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      The in vitro and ex vivo effect of Auranta 3001 in preventing Cryptosporidium hominis and Cryptosporidium parvum infection

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          Abstract

          Background

          Cryptosporidium is a major cause of diarrhea worldwide in both humans and farm animals with no completely effective treatment available at present. In this study, we assessed the inhibitory effect of different concentrations of Auranta 3001 (0.1, 0.5 and 1%), a novel natural feed supplement, on C. hominis and C. parvum invasion of human ileocecal adenocarcinoma (HCT-8), bovine primary cells and C. parvum invasion of HCT-8, bovine primary cells and bovine intestinal biopsies. The effect of the feed supplement on the production of pro-inflammatory cytokines IL-8 and INF-γ, the anti-inflammatory cytokine IL-10, the expression of CpSUB1 protease gene during infection was also assessed by quantitative PCR (q-PCR). Transepithelial electrical resistance (TEER) was employed to measure the integrity of tight junction dynamics of the culture models.

          Results

          Pre-treatment of intestinal cells or oocysts with the Auranta 3001 significantly reduced the invasiveness of C. hominis and C. parvum against HCT-8 and bovine primary cells in a dose dependent manner. The most pronounced reduction in the invasiveness of both parasites was observed when Auranta 3001 was present during infection. Levels of IL-8 were significantly reduced in both HCT-8 and bovine primary cells, while the levels of INF-γ and IL-10 showed opposite trends in the two cell lines during infection in the presence of Auranta 3001. CpSUB1 gene protease expression, which mediates infection, was significantly reduced suggesting that this enzyme is a possible target of Auranta 3001.

          Conclusions

          Although, C. hominis and C. parvum use different invasion mechanisms to infect cells, the novel feed additive can significantly attenuate the entry of Cryptosporidium in HCT-8 cells, primary bovine cells and bovine intestinal biopsies and thus provide an alternative method to control cryptosporidiosis.

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          Most cited references33

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          A review of the global burden, novel diagnostics, therapeutics, and vaccine targets for cryptosporidium.

          Cryptosporidium spp are well recognised as causes of diarrhoeal disease during waterborne epidemics and in immunocompromised hosts. Studies have also drawn attention to an underestimated global burden and suggest major gaps in optimum diagnosis, treatment, and immunisation. Cryptosporidiosis is increasingly identified as an important cause of morbidity and mortality worldwide. Studies in low-resource settings and high-income countries have confirmed the importance of cryptosporidium as a cause of diarrhoea and childhood malnutrition. Diagnostic tests for cryptosporidium infection are suboptimum, necessitating specialised tests that are often insensitive. Antigen-detection and PCR improve sensitivity, and multiplexed antigen detection and molecular assays are underused. Therapy has some effect in healthy hosts and no proven efficacy in patients with AIDS. Use of cryptosporidium genomes has helped to identify promising therapeutic targets, and drugs are in development, but methods to assess the efficacy in vitro and in animals are not well standardised. Partial immunity after exposure suggests the potential for successful vaccines, and several are in development; however, surrogates of protection are not well defined. Improved methods for propagation and genetic manipulation of the organism would be significant advances. Copyright © 2015 Elsevier Ltd. All rights reserved.
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            Cryptosporidium pathogenicity and virulence.

            Cryptosporidium is a protozoan parasite of medical and veterinary importance that causes gastroenteritis in a variety of vertebrate hosts. Several studies have reported different degrees of pathogenicity and virulence among Cryptosporidium species and isolates of the same species as well as evidence of variation in host susceptibility to infection. The identification and validation of Cryptosporidium virulence factors have been hindered by the renowned difficulties pertaining to the in vitro culture and genetic manipulation of this parasite. Nevertheless, substantial progress has been made in identifying putative virulence factors for Cryptosporidium. This progress has been accelerated since the publication of the Cryptosporidium parvum and C. hominis genomes, with the characterization of over 25 putative virulence factors identified by using a variety of immunological and molecular techniques and which are proposed to be involved in aspects of host-pathogen interactions from adhesion and locomotion to invasion and proliferation. Progress has also been made in the contribution of host factors that are associated with variations in both the severity and risk of infection. Here we provide a review comprised of the current state of knowledge on Cryptosporidium infectivity, pathogenesis, and transmissibility in light of our contemporary understanding of microbial virulence.
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              Parasitic infections: Time to tackle cryptosporidiosis.

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                Author and article information

                Contributors
                Alexandros.stratakos@afbini.gov.uk
                Filip.sima@afbini.gov.uk
                pat@auranta.ie
                Mark.linton@afbini.gov.uk
                Carmel.Kelly@afbini.gov.uk
                Laurette.pinkerton@afbini.gov.uk
                Lavi_stef@animalsci-tm.ro
                IoanPet@eurofins.com
                tiberiuiancu@usab-tm.ro
                gratiela87@gmail.com
                Nicolae.corcionivoschi@afbini.gov.uk
                Journal
                Gut Pathog
                Gut Pathog
                Gut Pathogens
                BioMed Central (London )
                1757-4749
                31 August 2017
                31 August 2017
                2017
                : 9
                : 49
                Affiliations
                [1 ]ISNI 0000 0000 9965 4151, GRID grid.423814.8, Bacteriology Branch, Veterinary Sciences Division, , Agri-Food and Biosciences Institute, ; Newforge Lane, Belfast, BT9 5PX Northern Ireland, UK
                [2 ]ISNI 0000 0001 2322 497X, GRID grid.5100.4, School of Biology, , University of Bucharest, ; Splaiul Independentei 91-95, Bucharest, Romania
                [3 ]Auranta, NovaUCD, Belfield Innovation Park, Belfield, Dublin 4, Ireland
                [4 ]ISNI 0000 0001 1033 9276, GRID grid.472275.1, Banat’s University of Agricultural Sciences and Veterinary Medicine, King Michael I of Romania, ; Calea Aradului 119, 300645 Timisoara, Romania
                [5 ]ISNI 0000 0001 2322 497X, GRID grid.5100.4, Research Institute of University of Bucharest, ; 36-46 Bd. M. Kogalniceanu, 5th District, 050107 Bucharest, Romania
                Article
                192
                10.1186/s13099-017-0192-y
                5580208
                8f441f4f-db95-41ac-9d50-97085235f753
                © The Author(s) 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 23 June 2017
                : 27 July 2017
                Funding
                Funded by: Auranta
                Categories
                Research
                Custom metadata
                © The Author(s) 2017

                Gastroenterology & Hepatology
                cryptosporidium hominis,cryptosporidium parvum,infection,natural antimicrobials

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