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A novel negative-stranded RNA virus mediates sex ratio in its parasitoid host

Parasitoid wasps are important natural enemies of arthropod hosts in natural and agricultural ecosystems and are often associated with viruses or virion-like particles. Here, we report a novel negative-stranded RNA virus from a parasitoid wasp (Pteromalus puparum). The complete viral genome is 12,23...

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Autores principales: Wang, Fei, Fang, Qi, Wang, Beibei, Yan, Zhichao, Hong, Jian, Bao, Yiming, Kuhn, Jens H., Werren, John H., Song, Qisheng, Ye, Gongyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344506/
https://www.ncbi.nlm.nih.gov/pubmed/28278298
http://dx.doi.org/10.1371/journal.ppat.1006201
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author Wang, Fei
Fang, Qi
Wang, Beibei
Yan, Zhichao
Hong, Jian
Bao, Yiming
Kuhn, Jens H.
Werren, John H.
Song, Qisheng
Ye, Gongyin
author_facet Wang, Fei
Fang, Qi
Wang, Beibei
Yan, Zhichao
Hong, Jian
Bao, Yiming
Kuhn, Jens H.
Werren, John H.
Song, Qisheng
Ye, Gongyin
author_sort Wang, Fei
collection PubMed
description Parasitoid wasps are important natural enemies of arthropod hosts in natural and agricultural ecosystems and are often associated with viruses or virion-like particles. Here, we report a novel negative-stranded RNA virus from a parasitoid wasp (Pteromalus puparum). The complete viral genome is 12,230 nucleotides in length, containing five non-overlapping, linearly arranged open reading frames. Phylogenetically, the virus clusters with and is a novel member of the mononegaviral family Nyamiviridae, here designated as Pteromalus puparum negative-strand RNA virus 1 (PpNSRV-1). PpNSRV-1 is present in various tissues and life stages of the parasitoid wasp, and is transmitted vertically through infected females and males. Virus infections in field populations of P. puparum wasps ranged from 16.7 to 37.5%, without linearly correlating with temperature. PpNSRV-1 increased adult longevity and impaired several fitness parameters of the wasp, but had no influence on successful parasitism. Strikingly, PpNSRV-1 mediated the offspring sex ratio by decreasing female offspring numbers. RNA interference knockdown of virus open reading frame I eliminated these PpNSRV-1-induced effects. Thus, we infer that PpNSRV-1 has complex effects on its insect host including sex ratio distortion towards males, as well as possible mutualistic benefits through increasing wasp longevity.
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spelling pubmed-53445062017-03-29 A novel negative-stranded RNA virus mediates sex ratio in its parasitoid host Wang, Fei Fang, Qi Wang, Beibei Yan, Zhichao Hong, Jian Bao, Yiming Kuhn, Jens H. Werren, John H. Song, Qisheng Ye, Gongyin PLoS Pathog Research Article Parasitoid wasps are important natural enemies of arthropod hosts in natural and agricultural ecosystems and are often associated with viruses or virion-like particles. Here, we report a novel negative-stranded RNA virus from a parasitoid wasp (Pteromalus puparum). The complete viral genome is 12,230 nucleotides in length, containing five non-overlapping, linearly arranged open reading frames. Phylogenetically, the virus clusters with and is a novel member of the mononegaviral family Nyamiviridae, here designated as Pteromalus puparum negative-strand RNA virus 1 (PpNSRV-1). PpNSRV-1 is present in various tissues and life stages of the parasitoid wasp, and is transmitted vertically through infected females and males. Virus infections in field populations of P. puparum wasps ranged from 16.7 to 37.5%, without linearly correlating with temperature. PpNSRV-1 increased adult longevity and impaired several fitness parameters of the wasp, but had no influence on successful parasitism. Strikingly, PpNSRV-1 mediated the offspring sex ratio by decreasing female offspring numbers. RNA interference knockdown of virus open reading frame I eliminated these PpNSRV-1-induced effects. Thus, we infer that PpNSRV-1 has complex effects on its insect host including sex ratio distortion towards males, as well as possible mutualistic benefits through increasing wasp longevity. Public Library of Science 2017-03-09 /pmc/articles/PMC5344506/ /pubmed/28278298 http://dx.doi.org/10.1371/journal.ppat.1006201 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Wang, Fei
Fang, Qi
Wang, Beibei
Yan, Zhichao
Hong, Jian
Bao, Yiming
Kuhn, Jens H.
Werren, John H.
Song, Qisheng
Ye, Gongyin
A novel negative-stranded RNA virus mediates sex ratio in its parasitoid host
title A novel negative-stranded RNA virus mediates sex ratio in its parasitoid host
title_full A novel negative-stranded RNA virus mediates sex ratio in its parasitoid host
title_fullStr A novel negative-stranded RNA virus mediates sex ratio in its parasitoid host
title_full_unstemmed A novel negative-stranded RNA virus mediates sex ratio in its parasitoid host
title_short A novel negative-stranded RNA virus mediates sex ratio in its parasitoid host
title_sort novel negative-stranded rna virus mediates sex ratio in its parasitoid host
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5344506/
https://www.ncbi.nlm.nih.gov/pubmed/28278298
http://dx.doi.org/10.1371/journal.ppat.1006201
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