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      Three-dimensional (3D) culture of adult murine colon as an in vitro model of cryptosporidiosis: Proof of concept

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          Abstract

          Cryptosporidium parvum is a major cause of diarrheal illness and was recently potentially associated with digestive carcinogenesis. Despite its impact on human health, Cryptosporidium pathogenesis remains poorly known, mainly due to the lack of a long-term culture method for this parasite. Thus, the aim of the present study was to develop a three-dimensional (3D) culture model from adult murine colon allowing biological investigations of the host-parasite interactions in an in vivo-like environment and, in particular, the development of parasite-induced neoplasia. Colonic explants were cultured and preserved ex vivo for 35 days and co-culturing was performed with C. parvum. Strikingly, the resulting system allowed the reproduction of neoplastic lesions in vitro at 27 days post-infection (PI), providing new evidence of the role of the parasite in the induction of carcinogenesis. This promising model could facilitate the study of host-pathogen interactions and the investigation of the process involved in Cryptosporidium-induced cell transformation.

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          Most cited references43

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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 species in humans and animals: current understanding and research needs.

            Cryptosporidium is increasingly recognized as one of the major causes of moderate to severe diarrhoea in developing countries. With treatment options limited, control relies on knowledge of the biology and transmission of the members of the genus responsible for disease. Currently, 26 species are recognized as valid on the basis of morphological, biological and molecular data. Of the nearly 20 Cryptosporidium species and genotypes that have been reported in humans, Cryptosporidium hominis and Cryptosporidium parvum are responsible for the majority of infections. Livestock, particularly cattle, are one of the most important reservoirs of zoonotic infections. Domesticated and wild animals can each be infected with several Cryptosporidium species or genotypes that have only a narrow host range and therefore have no major public health significance. Recent advances in next-generation sequencing techniques will significantly improve our understanding of the taxonomy and transmission of Cryptosporidium species, and the investigation of outbreaks and monitoring of emerging and virulent subtypes. Important research gaps remain including a lack of subtyping tools for many Cryptosporidium species of public and veterinary health importance, and poor understanding of the genetic determinants of host specificity of Cryptosporidium species and impact of climate change on the transmission of Cryptosporidium.
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              Three-dimensional tissue culture models in cancer biology.

              Jong Kim (2005)
              Three-dimensional (3D) tissue culture models have an invaluable role in tumour biology today providing some very important insights into cancer biology. As well as increasing our understanding of homeostasis, cellular differentiation and tissue organization they provide a well defined environment for cancer research in contrast to the complex host environment of an in vivo model. Due to their enormous potential 3D tumour cultures are currently being exploited by many branches of biomedical science with therapeutically orientated studies becoming the major focus of research. Recent advances in 3D culture and tissue engineering techniques have enabled the development of more complex heterologous 3D tumour models.
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                Author and article information

                Contributors
                gabriela.certad@pasteur-lille.fr
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                11 December 2017
                11 December 2017
                2017
                : 7
                : 17288
                Affiliations
                [1 ]ISNI 0000 0004 0471 8845, GRID grid.410463.4, Univ. Lille, CNRS, Inserm, CHU Lille, Institut Pasteur de Lille, U1019 – UMR 8204 – CIIL – Centre d’Infection et d’Immunité de Lille, ; Lille, France
                [2 ]ISA-YNCREA Hauts-de-France, Lille, France
                [3 ]ISNI 0000 0004 0640 572X, GRID grid.424753.3, Univ. Lille, CNRS, ISEN, UMR 8520 - IEMN, ; Lille, France
                [4 ]ISNI 0000 0001 2165 6146, GRID grid.417666.4, Laboratoire Ecologie et Biodiversité, Faculté de Gestion Economie et Sciences, , Institut Catholique de Lille, ; Lille, France
                [5 ]ISNI 0000 0001 2165 6146, GRID grid.417666.4, Service d’Anatomie et de Cytologie Pathologiques, Groupement des Hopitaux de l’Institut Catholique de Lille (GHICL), ; Lille, France
                [6 ]ISNI 0000 0001 2186 1211, GRID grid.4461.7, Faculté de Pharmacie, Univ. de Lille, ; Lille, France
                [7 ]ISNI 0000 0001 2159 9858, GRID grid.8970.6, Plateforme d’Expérimentations et de Hautes Technologies Animales, Institut Pasteur de Lille, ; Lille, France
                [8 ]ISNI 0000 0001 2164 3847, GRID grid.67105.35, Department of Internal Medicine, Case Western Reserve University School of Medicine, ; Cleveland, OH USA
                [9 ]ISNI 0000 0004 0420 190X, GRID grid.410349.b, Department of Internal Medicine, Louis Stokes VA Medical Center, ; Cleveland, OH USA
                [10 ]ISNI 0000 0001 2164 3847, GRID grid.67105.35, Department of Biomedical Engineering, , Case Western Reserve University, ; Cleveland, OH USA
                [11 ]Laboratoire de Biologie Médicale, Groupement des Hospitaux de l’Institut Catholique de Lille (GHICL), Lille, France
                [12 ]ISNI 0000 0001 2165 6146, GRID grid.417666.4, Département de la Recherche Médicale, Groupement des Hopitaux de l’Institut Catholique de Lille (GHICL), , Faculté de Médecine et Maïeutique, Université Catholique de Lille, ; Lille, France
                Author information
                http://orcid.org/0000-0002-6732-6772
                Article
                17304
                10.1038/s41598-017-17304-2
                5725449
                28127051
                88f490e0-d307-4776-a453-c740053a08f5
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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                : 20 September 2017
                : 19 November 2017
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