Effect of starch gelatinisation on nutrient digestibility and plasma metabolites in pigeons

Feed manufacturing exerts physical and chemical changes in ingredients, including the gelatinisation of starch. Studies on the effect of the degree of starch gelatinisation on nutrient digestibility, metabolism and subsequent performance show inconsistent results, and no data are available in pigeons. In a cross‐over trial, fourteen adult pigeons were randomly divided into two groups, in which two extruded pellet diets were tested. Both the diets were similar in ingredient composition and nutrient content, but differed in extrusion conditions, resulting in a different degree of starch gelatinisation: pellets with high gelatinisation degree (HG; 73.6% gelatinisation) and low gelatinisation degree (LG; 53.1% gelatinisation). After a 14‐day adaptation period, all excreta were gathered per bird during a 5‐day collection period. Coefficients of apparent digestibility of dry matter (DM), crude protein (CP), ether extract (EE), crude fibre (CF), crude ash (CA) and nitrogen free extract (NFE) as well as apparent nitrogen retention were calculated from proximate analyses of feed and excreta. Further, excreta consistency was subjectively scored. Blood samples were taken at the end of each period and plasma samples were analysed for glucose, fructosamine and triglycerides. Feed intake and body weight changes were recorded weekly. The apparent digestibility coefficients (ADCs) of DM, OM, CP, EE, CA and NFE were significantly higher in the LG group (p ≤ 0.05). The ADC of crude fibre was numerically higher in the LG group but not significant, and no significant differences were found in starch digestibility. Excreta consistency score tended to be higher in the LG diet group. Neither plasma glucose nor plasma fructosamine values were significantly different between the two test diets. The results of this study show that lower degree of starch gelatinisation in extruded diets can enhance digestibility in pigeons.     

Structural changes in kafirin extracted from a white type II tannin sorghum during germination

Kafirin proteins were extracted from a Sudanese cultivar of sorghum (Feterita). The extracted materials were characterized by SDS PAGE. Under non-reducing conditions as germination was progressing from 0 to 72 h, there was visually a decrease in β-kafirins whereas a small effect was observed on α-kafirins. The occurrence of interactions between tannins and kafirin might explain this behavior when compared to other cultivars. Thermogravimetric analysis (TGA) revealed that the first change in weight between room temperature and 100 °C was due to the loss of water. The protein extract started to degrade thereafter with the decomposition rate increasing with germination time. Fourier Transform Infrared (FT-IR) analysis showed that the secondary structure of kafirin was found to be mainly governed by α-helices with some β-sheets. Upon germination, there was a change in protein conformation, mainly an increase in α-helices. Scanning Electron Microscopy (SEM) showed that after extraction, kafirin proteins formed aggregated particles. This study is the first to show in the case of Feterita cultivar that upon germination, the physical properties of the kafirin proteins were significantly affected and relied on composition. This could shed some light on the effect of processing such as germination on sorghum kafirin proteins originated from Feterita.     

Pharmacokinetics and tissue residue profiles of erythromycin in broiler chickens after different routes of administration

This study investigated the disposition kinetics and plasma availability of erythromycin in broiler chickens after single intravenous (i.v.), intramuscular (i.m.), subcutaneous (s.c.) and oral administrations (p.o.) of 30 mg kg(-1) b. wt. Tissue residue profiles were also studied after multiple intramuscular, subcutaneous, and oral administration of 30 mg kg(-1) b. wt., twice daily for three consecutive days. Plasma and tissue concentrations of erythromycin were determined using microbiological assay methods with Micrococcus luteus as the test organism. Following intravenous injection, plasma concentration-vs-time curves were best described by a two compartment open model. The decline in plasma drug concentration was bi-exponential with half-lives of (t(1/2alpha)) 0.19 h and (t(1/2beta)) 5.3 h for distribution and elimination phases, respectively. After intramuscular, subcutaneous and oral administration erythromycin at the same dose was detected in plasma at 10 min and reached its minimum level 8 h post-administration. The peak plasma concentration (Cmax) were 5.0, 5.3, and 6.9 microg x ml(-1) and were attained at 1.7, 1.4, and 1.3 h (Tmax), respectively. The elimination half-lives (T(1/2el)) were 3.9, 2.6, and 4.1 h and the mean residence times (MRT) were 3.5, 3.2, and 3.6 h, respectively. The systemic bioavailabilities were 92.5, 68.8, and 109.3%, respectively. In vitro protein binding percent of erythromycin in broiler plasma was ranged from 21 to 31%. The limit of quantification (LOQ) for the assay was 0.03 microg x ml(-1) in plasma and tissues. The tissue level concentrations were highest in the liver, and decreased in the following order: plasma > kidney > lung > muscle and heart. No erythromycin residues were detected in tissues and plasma after 24 h except in liver and kidney where it persisted during 48 h following intramuscular and oral administrations.     

Status of autophagy,lysosome activity and apoptosis during corpus luteum regression in cattle

Corpus luteum (CL) regression is required during the estrous cycle. During CL regression, luteal cells stop producing progesterone and are degraded by apoptosis. However, the detailed mechanism of CL regression in cattle has not been fully elucidated. The aim of this study was to evaluate autophagy, lysosome activity, and apoptosis during CL regression in cattle. The expression of autophagy-related genes (LC3α, LC3β, Atg3, and Atg7) and the protein LC3-II was significantly higher in the late CL than in the mid CL. In addition, autophagy activity was significantly increased in the late CL. Moreover, gene expression of the autophagy inhibitor mammalian target of rapamycin (mTOR) was significantly lower in the late CL than in the mid CL. Lysosome activation and expression of cathepsin-related genes (CTSB, CTSD, and CTSZ) showed significant increases in the late CL and were associated with an increase in cathepsin B protein. In addition, mRNA expression and activity of caspase 3 (CASP3), an apoptotic enzyme, were significantly higher in the late CL than in the mid CL. These results suggest simultaneous upregulation of autophagy-related factors, lysosomal enzymes and apoptotic mediators, which are involved in regression of the bovine CL.     

A novel 57-kDa merozoite protein of Babesia gibsoni is a prospective antigen for diagnosis and serosurvey of canine babesiosis by enzyme-linked immunosorbent assay

We isolated a novel single copy gene encoding a 57-kDa merozoite protein of Babesia gibsoni (BgP57). The nucleotide sequence of the cDNA was 2387 bp with an open reading frame (ORF) of 1644 bp encoding a 57-kDa predicted polypeptide having 547 amino acid residues. The recombinant BgP57 (rBgP57) without a predicted signal peptide was expressed in Escherichia coli as a soluble glutathione S-transferase (GST) fusion protein. Western blotting showed that the corresponding native protein was 57-kDa, consistent with molecular weight of predicted mature polypeptide. An indirect enzyme-linked immunosorbent assay (ELISA) using the rBgP57 detected specific antibodies in the sequential sera from a dog experimentally infected with B. gibsoni. Moreover, the antigen did not cross-react with antibodies to B. canis sub-species and closely related apicomplexan parasites indicating that the rBgP57 was a specific antigen for B. gibsoni antibodies. The diagnostic performance of ELISA based on rBgP57 using 107 sera from B. gibsoni-naturally infected dogs was the same as the previously identified rBgP32 but performed better than the previously studied rBgP50. Although, seminested PCR detected higher proportions (82%) of positive samples than the ELISAs, the Mcnemar's chi-square test showed that there was no significant difference in relative effectiveness of rBgP57-ELISA and seminested PCR (chi(2)=2.70; P=0.1003) in identifying positive samples. The rBgP57-ELISA when used in combination with rBgP32-ELISA and rBgP50-ELISA appeared to improve sensitivity of the rBgP57-ELISA for detection of B. gibsoni antibodies. Overall, the rBgP57-ELISA and seminested PCR when used in combination, could improve epidemiological surveys and clinical diagnosis of B. gibsoni infection.