scholarly journals Structure and Development of the Legume-Rhizobial Symbiotic Interface in Infection Threads

Cells ◽  
2021 ◽  
Vol 10 (5) ◽  
pp. 1050
Author(s):  
Anna V. Tsyganova ◽  
Nicholas J. Brewin ◽  
Viktor E. Tsyganov
Keyword(s):  
Cell Wall ◽  
Plant Cell Wall ◽  
Host Cells ◽  
Infection Thread ◽  
Root Hair Cell ◽  
Infection Threads ◽  
Legume Symbiosis ◽  
And Control ◽  
Insight Into

The intracellular infection thread initiated in a root hair cell is a unique structure associated with Rhizobium-legume symbiosis. It is characterized by inverted tip growth of the plant cell wall, resulting in a tunnel that allows invasion of host cells by bacteria during the formation of the nitrogen-fixing root nodule. Regulation of the plant-microbial interface is essential for infection thread growth. This involves targeted deposition of the cell wall and extracellular matrix and tight control of cell wall remodeling. This review describes the potential role of different actors such as transcription factors, receptors, and enzymes in the rearrangement of the plant-microbial interface and control of polar infection thread growth. It also focuses on the composition of the main polymers of the infection thread wall and matrix and the participation of reactive oxygen species (ROS) in the development of the infection thread. Mutant analysis has helped to gain insight into the development of host defense reactions. The available data raise many new questions about the structure, function, and development of infection threads.

scholarly journals Identification of Symbiotically Defective Mutants of Lotus japonicus Affected in Infection Thread Growth

2006 ◽  
Vol 19 (12) ◽  
pp. 1444-1450 ◽  
Author(s):  
Fabien Lombardo ◽  
Anne B. Heckmann ◽  
Hiroki Miwa ◽  
Jillian A. Perry ◽  
Koji Yano ◽  
...  
Keyword(s):  
Root Hair ◽  
Plant Cell Wall ◽  
Plant Root ◽  
Lotus Japonicus ◽  
Cortical Cell ◽  
Host Cells ◽  
Infection Thread ◽  
Mycorrhizal Symbiosis ◽  
Symbiotic Interaction ◽  
Infection Threads

During the symbiotic interaction between legumes and rhizobia, the host cell plasma membrane and associated plant cell wall invaginate to form a tunnel-like infection thread, a structure in which bacteria divide to reach the plant root cortex. We isolated four Lotus japonicus mutants that make infection pockets in root hairs but form very few infection threads after inoculation with Mesorhizobium loti. The few infection threads that did initiate in the mutants usually did not progress further than the root hair cell. These infection-thread deficient (itd) mutants were unaffected for early symbiotic responses such as calcium spiking, root hair deformation, and curling, as well as for the induction of cortical cell division and the arbuscular mycorrhizal symbiosis. Complementation tests and genetic mapping indicate that itd2 is allelic to Ljsym7, whereas the itd1, itd3, and itd4 mutations identified novel loci. Bacterial release into host cells did occur occasionally in the itd1, itd2, and itd3 mutants suggesting that some infections may succeed after a long period and that infection of nodule cells could occur normally if the few abnormal infection threads that were formed reached the appropriate nodule cells.

Frankia forms infection threads

1999 ◽  
Vol 77 (9) ◽  
pp. 1327-1333 ◽  
Author(s):  
R Howard Berg
Keyword(s):  
Cell Wall ◽  
Plant Cell ◽  
Plant Cell Wall ◽  
Infection Thread ◽  
Nodule Development ◽  
Wall Material ◽  
Cell Wall Material ◽  
Infection Threads ◽  
Nodule Symbiosis ◽  
Plant Control

Frankia forms symbioses with a great variety of plant hosts, and because nodule development is under plant control, this results in an interesting diversity in the structure of developing symbiotic cells. However, it is apparent that, in all these symbioses, the microsymbiont Frankia follows a similar pattern of development within symbiotic cells of the nodule: the cell is invaded by formation of an infection thread containing invasive hyphae sheathed in plant cell wall material, parasitic vegetative hyphae proliferate by branching from this infection thread, and N2-fixing symbiotic vesicles differentiate from tips of these vegetative hyphae. Infection threads are recognized by their ontogeny and morphology, being the cell-invasive structures in the case of the former and straight-growing hyphae in the case of the latter. Formation of infection threads is a feature shared in common with legumes. Unlike in legumes, the infection thread in actinorhizae is not defined by the presence of sheathing plant cell wall material; all forms of the bacterium have this. Rather than using the term "encapsulation," which suggests a bacterial origin, it is proposed the term "interfacial matrix" be used to describe this plant cell wall material separating Frankia from host cytoplasm.Key words: Frankia, infection thread, interfacial matrix, microsymbiont, nodule, symbiosis.

scholarly journals Mycobacterium tuberculosis adhesins: potential biomarkers as anti-tuberculosis therapeutic and diagnostic targets

Microbiology ◽  
2014 ◽  
Vol 160 (9) ◽  
pp. 1821-1831 ◽  
Author(s):  
Viveshree S. Govender ◽  
Saiyur Ramsugit ◽  
Manormoney Pillay
Keyword(s):  
Immune Response ◽  
Mycobacterium Tuberculosis ◽  
Control Strategies ◽  
Host Cells ◽  
Tuberculosis Control ◽  
Surface Molecules ◽  
Host Pathogen Interaction ◽  
Bacterial Aggregation ◽  
Insight Into

Adhesion to host cells is a precursor to host colonization and evasion of the host immune response. Conversely, it triggers the induction of the immune response, a process vital to the host’s defence against infection. Adhesins are microbial cell surface molecules or structures that mediate the attachment of the microbe to host cells and thus the host–pathogen interaction. They also play a crucial role in bacterial aggregation and biofilm formation. In this review, we discuss the role of adhesins in the pathogenesis of the aetiological agent of tuberculosis, Mycobacterium tuberculosis. We also provide insight into the structure and characteristics of some of the characterized and putative M. tuberculosis adhesins. Finally, we examine the potential of adhesins as targets for the development of tuberculosis control strategies.

scholarly journals Role of cytoskeleton in plant cell wall formation

2020 ◽  
Vol 50 (2) ◽  
pp. 176-186
Author(s):  
Yi MAN ◽  
RuiLi LI ◽  
YuFen BU ◽  
Na SUN ◽  
YanPing JING ◽  
...  
Keyword(s):  
Cell Wall ◽  
Plant Cell ◽  
Plant Cell Wall ◽  
Cell Wall Formation ◽  
Wall Formation

scholarly journals Sheep Digestive Physiology and Constituents of Feeds

2021 ◽  
Author(s):  
Samir Medjekal ◽  
Mouloud Ghadbane
Keyword(s):  
Cell Wall ◽  
Plant Cell ◽  
Plant Cell Wall ◽  
Early Stage ◽  
Growth Period ◽  
Cell Plate ◽  
Soluble Carbohydrates ◽  
Winter Period ◽  
The Common

Sheep have a gastrointestinal tract similar to that of other ruminants. Their stomach is made up of four digestive organs: the rumen, the reticulum, the omasum and the abomasum. The rumen plays a role in storing ingested foods, which are fermented by a complex anaerobic rumen microbiota population with different types of interactions, positive or negative, that can occur between their microbial populations. Sheep feeding is largely based on the use of natural or cultivated fodder, which is exploited in green by grazing during the growth period of the grass and in the form of fodder preserved during the winter period. Ruminant foods are essentially of plant origin, and their constituents belong to two types of structures: intracellular constituents and cell wall components. Cellular carbohydrates play a role of metabolites or energy reserves; soluble carbohydrates account for less than 10% dry matter (DM) of foods. The plant cell wall is multi-layered and consists of primary wall and secondary wall. Fundamentally, the walls are deposited at an early stage of growth. A central blade forms the common boundary layer between two adjacent cells and occupies the location of the cell plate. Most of the plant cell walls consist of polysaccharides (cellulose, hemicellulose and pectic substances) and lignin, these constituents being highly polymerized, as well as proteins and tannins.

Impact of plant cell wall network on biodegradation in soil: Role of lignin composition and phenolic acids in roots from 16 maize genotypes

2011 ◽  
Vol 43 (7) ◽  
pp. 1544-1552 ◽  
Author(s):  
Gaylord Erwan Machinet ◽  
Isabelle Bertrand ◽  
Yves Barrière ◽  
Brigitte Chabbert ◽  
Sylvie Recous
Keyword(s):  
Cell Wall ◽  
Plant Cell ◽  
Phenolic Acids ◽  
Plant Cell Wall ◽  
Maize Genotypes ◽  
Lignin Composition ◽  
Biodegradation In Soil

scholarly journals Induction of Fusarium lytic Enzymes by Extracts from Resistant and Susceptible Cultivars of Pea (Pisum sativum L.)

Pathogens ◽  
2020 ◽  
Vol 9 (11) ◽  
pp. 976
Author(s):  
Lakshmipriya Perincherry ◽  
Chaima Ajmi ◽  
Souheib Oueslati ◽  
Agnieszka Waśkiewicz ◽  
Łukasz Stępień
Keyword(s):  
Cell Wall ◽  
Plant Extracts ◽  
Plant Cell Wall ◽  
Pathogenic Fungi ◽  
Human Beings ◽  
Cell Wall Degrading Enzymes ◽  
Lytic Enzymes ◽  
Mycelium Growth ◽  
Oat Bran

Being pathogenic fungi, Fusarium produce various extracellular cell wall-degrading enzymes (CWDEs) that degrade the polysaccharides in the plant cell wall. They also produce mycotoxins that contaminate grains, thereby posing a serious threat to animals and human beings. Exposure to mycotoxins occurs through ingestion of contaminated grains, inhalation and through skin absorption, thereby causing mycotoxicoses. The toxins weaken the host plant, allowing the pathogen to invade successfully, with the efficiency varying from strain to strain and depending on the plant infected. Fusariumoxysporum predominantly produces moniliformin and cyclodepsipeptides, whereas F. proliferatum produces fumonisins. The aim of the study was to understand the role of various substrates and pea plant extracts in inducing the production of CWDEs and mycotoxins. Additionally, to monitor the differences in their levels when susceptible and resistant pea plant extracts were supplemented. The cultures of F. proliferatum and F. oxysporum strains were supplemented with various potential inducers of CWDEs. During the initial days after the addition of substrates, the fungus cocultivated with pea extracts and other carbon substrates showed increased activities of β-glucosidase, xylanase, exo-1,4-glucanase and lipase. The highest inhibition of mycelium growth (57%) was found in the cultures of F. proliferatum strain PEA1 upon the addition of cv. Sokolik extract. The lowest fumonisin content was exhibited by the cultures with the pea extracts and oat bran added, and this can be related to the secondary metabolites and antioxidants present in these substrates.

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