Pyroptosis induced by lipopolysaccharide (LPS) has an obvious impact on intestinal inflammation and immune regulation. Enterotoxigenic Escherichia coli (ETEC) K88 has been proved to induce inflammatory responses in several models, but whether E. coli K88 participates in the same process of pyroptotic cell death as LPS remains to be identified. We conducted a pilot experiment to confirm that E. coli K88, instead of Escherichia coli O157 and Salmonella typhimurium, promotes the secretion of interleukin-1 beta (IL-1β) and interleukin-18 (IL-18) in macrophages. Further experiments were carried out to dissect the molecular mechanism both in vitro and in vivo. The Enzyme-Linked Immunosorbent Assay (ELISA) results suggested that E. coli K88 treatment increased the expression of pro-inflammatory cytokines IL-18 and IL-1β in both C57BL/6 mice and the supernatant of J774A.1 cells. Intestinal morphology observations revealed that E. coli K88 treatment mainly induced inflammation in the colon. Real-time PCR and Western blot analysis showed that the mRNA and protein expressions of pyroptosis-related factors, such as NLRP3, ASC, and Caspase1, were significantly upregulated by E. coli K88 treatment. The RNA-seq results confirmed that the effect was associated with the activation of NLRP3, ASC, Caspase1, GSDMD, IL-18, and IL-1β, and might also be related to inflammatory bowel disease and the tumor necrosis factor pathway. The pyroptosis-activated effect of E. coli K88 was significantly blocked by NLRP3 siRNA. Our data suggested that E. coli K88 caused inflammation by triggering pyroptosis, which provides a theoretical basis for the prevention and treatment of ETEC in intestinal infection.

The widespread use of antibiotics has led to the emergence of multidrug-resistant bacteria, which pose significant threats to animal health and food safety

The biosynthetic process of selenium nanoparticles (SeNPs) by specific bacterial strain, whose growth directly affects the synthesis efficiency, has attracted great attentions. We previously reported that Bacillus paralicheniformis SR14, a SeNPs-producing bacteria, could improve intestinal antioxidative function in vitro. To further analyze the biological characteristics of SR14, whole genome sequencing was used to reveal the genetic characteristics in selenite reduction and sugar utilization. The results reviewed that the genome size of SR14 was 4,448,062 bp, with a GC content of 45.95%. A total of 4300 genes into 49 biological pathways was annotated to the KEGG database. EC: 1.1.1.49 (glucose-6-phosphate 1-dehydrogenase) and EC: 5.3.1.9 (glucose-6-phosphate isomerase), were found to play a potential role in glucose degradation and EC:2.7.1.4 (fructokinase) might be involved in the fructose metabolism. Growth profile and selenite-reducing ability of SR14 under different sugar supplements were determined and the results reviewed that glucose had a better promoting effect on the reduction of selenite and growth of bacteria than fructose, sucrose, and maltose. Moreover, RT-qPCR experiment proved that glucose supplement remarkably promoted the expressions of thioredoxin, fumarate reductase, and the glutathione peroxidase in SR14. Analysis of mRNA expression showed levels of glucose-6-phosphate dehydrogenase and fructokinase significantly upregulated under the supplement of glucose. Overall, our data demonstrated the genomic characteristics of SR14 and preliminarily determined that glucose supplement was most beneficial for strain growth and SeNPs synthesis.

To provide a safe and effective supplement of the essential trace element selenium, we focused on the biosynthesis of nanoselenium (SeNPs) via probiotics. A novel kind of exopolymer-functionalized nanoselenium (SeEPS), whose average size was 67.0 ± 0.6 nm, was produced by Bacillus subtilis SR41, whereas the control consisted of exopolymers without selenium (EPS). Chemical composition analysis, Fourier transform infrared (FTIR) spectroscopy and high-performance liquid chromatography (HPLC) confirmed that SeEPS and EPS shared similar polysaccharide characteristic groups, such as COO- and C=O, and contained not only 45.2–45.4% of sugars but also 23.5–24.7% of proteins and some lipids. Both SeEPS and EPS were primarily composed of mannose, amino glucose, ribose, glucose and galactose. Furthermore, to identify the biologically active component of SeEPS, three kinds of selenium particles with different stabilizers [Se(0), bovine serum albumin-Se and EPS-Se] were synthesized chemically, and their ability to scavenge free radicals in vitro was compared with that of SeEPS and EPS. The results revealed that EPS itself exhibited weak superoxide and hydroxyl radical scavenging abilities. Nevertheless, SeEPS had superior antioxidant properties compared to all other products, possibly due to the specific structure of SeNPs and exopolymers. Our results suggested that exopolymer-functionalized SeNPs with specific monosaccharide composition and structure could eventually find a potential application as an antioxidant.

This study investigated the effects of a low-protein diet without soybean meal on the growth performance, nutrient digestibility, plasma-free amino acids, and meat quality of finishing pigs. A total of 81 barrows and 81 gilts ([Yorkshire × Landrace] × Duroc) of 150 days old with similar body weights (103.64 ± 3.65 kg) were selected and randomly allocated into three groups with three replicates in each group and 18 finishing pigs in each pen (4.5 m × 8.5 m). Three dietary formulations were established in this experiment: (1) 14% crude protein, and 14% soybean meal for the control group diet (CON); (2) 13% crude protein, and 7% soybean meal for half soybean meal group diet (HSB); (3) 12% crude protein, and 0% soybean meal for soybean meal free group diet (SBF). Three groups of diets were equal to standard ileal digestible amino acids and swine net energy. Results showed that (1) there was no significant difference in final body weight, average daily feed intake, and average daily gain in CON, HSB, and SBF groups (p > 0.05). However, the feed conversion rate was higher in the SBF but the differences were not significant (p = 0.08). (2) Compared with the CON group, the apparent digestibility of dry matter, crude protein, and calcium in the SBF group was significantly increased by 6.42%, 4.78%, and 9.82%, respectively (p < 0.05). However, ether extract and phosphorus did not differ significantly between the three groups (p > 0.05). All groups had no significant differences in serum biochemical indexes (p > 0.05). (3) Compared with the CON group, the plasma-free contents of glycine and glutamate in the HSB and SBF groups were significantly decreased by 42.90% and 37.06%, respectively (p < 0.05). Compared with the CON group, the contents of plasma-free histidine and valine in the SBF group were significantly decreased by 16.72% and 16.21%, respectively (p < 0.05), but there was no significant difference compared with the HSB group (p > 0.05). Compared with the CON group, plasma-free isoleucine content in the HSB group was significantly decreased by 50.39% (p < 0.05), but there was no significant difference compared with the SBF group (p > 0.05). (4) Backfat thickness in the SBF group was significantly increased by 3.53% compared with that in the CON group (p < 0.05), but there was no significant difference compared with the HSB group (p > 0.05). Compared with the CON group, lean meat percentage in the HSB and SBF groups showed a tendency to increase and decrease, respectively (p = 0.09). (5) The urine ammonia-nitrogen content of finishing pigs in the SBF group was significantly lower than that of the CON (p < 0.05), at a rate of 28.80%. H₂S content in the urine of the SBF group tended to decrease (p = 0.06). This study demonstrates that a low-protein diet without soybean meal can be applied as a dietary strategy for finishing pigs with no adverse influence on growth performance.