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Objectives: The World Health Organization recommends that human immunodeficiency virus (HIV)-infected children increase energy intake and maintain a balanced macronutrient distribution for optimal growth and nutrition. Few studies have evaluated dietary intake of HIV-infected children in resource-limited settings., Methods: We conducted a cross-sectional analysis of the dietary intake of 220 perinatally HIV-infected children and 220 HIV-uninfected controls ages 5 to 9 years in Johannesburg, South Africa. A standardized 24-hour recall questionnaire and software developed specifically for the South African population were used to estimate intake of energy, macronutrients, and micronutrients. Intake was categorized based on recommendations by the World Health Organization and Acceptable Macronutrient Distribution Ranges established by the IOM., Results: The overall mean age was 6.7 years and 51.8% were boys. Total energy intake was higher in HIV-infected than HIV-uninfected children (1341 vs 1196 kcal/day, P = 0.002), but proportions below the recommended energy requirement were similar in the 2 groups (82.5% vs 85.2%, P = 0.45). Overall, 51.8% of the macronutrient energy intake was from carbohydrates, 13.2% from protein, and 30.8% from fat. The HIV-infected group had a higher percentage of their energy intake from carbohydrates and lower percentage from protein compared with the HIV-uninfected group. Intakes of folate, vitamin A, vitamin D, calcium, iodine, and selenium were suboptimal for both groups., Conclusions: Our findings suggest that the typical diet of HIV-infected children and uninfected children in Johannesburg, South Africa, does not meet energy or micronutrient requirements. There appear to be opportunities for interventions to improve dietary intake for both groups.

Two growth experiments were conducted to estimate the minimal dietary vitamin A requirement for juvenile grass shrimp, Penaeus monodon. In expt. 1, purified diets containing 0, 1,500, 3,000, 15, 000, 30,000, 45,000 and 60,000 retinol equivalent (RE)/kg (i.e., 0, 5,000, 10,000, 50,000, 100,000, 150,000, 200,000 IU/kg) of supplemental vitamin A (retinyl acetate) were fed to P. monodon (mean initial weight 0.97 +/- 0.01 g) for 8 wk. In expt. 2, diets with 0, 600, 1,200, 1,800, 2,400, 3,000, 3,600, and 4,500 RE/kg (i.e. , 0, 2,000, 4,000, 6,000, 8,000, 10,000, 12,000, 15,000 IU/kg) of supplemental vitamin A were fed to the shrimp (mean weight 0.68 +/- 0.01 g) for 6 wk. The basal unsupplemented diet contained 54 RE vitamin A/kg, and supplemental levels were confirmed by analysis. Each diet was fed to three replicate groups of shrimp. In expt. 1, shrimp fed diets supplemented with 300 RE vitamin A/kg had significantly greater weight gain (P < 0.05) than those fed the unsupplemented control diet and diets supplemented with >===" BORDER="0">30,000 RE vitamin A/kg. Survival rate was higher in shrimp fed diets supplemented with 1,500-30,000 RE vitamin A/kg than shrimp fed the control diet. Highest blood triglyceride concentration and body lipid concentration were in shrimp fed diets supplemented with 45,000 and 60,000 RE vitamin A/kg, respectively. Eye vitamin A concentration and hepatopancreatic total lipid concentration in shrimp generally increased as dietary vitamin A supplementation increased. In expt. 2, feed efficiency was highest in shrimp fed diets supplemented with 2,400, 3,000, 3,600 and 4,500 RE vitamin A/kg, followed by shrimp fed diets with 600 and 1,200 RE vitamin A/kg and finally the unsupplemented control group. Shrimp fed diets supplemented with vitamin A had significantly higher survival percentages than those fed the unsupplemented control diet. Weight gain percentage of the shrimp analyzed by broken-line regression indicated that the minimal dietary vitamin A concentration in growing P. monodon is 2,511 RE/kg ( approximately 8, 400 IU/kg).

An 8-wk feeding trial was conducted to determine the dietary choline requirement for juvenile hybrid tilapia, Oreochromis niloticus x O. aureus. Purified basal diets were formulated using vitamin-free casein (contained 370 mg choline/kg) as the protein source. Graded levels (0, 100, 200, 400, 600, 800, 1,000 and 2,000 mg choline/kg diet) of choline chloride were added to the basal diet, resulting in eight dietary treatments in the experiment. Each diet was fed to three replicate groups of tilapia initially averaging 0.62 +/- 0.01 g/fish in a closed, recirculating rearing system. Feed efficiency, survival and blood triglyceride, cholesterol and phospholipid concentrations were generally high in fish fed choline-supplemented diets compared to fish fed the control diet. Analysis by broken-line regression of weight gain and body choline concentration and by polynomial regression of liver lipid concentration of the fish indicated that the dietary choline concentration for tilapia is about 900 mg/kg. Taking into account the choline concentration of the unsupplemented basal diet, the optimal dietary choline requirement for growing tilapia is about 1,000 mg/kg.

A 12-wk feeding trial was conducted to study the influence of chromic oxide (Cr2O3) on carbohydrate utilization and digestibility by tilapia, Oreochromis niloticus x O. aureus. Two levels of chromic oxide (0.5 and 2%) were each incorporated into diets containing glucose or starch. Chromic oxide was added at 0 or 8 wk. The diets were fed to triplicate groups of fish weighing 1.11 +/- 0.05 g. Fish fed the starch diet had greater (P < 0.05) weight gain, feed efficiency ratio, protein efficiency ratio, protein deposition and digestibility of protein, lipid, carbohydrate and dry matter than fish fed the glucose diet irrespective of the time and level of chromic oxide supplementation. Fish fed the glucose diet with 0.5% chromic oxide had higher weight gain, feed efficiency ratio, protein efficiency ratio and protein deposition than fish fed the glucose diet with 2% chromic oxide. The ingredient digestibility estimated using 0.5% chromic oxide as the marker was greater than that estimated with 2% chromic oxide. Higher phosphofructokinase and lower glucose-6-phosphatase activity was found in fish fed the starch diet than in fish fed the glucose diet regardless of the time and level of chromic oxide inclusion. Fish fed the glucose diet with 0.5% chromic oxide had higher phosphofructokinase activity and lower tissue chromium concentration than fish fed the glucose diet with 2% chromic oxide irrespective of chromic oxide inclusion time. These data suggest that the level of chromic oxide in the diet alters glucose utilization by tilapia and affects nutrient digestibility by tilapia. The time of chromic oxide inclusion had no effect on carbohydrate utilization and digestibility.

1. To either an agar-containing diet or an agar-free diet, 0, 0.3 and 2.0 mg/100 g of beta-carotene were incorporated and fed to groups of five rats for 28 days. 2. Weight gain and food consumption of rats fed different dietary groups did not show a significant difference (P > 0.05). 3. Colon weight, colonic mucosal DNA and RNA were generally higher in rats fed agar diets than rats fed agar-free diets at either beta-carotene supplementation level. 4. Mucinase activity was higher (P < 0.05) in rats fed the agar diet than in rats fed an agar-free diet without beta-carotene. However, the difference was not observed (P > 0.05) when beta-carotene was incorporated. 5. These data suggest that colonic mucin degradation in rats fed an agar diet decreased when the dietary beta-carotene inclusion level increased.

A feeding trial was conducted to estimate the minimal dietary pantothenic acid (PA) requirement for juvenile grass shrimp, Penaeus monodon. Purified diets with seven levels (0, 20, 40, 60, 120, 240, and 480 mg/kg) of supplemental PA were fed to P. monodon (mean weight 0.88 +/- 0.01 g) for 8 wk. The level of PA detected in the unsupplemented diet was 0.02 mg/kg. Each diet was fed to three replicate groups of shrimp. Feed efficiencies (FE) and protein efficiency ratios were highest in shrimp fed the diets supplemented with 120, 240, and 480 mg PA/kg diet, followed by the groups fed 60 mg/kg, then 40 mg/kg, and finally the unsupplemented control group (P < 0.05). Shrimp fed diets supplemented with PA had significantly higher survival percentages and lower hepatopancreatic lipid concentration than those fed the unsupplemented, control diets. Broken-line regression analyses of weight gain percentage and hepatopancreatic CoA and PA concentrations of the shrimp indicated that the adequate dietary PA concentration in growing P. monodon is 101-139 mg/kg. [ABSTRACT FROM AUTHOR]

A feeding trial was conducted to estimate the minimal dietary biotin requirement for juvenile grass shrimp, Penaeus monodon. Purified diets with eight levels (0, 0.2, 0.5, 1.0, 3.0, 6.0, 10.0 and 20.0 mg/kg) of supplemental biotin were fed to P. monodon (mean weight 0. 26 +/- 0.01 g) for 8 wk. Each diet was fed to three replicate groups of shrimp. Shrimp fed diets supplemented with biotin (0.2-20.0 mg/kg) had significantly (P < 0.05) higher weight gain, feed efficiency and protein efficiency ratio than those fed the unsupplemented control diet. Weight gain was high in shrimp fed 3. 0-10.0 mg biotin/kg diet and lowest in shrimp fed