BackgroundThe chicken gut microbiota is an important and complicated ecosystem for the host. They play an important role in converting food into nutrient and energy. The coding capacity of microbiome vastly surpasses that of the host’s genome, encoding biochemical pathways that the host has not developed. An optimal gut microbiota can increase agricultural productivity. This study aims to explore the composition and function of cecal microbiota in Dagu chicken under two feeding modes, free-range (outdoor, OD) and cage (indoor, ID) raising.ResultsCecal samples were collected from 24 chickens across 4 groups (12-w OD, 12-w ID, 18-w OD, and 18-w ID). We performed high-throughput sequencing of the 16S rRNA genes V4 hypervariable regions to characterize the cecal microbiota of Dagu chicken and compare the difference of cecal microbiota between free-range and cage raising chickens. It was found that 34 special operational taxonomic units (OTUs) in OD groups and 4 special OTUs in ID groups. 24 phyla were shared by the 24 samples. Bacteroidetes was the most abundant phylum with the largest proportion, followed by Firmicutes and Proteobacteria. The OD groups showed a higher proportion of Bacteroidetes (>50 %) in cecum, but a lower Firmicutes/Bacteroidetes ratio in both 12-w old (0.42, 0.62) and 18-w old groups (0.37, 0.49) compared with the ID groups. Cecal microbiota in the OD groups have higher abundance of functions involved in amino acids and glycan metabolic pathway.ConclusionThe composition and function of cecal microbiota in Dagu chicken under two feeding modes, free-range and cage raising are different. The cage raising mode showed a lower proportion of Bacteroidetes in cecum, but a higher Firmicutes/Bacteroidetes ratio compared with free-range mode. Cecal microbiota in free-range mode have higher abundance of functions involved in amino acids and glycan metabolic pathway.Electronic supplementary materialThe online version of this article (doi:10.1186/s12866-016-0877-2) contains supplementary material, which is available to authorized users.
Effects of three dietary lysine (protein) concentrations during lactation on metabolic state, protein metabolism, reproductive hormones, and performance were investigated in 36 primiparous sows. Sows were assigned randomly to one of three diets containing .4% (low lysine, LL), 1.0% (medium lysine, ML), or 1.6% (high lysine, HL) total lysine from intact protein sources. All diets contained 2.1 Mcal NE/kg and exceeded the recommended requirements for all other nutrients. Actual lysine intakes over an 18-d lactation were 16, 36, and 56 g/d for sows fed LL, ML, and HL, respectively. Fractional breakdown rate of muscle was determined on d 4 and 15 of lactation by using a three-compartment kinetic model of 3-methylhistidine metabolism. Increasing lysine intake during lactation did not affect fractional breakdown rate of muscle on d 4 of lactation but decreased it on d 15 (P < .05). Sows fed LL had a reduced number of LH pulses on d 12 and 18 (P < .05) and reduced serum estradiol (E2) concentration on d 18 of lactation compared with sows fed ML and HL treatments. However, LH pulses and E2 concentrations were similar between ML and HL treatments (P > .35). Increasing lysine intake increased serum urea nitrogen (SUN) and postprandial insulin concentrations (P < .05) during lactation but had no effect on plasma glucose concentrations (P > .20). Sows fed HL had greater serum IGF-I on d 6 and 18 than sows fed ML (P < .05). Number of LH peaks was correlated with serum insulin concentration 25 min after feeding on d 6 and 18 (r = .31 to .41; P < .1) and pre- (r = .33 to .46) and postprandial (r = .30 to .58) SUN concentrations (P < .05) during different stages of lactation. Results indicate that, compared with medium lysine intake, low lysine intake increased muscle protein degradation and decreased concentrations of insulin, SUN, and estradiol and LH pulsatility. In contrast, high lysine (protein) intake increased SUN, insulin, and IGF-I, but did not increase secretion of estradiol and LH compared with medium lysine intake. Furthermore, nutritional impacts on reproduction may be mediated in part through associated effects on circulating insulin concentration.
The physical and chemical composition of sows was determined at first mating (no. = 6), weaning the first litter (12) and 14 days after weaning the fourth litter (24). The sows were from 108 Large White/Landrace Fl hybrid gilts allocated in a factorial arrangement according to two levels of subcutaneous fatness at parturition (12 v. 22 mm P2), two levels of lactation feeding (3 v. 7 kg) and two sizes of sucking litter (six v. 10). Treatments significantly influenced the composition of dissected carcass fat and chemical lipid, but not composition of dissected lean and chemical protein. The final body protein mass of well fed sows at the termination of parity 4 was 41 kg, and the total content of gross energy (GE) in excess of 3000 MJ, with an average of 12·4 MJ GE per kg live weight; equivalent values for the less well fed sows were 33 kg and 9·4 MJ GE per kg live weight respectively. The weights of chemical lipid and protein could be predicted from the equations: lipid (kg) = -20·4 (s.e. 4·5) + 0·21 (s.e. 0·02) live weight + 1·5 (s.e. 0·2) P2; protein (kg) = -2·3 (s.e. 1·6) + 0·19 (s.e. 0·01) live weight - 0·22 (s.e. 0·07) P2. On average, sows lost 9 kg lipid and 3 kg protein in the course of the 28-day lactation; these being proportionately about 0·16 and 0·37 of the live-weight losses respectively. Maternal energy requirement for maintenance was estimated as 0·50 MJ digestible energy (DE) per kg M0·75, while the efficiency of use of DE for energy retention was 0·28.
One hundred and two Large White × Landrace Fl hybrid sows were allocated over four parities in a factorial design to two levels of target P2 backfat thickness at parturition (20 mm, F v. 12 mm, T), two levels of lactation feeding {ad libitum, H v. 3 kg/day, L), and two sizes of sucking litter (six v. 10). Sows attained 13 mm P2 when first mated at 126 kg live weight. Fatness (P2, mm) at weaning was significantly influenced by target fatness at parturition (14·2 v. 9·3), lactation feeding level (13·7 v. 10·0), and litter size (12·7 v. 11·0). Changes in backfat (P2, mm) during 28-day lactation were significantly influenced by target fatness at parturition (—5·0 v. —2·5), lactation feeding (-2 0 v. —5·4), and litter size (—2·9 v. -4·6). Sow live weight (kg) at weaning was significantly influenced by target fatness at parturition (211 v. 192), lactation feeding (218 v. 186), and litter size (208 v. 196). Changes in live weight (kg) during 28-day lactation were significantly influenced by target fatness at parturition (—26 v. — 12), lactation feeding (—5 v. —31), and litter size (—12 v. —25). With multiparous sows only, total food intake during 28-day lactation was negatively related to total food intake in pregnancy. Change in backfat (P2, mm) during 28-day lactation = -0·28 - 0·27 P2 at parturition + 0·04 lactation food intake — 0·50 litter size. Change in live weight (kg) during 28-day lactation = -3·8 — 0·15 live weight post partum + 0·36 lactation food intake — 3·3 litter size. Sows with target fat levels of 20 mm P2 at parturition had better food conversion efficiencies than sows with target fat levels of 12 mm. Target fatness at parturition, and especially lactation food intake, but not litter size, significantly influenced the interval (days) from weaning to oestrus in parity 1 (9·1 v. 14·2 and 7·8 v. 15·3, but 11·6 v. 11·5), while n i subsequent parities only litter size influenced the interval (days) from weaning to oestrus (6·0 v. 8·0). Birth weight (kg) of piglets was influenced only marginally by target fatness at parturition (1·4 v. 1·2) in parity 1, and not by the other factors, or in subsequent parities. Piglet growth rate was affected by both target fatness at parturition and litter size, but by lactation feeding level only in the last week of lactation. The relationship between fatness at weaning (mm) and the weaning to oestrus interval (days) for primiparous sows can be expressed as 26·6 — 1·28 P2. High level feeding in lactation imparted production and efficiency benefit in both primiparous and multiparous sows, while pregnancy feeding to a target of 20 mm rather than 12 mm at parturition was of benefit for primiparous sows.
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