Acute intoxication with single oral dose of ochratoxin A (OTA) causes leukopenia, heteropenia, lymphopenia and lymphoid depletion in the bursa of Fabricius in broiler chicks / Intoxicação aguda com dose oral única de ocratoxina A (OTA) causa leucopenia, heteropenia, linfopenia e depleção linfoide na bolsa de Fabricius em pintainhos de corte

Ochratoxin A (OTA) is a mycotoxin produced by species of Penicillium and Aspergillus, agricultural product contaminants. Chronic and sub-chronic OTA intoxication by chickens ingesting contaminated feed, leads to health damages due to its hepatotoxic, nephrotoxic, cytotoxic, immunotoxic, gastrotoxic, and possibly carcinogenic effects. As there are few data on acute intoxication, the present study evaluated the effects of a single acute OTA intoxication dose on immunological and hematological parameters in chicks. Sixteen one-day-old chicks were used, separated into two groups (n=8). A single dose of OTA (1400 µg kg-1 body weight) was administered, via gavage, for the OTA group and one dose of sterile PBS for the control group. On the 13th day, blood samples were collected to assess hematological and biochemical parameters, and on the 14th day, euthanasia and collection of lymphoid organs were performed. The animals of the OTA group demonstrated a significant decrease in total circulating leukocytes (p<0.001) with heteropenia (p<0.001) and lymphopenia (p=0.023), decrease hematocrit (p=0.020), hemoglobin (p=0.032), and plasma IgA (p =0.044), and increased plasma uric acid level (p=0.045), in relation to the control group. In addition, the animals intoxicated with OTA showed depletion of lymphoid cells in the bursa of Fabricius (p=0.016), but not in the thymus or spleen (p>0.05), compared to the control. For the other parameters: total plasma proteins, plasma IgY levels, and anti-Newcastle Disease Virus (NDV) vaccine titers from matrices, there were no significant differences between the analyzed groups (p>0.05), although there was a worsening tendency in contaminated animals. In conclusion, even a single acute OTA intoxication at a high dose, leads to the suppression of the systemic immune response, also affecting some hematological or biochemical parameters in chicks.

Ocratoxina A (OTA) é uma micotoxina produzida por espécies de Penicillium e Aspergillus, contaminantes de produtos agrícolas. Intoxicação crônica e subcrônica por OTA em frangos que ingerem ração contaminada, levam à danos à saúde devido aos seus efeitos hepatotóxicos, nefrotóxicos, citotóxicos, imunotóxicos, gastrotóxicos e possivelmente carcinogênicos. Como há poucos dados sobre intoxicação aguda, o presente estudo avaliou os efeitos de uma dose única de intoxicação aguda por OTA sobre parâmetros imunológicos e hematológicos em pintainhos. Foram utilizados 16 pintainhos de um dia de idade, separados em dois grupos (n=8). Uma dose única de OTA (1400 µg kg-1 de peso corporal) foi administrada, via gavagem, para o grupo OTA e uma dose de PBS estéril para o grupo controle. No 13º dia foram coletadas amostras de sangue para avaliação dos parâmetros hematológicos e bioquímicos, e no 14º dia foi realizada a eutanásia e coleta de órgãos linfoides. Os animais do grupo OTA demonstraram diminuição significativa do total de leucócitos circulantes (p<0,001) com heteropenia (p<0,001) e linfopenia (p=0,023), diminuição do hematócrito (p=0,020), hemoglobina (p=0,032) e IgA plasmática (p=0,044) e aumento do nível plasmático de ácido úrico (p=0,045), em relação ao grupo controle. Além disso, os animais intoxicados com OTA apresentaram depleção de células linfóides na bolsa de Fabricius (p=0,016), mas não no timo ou baço (p>0,05), em relação ao controle. Para os demais parâmetros: proteínas totais do plasma, níveis plasmáticos de IgY e títulos de vacinas contra o Vírus da Doença de Newcastle (NDV) das matrizes, não houve diferenças significativas entre os grupos analisados (p>0,05), embora tenha havido uma tendência de piora nos animais contaminados. Em conclusão, mesmo uma intoxicação única aguda por OTA em alta dose, leva à supressão da resposta imune sistêmica, afetando também alguns parâmetros hematológicos ou bioquímicos em pintainhos.

The Protective Role of Silymarin to Ameliorate the Adverse Effects of Ochratoxin-A in Laying Hens on Productive Performance, Blood Biochemistry, Hematological and Antioxidants Status

This study was planned to examine the effect of silymarin on diminishing adverse effects of ochratoxin-A (OTA) in laying hens. A total number of 300 Inshas, local layer hens of 28 weeks of age were randomly distributed into 4 groups with 5 replicates each (15 hens). The birds were fed on the following treatments, (Control): fed a hen diet without any supplementation; (SL): fed the control diet supplemented with SL (1000 mg/kg feed); (OTA-diet): was fed the control diet contaminated with 1 ppm of OTA/kg diet, and (OTA+SL): fed the OTA-diet plus SL (1ppm OTA+1000 mg SL/kg feed). Results showed that feeding OTA at 1 ppm reduced productive performance compared with those fed the control diet. In OTA treated groups the total erythrocytes count, leukocytes count, PCV and Hb were decreased when compared to the control and SL groups. Albumin, globulin and serum total proteins in OTA treated groups were significantly lower when compared to the control and SL groups. Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were significantly increased in OTA fed groups in comparison with the control and SL groups. Creatinine and uric acid were increased in OTA treated groups but were almost normal in the SL group. The results showed that OTA had a severe effect on liver and kidney, but SL treated group had normal liver and kidneys showing its hepatoprotective effects.(AU)

Effect of Modified Clinoptilolite to Counteract the Deleterious Effects of Ochratoxin A on Egg Production and Quality

The objective of this study was to evaluate the efficacy of modified clinoptilolite as mycotoxins adsorbent in preventing negative effects of ochratoxin A (OTA) on egg production and egg quality of laying hens exposed to this mycotoxin. Forty-eight (n=48) laying hens (27 weeks old) were used in this study. The hens were randomly divided into six equal groups and were fed for 7 weeks with a standard diet in addition to: E-I group - 1 mg/kg OTA; E-II group 0.25 mg/kg OTA; E-III group 1mg/kg OTA + 0.2% of MZ; E-IV group 0.25 mg/kg OTA + 0.2% of MZ. MZ group of hens was fed with standard diets containing 0.2% of the adsorbent (MZ). The control group of hens was fed with standard diet, without any addition of OTA or MZ. The present study showed that laying hens fed with 1 mg/kg of OTA (E-I), had a significant decrease (p<0.05) of all performance parameters during the trial, while group fed with 0.25 mg/kg OTA have shown no adverse effects on egg production and egg quality. Addition of modified clinoptilolite (0.2%) to the diet containing the OTA, minimized these effects bringing values not significantly different from the control diet for most of the parameters. These findings clearly indicate the protective potential of modified clinoptilolite against the toxic effects of OTA in laying hens.(AU)

Micotoxinas e adsorventes na alimentação animal / Mycotoxins and adsorbents in animal feed

As micotoxinas são substâncias produzidas durante o processo metabólico de alguns fungos, elas são extremamente nocivas aos animais. Esses fungos estão presentes em diversos tipos de cereais e frutas. O milho, principal cereal utilizado na alimentação animal, pode ser acometido por fungos dos gêneros Aspergillus e Fusarium, que quando submetidos à umidade e temperaturas específicas produzem aflatoxinas, ocratoxina, fumonisinas e zearalenona que causam problemas no desempenho e produção dos animais. Os animais monogástricos, como aves e suínos, e de ceco funcional, como os equinos, são mais susceptíveis aos efeitos que essas substâncias podem causar, quando comparados aos animais ruminantes, pois estes apresentam no rúmen microrganismos que são capazes de digerir as micotoxinas. No entanto, animais como vacas leiteiras de alta produção e animais monogástricos, quando consomem alimentos contaminados durante um longo período, podem desenvolver problemas digestivos, neurológicos, queda na produção e até mesmo chegar a óbito. Diante disso, algumas técnicas vêm sendo utilizadas pelos produtores e fábricas de ração, visando o não fornecimento de grãos contaminados aos animais, como um controle de qualidade dos alimentos e o uso de adsorventes. Os adsorventes são aditivos adicionados à dieta dos animais com o objetivo de inativar as micotoxinas. Eles podem ser de origem orgânica, como as leveduras, ou inorgânicos derivados de argila. Esses aditivos se ligam à substância impedindo que estas sejam absorvidas pelo enterócito e, assim, sejam excretadas sem causar prejuízos ao metabolismo dos animais.

Mycotoxins are substances produced during the metabolic process of some fungi, they are extremely harmful to animals. These fungi are present in several types of cereals and fruits. The main cereal corn used in animal feed can be affected by fungi of the genera Aspergillus and Fusarium that when subjected to humidity and specific specifications such as aflotoxins, ochratoxin, fumonisins and zearalenone that cause problems in the performance and production of animals. Monogastric animals, such as poultry, pigs and functional dry animals such as horses, are more susceptible to the effects that these occurrences can cause, when compared to ruminant animals, as they present in the rumen, microorganisms that are capable of digesting as mycotoxins. However, animals such as high production dairy cows and monogastric animals, when consuming contaminated food for a long period can develop digestive, neurological problems, drop in production and even die. In view of this, some techniques have been used by producers and feed factories, adding the non supply of contaminated grains to animals, such as food quality control and the use of adsorbents. Adsorbents are suitable additives to the animals' diet in order to inactivate as mycotoxins. They can be of organic origin, like yeasts or inorganic derived from clay. These additives bind to a substance preventing them from being absorbed by the enterocyte, thus being excreted without causing damage to the animals' metabolism.

Determination of Aflatoxin M1 and Ochratoxin A in raw, pasteurizedand UHT milk in Turkey

Background: Mycotoxins produced by yeast and fungi have toxic effects on human and animal health. Aflatoxin B1 (AFB1)is the most toxic hepatocarcinogen to mammals. Aflatoxin M1 (AFM1), which has been found in milk and dairy products,is the hydroxylated metabolite of AFB1. Aflatoxin M1 is formed by the cytochrome P450 enzyme in the liver. OchratoxinA (OTA) is synthesized by Aspergillus and Penicillium species. Ochratoxin A is known to cause teratogenic, immunotoxic,nephrotoxic and carcinogenic effects. Due to the potential harmful effects on human and animal health, OTA has also beenreceiving increased attention globally; however, there is limited information on the presence of OTA in milk and dairy products. The aim of this study was to determine how mycotoxins impact the hygienic quality of raw and heat-processed milk.Materials, Methods & Results: In this study, a total of 105 milk samples were analyzed (35 raw, 35 pasteurized and 35UHT) to identify AFM1 and OTA in raw, pasteurized and ultra-high temperature processing (UHT) milk. The levels ofAFM1 were detected by using the enzyme-linked immunosorbent assay (ELISA). The milk samples were centrifuged inorder to remove the fat content from the milk. After centrifugation, the upper cream layer was withdrawn with a pipette.The non-fat liquid portion was placed in wells at 100 μL for analysis. The concentration of AFM1 in the milk sampleswas analyzed by AFM1 test kit. The milk samples with AFM1 levels greater than 50 ng/L were confirmed by using HighPerformance Liquid Chromatography (HPLC). An Ochratoxin A Serum / Milk ELISA test kit was used for the analysesof OTA. The analyses were made according to the manufacturer’s instructions, and samples were analyzed in duplicate.The absorbance value of milk samples was obtained from the ELISA plate reader at 450 nm...

Determination of Aflatoxin M1 and Ochratoxin A in raw, pasteurizedand UHT milk in Turkey

Background: Mycotoxins produced by yeast and fungi have toxic effects on human and animal health. Aflatoxin B1 (AFB1)is the most toxic hepatocarcinogen to mammals. Aflatoxin M1 (AFM1), which has been found in milk and dairy products,is the hydroxylated metabolite of AFB1. Aflatoxin M1 is formed by the cytochrome P450 enzyme in the liver. OchratoxinA (OTA) is synthesized by Aspergillus and Penicillium species. Ochratoxin A is known to cause teratogenic, immunotoxic,nephrotoxic and carcinogenic effects. Due to the potential harmful effects on human and animal health, OTA has also beenreceiving increased attention globally; however, there is limited information on the presence of OTA in milk and dairy products. The aim of this study was to determine how mycotoxins impact the hygienic quality of raw and heat-processed milk.Materials, Methods & Results: In this study, a total of 105 milk samples were analyzed (35 raw, 35 pasteurized and 35UHT) to identify AFM1 and OTA in raw, pasteurized and ultra-high temperature processing (UHT) milk. The levels ofAFM1 were detected by using the enzyme-linked immunosorbent assay (ELISA). The milk samples were centrifuged inorder to remove the fat content from the milk. After centrifugation, the upper cream layer was withdrawn with a pipette.The non-fat liquid portion was placed in wells at 100 μL for analysis. The concentration of AFM1 in the milk sampleswas analyzed by AFM1 test kit. The milk samples with AFM1 levels greater than 50 ng/L were confirmed by using HighPerformance Liquid Chromatography (HPLC). An Ochratoxin A Serum / Milk ELISA test kit was used for the analysesof OTA. The analyses were made according to the manufacturers instructions, and samples were analyzed in duplicate.The absorbance value of milk samples was obtained from the ELISA plate reader at 450 nm...(AU)

Oxidative Stress of in-Ovo Ochratoxin A Administered during Chick Embryonic Development

The present work was carried out to study the effect of in-ovo injection of ochratoxin A (OTA) as an oxidative stress and its consequences on hepatic and kidney functions, thyroid activity, and histological examination of brain and liver in chicken embryos and subsequently in the hatching chicks. On the 10th day of incubation, one hundred and sixty-two fertile eggs were randomly divided into two equal treatments. Control treatment, (injected by 50 µl sodium carbonate) and OTA treatment (injected by 12.5 ng OTA dissolved in 50 µl sodium carbonate). OTA treatement group significantly reduced glutathione (GSH) and significantly increased thiobarbituric acid reactive substances production (TBARS) in embryonic and hatched chicks regarding livers, spleen, bursa of Fabricius, heart, and brain as an indicator of oxidative stress. OTA injection increased TBARS and decreased GSH levels in both allantoic and amniotic fluids. On the 14th and 16th days of incubation and at the hatch, a significant lower concentration in cholesterol and higher concentrations of alanine amino transferase, aspartate amino transferase, alkaline phosphatase, gamma glutamyl transferase, acid phosphatase enzymes activities and triglycerides in the hepatic tissues of the OTA group were observed. Histological examination of OTA group of brain and liver tissues showed some degenerative changes through the experimental period. In conclusion, in-ovo OTA treated had teratogenic and embryotoxic effects.(AU)

Oxidative Stress of in-Ovo Ochratoxin A Administered during Chick Embryonic Development

The present work was carried out to study the effect of in-ovo injection of ochratoxin A (OTA) as an oxidative stress and its consequences on hepatic and kidney functions, thyroid activity, and histological examination of brain and liver in chicken embryos and subsequently in the hatching chicks. On the 10th day of incubation, one hundred and sixty-two fertile eggs were randomly divided into two equal treatments. Control treatment, (injected by 50 µl sodium carbonate) and OTA treatment (injected by 12.5 ng OTA dissolved in 50 µl sodium carbonate). OTA treatement group significantly reduced glutathione (GSH) and significantly increased thiobarbituric acid reactive substances production (TBARS) in embryonic and hatched chicks regarding livers, spleen, bursa of Fabricius, heart, and brain as an indicator of oxidative stress. OTA injection increased TBARS and decreased GSH levels in both allantoic and amniotic fluids. On the 14th and 16th days of incubation and at the hatch, a significant lower concentration in cholesterol and higher concentrations of alanine amino transferase, aspartate amino transferase, alkaline phosphatase, gamma glutamyl transferase, acid phosphatase enzymes activities and triglycerides in the hepatic tissues of the OTA group were observed. Histological examination of OTA group of brain and liver tissues showed some degenerative changes through the experimental period. In conclusion, in-ovo OTA treated had teratogenic and embryotoxic effects.

Simultaneous determination of mycotoxins in peruvian purple maize / Determinação simultânea de micotoxinas em milho roxo peruano

Purple maize is an important foodstuff for the Peruvian people. Its unique nutritional and antioxidant characteristics makes it widely exported to other countries. However, when contaminated by fungi, it can trigger numerous health problems in the consumers. This study aimed to evaluate the presence of 27 mycotoxins in 63 samples of purple maize collected in Peru. Frequency of occurrence and mean concentration of the following mycotoxins were determined: alternariolmetileter (AME), alternariol (AOH), tentoxin, neosolaniol, nivalenol, wortmannin, deoxynivalenol, 3-acetyl deoxynivalenol, 15-acetyl deoxynivalenol, zearalenone, aflatoxin B1, aflatoxin B2, aflatoxin G1, aflatoxin G2, fumonisin B1, fumonisin B2, fumonisin B3, ochratoxin A, ochratoxin , T-2 toxin, HT-2 toxin, fusarenon x, cyclopiazonic acid, gliotoxin, agroclavin and citreoviridin. The main mycotoxins reported in purple maize were AME and AOH, with a frequency of occurrence of 14.3 and 7.9%, and mean concentration of 23.3% and 1.8%, respectively. AME and AOH do not have guidance levels in the Brazilian legislation. Contrastingly, levels of mycotoxins which are within the standards of the countrys regulations were below the limit of quantification. The present results suggested that purple maize is a raw material with a great potential for the production and industrialization of special products.(AU)

O milho roxo é um alimento importante para o povo peruano. Suas características nutricionais e antioxidantes únicas fazem com que seja amplamente exportado para outros países. No entanto, quando contaminado por fungos, pode desencadear inúmeros problemas de saúde nos consumidores. Este estudo teve como objetivo avaliar a presença de 27 micotoxinas em 63 amostras de milho roxo coletadas no Peru. A frequência de ocorrência e a concentração média das seguintes micotoxinas foram determinadas: alternariolmetileter (AME), alternariol (AOH), tentoxina, neosolaniol, nivalenol, wortmanina, desoxinivalenol, 3-acetil desoxinivalenol, 15-acetil desoxinivalenol, zearalenona, aflatoxina B1, aflatoxina B2 , aflatoxina G1, aflatoxina G2, fumonisina B1, fumonisina B2, fumonisina B3, ocratoxina A, ocratoxina, toxina T-2, toxina HT-2, fusarenona x, ácido ciclopiazonico, gliotoxina, agroclavina e citreoviridina. As principais micotoxinas encontradas no milho roxo foram AME e AOH, com frequência de ocorrência de 14,3% e 7,9% e concentração média de 23,3% e 1,8%, respectivamente. AME e AOH não possuem níveis de orientação na legislação brasileira. Contrastantemente, os níveis de micotoxinas que estão dentro dos padrões das regulamentações do país estavam abaixo do limite de quantificação. Os presentes resultados sugerem que o milho roxo é uma matéria-prima com grande potencial para a produção e industrialização de produtos especiais.(AU)

Efeito da ocratoxina A em suco de uva tinto sobre sobrevivência e geração de EROs em Caenoaerbiditis elegans / Effects of ochratoxin A in red grape juice on survival rate and ROs generation in Caenoaerbiditis elegans

O consumo do suco de uva vem crescendo ao longo dos anos em função das suas propriedades funcionais. No entanto, este produto não está livre de contaminantes como a ocratoxina A (OTA). O presente trabalho teve por objetivo avaliar o efeito da presença de OTA em suco de uva Concord sobre geração de espécies reativas de oxigênio (EROs) e taxa de sobrevivência em Caenoarbiditis elegans. Os vermes foram expostos por 30 minutos ao suco na presença de OTA (0, 1, 2 e 4 µg∙L-1). O suco em presença de OTA não afetou a sobrevivência do C. Elegans. A adição de suco livre de OTA reduziu a sobrevivência dos nematoides, embora não tenha influenciado a geração de EROs. Contudo o suco com a concentração mais elevada de OTA reduziu a geração de EROs. Assim, são necessários maiores estudos para entender os mecanismos de toxicidade da OTA neste modelo vivo.(AU)

Efeito da ocratoxina A em suco de uva tinto sobre sobrevivência e geração de EROs em Caenoaerbiditis elegans / Effects of ochratoxin A in red grape juice on survival rate and ROs generation in Caenoaerbiditis elegans

O consumo do suco de uva vem crescendo ao longo dos anos em função das suas propriedades funcionais. No entanto, este produto não está livre de contaminantes como a ocratoxina A (OTA). O presente trabalho teve por objetivo avaliar o efeito da presença de OTA em suco de uva Concord sobre geração de espécies reativas de oxigênio (EROs) e taxa de sobrevivência em Caenoarbiditis elegans. Os vermes foram expostos por 30 minutos ao suco na presença de OTA (0, 1, 2 e 4 µg∙L-1). O suco em presença de OTA não afetou a sobrevivência do C. Elegans. A adição de suco livre de OTA reduziu a sobrevivência dos nematoides, embora não tenha influenciado a geração de EROs. Contudo o suco com a concentração mais elevada de OTA reduziu a geração de EROs. Assim, são necessários maiores estudos para entender os mecanismos de toxicidade da OTA neste modelo vivo.

Determination of Ochratoxin A levels in mixed feed and feed stuffs used in some laying hens and ruminant interprises of Sivas City

Mycotoxins, which are produced by some fungi under improper storage conditions before or after harvesting in plant products, cause acute or chronic toxicities. Ochratoxin A (OA) which is also one of the harmful mycotoxins pose a threat to animal and human health. This study was carried out in order to determine OA levels in mixed feed and feedstuffs materials used in livestock enterprises throughout Sivas province. The 59 mixed feeds and 30 feedstuffs materials collected from different enterprises was analysed. Ochratoxin A concentrations were quantified using immunoassay (ELISA). In result, OA was found to be positive in 64 (71.91%) of the 89 samples analysed, whereas OA was not found in 25 samples (28.09%).(AU)

Determination of Ochratoxin A levels in mixed feed and feed stuffs used in some laying hens and ruminant interprises of Sivas City

Mycotoxins, which are produced by some fungi under improper storage conditions before or after harvesting in plant products, cause acute or chronic toxicities. Ochratoxin A (OA) which is also one of the harmful mycotoxins pose a threat to animal and human health. This study was carried out in order to determine OA levels in mixed feed and feedstuffs materials used in livestock enterprises throughout Sivas province. The 59 mixed feeds and 30 feedstuffs materials collected from different enterprises was analysed. Ochratoxin A concentrations were quantified using immunoassay (ELISA). In result, OA was found to be positive in 64 (71.91%) of the 89 samples analysed, whereas OA was not found in 25 samples (28.09%).

In vivo detoxification of ochratoxin A by highly porous magnetic nanocomposites prepared from coconut shell

The current study was conducted to elucidate the clinical effect of ochratoxin A in Gallus gallus domesticus and to ameliorate its toxic effects by the development and characterization of highly porous carbon-based adsorbent derived from coconut shell. A series of experiments were performed on one day-old chicks (Group A to F). Clinical signs of the positive control (group B fed on 400 ppb ochratoxin A contaminated feed) included depression, diarrhea, increased water intake, low body weight, high degree of genotoxicity, swollen and hemorrhagic kidneys and liver. Serum alanine amino transferase (ALT), alkaline phosphatase (ALP), creatinine and urea concentration significantly increased while albumin, globulin and total proteins were found significantly low. All these lead to increased mortality. Among adsorbents treated groups, chickens in group C (0.3% of the prepared adsorbent mixed in OTA contaminated feed) and D (0.6% of the prepared adsorbent mixed in Ochratoxin A (OTA) contaminated feed) showed very low pathological effects while group E (0.9% of the prepared adsorbent mixed in OTA contaminated feed) and F (1.2% of the prepared adsorbent mixed in OTA contaminated feed) showed normal behavior, blood biochemistry and well maintained histological structure like that in group A. As a whole, the adsorbents treated groups fed with ochratoxin A contaminated feed, supplemented with different levels of the prepared adsorbent helped to ameliorate the toxic effects of OTA and nearly showed normal clinical signs.(AU)

In vivo detoxification of ochratoxin A by highly porous magnetic nanocomposites prepared from coconut shell

The current study was conducted to elucidate the clinical effect of ochratoxin A in Gallus gallus domesticus and to ameliorate its toxic effects by the development and characterization of highly porous carbon-based adsorbent derived from coconut shell. A series of experiments were performed on one day-old chicks (Group A to F). Clinical signs of the positive control (group B fed on 400 ppb ochratoxin A contaminated feed) included depression, diarrhea, increased water intake, low body weight, high degree of genotoxicity, swollen and hemorrhagic kidneys and liver. Serum alanine amino transferase (ALT), alkaline phosphatase (ALP), creatinine and urea concentration significantly increased while albumin, globulin and total proteins were found significantly low. All these lead to increased mortality. Among adsorbents treated groups, chickens in group C (0.3% of the prepared adsorbent mixed in OTA contaminated feed) and D (0.6% of the prepared adsorbent mixed in Ochratoxin A (OTA) contaminated feed) showed very low pathological effects while group E (0.9% of the prepared adsorbent mixed in OTA contaminated feed) and F (1.2% of the prepared adsorbent mixed in OTA contaminated feed) showed normal behavior, blood biochemistry and well maintained histological structure like that in group A. As a whole, the adsorbents treated groups fed with ochratoxin A contaminated feed, supplemented with different levels of the prepared adsorbent helped to ameliorate the toxic effects of OTA and nearly showed normal clinical signs.

Mycotoxins in broiler production / Micotoxinas na produção de frangos de corte

The occurrence of mycotoxins has become a problem to be discussed, due to its harmfulness to humans and animals health, and may be an obstacle to the poultry economy. Mycotoxins are toxic metabolites produced by certain species of fungi and may contaminate food. Aflatoxins are mainly produced by Aspergillus flavus and Aspergillus parasiticus, and B1, B2, G1 and G2 are its best known types. Fumonisin, with its B1, B2 or B3 types, are produced by Fusarium, while ochratoxin A is produced by Penicillium and Aspergillus. The main trichothecenes mycotoxins are T-2 toxin, deoxynivalenol and diacetoxyscirpenol. Zearalenone, produced by different species of Fusarium fungi affects chickens only when they are exposed to extremely high levels of contamination. Generally, immunosuppression, hepatotoxicity and nephrotoxicity as a decrease in performance and production gains are the most observed effects. There are several laboratory methods that can be used for the determination of mycotoxins. In order to control the contamination, it is necessary to adopt proper farming practices which prevent fungi growth. Once grains and feed are contaminated, biological, physical and/or chemical decontamination methods may be employed, although the physical process with adsorbents mixed to the feed is more widely used. Due to the importance of mycotoxins to poultry production, it is necessary to adopt measures to prevent contamination, and also develop a control and an anti-fungal growth and toxin production program by reviewing the critical points favorable to the emergence of toxin-producing fungi.

A ocorrência de micotoxinas tornou-se um problema a ser discutido, pois representa riscos à saúde dos animais e humanos, podendo constituir um obstáculo à economia avícola. Micotoxinas são metabólitos tóxicos produzidos por algumas espécies de fungos e podem contaminar os alimentos. Aflatoxinas são majoritariamente produzidas por Aspergillus flavus e Aspergillus parasiticus, sendo B1, B2, G1 e G2 os tipos mais conhecidos. Fumonisinas são do tipo B1, B2 e B3, e produzidas pelo gênero Fusarium, enquanto a ocratoxina A é produzida por fungos da espécie Penicillium e Aspergillus. As principais micotoxinas dos tricotecenos são toxina T-2, deoxynivalenol e diacetoxyscirpenol. A zearalenona, produzida por diferentes espécies de fungos do gênero Fusarium, afeta os frangos apenas quando estes são expostos a níveis extremamente altos de contaminação. De modo geral, são observados efeitos imunossupressores, hepatotóxicos e nefrotóxicos, com queda no desempenho e nos ganhos de produção. Vários são os métodos laboratoriais que podem ser utilizados para a determinação de micotoxinas. Para o controle da contaminação, é necessário adoção de práticas agrícolas correta, com vistas à prevenção do crescimento de fungos. Após a contaminação de grãos e rações, métodos de descontaminação, biológicos, físicos e/ou químicos podem ser empregados, embora o processo físico com adsorventes misturados às rações seja o mais utilizado. Pela importância que as micotoxinas representam à produção de frangos, é necessário adotar medidas que previnam a contaminação e desenvolver programas de controle e combate ao desenvolvimento fúngico e produção de toxinas, revendo os pontos críticos propícios ao aparecimento dos fungos geradores das toxinas.

Mycotoxins in broiler production / Micotoxinas na produção de frangos de corte

The occurrence of mycotoxins has become a problem to be discussed, due to its harmfulness to humans and animals health, and may be an obstacle to the poultry economy. Mycotoxins are toxic metabolites produced by certain species of fungi and may contaminate food. Aflatoxins are mainly produced by Aspergillus flavus and Aspergillus parasiticus, and B1, B2, G1 and G2 are its best known types. Fumonisin, with its B1, B2 or B3 types, are produced by Fusarium, while ochratoxin A is produced by Penicillium and Aspergillus. The main trichothecenes mycotoxins are T-2 toxin, deoxynivalenol and diacetoxyscirpenol. Zearalenone, produced by different species of Fusarium fungi affects chickens only when they are exposed to extremely high levels of contamination. Generally, immunosuppression, hepatotoxicity and nephrotoxicity as a decrease in performance and production gains are the most observed effects. There are several laboratory methods that can be used for the determination of mycotoxins. In order to control the contamination, it is necessary to adopt proper farming practices which prevent fungi growth. Once grains and feed are contaminated, biological, physical and/or chemical decontamination methods may be employed, although the physical process with adsorbents mixed to the feed is more widely used. Due to the importance of mycotoxins to poultry production, it is necessary to adopt measures to prevent contamination, and also develop a control and an anti-fungal growth and toxin production program by reviewing the critical points favorable to the emergence of toxin-producing fungi.(AU)

A ocorrência de micotoxinas tornou-se um problema a ser discutido, pois representa riscos à saúde dos animais e humanos, podendo constituir um obstáculo à economia avícola. Micotoxinas são metabólitos tóxicos produzidos por algumas espécies de fungos e podem contaminar os alimentos. Aflatoxinas são majoritariamente produzidas por Aspergillus flavus e Aspergillus parasiticus, sendo B1, B2, G1 e G2 os tipos mais conhecidos. Fumonisinas são do tipo B1, B2 e B3, e produzidas pelo gênero Fusarium, enquanto a ocratoxina A é produzida por fungos da espécie Penicillium e Aspergillus. As principais micotoxinas dos tricotecenos são toxina T-2, deoxynivalenol e diacetoxyscirpenol. A zearalenona, produzida por diferentes espécies de fungos do gênero Fusarium, afeta os frangos apenas quando estes são expostos a níveis extremamente altos de contaminação. De modo geral, são observados efeitos imunossupressores, hepatotóxicos e nefrotóxicos, com queda no desempenho e nos ganhos de produção. Vários são os métodos laboratoriais que podem ser utilizados para a determinação de micotoxinas. Para o controle da contaminação, é necessário adoção de práticas agrícolas correta, com vistas à prevenção do crescimento de fungos. Após a contaminação de grãos e rações, métodos de descontaminação, biológicos, físicos e/ou químicos podem ser empregados, embora o processo físico com adsorventes misturados às rações seja o mais utilizado. Pela importância que as micotoxinas representam à produção de frangos, é necessário adotar medidas que previnam a contaminação e desenvolver programas de controle e combate ao desenvolvimento fúngico e produção de toxinas, revendo os pontos críticos propícios ao aparecimento dos fungos geradores das toxinas.(AU)

Toxic Effects of Ochratoxin A on Calcium Metabolism during Chick Embryo Developmentand in Hatched Chicks

ABSTRACT The present study was carried out to study the effect of in-ovo ochratoxin A (OTA) injection in Highline layer eggs on calcium metabolism and blood biochemical parameters of embryos and after the hatch. At day 10 of embryonic development, one hundred and sixty-two fertile eggs were individually weighed and divided into two equal treatments. The first treatment (control) consisted of the individual injection of fertile eggs with 50 µL sodium carbonate. In the second treatment (OTA), fertile eggs were individually injected with 12.5 ng OTA dissolved in 50 µL sodium carbonate. On days 12, 14, and 16 of incubation and at the hatch, serum calcium and inorganic phosphorus concentrations were lower (p 0.05), while sodium, alkaline phosphatase and triiodothyronine concentrations were higher (p 0.05) in the OTA-injected eggs compared with the controls. Serum potassium concentration was not affected (p 0.05) by OTA treatment. Lower calcium and phosphorus levels were determined (p 0.05) in the allantoic fluid of OTA-injected eggs compared with the controls. On days 12, 14, and 16 of incubation and at the hatch, lower whole body and yolk calcium and phosphorus, but not sodium levels, were measured (p 0.05) in the OTA treatment compared with the controls. In conclusion, the injection of eggs with OTA reduced blood calcium and phosphorus levels, which were associated with reduced whole body and yolk content from these electrolytes. Therefore, ochratoxin A had a negative effect on calcium metabolism.(AU)

Toxic Effects of Ochratoxin A on Calcium Metabolism during Chick Embryo Developmentand in Hatched Chicks

ABSTRACT The present study was carried out to study the effect of in-ovo ochratoxin A (OTA) injection in Highline layer eggs on calcium metabolism and blood biochemical parameters of embryos and after the hatch. At day 10 of embryonic development, one hundred and sixty-two fertile eggs were individually weighed and divided into two equal treatments. The first treatment (control) consisted of the individual injection of fertile eggs with 50 µL sodium carbonate. In the second treatment (OTA), fertile eggs were individually injected with 12.5 ng OTA dissolved in 50 µL sodium carbonate. On days 12, 14, and 16 of incubation and at the hatch, serum calcium and inorganic phosphorus concentrations were lower (p 0.05), while sodium, alkaline phosphatase and triiodothyronine concentrations were higher (p 0.05) in the OTA-injected eggs compared with the controls. Serum potassium concentration was not affected (p 0.05) by OTA treatment. Lower calcium and phosphorus levels were determined (p 0.05) in the allantoic fluid of OTA-injected eggs compared with the controls. On days 12, 14, and 16 of incubation and at the hatch, lower whole body and yolk calcium and phosphorus, but not sodium levels, were measured (p 0.05) in the OTA treatment compared with the controls. In conclusion, the injection of eggs with OTA reduced blood calcium and phosphorus levels, which were associated with reduced whole body and yolk content from these electrolytes. Therefore, ochratoxin A had a negative effect on calcium metabolism.

Survey of mycotoxins in Southern Brazilian wheat and evaluation of immunoassay methods

One hundred commercial wheat grain samples were collected during the 2015 sea-son across 78 municipalities in the states of Paraná (PR), Rio Grande do Sul (RS), and São Paulo (SP), Brazil. Separate subsamples were analyzed for the concentration of deoxynivalenol (DON), zearalenona (ZEA) and ochratoxin A (OTA) mycotoxins using two methods: UHPLC-MS/MS (reference method) and a commercial enzyme-linked immunosorbent assay (ELISA) (AgraQuant®). The OTA mycotoxin was not found in the samples by both methods. DON and ZEA were detected in 55 % and 39 % of the samples by the reference method, with overall mean levels of 795.2 g kg1 and 79.78 g kg1, respectively. There was a significant and positive correlation (Spearman rank) between DON and ZEA estimates by the reference method (r = 0.77, p 0.001). The DON levels estimated by the immunoassay agreed poorly with the reference, being largely overestimated. Based on a cut-off level of 1000 g kg1, the immunoassay correctly classified 57 samples as true negatives and 15 as true positives. Only 28 were classified as false positives. For ZEA, the levels estimated by the two methods were in better agreement than for DON. Using the cut-off level of 200 g kg1, 96 % of the samples were classified correctly as true positives and only one sample was classified as false positive. The levels for both mycotoxins were mostly acceptable for human consumption. Further studies should focus on multi-toxin methods compared with immunoassays to understand the reasons of overestimation and the role of immunoassays as a cost-effective solution for fast screening of mycotoxins in the food chain.