Morphology and Anatomy of the Haustorium of the Root Hemiparasite Olax phyllanthi (Olacaceae), with Special Reference to the Haustorial Interface

Gross morphology and internal structure of haustoria of Olaxphyllanthi are described in parasitism with a range of hosts,including roots of woody and herbaceous dicotyledons and certainmonocotyledons, and occasional instances of autoparasitism andhaustorial formation on monocotyledon rhizomes. Successful penetrationto xylem occurs on virtually all hosts across broad diameters,ages and anatomies of host root, but anatomical impedimentsto haustorial establishment and penetration are recorded forcertain host taxa. Each haustorium is a comparatively simpleand ephemeral structure. Its developing sucker (endophytic regionof the haustorium) spreads laterally around the surface of thehost xylem, yet never completely encircles the host stele. Damageto hosts is minimal and secondary thickening (of hosts) continueson the side of a host root opposite to a haustorium. The haustorialsucker lacks phloem and its interface with host xylem is comprisedalmost entirely (more than 98.7%) of parenchyma. The few terminatingtracheids at an interface lie in very close proximity to oroccasionally directly against exposed xylem vessels, but lumento lumen continuity between tracheary elements of the partnersis not achieved. Three dimensional reconstructions based onserial transverse sectioning indicate that well defined filesof tracheids connect back from an interface to the core of graniferoustracheary elements in the external body of the haustorium, andthence to the xylem of the parent parasite root. The findingsare discussed in relation to existing studies on haustorialanatomy. Root parasite, Olacaceae, haustorial anatomy, host specificity     

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.     

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.     

ELECTRON MICROSCOPY OF THE HOST-PARASITE RELATIONSHIPS IN STEM RUST OF WHEAT

Ehrlich , H. G., and Mary A. Ehrlich . (Duquesne U., Pittsburgh, Pa.) Electron microscopy of the host-parasite relationships in stem rust of wheat.—Amer. Jour. Bot. 50(2): 123–130. Illus. 1963.—A series of micrographs showing intercellular dikaryotic mycelium, haustorial mother cells, stages in haustorial formation, and haustoria within host cells are presented in the present report. Of special interest and potential significance in a study of obligate parasitism is an encapsulation ranging from 800 to 3400 A in thickness which surrounds the haustorium, but which is not present around the intercellular hyphae. The encapsulation completely encases the haustorium proper; it is bounded on the inside by the cell wall of the haustorium, and its thin membranous outer margin abuts directly on the protoplast of the host cell. The nature of the material composing the encapsulation is uncertain, but it appears to originate from the haustorial protoplast, and at least a portion of it may be fungal cytoplasm. This newly described structure represents the actual interface between the host and pathogen. Small vesicles which seem to originate from the outer margin of the encapsulation are sometimes found in the host cytoplasm surrounding apparently vigorous haustoria. The vesicles are bounded by a membrane and contain particulate material.     

Endogenous hormone levels and anatomical characters of haustoria in Santalum album L. seedlings before and after attachment to the host

The physiological and anatomical attributes of haustoria tissues in hemi-parasitic Santalum album L. seedlings, growing on the potential host, Kuhnia rosmarnifolia Vent., were investigated before and after attachment to the host. Quantization of endogenous levels of indole-3-acetic acid (IAA), zeatin (Z), zeatin riboside (ZR), GA-like substances (GAs) and abscisic acid (ABA) was performed by HPLC. Histological preparations were used to characterize structural differences between pre- and post-attachment haustoria. The contents of GAs and ABA were higher in attached haustoria, with 3.61 and 3.50μgg(-1) fresh weight, respectively, and three times higher than in non-attached haustoria. Cytokinins, Z, ZR and IAA levels were also high, and their contents in attached haustoria increased 2.04-, 2.17-, and 2.82-fold more, respectively, than in non-attached haustoria. A high auxin-to-cytokinin ratio contributed to haustorial development of S. album. A numerous amount of starch in parenchyma cells around the meristematic region above the haustorial gland and the endophyte tissue of the post-attachment haustoria were reported in a Santalaceae member for the first time. Many lysosomes were present and large-scale digestion of host cells occurred at the interface between the parasite and host. The haustorial penetration in S. album into the host stele was suggested to be a function of mechanical force and enzymatic activity. Analysis of the endogenous hormone levels and the structural characters in S. album haustoria indicated that the haustoria were able to synthesize phytohormones, which appeared to be necessary for cell division and differentiation during haustorial development. These results suggest that endogenous hormones are involved in the haustorial development of S. album and in water and nutrient transport in the host-parasite association.     

Haustorial Structure and Functioning of the Root Hemiparastic Tree Nuytsia floribunda(Labill.) R.Br. and Water Relationships with its Hosts

Observations on the origin and mature structure of the haustoriumof the Western Australian Christmas tree (Nuytsia floribunda)corroborate and extend the findings of earlier workers. We showthat the previously described sclerenchymatous ‘horn’or ‘prong’ formed within the haustorium acts asa sickle-like cutting device which transversely severs the hostroot and then becomes lodged in haustorial collar tissue directlyopposite to that where it originated. The cutting process isdeduced to be rapid and the gland-like fluid filled structurein the haustorium is suggested to generate a hydrostatic forcedriving the device through the host root. The haustorial parenchymacells at the tight junction between the endophytic part of thehaustorium and the cut face of the host root develop balloon-likeoutgrowths which intrude into the lumina of severed xylem vesselsof the host. Experiments feeding 0.05% (w/v) basic fuchsin tofreshly cut ends of host root segments distal to terminally-attachedmature haustoria demonstrate an apoplastic pathway from hostxylem elements fractured at the interface into haustorial parenchyma,and thence through vascular tissue to the haustorium into thetranspiring plant of Nuytsia. Application of labelled water(D₂O) to uncut basal roots of potted plants ofAcacia acuminataparasitized by Nuytsia results in labelling of leafy shootsof parasite and host, indicative of haustorial uptake of waterby Nuytsia from host root xylem in the intact association. Measurementsof xylem water potentials of pot-cultured seedling Nuytsia associatedwith a range of hosts, or of mature trees of Nuytsia and partnerwoody hosts in the native habitat, demonstrate consistentlymore negative potentials in the parasite than host, suggestingthat the parasite may regularly obtain xylem water through itshaustorial apparatus. Copyright 2000 Annals of Botany Company Root hemiparasite, Nuytsia floribunda, Loranthaceae, haustorial structure, host–parasite water relations     

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     

The Initiation of the Secondary Haustorium in Alectra vogelii Benth

Anatomical studies were carried out on initiation of the secondaryhaustorium in Alectra vogelii, a root parasite of leguminouscrops in Nigeria. In both the normal and self-haustorium, theformation of the haustorial initial on the parasite root soonafter initial contact between the host and parasite roots isfollowed by the penetration of the host root by the haustorium.Specialized penetrating cells (intrusive cells) at the haustorialfront prise apart and loosen the host root cortical cells, whichlater become digested. Through the same processes, a few ofthese columnar intrusive cells at the haustorial front piercethe endodermis to make contact with the xylem of the host root.Thereafter, a true conductive bridge consisting of short, isodiametric,reticulate vessel elements is established between the parasiteand host roots through the secondary haustorium. No pholem tissuewas observed in the connection. There is a close similaritybetween the mode of initiation of the secondary haustorium ofAlectra vogelii and that previously described for its primaryhaustorium. Alectra vogelii Benth, haustorium, self-haustorium, root parasite, hemiparasitism, Vigna unguiculata, Arachis hypogaea     

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.     

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.     

Anatomical and Histochemical Studies of Haustrial Development of Cassytha filiformis L.

This paper deals with the haustorium development of parasitic plant (Cassytha filiformis L.) parasitized on purple willow (Salix purpurea L.).The polarity occurred in the portion near the host; and the cushion-shaped haustorial plate formed, and then the haustorial primordium initiated in the cortex. Finally, the haustoria reached the cortex of pith of the host, penetrating through its own cortex and epidermis. Tracheary elements were differentiated from the base of the haustoria and the sieve elements were not observed in the haustoria. Histochemical studies revealed that there were starch grains in normal stem cortex. The starch grains were increased in the portion near the axis after twisting on host. After the haustorial plate was formed, the starch grains were richly accumulated in the central group of cells, which were followed by the haustorial development; The starch disappeared in the meristem, in which protein stained deeply; The dynamic change of protein turned oK to be contrary to the tendency of starch accumulation. The structure and parasitic mechanism and the dynamic change of starch and protein are discussed.     

Structure and Development of the Mature Secondary Haustorium in Alectra vogelii Benth

Anatomical investigations were carried out on the structureand development of the mature secondary haustorium in Alectravogelii growing on Arachis hypogaea or Vigna unguiculata. Followingthe formation of the young secondary haustorium, both the cambiumand pericycle of the host root directly opposite the young secondaryhaustorium are stimulated to divide and form new tissues andorgans including haustorial roots. Further proliferations ofthe host root pericycle and the haustorial cortex give riseto a large, tuberous and complex mature secondary haustoriumwithin which the tissues of the host and parasite remain inintimate contact forming a perfect graft union with a wide zoneof contact. Apart from the haustorial axial xylcm strand whichnormally connects the xylem of the parasite secondary root withthat of the host, direct xylary connections are also establishedbetween the axial xylem of the haustorium and the xylem of thehaustorial roots. The entire surface of the mature secondaryhaustorium of Alectrais covered with these haustorial rootsas was previously observed in its mature primary haustorium. Alectra vogelii Benth, secondary haustorium, haustorium, haustorial roots, root parasite, hemiparasitism, Arachis hypogaea, Vigna unguiculata     

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.     

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。     

Structure and development of the upper haustorium in the parasitic flowering plant Cuscuta japonica (Convolvulaceae)

The anatomical and ultrastructural development of the haustorium of the Cuscuta japonica, a holoparasitic angiosperm, growing on the host plant Impatiens balsamina was studied. After the shoot tips of light-grown parasite seedlings contacted the host, the upper haustorium (external to the host organ) developed through three main successive stages of the haustorial initials, the meristem, and the endophyte primoridium (EP) within the middle layer of the cortex of the parasite stem. The haustorial initial cells were characterized by abundant starch-bearing amyloplasts and mitochondria with an expanded intermembrane space. The meristem cells had numerous large chloroplasts with well-developed thylakoids, reflecting the capability for photosynthesis. Commonly, all three stages of haustorial cells contained conspicuous, large nuclei with enlarged nucleoli and dense cytoplasm including many other organelles, indicating a very active metabolism. In the final stage of upper haustorium development, the meristem cells differentiated into the EP, a host-penetrating tissue. The primordium had smaller file cells at the proximal end and elongate digitate cells at the distal end. The file cells divided actively, while the digitate cells contained abundant chloroplasts, dictyosomes, rough endoplasmic reticulum, and other organelles, suggesting that the EP was cytohistologically well organized for penetration into the host tissue.     

不同抗病性小麦品种上白粉菌吸器发育超微结构研究

利用电镜技术对不同抗病性小麦品种上白粉菌吸器发育及相应寄主细胞变化的超微结构进行了研究,并对吸器的Ca2+－ATP酶活性及几丁质的分布进行了细胞化学定位分析。结果表明,小麦白粉菌（Blumeriagraminisf．sp.tritici）成熟吸器在内部结构上类似一个代谢活跃的菌丝细胞,有大量的线粒体和多聚核糖体;Ca2+－ATP酶主要被定位在寄主质膜及病菌核膜上;随吸器的不断发育,吸器外膜厚度增加,同时Ca2+-ATP酶活性增强。几丁质均匀地分布在吸器壁上,其含量随吸器的成熟而增加。在不同抗病性小麦品种上,吸器细胞核最先退化,然后是线粒体的液泡化和多聚核糖体的解聚。中抗寄主细胞内的吸器普遍退化较早,相当一部分在吸器中心体阶段已解体。此外,高感寄主表皮细胞与叶肉细胞之间有发达的胞间连丝;而且在吸器形成后,能比中抗寄主细胞更快地增殖和聚积大量与能量代谢、物质合成及分泌活动有关的细胞器。     

An anatomical study of the haustoria of Rhinanthus minor attached to roots of different hosts

Roots of a range of potential hosts responded differently when Rhinanthus minor attempted to form haustoria. Roots of Fabaceae show the weakest reaction as apart from slight lignification, no reaction was observed at the interface between the endophyte and the cortical tissue of the host root. Grass roots react with strong lignification of all cells within the stele with the exception of a small number of phloem cells whilst the endodermis fully enters the tertiary stage. In the case of Phleum bertolonii the cortical cells also become lignified. The lignification is even observed in the host root tissue in a distance of about 1 mm from the haustorium (both apically and basipetally). In the case of Leucanthemum vulgare, strong suberisation can be observed in the cell walls of the interface between endophyte (tip of the sucker) and host. Plantago lanceolata exhibits the strongest reactions against the haustorial tissues. Cells of the interface between the endophyte and the host cortex are completely destroyed, as well as a few cell layers outside the central xylem cylinder, even in some distance from the haustorium. Thus, host xylem is completely isolated from the haustorium in this case. Extraction of sap from xylem vessels is likely to be drastically impaired in such a situation.     

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.     

Ultrastructure of the haustorium of Trenomyces histophthorus and adjacent host cells

The haustorium of Trenomyces histophthorus (Ascomycetes, Laboulbeniales) appears to be enucleate and aseptate; its bulbs, isthmuses, and tubules contain abundant mitochondria and are often vacuolate. Although host cells around some bulbs appear to be unaffected, most host cells in contact with the haustorial tubules are in various stages of degeneration. In some instances deterioration of the tissues of the mallophagan host apparently occurs in advance of the haustorial tips.     

The structure and development of the haustorium in parasitic Scrophulariaceae*

The structure and development of roots and haustoria in 37 species of parasitic Scrophulariaceae was studied using light microscopy. The mature haustorium consists of two regions: the swollen “body” and the parent root, which resembles non-haustorial roots in structure. The body arises from the parent root and is composed of an epidermis, cortex, central region of xylem (the vascular core), a region of parenchyma (the central parenchymatous core), and the portion of the haustorium contained in the host tissue (the endophyte). The xylem of the vascular core is composed predominately of vessel elements. The central parenchymatous core is composed of parenchyma and col-lenchyma. Vessels extend from the vascular core through the central parenchymatous core to the endophyte. The endophyte is composed of parenchyma cells and vessel elements. No phloem is present in the body of the haustorium. Early stages in the development of the haustorium are exogenous. Initial periclinal divisions in the epidermis or outer cortex are followed by hypertrophy of cortical parenchyma. These events are followed by development of the vascular core from the pericycle, attachment of haustorium to the host by a specialized layer of cementing cells or root hairs, and penetration of the host by dissolution of host cells.