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Corn gluten meal (CGM) is used as a protein source in aquafeeds. However, the potential for replacing fish meal (FM) with CGM in abalone feeds has not been adequately evaluated. A 110-day feeding trial was conducted to evaluate effects of replacing FM with CGM on abalone Haliotis discus hannai (initial weight: 21.83 ± 0.25 g). The control diet (CGM0) was designed to contain 20% of FM. The other four isonitrogenous (about 30% of crude protein) and isolipidic (about 4% of crude lipid) experimental diets were formulated with CGM protein replacing 25%, 50%, 75% and 100% of dietary FM protein, respectively. The five experimental diets were named as CGM0, CGM25, CGM50, CGM75 and CGM100, respectively. Results showed that no significant differences were found in survival rate among all the groups. Weight gain rate (WGR) of abalone in the CGM100 group was significantly lower than that in the control group. There were no significant differences in WGR among the CGM25, CGM50, CGM75 and the control groups. The increasing dietary CGM inclusion level elevated the operational taxonomic units, ACE estimator and Chao1 estimator, and changed the intestinal microbiota composition in abalone. The activities of trypsin, alanine transaminase, aspartate transaminase and Na+, K+-ATPase in digestive gland were significantly decreased when replacement level over 50%. The increasing dietary CGM inclusion level significantly downregulated the expressions of ribosomal S6 protein kinase (s6k), mammalian target of rapamycin (mtor) and eukaryotic translation initiation factor 4E (eif4e) in digestive gland. The CGM75 and CGM100 groups had significant lower activities of catalase and lysozyme in cell-free hemolymph and digestive gland. In conclusion, CGM could replace 75% of dietary FM (equivalent to 16.2% of CGM inclusion level in the diet) without significantly affecting the growth of abalone. However, high inclusion levels of CGM in diets (> 10.8%) had negative effects on intestinal microbiota, mTOR pathway and immunity in abalone.

Cell-selective biomaterials, i.e. favoring the functions of gingival cells and simultaneously reducing the adhesion of pathogenic bacteria, is highly desired in dental implants. However, due to the same mechanisms shared in attachment by mammalian and microbial cells, it is hard to increase the functions of the former while acting against the latter. Herein, a cell-selectivity was established on titanium oxide coatings by combining a plasma immersion ion implantation & deposition (PIII) and a UV pre-illumination. The titanium oxide coatings were produced on pure titanium substrates by using a plasma electrolytic oxidation technique and then doped of hafnium (Hf) by using a cathodic arc sourced PIII. The Hf-doped titanium oxide coatings (Hf-PIII groups) were capable of delaying the recombination of UV-illumination generated electron-hole pairs, which decreased the adhesion of bacterial cells at the later period (cultured for 24 h). Titanium oxide coating doped of 4.87 at.% hafnium (Hf) gained the biggest decrease (decreased 52.9% compared to its UV negative counterparts) in bacterial adhesion among the UV positive (UV+) groups. This study demonstrates that coupling Hf-doping and UV pre-illumination is promising for improving the cell-selective performance of titanium-based dental implants. Keywords: Titanium, Surface modification, Ultraviolet, Bacteria, Hafnium