Using fatty acid markers to distinguish between effects of salmon (Salmo salar) and halibut (Hippoglossus hippoglossus) farming on mackerel (Scomber scombrus) and whiting (Merlangius merlangus)

Presence of coastal aquaculture activities in marine landscapes is growing with impacts on the wild fish that share these habitats. However, it is difficult to disentangle subsequent ecological interactions between these activities and marine fish communities. We evaluated the impact of both salmon and halibut farms on mackerel (Scomber scombrus) and whiting (Merlangius merlangus) sampled near sea cages using condition indices and fatty acid (FA) biomarkers. Results of the stomach content analysis indicated that mackerel and whiting consumed waste feed which was also reflected in their modified FA profiles. Both mackerel and whiting had elevated levels of FAs that are of vegetable oils origin. The use of vegetable oils as replacement for marine oils is a lot more common in salmon farming than halibut farming. Additionally, the overall effects of the two fish farms were more pronounced in whiting than in mackerel sampled near the sea cages. By allowing discrimination between sources of trophic interactions, this method could lead to more informed decisions in managing different farming activities.     

Effects of dimethoate and beta-naphthoflavone on selected biomarkers of Poecilia reticulata

The main objective of the present study was to investigate if a battery of enzymatic biomarkers was suitable for use as effect criteria in acute toxicity tests with Poecilia reticulata. To attain this objective, the in vivo effects of dimethoate and beta-naphthoflavone on acetylcholinesterase (AChE), cytochrome P4501A-dependent monooxygenase activity of 7-ethoxyresorufin O-deethylase (EROD), glutathione S-transferases (GST), lactate dehydrogenase (LDH) and Na⁺-K⁺-ATPase activities of P. reticulata were studied. After 96 h of exposure to sublethal concentrations (0.063 mg l⁻¹ to 1 mg l⁻¹) of the pesticide, an inhibition of the enzymes AChE and GST, as well as an induction of LDH was observed. The compound beta-naphthoflavone significantly induced both EROD and GST. The remaining enzymes analysed were not significantly altered by the exposure to beta-naphthoflavone (0.82 mg l⁻¹ to 1.7 mg l⁻¹). These results suggest that in vivo toxicity tests based on the biomarkers used in this study are sensitive and present advantages to conventional acute tests based on mortality, since they were able to detect sublethal effects in a short-period of time (96 h) indicating target and/or detoxification mechanisms. This revised version was published online in July 2006 with corrections to the Cover Date.     

Microbial phospholipid biomarkers and stable isotope methods help reveal soil functions

This review targets microbial phospholipid biomarkers, their isotope analysis and their ability to reveal soil functions. The amount and composition of phospholipid fatty acids (PLFAs) measured in environmental samples strongly depend on the methodology. To achieve comparable results the extraction, separation and methylation method must be kept constant. PLFAs patterns are sensitive to microbial community shifts even though the taxonomic resolution of PLFAs is low. The possibility to easily link lipid biomarkers with stable isotope techniques is identified as a major advantage when addressing soil functions. Measurement of PLFA isotopic ratios is sensitive and enables detecting isotopic fractionation. The difference between the carbon isotopic ratio of single PLFAs and their substrate (Δ¹³C) can vary between −6 and +11‰. This difference derives from the fractionation during biosynthesis and from substrate inhomogeneity. Consequently, natural abundance studies are restricted to quantifying substrate uptake of the total microbial biomass. In contrast, artificial labelling enables quantifying carbon uptake into single PLFAs, but labelling success depends on homogeneous and undisturbed label application. Current developments in microbial ecology (e.g. ¹³C and ¹⁵N proteomics) and isotope techniques (online monitoring of CO₂ isotope ratios) will likely improve soil functional interpretations in the future. ¹³C PLFA analysis will continue to contribute because it is affordable, sensitive and allows frequent sampling combined with the use of small amounts of ¹³C label.     

Phenoloxidase and peroxidase activity in the shrimp Litopenaeus schmitti,Pérez‐Farfante and Kensley (1997) exposed to low salinity

Phenoloxidase and peroxidase activity were analysed in haemolymph of juvenile shrimp, Litopenaeus schmitti, exposed to different salinity levels (35%, 18%, 8%) for 48 h. A significant reduction (P<0.05) in total glucose and phenoloxidase activity in animals exposed to lower salinities (18% and 8%) was recorded, while peroxidase activity and total protein concentration did not vary. Histology revealed the occurrence of oedema in gills in shrimp exposed to 8%. The work demonstrates for the first time that in L. schmitti, low salinities can decrease glucose levels in haemolymph and create an immunosuppressive state by reducing phenoloxidase activity.     

European veterinary dissertations

Diseases affecting synovial joints are a major cause of chronic disability both in humans and in companion animal species, most notably dogs and horses. As progressive deterioration of the articular cartilage is the hallmark of degenerative joint disease or osteoarthritis, research efforts traditionally tended to focus primarily on cartilage pathology. However, in recent years it has become clear that synovial joints should be considered intricate organs in their own right, with each of the constituent tissues (cartilage, bone, and synovial membrane) interacting with each other both in health and disease. Moreover, with the advent of modern molecular biology techniques, the importance of synovial inflammation in disease development and progression has become increasingly recognized. These realizations have spurred the need for tools that allow a more comprehensive, integral study of synovial joint homeostasis. This review provides a brief overview of synovial joint biology and the concept of joint homeostasis, followed by a discussion of methods that may be used to study joint homeostasis (varying from in vitro tissue culture to in vivo imaging) including specific advantages and limitations of each approach. It then zooms in on one such approach, synovial fluid biomarker analysis, as a promising avenue in synovial joint research, highlighting some results from equine studies performed in the author's own laboratory that illustrate how such studies may help shed light on in vivo joint homeostasis and therapeutic modulation thereof. The review concludes with some future perspectives and promising developments in the field.     

Assessment of the diagnostic accuracy of circulating cardiac troponin I concentration to distinguish between cats with cardiac and non-cardiac causes of respiratory distress

Objective

To determine if serum cardiac troponin I (cTnI) concentrations can distinguish cardiac from non-cardiac causes of respiratory distress (RD) in cats.

Animals, materials and methods

53 cats. cTnI concentrations were measured in 30 cats with non-cardiac respiratory distress (RD-NC) and compared to 23 cats with RD due to congestive heart failure (RD + CHF).

Results

The RD + CHF group had higher median cTnI concentration (0.94 ng/ml interquartile range IQR 0.54-4.00, range <0.20 - 90.14) than the RD-NC group (<0.2 ng/ml IQR < 0.2-0.33, range <0.20-41.1, p < 0.001). The area under the curve (AUC) was 0.842 (95% CI 0.728-0.955) for the receiver operator curve (ROC) analysis of the accuracy of cTnI concentrations to discriminate RD + CHF from RD-NC cats. A cut-off of ≥ 0.81 ng/ml discriminated RD + CHF from RD-NC cats with a sensitivity and specificity of 65.2% and 90.0% respectively. However considerable overlap in cTnI concentrations between the 2 groups was identified.

Conclusions

Serum cTnI concentrations were different in RD + CHF compared to RD-NC cats. However the overlap in cTnI concentrations between the 2 groups reduced the clinical efficacy of the assay which therefore should not be used as a stand-alone test but in combination with other diagnostics such as echocardiography and radiography.     

Cardiac Troponin I as Compared to Troponin T for the Detection of Myocardial Damage in Horses

Background

Different cardiac troponin I (cTnI) assays give different results. Only 1 manufacturer has marketed troponin T (cTnT) assays. Therefore, cTnT often is preferred for detection of myocardial infarction in human patients. Studies of cTnT in horses are limited.

Objectives

To compare a cTnI and a high‐sensitive cTnT assay (hs‐cTnT) in horses.

Animals

Cardiac troponin I and cTnT were determined in 35 healthy horses (group 1), 23 horses suspected to have primary myocardial damage (group 2a), and 41 horses with secondary myocardial damage caused by structural heart disease (group 2b).

Methods

All cTnI samples were analyzed at laboratory A (limit of detection [LOD]: 0.03 ng/mL), whereas cTnT samples were analyzed at 2 laboratories with the same hs‐cTnT assay (laboratory B, LOD: 10.0 pg/mL; laboratory C, LOD: 4.0 pg/mL).

Results

The median cTnI concentration in group 2a (0.90 ng/mL; range, 0.03–58.27 ng/mL) was significantly higher (P < .001) than in group 1 (0.03 ng/mL; range, 0.03–0.09 ng/mL) or group 2b (0.05 ng/mL; range, 0.03–30.92 ng/mL), and the optimal cut‐off for detection of primary myocardial damage was 0.095 ng/mL (sensitivity: 90.5%, specificity: 100%). Using an LOD of 10.0 pg/mL for all cTnT samples, a cut‐off value of 10.5 pg/mL was found, but sensitivity was low (42.9%). When only samples analyzed at laboratory C (n = 58) were included, a cut‐off of 6.6 pg/mL was found (sensitivity: 81%, specificity: 100%).

Conclusions and Clinical Importance

Despite large quantitative differences, cTnI and cTnT are both useful for detection of myocardial damage in horses.     

Soil carbon pools, plant biomarkers and mean carbon residence time after afforestation of grassland with three tree species

Afforestation of grassland has been globally identified as being an important means for creating a sink for atmospheric carbon (C). However, the impact of afforestation on soil C is still poorly understood, due to the paucity of well designed long-term experiments and the lack of investigation into the response of different soil C fractions to afforestation. In addition, little is known about the origins of soil C and soil organic matter (SOM) stability after afforestation. In a retrospective study, we measured C mass in the soil light and heavy fractions in the first 10 years after afforestation of grassland with Eucalyptus nitens, Pinus radiata and Cupressus macrocarpa. The results suggest that C mass in the soil heavy fraction remained stable, but the C mass in the light fraction decreased at year 5 under three species. Soil δ¹³C analysis showed that the decrease in the light fraction may be due to reduced C inputs from grassland species litter and low inputs from the still young trees. After the initial reduction, the recovery of soil C in the light fraction depended on tree species. At year 10, an increase of 33% in light fraction soil C was observed at the 0-30 cm depth under E. nitens, compared to that under the original grassland (year 0). Planting P. radiata restored light fraction soil C to the original level under grassland, whereas planting C. macrocarpa led to a decrease of 33%. We concluded that the increase of light fraction soil C between year 5 and 10 is most likely due to C input from tree residues. Most of the increased C was derived from root turnover under pine and from both root and leaf turnover under E. nitens, as indicated by plant C biomarkers such as lignin-derived phenols and suberin and cutin-derived compounds in the 0-5 cm soil layer. Modelling of soil ?¹⁴C‰ suggested that SOM had a greater mean residence time at year 10 than year 0 and 5 due to increased relative abundance of recalcitrant plant biopolymers.