Vaccine efficacy for reducing turbinate atrophy and improving growth rate in piggeries with endemic atrophic rhinitis

Two vaccines, based on formalin-killed whole cells of toxigenic Pasteurella multocida type D and Bordetella bronchiseptica combined with a partially toxoided cell extract of P multocida, were prepared with Freund's incomplete adjuvant (vaccine 1) or by alum precipitation (vaccine 2). Each was tested for safety and efficacy in reducing the severity of nasal turbinate atrophy and improving the growth rate of pigs in three Western Australian commercial piggeries with endemic atrophic rhinitis. In safety experiments with vaccine 1, no adverse clinical effects were observed in vaccinated sows or their progeny. Piglets receiving vaccine 2 showed no injection site abnormalities, pyrexia or turbinate atrophy. In field trials, vaccine 1 significantly reduced the prevalence of moderate to severe nasal turbinate atrophy (Done score 3 to 5) when used in two piggeries (A and B). Progeny from vaccinated sows in piggery B also grew significantly faster than controls. When vaccine 2 was used in piggery A at a later date and in another piggery (C), growth rate was not improved in either piggery and the prevalence of moderate to severe turbinate atrophy was reduced only in piggery C.     

Diagnosing feline immunodeficiency virus (FIV) and feline leukaemia virus (FeLV) infection: an update for clinicians

With the commercial release in Australia in 2004 of a vaccine against feline immunodeficiency virus (FIV; Fel‐O‐Vax FIV®), the landscape for FIV diagnostics shifted substantially. Point‐of‐care (PoC) antibody detection kits, which had been the mainstay for diagnosing FIV infection since the early 1990s, were no longer considered accurate to use in FIV‐vaccinated cats, because of the production of vaccine‐induced antibodies that were considered indistinguishable from those produced in natural FIV infections. Consequently, attention shifted to alternative diagnostic methods such as nucleic acid detection. However, over the past 5 years we have published a series of studies emphasising that FIV PoC test kits vary in their methodology, resulting in differing accuracy in FIV‐vaccinated cats. Importantly, we demonstrated that two commercially available FIV antibody test kits (Witness? and Anigen Rapid?) were able to accurately distinguish between FIV‐vaccinated and FIV‐infected cats, concluding that testing with either kit offers an alternative to PCR testing. This review summarises pertinent findings from our work published in a variety of peer‐reviewed research journals to inform veterinarians (particularly veterinarians in Australia, New Zealand and Japan, where the FIV vaccine is currently commercially available) about how the approach to the diagnosis of FIV infection has shifted. Included in this review is our work investigating the performance of three commercially available FIV PoC test kits in FIV‐vaccinated cats and our recommendations for the diagnosis of FIV infection; the effect of primary FIV vaccination (three FIV vaccines, 4 weeks apart) on PoC test kit performance; our recommendations regarding annual testing of FIV‐vaccinated cats to detect ‘vaccine breakthroughs’; and the potential off‐label use of saliva for the diagnosis of FIV infection using some FIV PoC test kits. We also investigated the accuracy of the same three brands of test kits for feline leukaemia virus (FeLV) diagnosis, using both blood and saliva as diagnostic specimens. Based on these results, we discuss our recommendations for confirmatory testing when veterinarians are presented with a positive FeLV PoC test kit result. Finally, we conclude with our results from the largest and most recent FIV and FeLV seroprevalence study conducted in Australia to date.     

Factors influencing farmers' responses to welfare legislation: A case study of gestation sow housing in Flanders (Belgium)

In the light of the EU ban on individual confinement of gestating sows which will have to be fully implemented by 2013, a survey was conducted among a representative sample of Flemish pig producers. The questionnaire was sent by post to 250 farmers in 2003 and 352 farmers in 2005 of which 219 and 296, respectively, provided valid responses via telephone. The percentage of respondents housing (some of) their sows in group was 10.5% in 2003 and 16.2% in 2005. These farmers were more likely to have a successor than farmers housing their sows individually. The most common group housing systems were free access stalls (24%) followed by electronic feeding stations (21%), ad libitum feeding (20%), feeding stalls/troughs (18%), and drop/trickle feeding systems (13%). Interval (4%) and electronic feed dispensers (0%) were very rare in Flanders. The main criteria for having chosen a particular group housing system related to sow health and welfare, investment costs and amount of labour. The relative importance of economic reasons has increased over time. Users were generally rather satisfied with their group housing system. Farmers using group housing for all their sows were more satisfied than farmers using both group and individual housing. Users of ad libitum feeding systems (and feeding stalls/troughs) were more satisfied than users of electronic feeding stations. A minority of respondents was planning to change to group housing within two years time (4.1% in 2003 and 7.4% in 2005). These tended to be young farmers with a large sow herd and 58% reported to opt for free access stalls. The main reason why the remaining respondents were not planning to change to group housing yet is that they will stop farming activities before 2013. This reason was particularly important for older small-scale farmers without a successor. In contrast, the lack of financial resources and security was particularly important for young farmers of a large sow herd with a likely successor. An increasing group of farmers (often without a successor) reported to delay changing to group housing because they consider individual housing more profitable. These results show that, in Flanders, the conversion to group housing is taking place slowly, that the reasons for not converting yet vary according to the farmers' age, the likelihood of a successor and herd size, and that there are differences between operational group housing systems concerning herd size, age of the system, sow management and user satisfaction.     

Pyometra and unilateral uterine horn torsion in a sheep

A 13‐year‐old Romanov sheep presented for evaluation of vaginal discharge, depression and anorexia. Blood work demonstrated mature neutrophilia and marked hyperlactatemia. Transrectal and transabdominal ultrasound revealed echogenic fluid (pus) within the uterus. Purulent uterine fluid culture yield Escherichia coli. A diagnosis of pyometra was made. After medical treatment without clinical improvement, an exploratory laparotomy was performed, and a 360‐degree uterine left horn torsion was identified with the pyometra and multiple corpora lutea on both ovaries. Ovariohysterectomy was performed and the ewe recovered uneventfully.     

Postharvest quality of apple predicted by NIR-spectroscopy: Study of the effect of biological variability on spectra and model performance

The effect of cultivar, season, shelf-life and origin on the accuracy of near infrared (NIR) calibration models for the soluble solids content (SSC) and firmness of apple was studied based on a large spectral data set based on approximately 6000 apple fruit from different cultivars, origins, shelf-life exposure time and seasons. To interpret the variance in the spectra with respect to biological variability, functional analysis of variance (FANOVA) was used. From the FANOVA analysis it was concluded that the effects of cultivar, origin and shelf-life exposure time on the NIR spectra were all significant. The largest differences in the spectra were found around the water absorption peaks (970, 1170 and 1450 nm). External validations using independent data sets showed that the accuracy of the models increased considerably when more variability was included in the calibration data set. In general the RMSEP for predictions of the SSC were in the range 0.6–0.8 °Brix, while for Magness Taylor firmness it was 5.9–8.8 N, depending on the cultivar. It was shown that atypical data can lead to large validation errors. It is, therefore, important to collect a calibration data set which is sufficiently representative for future samples to be analyzed with the developed calibration models and to develop simple procedures for model adaptation during practical use.     

Restoring dry Afromontane forest using bird and nurse plant effects: Direct sowing of Olea europaea ssp. cuspidata seeds

To identify the perspectives of seed sowing for reforestation of degraded dry Afromontane savanna in exclosures in northern Ethiopia, seeds of a fleshy-fruited, secondary climax tree, Olea europaea ssp. cuspidata, were placed under two pioneer shrub species (Euclea racemosa and Acacia etbaica) and in open microhabitats. Seed removal and germination rates were examined. The effects of bird ingestion, manual pulp removal and mechanical endocarp treatments on germination rates were also studied.

Pulp removal promoted seed germination, in particular in seeds without endocarp manipulation. Seed removal, presumably by rodents, was concentrated in narrow strips along linear soil conservation structures, and not different between shrubs and open microhabitats. In the absence of water stress, humus types did not have a significant effect on germination rates. Under field conditions however, germination was higher under Euclea canopies. The observed facilitative effect of Euclea shrubs on germination may be attributed to moisture retention effects, related to the deep humus layer and canopy architecture, preventing desiccation and promoting imbibition of seeds. When readily available Olea seeds are not used for seedling production, direct sowing of seeds in the humus under dense Euclea shrubs could offer a cheap complement to planting of nursery-raised seedlings for forest restoration projects in recovering Afromontane savanna.