scholarly journals Structure and development of root gall induced by Meloidogyne javanica in Glycine max L.

2019 ◽  
Vol 40 (3) ◽  
pp. 1033
Author(s):  
Roberta Mendes Isaac Ferreira Vilela ◽  
Vitor Campana Martini ◽  
Letícia de Almeida Gonçalves ◽  
Vinícius Coelho Kuster ◽  
Denis Coelho de Oliveira
Keyword(s):  
Glycine Max ◽  
Host Plant ◽  
Light And Electron Microscopy ◽  
Meloidogyne Javanica ◽  
Giant Cells ◽  
Infection Process ◽  
Site Formation ◽  
Thick Wall ◽  
Vascular Cylinder ◽  
Root Cortex

Galls formed by root-knot nematodes have been studied in several cultivated species focusing on understanding the intimate relationship between parasite and the host plant. Species of Meloidogyne induce the development of a feeding site in the cortex or vascular cylinder of the host plant and are totally dependent on this site formation to complete their life cycle. Therefore, we focused on anatomical, cytological and histochemical changes during the establishment and development of galls and giant cells induced by Meloidogyne javanica in the roots of Glycine max. Seeds of soybean (susceptible cultivar M8372 IPRO) were sown in trays with coconut fibre substrate and the seedlings were removed ten days after the seeds emerged for nematode inoculation. The roots from inoculated and non-inoculated (control) were sampled at different stages of development until 55 days after inoculation. Histological, cytological, histochemical analysis were performed in light and electron microscopy in non-galled tissue and galls induced by M. javanica. The galls showed different shapes and abundance in the roots inoculated by M. javanica. The induction of galls occurs by hypertrophy of the root cortex shortly after the initial infection process. Giant cells were formed 18 days after nematode inoculation. These giant or nourishing cells are multinucleated, and have a dense cytoplasm, a thick wall with invaginations, many mitochondria and small vacuoles. The anatomical sections indicated a disorganisation of the cells of the cortex and vascular cylinder in relation to the control root.

Fine structure of the giant cells induced by Meloidogyne javanica in lima bean

1984 ◽  
Vol 62 (3) ◽  
pp. 429-436 ◽  
Author(s):  
F. Fattah ◽  
J. M. Webster
Keyword(s):  
Electron Microscopy ◽  
Fine Structure ◽  
Light And Electron Microscopy ◽  
Lima Bean ◽  
Meloidogyne Javanica ◽  
Giant Cells ◽  
Egg Laying ◽  
Phaseolus Lunatus ◽  
Wide Range

Giant cells associated with egg-laying females of Meloidogyne javanica in lima bean, Phaseolus lunatus cv. L-136, were examined by light and electron microscopy. These giant cells have characteristics that are typical of nematode-induced giant cells in a wide range of hosts, but they differ in that they (i) are less closely associated with xylem vessels, (ii) contain a very large number of plastids which are devoid of starch grains, and (iii) contain several different forms of cytoplasmic crystals. One form of the crystal is associated with a large number of "spiny" vesicles. The possible role of these features, especially the crystals, in the giant cell response of lima bean is discussed.

scholarly journals Xanthomonas campestris Promotes Diffusible Signal Factor Biosynthesis and Pathogenicity by Utilizing Glucose and Sucrose from Host Plants

2019 ◽  
Vol 32 (2) ◽  
pp. 157-166 ◽  
Author(s):  
Chunyan Zhang ◽  
Mingfa Lv ◽  
Wenfang Yin ◽  
Tingyan Dong ◽  
Changqing Chang ◽  
...  
Keyword(s):  
Host Plant ◽  
Xanthomonas Campestris ◽  
Infection Process ◽  
Plant Metabolites ◽  
Multiple Strategies ◽  
Exogenous Addition ◽  
Diffusible Signal Factor ◽  
Signal Production ◽  
Induced Changes ◽  
Encoding Genes

The plant pathogen Xanthomonas campestris pv. campestris produces diffusible signal factor (DSF) quorum sensing (QS) signals to regulate its biological functions and virulence. Our previous study showed that X. campestris pv. campestris utilizes host plant metabolites to enhance the biosynthesis of DSF family signals. However, it is unclear how X. campestris pv. campestris benefits from the metabolic products of the host plant. In this study, we observed that the host plant metabolites not only boosted the production of the DSF family signals but also modulated the expression levels of DSF-regulated genes in X. campestris pv. campestris. Infection with X. campestris pv. campestris induced changes in the expression of many sugar transporter genes in Arabidopsis thaliana. Exogenous addition of sucrose or glucose, which are the major products of photosynthesis in plants, enhanced DSF signal production and X. campestris pv. campestris pathogenicity in the Arabidopsis model. In addition, several sucrose hydrolase–encoding genes in X. campestris pv. campestris and sucrose invertase–encoding genes in the host plant were notably upregulated during the infection process. These enzymes hydrolyzed sucrose to glucose and fructose, and in trans expression of one of these enzymes, CINV1 of A. thaliana or XC_0805 of X. campestris pv. campestris, enhanced DSF signal biosynthesis in X. campestris pv. campestris in the presence of sucrose. Taken together, our findings demonstrate that X. campestris pv. campestris applies multiple strategies to utilize host plant sugars to enhance QS and pathogenicity.

The illustrated life cycle of Microbotryum on the host plant Silene latifolia

Botany ◽  
2010 ◽  
Vol 88 (10) ◽  
pp. 875-885 ◽  
Author(s):  
Angela Maria Schäfer ◽  
Martin Kemler ◽  
Robert Bauer ◽  
Dominik Begerow
Keyword(s):  
Life Cycle ◽  
Light And Electron Microscopy ◽  
Laboratory Data ◽  
Infection Process ◽  
Host Cells ◽  
Silene Latifolia ◽  
Long Distance ◽  
Biological Studies ◽  
Plant Parasitic

The plant-parasitic genus Microbotryum (Pucciniomycotina) has been used as a model for various biological studies, but fundamental aspects of its life history have not been documented in detail. The smut fungus is characterized by a dimorphic life cycle with a haploid saprophytic yeast-like stage and a dikaryotic plant-parasitic stage, which bears the teliospores as dispersal agents. In this study, seedlings and flowers of Silene latifolia Poir. (Caryophyllaceae) were inoculated with teliospores or sporidial cells of Microbotryum lychnidis-dioicae (DC. ex Liro) G. Deml & Oberw. and the germination of teliospores, the infection process, and the proliferation in the host tissue were documented in vivo using light and electron microscopy. Although germination of the teliospore is crucial for the establishment of Microbotryum, basidium development is variable under natural conditions. In flowers, where the amount of nutrients is thought to be high, the fungus propagates as sporidia, and mating of compatible cells takes place only when flowers are withering and nutrients are decreasing. On cotyledons (i.e., nutrient-depleted conditions), conjugation occurs shortly after teliospore germination, often via intrapromycelial mating. After formation of an infectious hypha with an appressorium, the invasion of the host occurs by direct penetration of the epidermis. While the growth in the plant is typically intercellular, long distance proliferation seems mediated through xylem tracheary elements. At the beginning of the vegetation period, fungal cells were found between meristematic shoot host cells, indicating a dormant phase inside the plant. By using different microscopy techniques, many life stages of Microbotryum are illustrated for the first time, thereby allowing new interpretations of laboratory data.

scholarly journals Oryza glumaepatula, a New Source of Resistance to Meloidogyne graminicola and Histological Characterization of Its Defense Mechanisms

2019 ◽  
Vol 109 (11) ◽  
pp. 1941-1948 ◽  
Author(s):  
Vanessa S. Mattos ◽  
Raycenne R. Leite ◽  
Juvenil E. Cares ◽  
Ana Cristina M. M. Gomes ◽  
Antonio W. Moita ◽  
...  
Keyword(s):  
Defense Mechanisms ◽  
Resistance Mechanism ◽  
Giant Cells ◽  
Wild Accession ◽  
Sources Of Resistance ◽  
Root Cortex ◽  
Meloidogyne Graminicola ◽  
Significant Damage ◽  
Resistant Accession ◽  
Moderately Resistant

Meloidogyne graminicola causes significant damage to rice fields worldwide. Sources of resistance to M. graminicola reported in Oryza sativa are limited. Resistance to this species has been found in other Oryza species such as O. glaberrima and O. longistaminata. This study aimed to evaluate the reaction of four wild species of Oryza from the Embrapa Rice and Bean Germplasm Bank (Goiás, Brazil) to a pool of M. graminicola populations and determine the resistance mechanism in O. glumaepatula. Two genotypes of O. glaberrima, one of O. alta, three of O. glumaepatula, one of O. grandiglumis, one of O. longistaminata, and one of O. sativa (control) were included in the study. The results showed that O. glumaepatula was highly resistant (reproduction factor [RF] < 1). O. glaberrima, O. alta, and O. grandiglumis were considered moderately resistant. O. longistaminata was susceptible, although values of RF remained lower than the control O. sativa ‘BR-IRGA 410’, considered highly susceptible. Histological observations on the interaction of O. glumaepatula and M. graminicola showed reduced penetration of second-stage juveniles (J2s) when this resistant wild accession was compared with O. sativa. An intense hypersensitivity response-like reaction occurred at 2 days after inoculation in the root cortex of the resistant accession. Few J2s established in the central cylinder, and rare collapsed giant cells were observed surrounded by degenerate females. Fluorescence microscopy in O. glumaepatula revealed giant cells and the female body presumably exhibiting accumulation of phenolic compounds. Our study suggests that wild rice accessions, especially from the AA genotype (e.g., O. glumaepatula), are of great interest for use in future breeding programs with Oryza spp.

Ultrastructure of eastern cottonwood clones susceptible or resistant to leaf rust

1987 ◽  
Vol 65 (8) ◽  
pp. 1586-1598 ◽  
Author(s):  
L. Shain ◽  
U. Järlfors
Keyword(s):  
Electron Microscopy ◽  
Leaf Rust ◽  
Light And Electron Microscopy ◽  
Infection Process ◽  
The Other ◽  
Host Cells ◽  
Eastern Cottonwood ◽  
Melampsora Medusae ◽  
Wall Appositions ◽  
Infected Cells

The infection process in four clones of eastern cottonwood susceptible or resistant to leaf rust caused by Melampsora medusae was studied by light and electron microscopy. Infection was initiated by stomatal rather than direct entry. Typical dikaryotic haustoria were observed in all clones within 1 day of inoculation. Some healthy-appearing haustoria were observed in susceptible clones throughout the duration of the study, which was terminated during the initiation of uredial production. Incompatibility was expressed differently in the two resistant clones. In clone St 75, most haustoria and invaded host cells that were observed appeared necrotic within 2 days of inoculation. Cell wall appositions appeared during this time in cells adjoining necrotic host cells. Some infected cells disintegrated within 4 days of inoculation. Affected host cells of clone St 92, on the other hand, plasmolyzed during the first 2 to 3 days after inoculation. Necrotic host cells were not observed in this clone until the 4th day after inoculation. Hyphal ramification and host plasmolysis were extensive at 6 days after inoculation.

scholarly journals Nodulation of Aeschynomene afraspera and A. indica by Photosynthetic Bradyrhizobium Sp. Strain ORS285: The Nod-Dependent Versus the Nod-Independent Symbiotic Interaction

2011 ◽  
Vol 24 (11) ◽  
pp. 1359-1371 ◽  
Author(s):  
Katia Bonaldi ◽  
Daniel Gargani ◽  
Yves Prin ◽  
Joel Fardoux ◽  
Djamel Gully ◽  
...  
Keyword(s):  
Fluorescent Protein ◽  
Lateral Roots ◽  
Root Hairs ◽  
Infection Process ◽  
Cortical Cells ◽  
Symbiotic Interaction ◽  
Root Cortex ◽  
Bradyrhizobium Sp ◽  
Infected Cells ◽  
Green Fluorescent

Here, we present a comparative analysis of the nodulation processes of Aeschynomene afraspera and A. indica that differ in their requirement for Nod factors (NF) to initiate symbiosis with photosynthetic bradyrhizobia. The infection process and nodule organogenesis was examined using the green fluorescent protein–labeled Bradyrhizobium sp. strain ORS285 able to nodulate both species. In A. indica, when the NF-independent strategy is used, bacteria penetrated the root intercellularly between axillary root hairs and invaded the subepidermal cortical cells by invagination of the host cell wall. Whereas the first infected cortical cells collapsed, the infected ones immediately beneath kept their integrity and divided repeatedly to form the nodule. In A. afraspera, when the NF-dependent strategy is used, bacteria entered the plant through epidermal fissures generated by the emergence of lateral roots and spread deeper intercellularly in the root cortex, infecting some cortical cells during their progression. Whereas the infected cells of the lower cortical layers divided rapidly to form the nodule, the infected cells of the upper layers gave rise to an outgrowth in which the bacteria remained enclosed in large tubular structures. Together, two distinct modes of infection and nodule organogenesis coexist in Aeschynomene legumes, each displaying original features.

Resistance to the root-knot nematode Meloidogyne fallax in Solanum sparsipilum: analysis of the mechanisms

Nematology ◽  
2004 ◽  
Vol 6 (3) ◽  
pp. 389-400 ◽  
Author(s):  
Abou Bakari Kouassi ◽  
Marie-Claire Kerlan ◽  
Miroslaw Sobczak ◽  
Jean-Paul Dantec ◽  
Claudia Rouaux ◽  
...  
Keyword(s):  
Female Parent ◽  
Giant Cells ◽  
F1 Hybrids ◽  
Vascular Cylinder ◽  
Root Knot Nematode ◽  
Resistant Parent ◽  
Defence Reaction ◽  
Invasion And Migration ◽  
Solanum Sparsipilum ◽  
And Migration

AbstractThe genotype 88S.329.15 of Solanum sparsipilum was studied in order to analyse the genetic basis and the mechanisms of its resistance to Meloidogyne fallax. In infected plants grown at 20°C, juveniles invaded the root system with a clear delay and a lower infection rate in comparison to the susceptible S. tuberosum genotype BF15 H1. No defence reaction occurred during root invasion and migration toward the vascular cylinder. The juveniles induced development of feeding sites usually composed of several giant cells, which contained condensed cytoplasm, only small vacuoles, enlarged nuclei with pronounced nucleoli and almost no endoplasmic reticulum. Abundant necrosis of surrounding parenchymatous vascular cylinder cells lead to the degeneration of the giant cells. More than 90% of the invading juveniles failed to develop. The others developed as males. The resistance inheritance was analysed on 128 F1 hybrids obtained using the susceptible line BF15 H1 as the female parent and 88S.329.15 as the male parent. Among the progenies, 68 genotypes produced a necrotic reaction to nematode infection and 60 produced no necrosis. This 1 : 1 segregation pattern suggests a monogenic control of this defence reaction. Unlike the resistant parent 88S.329.15, some M. fallax females developed in the roots of necrotically responding hybrids. There was a normal distribution of mean numbers of adult females found in the roots of these genotypes. This result suggests that the ability of the resistant genotype 88S.329.15 to suppress development of females is quantitatively inherited and likely to be controlled by more than one locus. These data indicate that the mechanism of resistance is different from the resistance to Meloidogyne incognita conferred by the Mi gene of tomato.

The interaction between the gelatin-binding domain of fibronectin and the attachment ofPasteuria penetransendospores to nematode cuticle

Parasitology ◽  
2001 ◽  
Vol 123 (3) ◽  
pp. 271-276 ◽  
Author(s):  
S. MOHAN ◽  
S. FOULD ◽  
K. G. DAVIES
Keyword(s):  
Polyclonal Antibodies ◽  
Meloidogyne Javanica ◽  
Infection Process ◽  
Binding Domain ◽  
Heparin Binding ◽  
Pasteuria Penetrans ◽  
Heparin Binding Domain ◽  
Human Fibronectin ◽  
Nematode Cuticle ◽  
Pre Treatment

Pasteuria penetransis a Gram-positive endospore-producing bacterium that is a parasite of root-knot nematodes. Attachment of endospores to the cuticle of the nematode is the first stage in the infection process. Western blot analysis with monoclonal and polyclonal antibodies that recognize the 30 kDa heparin-binding domain (HBD) and the 45 kDa gelatin-binding domain (GBD) fragments of human fibronectin (Fn) revealed a series of polypeptides of approximately 40, 45 and 55 kDa present in crude cuticle extracts ofMeloidogyne javanica2nd-stage juveniles. The results suggest that the structure of the nematode fibronectin is different to the fibronectins so far characterized. Pre-treatment of endospores ofPasteuriawith either the HBD or the GBD was found to inhibit binding to the nematode cuticle. The larger GBD fragment was the most effective at blocking adhesion. Pre-treatment of the GBD fragment with gelatin prevented the GBD fragment from inhibiting endospore attachment to the nematode cuticle.

Light and electron microscopic studies of nodule structure of alfalfa

1981 ◽  
Vol 27 (1) ◽  
pp. 36-43 ◽  
Author(s):  
J. J. Patel ◽  
A. F. Yang
Keyword(s):  
Light And Electron Microscopy ◽  
Infection Process ◽  
Infection Thread ◽  
Nodule Development ◽  
Electron Microscopic ◽  
Meristematic Region ◽  
Microscopic Studies ◽  
A Site ◽  
Ongoing Infection ◽  
Nodule Tissue

Light and electron microscopy was used to establish the structural organisation of the developing nodule of alfalfa. In these nodules three distinct regions were noted: (1) the base region, site of original infection where the nodule is attached to the root and now composed of degenerating nodule tissue, (2) the central region, or active region composed of nodule cells containing tightly packed bacteroids surrounding a central vacuole, and (3) the meristematic region, a site of new growth, behind which newly formed cells are continually invaded. The ongoing infection process accompanying continued nodule development provided the opportunity to study the release of Rhizobium cells from the infection threads.In the nodules of alfalfa it would appear that the Rhizobium cells are released from infection thread into the nodule tissue in two different ways: (i) release with infection thread membrane and (ii) release in thin-walled vesicular structures. Thus it is concluded that Rhizobium cells are surrounded by the infection thread membrane when they are released from the infection thread into nodule tissue.

Sign in / Sign up

Export Citation Format

Share Document