Uncommon, opaque particles (of approximately 20-22 nm, referred to as OP), aggregating into paracrystalloids occurred only next to colonized cells in carnation plants of either a susceptible or resistant cultivar (cv.) infected with Fusarium oxysporum f.sp. dianthi. In the susceptible plant, those structures occurred in vessel lumina and host walls, apparently associated with their alterations, but not in parenchyma cells, a situation which was the exact opposite of that observed in resistant plants. In comparison with apparently similar structures reported in other systems, paracrystalloids and their OPs did not seem to have exact counterparts in plants infected with viruses or fungi, although similar paracrystalloids were observed in nematode-infected plants. The OPs were associated in both cvs. with fine opaque matter, often displaying fine filamentous structures, and were in addition connected to fungal cells in the susceptible cv. Similar structures also extended through host walls into adjoining cells; these relations with parenchyma cells in resistant plants were interpreted as if the particles therein were akin to, if not exactly of the same nature as those in susceptible plants. As the opaque matter, the filamentous structures and the OPs were interrelated and associated with pathogen cells, it seemed warranted to assume that the OPs were issued from the pathogen.
Étude comparative de la présence de corps cristallins et de leurs particules dans des plants d’oeillet sensibles ou résistants à l’infection par le Fusarium oxysporum f.sp. dianthi race 2
Des structures cristallines opaques formées de particules singulières (d’environ 20-22 nm en diamètre désignées OP) ont été observées uniquement dans le voisinage de cellules colonisées dans des plants d’oeillet sensibles ou résistants à l’infection par le Fusarium oxysporum f.sp. dianthi. Dans les plants sensibles, les OPs se trouvaient dans les éléments de vaisseaux et les parois cellulaires, et rattachées à l’altération de celles-ci, mais elles étaient absentes dans les cellules de parenchyme du xylème. Par contre, dans les plants résistants, les OPs ne se trouvaient que dans ces cellules. En comparaison avec des structures vraisemblablement similaires rapportées pour d’autres systèmes, les OPs et les corps cristallins semblent tout à fait différents de ceux observés dans des plantes atteintes de virus ou de champignons, mais montrent une similitude avec des corps observés dans des plants parasités par des nématodes. Les OPs ont montré un rapport évident avec de la matière opaque, souvent parsemée de structures filamenteuses dans les plants des deux cvs., et en plus avec des cellules de l’agent pathogène dans le cas du cv. sensible. Des structures semblables se trouvaient souvent dans les parois de l’hôte, reliant en quelque sorte les cellules, incluant les cellules de parenchyme dans les plants résistants; ainsi, les OPs et les corps crystallins dans ces cellules semblaient pouvoir se rattacher à ces filaments comme dans les plants sensibles. En raison de l’affinité entre la matière opaque, les structures filamenteuses et les OPs, et de chacun de ces éléments avec les cellules fongiques, il a semblé pertinent d’attribuer la genèse des particules à l’agent pathogène.
Histopathological and cytochemical studies of fusarium wilt of carnation (Dianthus caryophyllus L.) have shown marked differences between plants of a susceptible cv. and those of a resistant one, inoculated with the same pathogen isolate, Fusarium oxysporum Schlechtend.:Fr. f.sp. dianthi (Prill. & Delacr.) Snyder & Hans. race 2 (Baayen et al. 1996; Ouellette et al. 1999a, 2002, and citations therein). One main difference was the confinement of the pathogen by host cell wall modifications and barrier zone formation in resistant plants as compared with its extensive intercellular invasion in the susceptible plants, favoured by the lack of similar wall modifications. The deposition of layers or patches of opaque matter on vessel walls occurred in both types of plants.
Another characteristic feature of infection specific to susceptible plants was the eventual occurrence, in primary walls and middle lamella of invaded vessel elements, of numerous opaque particles (referred to hereafter as OP), and their aggregations into paracrystalloids (Ouellette and Baayen 2000); these were absent in parenchyma cells. In the resistant plants, a reverse situation was observed, with numerous similar OPs and paracrystalloids found only in paratracheal cells (Ouellette et al. 2002). In that article, the illustrations of these structures were shown at low magnifications, making it difficult to pinpoint the particle arrangements and to describe accurately how they differed from normal host cell content.
Another yet undescribed feature concerned the occurrence in the susceptible plants of similar particles and aggregates in vessel elements, and their connections with fungal cells. For the present study, our goal was to describe more broadly the occurrence of these structures in cell walls and vessel lumina in the susceptible plants, in comparison with their different occurrence in the resistant plants, including indications of their possible origin and significance in the infection process. This work is a complement to reports of other types of matter present on vessel walls in the susceptible plants (Ouellette et al. 2004a).
Materials and methods
They are described in Ouellette et al. (2004a). Some of the photomicrographs presented here are from sections labelled for pectin (Ouellette et al. 1999a) but this labelling was not presented for purposes related to this study.
In early infection (Ouellette et al. 1999a), vessel walls became coated with layers of opaque matter. Some of this material contained small particles which were initially suspected to correspond to remnants of host vessel cytoplasm, although these particles were mixed with structures that seemed associated with vessel wall alterations (Fig. 1a); the possible relationship of these structures to fungal cells was similarly not investigated. Likewise, as the coating generally appeared as homogeneous, opaque matter (Fig. 1b), it was not frequently scrutinized at higher magnifications. Then, these particles (referred to hereafter as OPs) were noticed at different but mostly later stages of infection in lumina and on walls of vessels, associated with their alterations, and forming aggregates (Fig. 1c-e). The coating was often confluent with the outer opaque layer of fungal cells (Fig. 1e). Fine filamentous structures were noticeable that extended through these walls and into the host walls (Fig. 1e). Similar filaments also extended from intercellular fungal cells into host walls reaching vessel lumina (Fig. 1c, d) and bridged the occasionally localized additional fungal wall layers with their outer opaque layer (Fig. 1f).
Rows or confluent masses of OPs were closely connected to fungal walls by means of filamentous structures (Fig. 2a, b). The OPs were also frequently mixed with fine opaque material (Figs. 1d, 2b, 3a-b) that, in the clearest cases, likewise displayed filamentous structures (Fig. 2c). Vessel lumina often contained numerous OPs that were occasionally bound to membranous structures (Fig. 3b). Compared with the more opaque particles of the gold-complexed probes, OPs were less opaque and slightly larger (15 vs. 20-22 nm; see in particular the OPs included in the vessel wall overlaid with gold particles, Fig. 3b). Cross sections of the aggregates have shown them to be formed of spherical units, embedded in fine material, (Figs. 1d, 2c, 3b). These aggregates were frequently arranged in non-parallel arrays that formed paracrystalloids (Figs. 1d, 3b).
As mentioned above, the masses of matter appearing as homogeneously opaque at low magni-fications and contrast were shown to be a mixture of OPs and fine material. A similar association was observed in invaded vessel walls and adjoining parenchyma cell walls (Fig. 3c, d). This matter frequently spanned long distances in the walls, connected to fungal cells having thin and locally chitin-labelled walls or bordered by unlabelled bands (Fig. 3e). It also occurred in the vicinity of chitin-labelled large or irregular fungal cells (Figs. 3e, 4).
OPs and crystalline bodies were not detected in intact or altered host cell content, except in the immediate presence of pathogen cells (Fig. 5a-e). Even then, areas showing strongly degraded host cell contents in severely altered tissue, mostly in newly differentiated cells, could be distinguished from the OP-containing areas (Fig. 5c, e). Often, masses of OP-containing material extended over long distances, and could have been interpreted as being part of a host cell. However, this material was shown to be intraparietal (Fig. 5c). Individual parenchyma cells containing numerous OPs, similar to those surrounding fungal cells and free of other normal cytoplasmic structures, were only exceptionally observed in susceptible plants (Fig. 6a, b). The presence of similar OPs in the pathogen cells was not detected, but globoid bodies, twice as large as OPs, were sometimes observed therein (Fig. 6c).
Particles comparable to OPs were few and occasional in vessel lumina of resistant plants (see Ouellette et al. 1999a). Similarly, paracrystalloids and OPs were not detected in vessel lumina in these plants or in cells with normal content and in altered cells remote from colonized cells, in newly differentiated tissue in which collapsed and distorted cells including vessel elements occurred (not illustrated). However, particles were observed in paratracheal cells neighbouring invaded vessel elements or the rarely colonized paratracheal cells (Fig. 7a-d). With rare exceptions, OPs were not observed in host walls (Fig. 7d). The paracrystalloids were again formed of chains of OPs, oriented at diverging angles. Most of these cells contained appositions or new, opaque wall layers, which labelled for cellulose (Fig. 7a, b), or inner lucent, unlabelled layers (Fig. 8a, b). These new layers, which were often separated from the native cell wall layer by masses of seemingly homogeneous, opaque matter (Figs. 7b, 8c), were often eroded in association with these particles, or contained some of them (Fig. 7b, d).
The preceding illustrations of accumulation of the paracrystalloid-forming particles pertained to advanced stages of infection, either in young or older tissue. In Ouellette et al. (2002), an indication was provided that the OPs often accumulated in vacuolar-like areas, surrounded by still normal host cell cytoplasm. The following illustrations expand on this and other particularities of structures occurring in parenchyma cells.
Figures 8c and 9a show a ring of OP-like particles, some apparently aggregating, surrounded by recognizable host cell cytoplasm, but in which the particles corresponding to ribosomes are less opaque and mostly smaller and displaying a lucent core. Many cells contained only similar particles with lucent cores (Fig. 9b, c). New wall layers had likewise been deposited in these cells, and filamentous-like structures could be distinguished pervading the native walls (Fig. 9a). In some cells, bordered by invaded vessels or by other seemingly recently deposited, strongly reacting cells, many OP-like particles occurred in lacunar areas, showing links with the surrounding, still relatively normal cell cytoplasm (Fig. 9d, e).
The present observations concerned the occurrence of particles (OPs) and paracrystalloids in carnation plants infected with fusarium wilt. In considering whether these structures were real and free of artefacts, there is no reason to surmise that improper sample fixation and manipulation could have induced the build up of so many particles and paracrystalloids in both the susceptible and resistant plants. As far as it could be determined, these structures and their arrangements have no clear equivalents in the existing literature. A few lines of reasoning may be expressed that eventually may help unravel the nature and mode of formation of these structures. The paracrystalloids formed of OPs did not show a peroxisome-like microbody origin, as do crystals or paracrystalloids which have often been observed in plants, including those affected with wilt diseases (Coffey et al. 1972; Lazarovits and Higgins 1976; Liu and Boyle 1972; Robb et al. 1975) and in etioplasts (Bowman 1994).
A search for reports of similar bodies, unbound and mixed with other cell components, in plants, have yielded only a few examples. Unbound crystalline bodies have likewise been illustrated from plants infected by viruses, for example in oats infected with the blue dwarf virus (Zeyen and Banttari 1972), solely insect-transmitted, or by other pathogens (Fattah and Webster 1984; Sanger et al. 1998). The 28-30 nm virus particles forming the crystalline bodies described by Zeyen and Banttari (1972) were equally numerous in phloem cells, even intermixed with degraded host tissue, and in this respect may show features analogous to those described here. However, the OPs were smaller, and not detected in cells remote from colonized tissue, occurring even in cell walls in the susceptible cv., a location where virus particles are not expected to occur. Bodies, which at first sight might have corresponded to OPs, were occasionally observed in some pathogen cells, a fact which hinted to the possibility that a plant fungus-transmitted virus might nevertheless have been involved (Hiruki 1994; Temmink et al. 1970). However, these bodies were larger than OPs.
Fattah and Webster (1984) illustrated in nematode-infected plants paracrystalloid bodies similar to those described here. They suggested that these bodies could have corresponded to protein crystals formed by cuboid subunits. The present paracrystalloids were formed from apparently spherical particles that aggregated into lattices, and therefore do not correspond exactly to known icosehedral forms. Nevertheless, it is interesting to note that cylindrical crystalline structures in cells of nematode-feeding plants have been linked to the nematode-feeding tubes (in Fattah and Webster 1984). Besides the possibility that these bodies represented secretion products from the nematode, they could still have had a link with a fungal pathogen, as a companion infectious agent (Fattah and Webster 1983; Mai and Abawi 1987).
Other types of crystalline bodies have been reported in chloroplasts of fungal-infected plants (Tariq and Jeffries 1985), and considered as Rubisco crystals, composed of enzyme complexes and metals, and possibly analogous to Rubisco crystals formed in an intact system (Taylor et al. 2001).
Concerning the origin and nature of the lattice-forming particles themselves, it is important to stress that the same pathogen isolate was used to inoculate both the susceptible and resistant plants. In the susceptible plants, the OPs and paracrystalloids were present at the site of alterations of vessel secondary walls as well as in the compound middle lamellae adjoining invaded cells but were generally absent in the parenchyma cells. In opposition, in the resistant plants, OPs and paracrystalloids abounded in parenchyma cells and were absent elsewhere except for a few questionable cases (as in Fig. 7d, for example). These observations reinforced the previously expressed ones (Baayen et al. 1996; Ouellette et al. 2002) that host wall modifications and deposition of new wall material in host cells were the main factors impeding extensive pathogen ingress in the resistant plant. In this plant also, in an exact reverse situation with the susceptible plant, was the abundance of paracrystalloids and associated OPs in parenchyma cells and their lack in vessel lumina. One may thus suspect that the OPs, although structurally alike in both hosts, might not be exactly of the same nature, due to putative interaction with host cell content(s) in one case, but seemingly not in the other. In both instances, however, the same triggering action might have been involved. Indeed, both have in common the filamentous-like structures which extended from pathogen cells into the surrounding medium, in vessel lumina and host walls, mainly the pit membranes in the case of resistant plants, reaching the cell content.
Similar structures also appeared to extend into the opaque matter ensuing from fungal cells. Although the OPs were not detected in that matter in vessel lumina in the resistant plants, they were associated with it in parenchyma cells. As shown here and in previous reports (Charest et al. 2004; Ouellette and Rioux 1993; Ouellette et al. 1995, 1999a, 1999b, 2001, 2002, 2004a, 2004b, 2004c, 2004d), the release of fungal components would also be facilitated by modifications or the local absence of fungal walls. In elms, eggplant, and staghorn sumac, large masses and long stretches of opaque matter also occur, related to tissue alterations, and small particles are likewise connected to the coating as well as to fungal cells. Overall, it is difficult to visualize how the abundance of OPs in lumina of mature vessel elements could have been formed directly by the host. Similarly, the prolific occurrence of these OPs and paracrystalloids in parenchyma cells in resistant plants can hardly be ascribed to a boosted production of ribosomes, also different from the particles, to a plant virus that would develop independently of host cell cytoplasm (in vessels and host walls), or seemingly subsequently to the deposition of new wall layers in xylem cells and in the absence of intact organelles. In fact, these particles have not been observed in nuclei.
Whether in conjunction with the presently described structures or with other elements present on vessel walls, as described in the companion paper (Ouellette et al. 2004a), the host disturbances appear to be primarily related to the presence of fine filamentous structures and opaque matter extending from pathogen cells. In this perspective, many fungi have been shown to produce structures termed “fungal fimbriae” (Poon and Day 1975) that extend from the fungal cell into the surrounding medium, as units containing RNA and collagen (Celerin et al. 1994, 1996). Present observations may also concur with reports that in some bacteria, ribosomes may form crystals (Clark et al. 1982; Sutcliffe 2004) or “special protein-DNA cocrystals” (Frenkiel-Krispin and Minsky 2002).
In the susceptible carnation plants, the coating may thus occur either as OP-containing matter, as layers labelling for chitin, depending on the stage of infection (Ouellette et al. 2004a), or as layers of compact opaque matter. These constituents all have in common their association with vessel wall alterations, and the opaque matter in each may be congruous. The general occurrence of the features described shows their importance but, obviously, pursuing this study with other techniques, for example the production and use of other specific probes, would be commendable to discriminate more widely between host and pathogen components, particularly regarding the extraneous material present in vessel lumina.
In addition to the contributors mentioned in the companion paper, we are indebted to Dr. Alain Asselin, FSAA, Université Laval, and to Dr. Michel Cusson, Laurentian Forestry Centre, for their valuable criticism and suggestions in the preparation of the manuscript.
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