1. The effect of stocking density on welfare traits of turkeys was studied in 2 experiments. In each experiment 2,633 sexed BUT turkey poults were assigned to 3 rooms, 135 m2 with 1 treatment per room. Because of the large flock size (675,878 and 1080 birds in T1, T2 and T3 respectively) treatments were not replicated 2. Floor space allowances varied according to treatment; for the males: 24 dm2, 18.5 dm2 and 15 dm2 until week 12 and 40 dm2, 31 dm2 and 25 dm2 from week 12; for the females: 16 dm2, 12.3 dm2 and 10 dm2. 2. The scan sampling method in experiment 1 and the focal sampling method in experiment 2 were used to record behaviour at week 6, 9, 12 (males and females), and 16 (males). Birds' ethogram was divided into 7 mutually exclusive behaviours: standing/walking, resting, feeding, drinking, pecking at the environment, pecking at another bird, and preening. Position changes in the pen and the frequency of disturbances of resting birds by other birds were recorded in experiment 2. 3. Gait was assessed at week 12 (females) and week 16 (males). Prevalence of lesions, breast (males), hip and foot (males and females), were recorded at slaughter. Birds were weighed at week 12 (males and females) and week 16 (males). 4. Stocking density had little influence on behaviour except on the frequency of disturbances of resting birds by other birds, which tended to be more frequent at the highest density. 5. Gait deteriorated as stocking density increased. Hip and foot lesions were more frequent at the highest density. Bodyweight decreased significantly with decreasing floor space. 6. The results suggest that turkey welfare was poorer at the highest density than at the 2 lower stocking densities.

The objective of this study was to measure the effects of chronic exposure to fumonisins via the ingestion of feed containing naturally contaminated corn in growing pigs infected or not with Salmonella spp. This exposure to a moderate dietary concentration of fumonisins (11.8 ppm) was sufficient to induce a biological effect in pigs (Sa/So ratio), but no mortality or pathology was observed over 63 days of exposure. No mortality or related clinical signs, even in cases of inoculation with Salmonella (5 × 104 CFU), were observed either. Fumonisins, at these concentrations, did not affect the ability of lymphocytes to proliferate in the presence of mitogens, but after seven days post-inoculation they led to inhibition of the ability of specific Salmonella lymphocytes to proliferate following exposure to a specific Salmonella antigen. However, the ingestion of fumonisins had no impact on Salmonella translocation or seroconversion in inoculated pigs. The inoculation of Salmonella did not affect faecal microbiota profiles, but exposure to moderate concentrations of fumonisins transiently affected the digestive microbiota balance. In cases of co-infection with fumonisins and Salmonella, the microbiota profiles were rapidly and clearly modified as early as 48 h post-Salmonella inoculation. Therefore under these experimental conditions, exposure to an average concentration of fumonisins in naturally contaminated feed had no effect on pig health but did affect the digestive microbiota balance, with Salmonella exposure amplifying this phenomenon.

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In order to evaluate genetic variation between rabbit haemorrhagic disease virus (RHDV) isolates and to derive phylogenetic relationships, 56 virus isolates collected from various parts of France over a 7 year period (1988 to 1995) were examined. Analyses were carried out by direct nucleotide sequencing of PCR fragments of three genomic regions encoding the capsid protein (VP60) (regions A and B) and a non-structural protein (region C). Multiple sequence alignments revealed maximum nucleotide divergence of 7n6, 9n4 and 8n7 % for regions A, B and C, respectively, indicating a high level of conservation between isolates. Irrespective of the genomic region analysed, phylogenetic analyses carried out using various methods allowed the identification of three genogroups ; distribution of isolates within these genogroups appears to be more related to the year of their collection than to their geographical origin. The possible evolution of RHDV is discussed.Rabbit haemorrhagic disease (RHD) is a highly contagious and fatal viral disease of both domestic and wild rabbits. The disease is characterized by a short incubation period (24 to 48 h) and a high rate of mortality (60 to 90 %). Only young animals (less than 2 months old) remain unaffected.RHD was first described in China in 1984(Liu et al., 1984 and then in Korea following rabbit fur importation from China. Subsequently, the virus has spread from Asia to continental European countries and by 1989 the virus was widespread throughout Europe (Morisse et al., 1991). RHD was also described

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