Ultrastructure of sperm development in the genus Ditylenchus (Nematoda: Anguinidae)

Nematology ◽  
2015 ◽  
Vol 17 (3) ◽  
pp. 313-324 ◽  
Author(s):  
Dieter Slos ◽  
Pooria Ensafi ◽  
Myriam Claeys ◽  
Vladimir V. Yushin ◽  
Wilfrida Decraemer ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Outer Membrane ◽  
Higher Plants ◽  
Transmission Electron ◽  
Sperm Development ◽  
Ditylenchus Dipsaci ◽  
Mature Spermatozoa ◽  
Formation Of Complexes

Spermatogenesis in Ditylenchus arachis and D. dipsaci was studied using transmission electron microscopy. Spermatogenesis includes the formation of complexes of fibrous bodies (FB) and membranous organelles (MO) in the spermatocytes, which dissociate in separated MO and FB in the spermatids. Immature spermatozoa are unpolarised cells with separate FB and MO. Mature spermatozoa are arranged in chains. Ditylenchus dipsaci is unique in having MO that have already fused with the outer membrane in immature spermatozoa and have mature spermatozoa in the male testis, proving that not only insemination plays a role in spermiogenesis. Contrary to what has been described before, spermatogenesis in Ditylenchus, and other early diverging Tylenchomorpha, follow the typical ‘rhabditid’ pattern, while the absence of MO within Tylenchomorpha appears to be an apomorphic trait for the molecular defined clade of tylenchids that exclusively parasitise higher plants. This confirms the value of traits related to spermatogenesis in nematode phylogeny.

The comparative ultrastructure of spermatozoa from Bothrimonus sturionis Duv. 1842 (Pseudophyllidea), Pseudanthobothrium hanseni Baer, 1956 (Tetraphyllidea), and Monoecocestus americanus Stiles, 1895 (Cyclophyllidea)

1984 ◽  
Vol 62 (6) ◽  
pp. 1059-1066 ◽  
Author(s):  
Barbara M. MacKinnon ◽  
Michael D. B. Burt
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Plasma Membrane ◽  
Main Body ◽  
Posterior Portion ◽  
Transmission Electron ◽  
Dense Nucleus ◽  
Comparative Ultrastructure ◽  
Electron Lucent ◽  
Mature Spermatozoa

The mature spermatozoa from Bothrimonus sturionis (Pseudophyllidea), Pseudanthobothrium hanseni (Tetraphyllidea), and Monoecocestus americanus (Cyclophyllidea) were examined using transmission electron microscopy. Transverse sections of the sperm of B. sturionis indicate that the number of sperm axonemes varies from one to eight, with approximately one-third of the sperm containing two axonemes. Likewise, the number of peripheral microtubules lying just within the external plasma membrane varies from 12 to 20. The nucleus is electron lucent and fibrous in appearance. The spermatozoa of B. sturionis show great variation in the material examined and the majority of them are believed to be aberrant. The spermatozoon of P. hanseni contains a single axoneme with the nucleus wrapped in a crescent around it in the anterior region of the sperm. The posterior portion of the spermatozoon is characterized by a helical flange which projects from the main body of the sperm. The spermatozoon of M. americanus is elongate and slender, containing a single axoneme with an electron-dense nucleus coiled around it in the anterior one-third of the sperm. Electron-opaque bodies, which may be glycogen, fill the cytoplasm. The spermatozoa of all three species contain neither an acrosome nor mitochondria. The flagella of all the spermatozoa have a 9 + "1" arrangement of microtubules. The importance of the ultrastructure of spermatozoa in the phylogeny and taxonomy of cestodes is discussed.

scholarly journals Isolation and Characterization of Outer Membrane Vesicles of Pectobacterium brasiliense 1692

2021 ◽  
Vol 9 (9) ◽  
pp. 1918
Author(s):  
Silindile Maphosa ◽  
Lucy Novungayo Moleleki
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Outer Membrane ◽  
Critical Role ◽  
Membrane Vesicles ◽  
Outer Membrane Vesicles ◽  
Broad Host Range ◽  
Isolation And Characterization ◽  
Transmission Electron ◽  
Animal Pathogens

Pectobacterium brasiliense (Pbr) 1692 is an aggressive phytopathogen affecting a broad host range of crops and ornamental plants, including potatoes. Previous research on animal pathogens, and a few plant pathogens, revealed that Outer Membrane Vesicles (OMVs) are part of Gram-negative bacteria’s (GNB) adaptive toolkit. For this reason, OMV production and subsequent release from bacteria is a conserved process. Therefore, we hypothesized that OMVs might transport proteins that play a critical role in causing soft rot disease and in the survival and fitness of Pbr1692. Here, we show that the potato pathogen, Pbr1692, releases OMVs of various morphologies in Luria Bertani media at 31 °C. Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) confirmed the production of OMVs by Pbr1692 cells. Transmission Electron Microscopy showed that these exist as chain-, single-, and double-membrane morphologies. Mass spectrometry followed by Gene Ontology, Clusters of Orthologous Groups, Virulence Factor, CAZymes, Antibiotic Resistance Ontology, and Bastion6 T6SE annotations identified 129 OMV-associated proteins with diverse annotated roles, including antibiotic stress response, virulence, and competition. Pbr1692 OMVs contributed to virulence in potato tubers and elicited a hypersensitive response in Nicotiana benthamiana leaves. Furthermore, Pbr1692 OMVs demonstrated antibacterial activity against Dickeya dadantii.

Centromere structure and chromosome number in mitosis of the colourless phytoflagellate Polytoma papillatum (Chlorophyceae, Volvocales, Chlamydomonadaceae)

Genome ◽  
1995 ◽  
Vol 38 (6) ◽  
pp. 1249-1254 ◽  
Author(s):  
Klaus Werner Wolf
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Chromosome Number ◽  
Higher Plants ◽  
Attachment Site ◽  
Dense Layer ◽  
Mitotic Metaphase ◽  
Serial Sections ◽  
Transmission Electron ◽  
Alternative Approach

Centromere structure is described in mitosis of the unicellular biflagellate alga Polytoma papillatum using transmission electron microscopy. The kinetochores are five-layered elements at the poleward surface of the chromosomes. The five layers consist of three dense plates interspersed by two transparent zones. The polemost dense layer serves as the attachment site for kinetochore microtubules and the innermost dense layer is intimately associated with the chromatin. The five-layered organization of the kinetochore in the alga is unusual. In animals, three-layered kinetochores are the rule. This type has also been found in some algae, while higher plants do not possess striated kinetochores. An attempt was made to determine the chromosome number of P. papillatum. Individual chromosomes could not be recognized with confidence, since there were numerous lateral contacts between the chromosomes throughout mitosis. An alternative approach, however, was successful. Counting the kinetochores in serial sections through mitotic metaphase and anaphase plates revealed a number of 15 chromosomes.Key words: anaphase, kinetochore, metaphase, microtubule.

Topography and Ultrastructure of the tegument of adultSchistosoma mekongi

Parasitology ◽  
1984 ◽  
Vol 89 (3) ◽  
pp. 511-521 ◽  
Author(s):  
P. Sobhon ◽  
E. S. Upatham ◽  
Diane J. McLaren
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Outer Membrane ◽  
Inclusion Bodies ◽  
Unique Feature ◽  
Basal Membrane ◽  
The Body ◽  
Transmission Electron ◽  
Schistosoma Mekongi ◽  
Membrane Infoldings

SUMMARYThe tegument of adultSchistosoma mekongihas been studied by both scanning and transmission electron microscopy. The gross surface topography of the parasite resembles that ofS. japonicum, in that branched ridges, microvilli and sensory papillae predominate; such characteristics distinguish these two species from the non-oriental schistosomes. A unique feature ofS. mekongi, however, is the numerous pleomorphic protruberances which are concentrated particularly on the middle three-fourths of the body surface. Transmission electron microscopy has revealed that these protruberances enclose bundles of microfilaments which appear to insert into the tegumental outer membrane. The microfilaments are suggested to have a supportive or stabilizing function, and may compensate for the absence of more typical crystalline spines. The tegumental outer membrane is typically heptalaminate in section, while the basal membrane infoldings are surrounded by concentrations of mitochondria. Three types of tegumental inclusion bodies have been recognized. Discoid bodies and membraneous bodies are morphologically identical to those described in all other schistosome species, except that the latter inclusions have been seen connected to each other and to the tegumental outer membrane by unique channels lined with trilaminate membrane. The third inclusion takes the form of spherical, lucent vesicles containing membrane fragments; these may represent the remains of spent membraneous bodies.

Tem Study of Wound-Induced Vessel Occlusions in European Ash (Fraxinus Excelsior L.)

IAWA Journal ◽  
1997 ◽  
Vol 18 (4) ◽  
pp. 401-404 ◽  
Author(s):  
Uwe Schmitt ◽  
Hans Georg Richter ◽  
Claudia Muche
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Outer Membrane ◽  
Fraxinus Excelsior ◽  
Axial Parenchyma ◽  
Transmission Electron ◽  
Parenchyma Cells ◽  
Means Of Transmission ◽  
European Ash

Vessel occlusions in branches of Fraxinus excelsior L. were investigated by means of transmission electron microscopy. The vessel occlusions are formed by exudates released from adjacent ray and axial parenchyma cells through the intact pit membranes. Initial stages mostly display balloon- like structures protruding from the pit aperture into the vessellumen. These inclusions possess a very electron dense outer membrane and dispersed exudates in their interior. Therefore, the vessel occlusions in F. excelsior do not represent true tyloses.

Sexual reproduction in Chondrilla australiensis (Porifera:Demospongiae)

2004 ◽  
Vol 55 (2) ◽  
pp. 123 ◽  
Author(s):  
Kayley M. Usher ◽  
David C. Sutton ◽  
Simon Toze ◽  
John Kuo ◽  
Jane Fromont
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Late Summer ◽  
Maximum Height ◽  
Nurse Cells ◽  
Transmission Electron ◽  
Large Numbers ◽  
Wide Range ◽  
Sperm Development ◽  
Entire Matrix

Increasingly, sponges are being used as models for a wide range of biological systems. However, little is known about the reproductive biology of a group that has been shown to lack gonads or gonadal ducts. The development of gametes in the oviparous demosponge Chondrilla australiensis at Fremantle, Western Australia, was investigated using light microscopy and transmission electron microscopy over 5 years. Results indicate that C. australiensis is gonochoric and oviparous. Egg and sperm development were first apparent inside choanocyte chambers, with both types of gamete apparently developing from choanocytes. During egg development, large numbers of nurse cells appeared attached to eggs, with which they fused at the time of spawning. The origin of the nurse cells remains unclear, but they may also have a choanocyte origin. Eggs took 4 weeks to develop and sperm took approximately 2 weeks, during which time the nucleus condensed and the cytoplasm reduced. Mature sperm could occupy almost the entire matrix of fecund males and were not contained in cysts. Spawning occurred in late summer and autumn over a period of 4–5 days, when the tides were at the maximum height for the month.

scholarly journals Immunogold-labelling localization of chlorophyllase at different developmental stages of Pachira macrocarpa leaves

2021 ◽  
Author(s):  
Tzan-Chain Lee ◽  
Kuan-Hung Lin ◽  
Chang-Chang Chen ◽  
Tin-Han Shih ◽  
Meng-Yuan Huang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Cell Wall ◽  
Plasma Membrane ◽  
Thylakoid Membrane ◽  
Developmental Stages ◽  
Higher Plants ◽  
Plant Cells ◽  
Immunogold Labelling ◽  
Transmission Electron

Abstract Background: Chlorophyllases (Chlases) are housekeeping proteins in plant cells. The dephytylating enzymes can catalyze chlorophyll (Chl) to form chlorophyllide, but the distribution of Chlases in plant cells is still an interesting debate. In this study, antibody of PmCLH2 was made and used by immunogold-labelling technique to detect the location of Chlase of Pachira macrocarpa (Pm) leaves at four developmental stages, including young, mature, yellowing, and senesced stages. Results: The transmission electron microscopy results show that Chlases were comprehensively found in portions of chloroplast, such as the inner membrane of the envelope, grana, and the thylakoid membrane of the chloroplast, cytosol, and vacuoles at young, mature, and yellowing stages of Pm leaves, but not in the cell wall, plasma membrane, mitochondria, and nucleus. Conclusions: PmChlases were mainly detected in vacuoles at the senescent stage, but a few were found in the chloroplasts. A pathway is proposed to explain the birth and death of Chl, Chlase, and chloroplasts in higher plants.

A Differential Centrifugation Procedure for Obtaining Unstretched Metaphase Chromosomes from Higher Plants for Transmission Electron Microscopy

1977 ◽  
Vol 35 ◽  
pp. 402-403 ◽  
Author(s):  
Philip S. Woods ◽  
Jack Van't Hof ◽  
Myron C. Ledbetter
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Higher Plants ◽  
Plant Root ◽  
Root Tip ◽  
Natural State ◽  
Differential Centrifugation ◽  
Metaphase Chromosomes ◽  
Transmission Electron ◽  
Water Spreading

Metaphase chromosomes prepared as whole mounts for transmission electron microscopy have been studied by many workers using a variety of methods(1,2,3, 4). While satisfactory for some purposes these methods usually result in distortions which complicate interpretation of chromosome fine structure. In addition, most procedures were adapted for animal chromosomes and were inappropriate for plants in which cell walls present a barrier to isolation. Recently, Wolfe and Martin(5) used a pressing procedure devised by McLeish(6) to obtain plant root tip chromosomes and used this in combination with the water spreading method of Gall(3). Their electron micrographs, though unique in showing plant chromosomes essentially for the first time, nevertheless showed chromosomal distortions typical of water spreading. Chromosomes in the nearly natural state can be obtained by modifying Wolfe and Martin's procedure to the extent of replacing surface spreading with differential centrifugation of the broken-cell suspension.

Techniques for Transmission Electron Microscopy of Fiber-Matrix Interfaces in Aluminum Alloy-Boron Composites by Ion Erosio

1971 ◽  
Vol 29 ◽  
pp. 204-205
Author(s):  
G. G. Shaw
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Aluminum Alloy ◽  
Electron Beam ◽  
Pure Aluminum ◽  
Ion Milling ◽  
Transmission Electron ◽  
Fiber Matrix ◽  
Ion Erosion ◽  
Row Of Fibers

The morphology and composition of the fiber-matrix interface can best be studied by transmission electron microscopy and electron diffraction. For some composites satisfactory samples can be prepared by electropolishing. For others such as aluminum alloy-boron composites ion erosion is necessary.When one wishes to examine a specimen with the electron beam perpendicular to the fiber, preparation is as follows: A 1/8 in. disk is cut from the sample with a cylindrical tool by spark machining. Thin slices, 5 mils thick, containing one row of fibers, are then, spark-machined from the disk. After spark machining, the slice is carefully polished with diamond paste until the row of fibers is exposed on each side, as shown in Figure 1.In the case where examination is desired with the electron beam parallel to the fiber, preparation is as follows: Experimental composites are usually 50 mils or less in thickness so an auxiliary holder is necessary during ion milling and for easy transfer to the electron microscope. This holder is pure aluminum sheet, 3 mils thick.

Direct Observation of Heat Exchanger Deposits by Cross Sectioning

1967 ◽  
Vol 25 ◽  
pp. 364-365
Author(s):  
R. W. Anderson ◽  
D. L. Senecal
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Heat Exchanger ◽  
Direct Observation ◽  
Cross Sections ◽  
Preparation Method ◽  
Specimen Preparation ◽  
Flowing Water ◽  
Transmission Electron ◽  
Deposit Layer

A problem was presented to observe the packing densities of deposits of sub-micron corrosion product particles. The deposits were 5-100 mils thick and had formed on the inside surfaces of 3/8 inch diameter Zircaloy-2 heat exchanger tubes. The particles were iron oxides deposited from flowing water and consequently were only weakly bonded. Particular care was required during handling to preserve the original formations of the deposits. The specimen preparation method described below allowed direct observation of cross sections of the deposit layers by transmission electron microscopy.The specimens were short sections of the tubes (about 3 inches long) that were carefully cut from the systems. The insides of the tube sections were first coated with a thin layer of a fluid epoxy resin by dipping. This coating served to impregnate the deposit layer as well as to protect the layer if subsequent handling were required.

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