Exposure to dexamethasone modifies transcriptomic responses of free-living stages of Strongyloides stercoralis.

Hyperinfection and disseminated infection by the parasitic nematode Strongyloides stercoralis can be induced by iatrogenic administration of steroids and immunosuppression and lead to an elevated risk of mortality. Responses of free-living stages of S. stercoralis to the therapeutic corticosteroid d...

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Autores principales: Rutchanee Rodpai, Oranuch Sanpool, Tongjit Thanchomnang, Pokkamol Laoraksawong, Lakkhana Sadaow, Patcharaporn Boonroumkaew, Arporn Wangwiwatsin, Chaisiri Wongkham, Porntip Laummaunwai, Wannaporn Ittiprasert, Paul J Brindley, Pewpan M Intapan, Wanchai Maleewong
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Publicado: Public Library of Science (PLoS) 2021
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spelling oai:doaj.org-article:c75df2a642854204a393ffcbe431656c2021-12-02T20:09:55ZExposure to dexamethasone modifies transcriptomic responses of free-living stages of Strongyloides stercoralis.1932-620310.1371/journal.pone.0253701https://doaj.org/article/c75df2a642854204a393ffcbe431656c2021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0253701https://doaj.org/toc/1932-6203Hyperinfection and disseminated infection by the parasitic nematode Strongyloides stercoralis can be induced by iatrogenic administration of steroids and immunosuppression and lead to an elevated risk of mortality. Responses of free-living stages of S. stercoralis to the therapeutic corticosteroid dexamethasone (DXM) were investigated using RNA-seq transcriptomes of DXM-treated female and male worms. A total of 17,950 genes representing the transcriptome of these free-living adult stages were obtained, among which 199 and 263 were differentially expressed between DXM-treated females and DXM-treated males, respectively, compared with controls. According to Gene Ontology analysis, differentially expressed genes from DXM-treated females participate in developmental process, multicellular organismal process, cell differentiation, carbohydrate metabolic process and embryonic morphogenesis. Others are involved in signaling and signal transduction, including cAMP, cGMP-dependent protein kinase pathway, endocrine system, and thyroid hormone pathway, as based on Kyoto Encyclopedia of Genes and Genomes analysis. The novel findings warrant deeper investigation of the influence of DXM on growth and other pathways in this neglected tropical disease pathogen, particularly in a setting of autoimmune and/or allergic disease, which may require the clinical use of steroid-like hormones during latent or covert strongyloidiasis.Rutchanee RodpaiOranuch SanpoolTongjit ThanchomnangPokkamol LaoraksawongLakkhana SadaowPatcharaporn BoonroumkaewArporn WangwiwatsinChaisiri WongkhamPorntip LaummaunwaiWannaporn IttiprasertPaul J BrindleyPewpan M IntapanWanchai MaleewongPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 6, p e0253701 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Rutchanee Rodpai
Oranuch Sanpool
Tongjit Thanchomnang
Pokkamol Laoraksawong
Lakkhana Sadaow
Patcharaporn Boonroumkaew
Arporn Wangwiwatsin
Chaisiri Wongkham
Porntip Laummaunwai
Wannaporn Ittiprasert
Paul J Brindley
Pewpan M Intapan
Wanchai Maleewong
Exposure to dexamethasone modifies transcriptomic responses of free-living stages of Strongyloides stercoralis.
description Hyperinfection and disseminated infection by the parasitic nematode Strongyloides stercoralis can be induced by iatrogenic administration of steroids and immunosuppression and lead to an elevated risk of mortality. Responses of free-living stages of S. stercoralis to the therapeutic corticosteroid dexamethasone (DXM) were investigated using RNA-seq transcriptomes of DXM-treated female and male worms. A total of 17,950 genes representing the transcriptome of these free-living adult stages were obtained, among which 199 and 263 were differentially expressed between DXM-treated females and DXM-treated males, respectively, compared with controls. According to Gene Ontology analysis, differentially expressed genes from DXM-treated females participate in developmental process, multicellular organismal process, cell differentiation, carbohydrate metabolic process and embryonic morphogenesis. Others are involved in signaling and signal transduction, including cAMP, cGMP-dependent protein kinase pathway, endocrine system, and thyroid hormone pathway, as based on Kyoto Encyclopedia of Genes and Genomes analysis. The novel findings warrant deeper investigation of the influence of DXM on growth and other pathways in this neglected tropical disease pathogen, particularly in a setting of autoimmune and/or allergic disease, which may require the clinical use of steroid-like hormones during latent or covert strongyloidiasis.
format article
author Rutchanee Rodpai
Oranuch Sanpool
Tongjit Thanchomnang
Pokkamol Laoraksawong
Lakkhana Sadaow
Patcharaporn Boonroumkaew
Arporn Wangwiwatsin
Chaisiri Wongkham
Porntip Laummaunwai
Wannaporn Ittiprasert
Paul J Brindley
Pewpan M Intapan
Wanchai Maleewong
author_facet Rutchanee Rodpai
Oranuch Sanpool
Tongjit Thanchomnang
Pokkamol Laoraksawong
Lakkhana Sadaow
Patcharaporn Boonroumkaew
Arporn Wangwiwatsin
Chaisiri Wongkham
Porntip Laummaunwai
Wannaporn Ittiprasert
Paul J Brindley
Pewpan M Intapan
Wanchai Maleewong
author_sort Rutchanee Rodpai
title Exposure to dexamethasone modifies transcriptomic responses of free-living stages of Strongyloides stercoralis.
title_short Exposure to dexamethasone modifies transcriptomic responses of free-living stages of Strongyloides stercoralis.
title_full Exposure to dexamethasone modifies transcriptomic responses of free-living stages of Strongyloides stercoralis.
title_fullStr Exposure to dexamethasone modifies transcriptomic responses of free-living stages of Strongyloides stercoralis.
title_full_unstemmed Exposure to dexamethasone modifies transcriptomic responses of free-living stages of Strongyloides stercoralis.
title_sort exposure to dexamethasone modifies transcriptomic responses of free-living stages of strongyloides stercoralis.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/c75df2a642854204a393ffcbe431656c
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