Central Venous Pressure Measurements in the Caudal Vena Cava of Sedated Cats

The caudla vena cava (CVA) was evaluated as an laternative site for the measurement of central venous pressure (CPV) in six healthy, sedated (ketamine 10 mg/km, midazolam 0.1 mg/kg, and atropine 0.04 mg/kg IM) cats. The CVC was cathererized via medial saphenous puncture, and estimates of CPV from this site compared to those obtained via a jugular catheter. Simulataneous CPV values were recorded electronically (mmgh), via calibrated pressure transducer positioned at the level of the manubrium in cats in lateral recumbency. Five readings, performed at 1 minute intervals, were collected from the jugular and CVC catheters at rest (baseline) and following a rapid fluid bolus. Twenty-four hours later, cats were resedated, baseline measurements repeated, and CVPs recorded following a rapid, 25% whole-blood volume bleed. CVP measurements from the jugular and CVC were statistically compared using repeated measures ANOVA (p<0.05). There were no significant differences between the two sites in the baseline and bleed trials. Significant defferences between jugular and CVC CVPs were noted at 1 and 2 minutes following the fluid bolus. It was concluded that CVC is an alternative site for measurement of CPV in sedated cats.     

Resistance to root-lesion nematode Pratylenchus neglectus identified in a new collection of two wild chickpea species (Cicer reticulatum and C. echinospermum) from Turkey

Chickpea (Cicer arietinum) is a major legume crop, with Australia being the second largest producer worldwide. Pratylenchus neglectus is a root-lesion nematode that invades, feeds and reproduces in roots of pulse and cereal crops. In Australia, chickpea and wheat (Triticum aestivum) are commonly grown in rotation and annual damage by P. neglectus accounts for large economic losses to both crops. Cultivated chickpea has narrow genetic diversity that limits the potential for improvement in resistance breeding. New collections of wild chickpea species, C. reticulatum and C. echinospermum, have substantially increased the previously limited world collection of wild Cicer germplasm and offer potential to widen the genetic diversity of cultivated chickpea through the identification of accessions with good resistance. This research assessed 243 C. reticulatum and 86 C. echinospermum accessions for response to P. neglectus in replicated experiments under controlled glasshouse conditions from 2013 and 2014 collection missions that were received, tested and analysed in two experimental sets. Multi-experiment analyses showed lower P. neglectus population densities in both sets of wild Cicer accessions tested than Australia's elite breeding cultivar PBA HatTrick at the significance level p < 0.05. Provisional resistance ratings were given to all genotypes tested in both experimental sets, with C. reticulatum accessions CudiB_008B and Kayat_066 rated as resistant in both Set 1 and Set 2. New sources of resistance to P. neglectus observed in this study can be introgressed into commercial chickpea cultivars to improve their resistance to this nematode.     

Defense chemistry of cyanogenic Eucalyptus cladocalyx seedlings is affected by water supply

Cyanogenesis is a widespread and effective defense mechanism in plants. Published evidence suggests that cyanogenic capacity (i.e., cyanogenic glycoside concentration) is enhanced in response to water stress, although potentially confounding variables preclude a definite conclusion. We used highly cyanogenic Eucalyptus cladocalyx var. nana F. Muell. seedlings grown with varying amounts of water and nitrogen (N) to determine the relationship between cyanogenic capacity and water stress. We also examined whether variation in cyanogenic capacity affects phenolic biosynthesis because both pathways use phenylalanine as a substrate. Cyanogenic capacity in fully expanded leaves increased 70% in response to moderate water stress when N availability was high but only 30% when growth was N-limited. Absolute cyanogenic capacity also increased with increasing N supply. Total phenolics and condensed tannins decreased with increasing N supply, but these compounds were unaffected by water stress. We conclude that, under the influence of water stress, the enhanced demand for phenylalanine for cyanogenic glycoside biosynthesis can be sustained by enhanced shikimate pathway flux without affecting phenolic metabolism.     

Characterisation of bovine strains of Pasteurella multocida and comparison with isolates of avian, ovine and porcine origin

One hundred and fifty-three bovine Pasteurella multocida strains recovered primarily from cases of pneumonia and mastitis in England and Wales over an 11-year period were characterised by capsular PCR typing, comparison of outer membrane protein (OMP) profiles, and multilocus sequence analysis. All of the strains were of capsular type A with the exception of a single capsular type F isolate. Thirteen distinct OMP profiles (OMP-types) were identified based mainly on molecular mass heterogeneity of the heat-modifiable (OmpA) and porin (OmpH) proteins. However, 85% of the isolates were represented by just five OMP-types and 39% of the strains were of a single OMP-type. Multilocus sequence analysis revealed a limited degree of genetic diversity among bovine P. multocida isolates; strains of the same OMP-type have identical genetic backgrounds and represent distinct clones. Analysis of OMP variation was more discriminating than multilocus sequence analysis because strains of different OMP-types had the same, or similar, genetic backgrounds. The association of a small number of clones with the majority of cases of bovine pneumonia suggests that these clones have an increased capacity to cause disease compared to less frequently recovered clones. Molecular mass heterogeneity of OmpA and OmpH, in strains of the same or similar genetic background, suggests that these proteins are subject to diversifying selection within the host and might play important roles in host-pathogen interactions. Comparison of the OMP profiles of bovine isolates with those of avian, ovine and porcine strains showed that a high proportion of the respiratory tract infections in each of these species are caused by different strains of P. multocida. However, the presence of small numbers of closely related strains in more than one host species suggests that transmission of bacteria between different host species is also a factor in the population biology of P. multocida.     

Diversity of avian Pasteurella multocida strains based on capsular PCR typing and variation of the OmpA and OmpH outer membrane proteins

One hundred avian Pasteurella multocida isolates recovered from cases of fowl cholera and related infections in England and Wales over a 13-year period were characterised by capsular PCR typing and analysis of outer membrane protein (OMP) profiles. Sixty-eight percent of the strains were of capsular type A, 14% were type F, 5% were type D, 4% were type B and 9% were untypable. Nineteen distinct OMP profiles (OMP-types) were identified based mainly on molecular mass heterogeneity of the heat-modifiable (OmpA) and porin (OmpH) proteins. Fifty-six percent of the isolates were represented by 15 OMP-types, whereas 44% of the isolates were associated with four OMP-types. The extensive molecular mass heterogeneity of the OmpA and OmpH proteins supports previous findings that avian P. multocida strains are very diverse. Furthermore, the isolates studied were associated with different clinical symptoms and were recovered from a wide range of lesions and tissues. The high degree of strain diversity together with the wide variety of clinical symptoms suggest that certain avian strains of P. multocida are opportunistic pathogens of relatively low virulence. Strains of capsular types B, D and F, as well as the untypable isolates, were associated exclusively with specific OMP-types and represent distinct and widely disseminated clonal groups. These observations support the view that avian strains of P. multocida have a clonal population structure. Based on previous studies, the molecular mass heterogeneity of the OmpA and OmpH proteins might provide a selective advantage to P. multocida by generating antigenic variation.     

A column perfusion test to assess the kinetics of nutrient release by soluble,sparingly soluble and coated granular fertilizers

In recent years, innovations in fertilizer research have principally been in the design of products to supply more timely plant nutrients and mitigate detrimental losses to the environment. In the development of these fertilizers, a laboratory method to comparatively screen a large number of formulations for the rate of nutrient release is a critical first step in formulation optimization to significantly reduce time spent on pot and field trials, reducing costs considerably. Currently, given the absence of a standard laboratory method for all fertilizers, adaptions of a method for coated fertilizers from the International Organization for Standardization (2017) ISO 21263 and other column tests are being used which are often complex and/or require manual sampling which can be laborious, time consuming and costly. The method presented here evaluates the dynamic release in real time by continuously perfusing samples in columns utilizing an automated sample accumulation system for short‐term and long‐term release studies and eliminates the need for soil/sand packing of columns. Mass balance is accounted for by analysing the residue after dissolution and the amount released is expressed as a % of the total nutrient content in the product. This method is reliable, uncomplicated and cost‐effective and has been used to test uncoated soluble fertilizers, nanofertilizers, fertilizers with newly developed coating technologies and other slowly soluble fertilizers, to assess the effect of variables like coating chemistry and thickness, fertilizer composition or fertilizer particle size on release rate.     

Warming With a Forced Air Warming Blanket Minimizes Anesthetic-Induced Hypothermia in Cats

OBJECTIVE: To evaluate the effectiveness of a forced-air warming blanket (FAWB) in minimizing anesthetic-induced hypothermia in cats, and to examine the relationship between esophageal and other estimates of body temperature during skin surface warming. STUDY DESIGN: Prospective, randomized cross-over trial. ANIMALS: Eight adult domestic shorthair cats (four males and four females) weighing 2.3 to 4.5 kg. METHODS: Each cat was anesthetized with halothane in oxygen on four occasions and covered with a modified FAWB. Air delivered to the cats by the FAWB was warmed to approximately 43 degrees C. Each trial lasted 90 minutes and was divided into two consecutive 45-minute periods, during which the FAWB was activated or inactivated thus creating four treatment trials: off/off, on/off, on/on, off/on. Measurements of body temperature from the caudal esophagus, deep rectum, toe-web, and tympanic membrane were recorded at regular intervals throughout each trial and compared. RESULTS: A steady decline in body temperature was observed throughout each trial. Mean body temperature in the cats receiving continual skin surface warming (on/on) was significantly higher than in those receiving no active warming (off/off) and those receiving delayed warming (off/on), from 45 minutes onwards. By 90 minutes, the mean body temperature of cats warmed continuously was 0.9 degrees C higher than in those with no active warming. Notable differences in body temperature were detected between all measurement sites, with the exception of esophagus versus rectum. Rectal and esophageal temperatures did not differ at any time point. Tympanic membrane temperatures measured with either device were lower than esophageal temperatures. CONCLUSIONS: The modified FAWB was effective in minimizing the degree of hypothermia experienced in cats anesthetized with halothane for 90 minutes. Deep rectal temperature was an accurate reflection of esophageal temperature in these cats. CLINICAL RELEVANCE: Forced air warming blankets may prove successful in minimizing anesthetic-induced hypothermia in cats.     

Formulation,synthesis and characterization of boron phosphate (BPO4) compounds as raw materials to develop slow‐release boron fertilizers

We investigated the use of boron phosphate (BPO₄) as a slow‐release boron (B) source. Boron phosphate compounds were synthesized by mixing boric acid (H₃BO₃) and phosphoric acid (H₃PO₄) and heating at temperatures of 25 to 1000°C for 1 or 24 h. X‐ray diffraction (XRD) patterns and chemical analysis confirmed the formation of BPO₄. The crystallinity of these compounds increased with increasing temperature and heating time. The compounds synthesized at 300°C or less were hygroscopic and clumped together, while those synthesized at 500 to 1000°C were non‐hygroscopic and free‐flowing. The solubility of these compounds was assessed at different pH and P concentrations, and compared to the solubility of ulexite and colemanite. The solubility of the BPO₄ compounds decreased with increasing synthesis temperature and with decreasing pH. The solubility and the kinetics of B release from BPO₄ compounds synthesized at 500 and 800°C were slower than for most commonly used B sources. Given their slow dissolution, the BPO₄ compounds may have potential to continuously supply B to crops in environments where B leaching is a problem. The compounds synthesized at 500 and 800°C show potential for co‐granulation with macronutrient fertilizers such as mono‐ammonium phosphate to produce slow‐release B‐enriched granules.     

Temporal and spatial variation in cyanogenic glycosides in Eucalyptus cladocalyx

The release of hydrogen cyanide from endogenous cyanide-containing compounds in plants is an effective herbivore deterrent. We investigated temporal and spatial variations in cyanogenic glycoside concentration in greenhouse-grown seedlings and 6-year-old plantation trees of Eucalyptus cladocalyx F. Muell., which allocates up to 20% of leaf nitrogen to the cyanogenic glycoside, prunasin. The highest cyanogenic glycoside concentrations were in the young, developing vegetative and reproductive tissues. Both the overall cyanogenic glycoside concentration and the proportion of nitrogen allocated to cyanogenic glycoside decreased as tissues matured. Cyanogenic glycoside and nitrogen concentrations were similar at all positions on the leaf blade. There was no change in concentration of cyanogenic glycosides either diurnally or following wounding of the tissue, suggesting that these compounds are constitutive. Cyanogenic glycoside concentration varied seasonally in young leaf tips of field-grown E. cladocalyx, but not in mature, fully expanded leaves. Although some of the changes in cyanogenic glycoside concentration in young leaf tips may have been driven by changes in leaf nitrogen, there was a significant decrease in the proportion of nitrogen allocated to cyanogenic glycosides in young leaves during the summer, coinciding with the peak flowering period. Mobilization of cyanogenic glycosides may have occurred to provide nitrogen for reproduction. Most of the observed temporal and spatial variations in cyanogenic glycosides are consistent with the optimal use of resources, particularly nitrogen.