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Parasitic insect-derived miRNAs modulate host development
Parasitic wasps produce several factors including venom, polydnaviruses (PDVs) and specialized wasp cells named teratocytes that benefit the survival of offspring by altering the physiology of hosts. However, the underlying molecular mechanisms for the alterations remain unclear. Here we find that t...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992160/ https://www.ncbi.nlm.nih.gov/pubmed/29880839 http://dx.doi.org/10.1038/s41467-018-04504-1 |
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author | Wang, Zhi-zhi Ye, Xi-qian Shi, Min Li, Fei Wang, Ze-hua Zhou, Yue-nan Gu, Qi-juan Wu, Xiao-tong Yin, Chuan-lin Guo, Dian-hao Hu, Rong-min Hu, Na-na Chen, Ting Zheng, Bo-ying Zou, Jia-ni Zhan, Le-qing Wei, Shu-jun Wang, Yan-ping Huang, Jian-hua Fang, Xiao-dong Strand, Michael R. Chen, Xue-xin |
author_facet | Wang, Zhi-zhi Ye, Xi-qian Shi, Min Li, Fei Wang, Ze-hua Zhou, Yue-nan Gu, Qi-juan Wu, Xiao-tong Yin, Chuan-lin Guo, Dian-hao Hu, Rong-min Hu, Na-na Chen, Ting Zheng, Bo-ying Zou, Jia-ni Zhan, Le-qing Wei, Shu-jun Wang, Yan-ping Huang, Jian-hua Fang, Xiao-dong Strand, Michael R. Chen, Xue-xin |
author_sort | Wang, Zhi-zhi |
collection | PubMed |
description | Parasitic wasps produce several factors including venom, polydnaviruses (PDVs) and specialized wasp cells named teratocytes that benefit the survival of offspring by altering the physiology of hosts. However, the underlying molecular mechanisms for the alterations remain unclear. Here we find that the teratocytes of Cotesia vestalis, an endoparasitoid of the diamondback moth Plutella xylostella, and its associated bracovirus (CvBV) can produce miRNAs and deliver the products into the host via different ways. Certain miRNAs in the parasitized host are mainly produced by teratocytes, while the expression level of miRNAs encoded by CvBV can be 100-fold greater in parasitized hosts than non-parasitized ones. We further show that one teratocyte-produced miRNA (Cve-miR-281-3p) and one CvBV-produced miRNA (Cve-miR-novel22-5p-1) arrest host growth by modulating expression of the host ecdysone receptor (EcR). Altogether, our results show the first evidence of cross-species regulation by miRNAs in animal parasitism and their possible function in the alteration of host physiology during parasitism. |
format | Online Article Text |
id | pubmed-5992160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59921602018-06-11 Parasitic insect-derived miRNAs modulate host development Wang, Zhi-zhi Ye, Xi-qian Shi, Min Li, Fei Wang, Ze-hua Zhou, Yue-nan Gu, Qi-juan Wu, Xiao-tong Yin, Chuan-lin Guo, Dian-hao Hu, Rong-min Hu, Na-na Chen, Ting Zheng, Bo-ying Zou, Jia-ni Zhan, Le-qing Wei, Shu-jun Wang, Yan-ping Huang, Jian-hua Fang, Xiao-dong Strand, Michael R. Chen, Xue-xin Nat Commun Article Parasitic wasps produce several factors including venom, polydnaviruses (PDVs) and specialized wasp cells named teratocytes that benefit the survival of offspring by altering the physiology of hosts. However, the underlying molecular mechanisms for the alterations remain unclear. Here we find that the teratocytes of Cotesia vestalis, an endoparasitoid of the diamondback moth Plutella xylostella, and its associated bracovirus (CvBV) can produce miRNAs and deliver the products into the host via different ways. Certain miRNAs in the parasitized host are mainly produced by teratocytes, while the expression level of miRNAs encoded by CvBV can be 100-fold greater in parasitized hosts than non-parasitized ones. We further show that one teratocyte-produced miRNA (Cve-miR-281-3p) and one CvBV-produced miRNA (Cve-miR-novel22-5p-1) arrest host growth by modulating expression of the host ecdysone receptor (EcR). Altogether, our results show the first evidence of cross-species regulation by miRNAs in animal parasitism and their possible function in the alteration of host physiology during parasitism. Nature Publishing Group UK 2018-06-07 /pmc/articles/PMC5992160/ /pubmed/29880839 http://dx.doi.org/10.1038/s41467-018-04504-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Zhi-zhi Ye, Xi-qian Shi, Min Li, Fei Wang, Ze-hua Zhou, Yue-nan Gu, Qi-juan Wu, Xiao-tong Yin, Chuan-lin Guo, Dian-hao Hu, Rong-min Hu, Na-na Chen, Ting Zheng, Bo-ying Zou, Jia-ni Zhan, Le-qing Wei, Shu-jun Wang, Yan-ping Huang, Jian-hua Fang, Xiao-dong Strand, Michael R. Chen, Xue-xin Parasitic insect-derived miRNAs modulate host development |
title | Parasitic insect-derived miRNAs modulate host development |
title_full | Parasitic insect-derived miRNAs modulate host development |
title_fullStr | Parasitic insect-derived miRNAs modulate host development |
title_full_unstemmed | Parasitic insect-derived miRNAs modulate host development |
title_short | Parasitic insect-derived miRNAs modulate host development |
title_sort | parasitic insect-derived mirnas modulate host development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992160/ https://www.ncbi.nlm.nih.gov/pubmed/29880839 http://dx.doi.org/10.1038/s41467-018-04504-1 |
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