Detection of Ureaplasma diversum in the upper airways of Australian feedlot cattle

Bovine respiratory disease (BRD) exerts a major impact on the beef cattle industry nationally and worldwide, with a range of aetiological factors impacting its pathogenesis. Previous research has focussed on an increasing number of bacteria and viruses that have been shown to play a role in eliciting disease. Recently, additional agents have been emerging as potential contributors to BRD, including the opportunistic pathogen Ureaplasma diversum. To determine if U. diversum was present in Australian feedlot cattle and if that presence was linked to BRD, nasal swabs were collected from a cohort of 34 hospital pen animals and compared to 216 apparently healthy animals sampled contemporaneously at feedlot induction and again after 14 days on feed at an Australian feedlot. All samples were subjected to a de novo polymerase chain reaction (PCR) assay targeting U. diversum in combination with other BRD agents. U. diversum was detected at a low prevalence in cattle at induction (Day 0: 6.9%, Day 14: 9.7%), but in a significantly greater proportion of cattle sampled from the hospital pen (58.8%). When considering the presence of other BRD-associated agents, co-detection of U. diversum and Mycoplasma bovis was most common in hospital pen animals receiving treatment for BRD. These findings suggest that U. diversum may be an opportunistic pathogen involved in the aetiology of BRD in Australian feedlot cattle, in combination with other agents, with further studies are warranted to identify if a causal relationship exists.     

Significance for exercise capacity of some electrocardiographic findings in racehorses

Summary Various cardiorespiratory and metabolic indices were assessed during treadmill exercise in Thoroughbred and Standardbred racehorses with T wave changes in 4 or more leads on the electrocardiogram or second-degree atrio-ventricular (AV) block, and in horses that had no abnormalities on clinical examination, resting electrocardiography or upper respiratory tract endoscopy. No significant differences in heart rate, plasma lactate concentration, arterial blood gases, oxygen uptake, run time, peak velocity, or blood and red cell volumes were found between normal horses and horses with T wave changes or second-degree AV block. These results indicate that some electrocardiographic findings that are considered by some clinicians to indicate cardiac dysfunction, may have little effect on exercise capacity.     

The relationship of various muscular and skeletal scores and ultrasound measurements in the live animal,and carcass classification scores with carcass composition and value of bulls

The relationships of live animal muscular and skeletal scores and ultrasound measurements and carcass conformation and fat scores with carcass composition and value were determined using 74 bulls. The animals consisted of 53 late-maturing breed crosses and 21 Holstein–Friesian slaughtered at 13 to 17 months of age. They were offered concentrates ad-libitum and 1 kg of grass silage dry matter per head daily for the final 139 day finishing period. Live animal muscular and skeletal scores and ultrasonic muscle and fat depth measurements of the M. longissimus dorsi were recorded at 8 to 12 months of age and pre-slaughter. Following slaughter, carcasses were classified for conformation and fatness and the right side of each carcass was dissected into meat, fat and bone. Carcass conformation and fat scores, (scale 1 to 15) ranged from 4.7 to 14.4 and 2.7 to 11.5, respectively. Pre-slaughter muscular scores showed significant positive correlations with kill-out proportion (r = 0.82), carcass meat proportion (r = 0.72), conformation score (r = 0.94), carcass value (r = 0.72), and the proportion of high-value meat cuts in the carcass (r = 0.49), and significant negative correlations with carcass bone (r = − 0.89) and fat (r = − 0.32) proportions. The associations between pre-slaughter muscular scores and proportion of high-value cuts in meat, perinephric plus retroperitoneal fat and fat score were not significant. Corresponding correlations with muscular scores at 8 to 12 months of age were generally lower than those recorded pre-slaughter. Correlations of ultrasound muscle depth with carcass traits showed similar trends but lower values to those obtained using the muscular scoring procedure. Ultrasound fat depth pre-slaughter was positively correlated with carcass fat proportion (r = 0.56) and fat score (r = 0.54), and negatively correlated with carcass meat proportion, proportion of high-value cuts and carcass value. Correlations with other carcass traits were not significant. Correlations of live animal skeletal scores with carcass traits were generally non-significant. A one unit (scale 1–15) increase in carcass conformation score was associated with significant increases in kill-out proportion, meat yield and carcass value of 11.9 g/kg, 11.9 g/kg and 5.8 cent/kg, respectively. Corresponding effects for a one unit change in fat score were − 2.9 g/kg, − 11.1 g/kg and − 4.9 c/kg. In conclusion, live animal muscular scores and ultrasound measurements and carcass conformation and fat scores were shown to be useful predictors of carcass composition and value.     

Alpha-amylase/subtilisin Inhibitor Levels in Australian Barleys

An enzyme-linked immunosorbent assay (ELISA) was used to determine the bifunctional alpha-amylase/subtilisin inhibitor (BASI) content of barley grain from 11 cultivars grown in six diverse locations in Australia. The inhibitor ranged from 119 to 254 μg/g in 57 barley samples. Genotype had a significant (P<0·05) effect on BASI content but there was no effect due to environment. Total protein varied independently of BASI and was influenced by environment and genotype. BASI content was higher (P<0·05) in malting barley than in feed barley and was correlated positively (r=0·29;P<0·05) with alpha-amylase activity in corresponding malts. The ELISA used monoclonal and polyclonal antibodies raised against purified BASI. In immunoblot analysis the monoclonal antibody showed high specificity for the inhibitor in barley and also detected the inhibitor in wheat. Low levels of inhibitor (mean 3·2 μg/g) were found in 12 Australian wheat cultivars using the ELISA developed for barley. The assay had a linear working range of 5–50 ng/mL with a detection limit of 2 ng/mL. Reproducibility between assays was good (CV=4·9%) but mean recoveries were high, ranging from 116–129% when purified inhibitor was added to barley extracts. The ELISA may have useful applications in brewing research and barley breeding programmes.