Jednonukleotidni polimorfizmi gena za β-laktoglobulin, k-kazein i DGAT1 kao kandidati za stroge selekcijske kriterije holštajnskih krava s obzirom na sastav i proizvodnost mlijeka

The aim of this study was to investigate β-Lactoglobulin, k-casein and DGAT1 gene polymorphism and to associate this polymorphism with milk composition and performance traits in Holstein cattle using the PCR-DNA sequencing approach. On the basis of farm records, accurate phenotypic data for milk composition and performance traits were obtained for seventy Holstein dairy cows. Blood samples were collected from each animal into tubes containing disodium EDTA as an anticoagulant for DNA extraction. PCR was carried out for amplification of fragments of exon 4 (301-bp) of β-Lactoglobulin, exon 4 (373-bp) of k-casein, and exon 7 (321-bp) of DGAT1 genes. DNA sequencing assessment elaborated single nucleotide polymorphisms (SNPs) in the investigated genes amongst the enrolled dairy cows. On the basis of the dairy cows that harbored identified SNPs in each gene, the animals were allocated into different groups. The least square means of the groups revealed a significant association (P ≤ 0.05) between SNPs and milk production and performance traits. Logistic regression model confirmed a highly significant effect of the identified SNPs on the studied traits, where a moderate to strong relationship was detected between the predictor (SNPs) and the grouping variable (Milk composition and performance traits). Consequently, the identified SNPs in β-Lactoglobulin, k-casein and DGAT1 genes could be used as candidates for developing marker assisted selection (MAS) for milk composition and performance traits in Holstein dairy cattle.Cilj rada bio je, primjenom PCR-DNA metode i analize sljedova, istražiti polimorfizme gena za β-Lactoglobulin, k-kazein i DGAT1 te procijeniti njihovu povezati sa sastavom mlijeka i svojstvima proizvodnosti goveda holštajnske pasmine. Na temelju evidencija s farmi dobiveni su točni fenotipski podaci o sastavu mlijeka i proizvodnosti 70 muznih krava. Za ekstrakciju DNK prikupljeni su uzorci krvi pojedinačnih krava u epruvete koje su sadržavale dinatrijev EDTA kao antikoagulans. PCR je proveden za amplifikaciju fragmenata egzona 4 (301-bp) β-laktoglobulina, egzona 4 (373-bp) k-kazeina i egzona 7 (321-bp) gena DGAT1. Analiza sljedova DNK prikazala je jednonukleotidne polimorfizme (SNPs) u istraženim genima. Uzevši u obzir krave kod kojih su utvrđeni SNP-ove u svakom genu, životinje su raspoređene u različite skupine. Srednje vrijednosti (LSM) skupina pokazale su znakovitu povezanost (P<0,05) između SNP-ova i svojstava proizvodnosti mlijeka. Model logističke regresije potvrdio je visoko znakovit učinak identificiranih SNP-ova na istraživana svojstva, pri čemu je ustanovljena umjerena do jaka povezanost između prediktora (SNP-ovi) i varijabli grupiranja (sastav mlijeka i proizvodnost mlijeka). Posljedično, identificirani SNP-ovi u genima β-Lactoglobulina, k-kazeina i DGAT1 mogli bi se koristiti kao kandidatni pri razvoju postupaka selekcije uz pomoć markera (MAS) za sastav mlijeka i svojstva proizvodnosti u mliječnih goveda pasmine holštajn

Prevalence and Antibiogram of Vibrio parahaemolyticus and Aeromonas hydrophila in the Flesh of Nile Tilapia, with Special Reference to Their Virulence Genes Detected Using Multiplex PCR Technique

Vibrio parahaemolyticus and Aeromonas hydrophila are major public health problems and the main cause of bacterial disease in Nile tilapia (Oreochromis niloticus). This study was conducted to determine the prevalence, antibiotic resistance and some virulence genes of both V. parahaemolyticus and A. hydrophila isolates from Nile tilapia. From Manzala Farm at Dakahlia governorate, 250 freshwater fish samples were collected. The confirmed bacterial isolates from the examined Nile tilapia samples in the study were 24.8% (62/250) for V. parahaemolyticus and 19.2% (48/250) for A. hydrophila. multiplex PCR, revealing that the tlh gene was found in 46.7% (29/62) of V. parahaemolyticus isolates, while the tdh and trh virulence genes were found in 17.2% (5/29). Meanwhile, 39.5% (19/48) of A. hydrophila isolates had the 16s rRNA gene and 10.5% (2/19) had the aerA and ahh1 virulence genes. The Multiple Antibiotic Resistance indices of V. parahaemolyticus and A. hydrophila were 0.587 and 0.586, respectively. In conclusion, alternative non-antibiotic control strategies for bacterial infections in farmed fish should be promoted to avoid multidrug-resistant bacteria. Therefore, it is suggested that farmers should be skilled in basic fish health control and that molecular detection methods are more rapid and cost-effective than bacteriological methods

Thiacloprid Induced Developmental Neurotoxicity via ROS-Oxidative Injury and Inflammation in Chicken Embryo: The Possible Attenuating Role of Chicoric and Rosmarinic Acids

Insecticides are widely employed in agriculture to control pests and as major factors for enhancing crop productivity. Thiacloprid (TH) is one of the most-used insecticides worldwide. In this study, the negative impact of TH on the brain tissue of developing chicken embryo models and the modulatory effect of chicoric (CA) and rosmarinic (RA) acids were investigated. The eggs were injected in ovo with different doses of TH (0.1, 1, 10, and 100  g/egg). TH significantly increased the oxidative damage in the brain of exposed embryos in a dose-dependent manner (p &lt; 0.05). TH significantly elevated the oxidative stress markers; protein carbonyl, malondialdehyde content, and DNA damage (p &lt; 0.05). Myeloperoxidase activity and nitric oxide significantly increased with overexpression of the pro-inflammatory cytokines (interferon gamma, tumor necrosis factor alpha, and interleukin-1 beta) and stress-related and apoptotic genes (NF-KB, Caspase-3) in the brain tissue on both biochemical and molecular levels (p &lt; 0.05), while downregulating the expression of antiapoptotic Bcl-2. Co-treatment of CA and RA with TH markedly decreased the insecticide-induced toxicity with a prominent synergistic effect (p &lt; 0.05). In conclusion, TH is suggested to be a possible neurotoxic to embryos of vertebrates including human. The study also revealed the antioxidant, anti-inflammatory, genoprotective, and antiapoptotic property of CA and RA against TH toxicity

Insight View on the Role of in Ovo Feeding of Clenbuterol on Hatched Chicks: Hatchability, Growth Efficiency, Serum Metabolic Profile, Muscle, and Lipid-Related Markers

The present study aimed to assess the in ovo administration of clenbuterol on chick fertility, growth performance, muscle growth, myogenic gene expression, fatty acid, amino acid profile, intestinal morphology, and hepatic lipid-related gene expressions. In this study, 750 healthy fertile eggs from the local chicken breed Dokki-4 strain were analyzed. Fertile eggs were randomly divided into five experimental groups (150 eggs/3 replicates for each group). On day 14 of incubation, in addition to the control group, four other groups were established where 0.5 mL of worm saline (30 °C) was injected into the second group of eggs. In the third, fourth, and fifth groups, 0.5 mL of worm saline (30 °C), 0.9% of NaCl, and 10, 15, and 20 ppm of clenbuterol were injected into the eggs. Results suggested that clenbuterol increased growth efficiency up to 12 weeks of age, especially at 15 ppm, followed by 10 ppm, decreased abdominal body fat mass, and improved hatchability (p &lt; 0.01). Clenbuterol also modulated saturated fatty acid levels in the breast muscles and improved essential amino acids when administered at 10 and 15 ppm. Additionally, clenbuterol at 15 ppm significantly decreased myostatin gene expression (p &lt; 0.01) and considerably increased IGF1r and IGF-binding protein (IGFBP) expression. Clenbuterol administration led to a significant upregulation of hepatic PPARα, growth hormone receptor, and Lipoprotein lipase (LPL) mRNA expression with a marked decrease in fatty acid synthase (FAS) and sterol regulatory element-binding protein 1 (SREBP-1c) expression. In conclusion, the current study revealed that in ovo injection of clenbuterol showed positive effects on the growth of hatched chicks through reduced abdominal fat deposition, improved intestinal morphology, and modulation of hepatic gene expressions in myogenesis, lipogenesis, and lipolysis

Ameliorative Effect of Pomegranate Peel Extract (PPE) on Hepatotoxicity Prompted by Iron Oxide Nanoparticles (Fe2O3-NPs) in Mice

An evaluation of the ameliorative effect of pomegranate peel extract (PPE) in counteracting the toxicity of iron oxide nanoparticles (Fe2O3-NPs) that cause hepatic tissue damage is focused on herein. Forty male albino mice were haphazardly grouped into four groups as follows: the first control group was orally gavage daily with physiological saline; the second group received 100 mg/kg of PPE by the oral route day after day; the third group received 30 mg/kg Fe2O3-NPs orally; and the fourth group received both PPE and Fe2O3-NPs by the oral route, the same as the second and third sets. Later, after the completion of the experiment, we collected the liver, blood, and bone marrow of bone specimens that were obtained for further laboratory tests. For instance, exposure to Fe2O3-NPs significantly altered serum antioxidant biomarkers by decreasing the levels of total antioxidant capacity (TAC), catalase (CAT), and glutathione s-transferase (GST). Additionally, it caused changes in the morphology of hepatocytes, hepatic sinusoids, and inflammatory Kupffer cells. Furthermore, they significantly elevated the number of chromosomal aberrations including gaps, breaks, deletions, fragments, polyploidies, and ring chromosomes. Moreover, they caused a significant overexpression of TIMP-1, TNF-&alpha;, and BAX mRNA levels. Finally, the use of PPE alleviates the toxicity of Fe2O3-NPs that were induced in the hepatic tissues of mice. It is concluded that PPE extract has mitigative roles against the damage induced by Fe2O3-NPs, as it serves as an antioxidant and hepatoprotective agent. The use of PPE as a modulator of Fe2O3-NPs&rsquo; hepatotoxicity could be considered as a pioneering method in the use of phytochemicals against the toxicity of nanoparticles