Effect of various levels of aflatoxin and ochratoxin A and combinations thereof on protein and energy utilisation in broilers

Studies were conducted to evaluate protein and energy utilisation in broilers fed diets containing various levels of aflatoxin (AF; 0, 0.5, 1 and 2 mg kg^?1) and ochratoxin A (OA; 0, 1, 2 and 4 mg kg^?1) either singly or in different combinations. Total protein efficiency (TPE) was reduced by 50.97, 76.52 and 132.75% at 2 mg kg^?1 AF and 2 and 4 mg kg^?1 OA respectively. Co‐toxicity at two levels, 1 mg kg^?1 AF + 2 mg kg^?1 OA and 2 mg kg^?1 AF + 4 mg kg^?1 OA, resulted in significant reductions of 78.58 and 127.43% respectively in TPE. AF at all three levels and OA at 2 and 4 mg kg^?1 caused significant decreases in net protein utilisation (NPU). Co‐toxicity at all three levels led to significantly lower NPU. The reduction in NPU ranged from 18.68% at 0.5 mg kg^?1 AF to 75.12% at 2 mg kg^?1 AF + 4 mg kg^?1 OA. Significant reductions in metabolisable energy (ME) content were recorded at 1 and 2 mg kg^?1 AF and all three levels of OA. ME content was reduced drastically when both toxins were fed simultaneously. It is suggested that both AF and OA adversely affect energy and protein utilisation in broilers, and this effect is exacerbated when both toxins are fed simultaneously. © 2002 Society of Chemical Industry     

Residues of ethoxyquin in poultry tissues and eggs

Tissues of broilers raised experimentally on diets containing the feed antioxidant ethoxyquin (6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline) contained very low levels of this compound (<0.005 mg kg^?1) both raw and after roasting. Residues were higher in liver (up to 0.063 mg kg^?1) and highest in what appeared to be the major deposition site, the body fat (0.215 mg kg^?1). The body fat of commercial broiler samples showed much lower levels (0.015-0.051 mg kg^?1). Leg and breast muscles from laying hens after 30 weeks on the experimental diets had low ethoxyquin levels (< 0.005 mg kg^?1) with a higher liver content (0.048 mg kg^?1) and again the highest level in the body fat (0.238 mg kg^?1). Eggs from these hens contained 0.031 mg kg^?1 ethoxyquin, probably all in the yolk. Market samples of eggs from five major producers gave an average value of 0.011 mg kg^?1. A rapid and considerable loss of ethoxyquin occurred in the feed troughs, the concentration dropping from 125 mg kg^?1 to 90 mg kg^?1 in four hours.     

Natural occurrence of zearalenone and trichothecene toxins in maize-based animal feeds in zambia

A year-long collection of maize-based animal feed samples from the National Milling Company and mouldy maize collected from farmers fields near Lusaka were analysed for Fusarium mycotoxins. In the survey, 148 samples were tested for zearalenone, deoxynivalenol and nivalenol, and 60 samples for T-2 toxin and diacetoxyscirpenol. Zearalenone was present up to 0.6 mg kg^?1 in 17% of the feed samples, and deoxynivalenol was found at I-0 mg kg^?1 in 1.4 % of these samples. This is the first report of these toxins in animal feeds in Zambia. Zearalenone was also found in 57.6 % of the 33 mouldy maize samples collected at levels ranging from 0.08 to 6.0 mg kg^?1 (mean concentration 1.11 mg kg^?1), and 49.5% of these samples contained deoxynivalenol at levels ranging from 0.5 to 16.0 mg kg^?1 (mean concentration 5.56 mg kg ^?1). T-2 toxin and diacetoxyscirpenol were not detected.     

Aflatoxin and its metabolites in tissues from laying hens and broiler chickens fed a contaminated diet

Two groups of 32 hens and broiler chickens were contaminated with 2.5 and 5 mg of aflatoxin (AF) kg^?1 feed for a period of 32 days. During this contamination 16 birds were sacrificed and aflatoxin and its metabolites were detected using thin-layer chrotnatography and fluorescence densisometry. The tissues analysed (liver, muscle, kidney, gizzard and eggs) gave a wide range of concentrations, the lowest was found in ben muscle (0.05 μg kg^?1 of AFB₁) and the highest in gizzards from the 5 mg kg^?1 group of the hens (9.01 μg kg^?1 of AFB₁). Metabolites of AFB₁, AFM, and AFB_2a appeared in the liver but not in other tissues. In broiler's tissues, the following metabolities were isolated: AFM₁ and AFB_2a, in liver, aflatoxicol in muscle and AFM₁ and AFB_2a in kidneys, all having concentrations lower than AFB₁. Aflatoxicol was isolated from one egg sample (0.32 μg kg^?1). For both types of birds, aflatoxin clearance time was only 24 h for muscle and kidneys. In livers from the 5 mg kg^?1 group, AFM₁ and AFB_2a were still found 4 days after removal of the contaminated feed. In eggs and gizzards, aflatoxin residue was still detected on the 8th day of the clearance period although in low quantities. In the broiler's gizzards, clearance time was only 24 h. These results suggest that aflatoxin transfer to edible tissues is very small and the danger of contaminations to humans is also very small, except in the case of gizzards.     

Lipophilic toxin profiles detected in farmed and benthic mussels populations from the most relevant production zones in Southern Chile

Lipophilic toxins associated with diarrhoeic toxins were found in Mytilus chilensis (Blue mussels) and Aulacomya ater (Ribbed mussels). These shellfish samples were collected from Chiloe Island, Southern Chile. The samples were tested by liquid chromatography–tandem mass spectrometry (LC-MS/MS). After the analysis, four toxins were found: DTX-1, DTX-3, YTX and PTX. All toxins were identified by comparing their HPLC retention times with those of analytical standards and confirmed by LC-MS/MS. Dinophysistoxin-1 (DTX-1) and dinophysistoxin-3 (DTX-3) toxins were the major components within the mussel extracts. Nevertheless, the percentages of these toxins differed depending on the area they were collected from and/or the sampling date. The levels detected in Butacheuques Island for okadaic acid (OA) was 267?±?3.5?µg OA?eq?kg^?1 (p?<?0.05) and for DTX-3 was 183.4?±?7.5?µg?kg^?1 in ribbed mussels. Pectenotoxin (PTX) and yessotoxin (YTX) were the toxins detected in minor proportions in the toxic profile of the bivalves. The maximum concentration of YTX detected in ribbed mussels was 85.2?±?2.8?µg?kg^?1 in Mechuque Island, whereas the PTX-2 level in ribbed mussels was 82.0?±?2.4?µg?kg^?1 in Cailin Island. Analogues of YTX and PTX-2 were not detected in any of the analysed mussels, which did not support the supposed presence of isomers of toxins as a result of the enzymatic metabolism of bivalves. This study found evidence proving co-occurrence of lipophilic toxins – like PTX and YTX – with diarrhoeic toxin in samples collected in Southern Chile, which is, to date, the more complex mix of lipophilic toxins ever found in mussels samples from Southern Chile.     

Effects of individual and combined administration of ochratoxin A and aflatoxin B1 in tissues and eggs of White Leghorn breeder hens

BACKGROUND: Mycotoxins, the secondary fungal metabolites, are unavoidable contaminants of human and animal food and feeds. The objectives of this study were to evaluate the effect of concurrent feeding of ochratoxin A (OTA) and aflatoxin B₁ (AFB₁) to breeder hens, upon their deposition in different tissues and eggs. RESULTS: Residues of OTA and AFB₁ in (ng g^?1) were significantly higher in liver followed by kidneys and breast muscles by 22.54 ± 1.48, 4.22 ± 0.93 and 0.56 ± 0.06 for OTA (group fed OTA at 5 mg kg^?1 diet) and 1.44 ± 0.21, 0.25 ± 0.01 and 0.03 ± 0.01 for AFB₁ (group fed AFB₁ at 5 mg kg^?1 diet), respectively. Residues of OTA and AFB₁ in eggs appeared at days 3 and 5 of toxin feeding and disappeared at days 5 and 6 of withdrawal of mycotoxins contaminated feed, respectively. The residues of OTA and AFB₁ were significantly lower in the tissues of hens fed these toxins concurrently compared with the groups fed OTA and AFB₁ independently. CONCLUSIONS: Residues of OTA and AFB₁ appeared in the tissues and eggs of laying hens kept on OTA‐ and AFB₁‐contaminated diets. Concurrent feeding of OTA and AFB₁ to hens significantly decreased the concentration of OTA and AFB₁ residues in the tissues and eggs. Copyright © 2011 Society of Chemical Industry     

Effects of dietary yeast autolysate (Saccharomyces cerevisiae) on performance,egg traits,egg cholesterol content,egg yolk fatty acid composition and humoral immune response of laying hens

BACKGROUND: The objective of this study was to determine the effects of dietary yeast autolysate on performance, egg traits, egg cholesterol content, egg yolk fatty acid composition, lipid oxidation of egg yolk, some blood parameters and humoral immune response of laying hens during a 16 week period. A total of 225 Hyline Brown laying hens, 22 weeks of age, were allocated equally to one control group and four treatment groups. Yeast autolysate (Saccharomyces cerevisiae, InteWall) was used at levels of 1, 2, 3 and 4 g kg^?1 in the diets of the first, second, third and fourth treatment groups respectively. RESULTS: Dietary treatments did not significantly affect body weight, feed intake and egg traits. Yeast autolysate supplementation increased egg production (P < 0.001) and egg weight (P < 0.001) and improved feed efficiency (P < 0.05). Yeast autolysate at levels of 2, 3 and 4 g kg^?1 decreased egg yolk cholesterol level as mg g^?1 yolk (P < 0.01) and blood serum levels of cholesterol and triglyceride (P < 0.05) and increased antibody titres to sheep red blood cells (P < 0.01). Total saturated fatty acids and the ratio of saturated/unsaturated fatty acids increased (P < 0.01) and total monounsaturated fatty acids (P < 0.001) decreased with yeast autolysate supplementation. CONCLUSION: Dietary yeast autolysate at levels of 2, 3 and 4 g kg^?1 had beneficial effects on performance, egg cholesterol content and humoral immune response. It is concluded that 2 g kg^?1 yeast autolysate will be enough to have beneficial effects in laying hens. Copyright © 2010 Society of Chemical Industry     

Residues of sulfadiazine and doxycycline in egg matrices due to cross-contamination in the feed of laying hens and the possible correlation with physicochemical,pharmacokinetic and physiological parameters

In the poultry industry, the widespread use of veterinary drugs such as antimicrobial compounds may lead to the presence of residues in whole eggs, egg white and egg yolk. During this study, laying hens received experimental feed containing sulfadiazine or doxycycline at cross-contamination levels of 2.5%, 5% and 10% of the therapeutic concentration. Since the therapeutic dose is 250?mg?kg^?1 for both substances, cross-contamination concentrations in the feed of 6.25, 12.5 and 25?mg?kg^?1 were expected. Whole egg, egg white and egg yolk samples were collected during the treatment and depletion period and were analysed via liquid chromatography-tandem mass spectrometry. For both drugs, a plateau phase was reached within 3–5 days and residue concentrations were detected in all egg matrices. For the 10% cross-contamination group, residual sulfadiazine concentrations of 208, 299 and 60?µg?kg^?1 and residual doxycycline concentrations of 455, 332, 206?µg?kg^?1 were detected in whole egg, egg white and egg yolk on day 13 of the treatment period, respectively. Both sulfadiazine and doxycycline had higher concentrations in egg white than in egg yolk, but the egg white–egg yolk ratio was higher for sulfadiazine than for doxycycline. As neither drug is allowed in Belgium for use in laying hens, residues may pose food safety concerns.     

Saxitoxins and okadaic acid group: accumulation and distribution in invertebrate marine vectors from Southern Chile

Harmful algae blooms (HABs) are the main source of marine toxins in the aquatic environment surrounding the austral fjords in Chile. Huichas Island (Aysén) has an history of HABs spanning more than 30 years, but there is limited investigation of the bioaccumulation of marine toxins in the bivalves and gastropods from the Region of Aysén. In this study, bivalves (Mytilus chilenses, Choromytilus chorus, Aulacomya ater, Gari solida, Tagelus dombeii and Venus antiqua) and carnivorous gastropods (Argobuccinum ranelliformes and Concholepas concholepas) were collected from 28 sites. Researchers analysed the accumulation of STX-group toxins using a LC with a derivatisation post column (LC-PCOX), while lipophilic toxins (OA-group, azapiracids, pectenotoxins and yessotoxins) were analysed using LC-MS/MS with electrospray ionisation (+/–) in visceral (hepatopancreas) and non-visceral tissues (mantle, adductor muscle, gills and foot). Levels of STX-group and OA-group toxins varied among individuals from the same site. Among all tissue samples, the highest concentrations of STX-group toxins were noted in the hepatopancreas in V. antiqua (95 ± 0.1 μg STX-eq 100 g^?1), T. dombeii (148 ± 1.4 μg STX-eq 100 g^?1) and G. solida (3232 ± 5.2 μg STX-eq 100 g^?1; p < 0.05); in the adductor muscle in M. chilensis (2495 ± 6.4 μg STX-eq 100 g^?1; p < 0.05) and in the foot in C. concholepas (81 ± 0.7 μg STX-eq 100 g^?1) and T. dombeii (114 ± 1.2 μg STX-eq 100 g^?1). The highest variability of toxins was detected in G. solida, where high levels of carbamate derivatives were identified (GTXs, neoSTX and STX). In addition to the detected hydrophilic toxins, OA-group toxins were detected (OA and DTX-1) with an average ratio of ≈1:1. The highest levels of OA-group toxins were in the foot of C. concholepas, with levels of 400.3 ± 3.6 μg OA eq kg^?1 (p < 0.05) and with a toxic profile composed of 90% OA. A wide range of OA-group toxins was detected in M. chilensis with a toxicity < 80 μg OA eq kg^?1, but with 74% of those toxins detected in the adductor muscle. In all evaluated species, there was no detection of lipophilic toxins associated with biotransformation in molluscs and carnivorous gastropods. In addition, the STX-group and OA-group toxin concentrations in shellfish was not associated with the presence of HAB. The ranking of toxin concentration in the tissues of most species was: digestive glands > mantle > adductor muscle for the STX-group toxins and foot > digestive gland for the OA-group toxins. These results gave a better understanding of the variability and compartmentalisation of STX-group and OA-group toxins in different bivalve and gastropod species from the south of Chile, and the analyses determined that tissues could play an important role in the biotransformation of STX-group toxins and the retention of OA-group toxins.     

Hepatoprotection of silymarin against thioacetamide-induced chronic liver fibrosis

BACKGROUND: Liver fibrosis is chronic liver damage usually caused by alcohol, viruses or other toxins and is characterised by an excessive accumulation of extracellular matrix proteins such as collagen. The aim of this study was to establish an animal model of chronic liver damage and investigate molecular mechanisms of silymarin hepatoprotective effects. RESULTS: Thioacetamide (TAA; 100 mg kg^?1 intraperitoneal (i.p.) injection three times weekly) effectively induced chronic liver fibrosis in male ICR mice. Then 24 ICR mice were randomly divided into four groups: (1) saline (i.p.) + water (gavage); (2) saline (i.p.) + 150 mg kg^?1 silymarin (gavage); (3) 100 mg kg^?1 TAA (i.p.) + water (gavage); (4) 100 mg kg^?1 TAA (i.p.) + 150 mg kg^?1 silymarin (gavage). Eight weeks of TAA treatment resulted in lower body weight, serum cholesterol and triglycerides as well as increased liver size, ALT, AST and LDH values (P < 0.05). These TAA‐induced effects were attenuated by silymarin (P < 0.05); therefore silymarin also ameliorated TAA‐induced liver lesions. Effects of silymarin on TAA‐induced chronic liver damage may be attributed to down‐regulation of hepatic MMP‐2, MMP‐13, TIMP‐1, TIMP‐2, AP‐1, KLF6, TGF‐β1, α‐SMA and COL‐α1. CONCLUSION: A mouse model of chronic liver fibrosis was successfully established by injecting 100 mg kg^?1 TAA three times weekly in male ICR mice. Meanwhile, silymarin showed hepatoprotection against TAA‐induced damage. Copyright © 2011 Society of Chemical Industry     

Inorganic and organic arsenic in some commercial east australian crustacea

The levels of inorganic and organic arsenic have been determined in a total of 86 samples of crustacea which included School prawns (Metapenaeus macleayi), King prawns (Penaeus plebejus), Royal Red prawns (Hymenopenaeus sibogae), Eastern Common crayfish (Jasus verreauxii), Blue Swimmer crab (Portunus pelagicus) and Mud crab (Scylla serrata). Most samples were obtained from New South Wales coastal waters and the remainder were purchased at the Sydney fish markets. Inorganic arsenic was isolated by distillation as the chloride and determined by an atomic absorption-hydride generation method. Organic arsenic was determined on the remaining solution by flame atomic absorption spectrophotometry after digestion of the organic matter with a mixture of nitric, perchloric and sulphuric acids (25 + 5 +1). The Eastern Common crayfish contained the highest levels of inorganic and organic arsenic with ranges of 0.12–0.41 mg kg^?1 and 11.9–54.1 mg kg^?1 (wet basis), respectively. Of the remaining samples, 85% contained inorganic arsenic at <0.1 mg kg^?1 and 97% contained organic arsenic at <7 mg kg^?1. The absolute sensitivity and detection limit of the inorganic arsenic method was estimated to be 3 ng (0.03 mg kg^?1). For the organic arsenic method the sensitivity and detection limits were estimated as 0.5 and 0.8 mg kg^?1, respectively.     

Occurrence of Fusarium T-2 and HT-2 toxins in oats from cultivar studies in Germany and degradation of the toxins during grain cleaning treatment and food processing

For the Fusarium trichothecene mycotoxins T-2 and HT-2, a combined (T-2 + HT-2) temporary tolerable daily intake (tTDI) of 0.06 µg kg^?1 body weight day^?1 was proposed at the European level in 2001 (Opinion of the Scientific Committee on Food). In the near future, maximum levels for these trichothecenes will be regulated by the European Commission as announced in EU (VO) 1881/2006. For the implementation of these maximum levels, more data on occurrence and behaviour of T-2 and HT-2 toxins in primary agricultural products as well as during cleaning treatment and food processing are needed. In the current work, we determined the T-2/HT-2 concentrations in four oat cultivars (Aragon, Dominik, Ivory, Pergamon) from ten different agricultural sites in Germany, grown in cultivar studies in 2007. The grains were de-hulled, oat meal was prepared, and bread with 20% oat meal and 80% wheat flour was baked. In the cereal-processing chain, samples were taken at various steps and subsequently analysed for their T-2/HT-2 content. We employed liquid chromatography-mass spectrometry (LC-MS) and an immunological screening method (enzyme-linked immunoabsorbant assay (ELISA)) for T-2/HT-2 determination. Detection limits were between 1 and 10 µg kg^?1 in different matrices. T-2/HT-2 concentrations determined by ELISA in oat samples from ten different agricultural sites in Germany were between 9 and 623 µg kg^?1. The median and 90th percentile were 48 and 191 µg kg^?1 T-2/HT-2, respectively. One site showed six times higher T-2/HT-2 levels than the other sites, where concentrations ranged from 322 to 623 µg kg^?1. In 80% of the samples the cultivars Pergamon and Ivory had the lowest concentration of T-2 and HT-2 toxins. Using LC-MS for T-2/HT-2 determination, cleaning of the raw material did not lead to significant reductions of T-2 and HT-2 levels, whereas de-hulling led to a reduction of over 90%. Boiling of oat meal produced from cleaned raw material to yield ‘porridge’ resulted in varying T-2/HT-2 levels in experimental replicates. No major reduction of T-2/HT-2 levels in cooked porridge was obtained. Standardized baking experiments using 20% oat meal showed that T-2 and HT-2 toxins are relatively stable during the baking process, probably due to their temperature stability.     

Fatty acid profile and cholesterol content of egg yolk from chickens fed diets supplemented with purslane (Portulaca oleracea L.)

BACKGROUND: The aim of the present study was to evaluate the effects of purslane on egg production, egg weight, feed efficiency, yolk fatty acid composition, and egg cholesterol content in laying hens. MATERIAL AND METHODS: Sixty 80‐week‐old layers were allocated randomly to receive diets supplemented with 0 (control), 10 g kg^?1 or 20 g kg^?1 dried purslane for 84 days. Egg weights and egg production in the groups were recorded daily, whereas feed intake was measured weekly. RESULTS: Diet supplemented with 20 g kg^?1 purslane significantly decreased body weight of the chickens compared to the control. Inclusion of purslane at the level of 10 g kg^?1 or 20 g kg^?1 into the diet significantly (P < 0.05) improved egg weight compared to the control. Chickens fed the diet including 20 g kg^?1 purslane had a significantly (P < 0.05) higher egg production and improved feed efficiency compared to the control. Cholesterol content of eggs from the hens fed 0, 10 or 20 g kg^?1 did not differ and was 10.45, 9.51 or 9.51 mg g^?1 dried egg yolk, respectively. Inclusion of purslane at the level of 20 g kg^?1 into the diet significantly (P < 0.05) increased ω‐3 fatty acids such as C18:3(ω‐3) and C22:6(ω‐3). The ratio of ω‐6 to ω‐3 also was significantly (P < 0.05) lower in the eggs from chickens fed 10 g kg^?1 or 20 g kg^?1 purslane supplemented diets compared to the control. CONCLUSION: This study showed that adding dried purslane to the diet of laying hens significantly increased egg production and egg weights although there was no reduction in the egg cholesterol concentration. This study also showed that inclusion of purslane into diet enriched eggs with ω‐3 fatty acids and decreased the ratio of ω‐6/ω‐3 in the yolk. Copyright © 2010 Society of Chemical Industry     

Natural occurrence of Fusarium toxins in peanut,sorghum and maize from Mysore (India)

Peanut, sorghum and maize samples were collected from the wholesale market in Mysore, India, over a period of one year (October 1984 to September 1985). The samples were analysed for the natural occurrence of T-2 toxin (T-2), diacetoxyscirpenol (DAS) and zearalenone by thin-layer chromatography, dermal toxicity test and gas chromatography. Of the total number of peanut samples analysed, 6.9% were positive for the toxic trichothecene(s) (T-2, up to 38.89 mg kg^?1; DAS, up to 2.03 mg kg^?1); 4.8% of total sorghum samples analysed contained T-2 up to 15 mg kg^?1. Zearalenone was not found in any of the samples tested, and no toxins were detected in any of the maize samples. Samples marketed during winter and summer periods were contaminated with the toxins. All the toxin-positive samples except one peanut sample were found in produce stored for more than a week.     

Inter-species variability of okadaic acid group toxicity in relation to the content of fatty acids detected in different marine vectors

Okadaic acid group (OA-group) is a set of lipophilic toxins which are characterised by being produced by species associated with the genera Dinophysis and Prorocentrum. OA-group has been regularly detected in endemic shellfish species from the southern zone of Chile only through the mouse bioassay. The purpose of this work was to determine the variability of OA-group toxins in endemic aquatic organisms (bivalves, crabs, gastropods and fish) and to establish the relationship with the concentration of fatty acids (FAs) detected in the evaluated species. The toxicity of OA-group and the FA profiles were determined using LC-MS/MS and gas chromatography with flame-ionisation detection, respectively. In the study area, the dinoflagellate Dinophysis acuta was detected in densities ≈2000 cells ml^?1 with a toxicity ≈18.3 pg OA equiv cel^?1. The analysis identified OA and dinophysistoxin-1 in shellfish in a range of ≈90 to ≈225 μg OA eq kg^?1, where no toxins in fish were detected. A positive relationship between the FA level and the concentration of OA-group toxins in the digestive glands of bivalves and gastropods was established, noted for high levels of saturated FAs (C14:0 and C16:0). The toxic variability of OA-group toxins determined in the different species allowed us to establish that the consumption of these vectors, regulated by non-analytical methods, can be harmful when consumed by humans, thus suggesting that the sanitary regulations for the control of OA-group in Chile should be updated.     

Improvement by oxidising agents of the baking performance of pure and composite flours from nigerian-grown wheats (Lee X and Inia 66)

The feasibility of improving the bread-baking performance of two varieties of Nigerian-grown wheat (Lee X and Inia 66) in pure and composite flour, using the oxidising agents potassium bromate and ascorbic acid was studied. Composite flour was prepared by mixing pre-cooked bambara bean (Voandzeia subterranean) flour at levels between 0 and 50% with each of commercial (control), Lee X and Inia 66 wheat flour. Physical and sensory evaluations showed that the performance of straight Lee X and Inia 66 flours was inferior to that of the commercial flour. The commercial flour showed better tolerance to blending with bambara flour, producing acceptable loaves at up to 20% substitution with bean flour; Lee X and Inia 66 could not tolerate blending beyond 15% and 5% levels, respectively. Physical properties and baking performance of the Lee X and Inia 66 flours were improved by treatment with various levels of the oxidising agents KBrO₃, ascorbic acid and KBrO₃/ascorbic acid combinations. Lee X flour was more responsive to the treatments than Inia 66. Concentrations of 25 mg kg^?1 KBrO₃ and 80 mg kg^?1 ascorbic acid singly were found to improve Lee X flours adequately, but a combination of the two agents at a level of 25/60 mg kg^?1 KBrO₃/ascorbic acid was optimal. When treated with the optimal level of improver combination, Lee X flour performed as well as the commercial flour; and treated Lee X composite flours containing up to 30% pre-cooked bambara flour were found to produce loaves not significantly different from 100% commercial wheat bread (P≤0.05).     

The interaction between threonine and avilamycin on piglet performance and diet digestibility post weaning

A 3 × 2 factorial experimental design was used to investigate the interaction between threonine level (8.6, 10.5 or 12.1 g kg^?1) and an antimicrobial growth promoter (0 or 60 mg kg^?1 avilamycin) in piglet starter diets. Three hundred and sixty weaned piglets (24 d of age; 5.9 kg live weight) were blocked on the basis of live weight and assigned to one of six dietary treatments. The treatments were (1) 8.6 g kg^?1 threonine and avilamycin, (2) 10.5 g kg^?1 threonine and avilamycin, (3) 12.1 g kg^?1 threonine and avilamycin, (4) 8.6 g kg^?1 threonine and no avilamycin, (5) 10.5 g kg^?1 threonine and no avilamycin and (6) 12.1 g kg^?1 threonine and no avilamycin. The diets were formulated to have identical concentrations of digestible energy (16 MJ kg^?1) and total lysine (16 g kg^?1). There was no interaction between threonine and avilamycin in any performance variable measured. Neither the level of threonine nor the inclusion of avilamycin in the diet had any effect on feed intake, average daily gain or food conversion ratio. There was a significant interaction between threonine level and avilamycin inclusion in the apparent digestibility of dry matter, organic matter, nitrogen, ash, neutral detergent fibre and gross energy and also digestible energy content. In the absence of avilamycin, there was a linear increase in nutrient digestibility to increased threonine levels in the diet. However, in the presence of avilamycin there was a quadratic response to increased threonine levels. In conclusion, optimum piglet performance was achieved at a threonine level of 8.6 g kg^?1 and there was no advantage to avilamycin inclusion under current conditions. Copyright © 2005 Society of Chemical Industry     

Chemical composition and toxic trace element composition of some Nigerian edible wild mushrooms

Two essential amino acids (methionine and tryptophan); anti‐nutritional factors (tannin and trypsin inhibitor) and toxic elements (Pb, Cd, Ni, As, Hg and Cr) were determined spectrophotometrically from five edible wild mushrooms. The tryptophan content was between 1.00 and 1.82 g (100 g)^?1 but methionine was low at 0.26–1.38 g (100 g)^?1. Tannin content was high (30.3–40.0 mg g^?1) but trypsin inhibitor was low (22.0–39.5 TIU g^?1). Trace elements analysis reviled Pb (0.34–5.06 mg kg^?1) to be the highest of all the trace elements. Cd was (0.06–1.70 mg kg^?1), Ni (0.26–2.08 mg kg^?1), As (0.17–0.92 mg kg^?1), Hg (0.01–0.05 mg kg^?1) and Cr (0.04–0.22 mg kg^?1). These mushrooms are nutritious but must be well processed to eliminate or at least reduce the levels of tannin and Pb to improve their nutritional values.     

Validation of the procedure for the determination of maduramicin in concentrates,premixes, and feeds by liquid chromatography

A single laboratory validation was carried out for the determination of maduramicin in concentrates, premixes, and feed. The method comprised sample extraction of maduramicin, derivatization with dansylhydrazine and liquid chromatography with ultraviolet light detection. The limit of detection (LOD) and limit of quantification (LOQ) were 0.4 and 1.0 mg kg^?1, respectively. The repeatability expressed as the average difference between the results of duplicate measurements was 5.9% at the concentration level of 1% (concentrate), 7.1% at the concentration level of 1 g kg^?1 (premix), and 11% with the feed containing maduramicin with the nominal concentration of 5 mg kg^?1 and feed spiked at the concentration level of 1 mg kg^?1. The relative standard deviations for the within-laboratory reproducibility (RSD_W) were 9.2%, 16%, 18%, and 17% at the concentration levels of 1%, 1 g kg^?1, 5 mg kg^?1, and 1 mg kg^?1, respectively. The measurement uncertainties were ±0.2%, ±0.3 g kg^?1, ±1.9 mg kg^?1, and ±0.3 mg kg^?1 at the same concentration levels, respectively.     

Organochlorine pesticide residues in domestic fowl (Gallus domesticus) eggs from central Kenya

In 367 domestic fowl (Gallus domesticus) eggs collected from 61 farms, residues of 10 pesticides were detected in various combinations and in the following order of frequency: p,p′-DDE (in 100% of the eggs), p,p′-DDT (98%), dieldrin (95%), Indiane (66%), p,p′-DDD (46%), o,p′-DDT (17%), β-HCH (9%), γ-HCH (5%), endrin (4%) and aldrin (0–5%). No residues of heptachlor, heptachlor epoxide, HCB or PCBs were found. The mean concentration (0–70 mg kg^?1 eggs; range <0–01–10–25) of total DDT exceeded the extraneous residue limit (ERL) of 0–50 mg kg^?1. The mean dieldrin residue level (0–35 mg kg^?1; range 0–01–14–90) was 3–5 times higher than the ERL (0–10 mg kg^?1). Only 3% of the eggs exceeded the ERL for Indane. The 156 eggs from free-range hens had significantly (P<0–05) higher residue concentrations of total DDT, dieldrin and Iindane than eggs collected from hens kept in enclosures. The mean ratio [p,p′-DDT]/[p,p′-DDE] in eggs from enclosed hens (0–97) was significantly higher (P<0–01) than in eggs from free-range hens (0–53), indicating that the former had a more direct exposure to p,p′-DDT, whereas the latter obtained more of it after environmental conversion to p,p′-DDE. Eggs from a rice-growing area had the highest concentrations of all pesticide residues detected. Accumulation ratios indicated that the levels of DDT and Iindane in the feed of enclosed hens could account for the levels in the corresponding eggs. The much higher accumulation ratios calculated for the free-range hens demonstrated that the feed ingested by these chickens obviously contained ingredients additional to those sampled, and revealed probable extensive environmental contamination by these persistent pesticides. The present results indicate that there is a need to identify sources of dieldrin in the eggs of domestic fowls and, where necessary to investigate local wildlife samples. The amounts of total DDT and dieldrin in eggs in this study seem to be higher than reported from any other country. Toxicological evaluation of the results indicates that, at lest in parts of KEnya there is a need for improved practices in the use of some organochlorine pesticides.