-stacks (approximately 150 optical sections depending on the spore size, with an interval of 0.2 μm) were recorded. Z-stacks were then merged into 2D images in which optical sections were colour indexed in order to facilitate manual counting of nuclei. Time-lapse experiments were performed using (x, y, t) mode and 10 optical sections were collected at each 5 min interval for each series.
Two compartment 100 × 15 mm Petri dishes  were used in this experiment with the AMF G. irregulare. One compartment was filled with 25 ml of M medium to the top level of the dividing wall, while the other compartment was filled with only 10 ml of M medium lacking sugar and complemented axenically with 150 μM of aphidicolin  in DMSO (Sigma, Canada) after it had been autoclaved and allowed to cool to 45°C. After solidification of the medium, an additional 1 ml of sugarless M medium containing aphidicolin was deposited on the dividing wall in the sugarless compartment, placed at an angle in order to form a bridge and facilitate hyphal crossing between the two compartments but without continuous connection between growth media . Control plates were prepared in the same conditions, except the second compartment was filled with sugarless M medium complemented with an equal volume of DMSO only. G. irregulare colonized transformed carrot roots were added to the compartment containing sugar. Plates were then incubated in the dark at 25°C until the mycelium had crossed the dividing wall and grown on the second compartment. The cultures were examined weekly. The number of newly formed spores was counted weekly on the second compartment containing aphidicolin or DMSO as a control. After 3 months of culture, spores from this compartment were collected by dissolving the gel, rinsed with sterile and stained with SytoGreen as described above. Spores were examined as described in the confocal microscope section.
Hyphal swellings differentiated along AMF mycelium filaments on the fungal side of two-compartment plates were marked by pen on the plate bottom and their development followed under episcopic light with a dissecting microscope (Nikon SMZ 10A). Twenty-five marked 15, 30, 60 and 90 day-old spores, respectively, were recovered manually from the fungal colonies and mounted on microscopic slides in PVLG mounting medium . Cross diameters of mounted spores were measured at magnification 600X (Nikon Eclipse 800), photographed (Digital camera Nikon Coolpix 950) and spore wall development sequentially described.
Spore viability was estimated by the MTT 3-(4,5-dimethylthiazol-yl-2,5-diphenyl-2H-tetrazolium bromide) vital stain procedure . Using separate cavity slides, 25 spores were treated with MTT for 40 hours to allow maximum staining response. Treated spores were observed under dissecting microscope. Red and blue stained spores were considered viable. At 15 days old, the majority of spore primordia tested positive for viability and the level of viability remained unchanged throughout the spore maturation period (15-90 days old). The high level of viability and the uniformity of results may be attributed to the fact that spores were produced in vitro, under uniform environmental conditions and with no growth constraints. As such, the fungal material may have been less susceptible to mortality or abortion compared to spores isolated directly from soil .
Twenty-five spores of each selected age category (15, 30, 60, 90 days) were extracted from two-compartment in vitro cultures, deposited on H2O agar medium (pH 6.0) and incubated for a maximum of 30 days at 27°C in darkness. Spores bearing germinating hyphae longer than 150 μm were considered germinated. Thirty day-old spores already showed a 40% germination potential and the capacity to regenerate an in vitro functioning colony when associated with transformed carrot roots. This germination potential, whatever the level of spore maturity, never reached more than 50% of the spores, even in those considered viable according to the MTT staining test. The 30 days incubation period chosen may not have been sufficient to demonstrate the full germination capability. However, most of the spore germination observed occurred in the first 3-6 days after incubation, indicating a sufficient maturity to undergo the germination process.
The extraradical symbiotic mycelium of AMF exhibits three distinguishable morphological structures: large-diameter, relatively unbranched, thick-walled hyphae called runner hyphae (RH) , small-diameter thin-walled branched hyphae called arbuscule-like structures  or fine branching (FB)  and spores. To assess for the presence of uninucleate structures, the mycelium of G. diaphanum was carefully examined. Mycelia samples were harvested from five different plate cultures by dissolving the gellan gum in citrate buffer , washed with sterile water and immediately stained with 10 μM SytoGreen 13 for 60 min at 35°C in the dark. Stained mycelia were mounted in 50% glycerol solution on a glass plate and 20-22 RH, FB and spores were randomly chosen and visualized using a Zeiss confocal microscope as described above. The nuclei were counted and the volume was calculated from the diameter (for all structures) and length (for RH and FB).
Statistical analyses were conducted using the using JMP 7.0 and Statgraphics Plus v3 statistical software. Since no transformation produced a normal distribution of the residuals, Kruskal-Wallis non-parametric one-way analysis of variance by ranks were conducted to determine the effect of aphidicolin on spore diameter and number of nuclei per spore, and to compare the number of nuclei between morphological structures of G. diaphanum symbiotic extraradical mycelia, while a posteriori comparisons between means were done using Tukey-Kramer honestly significant difference tests. In order to determine the relationship between the number of nuclei per spore and the diameter of spores, a linear regression model (y = ax + b) was fitted to the number of nuclei (y) with respect to spore diameter (x) for each AMF species.
Arbuscular Mycorrhizal Fungi
National Mycological Herbarium.
This work was supported by NSERC discovery grant to MH. We thank the Canada Foundation for Innovation (CFI) grant to MH for the confocal microscopy facility and FQRNT for award of a scholarship to JM. We thank Dr I.R. Sanders for allowing part of this work to be conducted in his lab at the University of Lausanne. We also thank K. Coquart for technical assistance, Dr R. Lahlali for assistance on statistics, Dr D. Morse, Dr. C. Cameron and Dr. R. Maranger for comments and discussions.
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