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Scrapie is a fatal prion protein disease stiffly associated with single nucleotide polymorphism (SNPs) of the prion protein gene (PRNP). The prevalence of this deadly disease has been reported in small ruminants, including goats. The Nigerian goats are hardy, trypano-tolerant, and contribute to the protein intake of the increasing population. Although scrapie has been reported in Nigerian goats, there is no study on the polymorphism of the PRNP gene. Herein, we evaluated the genetic and allele distributions of PRNP polymorphism in 132 Nigerian goats and compared them with publicly available studies on scrapie-affected goats. We utilized Polyphen-2, PROVEAN and AMYCO programs to examine structural variations produced by the non-synonymous SNPs. Our study revealed 29 SNPs in Nigerian goats, of which 14 were non-synonymous, and 23 were novel. There were significant differences (P 0.001) in the allele frequencies of PRNP codons 139, 146, 154 and 193 in Nigerian goats compared with scrapie-affected goats, except for Northern Italian goats at codon 154. Based on the prediction by Polyphen-2, R139S and N146S were 'benign', R154H was 'probably damaging', and T193I was 'possibly damaging'. In contrast, PROVEAN predicted 'neutral' for all non-synonymous SNPs, while AMYCO showed a similar amyloid propensity of PRNP for resistant haplotype and two haplotypes of Nigerian goats. Our study is the first to investigate the polymorphism of scrapie-related genes in Nigerian goats.

In this study, we present a simple, fast and cost-effective sonochemical growth method for the synthesis of zinc oxide (ZnO) nanorods. ZnO nanorods were grown on glass substrates at room temperature without the addition of surfactants. The successful coating of substrates with ZnO nanorods was demonstrated by Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS). The antimicrobial properties of ZnO nanorods against the planktonic Bacillus subtilis and Escherichia coli and their respective biofilms were investigated. The cytotoxicity of ZnO nanorods were evaluated using the NIH 3T3 mammalian fibroblast cell line. Moreover, to understand the possible mechanisms of ZnO nanorod toxicity, glutathione oxidation, superoxide production, and release of Zn2+ ions by the ZnO nanorods were determined, and the LIVE/DEAD assay was employed to investigate cell membrane damage. The results showed that sonochemically grown ZnO nanorods exhibited significant antimicrobial effects to both bacteria and prevented biofilm formation. ZnO nanorods did not present any significant toxicity to fibroblast cells. The main anti-microbial mechanisms of ZnO nanorods were determined to be H2O2 production and cell membrane disruption.

Sonochemical growth technique is based upon the chemical effect of ultrasound on chemical reactions. This process is carried out at an ambient atmosphere without the need for a complex experimental set up and additional heating. This method is of significant importance because of it's vital application in various fields. ZnO nanorods were grown on glass substrates without any additional heat or surfactance by sonochemical growth technique. The grown nanostructures were characterized by Raman spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). Sonochemically grown ZnO nanorod networks were characterized for their antibacterial properties toward B.subtilis. These structures were also characterized for their CO sensing properties and photovoltaic performances for dye sensitized solar cell (DSSC) application. All material characterization and device performances suggest that sonochemsitry can be utilized as an alternative growth method for 1D ZnO nanostructures.