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Nuclear hormone receptors promote gut and glia detoxifying enzyme induction and protect C. elegans from the mold P. brevicompactum

Animals encounter microorganisms in their habitats, adapting physiology and behavior accordingly. The nematode Caenorhabditis elegans is found in microbe-rich environments; however, its responses to fungi are not extensively studied. Here, we describe interactions of C. elegans and Penicillium brevi...

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Autores principales: Wallace, Sean W., Lizzappi, Malcolm C., Magemizoğlu, Elif, Hur, Hong, Liang, Yupu, Shaham, Shai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733895/
https://www.ncbi.nlm.nih.gov/pubmed/34965433
http://dx.doi.org/10.1016/j.celrep.2021.110166
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author Wallace, Sean W.
Lizzappi, Malcolm C.
Magemizoğlu, Elif
Hur, Hong
Liang, Yupu
Shaham, Shai
author_facet Wallace, Sean W.
Lizzappi, Malcolm C.
Magemizoğlu, Elif
Hur, Hong
Liang, Yupu
Shaham, Shai
author_sort Wallace, Sean W.
collection PubMed
description Animals encounter microorganisms in their habitats, adapting physiology and behavior accordingly. The nematode Caenorhabditis elegans is found in microbe-rich environments; however, its responses to fungi are not extensively studied. Here, we describe interactions of C. elegans and Penicillium brevicompactum, an ecologically relevant mold. Transcriptome studies reveal that co-culture upregulates stress response genes, including xenobiotic-metabolizing enzymes (XMEs), in C. elegans intestine and AMsh glial cells. The nuclear hormone receptors (NHRs) NHR-45 and NHR-156 are induction regulators, and mutants that cannot induce XMEs in the intestine when exposed to P. brevicompactum experience mitochondrial stress and exhibit developmental defects. Different C. elegans wild isolates harbor sequence polymorphisms in nhr-156, resulting in phenotypic diversity in AMsh glia responses to microbe exposure. We propose that P. brevicompactum mitochondria-targeting mycotoxins are deactivated by intestinal detoxification, allowing tolerance to moldy environments. Our studies support the idea that C. elegans NHRs may be regulated by environmental cues.
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spelling pubmed-87338952022-01-06 Nuclear hormone receptors promote gut and glia detoxifying enzyme induction and protect C. elegans from the mold P. brevicompactum Wallace, Sean W. Lizzappi, Malcolm C. Magemizoğlu, Elif Hur, Hong Liang, Yupu Shaham, Shai Cell Rep Article Animals encounter microorganisms in their habitats, adapting physiology and behavior accordingly. The nematode Caenorhabditis elegans is found in microbe-rich environments; however, its responses to fungi are not extensively studied. Here, we describe interactions of C. elegans and Penicillium brevicompactum, an ecologically relevant mold. Transcriptome studies reveal that co-culture upregulates stress response genes, including xenobiotic-metabolizing enzymes (XMEs), in C. elegans intestine and AMsh glial cells. The nuclear hormone receptors (NHRs) NHR-45 and NHR-156 are induction regulators, and mutants that cannot induce XMEs in the intestine when exposed to P. brevicompactum experience mitochondrial stress and exhibit developmental defects. Different C. elegans wild isolates harbor sequence polymorphisms in nhr-156, resulting in phenotypic diversity in AMsh glia responses to microbe exposure. We propose that P. brevicompactum mitochondria-targeting mycotoxins are deactivated by intestinal detoxification, allowing tolerance to moldy environments. Our studies support the idea that C. elegans NHRs may be regulated by environmental cues. 2021-12-28 /pmc/articles/PMC8733895/ /pubmed/34965433 http://dx.doi.org/10.1016/j.celrep.2021.110166 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Wallace, Sean W.
Lizzappi, Malcolm C.
Magemizoğlu, Elif
Hur, Hong
Liang, Yupu
Shaham, Shai
Nuclear hormone receptors promote gut and glia detoxifying enzyme induction and protect C. elegans from the mold P. brevicompactum
title Nuclear hormone receptors promote gut and glia detoxifying enzyme induction and protect C. elegans from the mold P. brevicompactum
title_full Nuclear hormone receptors promote gut and glia detoxifying enzyme induction and protect C. elegans from the mold P. brevicompactum
title_fullStr Nuclear hormone receptors promote gut and glia detoxifying enzyme induction and protect C. elegans from the mold P. brevicompactum
title_full_unstemmed Nuclear hormone receptors promote gut and glia detoxifying enzyme induction and protect C. elegans from the mold P. brevicompactum
title_short Nuclear hormone receptors promote gut and glia detoxifying enzyme induction and protect C. elegans from the mold P. brevicompactum
title_sort nuclear hormone receptors promote gut and glia detoxifying enzyme induction and protect c. elegans from the mold p. brevicompactum
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8733895/
https://www.ncbi.nlm.nih.gov/pubmed/34965433
http://dx.doi.org/10.1016/j.celrep.2021.110166
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