Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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
_version_ 1783329958101254144
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
work_keys_str_mv AT wangzhizhi parasiticinsectderivedmirnasmodulatehostdevelopment
AT yexiqian parasiticinsectderivedmirnasmodulatehostdevelopment
AT shimin parasiticinsectderivedmirnasmodulatehostdevelopment
AT lifei parasiticinsectderivedmirnasmodulatehostdevelopment
AT wangzehua parasiticinsectderivedmirnasmodulatehostdevelopment
AT zhouyuenan parasiticinsectderivedmirnasmodulatehostdevelopment
AT guqijuan parasiticinsectderivedmirnasmodulatehostdevelopment
AT wuxiaotong parasiticinsectderivedmirnasmodulatehostdevelopment
AT yinchuanlin parasiticinsectderivedmirnasmodulatehostdevelopment
AT guodianhao parasiticinsectderivedmirnasmodulatehostdevelopment
AT hurongmin parasiticinsectderivedmirnasmodulatehostdevelopment
AT hunana parasiticinsectderivedmirnasmodulatehostdevelopment
AT chenting parasiticinsectderivedmirnasmodulatehostdevelopment
AT zhengboying parasiticinsectderivedmirnasmodulatehostdevelopment
AT zoujiani parasiticinsectderivedmirnasmodulatehostdevelopment
AT zhanleqing parasiticinsectderivedmirnasmodulatehostdevelopment
AT weishujun parasiticinsectderivedmirnasmodulatehostdevelopment
AT wangyanping parasiticinsectderivedmirnasmodulatehostdevelopment
AT huangjianhua parasiticinsectderivedmirnasmodulatehostdevelopment
AT fangxiaodong parasiticinsectderivedmirnasmodulatehostdevelopment
AT strandmichaelr parasiticinsectderivedmirnasmodulatehostdevelopment
AT chenxuexin parasiticinsectderivedmirnasmodulatehostdevelopment