RESUMEN
Rotaviruses cause diarrhea in infants and young children worldwide. Rotavirus outer capsid protein, VP7 is major neutralizing antigen that is important component of subunit vaccine to prevent rotavirus infection. Many efforts have been done to produce recombinant VP7 that maintain native characteristics. We used baculovirus expression system to produce rotavirus VP7 protein and to study its immunogenicity. Simian rotavirus SA11 full-length VP7 ORF was cloned into a cloning plasmid and then the cloned gene was inserted into the linear DNA of baculovirus Autographa californica Nuclear Polyhedrosis Virus [AcNPV] downstream of the polyhedrin promoter by in vitro recombination reactions. The expressed VP7 in the insect cells was recognized by rabbit hyperimmune serum raised against SA11 rotavirus by Immunofluorescence and western blotting assays. Rabbits were immunized subcutaneously by cell extracts expressing VP7 protein. Reactivity with anti-rotavirus antibody suggested that expressed VP7 protein had native antigenic determinants. Injection of recombinant VP7 in rabbits elicited the production of serum antibodies, which were able to recognize VP7 protein from SA11 rotavirus by Western blotting test and neutralized SA11 rotavirus in cell culture. Recombinant outer capsid glycoprotein [VP7] of rotavirus expressed in insect cells induces neutralizing antibodies in rabbits and may be a candidate of rotavirus vaccine
RESUMEN
The gram-negative bacterium Helicobacter pylori [H. pylori], identified in 1982, is now recognized as the primary etiological factor associated with the development of gastritis and peptic ulcer disease. The growing problem of antibiotic resistance by the organism demands the search for novel compounds from plant based sources. The present study is aimed at evaluating the anti-Helicobacter pylori activity of 10 Iranian plant extracts on clinical isolates of H. pylori. Gastric biopsy samples were obtained from patients presenting with gastroduodenal complications. H. pylori was isolated from the specimens following standard microbiology procedures. The disk diffusion method was used to determine the susceptibility of 12 isolates to methanol plant extracts [Fruit and leaves of Melia azedarach, Melia indica and aerial parts of Stachys setifera, Stachys turcomanica, Stachys trinervis, Stachys subaphylla, Stachys byzanthina, Stachys persica, Stachys inflata, Stachys laxa]. The plants tested at 8 mg/disc concentration demonstrated anti-Helicobacter pylori activity with zone diameters of inhibition ranging from 12-38 mm. Of these, Stachys setifera [aerial parts], Melia indica [Fruit] and Melia azedarach [leaves] showed the most potent anti -H. pylori activity on the isolates. Due to the rise in antibiotic resistance, new sources of anti-H. pylori drugs are needed. The use of medicinal plants may have potential benefit in eradicating such problems. According to the results of this study, further studies will be necessary to investigate the effects of other plants of Iran against H. pylori infectio