Authors studied the effect of sterigmatocystin from infected corn (STC), purified sterigmatocystin (PSTC), and aflatoxin B1 from infected corn (AFB₁) on lipid peroxidation and glutathione redox parameters, including the expression of their encoding genes in a sub-chronic (14 days) trial. A total of 144 three-week-old cockerels was divided into four experimental groups (n = 36 in each). Control feed was contaminated with STC or PSTC (1590 µg STC/kg or 1570.5 µg STC/kg feed), or with AFB₁ (149.1 µg AFB₁/kg feed). Six birds from each group were sampled at day 1, 2, 3, 7 and 14 of mycotoxin exposure. As parameters of lipid peroxidation, conjugated dienes (CD) and trienes (CT) were measured in the liver, while malondialdehyde (MDA) concentration was determined in blood plasma, red blood cell hemolysate and liver. Reduced glutathione (GSH) concentration and glutathione peroxidase (GPx) activity were determined in the same samples, and expression of glutathione peroxidase 4 (GPX4), glutathione synthetase (GSS) and glutathione reductase (GSR) genes was measured by RT-PCR in the liver. STC, PSTC or AFB₁ caused a slight, but not significant, increase in CD and CT levels; however, in the case of MDA, no increase was found in the liver. Glutathione redox system was activated in the liver by AFB₁, but less markedly by STC/PSTC. PSTC and AFB₁ resulted in a higher expression of GPX4, while GSS expression was down-regulated by AFB₁ on day 1, but up-regulated by STC on day 2 and by both mycotoxins on day 7. However, on day 14, GSS expression was down-regulated by PSTC. Expression of GSR was low on day 1 in AFB₁ and PSTC groups, but later it was up-regulated by AFB₁. The observed changes regarding gene expression strengthen the hypothesis that the mild oxidative stress, caused by the applied STC doses, activates the glutathione redox system of broiler chickens.

Due to global climate change, mould strains causing problems with their mycotoxin production in the tropical–subtropical climate zone have also appeared in countries belonging to the temperate zone. Biodetoxification of crops and raw materials for food and feed industries including the aflatoxin B1 (AFB1) binding abilities of lactobacilli is of growing interest. Despite the massive quantities of papers dealing with AFB1-binding of lactobacilli, there are no data for microbial binding of the structurally similar mycotoxin sterigmatocystin (ST). In addition, previous works focused on the detection of AFB1 in extracts, while in this case, analytical determination was necessary for the microbial biomass as well. To test binding capacities, a rapid instrumental analytical method using high-performance liquid chromatography was developed and applied for measurement of AFB1 and ST in the biomass of the cultured bacteria and its supernatant, containing the mycotoxin fraction bound by the bacteria and the fraction that remained unbound, respectively. For our AFB1 and ST adsorption studies, 80 strains of the genus Lactobacillus were selected. Broths containing 0.2 µg/mL AFB1and ST were inoculated with the Lactobacillus test strains. Before screening the strains for binding capacities, optimisation of the experiment parameters was carried out. Mycotoxin binding was detectable from a germ count of 10⁷ cells/mL. By studying the incubation time of the cells with the mycotoxins needed for mycotoxin-binding, co-incubation for 10 min was found sufficient. The presence of mycotoxins did not affect the growth of bacterial strains. Three strains of L. plantarum had the best AFB1 adsorption capacities, binding nearly 10% of the mycotoxin present, and in the case of ST, the degree of binding was over 20%.

Research on the ability of lactic acid bacteria (LAB) to bind aflatoxin B1 (AFB1) has mostly been focusing on lactobacilli and bifidobacteria. In this study, the AFB1 binding capacities of 20 Enterococcus strains belonging to E. casseliflavus, E. faecalis, E. faecium, E. hirae, E. lactis, and E. mundtii, 24 Pediococcus strains belonging to species P. acidilactici, P. lolii, P. pentosaceus, and P. stilesii, one strain of Lactococcus formosensis and L.garviae, and 3 strains of Weissella soli were investigated in MRS broth at 37 °C at 0.2 µg/mL mycotoxin concentration. According to our results, among non-lactobacilli LAB, the genera with the best AFB1 binding abilities were genus Pediococcus, with a maximum binding percentage of 7.6% by P. acidilactici OR83, followed by genus Lactococcus. For AFB1 bio-detoxification purposes, beside lactobacilli, pediococci can also be chosen, but it is important to select a strain with better binding properties than the average value of its genus. Five Pediococcus strains have been selected to compare their sterigmatocystin (ST) binding abilities to AFB1 binding, and a 2–3-fold difference was obtained similar to previous findings for lactobacilli. The best strain was P. acidilactici OR83 with 18% ST binding capacity. This is the first report on ST binding capabilities of non-Lactobacillus LAB strains.

Aflatoxin B1 (AFB1) is a potent mycotoxin and natural carcinogen. The primary producers of AFB1 are Aspergillus flavus and A. parasiticus. Sterigmatocystin (STC), another mycotoxin, shares its biosynthetic pathway with aflatoxins. While there are abundant data on the biological effects of AFB1, STC is not well characterised. According to published data, AFB1 is more harmful to biological systems than STC. It has been suggested that STC is about one-tenth as potent a mutagen as AFB1 as measured by the Ames test. In this research, the biological effects of S9 rat liver homogenate-activated and non-activated STC and AFB1 were compared using two different biomonitoring systems, SOS-Chromotest and a recently developed microinjection zebrafish embryo method. When comparing the treatments, activated STC caused the highest mortality and number of DNA strand breaks across all injected volumes. Based on the E. coli SOS-Chromotest, the two toxins exerted the same genotoxicities. Moreover, according to the newly developed zebrafish microinjection method, STC appeared more toxic than AFB1. The scarce information correlating AFB1 and STC toxicity suggests that AFB1 is a more potent genotoxin than STC. Our findings contradict this assumption and illustrate the need for more complex biomonitoring systems for mycotoxin risk assessment.

A novel Gram-reaction-negative bacterial strain, designated Ka43^T, was isolated from agricultural soil and characterised using a polyphasic approach to determine its taxonomic position. On the basis of 16S rRNA gene sequence analysis, the strain shows highest similarity (97.1 %) to Cellvibrio diazotrophicus E50^T. Cells of strain Ka43^T are aerobic, motile, short rods. The major fatty acids are summed feature 3 (C_16 : 1 ω7c and/or iso-C_15 : 0 2-OH), C_18 : 1  ω7c and C_16 : 0. The only isoprenoid quinone is Q-8. The polar lipid profile includes phosphatidylethanolamine, phosphatidylglycerol, four phospholipids, two lipids and an aminolipid. The assembled genome of strain Ka43^T has a total length of 4.2 Mb and the DNA G+C content is 51.6 mol%. Based on phenotypic data, including chemotaxonomic characteristics and analysis of the 16S rRNA gene sequences, it was concluded that strain Ka43^T represents a novel species in the genus Cellvibrio , for which the name Cellvibrio polysaccharolyticus sp. nov. is proposed. The type strain of the species is strain Ka43^T (=LMG 31577^T=NCAIM B.02637^T).

Probiotics are widely used in poultry farming and industry, as they offer numerous health and performance benefits for birds. Probiotic Lactobacilli maintain gut microbiota balance, aid nutrient utilization, boost the immune system, increase stress resistance and serve as antibiotic alternatives. However, their impact on male reproductive function is not yet fully understood. This study investigated the effect of a novel probiotic strain, Lactiplantibacillus plantarum SNI3 (LbSNI3), on the reproductive performance of roosters. Twenty adult roosters were used. LbSNI3 was administered orally (dose: 2 × 10⁷ CFU/animal/day) for 7 weeks to half of the animals. Control birds (10) received sterile tap water vehicle. Ejaculate volume, sperm concentration, sperm motility, number of IPVL penetration holes and testosterone plasma concentration have been measured weekly. Testis weight, dimensions and histology have been determined at the end of the experiment. mRNA levels of select genes, involved in spermatogenesis and sperm motility, oxidative and steroid synthesis have been measured in the testis samples by qRT-PCR. Total antioxidant capacity, superoxide dismutase (SOD) enzyme activity and malondialdehyde (MDA) levels were also analyzed. LbSNI3 administration increased the ejaculate volume, sperm concentration and the number of penetration holes, resulting in a significant improvement in the reproductivity index. In contrast, testosterone levels were not statistically different in control versus LbSNI3-treated groups. At the end of the experiment, testis size, the area, and the lumen of seminiferous tubuli were increased in LbSNI3-treated roosters. The testicular expression of Gpx1, Sepw1, Dio2, Birc5 and Rec8 genes was elevated following oral administration of LbSNI3. Total antioxidant activity, SOD activity significantly increased, while MDA concentration decreased, indicating enhanced antioxidant capacity in the testis. LbSNI3 produces a bacterial metabolite, γ-glutamyl-glutamate, which enters the glutathione cycle and strengthens the testicular defense mechanisms against oxidative stress. In conclusion, oral administration of probiotic LbSNI3 enhances antioxidant defense mechanisms in the testis, leading to increased reproductive index in adult roosters. This effect may be mediated through the gut-testis axis and could be utilized to improve productivity in the livestock industry.