Effect of strategic deworming on Ascaris suum exposure and technical performance parameters in fattening pigs.

The aim of this study was to investigate the effect of a strategic deworming program on Ascaris suum infection levels and technical performance parameters in fattening pigs. Eighteen fattening stables were selected and divided into two groups. Group 1 consisted of 9 stables in which the fattening pigs tested seropositive for Ascaris, indicative for the presence of Ascaris eggs in the stable, whereas group 2 consisted of 9 stables in which the fattening pigs tested seronegative for Ascaris, indicating of a low or absent environmental contamination with Ascaris eggs. The production in each stable was monitored for a period of 7 consecutive fattening rounds. The first of these 7 fattening rounds (i.e. round 0), during which no intervention took place in the deworming strategy applied in the stable, served as a historical control. A deworming program using 200 mg/ml fenbendazole oral suspension in drinking water for 2 days every 6 weeks was implemented for a period of 6 consecutive fattening rounds. For each fattening round and for each stable, technical performance parameters including average daily growth, feed conversion ratio, days in fattening and the percentage of affected livers were obtained from the producers. Blood was collected from 10 randomly selected animals per stable at the end of each fattening round and evaluated for the presence of anti-Ascaris antibodies using 2 different serological tests, namely the AsHb- and the L3-Lung ELISA. The serological results obtained indicated a lower exposure of the animals to Ascaris after the implementation of a strategic deworming program. A significant decline in anti-Ascaris antibody levels was detectable in the stables that originally tested positive for Ascaris and was already visible after one treatment round. The outcomes of hierarchical linear mixed models indicated that the level of L3-Lung antibody reactivity was a significant predictor of decreased ADG, increased FCR and prolonged DIF for the Ascaris-positive herds, indicating an effect of Ascaris infections on productivity.

Immune responses of a chimaeric protein vaccine containing Mycoplasma hyopneumoniae antigens and LTB against experimental M. hyopneumoniae infection in pigs.

A recombinant chimaeric protein containing three Mycoplasma hyopneumoniae antigens (C-terminal portion of P97, heat shock protein P42, and NrdF) fused to an adjuvant, the B subunit of heat-labile enterotoxin of Escherichia coli (LTB), was used to immunize pigs against enzootic pneumonia. The systemic and local immune responses, as well as the efficacy of the chimaeric protein in inducing protection against experimental M. hyopneumoniae infection were evaluated. In total, 60 male piglets, purchased from a M. hyopneumoniae-free herd, at 4 weeks of age were randomly allocated to six different experimental groups of 10 animals each: recombinant chimaeric protein by intramuscular (IM) (1) or intranasal (IN) (2) administration, commercial bacterin by IM administration (3), and the adjuvant LTB by IM (4, control group A) or IN (5, control group B) administration. All groups were immunized at 24 and 38 days of age and challenged at 52 days of age. The sixth group that was not challenged was used as the negative control (IN [n=5] or IM [n=5] administration of the LTB adjuvant). Compared with the non-challenged group, administration of the chimaeric protein induced significant (P<0.05) IgG and IgA responses against all individual antigens present in the chimaera, but it could not confer a significant protection against M. hyopneumoniae infection in pigs. This lack of effectiveness points towards the need for further studies to improve the efficacy of this subunit-based vaccine approach.

A longitudinal study of the diversity and dynamics of Mycoplasma hyopneumoniae infections in pig herds.

A longitudinal study was carried out to investigate the diversity and persistence of Mycoplasma hyopneumoniae (M. hyopneumoniae) strains in four infected pig herds. In each herd, 20 pigs were randomly selected and blood and/or bronchoalveolar lavage (BAL) fluid was collected at 6, 10, 14 and 26 weeks of age. In the BAL fluid, quantitative PCR and MLVA (multiple-locus variable number of tandem repeats (VNTR) analysis) testing were performed for detection and typing of M. hyopneumoniae strains, respectively. At 26 weeks of age, the prevalence and severity of lung lesions were recorded at slaughter (minimum 50 pigs belonging to the same batch as the investigated pigs). The percentage of pigs testing positive on qPCR increased from 35% at 6 weeks to 96% at 26 weeks of age. With MLVA testing, positive pigs were found from 14 weeks onwards. Within each herd, only one distinct strain was detected, although clonal variants were identified in two herds. In three of the herds, the strain remained present until slaughter age. The percentage of pigs with Mycoplasma-like lesions ranged from 38% to 98%, and the average pneumonia score ranged from 1.7 to 11.9, respectively. The present field study documented that within a herd, mainly one distinct M. hyopneumoniae strain was present that persisted in the same animals for at least 12 weeks. This implies that the immune response of the animals following infection is not able to rapidly clear the infection from the respiratory tract.