The emergence of a rapidly spreading and highly infectious COVID-19 outbreak by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), has caused a global pandemic with unprecedented, social and economic dimensions. Therefore, the development of effective strategies is urgent to control COVID-19 outbreak. According to the recent investigations, cell entry of coronaviruses relies on binding of the viral spike glycoprotein to the host cellular receptors. Therefore, in the present study aimed to predict immunogenic epitopes in silico by analyzed spike protein. In parallel, by screening the immunogenic SARS-CoV-2 spike derived epitopes provided in the literature, we chose a set of epitopes believed to induce immunogenic response. Next, we provided the selected epitopes from both approaches, we performed immunoinformatic analysis that map identically to antigen regions and have antigenic properties. Finally, by suggesting a screened set of epitopes, we designed a novel virus-like particle (VLP) vaccine, optimized to be produced in plants by using molecular farming biotechnology techniques. We anticipate our assay to be a starting point for guiding experimental efforts toward the development of a vaccine against SARS-CoV-2.
Highlights Virus-like particles -based vaccines have attracted great interest as the next generation of vaccines due to their safety profile, efficacy, shorter production times, and ability to induce both cellular and humoral immunity. The production of HBc-based virus-like particles in plants would thus greatly increase the efficiency of vaccine production. This review investigates the application of plant-based HBc VLP as a platform for vaccine production.
The aim of the present study was to determine the seroprevalence of CE among human referring to Health Centers in Mazandaran Province, northern Iran and to identify the risk factors involved in spreading the disease. Between 2013 and 2014, the serum samples were taken randomly from 600 subjects referring to health centers in Mazandaran Province. After obtaining informed consent for each participant, a questionnaire including demographic characteristics and associated risk factors was filled for each individual. Anti-CE antibody was tested by enzyme-linked immunosorbent assay (ELISA), using native antigen B. Our results showed 31.6% (n = 190) seropositivity. There were significant difference between seropositivity and sex and residence. Males were significantly more seropositive than females (24.6% versus 7%, P = 0.0001). Regression analysis showed that the subjects who are living in rural areas were 4.4 times more likely to be at risk to CE than urban areas (OR = 4.4; 95% CI = 2.91, 6.64). Contact with dogs, soil and consumed raw vegetables was appeared as main risk factors for CE among community in Mazandaran and it may increase the probability of infection. The high prevalence of CE among individuals indicated that hydatidosis is still a major health problem among community in the investigated areas.
Circular RNAs (circRNAs) are covalently closed non-coding RNAs that are usually derived from exonic regions of genes, but can also arise from intronic and intergenic regions. Studies of circRNAs in humans, animals and several plant species have shown an altered population of circRNAs in response to abiotic and biotic stress. Recently it was shown that circRNAs also occur in maize, but it is unknown if maize circRNAs are responsive to stress. Maize Iranian mosaic virus (MIMV, genus Nucleorhabdovirus, family Rhabdoviridae) causes an economically important disease in maize and other gramineous crops in Iran. In this study, we used data from RNA-Seq of MIMV-infected maize and uninfected controls to identify differentially expressed circRNAs. Such circRNAs were confirmed by two-dimensional polyacrylamide gel electrophoresis, northern blot, RT-qPCR and sequencing. A total of 1443 circRNAs were identified in MIMV-infected maize and 1165 circRNAs in uninfected maize. Two hundred and one circRNAs were in common between MIMV-infected and uninfected samples. Of these, 155 circRNAs were upregulated and 5 down-regulated in MIMV infected plants, compared to the uninfected control. This study for the first time identified and profiled circRNA expression in maize in response to virus infection. Moreover, we predict that 33 circRNAs may bind 23 maize miRNAs, possibly affecting plant metabolism and development. Our data suggest a role for circRNAs in plant cell regulation and response to biotic stress such as virus infection, and give new insights into the complexity of plant-microbe interactions.
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