Synthesis of some 3-(2-substituted sulfanyl-imidazo [2,1-b][1,3,4] thiadiazol-6-yl)-chromen-2-one and its derivatives

454-458A series of 3-(2-substituted sulfanyl-imidazo [2,1-b][1,3,4] thiadiazol-6-yl)-chromen-2-ones (3) have been synthesized from 3-(2-bromo acetyl) chromen-2-ones 1 and 2-amino-5-thio substituted[1,3,4]thiadiazole 2 in anhydrous ethanol. The 7,8-benzo analogs of 3-(2-substituted sulfanyl-imidazo[2,1-b][1,3,4] thiadiazol-6-yl)-chromen-2-ones 5 have been synthesized under similar conditions. All the synthesized compounds have been characteriszed by analytical and spectral data

A plant rhabdovirus associated with peanut veinal chlorosis disease in India

A disease of groundnut characterized by stunting of plants, veinal chlorosis, outward bending of leaflets and proliferation of axillary buds has been observed in several parts of Peninsular India since 1977. The disease was restricted to crops raised during the post-rainy season. A rhabdovirus was associated with this disease. This appears to be the first record of natural occurrence of a rhabdovirus in groundnut

Indian Peanut Clump Virus Isolates: Host Range, Symptomatology, Serological Relationships, and Some Physical Properties

The symptomatology of Indian peanut clump virus (IPCV) isolates collected from five different geographical locations, Bapatla (B), Chinnaganjam (C), Hyderabad (H), Ludhiana (L), and Talod (T), differed. B-IPCV and C-IPCV were indistinguishable by host range but could be distinguished from the other isolates by symptoms on Canavalia ensiformis, Nicotiana clevelandii × glutinosa, Phaseolus vulgaris, and Vigna unguiculata. B-IPCV, C-IPCV, and T-IPCV were related serologically, but could be distinguished from H-IPCV and L-IPCV isolates in serological tests. The five isolates could not be distinguished on the basis of particle size. Each isolate contained two RNA species of 1.90 × 106 and 1.65 × 106 Mr estimated under nondenaturing conditions and a single polypeptide of 24 × 103 Mr. Significance of these findings for the diagnosis of IPCV and for screening of peanut genotypes for resistance is discussed

Identification of Peanut Green Mosaic Virus Strains in India

During field surveys, three peanut green mosaic virus isolates differing in symptomatology on groundnut and a few other hosts were collected. Ultrathin sections of infected groundnut leaflets showed cytoplasmic inclusions with pin wheels and scrolls. In enzyme-linked immunosorbent assay they reacted strongly with antisera to peanut green mosaic and soybean mosaic virus antisera, and moderately with adzuki bean mosaic and peanut stripe virus antisera. All isolates also reacted positively with antisera to peanut eye spot, blackeye cowpea mosaic, pea seed-borne mosaic, potato virus Y and tobacco etch viruses, and did not react with antisera to peanut mottle, bean yellow mosaic, bean common mosaic, clover yellow vein and sugarcane mosaic viruses. SDS-PAGE analysis of purified virus preparations of the three isolates showed a single polypeptide with mol. wt. of 34,500 daltons. Based on these results, the three isolates are identified as biologically distinct strains of peanut green mosaic virus

Peanut Chlorotic Streak Virus, a New Caulimovirus Infecting Peanuts (Arachis hypogaea) in India

Peanut (Arachis hypogaea [groundnut]) plants with reduced leaflets, chlorotic streaks, and stunting were observed during surveys for diseases caused by peanut viruses in India. These peanut plants were infected with a new caulimovirus designated peanut chlorotic streak virus (PClSV). PClSV was mechanically transmissible to several plants in Leguminosae and Solanaceae but was not transmitted by Aphis craccivora or Myzus persicae. Purified from Nicotiana clevelandii leaves, PClSV contained isometric particles 52 ± 3 nm in diameter. The virus was not related to cauliflower mosaic, figwort mosaic, or soybean chlorotic mottle viruses. Inclusion bodies similar to those produced by caulimoviruses were observed in the cytoplasm of infected Nicotiana rustica and A. hypogaea leaves. Purified PClSV contained two polypeptides with relative molecular masses of 58 and 51 kDa. The size of double-stranded DNA was estimated as approximately 8.1 kbp, which contained two single-stranded discontinuities. The physical map of the PClSV genome was distinctly different from those of other caulimoviruses

Isolation and characterization of a potyvirus associated with bushy dwarf symptom in chickpea, Cicer arietinum, in India

A potyvirus that induced stunting and a characteristic bushy appearance at the apical region, due to proliferation of terminal branches with narrowed, reduced and deformed leaflets, was isolated from chickpea in India. The virus was sap-transmissible to 14 species of Chenopodiaceae, Leguminosae, Solanaceae and Malvaceae; Chenopodium amaranticolor was a good local lesion host. Virus particles, trapped by immunosorbent EM and stained with uranyl acetate, were 710±10 nm long. Purified virus preparations contained a single polypeptide species of 32 500 Da and one nucleic acid species of 3.1×106 Da. The virus was serologically related to soybean mosaic, azuki bean mosaic and peanut mottle potyviruses but not to clover yellow vein, pea seed-borne mosaic and bean yellow mosaic potyviruses. On the basis of these properties, the virus was identified as a previously undescribed potyvirus in chickpea, for which the name chickpea bushy dwarf virus is proposed

The occurrence of maize mosaic virus on sorghum in India

A leaf disease of sorghum (Sorghum bicolor) characterised by fine discontinuous chlorotic streaks between the veins, was observed on sorghum grown during the 1987/88 post-rainy season in peninsular India. Early-infected plants were stunted, had shortened internodes, and produced poorly developed panicles. The virus was transmitted by the delphacid planthopper, Peregrinus maidis. Negatively stained leaf dip preparations contained bullet-shaped virus particles (208 ± 4.4 × 66 ± 1.0 nm) resembling those of rhabdoviruses. In ultrathin sections, the particles budded through the inner nuclear membrane and were present in the cytoplasm within membrane-bound vesicles that were apparently contiguous with the distended outer nuclear membrane. A method for purifying the virus was developed utilising polyethylene glycol (PEG) precipitation, Celite filtration and sucrose densitygradient centrifugation. An antiserum was produced in rabbits with a titre of 1/2650 in the precipitin ring interphase test. The virus could be detected in infected sorghum leaf tissues using a direct antigen coating form of enzyme-linked immunosorbent assay (DAC-ELISA). In immuno-double diffusion tests, the virus reacted positively with antisera to maize mosaic virus (MMV) from Reunion (MMV-RN) and Hawaii (MMV-HI), but not with antisera to barley yellow striate mosaic (BYSMV), cereal chlorotic mottle (CCMV), and cynodon chlorotic streak (CCSV) viruses. Thus, the virus isolated from sorghum is designated the MMV-S isolate. In DAC-ELISA tests, MMV-S reacted positively with antisera to MMV-R, MMV-HI, MMV-Florida isolate, CCSV, and CCMV, and weakly with antiserum to BYSMV. SDS-polyacrylamide gel electrophoresis revealed four major proteins of relative mass Mr 70 000, 59 000, 32 000 and 28 000. In electro-blot immunoassay, MMV and CCSV antisera detected the G and N proteins. These data suggest that MMV-S should be placed in the sonchus yellow net virus subgroup of plant rhabdoviruse

Genome-wide in silico analysis of dehydrins in Sorghum bicolor , Setaria italica and Zea mays and quantitative analysis of dehydrin gene expressions under abiotic stresses in Sorghum bicolor

Dehydrins (DHNs) are highly hydrophilic, thermo stable, calcium dependent chaperons involved in plant developmental processes as well as in diverse abiotic stresses. A systematic survey resulted in the identification of 7 dehydrins (DHNs) in Setaria italica and Zea mays, but 6 in Sorghum bicolor. They are classified into 5 sub-groups, namely YnSKn, SKn, KnS, S, and YnS. DHNs of Sorghum exhibit 1 ortholog with Oryza sativa and Z. mays and 3 with S. italica. Unlike other DHNs, SbDHN5 has been found as an ordered protein with many phosphorylation sites. Network analyses of novel YnS subgroup showed interaction with HSP70 and FKBP genes. In silico promoter analysis revealed the presence of abscisic acid (ABA), drought, salt, low temperature stress-responsive elements. The miRNA target analysis revealed DHNs are targeted by 51 miRNAs responsive to abiotic stresses. High transcript expressions of DHNs were observed in root, stem and leaf compared to inflorescence in S. bicolor. All DHN genes exhibited high levels of expression in stem under cold, heat, salt, and drought stresses. In contrast to other DHNs, the SbDHN2 of YnS subgroup, exhibited the highest expression, under multiple stresses in all the tissues indicating its involvement against a wide array of abiotic stresses