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      Tryptophan Attenuates the Effects of OTA on Intestinal Morphology and Local IgA/IgY Production in Broiler Chicks

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          Abstract

          Ochratoxin A (OTA) is a mycotoxin produced by species of Penicillium and Aspergillus that can contaminate products of plant origin that are used as animal feed. Through oral exposure, this mycotoxin primarily affects the chicken gastrointestinal system. The present study evaluated the intestinal toxic effects of OTA and the introduction of L-tryptophan to alleviate these effects in chickens. One-day-old chicks were exposed to a single OTA dose (1.4 mg/kg body weight—b.w.) and treated with or without four daily doses of L-tryptophan (100 mg/kg b.w.). Duodenal villus height/crypt depth, fecal immunoglobulin A/immunoglobulin Y (IgA/IgY) levels, and duodenal positive immunoglobulin A cells (IgA +) were evaluated by histology, ELISA, and immunohistochemistry, respectively, on the 14th day. There were significant changes in the duodenal villus height, crypt depth, and levels of fecal IgA/IgY and duodenal IgA + cells ( p < 0.05) in groups exposed to OTA. On the other hand, groups exposed to OTA and treated with L-tryptophan showed similar levels of villus height, IgA/IgY levels, and duodenal IgA + cells to those of the control group ( p > 0.05). In conclusion, exposure to a single dose of OTA orally induces changes in intestinal morphology, levels of IgA/IgY antibodies, and IgA + cells. Thus, treatment with L-tryptophan may be a valid alternative means to reduce the harmful effects of OTA on the intestinal mucosa, which requires further study.

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          Most cited references39

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          Mycotoxins as human carcinogens-the IARC Monographs classification.

          Humans are constantly exposed to mycotoxins (e.g. aflatoxins, ochratoxins), mainly via food intake of plant and animal origin. The health risks stemming from mycotoxins may result from their toxicity, in particular their carcinogenicity. In order to prevent these risks, the International Agency for Research on Cancer (IARC) in Lyon (France)-through its IARC Monographs programme-has performed the carcinogenic hazard assessment of some mycotoxins in humans, on the basis of epidemiological data, studies of cancer in experimental animals and mechanistic studies. The present article summarizes the carcinogenic hazard assessments of those mycotoxins, especially aflatoxins (aflatoxin B1, B2, G1, G2 and M1), fumonisins (fumonisin B1 and B2) and ochratoxin A (OTA). New information regarding the genotoxicity of OTA (formation of OTA-DNA adducts), the role of OTA in oxidative stress and the identification of epigenetic factors involved in OTA carcinogenesis-should they indeed provide strong evidence that OTA carcinogenicity is mediated by a mechanism that also operates in humans-could lead to the reclassification of OTA.
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            The biology of intestinal immunoglobulin A responses.

            The gut mucosa is exposed to a large community of commensal bacteria that are required for the processing of nutrients and the education of the local immune system. Conversely, the gut immune system generates innate and adaptive responses that shape the composition of the local microbiota. One striking feature of intestinal adaptive immunity is its ability to generate massive amounts of noninflammatory immunoglobulin A (IgA) antibodies through multiple follicular and extrafollicular pathways that operate in the presence or absence of cognate T-B cell interactions. Here we discuss the role of intestinal IgA in host-commensal mutualism, immune protection, and tolerance and summarize recent advances on the role of innate immune cells in intestinal IgA production.
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              Modulation of Intestinal Functions Following Mycotoxin Ingestion: Meta-Analysis of Published Experiments in Animals

              Mycotoxins are secondary metabolites of fungi that can cause serious health problems in animals, and may result in severe economic losses. Deleterious effects of these feed contaminants in animals are well documented, ranging from growth impairment, decreased resistance to pathogens, hepato- and nephrotoxicity to death. By contrast, data with regard to their impact on intestinal functions are more limited. However, intestinal cells are the first cells to be exposed to mycotoxins, and often at higher concentrations than other tissues. In addition, mycotoxins specifically target high protein turnover- and activated-cells, which are predominant in gut epithelium. Therefore, intestinal investigations have gained significant interest over the last decade, and some publications have demonstrated that mycotoxins are able to compromise several key functions of the gastrointestinal tract, including decreased surface area available for nutrient absorption, modulation of nutrient transporters, or loss of barrier function. In addition some mycotoxins facilitate persistence of intestinal pathogens and potentiate intestinal inflammation. By contrast, the effect of these fungal metabolites on the intestinal microbiota is largely unknown. This review focuses on mycotoxins which are of concern in terms of occurrence and toxicity, namely: aflatoxins, ochratoxin A and Fusarium toxins. Results from nearly 100 published experiments (in vitro, ex vivo and in vivo) were analyzed with a special attention to the doses used.
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                Author and article information

                Journal
                Toxins (Basel)
                Toxins (Basel)
                toxins
                Toxins
                MDPI
                2072-6651
                23 December 2020
                January 2021
                : 13
                : 1
                : 5
                Affiliations
                [1 ]Department of Pathological Sciences, State University of Londrina, P.O. Box 10.011, Londrina, PR 86057-970, Brazil; fernandogricci@ 123456hotmail.com (F.G.R.); letterkelli@ 123456gmail.com (L.R.T.); emersonj@ 123456uel.br (E.J.V.); bianca_dorana@ 123456hotmail.com (B.D.d.O.S.)
                [2 ]Department of Preventive Veterinary Medicine, State University of Londrina, P.O. Box 10.011, Londrina, PR 86057-970, Brazil; larissa.justino@ 123456uel.br (L.J.); beatriz.queiroz@ 123456uel.br (B.Q.d.S.); anaangelita@ 123456uel.br (A.A.S.B.)
                [3 ]Department of Zootechny, State University Londrina, P.O. Box 10.011, Londrina, PR 86057-970, Brazil; oba@ 123456uel.br
                [4 ]Laboratory of Animal Pathology, State University of Londrina, P.O. Box 10.011, Londrina, PR 86057-970, Brazil; anapaula@ 123456uel.br
                [5 ]Department of Food Science and Technology, State University Londrina, P.O. Box 10.011, Londrina, PR 86057-970, Brazil; elisahirooka@ 123456hotmail.com
                Author notes
                [* ]Correspondence: itanoeiko@ 123456hotmail.com ; Tel.: +55-43-3371-4469
                Author information
                https://orcid.org/0000-0001-9195-1490
                https://orcid.org/0000-0002-3735-9207
                https://orcid.org/0000-0002-6552-0635
                https://orcid.org/0000-0002-0159-5494
                Article
                toxins-13-00005
                10.3390/toxins13010005
                7823272
                33374814
                d9b8fd04-d81e-486a-8e7c-51e22e7f5e27
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 18 November 2020
                : 18 December 2020
                Categories
                Article

                Molecular medicine
                iga,igy,mycotoxins,villi,crypts
                Molecular medicine
                iga, igy, mycotoxins, villi, crypts

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