INCORPORATION OF CYTIDINE-H3 INTO THE PRIMARY LEAF OF WHEAT FOLLOWING INFECTION WITH PUCCINIA RECONDITA ROB. EX DESM.

1963 ◽  
Vol 41 (10) ◽  
pp. 1501-1508 ◽  
Author(s):  
J. Nielsen ◽  
R. Rohringer
Keyword(s):  
Host Cell ◽  
Ribonucleic Acid ◽  
Host Tissue ◽  
Host Cells ◽  
Puccinia Recondita ◽  
Infected Leaf ◽  
Cell Nuclei ◽  
Short Term ◽  
Wheat Leaves ◽  
Host Parasite

In short-term experiments, cytidine-H3 was fed to rusted and healthy areas of wheat leaves. The incorporated activity, presumably residing in ribonucleic acid, was detected by microautoradiographic methods. Most of the label was found to be incorporated in host cell nuclei. Little incorporation occurred in extranuclear structures of host cells, including chloroplasts. Very long autoradiographic exposure times failed to reveal any incorporation into the fungus.Host cells in infected leaf areas contained considerably less label in their nuclei and cytoplasm than those in cells further from the site of infection. This effect of the fungus extended over some distance into uninvaded host tissue, but not beyond 100 μ from the periphery of the mycelium. The decreased cytidine incorporation in the affected host tissue is not caused by possible changes in pool size of endogenous cytidine. The significance of these results for the host–parasite interaction is briefly discussed.

scholarly journals Drug Discovery for Chagas Disease: Impact of Different Host Cell Lines on Assay Performance and Hit Compound Selection

2019 ◽  
Vol 4 (2) ◽  
pp. 82 ◽  
Author(s):  
Caio Haddad Franco ◽  
Laura Maria Alcântara ◽  
Eric Chatelain ◽  
Lucio Freitas-Junior ◽  
Carolina Borsoi Moraes
Keyword(s):  
Drug Discovery ◽  
Host Cell ◽  
Cell Lines ◽  
Chagas Disease ◽  
Host Cells ◽  
Mammalian Cell Lines ◽  
Starting Point ◽  
Disease Impact ◽  
Screening Assays ◽  
Host Parasite

Cell-based screening has become the major compound interrogation strategy in Chagas disease drug discovery. Several different cell lines have been deployed as host cells in screening assays. However, host cell characteristics and host-parasite interactions may play an important role when assessing anti-T. cruzi compound activity, ultimately impacting on hit discovery. To verify this hypothesis, four distinct mammalian cell lines (U2OS, THP-1, Vero and L6) were used as T. cruzi host cells in High Content Screening assays. Rates of infection varied greatly between different host cells. Susceptibility to benznidazole also varied, depending on the host cell and parasite strain. A library of 1,280 compounds was screened against the four different cell lines infected with T. cruzi, resulting in the selection of a total of 82 distinct compounds as hits. From these, only two hits were common to all four cell lines assays (2.4%) and 51 were exclusively selected from a single assay (62.2%). Infected U2OS cells were the most sensitive assay, as 55 compounds in total were identified as hits; infected THP-1 yielded the lowest hit rates, with only 16 hit compounds. Of the selected hits, compound FPL64176 presented selective anti-T. cruzi activity and could serve as a starting point for the discovery of new anti-chagasic drugs.

THE PHYSIOLOGY OF HOST–PARASITE RELATIONS: XVIII. DISTRIBUTION OF TRITIUM-LABELLED CYTIDINE, URIDINE, AND LEUCINE IN WHEAT LEAVES INFECTED WITH THE STEM RUST FUNGUS

1967 ◽  
Vol 45 (5) ◽  
pp. 555-563 ◽  
Author(s):  
P. K. Bhattacharya ◽  
Michael Shaw
Keyword(s):  
Stem Rust ◽  
Rust Fungus ◽  
Host Cells ◽  
Fungal Mycelium ◽  
Puccinia Graminis ◽  
Mesophyll Cells ◽  
Wheat Leaves ◽  
Host Parasite

Wheat leaves were detached 6 days after inoculation with the stem rust fungus (Puccinia graminis var. tritici Erikss. and Henn.) and fed with tritiated leucine, cytidine, uridine, or thymidine. Mesophyll cells in infected zones incorporated more leucine into protein and more cytidine and uridine into RNA than did cells in adjacent uninfected tissue. Leucine, cytidine, and uridine were also heavily incorporated by fungal mycelium and developing uredospores. Grain counts over host nuclei in the infected zone were two to three-fold of those over nuclei in adjacent uninfected zones. There was no detectable incorporation of thymidinemethyl-3H into either the fungus or the host cells. The results are discussed.

Ultrastructure of the Host-Parasite Relationships of Pseudoperonospora humuli on Hops

1977 ◽  
Vol 25 (6) ◽  
pp. 585 ◽  
Author(s):  
RD Pares ◽  
AD Greenwood
Keyword(s):  
Leaf Tissue ◽  
Host Cells ◽  
Wall Structure ◽  
Infected Leaf ◽  
Cell Penetration ◽  
Pseudoperonospora Humuli ◽  
Host Cell Wall ◽  
Staining Techniques ◽  
Host Parasite ◽  
Infected Leaf Tissue

Infected leaf tissue was examined at 3, 4, 5 and 6 days after inoculation, after different fixing and staining techniques. One example of stomata1 penetration was seen. Examples of cell penetration and haustorium development were examined in detail. Haustoria penetrate host cells by altering host cell wall structure, and lomasomes are frequently present in the haustorium neck. Haustoria do not have nuclei and in early stages have abundant mitochondria that gradually decrease in number as infection advances.

INCORPORATION OF P32 INTO RIBONUCLEIC ACID OF RUSTED WHEAT LEAVES

1961 ◽  
Vol 39 (2) ◽  
pp. 263-267 ◽  
Author(s):  
R. Rohringer ◽  
R. Heitefuss
Keyword(s):  
Ribonucleic Acid ◽  
Rna Synthesis ◽  
Specific Activity ◽  
Leaf Material ◽  
Resistant Reaction ◽  
Wheat Leaves ◽  
Host Parasite ◽  
Parasite Complex ◽  
Metabolic Significance

P32-labelled orthophosphate was fed to rusted and non-rusted wheat leaves. The ribonucleic acid (RNA) isolated from this material was purified and its specific activity determined. The specific activity of RNA from susceptible reacting tissue had increased 60–208% [Formula: see text] days after inoculation, but [Formula: see text] days after inoculation it was not markedly different from RNA preparations of uninoculated leaf material, indicating an increase and eventual decline in RNA synthesis of the host–parasite complex. In the resistant reaction incorporation of P32 into the RNA was unaltered by infection. The possible metabolic significance of these observations is discussed.

Cytochemical localization of acid phosphatase in endophyte cells of the semiparasitic angiosperm Comandra umbellata (Santalaceae)

1977 ◽  
Vol 55 (4) ◽  
pp. 470-475 ◽  
Author(s):  
Ronald Toth ◽  
Job Kuijt
Keyword(s):  
Acid Phosphatase ◽  
Host Cell ◽  
Lysosomal Enzymes ◽  
Large Scale ◽  
Turgor Pressure ◽  
Host Cells ◽  
Cytochemical Localization ◽  
Host Cell Membranes ◽  
Host Parasite ◽  
Tip Cells

Acid phosphatase (orthophosphoric-monoester phosphohydrolase (acid optimum), EC 3.1.3.2) has been localized in cells at the growing tips of the endophyte in the semiparasitic angiosperm Comandra umbellata. Lysosomes in tip cells release their contents into the apoplast at the host–parasite interface before any possible release of enzyme from disrupted host lysosomes. However, a large-scale digestion of host cells does not occur. Parasite cells release acid phosphatase and probably other lysosomal enzymes which appear to disrupt host cell membranes causing a loss in turgor pressure followed by the eventual crushing of host cells by the invading endophyte.

Host – parasite relationships between the fungus Leptosphaerulina crassiasca and peanut

1992 ◽  
Vol 70 (9) ◽  
pp. 1724-1733 ◽  
Author(s):  
Mei-Lee Wu ◽  
Richard T. Hanlin
Keyword(s):  
Cell Wall ◽  
Host Cell ◽  
Germ Tube ◽  
Light And Electron Microscopy ◽  
Host Cells ◽  
Detached Leaves ◽  
Host Cell Wall ◽  
Host Parasite ◽  
Germ Tubes ◽  
Infection Hypha

The mode of penetration and infection of the peanut leaf by Leptosphaerulina crassiasca were studied by means of light and electron microscopy. The attachment of the multicellular ascospores to the leaf surface was by a mucilagenous sheath that covered the ascospores at maturity. This sheath expanded rapidly in moisture and it extended along the germ tube as it elongated. Two types of germ tubes appeared to be formed, a short one and a relatively long one. Short germ tubes were not delimited by septa, and they penetrated the cuticle and host epidermal cell wall directly without appressorium formation. Penetration occurred 2–6 h after inoculation. The wall was breached by a relatively broad infection hypha that expanded in width inside the host cell wall. The lack of mechanical rupture at the infection site indicated that penetration may involve enzymatic activity. Intracellular hyphae were present in the epidermal cells, but only intercellular hyphae occurred in the palisade and spongy mesophyll tissues. The intercellular hyphae were frequently appressed to the outer surface of the host cell wall. Infected areas rarely exceeded 1 mm in diameter, and they were only sparsely colonized by hyphae of the pathogen. Host cells in the vicinity of hyphae underwent senescence and death. One to 2 months after inoculation, pseudothecia formed in the dead tissues of detached leaves. In some instances the presence of penetration hyphae by short germ tubes induced the formation of a papilla inside the host cell wall, which either restricted growth of the infection hypha or resulted in the death of the germ tube and the cell from which it arose. Long germ tubes were delimited by simple septa and they terminated in an appressorium; however, details of their behavior were not studied. Key words: Arachis hypogaea, Ascomycotina, Dothideales, leaf scorch, pepper spot.

THE PHYSIOLOGY OF HOST–PARASITE RELATIONS: III. THE PATTERN OF RESPIRATION IN RUSTED AND MILDEWED CEREAL LEAVES

1957 ◽  
Vol 35 (3) ◽  
pp. 389-407 ◽  
Author(s):  
Michael Shaw ◽  
D. J. Samborski
Keyword(s):  
Oxygen Uptake ◽  
Dry Weight ◽  
Significant Negative Correlation ◽  
Pentose Phosphate ◽  
Host Tissue ◽  
Infected Tissue ◽  
Short Term ◽  
Pasteur Effect ◽  
Host Parasite ◽  
Leaf Disks

The first leaves of resistant (Khapli) and susceptible (Little Club) species of wheat were heavily inoculated with stem rust (Race 15B). After infection, oxygen consumption per unit dry weight increased two- to three-fold and then fell off again. The R.Q. remained close to 1.0 until the respiratory peak was reached and then declined to 0.80 to 0.85, at least in Khapli. The INR/OR values (approximately 1.2) suggest the operation of a Pasteur effect in uninfected tissue. With infected tissue there was little or no increase in NR as oxygen uptake rose and the INR/OR values declined steadily to about 0.2 to 0.3. The oxygen uptake of rusted, mildewed, and uninfected tissue was stimulated by 2,4-dinitrophenol. The percentage stimulation was reduced by infection. The smallest percentage stimulations were observed, after the respiratory peak had been passed, with infected tissue of Khapli, in which chlorosis and other degenerative changes developed quickly. The actual increases in oxygen uptake obtained with 10−5 M dinitrophenol were about the same for infected as for uninfected tissue, but, in Khapli, fell sharply after the respiratory maximum. Leaf-disks were incubated separately with glucose-1-C14, glucose-6-C14, and glucose-UL-C14, and the relative activities of the carbon dioxide produced were measured. The C6/C1 ratio showed a significant negative correlation with the oxygen uptake of rusted tissue, suggesting that the pentose phosphate pathway is of increased importance in infected tissue. The C6/C1 ratio was also reduced in the host tissue at the loci of mildew infections. In short term experiments dinitrophenol raised the C6/C1 ratio. The significance of the results is discussed and it is concluded that infection with rust or mildew not only raises the respiration rate but alters the pathway of respiration in the host tissue.

scholarly journals Utilization of Host Cell Chromosome Conformation by Viral Pathogens: Knowing When to Hold and When to Fold

2021 ◽  
Vol 12 ◽  
Author(s):  
Kinjal Majumder ◽  
Abigail J. Morales
Keyword(s):  
Host Cell ◽  
Nuclear Dna ◽  
Life Cycles ◽  
Host Genome ◽  
Host Cells ◽  
Cell Nuclei ◽  
Chromosome Conformation ◽  
Dna Viruses ◽  
Viral Genomes ◽  
Virus Expression

Though viruses have their own genomes, many depend on the nuclear environment of their hosts for replication and survival. A substantial body of work has therefore been devoted to understanding how viral and eukaryotic genomes interact. Recent advances in chromosome conformation capture technologies have provided unprecedented opportunities to visualize how mammalian genomes are organized and, by extension, how packaging of nuclear DNA impacts cellular processes. Recent studies have indicated that some viruses, upon entry into host cell nuclei, produce factors that alter host chromatin topology, and thus, impact the 3D organization of the host genome. Additionally, a variety of distinct viruses utilize host genome architectural factors to advance various aspects of their life cycles. Indeed, human gammaherpesviruses, known for establishing long-term reservoirs of latent infection in B lymphocytes, utilize 3D principles of genome folding to package their DNA and establish latency in host cells. This manipulation of host epigenetic machinery by latent viral genomes is etiologically linked to the onset of B cell oncogenesis. Small DNA viruses, by contrast, are tethered to distinct cellular sites that support virus expression and replication. Here, we briefly review the recent findings on how viruses and host genomes spatially communicate, and how this impacts virus-induced pathology.

Effect of blasticidin S, ethionine, and polyoxin D on stem rust development and host-cell necrosis in wheat near-isogenic for gene Sr6

1977 ◽  
Vol 55 (5) ◽  
pp. 568-573 ◽  
Author(s):  
W. K. Kim ◽  
R. Rohringer ◽  
D. J. Samborski ◽  
N. K. Howes
Keyword(s):  
Host Cell ◽  
Stem Rust ◽  
Fungal Growth ◽  
Triticum Aestivum L ◽  
Hypersensitive Reaction ◽  
Host Cells ◽  
Puccinia Graminis ◽  
Cell Necrosis ◽  
Blasticidin S ◽  
Wheat Leaves

Seedlings of resistant (Sr6) and susceptible (sr6) near-isogenic lines of wheat (Triticum aestivum L.) were inoculated with an avirulent (P6) race of stem rust (Puccinia graminis (Pers.) f.sp. tritici Eriks. & Henn.) and kept for 2 days at 26 °C where the Sr6 gene is ineffective, treated with blasticidin S, ethionine, polyoxin D, or buffer, and transferred to 19 °C where the Sr6 gene is normally effective. One and 2 days later, leaves were stained with Calcofluor and examined by fluorescence microscopy to detect autofluorescing necrotic host cells and Calcofluor-stained stem rust colonies.Blasticidin S was phytotoxic to wheat leaves at concentrations that had no effect on fungal growth during the first 2 days after treatment. At later stages, extensive host necrosis, resulting from the phytotoxicity of this antibiotic, inhibited rust development.Ethionine and polyoxin D strongly inhibited rust development at concentrations that were not phytotoxic. In genotypically resistant leaves treated with ethionine and polyoxin D there were fewer necrotic cells associated with stem rust colonies than in leaves treated with buffer. The spacial distribution of necrotic cells was consistent with the view that necrosis occurs only in cells newly invaded after the temperature was lowered to 19 °C.The observations do not support the concept that host-cell necrosis in the hypersensitive reaction conditioned by this gene results from the death of the fungus.

The Alternaria brassicae – Nectria inventa host–parasite interface

1977 ◽  
Vol 55 (4) ◽  
pp. 448-454 ◽  
Author(s):  
A. Tsuneda ◽  
W. P. Skoropad
Keyword(s):  
Cell Wall ◽  
Host Cell ◽  
Host Cells ◽  
Alternaria Brassicae ◽  
Adhesive Material ◽  
Large Hole ◽  
Mature Conidium ◽  
Host Cell Wall ◽  
Host Parasite

The Verticillium state of Nectria inventa is a destructive parasite of Alternaria brassicae. Tropic growth of parasite hyphae towards hyphae and conidia of A. brassicae occurs in the vicinity of the host. Upon contact, the parasite hyphae often form appressorium-like bodies on the host cells and produce fibrous adhesive material at the host–parasite interface. Conidia are penetrated more commonly than hyphae. Penetration of the septa in hyphae results in a separation of cells. Penetration of a mature conidium also occurs commonly at a septum. The presence of a large hole in the wall of the host cell and the meshwork of material at the penetration site suggest that enzymatic breakdown of host cell wall occurs. Juvenile conidia are penetrated usually at the basal pore.

Sign in / Sign up

Export Citation Format

Share Document