Taxonomic Significance of Sclerenchyma Distribution in the Secondary Phloem of Some Indian Tropical Trees

Analysis of the relative amount and distribution pattern of phloem sclerenchyma in some 29 tropical trees of India was carried out with systematic considerations. Both the features exhibited considerable diversity among the species analyzed. The extent of area occupied by sclerenchyma in transections of the bark of these species varied from zero to 35% and 3 to 49% in the conducting and non-conducting phloem zones respectively, the overall amount constituting about 3 to 45% of the secondary phloem as a whole. The sclerenchyma cells differentiated either as isolated elements or in the form of bands or fascicles of diverse shape and size showing various distribution patterns.     

Histochemical IAA-oxidase localization in the shoot of wheat

A histochemical method for the determination of IAA-oxidase has been used in sections of various aerial parts of winter wheat plants. High IAA-oxidase activity was localized in the cell walls of sclerenchyma near the periphery of the stem, in the vascular bundle sheath of sclerenchyma and in xylem, both in the stem and in the leaf. The cell wall—bound IAA-oxidase activity therefore appeared in lignifying tissues. The staining was very weak or absent in the cell walls of parenchyma tissues and phloem. The positive reaction of the cytosol at the bulbous ends of guard cells and in the leaf primordia is presumed to be due to cytosolic IAA-oxidase. These results are discussed in relation to peroxidase localization and to our previousin vitro studies.     

Mechanism of resistance induced by plant activators against Colletotrichum falcatum in sugarcane

Abstract

A search for plant activators capable of inducing systemic resistance in sugarcane showed that plants pre-treated with synthetic signal inducers confer a high degree of resistance to Colletotrichum falcatum – the red rot pathogen. Among the various treatments, Acibenzolar S- methyl (ASM) was found to be very effective in restricting the pathogen colonization inside the inoculated cane stalk tissues. The induction of resistance was accompanied by a significant increase in peroxidases and polyphenoloxidases activities. A considerable decrease of pathogen titre in the pre-treated tissues as determined by ELISA, clearly demonstrated the restriction of pathogen colonization and proliferation in the sensitized cane stalks. Specific induction of new isoforms of peroxidases and polyphenoloxidases in C. falcatum elicitor treatment indicates the pathogen elicitor induced specific cellular response of sugarcane suspension-cultured cells.     

Structural modification of Quercus petraea leaf caused by Cynips quercusfolii – histological study of galls

Galls formed by the interaction of insects on plant tissues are an example of the unusual transformation and use of plants by insects. The aim of this study was to characterize the structure of galls formed by Cynips quercusfolii L. on sessile oak leaves. In the structure of galls, we distinguished the following: (1) the protective ‘first contact zone’ created by epidermal and sub-epidermal sclerenchyma rings, (2) the wide parenchymatous ring, (3) the internal protective zone created by the sclerenchyma ring, and (4) the nutritional zone consisting of cells filled with amyloplasts containing starch. A characteristic for galls in the development stage is the centripetal starch gradient in which starch accumulates in a ‘ring of amyloplasts’ in the larval chamber.     

CAREX GRACEII SP. N., CYPEROCARPUS ELIASII SP. N., CYPEROCARPUS TERRESTRIS SP. N., AND CYPEROCARPUS PULCHERRIMA SP. N. (CYPERACEAE) FROM THE MIOCENE OF NEBRASKA

Silicified achenes and some perigynia of four new sedges are described from the late middle or late Miocene Ash Hollow (Clarendonian or Hemphillian) and early middle Miocene Sheep Creek (Late Hemingfordian) Formations of Nebraska. Carex graceii, sp. n., Cyperocarpus terrestris, sp. n., and Cyperocarpus pulcherrima, sp. n., were collected from strata in Garden and Antelope Counties and Cyperocarpus eliasii, sp. n., was collected from strata in Sioux County. Certain of the newly discovered taxa exhibit considerable anatomical detail of the pericarp wall of the achene. In two taxa, Carex graceii and Cyperocarpus pulcherrima, the achene pericarp exhibits four topographic regions: a cuticle, an outer layer of pentagonally to hexagonally shaped epidermal cells containing silica bodies, a middle layer of sclerenchyma cells, and an inner layer of sclerenchyma cells whose long axes are perpendicular to the long axes of the cells of the middle layer. Similar pericarp anatomy was found in Cyperocarpus terrestris except that the inner layer was not observed. In the fourth taxon, Cyperocarpus eliasii, only an outer epidermal layer of elongate cells with small protuberances is preserved. The ultrastructure of the pericarp of the fossil taxa is similar to that of living forms. Associated flora and fauna indicate widespread savanna environments with significant riparian elements. This is the first systematic treatment of sedges from the Miocene of North America.     

Exit of intracellular Porphyromonas gingivalis from gingival epithelial cells is mediated by endocytic recycling pathway

Gingival epithelial cells function as an innate host defence system to prevent intrusion by periodontal bacteria. Nevertheless, Porphyromonas gingivalis, the most well‐known periodontal pathogen, can enter gingival epithelial cells and pass through the epithelial barrier into deeper tissues. However, it is poorly understood how this pathogen exits from infected cells for further transcellular spreading. The present study was performed to elucidate the cellular machinery exploited by P. gingivalis to exit from immortalized human gingival epithelial cells. P. gingivalis was shown to be internalized with early endosomes positive for the FYVE domain of EEA1 and transferrin receptor, and about half of the intracellular bacteria were then sorted to lytic compartments, including autolysosomes and late endosomes/lysosomes, while a considerable number of the remaining organisms were sorted to Rab11‐ and RalA‐positive recycling endosomes. Inhibition experiments revealed that bacterial exit was dependent on actin polymerization, lipid rafts and microtubule assembly. Dominant negative forms and RNAi knockdown of Rab11, RalA and exocyst complex subunits (Sec5, Sec6 and Exo84) significantly disturbed the exit of P. gingivalis. These results strongly suggest that the recycling pathway is exploited by intracellular P. gingivalis to exit from infected cells to neighbouring cells as a mechanism of cell‐to‐cell spreading.     

An Ultrastructural Study on the Development of Silicified Tissues in the Leaf Tip of Barley (Hordeum sativum Jess)

The development of silicified tissues in the tip of the fourthand fifth leaf of 7-week-old barley plants grown in nutrientsolution was investigated by transmission electron microscopy.The pattern of silicification was similar in the epidermal cells,sclerenchyma cells and intercellular spaces. Silica granulesfirst appeared around the periphery and eventually filled theentire cell lumen or space. The granules then polymerized toform a solid mass. The walls of the sclerenchyma cells alsobecame silicified but to a less extent than those of the epidermalcells, in which silicification sometimes occurred prior to thatin the lumen. The results are discussed in relation to the chemistry of silicaand possible mechanisms of silicification. Hordeum sativum Jess, barley, silica bodies, opalines, epidermal cells, sclerenchyma, ultrastructure     

Infection process of Gaeumannomyces graminis var. graminis on the roots and culms of rice

Crown sheath rot, caused by the ascomycete Gaeumannomyces graminis var. graminis that infects the root and the base of the culm of rice, causes early grains maturation, tiller death and reduced yield. As a paucity of information exists in the literature on the rice‐G. graminis var. graminis interaction at the microscopic level, this study aimed to gain novel insights into the infection process of this pathogen in the root and culm of rice using both light and scanning electron microscopy. In the roots, the fungus initially colonized the epidermal, exodermal and sclerenchyma cells. At 15 days after inoculation (dai), fungal hyphae colonized the cortex and clusters of perithecia were observed in the roots. At 20 dai, the fungus reached the central cylinder, and an intense fungal colonization at the base of the culm was observed that resulted in the formation of a mycelial mat on both adaxial and abaxial surfaces of the leaf sheaths. At 25 dai, fungal growth was noticed in the parenchyma cells, vascular bundles and airspaces. Perithecia emerged through the base of prophyllum and from the first leaf sheath at 30 dai. The results of this study provide new insights into the infection process of G. graminis var. graminis in rice and may help to find better control measures in reducing crown sheath rot development.     

互花米草、狐米草和大绳草茎秆的比较解剖观察

互花米草、狐米草和大绳草的表皮均由长细胞、短细胞(栓质细胞和硅质细胞)、盐腺和气孔器组成。它们成纵行交互排列。盐腺的结构与大米草相似,但三个种的盐腺和气孔器的数目不同,尤其以大绳草最多。它们的内部结构是由气道、不同大小的维管束、基本组织以及厚壁组织组成。然而,维管束的数目及厚壁组织的发育各不相同。狐米草和大绳草有高度木质化的厚壁组织细胞,而互花米草的厚壁组织木质化较弱。大绳草的维管束多于其他两种。     

Composition of the cell walls of different asparagus (Asparagus officinalis) tissues

Portions of stems from the base of asparagus spears (Asparagus officinalis L. cv. Connovor Collossus) were dissected to give the following tissues: (1) pith, which was free of vascular bundles, (2) two surrounding layers, parenchyma and fibre I and II (PFI and PFII), containing parenchyma and vascular bundles, (3) sclerenchyma sheath, (4) epidermis and sub-epidermal layers and (5) asparagus vascular fibre (AVF). The alcohol-insoluble residues (AIRs) from these tissues were shown to be free of starch. They were analysed for moisture and protein, and the component sugars were released by two hydrolytic procedures, which helped to distinguish the sugars from non-cellulosic polysaccharides and cellulose. The AIRs from pith and epidermal tissues were relatively low in xylose, but were rich in cellulosic glucose, and sugars associated with pectic polysaccharides such as galacturonic acid, galactose and arabinose. Their major component polysaccharides (in decreasing amounts) were inferred to be pectic polysaccharides, cellulose, and hemicelluloses. AIR from sclerenchyma was rich in glucose and xylose, suggesting the presence of much cellulose and (acidic) xylans. The AIRs of PFI, PFII and AVF contained significant amounts of xylose in addition tn other sugars, and the major polysaccharides inferred to be present were pectic polysaccharides, cellulose and hemicelluloses, a significant proportion of which may be acidic xylans. Methylation analysis of the AIRs confirmed the above inferences. The bulk of the glucosyl residues were (1–4)-linked, and there were small but significant amounts of (1–4, 6)-linked glucosyl residues (the linkage characteristic of xyloglucans) in all the preparations. The presence of (1–4)-linked galactosyl, (1–5)-linked arabinosyl, terminal galactosyl, terminal arabinosyl, (1–2)- and (1–2, 4)-linked rhamnosyl residues in all the AIRs except that from sclerenchyma, confirmed the presence of significant levels of pectic polysaccharides in all the parenchyma tissues. All the preparations containing vascular tissues contained significant amounts of (1–4)-linked xylosyl residues, probably derived from acidic xylans. Even in the AIR of pith, a significant amount of (1–4)-linked xylosyl residues were detected. This may be due to the ability of these cells and the parenchyma cells associated with the vascular bundles, to undergo lignification in mature asparagus plants.     

菰适应湿地环境的解剖和屏障结构特征研究

菰(Zizania latifolia)是一种多年生挺水植物,为了探讨该植物根、茎和叶的解剖结构、组织化学及其质外体屏障的通透性生理。该文利用光学显微镜和荧光显微镜,对菰的根、茎、叶进行了解剖学和组织化学研究。结果表明:(1)菰不定根解剖结构由外而内分别为表皮、外皮层、单层细胞的厚壁机械组织层、皮层、内皮层和维管柱;茎结构由外而内分别为角质层、表皮、周缘厚壁机械组织层、皮层、具维管束的厚壁组织层和髓腔。叶鞘具有表皮和具维管束皮层,叶片具有表皮,叶肉和维管束。(2)不定根具有位于内侧的内皮层及其邻近栓质化细胞和外侧的外皮层组成的屏障结构;茎具内侧厚壁机械组织层,外侧的角质层和周缘厚壁机械组织层组成的屏障结构,屏障结构的细胞壁具凯氏带、木栓质和木质素沉积的组织化学特点,叶表面具有角质层。(3)菰通气组织包括根中通气组织,茎、叶皮层的通气组织和髓腔。(4)菰的屏障结构和解剖结构是其适应湿地环境的重要特征,但其茎周缘厚壁层和厚壁组织层较薄。由此推测,菰适应湿地环境,但在旱生环境中分布有一定的局限性。     

<Emphasis Type="Italic">Coxiella burnetii</Emphasis> Nine Mile II proteins modulate gene expression of monocytic host cells during infection

Background  

Coxiella burnetii is an intracellular bacterial pathogen that causes acute and chronic disease in humans. Bacterial replication occurs within enlarged parasitophorous vacuoles (PV) of eukaryotic cells, the biogenesis and maintenance of which is dependent on C. burnetii protein synthesis. These observations suggest that C. burnetii actively subverts host cell processes, however little is known about the cellular biology mechanisms manipulated by the pathogen during infection. Here, we examined host cell gene expression changes specifically induced by C. burnetii proteins during infection.     

Streptococcal toxins: role in pathogenesis and disease

Group A Streptococcus (Streptococcus pyogenes), group B Streptococcus (Streptococcus agalactiae) and Streptococcus pneumoniae (pneumococcus) are host‐adapted bacterial pathogens among the leading infectious causes of human morbidity and mortality. These microbes and related members of the genus Streptococcus produce an array of toxins that act against human cells or tissues, resulting in impaired immune responses and subversion of host physiological processes to benefit the invading microorganism. This toxin repertoire includes haemolysins, proteases, superantigens and other agents that ultimately enhance colonization and survival within the host and promote dissemination of the pathogen.     

Colonization of root tissues and protection against Fusarium wilt of rye (Secale cereale) by nonpathogenic rhizosphere strains of Fusarium culmorum

Colonization of rye (Secale cereale) tissues by nonpathogenic rhizosphere Fusarium culmorum isolates DEMFc2 and DEMFc5 and a pathogenic strain DEMFc37, and their effect on plant fresh weight were studied in pot experiments. Both rhizosphere isolates colonized the epidermis and the cortex but were not found in vessels, while the pathogen colonized all three layers of root cells. The numbers of pathogen CFU isolated from plant tissues were much higher than those of the rhizosphere isolates in spite of the same number of macroconidia used as inoculum (1 × 10⁵ g⁻¹ of soil). Inoculation of seedlings with DEMFc2 resulted in a 20% increase, with DEMFc5 in more than a 20% reduction, and with DEMFc37 in a 38% reduction of shoot fresh weight of 14-day-old plants. Pre-colonization of plants with (either of) the rhizosphere isolates and subsequent inoculation with the pathogen resulted in plant weights the same as those observed in plants inoculated with the rhizosphere strain alone. The disease severity index for shoots of plants pre-colonized with DEMFc2 was reduced from class 4 (86% diseased plants) observed for plants inoculated with the pathogen alone to class 2 (average of 8% diseased plants) when pre-treated with the rhizosphere strain. The CFU number of the pathogen isolated from the interior of roots of plants pre-colonized with the rhizosphere isolates was as low as 10% of the number isolated from plants inoculated with the pathogen alone. A study of in vitro interactions between the rhizosphere isolates and the pathogen suggests that changes in plant colonization by the pathogen and its effect on fresh weight of plants pre-colonized with the rhizosphere isolates were not connected with inhibition of its growth by a direct action of the rhizosphere isolates. The results suggest that strain DEMFc2 can be considered as a potential biocontrol agent.     

Eradication of endophytic bacteria via treatment for axillary buds of <Emphasis Type="Italic">Petunia hybrida</Emphasis> using Plant Preservative Mixture (PPM<Superscript>TM</Superscript>)

Plant Preservative Mixture (PPM^TM), a proprietary mixture of two broad-spectrum isothiazolone biocides, was recently introduced as a prophylactic anti-bacterial agent in plant tissue culture. Its efficacy for eradicating endophytic Sphingomonas paucimobilis in Petunia hybrida was tested. The presence of bacterial cells in intercellular spaces of parenchyma tissues in the cortex and pith, in the lumen of xylem vessels and within sclerenchyma cells, could be detected in histo-sections by both light and transmission electron microscopy. The eradication protocol involved infiltration of infected axillary buds with PPM solution under vacuum. Quantitation by high performance liquid chromatography (HPLC) revealed that axillary buds from upper young nodes absorbed significantly more PPM compared with those from the lower nodes. Indexation indicated successful eradication of bacterial contaminants from upper young axillary buds after vacuum-infiltration with 5 ml l⁻¹ PPM.     

Comparative vegetative anatomy and systematics of Spiranthoideae (Orchidaceae)

STERN, W. L., MORRIS, M. W., JUDD, W. S., PRIDGEON, A. M. & DRESSLER, R. L. 1993. Comparative vegetative anatomy and systematics of Spiranthoideae (Orchidaceae). The anatomy of leaf, stem and root of plants in the orchid subfamily Spiranthoideae was studied and described from the viewpoint of systematics. Plants were available from most of the geographic range. Tribes Diceratosteleae and Tropidieae show sinuous anticlinal epidermal cell walls in leaves, glandular foliar hairs, tetracytic para-mesoperigenous stomata, unitary tracheary components in the foliar midrib, foliar and cauline stegmata and sclerenchyma, typical cruciate starch grains, thick-walled exodermal, endodermal, and pericyclic cells, and conductive strands of the root embedded in sclerenchyma. The tribe Cranichideae shows straight to curvilinear anticlinal epidermal cell walls in leaves, lack glandular foliar hairs, have variably patterned mesoperigenous stomata, lack sclerenchyma throughout the parts studied, have a binary tracheary component in the foliar midrib, store starch in specialized amyloplasts (spiranthosomes), lack stegmata, have thin-walled exodermal, endodermal, and pericyclic cells, show scalariform thickenings in exodermal cells, and have conductive strands of the root embedded in parenchyma. In Cryptostylis the tracheary component of the foliar midrib is unitary, stomata lack subsidiary cells, starch grains are of the typical cruciate configuration, and passage cells of the endodermis are apparently associated with tilosomes. Anatomical data, when analysed cladistically, support the hypothesis that Spiranthoideae, as currently delimited, are polyphyletic. Corymborkis, Tropidia, and Diceratostele are more closely related to Palmorchis, a likely representative of a basal clade within subfamily Epidendroideae, than to genera of Cranichideae. Likewise, members of Cranichideae are more closely related to Diuris, a representative of subfamily Orchidoideae-tribe Diurideae, than to Corymborkis, Tropidia and Diceratostele. The Corymborkis– Tropidia-Diceratostele-bassd epidendroid [Palmorchis) clade may be diagnosed by the foliar synapomorphies of sinuous anticlinal walls of epidermal cells and presence of glandular hairs. The Cranichideae-orchidoid (Diuris) clade may be diagnosed by its variably patterned, mesoperigenous stomata, lack of vascular bundle sclerenchyma, absence of stegmata, unthickened endodermal cell walls in roots, and conductive cells of roots embedded in parenchyma. Relationships within this clade are quite unresolved, when only anatomical data are employed; however, all studied genera of Cranichideae, except Cryptostylis, possess a binary tracheary component in the foliar midrib. Cranichideae, excluding Cryptostylis, may be considered monophyletic. All Cranichideae, except Helaeria and Cryptostylis, possess spiranthosomes. Hetaeria may be a basal member within Cranichideae. We consider the phylogenetic position of Cryptostylis, in relation to Cranichideae vs. Diurideae, to be equivocal.     

两种香荚兰茎的解剖学研究

对引自墨西哥的香荚兰ＶａｎｉｌａｐｌａｎｉｆｏｌｉａＡｎｄｒ．和生长于云南河口县城附近沟谷雨林下的滇南香荚兰Ｖ．ｓｉａｍｅｎｓｉｓＲｏｌｆｅｅｘＤｏｗｎｉｅ进行了茎的解剖研究。结果表明,两者在茎的解剖特征上有显著差异。从茎的横切面上看,引自墨西哥的香荚兰,在皮层最内方与维管区之间存在一环带状的厚壁组织,而滇南香荚兰茎则没有形成这种厚壁组织环;香荚兰茎的皮层细胞小,易于与维管区域的薄壁组织细胞相区别,而滇南香荚兰茎的皮层细胞较大,难与维管区域的薄壁组织细胞区分开来。在同属不同种植物茎中存在如此大的解剖学特征差异实属罕见。它不仅为区分这两个种提供重要的解剖特征依据,而且对于开展种间杂交和对杂种后代的识别具有指导意义     

Differentiation Between Tissues from Carnation (Dianthus caryophyllus) Stems by Pyrolysis-Mass Spectrometry

Small pieces of different tissues from stems of young and oldcarnation plants were analyzed for lignification (lignin/celluloseratios) and lignin composition by means of pyrolysis-(gas chromatography)-massspectrometry. The epidermis and phloem of young and old stemswere essentially non-lignified. Pith parenchyma was only lignifiedin mature and senescing tissues. The type of lignin in sclerenchymadiffered from that in xylem and pith. Lignification in the xylemof very young tissues was a mainly guaiacyl-type lignin, whichgradually changed into a mixed guaiacyl-syringyl lignin in oldertissues. In mature tissues, the sclerenchyma was more highlylignified than the xylem. All tissues yielded comparatively large amounts of dihydroferulicacid, a compound which may be specific for carnation. Carnation, Dianthus caryophyllus, epidermis, cortex, sclerenchyma, phloem, xylem, pith, lignification, aging, dihydroferulic acid, pyrolysis-(gas chromatography)-mass spectrometry     

Show and tell: cell biology of pathogen invasion

Because the initial stages of pathogen invasion are often confined to a limited number of host cells, measures of host responses that are averaged over attacked and non-attacked cells provide an unsatisfactory view of these events. To identify the earliest and often transient responses to pathogen attack, there is considerable interest in monitoring the subcellular events that occur specifically in living host cells. Recent improvements in live-cell imaging using fluorescent-tagged markers have expanded the scope of the experiments that can be performed. Changes in the subcellular distribution of organelles and of fluorescently tagged proteins can be monitored in real time in living tissues during pathogen attack, and the dynamic nature of such changes across space and over time can be determined. The application of these sensitive imaging methods has extended earlier observations, made with Nomarski microscopy or inferred from static transmission electron micrographs, about the focal accumulation of subcellular organelles at sites of pathogen attack. In addition, recent experiments have demonstrated the focused accumulation and interaction of specific plant proteins at penetration sites, opening a new window on early host responses and raising questions about the underlying plant processes that sense and direct this marshalling of host resources to block pathogen entry.