Biomedical subjects

J P Tewari

Publications and source records attributed to J P Tewari.

At least 19 recordsLinked to original sources

PubMed2005

Inheritance and QTL analysis of durable resistance to stripe and leaf rusts in an Australian cultivar, Triticum aestivum 'Cook'.

An F4-derived F6 recombinant inbred line population (n = 148) of a cross between the durable stripe (yellow) rust (caused by Puccinia striiformis) and leaf (brown) rust (caused by Puccinia triticina) resistant cultivar, Triticum aestivum 'Cook', and susceptible genotype Avocet-YrA was phenotyped at several locations in Canada and Mexico under artificial epidemics of leaf or stripe rusts and genotyped using amplified fragment length polymorphism (AFLP) and microsatellite markers. Durable adult plant resistance to stripe and leaf rusts in 'Cook' is inherited quantitatively and was based on the additive interaction of linked and (or) pleiotropic slow-rusting genes Lr34 and Yr18 and the temperature-sensitive stripe rust resistance gene, YrCK, with additional genetic factors. Identified QTLs accounted for 18% to 31% of the phenotypic variation in leaf and stripe rust reactions, respectively. In accordance with the high phenotypic associations between leaf and stripe rust resistance, some of the identified QTLs appeared to be linked and (or) pleiotropic for both rusts across tests. Although a QTL was identified on chromosome 7D with significant effects on both rusts at some testing locations, it was not possible to refine the location of Lr34 or Yr18 because of the scarcity of markers in this region. The temperature-sensitive stripe rust resistance response, conditioned by the YrCK gene, significantly contributed to overall resistance to both rusts, indicating that this gene also had pleiotropic effects.

Basidiomycota↗

PubMed2001

Detection of aster yellows phytoplasma in false flax based on PCR and RFLP.

False flax (Camelina sativa L.) plants were found to be infected with a yellows-type disease caused by a phytoplasma in experimental plots at the Edmonton Research station. Alberta, Canada. Typical phytoplasmas were detected in the phloem cells in ultrathin sections from leaf midrib tissues examined by electron microscopy. These observations were supported by polymerase chain reaction (PCR) using two primer pairs, R16 F2n/R2 and R16(1)F1/R1, derived from phytoplasma rDNA sequences. Aster yellows (AY) and potato witches'-broom (PWB) phytoplasma DNA samples served as controls and were used to study group relatedness. In a direct PCR assay, DNA amplification with universal primer pair R16F2n/R2 gave the expected PCR products of 1.2 kb. Based on a nested-PCR assay using the latter PCR products as templates, and a specific primer pair, R16(1)F1/R1, designed on the basis of AY phytoplasma rDNA sequences, a PCR product of 1.1 kb was obtained from each phytoplasma-infected false flax and AY sample, but not from PWB phytoplasma and healthy controls. DNA amplification with specific primer pair R16(1)F1/R1 and restriction fragment length polymorphism indicated the presence of AY phytoplasma in the infected false flax sample. This is the first reported characterization of AY phytoplasma in false flax.

Acholeplasmataceae↗

PubMed1991

Contact sites between mitochondrial membranes: comments.

Extensive contact sites between the two mitochondrial membranes are visualized particularly when tissues are prepared by freeze-substitution methods for electron microscopy. Such contacts rapidly diminish if animals are asphyxiated even for a relatively short period of 8 min. Thus contacts between the mitochondrial membranes are likely to be labile.

Animals↗

PubMed1990

Evaluation of soil microorganisms with inhibitory activity against Rhizoctonia solani causal agent of the damping-off of canola.

Pre- and post-emergence damping-off of canola seedlings caused by Rhizoctonia solani is a serious disease in Western Canada. Other fungi such as Fusarium spp. and Pythium spp. are also related to seedling damping-off. To-day, the search of soil bacteria is becoming a tool to use microorganisms as potential biocontrol agents for several plant diseases. The purpose of this research was to detect bacteria to biologically control R. solani, Pythium spp., and Fusarium spp. Soil samples were collected throughout Alberta during 1987 to isolate bacteria. Canola seedlings were also used to obtain bacteria from the same samples. Plant pathogenic fungi were tested to detect the antagonistic activity of the isolates. Tests were made with coated canola seeds, amendments and fresh of freeze-dried cells. Three hundred forty-one bacterial cultures were isolated. Only 16 inhibited fungal growth: 7 showed the same effects against R. solani and 9 showed uneven effects. Some isolates showed a weak action to Pythium spp. and Fusarium spp. Three isolates showed inhibitory effect on R. solani and Pythium spp. Isolate F1 improved by about 50% the germination of canola seeds in inoculated pots when compared with the inoculated control. Coated seeds had low germination and emergence was below the inoculated control. The emergence of canola seedlings was very much improved when isolate 147 was delivered as an amendment in inoculated pots. Identification showed that 3 bacterial belonged to Bacillus spp., 4 to green fluorescent Pseudomonas spp. and 2 were Streptomyces spp.

Analysis of Variance↗

PubMed1982

Microanalysis of the reaction product in Karnovsky and Roots histochemical localization of acetylcholinesterase.

X-ray energy dispersive microanalysis of the reaction product in Karnovsky and Roots histochemical localization of acetylcholinesterase indicated the presence of sulfur, iodine, copper, and iron. The reaction was run in vitro using purified acetylcholinesterase from the electric eel to confirm our previous results on similarly treated neuromuscular junction in situ.

Acetylcholinesterase↗

PubMed1981

Thiocholine methods for the demonstration of acetylcholinesterase in neuromuscular junctions.

The extensor digitorum longus muscles of rat were stained for the localization of acetylcholinesterase activity at the neuromuscular junctions. The modified methods of Koelle-Friedenwald and Karnovsky-Roots were used with acetylthiocholine iodide as the substrate. The merits and demerits of both these methods are discussed. TEM and SEM X-ray dispersive analyses of the muscle fibres treated histochemically by both the methods were also made in order to elucidate further the nature of the reaction products. Denervated muscles were subjected to similar treatment.

Acetylcholinesterase↗

PubMed1981

Subunit structure of the connexons in hepatocyte gap junctions.

The connexons in the mouse hepatocyte gap junctions consistently reveal a subunit structure in rotary shadowed replicas of quick frozen freeze-fractured material. Quick freezing eliminates treatment of the material with chemical fixatives and cryoprotectants and hence captures the structures in their native state. Previous biophysical studies have indicated that the connexon in hepatocyte gap junction is composed of 6 subunits. In rotary shadowed replicas, some connexons have 6 subunits while the rest reveal less than 6 subunits. Visualization of less than 6 subunits may be due to local variations in the angle of shadowing because of an uneven plane of fracturing and/or breaking of some of the subunits during freeze-fracturing. Markham's rotation technique reveals that some connexons have a hexameric symmetry while others approach a tetrameric symmetry. Using models of connexons and tilting experiments with the replicas it is shown that these apparent deviations from the hexameric symmetry result from inclination of the fractured face relative to the plane of viewing.

Animals↗

PubMed1980

Multilamellar surface layer of the cell wall of Albugo candida and Phycomyces blakesleeanus.

The surface layer of the cell wall of the sporangia of Albugo candida and of the sporangiophores of Phycomyces blakesleeanus was composed of a series of lamellae. The evidence from freeze-fracture, freeze-etch, and single-stage replicas indicated that the lamellae are organized as bilayers, an organization associated with the presence of lipids. The role of these lamellae in dispersibility and resistance is discussed.

Cell Wall↗

PubMed1975

Functional characterization of types of plasma membranes in cerebral cortex.

The cerebral cortex of normal oxygenated and of asphyxiated mice has been studied by freeze-fracturing technique with a twofold purpose. First, to investigate changes, if any, in the molecular organization of the plasma membrane of any specific cell type(s) that could be correlated with permeability changes thought to take place as a consequence of asphyxiation. Secondly, to attempt characterization of plasma membranes on the basis of the organization of their fractured faces. The decrease in the extracellular material in asphyxiated cerebral cortex seen in electron micrographs of thin sections could not be correlated with change(s), if any, in the molecular organization of the plasma membrane of any particular cell type. Plasma membranes of various types could be characterized on the basis of the arrangement of particles on the fractured faces. Some of these types correspond to identifiable cell processes, while others have not yet been identified with certainty. Fusion of synaptic vesicles with the presynaptic membrane is mediated through clustering of 100-150 A membrane-associated particles.

Animals↗

PubMed1974