2006). The effect of lactose and inulin on intestinal morphology, selected microbial populations and volatile fatty acid concentrations in the gastro-intestinal tract of the weanling pig. AbstractTwenty piglets (21 days, 7·8 kg live weight (LW)) were used in a 2 £ 2 factorial to investigate interactions between lactose and inulin on intestinal morphology, microbiology and volatile fatty acid (VFA) production of the weanling pig. The piglets were offered the following diets for 6 days and then sacrificed: (T1) 150 g/kg lactose, (T2) 150 g/kg lactose þ15 g/kg inulin, ( T3) 330 g/kg lactose, and ( T4) 330 g/kg lactose þ15 g/kg inulin. Tissue samples were taken from the duodenum, jejunum and ileum for morphological measurements. Digesta samples were taken from the ileum, caecum and colon. There was an interaction ( P , 0·05) between lactose and inulin in villous height in the jejunum. The inclusion of inulin at 150 g/kg lactose increased villous height compared with 150 g/kg lactose without inulin. However, inulin had no effect on villous height at 330 g/kg lactose inclusion. There was a linear relationship between food intake and villous height in the duodenum ( P , 0·001, R 2 ¼ 0·45) and the jejunum ( P , 0·01, R 2 ¼ 0·25). The inclusion of 330 g/kg lactose increased ( P , 0·05) total VFA compared with 150 g/kg lactose in the caecum and the population of lactobacilli in the caecum and colon ( P , 0·1). There was an interaction ( P , 0·05) between lactose and inulin for total VFA concentration in the colon. The pigs receiving 330 g/kg lactose had a higher total VFA concentration compared with pigs on 150 g/kg lactose. However, there was no difference between 150 g/kg and 330 g/kg lactose when the diets were supplemented with inulin. In conclusion, the inclusion of high dietary concentrations of lactose resulted in increased lactobacilli and short-chain fatty acid concentrations. The inclusion of inulin with low dietary concentrations of lactose resulted in improved intestinal health through a reduction of intestinal pH and increases in villous height.

Equine mitochondrial DNA (mtDNA) phylogeny reconstruction reveals a complex pattern of variation unlike that seen in other large domesticates. It is likely that this pattern reflects a process of multiple and repeated, although not necessarily independent, domestication events. Until now, no clear geographic affiliation of clades has been apparent. In this study, amova analyses have revealed a significant non-random distribution of the diversity among equine populations when seven newly sequenced Eurasian populations were examined in the context of previously published sequences. The association of Eastern mtDNA types in haplogroup F was highly significant using Fisher's exact test of independence (P = 0.00000). For the first time, clear biogeographic partitioning has been detected in equine mtDNA sequence.

Equine mitochondrial DNA sequence variation was investigated in three indigenous Irish horse populations (Irish Draught Horse, Kerry Bog Pony and Connemara Pony) and, for context, in 69 other horse populations. There was no evidence of Irish Draught Horse or Connemara Pony sequence clustering, although the majority of Irish Draught Horse sequences (47%) were assigned to haplogroup D. Conversely, 31% of the Kerry Bog Pony sequences were assigned to the rare haplogroup E. In addition to the extant population analyses, ancient DNA sequences were generated from three out of four Irish archaeological specimens, all of which were assigned to haplogroup A.

Summary A linear assessment trait evaluation system is proposed to allow quantitative description of the static conformation of the horse. Measurements were made on 27 selected traits. The system was tested initially for repeatability of measurements on 4 horses. Twenty‐one of the selected traits were satisfactory and 6 proved unsatisfactory in terms of reproducibility. A population of 101, superior 2‐ and 3‐year‐old Thoroughbreds and 19 premium Thoroughbred stallions were similarly assessed. More than 65% of the traits exhibited large (CV>10%) phenotypic variation within the sampled population. It is proposed that such a system of static conformation assessment, in conjunction with a similar system for dynamic linear assessment, would provide useful quantitative selection criteria in the description and breeding of horses.

Three experiments were carried out to evaluate the effects of varying levels of mineral and iodine supplements when offered to ewes in late pregnancy on lamb serum immunoglobulin G (IgG) concentrations. In experiment 1, 44 individually housed ewes were allocated to one of four treatments (no. = 11) and offered a basal diet of grass silage ad libitum which was supplemented with 500 g/day of a concentrate (190 g/kg of crude protein (CP)), in addition to mineral/vitamin fortification at the rate of 0 g (C), 17.3 g (LM), 34.6 g (MM) or 52.0 g (HM) per day for the final 7 weeks of pregnancy. The mineral/vitamin supplement contained Ca, P, Na, Mg, Mn, Se, I, Co, Mn and vitamin E. The ewes were milked at 1 h, 10 h and 18 h post partum and measured quantities of colostrum, proportional to lamb birth weight, were fed back to the lambs via a stomach tube. Treatment had no effect on total colostrum yield or total IgG yield to 18 h post partum (P > 0.05). There was a linear decrease in serum IgG concentration and IgG absorption efficiency as mineral supplementation increased (P < 0.001). In experiment 2, which was carried out in conjunction with experiment 1, 44 ewes were allocated to four treatments (no. = 11) and offered the same basal silage/concentrate diet as in experiment 1, in addition to receiving one of the following supplements : (C) control, as in experiment 1; (HM), as in experiment 1; (−I), ewes offered the same mineral/vitamin supplement as HM but with iodine excluded; (I0), ewes offered a daily mineral supplement of iodine only at a level of 40 mg per ewe, equivalent to the iodine inclusion in the 52 g of minerals offered in HM. The iodine-supplemented progeny (HM and IO) had lower (P < 0.001) serum IgG concentrations and higher soil scores (P < 0.05) than the C and −I progeny. In experiment 3, the effects of varying levels of iodine supplementation when offered to ewes during the final 6 weeks of pregnancy on lamb serum IgG values were examined. Forty-eight individually housed ewes were allocated to one of four treatments (no. = 12) and offered grass silage ad libitum, which was supplemented initially with 500 g of a concentrate (140 g/kg of CP) from days 99 to 130 of gestation and then replaced with 700 g/day of a concentrate (180 g/kg of CP) from day 131 of gestation until lambing. In addition, the diet of each ewe was supplemented on a daily basis with iodine at the rate of 0 mg (C), 8.9 mg (LI), 17.7 mg (MI) or 26.6 mg (HI). There was a negative linear reduction in serum IgG concentration and IgG absorption efficiency as maternal dietary iodine supplementation increased (P < 0.001). We conclude that supplementation of the ewe's diet in late pregnancy with 17.3 g of a mineral supplement as formulated in the current experiment lowers the lamb's ability to absorb colostral IgG, and offering only the iodine component of this mineral supplement, at a level which approximates to about one third of currently quoted toxicity levels, will result in reduced serum IgG concentration in the lamb. These findings suggest the need to re-examine current toxicity values for iodine.

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Ninety twin-bearing ewes were given food individually and allocated to five (no. = 18) treatments in order to determine the effects of supplementing their diet in late pregnancy with mineral-block components on colostrum production, lamb serum immunoglobulin G (IgG) concentration and colostral IgG absorption. Ewes were offered grass silage ad libitum, supplemented with 400 to 500 g per ewe per day of concentrates from day 99 of gestation, in addition to receiving one of the following supplements: C, (control) no supplement; B, mineral block; ML, liquid molasses; MN, granular minerals; ML + MN, liquid molasses and granular minerals. The experiment commenced on day 99 of gestation. Ewes were milked at lh, 10 h and 18 h post lambing and all lambs were fed measured quantities of colostrum, proportionate to birth weight, via stomach tube. Treatment had no effect (P > 0-05) on colostrum yield at lh, 10 h or 18 h post partum or on total colostrum yield to 18 h post partum. Ewes offered molasses (ML) or molasses plus minerals (ML + MN) had a lower colostral IgG concentration at lh post lambing than the control ewes (C) (P < 0-05). Ewes offered molasses (ML) also had a lower colostral IgG concentration than the control (C) at 10 h post partum (P < 0-05). Treatment had no effect on total IgG yield to 18 h post partum. When ewes were supplemented with minerals in any combination, with or without molasses (B, MN, ML + MN) it resulted in lambs having an impaired ability to absorb colostral IgG. Lambs from treatments B, MN and ML + MN had significantly poorer efficiency of colostral IgG absorption than lambs born to control ewes (C) or molasses (ML) supplemented ewes (P < 0-001). This in turn resulted in the progeny of mineral supplemented ewes (B, MN or ML + MN) having lower serum IgG concentration at 24 h post partum than either the control (C) or the molasses treatments (ML) (P < 0-001). When ewes were supplemented with molasses only (ML) lamb serum IgG content at 24 h was lower than in lambs born to control (C) ewes (P < 0-05) but this was as a result of a lower intake of colostral IgG (P < 0-05) and not a result of reduced IgG absorption efficiency. In conclusion, the data show that when ewe mineral intake is high in late pregnancy, as was the case in the current experiment, lamb serum IgG concentration and colostral IgG absorption efficiency are reduced. Further work is required to determine which component of the mineral formulation is responsible for this reduced IgG absorption efficiency and the mechanism through which this impaired efficiency operates.

Two experiments were conducted to investigate the use of dietary manipulation as a means of improving piglet postweaning performance and gastro-intestinal health. In experiment 1, 144 piglets (24 days old) in a 3 × 2 factorial arrangement were offered diets containing 65, 170 and 280 g lactose per kg with or without lactic acid (16 g/kg) for 28 days. In experiment 2, 20 piglets (24 days old) in a 2 × 2 factorial arrangement were offered the following diets for 7 days and then sacrificed: T1) basal diet; T2) basal diet + 15 g inulin per kg; T3) basal diet + 16 g lactic acid per kg and T4) basal diet + 15 g inulin per kg + 16 g lactic acid per kg. After slaughtering, tissue samples were taken from the duodenum, jejunum and ileum for morphological measurements. Digesta samples were taken from the ileum, caecum and colon for microbiology and volatile fatty acid analysis. In experiment 1, pigs offered diets containing lactic acid had improved daily gain ( P < 0·01) and food efficiency ( P < 0·05) from days 0 to 7 compared with pigs offered diets containing no lactic acid. There was a linear increase ( P < 0·05) in average daily gain (ADG) from days 0 to 28 and a linear decrease in faecal pH ( P < 0·01) with increasing lactose levels. There was a quadratic effect of lactose on food conversion ratio from days 0 to 28 ( P < 0·05). In experiment 2, there was a significant interaction between inulin and lactic acid in villous height in the jejunum ( P < 0·001) and the concentrations of lactobacilli ( P < 0·1) and E. coli ( P < 0·05) in the colon. The inclusion of inulin and lactic acid resulted in a significant increase in villous height compared with the inulin only diet ( P < 0·001). However, lactic acid had no effect on villous height in pigs offered diets without inulin supplementation. The inclusion of lactic acid and inulin caused a significant increase in both lactobacilli and E. coli concentrations compared with the inulin only diets ( P < 0·05). However, neither inulin nor lactic acid had an effect on lactobacilli and E. coli numbers in isolation of the other. In conclusion, in experiment 1, lactic acid improved performance in the 1st week post weaning. There was a linear increase in ADG with increasing lactose levels. In experiment 2, the combination of lactic acid and inulin increased villous height in the jejunum and concentrations of lactobacilli and E. coli in the colon.