Light and electron microscopy of teliospores and teliospore germination in the rust fungus Coleosporium ipomoeae

2005 ◽  
Vol 83 (5) ◽  
pp. 451-458 ◽  
Author(s):  
C W Mims ◽  
E A Richardson
Keyword(s):  
Electron Microscopy ◽  
Rust Fungus ◽  
Fungal Spores ◽  
Light And Electron Microscopy ◽  
Spore Wall ◽  
Morning Glory ◽  
Extracellular Material ◽  
Teliospore Germination ◽  
Transmission Electron ◽  
Ipomoea Coccinea

A combination of light, scanning, and transmission electron microscopy was used to examine teliospores and teliospore germination in the rust fungus Coleosporium ipomoeae (Schw.) Burrill, a parasite of the wild morning glory Ipomoea coccinea L. Telia developed on abaxial surfaces of infected leaves and appeared as orange, waxy crusts usually associated with uredinia. Mature teliospores were cylindrical to slightly clavate in shape and thin-walled. The presence of chitin in the spore wall was demonstrated using wheat germ agglutinin gold labeling. Teliospores were surrounded by an electron-dense extracellular material. Each spore possessed a large prominent nucleus containing synaptonemal complexes indicative of prophase I meiotic nuclei. Following hydration, the nucleus of each spore completed meiosis and the spore was divided into four uninucleate compartments by the formation of three transverse septa. Each compartment gave rise to a germ tube into which the nucleus and cytoplasm migrated. Germ tubes developed into long slender sterigmata that grew through the extracellular material within the telium to become exposed on the leaf surface. A basidiospore then developed at the tip of each sterigma. Once the nucleus moved from the sterigma into the spore, a septum formed to delimit the spore from the tip of the sterigma.Key words: fungal spores, transmission and scanning electron microscopy, high pressure freezing.

Light and Electron Microscopy of Teliospores and Teliospore Germination in the Rust Fungus Coleosporium ipomoeae

2004 ◽  
Vol 10 (S02) ◽  
pp. 1446-1447
Author(s):  
Charles W. Mims ◽  
Elizabeth A. Richardson
Keyword(s):  
Electron Microscopy ◽  
Rust Fungus ◽  
Light And Electron Microscopy ◽  
Teliospore Germination

Extended abstract of a paper presented at Microscopy and Microanalysis 2004 in Savannah, Georgia, USA, August 1–5, 2004.

Investigation of Tickborne Pathogens within Naturally Infected Brown Dog Tick (Ixodidae: Rhipicephalus Sanguineus) in Egypt by Light and Electron Microscopy

2020 ◽  
Keyword(s):  
Electron Microscopy ◽  
Salivary Gland ◽  
Light And Electron Microscopy ◽  
Rhipicephalus Sanguineus ◽  
Mammalian Host ◽  
Babesia Canis ◽  
Brown Dog Tick ◽  
Transmission Electron ◽  
Dog Tick ◽  
Theileria Spp

Tick borne pathogens present a significant health challenge to animals and human because a single tick may transmit multiple pathogens to a mammalian host during feeding. The present study detected tick-borne pathogens from pet dogs. A total of 666 ticks were collected from 144 pet and sheltered dogs in Egypt from April to September 2018. For hemolymph, midgut and salivary gland smears 546 ticks were used as well as 360 egg smears from 120 female tick were examined by light microscope. The infected ticks were prepared for transmission electron microscopy (TEM). Ticks were identified; Rhipicephalus sanguineus. Light microscopy showed infection rates of 44.69%, 68.50% & 15.75%, in hemolymph, midgut and salivary gland, respectively. H. canis recorded the highest rates in hemolymph and midgut (35.89% & 49.82%, respectively), but Theileria spp. was the lowest (0.73% & 2.93%, respectively). In salivary gland smears, Babesia canis. was detected in 13.55% and Theileria spp. in 1.83%. Mixed infection in same tick was recorded in 4.76% &0.37% in midgut and salivary gland smears, respectively. Babesia canis stages were recovered from 15% of egg smears. R. sanguineus was natural infected by Babesia, Theileria, Hepatozoon and Anaplasma phagocytophilum as well as mixed infections of protozoa accompanied by a complicated sign of diseases and failure in accurate diagnosis.

scholarly journals Localization of ‘Candidatus Liberibacter solanacearum’ and Evidence for Surface Appendages in the Potato Psyllid Vector

2016 ◽  
Vol 106 (2) ◽  
pp. 142-154 ◽  
Author(s):  
J. M. Cicero ◽  
T. W. Fisher ◽  
J. K. Brown
Keyword(s):  
Electron Microscopy ◽  
Light And Electron Microscopy ◽  
Fluorescence Labeling ◽  
Potato Psyllid ◽  
Bactericera Cockerelli ◽  
Visual Identification ◽  
Transmission Electron ◽  
Candidatus Liberibacter ◽  
Identification Of Bacteria

The potato psyllid Bactericera cockerelli is implicated as the vector of the causal agent of zebra chip of potato and vein-greening of tomato diseases. Until now, visual identification of bacteria in the genus ‘Candidatus Liberibacter’ has relied on direct imaging by light and electron microscopy without labeling, or with whole-organ fluorescence labeling only. In this study, aldehyde fixative followed by a coagulant fixative, was used to process adult psyllids for transmission electron microscopy (TEM) colloidal gold in situ hybridization experiments. Results indicated that ‘Ca. Liberibacter solanacearum’ (CLso)-specific DNA probes annealed to a bacterium that formed extensive, monocultural biofilms on gut, salivary gland, and oral region tissues, confirming that it is one morphotype of potentially others, that is rod-shaped, approximately 2.5 µm in diameter and of variable length, and has a rough, granular cytosol. In addition, CLso, prepared from shredded midguts, and negatively stained for TEM, possessed pili- and flagella-like surface appendages. Genes implicating coding capacity for both types of surface structures are encoded in the CLso genome sequence. Neither type was seen for CLso associated with biofilms within or on digestive organs, suggesting that their production is stimulated only in certain environments, putatively, in the gut during adhesion leading to multiplication, and in hemolymph to afford systemic invasion.

scholarly journals Ultrastructural analysis of the spermatogenesis in the guinea pig (Cavia porcellus)

2016 ◽  
Vol 36 (suppl 1) ◽  
pp. 89-94 ◽  
Author(s):  
Luciana S. Simões ◽  
Rose E.G. Rici ◽  
Phelipe O. Favaron ◽  
Taís Harumi de Castro Sasahara ◽  
Rodrigo S.N. Barreto ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Guinea Pig ◽  
Sexual Development ◽  
Morphological Changes ◽  
Light And Electron Microscopy ◽  
Management Systems ◽  
Cavia Porcellus ◽  
Reproductive Parameters ◽  
Development Stages ◽  
Transmission Electron

Abstract: al for both, the establishment of appropriate management systems, and for the use of new species as animal models. In this study, we used light and electron microscopy to characterize the sexual development stages of the guinea pig (Cavia porcellus) in specimens of 30, 45 and 90 days of age. We observed the differentiation of spermatocytes only through transmission electron microscopy in the leptotene, zygotene and pachytene phases of meiosis, in 30-day-old animals. During puberty, there was differentiation of the germinative epithelium and formation of the acrosome. Spermatozoa, however, were not detected. Thus, we could infer that puberty happens after 45 days of age. Sexual maturity was evident in 90-day-old specimens. Our results showed that changes in the testicular germinative epithelium during the postnatal sexual development in guinea pig led to morphological changes, including the ones related to the development of Leydig and Sertoli cells, which are directly related to puberty. In this work, we provide new morphological subsidies for a better understanding of reproductive parameters of this species, enabling its use as an animal model in the field of the reproductive biology.

scholarly journals The osmium tetroxide-p-phenylenediamine procedure reveals the chromatid cores and kinetochores of meiotic chromosomes by light and electron microscopy.

1996 ◽  
Vol 44 (11) ◽  
pp. 1279-1288 ◽  
Author(s):  
C Antonio ◽  
J M González-García ◽  
J Page ◽  
J A Suja ◽  
J C Stockert ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Reaction Mechanism ◽  
Osmium Tetroxide ◽  
Light And Electron Microscopy ◽  
X Ray ◽  
Meiotic Chromosomes ◽  
Transmission Electron ◽  
Ethanol Acetic Acid ◽  
Electron Imaging ◽  
Z Contrast

We analyzed first-metaphase meiotic chromosomes of the grasshopper Chorthippus jucundus by two different methods, i.e., a silver impregnation technique and the osmium tetroxide-p-phenylenediamine (Os-PPD) procedure. The former was applied on squashed testes previously fixed in ethanol-acetic acid, whereas for Os-PPD the material was not subjected to any previous extraction treatment but was fixed in OsO4, treated with PPD, and embedded in Epon 812. Both techniques revealed chromatid cores and kinetochores regardless of the processing of the material (squashed or sectioned). Unstained Os-PPD sections were analyzed by light microscopy and transmission electron microscopy (TEM). The Os-PPD technique provided a high contrast of chromatid cores and kinetochores in relation to the chromatin, which revealed a low electron density. To determine the Os-PPD reaction mechanism, the PAS procedure, as well as scanning electron microscopy (SEM) backscattering and SEM X-ray microanalysis, was performed on sections. By use of the Os-PPD-PAS procedure, glycol groups formed by oxidation of osmium bound to aromatic substrates were detected in chromatid cores and kinetochores by brightfield and fluorescence microscopy. A high Z contrast was detected in these structures by backscattered electron imaging. SEM X-ray microanalysis showed osmium and phosphorus to be the main elements present on the chromatid cores. Taking into account the known reactivity of OsO4 and the present results, the possible participation of nucleic acids as well as proteins in the Os-PPD reaction mechanism and in the composition of chromatid cores and kinetochores is discussed.

Ultrastructure of freeze-substituted appressoria produced by aeciospore germlings of the rust fungus Arthuriomyces peckianus

1991 ◽  
Vol 69 (8) ◽  
pp. 1655-1665 ◽  
Author(s):  
E. C. Swann ◽  
C. W. Mims
Keyword(s):  
Electron Microscopy ◽  
Plasma Membrane ◽  
Key Words ◽  
Direct Contact ◽  
Germ Tube ◽  
Rust Fungus ◽  
Mitotic Division ◽  
Extracellular Material ◽  
Dialysis Membrane ◽  
Fungus Infection

Aeciospores of Arthuriomyces peckianus germinated readily on moist strips of dialysis membrane and developing appressoria were observed within 3 to 6 h after spores were deposited on membranes. A single germ tube typically emerged from each binucleate spore and grew until its tip contacted the dialysis membrane. The germ tube tip was then transformed into a swollen appressorium that adhered tightly to the membrane, apparently as a result of an extracellular material that surrounded the appressorium base. Virtually all the spore cytoplasm and both nuclei moved into the germ tube and developing appressorium. Following a synchronous mitotic division of the two nuclei, a septum formed to delimit the now tetranucleate appressorium from the germ tube. As the appressorium matured, an apparently wall-less region developed in the central portion of the appressorium appressed against the dialysis membrane. In this region the fungus plasma membrane appeared to make direct contact with the underlying dialysis membrane. A funnel-like or cone-like structure referred to as the appressorial cone then developed in the wall-less region. The appressorial cone extended up into the cytoplasm of the appressorium and was lined by the fungal plasma membrane. Numerous branched elaborations of the plasma membrane were associated with the inner portion of the cone. Key words: rust fungus, infection structures, electron microscopy.

Teliospore wall structure in Entorrhiza (Tilletiaceae) and its relationship to taxonomy of the genus

1992 ◽  
Vol 70 (10) ◽  
pp. 1964-1983 ◽  
Author(s):  
Brian A. Fineran ◽  
Judith M. Fineran
Keyword(s):  
Electron Microscopy ◽  
Outer Zone ◽  
Spore Wall ◽  
Wall Structure ◽  
Dense Matrix ◽  
Thin Sections ◽  
Transmission Electron ◽  
Layer 2 ◽  
Layer 4 ◽  
Freeze Etching

Spore wall organization in the five species of Entorrhiza (Ustilaginales) has been investigated using thin sections for transmission electron microscopy, supported by light and scanning electron microscopy and some freeze-etching. Material was examined from herbaria, specimens preserved in fixative, and fresh host tissue. The wall has four main layers, numbered 1–4 from the outside to inside of the wall; some layers are further differentiated into zones. Layer 1 in E. aschersoniana, E. caspaiyana, and E. caricicola has two zones: a broad outer zone 2 of dense matrix and a narrow inner zone 1 of less compacted material. Zone 1 is absent in E. cypericola. In E. scirpicola, layer 1 is represented by discontinuous longitudinal ridges. In all spores, layer 2 is composed of a homogeneous electron-dense matrix. Layer 1 in E. aschersoniana, E. casparyana, and E. caricicola is uniformly thick, but in E. cypericola it is broad with an irregular outer margin. In E. scirpicola, layer 2 is differentiated into a distinctive pattern of longitudinal ribs. In all spores of Entorrhiza, layer 3 is resolvable into fine lamellae, corresponding to the mosaic of striations seen after freeze-etching. Layer 3 in Entorrhiza is equivalent to the partition layer described in other Tilletiaceae. Layer 4 has the same organization in all the species, consisting of a very narrow zone 2 abutting layer 3 and a broad zone 1 that forms the rest of the layer. Based on wall structure, E. aschersoniana and E. casparyana represent the most closely related species, followed by E. caricicola, with E. cypericola more distant again. Entorrhiza scirpicola is considered the least related of the species; only its layers 3 and 4 resemble the other species. Key words: Entorrhiza, Tilletiaceae, spore wall ultrastructure, species relationships.

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