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Symbiotic bracovirus of a parasite manipulates host lipid metabolism via tachykinin signaling

Parasites alter host energy homeostasis for their own development, but the mechanisms underlying this phenomenon remain largely unknown. Here, we show that Cotesia vestalis, an endoparasitic wasp of Plutella xylostella larvae, stimulates a reduction of host lipid levels. This process requires excess...

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Autores principales: Wang, Yanping, Wu, Xiaotong, Wang, Zehua, Chen, Ting, Zhou, Sicong, Chen, Jiani, Pang, Lan, Ye, Xiqian, Shi, Min, Huang, Jianhua, Chen, Xuexin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951984/
https://www.ncbi.nlm.nih.gov/pubmed/33647060
http://dx.doi.org/10.1371/journal.ppat.1009365
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author Wang, Yanping
Wu, Xiaotong
Wang, Zehua
Chen, Ting
Zhou, Sicong
Chen, Jiani
Pang, Lan
Ye, Xiqian
Shi, Min
Huang, Jianhua
Chen, Xuexin
author_facet Wang, Yanping
Wu, Xiaotong
Wang, Zehua
Chen, Ting
Zhou, Sicong
Chen, Jiani
Pang, Lan
Ye, Xiqian
Shi, Min
Huang, Jianhua
Chen, Xuexin
author_sort Wang, Yanping
collection PubMed
description Parasites alter host energy homeostasis for their own development, but the mechanisms underlying this phenomenon remain largely unknown. Here, we show that Cotesia vestalis, an endoparasitic wasp of Plutella xylostella larvae, stimulates a reduction of host lipid levels. This process requires excess secretion of P. xylostella tachykinin (PxTK) peptides from enteroendocrine cells (EEs) in the midgut of the parasitized host larvae. We found that parasitization upregulates PxTK signaling to suppress lipogenesis in midgut enterocytes (ECs) in a non-cell-autonomous manner, and the reduced host lipid level benefits the development of wasp offspring and their subsequent parasitic ability. We further found that a C. vestalis bracovirus (CvBV) gene, CvBV 9–2, is responsible for PxTK induction, which in turn reduces the systemic lipid level of the host. Taken together, these findings illustrate a novel mechanism for parasite manipulation of host energy homeostasis by a symbiotic bracovirus gene to promote the development and increase the parasitic efficiency of an agriculturally important wasp species.
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spelling pubmed-79519842021-03-22 Symbiotic bracovirus of a parasite manipulates host lipid metabolism via tachykinin signaling Wang, Yanping Wu, Xiaotong Wang, Zehua Chen, Ting Zhou, Sicong Chen, Jiani Pang, Lan Ye, Xiqian Shi, Min Huang, Jianhua Chen, Xuexin PLoS Pathog Research Article Parasites alter host energy homeostasis for their own development, but the mechanisms underlying this phenomenon remain largely unknown. Here, we show that Cotesia vestalis, an endoparasitic wasp of Plutella xylostella larvae, stimulates a reduction of host lipid levels. This process requires excess secretion of P. xylostella tachykinin (PxTK) peptides from enteroendocrine cells (EEs) in the midgut of the parasitized host larvae. We found that parasitization upregulates PxTK signaling to suppress lipogenesis in midgut enterocytes (ECs) in a non-cell-autonomous manner, and the reduced host lipid level benefits the development of wasp offspring and their subsequent parasitic ability. We further found that a C. vestalis bracovirus (CvBV) gene, CvBV 9–2, is responsible for PxTK induction, which in turn reduces the systemic lipid level of the host. Taken together, these findings illustrate a novel mechanism for parasite manipulation of host energy homeostasis by a symbiotic bracovirus gene to promote the development and increase the parasitic efficiency of an agriculturally important wasp species. Public Library of Science 2021-03-01 /pmc/articles/PMC7951984/ /pubmed/33647060 http://dx.doi.org/10.1371/journal.ppat.1009365 Text en © 2021 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Yanping
Wu, Xiaotong
Wang, Zehua
Chen, Ting
Zhou, Sicong
Chen, Jiani
Pang, Lan
Ye, Xiqian
Shi, Min
Huang, Jianhua
Chen, Xuexin
Symbiotic bracovirus of a parasite manipulates host lipid metabolism via tachykinin signaling
title Symbiotic bracovirus of a parasite manipulates host lipid metabolism via tachykinin signaling
title_full Symbiotic bracovirus of a parasite manipulates host lipid metabolism via tachykinin signaling
title_fullStr Symbiotic bracovirus of a parasite manipulates host lipid metabolism via tachykinin signaling
title_full_unstemmed Symbiotic bracovirus of a parasite manipulates host lipid metabolism via tachykinin signaling
title_short Symbiotic bracovirus of a parasite manipulates host lipid metabolism via tachykinin signaling
title_sort symbiotic bracovirus of a parasite manipulates host lipid metabolism via tachykinin signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951984/
https://www.ncbi.nlm.nih.gov/pubmed/33647060
http://dx.doi.org/10.1371/journal.ppat.1009365
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