Microsporidia are natural intracellular parasites of the nematode Caenorhabditis elegans.

For decades the soil nematode Caenorhabditis elegans has been an important model system for biology, but little is known about its natural ecology. Recently, C. elegans has become the focus of studies of innate immunity and several pathogens have been shown to cause lethal intestinal infections in C...

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Main Authors: Emily R Troemel, Marie-Anne Félix, Noah K Whiteman, Antoine Barrière, Frederick M Ausubel
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-12-01
Series:PLoS Biology
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19071962/?tool=EBI
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author Emily R Troemel
Marie-Anne Félix
Noah K Whiteman
Antoine Barrière
Frederick M Ausubel
author_facet Emily R Troemel
Marie-Anne Félix
Noah K Whiteman
Antoine Barrière
Frederick M Ausubel
author_sort Emily R Troemel
collection DOAJ
description For decades the soil nematode Caenorhabditis elegans has been an important model system for biology, but little is known about its natural ecology. Recently, C. elegans has become the focus of studies of innate immunity and several pathogens have been shown to cause lethal intestinal infections in C. elegans. However none of these pathogens has been shown to invade nematode intestinal cells, and no pathogen has been isolated from wild-caught C. elegans. Here we describe an intracellular pathogen isolated from wild-caught C. elegans that we show is a new species of microsporidia. Microsporidia comprise a large class of eukaryotic intracellular parasites that are medically and agriculturally important, but poorly understood. We show that microsporidian infection of the C. elegans intestine proceeds through distinct stages and is transmitted horizontally. Disruption of a conserved cytoskeletal structure in the intestine called the terminal web correlates with the release of microsporidian spores from infected cells, and appears to be part of a novel mechanism by which intracellular pathogens exit from infected cells. Unlike in bacterial intestinal infections, the p38 MAPK and insulin/insulin-like growth factor (IGF) signaling pathways do not appear to play substantial roles in resistance to microsporidian infection in C. elegans. We found microsporidia in multiple wild-caught isolates of Caenorhabditis nematodes from diverse geographic locations. These results indicate that microsporidia are common parasites of C. elegans in the wild. In addition, the interaction between C. elegans and its natural microsporidian parasites provides a system in which to dissect intracellular intestinal infection in vivo and insight into the diversity of pathogenic mechanisms used by intracellular microbes.
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spelling doaj.art-e5087661cfed49d58c1b39e87f7ad49b2022-12-21T19:10:42ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852008-12-016122736275210.1371/journal.pbio.0060309Microsporidia are natural intracellular parasites of the nematode Caenorhabditis elegans.Emily R TroemelMarie-Anne FélixNoah K WhitemanAntoine BarrièreFrederick M AusubelFor decades the soil nematode Caenorhabditis elegans has been an important model system for biology, but little is known about its natural ecology. Recently, C. elegans has become the focus of studies of innate immunity and several pathogens have been shown to cause lethal intestinal infections in C. elegans. However none of these pathogens has been shown to invade nematode intestinal cells, and no pathogen has been isolated from wild-caught C. elegans. Here we describe an intracellular pathogen isolated from wild-caught C. elegans that we show is a new species of microsporidia. Microsporidia comprise a large class of eukaryotic intracellular parasites that are medically and agriculturally important, but poorly understood. We show that microsporidian infection of the C. elegans intestine proceeds through distinct stages and is transmitted horizontally. Disruption of a conserved cytoskeletal structure in the intestine called the terminal web correlates with the release of microsporidian spores from infected cells, and appears to be part of a novel mechanism by which intracellular pathogens exit from infected cells. Unlike in bacterial intestinal infections, the p38 MAPK and insulin/insulin-like growth factor (IGF) signaling pathways do not appear to play substantial roles in resistance to microsporidian infection in C. elegans. We found microsporidia in multiple wild-caught isolates of Caenorhabditis nematodes from diverse geographic locations. These results indicate that microsporidia are common parasites of C. elegans in the wild. In addition, the interaction between C. elegans and its natural microsporidian parasites provides a system in which to dissect intracellular intestinal infection in vivo and insight into the diversity of pathogenic mechanisms used by intracellular microbes.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19071962/?tool=EBI
spellingShingle Emily R Troemel
Marie-Anne Félix
Noah K Whiteman
Antoine Barrière
Frederick M Ausubel
Microsporidia are natural intracellular parasites of the nematode Caenorhabditis elegans.
PLoS Biology
title Microsporidia are natural intracellular parasites of the nematode Caenorhabditis elegans.
title_full Microsporidia are natural intracellular parasites of the nematode Caenorhabditis elegans.
title_fullStr Microsporidia are natural intracellular parasites of the nematode Caenorhabditis elegans.
title_full_unstemmed Microsporidia are natural intracellular parasites of the nematode Caenorhabditis elegans.
title_short Microsporidia are natural intracellular parasites of the nematode Caenorhabditis elegans.
title_sort microsporidia are natural intracellular parasites of the nematode caenorhabditis elegans
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19071962/?tool=EBI
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