Adhesion of fungal spores and germlings to host plant surfaces

Summary Firm adhesion of fungal plant pathogens to their hosts is critical at several stages in the host-parasite interaction. Spores of many fungal species are capable of rapid, non-specific attachment to various surfaces. This early adhesion, which often occurs well before germ tube emergence, prevents spores from being blown or washed from the host surface before infection can take place. Adhesion is critical for proper sensing of topographic signals involved in thigmotropic responses and for differentiation and function of appressoria. Four fungal pathogens which exhibit a variety of adhesion mechanisms have been selected for discussion.Abbreviations EMC extracellular matrix - FSTEM freeze-substitution transmission electron microscopy - Con A concanavalin A - CryoSEM cryo scanning electron microscopy - MTM macroconidial tip mucilage - STM spore tip mucilage     

A MOLECULAR MOTOR FOR GLIDING MOTILITY IN CYANOBACTERIA

Motile microorganisms either swim, by using flagella or glide over surfaces by mechanisms that are poorly understood. In cyanobacteria, gliding motility appears as a relatively slow and smooth surface-associated translocation in the direction of the long axis of the filaments at rates up to a few micrometers a second. Many filamentous species translocate in a highly coordinated manner. Translational movements are usually accompanied by revolutions around the long axis of the filament. While moving, the cyanobacteria secrete slime which is left behind as a twisted and collapsed thin tube. The observation of the slime secretion process shows that the mucilage is formed as fine bands that emerge in close proximity to the cells cross walls. Ultrastructural studies have revealed that the cyanobacteria possess at their cross walls complex, pore-like organelles, which might be involved in slime secretion. As each cell possess two different sets of pores pointing in opposite direction, the coordinated activity of these structures could explain how the filament can reverse the direction of locomotion. Furthermore, ultrastructural studies have shown that rotating cyanobacteria possess cell surfaces formed by parallel, helically arranged surface fibrils. As the arrangement of these fibrils corresponds with the path of the filaments during locomotion, it might be imaginable that these fibrils serve as screw thread guiding the rotation of the filaments, with the necessary thrust for locomotion being derived from the secretion of slime using the pores at the cross walls.     

Purple acid phosphatases from bacteria: similarities to mammalian and plant enzymes

Mammalian and plant purple acid phosphatases have similar active site structures despite low sequence identity (<20%). Although no bacterial enzyme has been purified, a sequence database search revealed that genes that could encode potential purple acid phosphatases may be restricted to a small number of organisms (i.e. myco- and cyanobacteria). Analysis of their deduced amino acid sequences and predicted secondary structures indicates that the cyanobacterial enzyme is similar to both the mammalian and the recently discovered low-molecular-weight plant purple acid phosphatases, while the mycobacterial enzyme is homologous to the fungal and high-molecular-weight plant purple acid phosphatases. Homology models indicate that both bacterial proteins appear to be similar to mammalian purple acid phosphatases in the immediate vicinity of the active site. It is likely that these enzymes act as Fenton-type catalysts in order to prevent damage caused by reactive oxygen species generated by invaded host cells (M. tuberculosis) or by the light-harvesting complex (Synechocystis sp.).     

Mucilages and polysaccharides in Ziziphus species (Rhamnaceae): localization, composition and physiological roles during drought-stress.

The drought-tolerant tree species Ziziphus mauritiana Lamk. and Z. rotundifolia Lamk. were shown to have similar high mucilage concentrations (7-10% dry weight) in their leaves, with large numbers of mucilage-containing cells in the upper epidermis and extracellular mucilage-containing cavities in the leaf veins and stem cortex. The main sugar constituents of the water-soluble mucilage extract were rhamnose, glucose and galactose. During drought-stress in two independent studies, foliar mucilage content was unaffected in both species, but glucose and starch contents declined significantly in crude mucilage extracts from droughted leaves. Enzymatic hydrolysis of the mucilage extract using alpha-amylase and amyloglucosidase released glucose, indicating that a mucilage-associated water-soluble glucan, with alpha-1,4- and alpha-1,6-linkages, may exist which was extracted together with the mucilage. From the current data, it is not possible to localize the glucan to determine whether or not it is associated with mucilage-containing cells. Data from pressure-volume analyses of drought-stressed and control leaves showed that, in line with their similar mucilage contents, the relative leaf capacitance isotherm (change in relative water content per unit change in water potential) was similar in both species. During drought-stress, reduced relative capacitance resulted from osmotic adjustment and decreased wall elasticity. Data suggest that in Ziziphus leaves, intracellular mucilages play no part in buffering leaf water status during progressive drought. In Ziziphus species, growing in environments with erratic rainfall, the primary role of foliar mucilage and glucans, rather than as hydraulic capacitors, may be as sources for the remobilization of solutes for osmotic adjustment, thus enabling more effective water uptake and assimilate redistribution into roots and stems prior to defoliation as the drought-stress intensified.     

Factors affecting the immobilisation of plant cells on reticulated polyurethane foam particles

Summary Factors affecting the immobilisation and subsequent growth of plant cells in reticulated polyurethane foam particles have been studied using three plant species. Polyurethane foam from a number of commercial sources has been screened and a foam having a low phytotoxicity and good retention of plant cells selected for use. Particles (8×8×8 mm) of the material were seeded with plant cells from suspension culture and cells grown immobilised in particles until they occupied >80% of the available volume. For all species, foams containing small pores (60–80 ppi) were most effective in immobilising and retaining cells. For efficient use of the inoculum, high partial volumes of foam particles are required; with partial volumes above 40%, over 80% of the inoculum is taken up by the particles. While the initial immobilisation process presumably involves weak interactions between cells and the support material, factors such as inoculum size and the length of the loading period have been found to affect the immobilisation of cells and their subsequent growth within the matrix. A preliminary study of the requirements for the maintenance of viability of immobilised cultures at high cell densities has been made.     

Gliding motility in cyanobacteria: observations and possible explanations

Cyanobacteria are a morphologically diverse group of phototrophic prokaryotes that are capable of a peculiar type of motility characterized as gliding. Gliding motility requires contact with a solid surface and occurs in a direction parallel to the long axis of the cell or filament. Although the mechanistic basis for gliding motility in cyanobacteria has not been established, recent ultrastructural work has helped to identify characteristic structural features that may play a role in this type of locomotion. Among these features are the distinct cell surfaces formed by specifically arranged protein fibrils and organelle-like structures, which may be involved in the secretion of mucilage during locomotion. The possible role of these ultrastructural features, as well as consequences for understanding the molecular basis of gliding motility in cyanobacteria, are the topic of this review.     

Pericarp structure and myxocarpy in selected genera of Nepetoideae (Lamiaceae)

The pericarp structure has been analyzed in 37 species representing 13 genera from four tribes of Nepetoideae (Lamiaceae). 11 species are endemics of Balkan Peninsula or other Mediterranean regions. Basically, the pericarp was similar to other Nepetoideae by having exocarp, mesocarp s. str., vertically arranged bone cells and thin innermost cell layer. The ratio between pericarp thickness and nutlet size was the highest in Mentha spp. According to this parameter Micromeria species belonging to different sections could be distinguished. Acinos spp. were characterized by the thickest sclerenchyma in ratio to pericarp thickness. Crystals were present within sclerenchyma region in genera Mentha, Melissa, Nepeta and Prunella . The mucilage production has also been tested. Most of the studied species produced mucilage when becoming wet. The strongest mucilage reaction showed Acinos and Prunella . Pericarp characters studied are of taxonomical interest. They were mainly correlated with the generic or infrageneric classification of some genera.     

Integument cell differentiation in dandelions (<Emphasis Type="Italic">Taraxacum</Emphasis>, Asteraceae,Lactuceae) with special attention paid to plasmodesmata

The aim of the paper is to determine what happens with plasmodesmata when mucilage is secreted into the periplasmic space in plant cells. Ultrastructural analysis of the periendothelial zone mucilage cells was performed on examples of the ovule tissues of several sexual and apomictic Taraxacum species. The cytoplasm of the periendothelial zone cells was dense, filled by numerous organelles and profiles of rough endoplasmic reticulum and active Golgi dictyosomes with vesicles that contained fibrillar material. At the beginning of the differentiation process of the periendothelial zone, the cells were connected by primary plasmodesmata. However, during the differentiation and the thickening of the cell walls (mucilage deposition), the plasmodesmata become elongated and associated with cytoplasmic bridges. The cytoplasmic bridges may connect the protoplast to the plasmodesmata through the mucilage layers in order to maintain cell-to-cell communication during the differentiation of the periendothelial zone cells.     

Cyanobacteria in mangrove ecosystems

Mangroves are subject to the effects of tides and fluctuations in environmental conditions, which may reach extreme conditions. These ecosystems are severely threatened by human activities despite their ecological importance. Although mangroves are characterized by a highly specialized but low plant diversity in comparison to most other tropical ecosystems, they support a diverse microbial community. Adapted microorganisms in soil, water, and on plant surfaces perform fundamental roles in nutrient cycling, especially nitrogen and phosphorus. Cyanobacteria contribute to carbon and nitrogen fixation and their cells act as phosphorus storages in ecosystems with extreme or oligotrophic environmental conditions such as those found in mangroves. As the high plant productivity in mangroves is only possible due to interactions with microorganisms, cyanobacteria may contribute to these ecosystems by providing fixed nitrogen, carbon, and herbivory-defense molecules, xenobiotic biosorption and bioremediation, and secreting plant growth-promoting substances. In addition to water, cyanobacterial colonies have been detected on sediments, rocks, decaying wood, underground and aerial roots, trunks, and leaves. Some mangrove cyanobacteria were also found in association to algae or seagrasses. Few studies on mangrove cyanobacteria are available, but together they have reported a substantial number of species in these ecosystems. However, the cyanobacterial diversity in this biome has been traditionally underestimated. Though mangrove communities generally host cyanobacterial taxa commonly found in marine environments, unique microhabitats found in mangroves potentially harbor several undescribed cyanobacterial taxa. The relevance of cyanobacteria for mangrove conservation is highlighted in their use for the recovery of degraded mangroves as biostimulants or in bioremediation.     

An alternative explanation for cyanobacterial scum formation and persistence by oxygenic photosynthesis

The cause of persistent cyanobacteria scum formation in lakes is an unresolved subject. Scum refers to the event in which cyanobacteria are at the water surface of a lake. Factors like low turbulence levels, long day-light, high water temperatures and the buoyant capacity of cyanobacterial cells play a role in the occurrence of scums. However, they do not explain why scums are observed at periods during the day when according to theory they should have disappeared into the deeper water layers. In this study, we present an alternative explanation. The hypothesis we present here is that irreversible buoyancy of cyanobacteria colonies is created by the growth of gas bubbles on or within the mucilage of the colonies. These bubbles grow under oxygen super-saturated conditions. At low wind speed and high chlorophyll levels, the dissolved oxygen (DO) produced during photosynthesis by cyanobacteria, cannot escape sufficiently fast to the atmosphere hence a DO supersaturated condition arises in the water. At this stage, growth of oxygen bubbles may occur inside or attached to the mucilage. We present results of compression experiments to support our hypothesis. In a chamber, the pressure on lake water containing a natural cyanobacteria population is increased. At 3 × 10⁵ and 4 × 10⁵ Pa the cyanobacteria colonies were not able to float anymore and sank. This pressure is lower than the 10⁶ Pa needed to collapse all gas vacuoles inside the cyanobacteria cells (Walsby, 1994). The observed change from floating to sinking colonies due to increased water pressure suggests that gas bubbles were present inside the colonies. In lakes, these gas bubbles may lead to permanent buoyancy, i.e. a persistent scum.     

Sub-aerial biofilms as blockers of solar radiation: spectral properties as tools to characterise material-relevant microbial growth

Sub-aerial biofilms (SABs) are ubiquitous microbial communities that develop at the interface between hard surfaces and the atmosphere. Inherent SAB “core-settlers” include phototrophic algae, cyanobacteria, heterotrophic bacteria and microcolonial fungi (MCF). SABs do not simply cover hard surfaces; they interact with them in myriads of ways and bind to the underlying substrate. Secretion of extracellular mucilage aids adhesion, while organic acids and acidic polysaccharides weather the surface. As protection against solar radiation, many members of the SAB consortia produce shielding pigments while the phototrophic inhabitants are laden with photosynthetic pigments. All absorb light of many wavelengths and in addition, the cells themselves scatter light. Both effects change the spectra of incoming radiation (including wavelengths that are converted to electricity by photovoltaic cells) and decrease its intensity. To quantify these effects on SABs as complex entities of organisms and pigments, we measured the spectral properties of model and natural biofilms transferred to glass. Here we show that SABs growing on solar panels and other substrates scatter incident radiation between 250 nm up to 1800 nm and block up to 70% of its transmission. Model biofilms have the advantage that their microbial components can be “tuned” to resemble natural ones of different compositions thus providing a novel materials-testing tool.     

Cell-cell recognition of host surfaces by pathogens. The adsorption of maize (Zea mays) root mucilage by surfaces of pathogenic fungi.

The adsorption of radioactive mucilage by pathogenic fungi was shown to be dependent upon time, the composition of mucilage, the type of fungal surface (conidia, hyphae, hyphal apices), fungal species, pH and bivalent cations. All fungal adhesins were inactivated by either proteinase or polysaccharase treatments. Adsorption was not inhibited by the numberous mono-, di- and oligo-saccharides that were tested individually, but it was inhibited absolutely by several polysaccharides. This suggested that adsorption of mucilage by pathogens involved conformational and ionic interactions between plant and fungal polymers but not fungal lectins bound to sugar residues of mucilage. Several fractionation schemes showed that pathogens bound only the most acidic of the variety of polymers that comprise mucilage. There was not any absolute distinction between ability to bind radioactive mucilage and type of pathogen or non-pathogen. However, there were notable differences in characteristics of adsorption between two types of pathogen. Differences were revealed by comparison of the adsorption capacities of conidia and germinant conidia and chromatography of radioactive mucilage on germinant conidia. An ectotrophic root-infecting fungus (a highly specialized pathogen) bound a greater proportion of mucilage than did a vascular-wilt fungus (of catholic host and tissue range) with more than one class of site for adsorption. In contrast with the vascular-wilt fungus, sites for adsorption on the specialized pathogen were present solely on surfaces formed by germination.     

Spore attachment and extracellular mucilage of aquatic hyphomycetes

Stages in conidiun attachment to surfaces of Lemmoniera aquatica and Mycocentrospora filiformis (freshwater Hyphomycetes) were studied at the light microscope and scanning and transmission electron microscope levels. Sigmoid conidia of M. filiformis attach by pre-existing conidial mucilage at the spore pole and at a point along the conidial body. Tetraradiate conidia of L. aquatica attach by the thigmotropic release of mucilage at the tips of the three "arms";. Germination in both species is followed by the production of germ tubes, germ hyphae and appressoria. The chemical composition of the mucilage involved in attachment was determined by enzymatic studies and lectin-gold cytochemical studies. The major component was found to be acidic poly-saccharide, comprising mainly ?-1, 3-glucan, N-acetyl-D-glucosamine and N-acetyl-neuraminic acid. Variation in mucilage composition exists between the two species, among different structures of the same species, and on different regions of the same structure. This indicates that mucilage producton in the two species is a dynamic process.The ability to secure rapid spore attachment, often in turbulent condition, would be a competitive advantage to these saprobic fungi in the colonization of substrata.     

Evaluating specific adhesion of Plasmodium falciparum-infected erythrocytes to immobilised hyaluronic acid with comparison to binding of mammalian cells

A feature of infection with Plasmodium falciparum is the ability of parasite-infected erythrocytes to adhere to vascular endothelial cells and accumulate in vital organs, associated with severe clinical disease. Hyaluronic acid was recently identified as a receptor for adhesion and has been implicated in mediating the accumulation of parasites in the placenta. Here, we report in vitro assays to measure specific adhesion of infected erythrocytes to hyaluronic acid that is distinct from binding to chondroitin sulphate A, another glycosaminoglycan implicated as a receptor in placental malaria. In this study, specific adhesion of mature stage infected erythrocytes to hyaluronic acid of high purity immobilised on plastic surfaces was abolished by pre-treating hyaluronic acid with a specific hyaluronate lyase from Streptomyces, whereas the same treatment of chondroitin sulphate A had little effect. Adhesion to hyaluronic acid could not be explained by the presence of chondroitin sulphate A or other glycosaminoglycans in the hyaluronic acid preparations. Chinese hamster ovary cells bound in a similar manner in the assays and confirmed that hyaluronic acid was appropriately immobilised for cell adhesion. In contrast to parasites, these cells did not adhere to chondroitin sulphate A. The adsorption of hyaluronic acid onto plastic surfaces was also confirmed by the use of a specific hyaluronic acid-binding protein. Fixing cells with glutaraldehyde at the completion of adhesion assays reduced the number of parasites remaining adherent to hyaluronic acid, but not to chondroitin sulphate A or CD36. These findings have important implications for understanding and evaluating interactions between P. falciparum and hyaluronic acid that may be involved in disease pathogenesis.     

Life on a deadly trap: Buckleria paludum,a specialist herbivore of carnivorous sundew plants,licks mucilage from glands for defense

Caterpillars of Buckleria spp. (Lepidoptera: Pterophoridae) have a unique feeding habit of eating trap leaves of carnivorous sundew plants (Drosera spp.). We observed the foraging behavior of Buckleria paludum on trap leaves of Drosera spp. and discussed how the moth species avoided being caught by trap leaves. In 81.5% (66/81) of encounters with glandular hairs on adaxial surfaces of Drosera trap leaves, B. paludum larvae licked mucilage and crawled on the processed hairs. The frequency of licking mucilage was significantly higher than the frequency of other behaviors such as eating glandular hairs, chewing bases of them without eating and ignoring when encountering secreted mucilage. Licking mucilage enables the caterpillars to move safely on trap leaves and prevents bending of glandular hairs.     

Seed coat mucilage cells of Arabidopsis thaliana as a model for plant cell wall research

Plant cells are encased within a complex polysaccharide wall that strengthens the cell and has key roles in all aspects of plant cell growth, differentiation and interaction with the environment. This dynamic structure is under continual modification during plant development, and its synthesis and modification require the activity of a myriad of enzymes. The mucilage secretory cells (MSCs) of the Arabidopsis thaliana seed coat provide a model for the discovery of novel genes involved in the synthesis, secretion and modification of cell wall components, particularly pectin. These cells synthesize copious amounts of pectinaceous mucilage during development and, upon hydration of the desiccated seed, the mucilage rapidly swells, bursts from the MSCs and surrounds the seed in a gelatinous capsule. Several genes affecting MSC differentiation, pectin synthesis and mucilage release have been identified and additional genes involved in these and related processes including pectin secretion and the mechanical alteration of cell walls await to be discovered.Key words: cell wall, pectin, mucilage, arabidopsis, seed coat     

Homologous Comparisons of Photosynthetic System 1 Genes among Cyanobacteria and Chloroplasts

It has now believed that chloroplasts arose from cyanobacteria,however,during endosymbiosis,the photosynthetic genes in chloroplasts have been reduced.How these changes occurred during plant evolution was the focus of the present study.Beginning with photosystem Ⅰ (PSI) genes,a homologous comparison of amino acid sequences of 18 subunits of PSI from 10 species of cyanobacteria,chloroplasts in 12 species of eucaryotic algae,and 28 species of plants (including bryophytes,pteridophytes,gymnospermae,dicotyledon and monocotyledon) was undertaken.The data showed that 18 genes of PSIcan be divided into two groups: Part Ⅰ including seven genes (psaA,psaB,psaC,psaI,psaJ,yct3 and ycf4) shared both by cyanobacteria and plant chloroplasts;Part Ⅱ containing another 11 genes (psaD,psaE,psaF,psaK,psaL,psaM,btpA,ycf37,psaG,psaH and psaN) appeared to have diversified in different plant groups.Among Part I genes,psaC,psaA and psaB had higher homology in all species of cyanobacteria and chloroplasts.Among Part II genes,only psaG,psaH and psaN emerged in seed plants.     

Differentiation of mucilage secretory cells of the Arabidopsis seed coat

In some plant species, including Arabidopsis, fertilization induces the epidermal cells of the outer ovule integument to differentiate into a specialized seed coat cell type with a unique morphology and containing large quantities of polysaccharide mucilage (pectin). Such seed coat mucilage cells are necessary for neither viability nor germination under normal laboratory conditions. Thus, the Arabidopsis seed coat offers a unique system with which to use genetics to identify genes controlling cell morphogenesis and complex polysaccharide biosynthesis and secretion. As a first step in the application of this system, we have used microscopy to investigate the structure and differentiation of Arabidopsis seed coat mucilage cells, including cell morphogenesis and the synthesis, secretion, and extrusion of mucilage. During seed coat development in Arabidopsis, the epidermal cells of the outer ovule integument grow and differentiate into cells that produce large quantities of mucilage between the primary cell wall and plasma membrane. Concurrent with mucilage production, the cytoplasm is shaped into a column in the center of the cell. Following mucilage secretion the cytoplasmic column is surrounded by a secondary cell wall to form a structure known as the columella. Thus, differentiation of the seed coat mucilage cells involves a highly regulated series of events including growth, morphogenesis, mucilage biosynthesis and secretion, and secondary cell wall synthesis.     

Purification effects show seed and root mucilage's ability to respond to changing rhizosphere conditions

Mucilage, a polysaccharide-containing hydrogel, is hypothesized to play a key role in the rhizosphere as a self-organized system because it may vary its supramolecular structure with changes in the surrounding solution. However, there is currently limited research on how these changes are reflected in the physical properties of real mucilage. This study examines the role of solutes in maize root, wheat root, chia seed, and flax seed mucilage in relation to their physical properties. Two purification methods, dialysis and ethanol precipitation, were applied to determine the purification yield, cation content, pH, electrical conductivity, surface tension, viscosity, transverse ¹H relaxation time, and contact angle after drying of mucilage before and after purification. The two seed mucilage types contain more polar polymers that are connected to larger assemblies via multivalent cation crosslinks, resulting in a denser network. This is reflected in higher viscosity and water retention ability compared to root mucilage. Seed mucilage also contains fewer surfactants, making them better wettable after drying compared to the two root mucilage types. The root mucilage types, on the other hand, contain smaller polymers or polymer assemblies and become less wettable after drying. However, wettability not only depends on the amount of surfactants but also on their mobility, as well as the strength and mesh size of the network structure. The changes in physical properties and cation composition observed after ethanol precipitation and dialysis suggest that the polymer network of seed mucilage is more stable and specialized in protecting the seeds from unfavorable environmental conditions. In contrast, root mucilage is characterized by fewer cationic interactions and its network relies more on hydrophobic interactions. This allows root mucilage to be more flexible in responding to changing environmental conditions, facilitating nutrient and water exchange between root surfaces and the rhizosphere soil.     

More than just a coating: Ecological importance,taxonomic occurrence and phylogenetic relationships of seed coat mucilage

Studies on the ecological importance of seed coat mucilage have provided valuable information about its roles in critical stages of the plant life cycle. Seed mucilage may, by providing a moist environment and maintaining metabolic activity in the seed, promote seed development. In seed dispersal, seed mucilage influences topochory, epizoochory, endozoochory and hydrochory by anchorage of seeds to soil surface, lubrication or changing the specific weight of the seed. In arid environments, seed mucilage can prevent seeds from drying or initiate DNA repair mechanisms, thereby maintaining the soil seed bank. Seed mucilage reduces oxygen diffusion to the seed and thus has a role in regulating seed dormancy. Due to it being hydrophilous, acting as a physical barrier and containing chemicals, seed mucilage is proposed to promote seed germination in favorable environments. In seedling growth, seed mucilage may lubricate the radicle as it penetrates the soil and be degraded by soil microfloras and thus promote seedling growth. Further investigation of seed mucilage for more species in diverse habitats from the perspectives of evolution, genetics, proteomics, phylogeny and plant–microbe interactions would contribute substantially to our understanding about its ecological importance.