Assessment of Biological Activities and Genomic Changes on Microorganisms,Wheat, and Wilding Arise from Poly(pyrazole)

The rapidly growing human population has led to duplicate food production and also reduced product loss. Although the negative effects of synthetic chemicals were recorded, they are still used as agrochemical. The production of non-toxic synthetics makes their use particularly safe. The goal of our research is to evaluate antimicrobial activity of previously synthesized Poly(p-phenylene-1-(2,5-dimethylphenyl)-5-phenyl-1H-pyrazole-3,4-dicarboxy amide) (poly(PDPPD)) against selected Gram-negative, Gram-positive bacteria, and fungus. In addition, the possible genotoxic effects of the poly(PDPPD) were searched on Triticum vulgare and Amaranthus retroflexus seedlings using Random Amplified Polymorphic DNA (RAPD) marker. The binding affinity and binding energies of the synthesized chemical to B-DNA were simulated with AutoDock Vina. It was observed that the poly(PDPPD) affected most of the organisms in a dose-dependent manner. Pseudomonas aeruginosa was the most affected species in tested bacteria at 500 ppm with 21.5 mm diameters. Similarly, a prominent activity was observed for tested fungi. The poly(PDPPD) decreased root and stem length of the Triticum vulgare and Amaranthus retroflexus seedlings and also reduced the genomic template stability (GTS) value of Triticum vulgare more than Amaranthus retroflexus. The binding energy of poly(PDPPD) was found in range of −9.1 and −8.3 kcal/mol for nine residues of B-DNA.     

The immune system utilizes two distinct effector mechanisms of T cells depending on two different life cycle stages of a single pathogen,Toxoplasma gondii,to control its cerebral infection

Toxoplasma gondii takes two different life cycle stages within intermediate hosts including humans. Tachyzoites proliferate during the acute stage, and they transform into cysts to establish a chronic infection preferentially in the brain. IFN-γ production by infiltrated CD4⁺ and CD8⁺ T cells is required for the prevention of cerebral tachyzoite growth. IFN-γ production by brain-resident cells, most likely microglia, plays a key first line defense role to facilitate both innate and T cell-mediated protective immunity to control the tachyzoite growth. IFN-γ produced by brain-resident cells activates cerebral expression of IFN-dependent effector molecules to suppress tachyzoite growth during the early stage of infection. Their IFN-γ production also induces an expression of CXCL9 and CXCL10 chemokines to recruit immune T cells into the brain, and upregulates cerebral expression of MHC class I and II molecules for antigen presentation to the recruited T cells to activate their IFN-γ production. CD8⁺ T cells also have the activity to remove T. gondii cysts from the brains of infected hosts. Of interest, the anti-cyst activity of CD8⁺ T cells does not require their IFN-γ but does require perforin. Notably, we discovered that CD8⁺ cytotoxic T cells penetrate in the cysts in a perforin-mediated manner, which induces morphological deterioration and destruction of the cysts and an accumulation of microglia and macrophages for their elimination. Thus, the immune system employs two distinct effector mechanisms mediated by IFN-γ or perforin depending on two different life cycle stages of a single pathogen, T. gondii, to control its cerebral infection.     

Larvicidal activity of spinosad and its impact on oviposition preferences of the West Nile vector Culex pipiens biotype molestus – A comparison with a chitin synthesis inhibitor

In the present study, the larvicidal activity of ageing aqueous suspensions of spinosad against larvae of Culex pipiens biotype molestus, as well as their effect on the oviposition preferences of adult gravid females were evaluated in laboratory bioassays. Spinosad was applied at its label dose and the aqueous stock suspensions were stored for various ageing intervals up to 38 days. Untreated distilled water and diflubenzuron served as negative and positive control, respectively. Stock suspensions were taken after 0, 2, 6, 8, 16, 30 and 38 days of storage for diflubenzuron and after 0, 2, 6, 8, 20 and 27 days for spinosad, and were used for the bioassays. Furthermore, the effect of spinosad on the oviposition response of Cx. p. biotype molestus gravid females was investigated in two-choice oviposition preference bioassays. Spinosad was evaluated at half of its label dose and at its label dose, whereas diflubenzuron and distilled water served as positive and negative control, respectively. Results showed that both insecticides were found highly effective for the control of Cx. p. biotype molestus larvae, for ageing intervals up to 27 and 38 days for spinosad and diflubenzuron, respectively. Spinosad acted immediately after the preparation of the insecticidal solution (LT₅₀ = 1.5 h), whereas for aged samples, LT₅₀ values increased with the increase of the ageing interval (LT₅₀ = 5 days for the 27 days old sample). For diflubenzuron, ageing time increased its insecticidal activity, as for aged diflubenzuron-treated solutions, lower LT₅₀ values were achieved. In the oviposition preference bioassays, significantly fewer egg rafts were laid in water treated with spinosad at its label dose compared to control. However, this was not the case for water treated with spinosad at half of its label dose. Oviposition Activity Index (OAI) values were always comprised between −0.3 and 0.3, showing no relevant oviposition deterrence or attraction. The results of the present study contribute to our understanding of the effect of ageing on insecticidal solutions widely used in urban areas to control Cx. p. biotype molestus. Although an important vector of high public health importance, Cx. p. biotype molestus has been scarcely studied as target of environmentally and toxicologically reduced risk insecticides, such as spinosad.     

炭角菌科部分类群的生物地理学研究(英文)

与肉质真菌相比,大多数炭角菌科真菌的子实体结构和质地使其在自然环境中保持长久,不易腐变,这有利于记录该科采集物的分布信息,基于过去长达25年对该科的深厚工作积累,使我们有可能对其进行地理分布的研究。     

Strategies for oral delivery of macromolecule drugs

Advances in biotechnology, gene manipulation, and protein engineering for macromolecule drugs, such as insulin, parathyroid hormone (PTH), calcitonin, human growth hormone, erythropoietin (EPO), and peptide YY (PYY) allow commercial production in large scale for diverse therapeutic uses. Other macromolecules, such as mucopolysaccharide heparin, have expanded markets through improvements in their pharmacokinetic and pharmacological effects. However, most products are available only as injectable forms and are limited to patients with no alternative therapeutic choices. Orally available macromolecule formulations are still unmet needs for improving patient compliance and expanding administration paradigms and indications. Oral delivery technologies including carrier systems, absorption enhancers, protease inhibitors, and modification by conjugating transporter or receptor recognition molecules have been developed and some are undergoing clinical studies. In this review, we discuss major obstacles for oral absorption of macromolecule drugs and summarize recent strategies to overcome the huddles related to enhancing intestinal permeation.     

Molecular study of the genus Astraeus

The aim of the present work was to determine phylogenetic relationships among Astraeus species and to support macroscopic and microscopic characters of Astraeus with analysis of the ITS rDNA region. Collections of Astraeus basidiomes were made from different geographical areas in Thailand and compared with existing collections made worldwide. The marriage of observations on morphological features, including basidiospore ornamentation and molecular data demonstrated the presence of several Astraeus species. Sequences for 41 Astraeus collections were compared and the phylogenetic analyses grouped Thai Astraeus collections into two distinct groups. One contained A. odoratus and an Asian species described herein as A. asiaticus. There are at least two additional species: A. pteridis, and one so far un-named from North America. Our results show that molecular data can be used in combination with traditional morphological characteristics to resolve taxonomic uncertainties in the genus Astraeus.     

Modification of theophylline release with alginate gel formed in hard capsules

The aim of this work was to establish whether alginate gel formed spontaneously in hard gelatin capsules which modifies release of a model drug, theophylline. The effects of the alginate composition, the calcium addition, and the dissolution medium on drug release were also investigated. After the capsule shell dissolved in water, at neutral pH the gel layer of sodium alginate was formed immediately as the sodium alginate hydrated and swelled on contact with the aqueous medium. In acidic pH, the contents remained intact and the matrix shape was the same. Theophylline release from capsules containing different grades of alginate demonstrated different release patterns, depending on alginate composition and the pH of the medium. The capsules containing sodium/calcium salts of alginate showed the slowest drug release at neutral pH but the fastest in acidic medium. The presence of calcium acetate in the formulations influenced the drug release kinetics. The drug release in acidic medium showed a non-Fickian diffusion-controlled release, while those in water at neutral pH exhibited a Super Case II transport mechanism. The study also provides evidence that the behavior of alginate in forming the hydrated gel layer may explain the drug release behavior at different pHs. Published: July 6, 2007