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Persistently Transmitted Viruses Restrict the Transmission of Other Viruses by Affecting Their Vectors
Diverse pathogens, plant hosts, insect vectors, and non-vector herbivores coexist and interact in natural systems. An example is the cooccurrence of insects Bemisia tabaci Q and Frankliniella occidentalis and the pathogens tomato yellow leaf curl virus (TYLCV) and tomato spotted wilt virus (TSWV) on...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174246/ https://www.ncbi.nlm.nih.gov/pubmed/30327608 http://dx.doi.org/10.3389/fphys.2018.01261 |
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author | Chen, Gong Su, Qi Shi, Xiaobin Pan, Huipeng Jiao, Xiaoguo Zhang, Youjun |
author_facet | Chen, Gong Su, Qi Shi, Xiaobin Pan, Huipeng Jiao, Xiaoguo Zhang, Youjun |
author_sort | Chen, Gong |
collection | PubMed |
description | Diverse pathogens, plant hosts, insect vectors, and non-vector herbivores coexist and interact in natural systems. An example is the cooccurrence of insects Bemisia tabaci Q and Frankliniella occidentalis and the pathogens tomato yellow leaf curl virus (TYLCV) and tomato spotted wilt virus (TSWV) on the same plant. In addition, both TYLCV and TSWV are persistently transmitted in these insect species. However, TSWV reduces the fitness of B. tabaci Q; therefore, we investigated whether TSWV affects the transmission of TYLCV to tomato. Both TYLCV and TSWV are persistently transmitted. Although B. tabaci Q cannot transmit TSWV, we found that this insect species is able to acquire and retain this virus serotype, indicating that the effects of TSWV on TYLCV transmission in the current study result from effects on the vector. The acquisition, retention, and transmission of TYLCV by B. tabaci Q were reduced when the insect vector contained TSWV. Additionally, the TYLCV acquisition and transmission by B. tabaci Q were reduced when the host plant was inoculated with TSWV before TYLCV or simultaneously with TYLCV. We also found that F. occidentalis fecundity and transmission of TSWV were reduced when F. occidentalis contained TYLCV. Our findings are consistent with the hypothesis that persistently transmitted viruses can restrict the transmission of other viruses by affecting their insect vectors. |
format | Online Article Text |
id | pubmed-6174246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61742462018-10-16 Persistently Transmitted Viruses Restrict the Transmission of Other Viruses by Affecting Their Vectors Chen, Gong Su, Qi Shi, Xiaobin Pan, Huipeng Jiao, Xiaoguo Zhang, Youjun Front Physiol Physiology Diverse pathogens, plant hosts, insect vectors, and non-vector herbivores coexist and interact in natural systems. An example is the cooccurrence of insects Bemisia tabaci Q and Frankliniella occidentalis and the pathogens tomato yellow leaf curl virus (TYLCV) and tomato spotted wilt virus (TSWV) on the same plant. In addition, both TYLCV and TSWV are persistently transmitted in these insect species. However, TSWV reduces the fitness of B. tabaci Q; therefore, we investigated whether TSWV affects the transmission of TYLCV to tomato. Both TYLCV and TSWV are persistently transmitted. Although B. tabaci Q cannot transmit TSWV, we found that this insect species is able to acquire and retain this virus serotype, indicating that the effects of TSWV on TYLCV transmission in the current study result from effects on the vector. The acquisition, retention, and transmission of TYLCV by B. tabaci Q were reduced when the insect vector contained TSWV. Additionally, the TYLCV acquisition and transmission by B. tabaci Q were reduced when the host plant was inoculated with TSWV before TYLCV or simultaneously with TYLCV. We also found that F. occidentalis fecundity and transmission of TSWV were reduced when F. occidentalis contained TYLCV. Our findings are consistent with the hypothesis that persistently transmitted viruses can restrict the transmission of other viruses by affecting their insect vectors. Frontiers Media S.A. 2018-10-01 /pmc/articles/PMC6174246/ /pubmed/30327608 http://dx.doi.org/10.3389/fphys.2018.01261 Text en Copyright © 2018 Chen, Su, Shi, Pan, Jiao and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Chen, Gong Su, Qi Shi, Xiaobin Pan, Huipeng Jiao, Xiaoguo Zhang, Youjun Persistently Transmitted Viruses Restrict the Transmission of Other Viruses by Affecting Their Vectors |
title | Persistently Transmitted Viruses Restrict the Transmission of Other Viruses by Affecting Their Vectors |
title_full | Persistently Transmitted Viruses Restrict the Transmission of Other Viruses by Affecting Their Vectors |
title_fullStr | Persistently Transmitted Viruses Restrict the Transmission of Other Viruses by Affecting Their Vectors |
title_full_unstemmed | Persistently Transmitted Viruses Restrict the Transmission of Other Viruses by Affecting Their Vectors |
title_short | Persistently Transmitted Viruses Restrict the Transmission of Other Viruses by Affecting Their Vectors |
title_sort | persistently transmitted viruses restrict the transmission of other viruses by affecting their vectors |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174246/ https://www.ncbi.nlm.nih.gov/pubmed/30327608 http://dx.doi.org/10.3389/fphys.2018.01261 |
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