Study on metal-triggered callose deposition in roots of maize and soybean

Callose plays important roles in a variety of processes of plant development, and/or in a response to a range of biotic and abiotic stresses. In the current work we have studied and compared the effect of lead, cadmium and arsenic on accumulation of newly formed callose deposits in the roots of maize and soybean. We observed formation of characteristic callose deposits in the root cell walls, probably associated with plasmodesmata, depending on the type of metal and the plant species investigated. Further, the callose turnover was analysed by measuring of total callose content as well as activities of total β-(1,3)-glucanases in roots. The latter enzymes are responsible for callose depletion, and their possible role during metal stress has previously been proposed. However, neither of these biochemical values appeared to be sufficiently reliable for scoring the altered callose turnover (including local deposits) in plant tissue. The microscopical observations are discussed in light of the biochemical data obtained.     

Differences in early callose deposition during adapted and non-adapted powdery mildew infection of resistant Arabidopsis lines

The deposition of callose, a (1,3)-β-glucan cell wall polymer, can play an essential role in the defense response to invading pathogens. We could recently show that Arabidopsis thaliana lines with an overexpression of the callose synthase gene PMR4 gained complete penetration resistance to the adapted powdery mildew Golovinomyces cichoracearum and the non-adapted powdery mildew Blumeria graminis f. sp hordei. The penetration resistance is based on the transport of the callose synthase PMR4 to the site of attempted fungal penetration and the subsequent formation of enlarged callose deposits. The deposits differed in their total diameter comparing both types of powdery mildew infection. In this study, further characterization of these callose deposits revealed that size differences were especially pronounced in the core region of the deposits. This suggests that specific, pathogen-dependent factors exist, which might regulate callose synthase transport to the core region of forming deposits.     

Callose Deposition and Photoassimilate Export in Phaseolus vulgaris Exposed to Excess Cobalt, Nickel, and Zinc

Callose accumulated on sieve plates of phloem of white bean seedlings exposed to excess Co, Ni, or Zn. The callose deposits ranged in thickness and were most pronounced in midribs of unifoliate leaves and their subtending petioles. Lesser callose deposits were found in stems. Although translocation of ¹⁴C was reduced drastically in seedlings exposed to excess metal, no correlation was found between translocated ¹⁴C and the amount of callose in the petioles. It is concluded that the inhibition of phloem translocation in seedlings exposed to excess metal is due to effects other than callose deposition.     

ECTODESMATA AND FOLIAR ABSORPTION

Franke , Wolfgang . (U. Bonn, Germany.) Ectodesmata and foliar absorption. Amer. Jour. Bot. 48(8): 683–691. Illus. 1961.—Plasmodesmata, called ectodesmata, in the outer walls of epidermal cells, have been investigated. Their occurrence and distribution in the epidermis of leaves of Plantago major and Helxine soleirolii have been examined in connection with foliar absorption. Leaf structures such as guard-cells, conical hairs, anticlinal walls and the epidermal cells adjacent to the leaf veins have been shown consistently to contain large numbers of ectodesmata, while in neighboring cells ectodesmata may be low in number or lacking. The same areas also are known to be especially pervious to water and dissolved dyes applied to the surface of the leaf. From special investigations, it appears that certain solutions that form visible crystals and precipitates in the outer wall enter the epidermal cell wall in localized pathways. The localization of these bodies coincides with that of ectodesmata. Therefore, it is concluded that the ectodesmata may be the pathways for transport of substances from the outside to the interior of tissues and vice versa. Nutrients applied to the surface of leaves are thought to enter by the same pathways, i.e., the ectodesmata, as those in which the penetration can be visibly detected. Some phenomena of foliar absorption which confirm this theory are explained in connection with the presence of ectodesmata.     

Auxin promotes dormancy callose removal from the phloem ofMagnolia kobus and callose accumulation and earlywood vessel differentiation inQuercus robur

During winter, the phloem of the diffuse-porous tree magnolia (Magnolia kobus DC.) is dormant and is characterized by heavy deposits of dormancy callose. Application of 1-naphthaleneacetic acid (NAA) to either the top or the lower ends of excised dormant branches before bud break resulted in the removal of the dormancy callose from the sieve tubes. In both intact and auxintreated branches, callose degradation occurred first in the recently formed sieve tubes. There was no new vessel differentiation in magnolia before bud break. In contrast, the sieve tubes of the ring-porous oak (Quercus robur L.), which possess massive dormancy callose deposits during winter, were almost callose-free just before bud break. Application of auxin to the top of excised branches before bud break resulted in callose accumulation on the most recently formed sieve tubes. The first earlywood vessels were evident in oak before bud break, and their numbers were increased by auxin application. The early development of phloem and xylem (before bud break) in ring-porous species is an ecological adaptation which prepares the vascular system of these trees to function immediately at the beginning of their growing season which is relatively short.     

Histological study of the responses of two Vitis vinifera cultivars (resistant and susceptible) to Plasmopara viticola infections

Leaves of Vitis vinifera L. cvs. Chasselas (susceptible) and Solaris (resistant) were inoculated with Plasmopara viticola. Samples were then examined by scanning electron microscopy, light and epifluorescence microscopy. On the resistant cv. Solaris, stomatal deposits, identified as callose, were visible around the germinating zoospores 7 h after inoculation. Twenty-four hours after inoculation, infected stomata exhibited secretions that enveloped the zoospores. At this time, infected stomata were surrounded by necrotic tissues. At 120 h after inoculation, undefined material was deposited on the cuticle in the necrotic areas. Stomata in the vicinity of the infection sites contained callose deposits in and around the stomatal openings, but no necrotic zones were observed. On the sensitive cv. Chasselas neither secretion nor callose deposits were observed. Sporangiophores emerged about 96 h after inoculation and were fully developed 24 h later. Sporulation through small stomata-like apertures present all along the primary vein was also observed on the upper leaf surface. The role of stomatal callose deposits in the defense reactions of the Solaris grapevine cultivar against P. viticola is discussed.     

Co-Localization of β-1,3-Glucanases and Callose During Somatic Embryogenesis in Cichorium

During direct somatic embryogenesis in leaves of Cichorium hybrid clone ‘474’, 38 kDa β-1,3-glucanases are accumulated in the culture medium of the embryogenic hybrid to a higher level when compared with a non-embryogenic cultivar. In the same time, embryogenic cells were surrounded by a cell wall that was characterized by the presence of callose. This callosic deposition disappeared as embryos grew. Callose consisted of β-1,3-glucan linkages and so represented a possible substrate for β-1,3-glucanases. Using immunolocalization experiments, we demonstrated that from the three types of callose deposits observed during the culturing of Cichorium leaf explants, only the callose present in the walls surrounding reactivated cells seemed specifically related to somatic embryogenesis. Moreover, callose and the 38-kDa β-1,3-glucanases were co-localized dispersed throughout the thick and swelled walls of reactivated cells and embryo cell walls. This suggests that callose and β-1,3-glucanases are implicated in the process of somatic embryogenesis since they were always detected in or quite near embryogenic and embryo cell. This also suggested that β-1,3-glucanases could be involved in the degradation of this callose.Key Words: β-1,3-glucanases, callose, Cichorium, immunolocalizations, somatic embryogenesis     

Chlorantine Fast Green Bll as A Stain for Callose in Oak Phloem

Sections of oak bark were stained with chlorantine fast green BLL, rued u a 0.45% aqueous solution. All tissues were unstnined, except for local deposits of material associated with phloem cell walls, which stained deep green. This green-staining material also stained specifically with resorcinol blue and with the aniline blue fluorescence, technique, the usual histochemical tests for callose. The chlorantine fast green-staining material was removed from sections by treatment with a β-1,3-glucan hudrolase. It is concluded that chlorantine fast green BLL stains callose in plant sections and is a useful additional stain for the histochemical detection of this polymer.     

Diversity and evolution of microsporogenesis in Bromeliaceae

In this study, we explore the features of microsporogenesis in Bromeliaceae and, in particular, the diversity and evolution of additional callose deposits. Cytokinesis type, cell wall formation, tetrad form and patterns of additional callose deposition after intersporal wall formation were studied in 12 species of Bromeliaceae (each from a different genus) presenting four different aperture patterns. Microsporogenesis is highly conserved, with successive cytokinesis, centrifugal cell plate formation and predominantly tetragonal and decussate tetrads, as in many monocots, but five different patterns of additional callose deposition were recorded. The optimization of patterns of additional callose deposition on the phylogeny of Bromeliaceae reveals convergences. Additional callose deposition is a variable and labile feature of microsporogenesis in Bromeliaceae and is linked, to some extent, to aperture pattern. © 2014 The Linnean Society of London, Botanical Journal of the Linnean Society, 2014, 176 , 36–45.     

Ektodesmenstudien

Summary Lambertz (1954) did not mention Gramineae as plants containing ectodesmata, although he stated that ectodesmata are not bound to special groups of angiosperms but should occur in all families of angiosperms. Schnepe (1959) expressly pointed out that he never succeeded in demonstrating such structures in leaves of Gramineae with his method. In our studies, however, ectodesmata could be shown in leaves of wheat and maize if the fixation mixture contained nitric acid. As in other objects, including species of gymnosperms and pteridophytes, the same distribution of ectodesmata could be observed which was characterized by the formation of rows along the anticlinal walls, crowding in guard-cells and seattering in periclincal walls.     

Über die Beziehungen der Ektodesmen zur Stoffaufnahme durch Blätter

Summary When droplets of radioactive solutions are applied to the cuticle, micro-autoradiograms show that the guard cells and the anticlinal walls of the leaf epidermis ofSpinacia oleracea and ofViola tricolor are the favoured sites of absorption. Scattered black spots in the stripping film could also be observed above the periclinal walls of the epidermis.A comparison of such micro-autoradiograms with the distribution of the ectodesmata in the leaf epidermis of the same two species demonstrates that the areas of favoured foliar absorption correspond to the areas of the densest accumulation of the ectodesmata, while the ectodesmata in the less absorbing periclinal walls are more loosely dispersed. Thus, though ectodesmata cannot be localized exactly by the occurrence of silver grains in the stripping film, identity exists between the areas of foliar absorption and the distribution of ectodesmata in the leaves which proves that ectodesmata are functioning as pathways of transport in foliar absorption.The experiments reported cofirm earlier statements that guard cells participate essentially in foliar absorption. The micro-autoradiograms also clearly show that absorption does not take place through the pores of the guard cells.

---

---

Mit 20 Textabbildungen     

Abnormal callose response phenotype and hypersusceptibility to Peronospoara parasitica in defence-compromised arabidopsis nim1-1 and salicylate hydroxylase-expressing plants

To investigate the impact of induced host defenses on the virulence of a compatible Peronospora parasitica strain on Arabidopsis thaliana, we examined growth and development of this pathogen in nim1-1 mutants and transgenic salicylate hydroxylase plants. These plants are unable to respond to or accumulate salicylic acid (SA), respectively, are defective in expression of systemic acquired resistance (SAR), and permit partial growth of some normally avirulent pathogens. We dissected the P. parasitica life cycle into nine stages and compared its progression through these stages in the defense-compromised hosts and in wild-type plants. NahG plants supported the greatest accumulation of pathogen biomass and conidiophore production, followed by nim1-1 and then wild-type plants. Unlike the wild type, NahG and nim1-1 plants showed little induction of the SAR gene PR-1 after colonization with P parasitica, which is similar to our previous observations. We examined the frequency and morphology of callose deposits around parasite haustoria and found significant differences between the three hosts. NahG plants showed a lower fraction of haustoria surrounded by thick callose encasements and a much higher fraction of haustoria with callose limited to thin collars around haustorial necks compared to wild type, whereas nim1-1 plants were intermediate between NahG and wild type. Chemical induction of SAR in plants colonized by P. parasitica converted the extrahaustorial callose phenotype in NahG to resemble closely the wild-type pattern, but had no effect on nim1-1 plants. These results suggest that extrahaustorial callose deposition is influenced by the presence or lack of SA and that this response may be sensitive to the NIM1/NPR1 pathway. Additionally, the enhanced susceptibility displayed by nim1-1 and NahG plants shows that even wild-type susceptible hosts exert defense functions that reduce disease severity and pathogen fitness.     

Aluminum-induced deposition of (1,3)-β-glucans (callose) inTriticum aestivum L.

Aluminum (Al)-induced damage to leaves and roots of two Al-resistant (cv. Atlas 66, experimental line PT741) and two Al-sensitive (cv. Scout 66, cv. Katepwa) lines ofTriticum aestivum L. was estimated using the deposition of (1, 3)--glucans (callose) as a marker for injury. Two-day-old seedlings were grown for forty hours in nutrient solutions with or without added Al, and callose deposition was quantified by spectrofluorometry (0–1000 µM Al) and localized by fluorescence microscopy (0 and 400 µM Al). Results suggested that Al caused little damage to leaves. No callose was observed in leaves with up to 400 µM Al treatment. In contrast, root callose concentration increased with Al treatment, especially in the Al-sensitive lines. At 400 µM Al, root callose concentration of Al-sensitive Scout 66 was nearly four-fold that of Al-resistant Atlas 66. After Al treatment, large callose deposits were observed in the root cap, epidermis and outer cortex of root tips of Scout 66, but not Atlas 66. The identity of callose was confirmed by a reduced fluorescence in Al-treated roots: firstly, after adding an inhibitor of callose synthesis (2-deoxy-D-glucose) to the nutrient solution, and secondly, after incubating root sections with the callosedegrading enzyme -D-glucoside glucohydrolase [EC 3.2.1.21]. Root callose deposition may be a good marker for Al-induced injury due to its early detection by spectrofluorometry and its close association with stress perception.Abbreviations DDG 2-deoxy-D-glucose - PAS periodic acid - Schiffs reagent - PE pachyman equivalents     

Physiological Studies on Pea Tendrils : XIV. Effects of Mechanical Perturbation, Light, and 2-Deoxy-d-Glucose on Callose Deposition and Tendril Coiling

When excised tendrils of pea (Pisum sativum L. cv Alaska) are mechanically perturbed there is an immediate and transient increase in callose deposition in the sieve cells. Mechanical perturbation (MP) results in a coiling response in light-grown tendrils and in dark-adapted tendrils, provided, in the latter case, that they receive adequate illumination within a limited period of time after MP. In nonperturbed tendrils the number of callose deposits decreases to some minimum with increasing time in the dark, and their ability to coil in the dark in response to MP diminishes with time in the dark. The transient increase of callose deposition due to MP, however, occurs whether or not tendrils are dark adapted, and whether they receive light or are retained in the dark after MP. This indicates that if callose is directly involved in tendril coiling, then it exerts its effect on the sensory perception of the mechanical stimulus. In the present investigation, there is never tendril coiling without the transient increase in callose, and the time after MP at which the peak of callose deposition occurs precedes the time of the peak amount of coiling.     

Callose Deposition During Megagametogenesis in Two Species of Oenothera

Callose deposits are present both in degenerating megasporesof the heteropolar tetrad in Oenothera hookeri and in degeneratingembryo sacs of the homopolar developing tetrad in O biennis.They are partially continuous with the cell wall and partiallyenclosed in the degenerating cytoplasm and show electron opaquebands within a less electron opaque material Vesicles calledcallose grains are present in the degenerating cytoplasm ofthe embryo sac in O biennis These show an electron opaque fibnllaror granular core surrounded by a halo of low electron opacity Similarities in fine structure between callose deposits of femalegametophytes which follow the degenerating pathway of development,and callose plugs present in pollen tubes during their growth,are discussed. Oenothera, evening primrose, megagametogenesis, megasporogenesis, callose, ultrastructure     

The time course of the induction of callose in wounded pea roots

Summary Initial study indicated that much callose is produced in pea root tissues during the preparation of fresh hand-cut sections or during conventional fixation in formalin-acetic acid-alcohol, glutaraldehyde or acrolein. In contrast, there is little callose in freeze-substituted tissues and this is mostly in sieve tubes and considered endogenous. Freeze-substitution was subsequently used to monitor wound-induced callose development in the various tissues of pea roots. This development was fastest in the phloem, first detected 1 minute post-wounding and complete by 3 hours. In some parenchyma cells full development was delayed by 20 hours. By 100 hours, wound callose was no longer detectable in parenchyma cells but remained undiminished in the phloem. The implications of these results for all studies involving callose localization are discussed.Abbreviations C callose - FAA formalin-acetic acid-alcohol - GMA glycol methacrylate - P phloem - PAS periodic acid-Schiffs - PF phloem fibres - PP pith parenchyma - PW post-wounding     

Callose deposition in the phloem plasmodesmata and inhibition of phloem transport in citrus leaves infected with “Candidatus Liberibacter asiaticus”

Huanglongbing (HLB) is a destructive disease of citrus trees caused by phloem-limited bacteria, Candidatus Liberibacter spp. One of the early microscopic manifestations of HLB is excessive starch accumulation in leaf chloroplasts. We hypothesize that the causative bacteria in the phloem may intervene photoassimilate export, causing the starch to over-accumulate. We examined citrus leaf phloem cells by microscopy methods to characterize plant responses to Liberibacter infection and the contribution of these responses to the pathogenicity of HLB. Plasmodesmata pore units (PPUs) connecting companion cells and sieve elements were stained with a callose-specific dye in the Liberibacter-infected leaf phloem cells; callose accumulated around PPUs before starch began to accumulate in the chloroplasts. When examined by transmission electron microscopy, PPUs with abnormally large callose deposits were more abundant in the Liberibacter-infected samples than in the uninfected samples. We demonstrated an impairment of symplastic dye movement into the vascular tissue and delayed photoassimilate export in the Liberibacter-infected leaves. Liberibacter infection was also linked to callose deposition in the sieve plates, which effectively reduced the sizes of sieve pores. Our results indicate that Liberibacter infection is accompanied by callose deposition in PPUs and sieve pores of the sieve tubes and suggest that the phloem plugging by callose inhibits phloem transport, contributing to the development of HLB symptoms.     

Aluminum-induced 1-->3-beta-D-glucan inhibits cell-to-cell trafficking of molecules through plasmodesmata. A new mechanism of aluminum toxicity in plants

Symplastic intercellular transport in plants is achieved by plasmodesmata (PD). These cytoplasmic channels are well known to interconnect plant cells to facilitate intercellular movement of water, nutrients, and signaling molecules including hormones. However, it is not known whether Al may affect this cell-to-cell transport process, which is a critical feature for roots as organs of nutrient/water uptake. We have microinjected the dye lucifer yellow carbohydrazide into peripheral root cells of an Al-sensitive wheat (Triticum aestivum cv Scout 66) either before or after Al treatment and followed the cell-to-cell dye-coupling through PD. Here we show that the Al-induced root growth inhibition is closely associated with the Al-induced blockage of cell-to-cell dye coupling. Immunofluorescence combined with immuno-electron microscopic techniques using monoclonal antibodies against 1-->3-beta-D-glucan (callose) revealed circumstantial evidence that Al-induced callose deposition at PD may responsible for this blockage of symplastic transport. Use of 2-deoxy-D-glucose, a callose synthesis inhibitor, allowed us to demonstrate that a reduction in callose particles correlated well with the improved dye-coupling and reduced root growth inhibition. While assessing the tissue specificity of this Al effect, comparable responses were obtained from the dye-coupling pattern in tobacco (Nicotiana tabacum) mesophyll cells. Analyses of the Al-induced expression of PD-associated proteins, such as calreticulin and unconventional myosin VIII, showed enhanced fluorescence and co-localizations with callose deposits. These results suggest that Al-signal mediated localized alterations to calcium homeostasis may drive callose formation and PD closure. Our data demonstrate that extracellular Al-induced callose deposition at PD could effectively block symplastic transport and communication in higher plants.     

A Rapid Method for Macerating Phloem

Sieve cells and sieve tube members can be macerated from the phloem of various organs of woody and herbaceous species by au-toclaving the tissue in a mild macerating medium. This treatment does not digest the primary walls or the callose deposits on the sieve areas and sieve plates of the sieve elements. These cells can then be recognized by the fluorescence of their callose after staining with aniline blue. Sometimes adjacent sieve elements fail to separate and one can observe details of their junctures.     

Chlorantine fast green BLL as a stain for callose in oak phloem

Sections of oak bark were stained with chlorantine fast green BLL, used as a 0.25% aqueous solution. All tissues were unstained, except for local deposits of material associated with phloem cell walls, which stained deep green. This green-staining material also stained specifically with resorcinol blue and with the aniline blue fluorescence technique, the usual histochemical tests for callose. The chlorantine fast green-staining material was removed from sections by treatment with a beta-1,3-glucan hydrolase. It is concluded that chlorantine fast green BLL stains callose in plant sections and is a useful additional stain for the histochemical detection of this polymer.