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Cystoisospora suis – A Model of Mammalian Cystoisosporosis

Cystoisospora suis is a coccidian species that typically affects suckling piglets. Infections occur by oral uptake of oocysts and are characterized by non-hemorrhagic transient diarrhea, resulting in poor weight gain. Apparently, primary immune responses to C. suis cannot readily be mounted by neona...

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Autores principales: Shrestha, Aruna, Abd-Elfattah, Ahmed, Freudenschuss, Barbara, Hinney, Barbara, Palmieri, Nicola, Ruttkowski, Bärbel, Joachim, Anja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672278/
https://www.ncbi.nlm.nih.gov/pubmed/26664994
http://dx.doi.org/10.3389/fvets.2015.00068
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author Shrestha, Aruna
Abd-Elfattah, Ahmed
Freudenschuss, Barbara
Hinney, Barbara
Palmieri, Nicola
Ruttkowski, Bärbel
Joachim, Anja
author_facet Shrestha, Aruna
Abd-Elfattah, Ahmed
Freudenschuss, Barbara
Hinney, Barbara
Palmieri, Nicola
Ruttkowski, Bärbel
Joachim, Anja
author_sort Shrestha, Aruna
collection PubMed
description Cystoisospora suis is a coccidian species that typically affects suckling piglets. Infections occur by oral uptake of oocysts and are characterized by non-hemorrhagic transient diarrhea, resulting in poor weight gain. Apparently, primary immune responses to C. suis cannot readily be mounted by neonates, which contributes to the establishment and rapid development of the parasite, while in older pigs age-resistance prevents disease development. However, the presence of extraintestinal stages, although not unequivocally demonstrated, is suspected to enable parasite persistence together with the induction and maintenance of immune response in older pigs, which in turn may facilitate the transfer of C. suis-specific factors from sow to offspring. It is assumed that neonates are particularly prone to clinical disease because infections with C. suis interfere with the establishment of the gut microbiome. Clostridia have been especially inferred to profit from the altered intestinal environment during parasite infection. New tools, particularly in the area of genomics, might illustrate the interactions between C. suis and its host and pave the way for the development of new control methods not only for porcine cystoisosporosis but also for other mammalian Cystoisospora infections. The first reference genome for C. suis is under way and will be a fertile ground to discover new drugs and vaccines. At the same time, the establishment and refinement of an in vivo model and an in vitro culture system, supporting the complete life cycle of C. suis, will underpin the functional characterization of the parasite and shed light on its biology and control.
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spelling pubmed-46722782015-12-10 Cystoisospora suis – A Model of Mammalian Cystoisosporosis Shrestha, Aruna Abd-Elfattah, Ahmed Freudenschuss, Barbara Hinney, Barbara Palmieri, Nicola Ruttkowski, Bärbel Joachim, Anja Front Vet Sci Veterinary Science Cystoisospora suis is a coccidian species that typically affects suckling piglets. Infections occur by oral uptake of oocysts and are characterized by non-hemorrhagic transient diarrhea, resulting in poor weight gain. Apparently, primary immune responses to C. suis cannot readily be mounted by neonates, which contributes to the establishment and rapid development of the parasite, while in older pigs age-resistance prevents disease development. However, the presence of extraintestinal stages, although not unequivocally demonstrated, is suspected to enable parasite persistence together with the induction and maintenance of immune response in older pigs, which in turn may facilitate the transfer of C. suis-specific factors from sow to offspring. It is assumed that neonates are particularly prone to clinical disease because infections with C. suis interfere with the establishment of the gut microbiome. Clostridia have been especially inferred to profit from the altered intestinal environment during parasite infection. New tools, particularly in the area of genomics, might illustrate the interactions between C. suis and its host and pave the way for the development of new control methods not only for porcine cystoisosporosis but also for other mammalian Cystoisospora infections. The first reference genome for C. suis is under way and will be a fertile ground to discover new drugs and vaccines. At the same time, the establishment and refinement of an in vivo model and an in vitro culture system, supporting the complete life cycle of C. suis, will underpin the functional characterization of the parasite and shed light on its biology and control. Frontiers Media S.A. 2015-11-30 /pmc/articles/PMC4672278/ /pubmed/26664994 http://dx.doi.org/10.3389/fvets.2015.00068 Text en Copyright © 2015 Shrestha, Abd-Elfattah, Freudenschuss, Hinney, Palmieri, Ruttkowski and Joachim. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Shrestha, Aruna
Abd-Elfattah, Ahmed
Freudenschuss, Barbara
Hinney, Barbara
Palmieri, Nicola
Ruttkowski, Bärbel
Joachim, Anja
Cystoisospora suis – A Model of Mammalian Cystoisosporosis
title Cystoisospora suis – A Model of Mammalian Cystoisosporosis
title_full Cystoisospora suis – A Model of Mammalian Cystoisosporosis
title_fullStr Cystoisospora suis – A Model of Mammalian Cystoisosporosis
title_full_unstemmed Cystoisospora suis – A Model of Mammalian Cystoisosporosis
title_short Cystoisospora suis – A Model of Mammalian Cystoisosporosis
title_sort cystoisospora suis – a model of mammalian cystoisosporosis
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672278/
https://www.ncbi.nlm.nih.gov/pubmed/26664994
http://dx.doi.org/10.3389/fvets.2015.00068
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