Progress in parasitic plant biology: host selection and nutrient transfer

Host range varies widely among species of parasitic plants. Parasitic plants realize host selection through induction by chemical molecular signals, including germination stimulants and haustoria-inducing factors (HIFs). Research on parasitic plant biology has provided information on germination, haustorium induction, invasion, and haustorial structures and functions. To date, some molecular mechanisms have been suggested to explain how germination stimulants work, involving a chemical change caused by addition of a nucleophilic protein receptor, and direct or indirect stimulation of ethylene generation. Haustorium initiation is induced by HIFs that are generated by HIF-releasing enzymes from the parasite or triggered by redox cycling between electrochemical states of the inducers. Haustorium attachment is non-specific, however, the attachment to a host is facilitated by mucilaginous substances produced by haustorial hairs. Following the attachment, the intrusive cells of parasites penetrate host cells or push their way through the host epidermis and cortex between host cells, and some types of cell wall-degrading enzymes may assist in the penetration process. After the establishment of host-parasite associations, parasitic plants develop special morphological structures (haustoria) and physiological characteristics, such as high transpiration rates, high leaf conductance, and low water potentials in hemiparasites, for nutrient transfer and resource acquisition from their hosts. Therefore, they negatively affect the growth and development and even cause death of their hosts.     

Ultrastructure of the haustorial interface and apoplastic continuum between host and the root hemiparasiteOlax phyllanthi (Labill.) R. Br. (Olacaceae)

Summary Structural features of haustorial interface parenchyma of the root hemiparasiteOlax phyllanthi are described. Walls contacting host xylem are thickened non-uniformly with polysaccharides, not lignin, and show only a thin protective wall layer when abutting pits in walls of host xylem vessels or tracheids. Lateral walls of interface parenchyma exhibit an expanded middle layer of open fibrillar appearance, sometimes with, but mostly lacking adjoining layers of dense wall material. Free ribosomes and rough endoplasmic reticulum are prominent and occasional wall ingrowths present. Experiments involving transpirational feeding of the apoplast tracers lanthanum nitrate or uranyl acetate to host roots cut below haustorial connections, indicate effective apoplastic transfer from host to parasite root via the haustorium. Deposits of the tracers suggest a major pathway for water flow through host xylem pits, across the thin protective wall layer, and thence into the haustorium via the electronopaque regions of the terminal and lateral walls of the contact parenchyma. Graniferous tracheary elements and walls of parenchyma cells of the body of the haustorium appear to participate in tracer flow as do walls of cortical cells, stele parenchyma and xylem conducting elements of the parasite root, suggesting that both vascular and non-vascular routes are involved in extracytoplasmic transfer of xylem sap from host to parasite. The Casparian strip of the endodermis and the suberin lamella of the exodermis of theOlax root act as barriers to flow within the system.     

芡实种子萌发期子叶传递细胞发育的初步研究

芡实种子萌发期,子叶吸收外胚乳中养分供萌发和幼苗发育,具有吸器的功能。在种子萌发过程中,子叶的部分表皮细胞发育为传递细胞。其壁内突的生长以外切向壁为多,形成壁内突的造壁物质主要由高尔基体合成,并由其溢出的囊泡运送的。     

Development and functions of seed transfer cells

In secretion or absorption processes, solutes are transported across the plasmalemma between the symplastic and apoplastic compartments. For this purpose, certain plant cells have developed a specialised transfer cell morphology characterised by wall ingrowths, which amplify the associated plasmalemma surface area up to 20-fold. Detailed studies on the function and development of transfer cells in the context of seed filling have been carried out mainly in cereal endosperm, and for the cotyledon and seed coat cells of legumes. The major solutes transferred are amino acids, sucrose and monosaccharides. The contributions of recently identified symporter proteins to solute transfer are reviewed here, as is the role of apoplastic invertases in promoting solute assimilation. Expression of invertase and monosaccharide transporters early in both cereal and legume seed development orchestrates the distribution of free sugars which play an important role in regulating transfer cell function and determining final endosperm or embryo cell number. Transfer cell differentiation is subject to developmental control, and may also be modulated by sugar levels. The most abundant genes specifically expressed in the transfer layer of maize endosperm encode small antipathogenic proteins, pointing to a role for these cells in protecting the developing endosperm against pathogen ingress. The functional characterisation of the corresponding transfer layer-specific promoters has provided a tool for dissecting transfer cell functions. Transfer cells are highly polar in their organisation, the characteristic cell wall ingrowths developing on one face only. The presence of cytoskeletal components bordering wall ingrowths is documented, but their role in establishing transfer cell morphology remains to be established.     

Changes in lipid profiles in the developing haustorium of oil palm seeds

Germinated oil palm seeds were placed in special trays in the field and at different intervals the haustoria were harvested. Changes in haustorial lipids were followed until the eighth week after germination. The moisture content decreased while the lipids increased. The haustorial fatty acid profile was similar to that of the palm kernel. Changes in fatty acid composition at different weeks after germination were observed. The major haustorial lipids were triacylglycerols; free fatty acids and diacylglycerols were also present     

Establishment, Structure and Morphology of the Tuber of Balanophora

During germination of the ‘seed’ of Balanophora,endosperm cells at the radicular pole grow out as tubular structuresand anchor the ‘seed’ to the host rootlet. The radiculartier of cells of the embryo elongate as primary haustorial tubesand establish contact with the host root vasculature. A secondaryhaustorium arises from a meristem adjoining the primary haustorium.The remainder of the embryo contributes to the tuber proper. Host parenchyma in the immediate vicinity of the primary haustoriumreverts to meristematic activity. Some of the derivatives matureas perforate tracheary cells. The remainder, retaining meristematicactivity, squeeze themselves between secondary haustorial cellsand together initiate a composite conducting strand, which repeatedlydichotomizes as the tuber grows. The conducting strand of Balanophora is looked upon as the equivalentof combined adventitious root system of parasite and host. Theremaining part of the tuber is equivalent to the shoot. Balanophora, tuber, morphology, host-parasite relations, parasite     

Ultrastructural specialization at the host-pathogen interface in rust-infected flax

Summary Ultrastructure of the association between the rust fungus, Melampsora lini, and a compatible variety of flax, Linum usitatissimum, was studied to clarify the structural relationships and interactions at the site of host penetration and at the host-parasite interface. Results of freeze-etching as well as a special section-staining procedure consisting of periodate-chromate-phosphotungstate (PACP) are shown with a host-parasite combination for the first time. The host plasma membrane is invaginated by the fungus and forms a continuous boundary around the fungal haustoria which penetrate the host cells. No morphological continuities are observed linking the protoplasts of host and fungus. With both freeze-etching and the PACP stain, the invaginated portion of the host plasma membrane at the host-parasite interface shows distinctive features that are not characteristic of the non-invaginated portion of the membrane. This localized specialization of host plasma membrane in response to the fungus appears as a significant and consistent feature of the host-parasite interaction. The host plasma membrane is separated from the haustorial wall by an amorphous layer of sheath material which covers the body but not the neck of the haustorium. This sheath provides the environment in which the haustorium exists and functions during the course of the host-parasite association. Occasionally, a collar of wall-like material derived from the host cell forms around the haustorial neck. The collar is continuous with the host wall and is distinct and discontinuous from the haustorial sheath. In fewer than 5% of the infected cells this wall material encases entire haustoria. The fungal wall is structurally specialized around the site of host penetration, and it becomes intimately associated with the host wall where the fungus penetrates into the lumen of the host cell. During penetration, the host and fungal walls appear to be fused so that the interface between them is not clearly delineated. The haustorial wall is continuous, via the haustorial neck, with the wall of the haustorial mother cell which lies outside the host cell. Different staining properties reveal this wall continuum to consist of several well-defined regions having different structure or composition. A ring of fungal wall material midway along the haustorial neck stains densely with lead citrate, but is preferentially etched away by periodic acid. The neck ring denotes a transition in the staining reaction of the fungal wall, from that present in the region of host penetration to that of the wall surrounding the haustorium. The findings demonstrate specialization of the fungal wall in the area of host penetration as well as specialization of the host plasma membrane at the host-parasite interface to a degree not previously realized from ultrastructural information.     

Anatomy of the endophyte of Viscum album L. (Loranthaceae)

Anatomy of the endophyte of Viscum album L. (Loranthaceae). An anatomical investigation into the nature of the host-parasite interaction of V. album and several of its phanerogamic hosts using SEM and light microscopy was conducted. Three kinds of parasite cell (haustorial parenchyma cells, cells resembling transfer cells and haustorial tracheids) were identified at the host-parasite interface. The terms haustorial parenchyma and haustorial tracheid are defined. Haustorial tracheids were seen to have penetrated the walls of host vessel elements and it is suggested that V. album is able to establish on a wide range of hosts because of the anatomically plastic nature of its haustorium. The development of the haustorium depends to a large extent on the nature of the surrounding host tissues. Parasite-induced host abnormalities including hypertrophy, distorted xylem elements, vessel-wall penetration and tylosis-occluded vessels were observed. The macroanatomical features observed are discussed and interpreted by-proposing a new theory for the ontogenesis of the V. album haustorium. Cortical strands with 'chisel' and 'pencil' shaped apices were both found to be present at the same time on one plant and thus were not seasonally separated.     

PARASITISM IN PHOLISMA (LENNOACEAE). I. EXTERNAL MORPHOLOGY OF SUBTERRANEAN ORGANS

The external features of the subterranean organs of coastal Californian Pholisma depressum Greene are described. A dimorphic root system exists. Long, stout roots (pilot roots) serve for vegetative propagation in reaching other host roots. Short, unbranching, more slender roots originating from the pilot roots are haustorial in function. Shoots seem to arise only on pilot roots. Host attachment is achieved through the direct transformation of the apical meristem of haustorial roots into the haustorial organ. The basal part of the shoot is also able to produce roots when near host roots, and may form lateral branch shoots either directly or after new haustorial connections are formed. Both types of roots arise endogenously. The invaded host root undergoes considerable hypertrophy. The intrusive organ itself forms a massive but irregular body. More than one haustorial root may enter even a small host root. Self parasitism may occur but is not common.     

Adaptation of the parasitic plant lifecycle: germination is controlled by essential host signaling molecules

Parasitic plants are plants that connect with a haustorium to the vasculature of another, host, plant from which they absorb water, assimilates, and nutrients. Because of this parasitic lifestyle, parasitic plants need to coordinate their lifecycle with that of their host. Parasitic plants have evolved a number of host detection/host response mechanisms of which the germination in response to chemical host signals in one of the major families of parasitic plants, the Orobanchaceae, is a striking example. In this update review, we discuss these germination stimulants. We review the different compound classes that function as germination stimulants, how they are produced, and in which host plants. We discuss why they are reliable signals, how parasitic plants have evolved mechanisms that detect and respond to them, and whether they play a role in host specificity. The advances in the knowledge underlying this signaling relationship between host and parasitic plant have greatly improved our understanding of the evolution of plant parasitism and are facilitating the development of more effective control measures in cases where these parasitic plants have developed into weeds.

Root parasitic plants grow on the roots of other plants and germinate only in the presence of that host, on which they completely depend, through the perception of host presence signaling molecules called germination stimulants.

Outstanding questions

• Have we overlooked the role of germination stimulants in facultative parasites?
• What is the biological relevance of the observation that many plant species produce and secrete a range of different strigolactones?
• Have parasitic plants evolved mechanisms to compensate for low phosphorus availability, a condition that stimulates their germination?
• What is the contribution of the HTL strigolactone receptors to host specificity in parasitic plants or does downstream signaling play a role?
• What other, nonstrigolactone, germination stimulants can parasitic plants respond to and does this require adaptation in the HTL receptors?
• What is the role of germination and underlying mechanism in the rapid adaptation of (orobanchaceous) parasitic plants to a new host?

     

梨胶锈菌性孢子和锈孢子阶段吸器的超微结构研究

本文对梨胶锈菌性子期和锈子期菌丝吸器的形成方式、吸器及其与寄主细胞界面的超微结构进行了研究。观察结果表明：梨胶锈菌性子期和锈子期寄主胞间菌丝吸器的形成方式有两种：一种是由寄主胞间菌丝直接形成吸器;另一种是由寄主胞间菌丝先形成吸器母细胞,然后由吸器母细胞形成吸器。吸器在开始形成时只是一个乳头状的侵入楔,以后逐渐形成囊状、镰刀状、指状及其它不规则形状的吸器。多数吸器分化为颈和吸器主体两部分,在颈部及部分吸器主体外有一个由类似寄主细胞壁物质形成的领圈。吸器内部的超微结构与寄主胞间菌丝基本相同,但吸器壁比胞间菌丝或吸器母细胞的壁薄。吸器鞘的厚度随着吸器伸长膨大 而逐渐增厚。     

EXPERIMENTAL EVIDENCE FOR HOST RACES IN MISTLETOE (PHORADENDRON TOMENTOSUM)

In order to test the hypothesis that mistletoes (Phoradendron tomentosum) are differentially adapted for the host species that they occur on, mistletoe seeds from the three most common hosts in central Texas (hackberry, Celtis occidentalis, elm, Ulmus crassifolia, and mesquite, Prosopsis glandulosa) were planted onto different individuals of each of the three hosts. Germination of seeds and formation of haustorial disks by seedlings were followed in the subsequent 17 months. Germination of seeds was very high for all nine combinations of maternal (source) and seed (experimental) hosts (range 82%–98%). There were no significant differences in seed germination between the two groups when source and experimental hosts were the same species and when they were different species. In contrast, development of haustorial disks when source and experimental hosts were the same species was significantly greater than when experimental host and source host species were different. The data suggest that populations of mistletoes are genetically differentiated such that early seedling development is greatest when there is correspondence between maternal and seedling host species.     

Initiation, Development and Structure of the Primary Haustorim in Striga gesnerioides (Scrophulariaceae)

A light-microscopic study is reported on the initiation, establishmentand structure of the primary haustorium of Striga gesnerioideson the host, cowpea (Vigna unguiculata). The radicular apexof the germinated parasite seed dissolves its way through thehost root cortex to the stele. Thus, it is converted into aprimary haustorium. Some of the haustorial front-line cellsin contact with the host endodermis penetrate into the steleand make contact with the xylem vessels. Differentiation ofthese haustorial cells into xylem vessels occurs and extendsbackwards through the median axial region of the haustorialtract in the host cortex to connect with the conductive xylemof the radicle outside the host root. Subsequently the parasite'splumule develops into a leafy shoot. On penetrating the steleof the host, the haustorium stimulates cell division in thehost pericycle whose triggered proliferation together with expansionof the parasite haustorial tissues result in the formation ofa large, tuberous primary haustorium. At various points of thehost-parasite interface, differentiation of xylem elements occurs,presumably maximizing nutrient transfer from host to parasite.In spite of this, many proliferated host cells at the interfaceremain apparently meristematic showing densely-stained cytoplasmand prominent nuclei.     

EXPERIMENTAL STUDIES OF HAUSTORIUM INITIATION AND EARLY DEVELOPMENT IN AGALINIS PURPUREA (L.) RAF. (SCROPHULARIACEAE)

In parasitic angiosperms the haustorium, an organ specialized for attachment and penetration of host tissue, functions in the transport of water and nutrients from the host to the parasite. In Agalinis purpurea (L.) Raf. (Scrophulariaceae) these organs are initiated laterally along its roots, opposite a primary xylem pole. Analyses of haustoria distribution and cellular root profiles show that the portion of the root which is most sensitive to haustorial elicitor molecules is the area distal to the zone of elongation and near the root meristem. Sectioned material supports this finding and, further, indicates that the cells which are the first to respond to haustorial elicitors are located in the inner cortex. Haustoria develop rapidly in response to a host root or to isolated chemical elicitors (xenognosins) normally contained in host root exudate. By 6 hr, vacuolation and radial cellular enlargement are observed in the cortex, and a lateral swelling along the root is visible. By 12 hr, cells of the epidermis divide anticlinally to establish a group of densely cytoplasmic cells at the apex of the haustorial swelling. Accompanying these divisions is the differentiation of specialized hair cells which elongate from epidermal cells flanking the presumptive haustorial apex. Next, the internal, radially enlarged cortical cells divide periclinally. Periclinal divisions are subsequently initiated in the pericycle as early as 18 hr post-induction. Cellular division and enlargement continue so that by 24–36 hr a mature pre-contact haustorium is formed. There is a reduction in root elongation concomitant with haustorial initiation. Depending upon the number of haustoria produced, elongation typically returns to the preinduction level within 2 or 3 days.     

寄生药用植物管花肉苁蓉种子的离体萌发与吸器形成的形态学研究

研究了管花肉苁蓉(Cistanche tubulosa (Schenk) R. Wight)种子脱离寄主条件下的离体萌发和吸器形成的形态学,为其高产栽培提供参考。将经过层积处理的种子浸泡于赤霉素(1 000 mg.L-1)36小时,然后培养于1/2 MS(加500 mg.L-1酵母提取物、250 mg.L-1氯化钠和100 mg.L-1甘露醇,pH5.83)培养基上。培养两周后种子开始萌动,首先胚根从软化的内种皮的种孔端伸出,接着形成芽管状物,之后芽管状物逐渐伸长;17天后初生吸器开始发育,厚的带状表皮分化出若干吸根毛;在初生吸器顶端带状表皮围成窝状,表皮上的褶皱和窝内分布有乳头状突起。芽管状物延伸至4 mm就停止发育。吸根毛和乳突是黏着寄主根、刺穿寄主皮层发育为内生吸器最终建立寄生关系的基础。     

The apoplastic continuum,nutrient absorption and plasmatubules in the dwarf mistletoeKorthalsella lindsayi (Viscaceae)

Summary The transfer of nutrients between host and parasite in mistletoes has generally been considered to occur via the xylem to xylem contacts at the host-parasite interface in the haustorial organ of attachment. A few workers, however, have recently begun to question this assumption and have suggested an alternative pathway of transport involving the intervening parenchyma cells which are often abundant in the parasite at the interface. But no morphological experimental evidence has yet been forthcoming in support of an apoplastic continuum across this interface between parasite and host.Our observations on the dwarf mistletoeKorthalsella lindsayi first indicate an absence of plasmodesmata at the interface, with the conclusion that symplastic transport between the two plants is not involved. However, application of apoplastic markers, such as Calcofluor white and lanthanum and uranyl ions, to the stem of the host results in the transfer of these tracers across the interface and into the tissues of the parasite. This demonstrates the existence of an apoplastic continuum between the two plants, and a pathway that is probably used in the normal transfer of water and other nutrients from host to parasite.From the apoplastic continuum provided by the walls of the haustorial parenchyma tissue, nutrients are transferred to the symplast for eventual distribution to other parts of the plant. Evidence for the active uptake of substances from the apoplast by the protoplasts of the parenchyma cells is shown by the convoluted appearance of the plasmalemma and its differentiation often into plasmatubules.     

THE HOST-PARASITE INTERFACE OF ALBUGO CANDIDA ON RAPHANUS SATIVUS

The fine structure of the intercellular hyphae of the obligate parasite Albugo candida infecting radish does not differ markedly from that described previously for cells of Peronospora manshurica. The stalked, capitate haustoria do not contain nuclei and are packed with mitochondria and lomasomes. The fungal plasma membrane and cell wall are continuous from the intercellular hypha throughout the haustorium except that there is no evidence of fungal cell wall around a portion of the haustorial stalk proximal to the haustorial head. Within the vacuolate host mesophyll cell, the haustorium is always surrounded by host plasma membrane and with at least a thin layer of host cytoplasm. The host cell wall invaginates at the point of haustorial penetration to form a short sheath around the region of penetration, but normally there is no host cell wall around the balance of the haustorium. About 1% of the haustoria observed were necrotic, and these were invariably walled-off completely from host cytoplasm by host cell wall. An amorphous, moderately electron-dense encapsulation lies between the haustorium proper and the host plasma membrane and extends into the penetration region between the sheath and the fungal cell wall. Invaded host cells contain more ribosomal-rich ground cytoplasm than uninfected cells. Glandular-like systems of tubules and connecting vesicles are often numerous in host cytoplasm in the vicinity of haustorial heads. These tubules open into the encapsulation, their limiting unit membranes being continuous with the host plasma membrane. We suggest that these represent a secretory mechanism of the host specifically induced by the parasite.     

Tremelloid haustorial cells with haustorial filaments and potential host range of Tremella mesenterica

Zugmaier, W. & Oberwinkler, F. 1995. Tremelloid haustorial cells with haustorial and potential host ranges of Tremella mesenterica . - Nord. J. Bot. 15: 207–213. Copenhagen. ISSN 0107–055X.
In vitro and in vivo haustorial cells of Tremella mesenterica , consisting of a subglobose basal part with one or more thread-like haustorial filaments, were examined using light and electron microscopy. The haustorial cells developed from clamp connections of hyphal septa or intercalarily. Mostly such haustorial cells were monokaryotic, but in a few cases also dikaryotic haustorial cells were observed. In vitro, the host range of Tremella mesenterica was tested with the corticiaceous homobasidiomycetes Peniophora erikssonii, P. quercina and Phanerochaete eremea . The in vitro interaction of Tremella mesenterica with all these fungi was principally the same as in vivo with Peniophora laeta . A single micropore connected the cytoplasm of the haustorial filament with that of the respective host cell. The pore domain at the host side was delimited by curved ER cisternae only in Peniophora quercina , but not in Peniophora erikssonii and Phanerochaete cremea .     

Examining the interaction of light,nutrients and carbohydrates on seed germination and early seedling development of <Emphasis Type="Italic">Bletia purpurea</Emphasis> (Orchidaceae)

The effects of carbohydrate availability, carbohydrate source, nutrient availability and illumination on germination and early development of Bletia purpurea (Orchidaceae) seeds were investigated using asymbiotic seed germination. Of special interest was determining the minimum nutritional and light requirements for the completion of germination. Germination and development was limited when seeds were cultured in darkness without sucrose. Seeds were able to germinate under illuminated conditions even in the absence of sucrose and this effect was enhanced when mineral nutrients were incorporated into media. Sucrose, fructose, glucose and trehalose enhanced germination and seedling development while mannitol and sorbitol did not. These data suggest that carbohydrates, either as products of photosynthesis, from symbiotic fungi in situ or as exogenously supplied sugars in vitro, play an important role in regulating seed germination by fulfilling an energy requirement. This hypothesis has been often expressed but rarely satisfactorily tested. Mineral nutrients appear to be less important for germination than carbohydrates. The differential effect of sucrose, fructose, glucose and trehalose at two different concentrations on rhizoid production indicates carbohydrates may play a role in regulating rhizoid production.     

The Peptide pools of germinating barley grains: relation to hydrolysis and transport of storage proteins

A quantitative procedure for purifying small peptides from plant tissues, involving both ion-exchange and gel-exclusion chromatography, is described. Peptides were quantified and characterized by using the fluorescence reagents dansyl chloride and fluorescamine. Large pools of small peptides and amino acids have been identified in both the endosperm and embryo of germinating barley grains. The peptide pool of the endosperm increases during the first 3 days of germination, subsequently decreasing, an observation compatible with a role for peptides as intermediates in the breakdown of the storage proteins and their transfer to the embryo. The amino acid composition of these peptides indicates that all the major classes of storage protein contribute to the pool. The concentration of peptides produced in the endosperm during germination is sufficient for the efficient operation of the peptide transport system of the scutellar membrane characterized previously (Higgins and Payne, Planta 136: 71-76, 1977; Planta 138: 211-215 and 217-221, 1978). Data presented here indicate that peptides play at least as important a role as amino acids in the transfer of stored nitrogen from the endosperm to the embryo during germination.