Construction Materials and Dam Foundation While Memve’ele Dam Building in the Craton’s Region of South Cameroon

This chapter mainly focuses on engineering geology for dam construction from the Memve’ele region in Cameroon. Here, it deals with geotechnical and geological proprieties of both construction and dam foundation materials. This study is done at the aim to ensure that these materials need to be improved and how they have been used during dam construction. Field investigations, borehole information, density and seismic velocity measurements have been used, and results indicate that soil deposits have slightly clay content, mechanically well for dam construction and display a weak thickness layer particularly on the dam site. These conditions suggest that soil materials can be used as construction (cushion, transition layers, etc.) and foundation materials after few amendments. Ntem Formations appear weathered and fractured sometimes, though their mechanical behaviors display a good character for civil applications. However, engineering processes have been used to improve it by GIN (Grouting Intensity Number) methods. These formations have been used as construction (rip rap crushing aggregate, etc.) and dam foundation materials. Thus, this chapter contributes to highlight materials and dam foundation conditions which are crucial criteria encountered in the dam with emphasis on both theoretical study and practical application during dam construction

Physicochemical Properties of Chemical Pollutants Available in Food Contact Materials (FCM)

Health and welfare of population are priority reasons to study the toxic effects of chemical pollutants. These effects can directly produce deterioration of health or can cause less healthful environment toxicity and restricting food production. Thereby, preventing such a consequence is important for human health risk assessment. In recent times, the use of recycled materials for packaging has undeniably been intensified. Nevertheless, recycling systems could not effectively eliminate the potential effect of chemical pollutants (alkyl phenol, phthalates, aldehydes, etc.) existent in such packages. The migration process and/or the ability of these pollutants to be absorbed into the recycled material, subsequently released by the packaging material, and then trapped by the matrices they contain, has become a potential source of exposure to consumers. This process is controlled by the nature of the packaging, time, temperature, and the physicochemical properties of the contaminant. The literature suffers from a lack of data related to the physicochemical (aqueous solubility, vapor pressure, Henry’s constant, etc...) of these contaminants. In this work, we are going to describe the experimental devices used for aqueous solubility, vapor pressure and octanol/water partition coefficient determination

Metabolomic profiles of arsenic (+3 oxidation state) methyltransferase knockout mice: effect of sex and arsenic exposure

Arsenic (+3 oxidation state) methyltransferase (As3mt) is the key enzyme in the pathway for methylation of inorganic arsenic (iAs). Altered As3mt expression and AS3MT polymorphism have been linked to changes in iAs metabolism and in susceptibility to iAs toxicity in laboratory models and in humans. As3mt-knockout mice have been used to study the association between iAs metabolism and adverse effects of iAs exposure. However, little is known about systemic changes in metabolism of these mice and how these changes lead to their increased susceptibility to iAs toxicity. Here, we compared plasma and urinary metabolomes of male and female wild-type (WT) and As3mt-KO (KO) C57BL6 mice and examined metabolomic shifts associated with iAs exposure in drinking water. Surprisingly, exposure to 1 ppm As elicited only small changes in the metabolite profiles of either WT or KO mice. In contrast, comparisons of KO mice with WT mice revealed significant differences in plasma and urinary metabolites associated with lipid (phosphatidylcholines, cytidine, acyl-carnitine), amino acid (hippuric acid, acetylglycine, urea), and carbohydrate (L-sorbose, galactonic acid, gluconic acid) metabolism. Notably, most of these differences were sex-specific. Sex-specific differences were also found between WT and KO mice in plasma triglyceride and lipoprotein cholesterol levels. Some of the differentially changed metabolites (phosphatidylcholines, carnosine, and sarcosine) are substrates or products of reactions catalyzed by other methyltransferases. These results suggest that As3mt KO alters major metabolic pathways in a sex-specific manner, independent of iAs treatment, and that As3mt may be involved in other cellular processes beyond iAs methylation

Experimental Determination of Phase Equilibria and Occupancies for CO2, CH4, and N2 Hydroquinone Clathrates

Hydroquinone (HQ) forms organic clathrates in the presence of various gas molecules in specific thermodynamic conditions. For some systems, clathrate phase equilibrium and occupancy data are very scarce or inexistent in literature to date. This work presents experimental results obtained for the CO2–HQ, CH4–HQ, and N2–HQ clathrates, in an extended range of temperature from about 288 to 354 K. Formation/dissociation pressures, and occupancies at the equilibrium clathrate forming conditions, were determined for these systems. Experiments showing the influence of the crystallization solvent, and the effect of the gas pressure on HQ solubility, were also presented and discussed. A good agreement is obtained between our experimental results and the already published experimental and modeling data. Our results show a clear dependency of the clathrate occupancy with temperature. The equilibrium curves obtained for CO2–HQ and CH4–HQ clathrates were found to be very close to each other. The results presented in this study, obtained in a relatively large temperature range, are new and important to the field of organic clathrates with potential impact on gas separation, energy storage, and transport

Genome-wide diversity and gene expression profiling of Babesia microti isolates identify polymorphic genes that mediate host-pathogen interactions

Babesia microti, a tick-transmitted, intraerythrocytic protozoan parasite circulating mainly among small mammals, is the primary cause of human babesiosis. While most cases are transmitted by Ixodes ticks, the disease may also be transmitted through blood transfusion and perinatally. A comprehensive analysis of genome composition, genetic diversity, and gene expression profiling of seven B. microti isolates revealed that genetic variation in isolates from the Northeast United States is almost exclusively associated with genes encoding the surface proteome and secretome of the parasite. Furthermore, we found that polymorphism is restricted to a small number of genes, which are highly expressed during infection. In order to identify pathogen-encoded factors involved in host-parasite interactions, we screened a proteome array comprised of 174 B. microti proteins, including several predicted members of the parasite secretome. Using this immuno-proteomic approach we identified several novel antigens that trigger strong host immune responses during the onset of infection. The genomic and immunological data presented herein provide the first insights into the determinants of B. microti interaction with its mammalian hosts and their relevance for understanding the selective pressures acting on parasite evolution

Identifying SARS-CoV-2 antiviral compounds by screening for small molecule inhibitors of Nsp5 main protease

The coronavirus 2019 (COVID-19) pandemic, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), spread around the world with unprecedented health and socio-economic effects for the global population. While different vaccines are now being made available, very few antiviral drugs have been approved. The main viral protease (nsp5) of SARS-CoV-2 provides an excellent target for antivirals, due to its essential and conserved function in the viral replication cycle. We have expressed, purified and developed assays for nsp5 protease activity. We screened the nsp5 protease against a custom chemical library of over 5000 characterised pharmaceuticals. We identified calpain inhibitor I and three different peptidyl fluoromethylketones (FMK) as inhibitors of nsp5 activity in vitro, with IC(50) values in the low micromolar range. By altering the sequence of our peptidomimetic FMK inhibitors to better mimic the substrate sequence of nsp5, we generated an inhibitor with a subnanomolar IC(50). Calpain inhibitor I inhibited viral infection in monkey-derived Vero E6 cells, with an EC(50) in the low micromolar range. The most potent and commercially available peptidyl-FMK compound inhibited viral growth in Vero E6 cells to some extent, while our custom peptidyl FMK inhibitor offered a marked antiviral improvement