Cargando…
A proteomic approach reveals possible molecular mechanisms and roles for endosymbiotic bacteria in begomovirus transmission by whiteflies
BACKGROUND: Many plant viruses are vector-borne and depend on arthropods for transmission between host plants. Begomoviruses, the largest, most damaging and emerging group of plant viruses, infect hundreds of plant species, and new virus species of the group are discovered each year. Begomoviruses a...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662926/ https://www.ncbi.nlm.nih.gov/pubmed/33185242 http://dx.doi.org/10.1093/gigascience/giaa124 |
_version_ | 1783609508259430400 |
---|---|
author | Kliot, Adi Johnson, Richard S MacCoss, Michael J Kontsedalov, Svetlana Lebedev, Galina Czosnek, Henryk Heck, Michelle Ghanim, Murad |
author_facet | Kliot, Adi Johnson, Richard S MacCoss, Michael J Kontsedalov, Svetlana Lebedev, Galina Czosnek, Henryk Heck, Michelle Ghanim, Murad |
author_sort | Kliot, Adi |
collection | PubMed |
description | BACKGROUND: Many plant viruses are vector-borne and depend on arthropods for transmission between host plants. Begomoviruses, the largest, most damaging and emerging group of plant viruses, infect hundreds of plant species, and new virus species of the group are discovered each year. Begomoviruses are transmitted by members of the whitefly Bemisia tabaci species complex in a persistent-circulative manner. Tomato yellow leaf curl virus (TYLCV) is one of the most devastating begomoviruses worldwide and causes major losses in tomato crops, as well as in many agriculturally important plant species. Different B. tabaci populations vary in their virus transmission abilities; however, the causes for these variations are attributed among others to genetic differences among vector populations, as well as to differences in the bacterial symbionts housed within B. tabaci. RESULTS: Here, we performed discovery proteomic analyses in 9 whitefly populations from both Middle East Asia Minor I (MEAM1, formerly known as B biotype) and Mediterranean (MED, formerly known as Q biotype) species. We analysed our proteomic results on the basis of the different TYLCV transmission abilities of the various populations included in the study. The results provide the first comprehensive list of candidate insect and bacterial symbiont (mainly Rickettsia) proteins associated with virus transmission. CONCLUSIONS: Our data demonstrate that the proteomic signatures of better vector populations differ considerably when compared with less efficient vector populations in the 2 whitefly species tested in this study. While MEAM1 efficient vector populations have a more lenient immune system, the Q efficient vector populations have higher abundance of proteins possibly implicated in virus passage through cells. Both species show a strong link of the facultative symbiont Rickettsia to virus transmission. |
format | Online Article Text |
id | pubmed-7662926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76629262020-11-18 A proteomic approach reveals possible molecular mechanisms and roles for endosymbiotic bacteria in begomovirus transmission by whiteflies Kliot, Adi Johnson, Richard S MacCoss, Michael J Kontsedalov, Svetlana Lebedev, Galina Czosnek, Henryk Heck, Michelle Ghanim, Murad Gigascience Data Note BACKGROUND: Many plant viruses are vector-borne and depend on arthropods for transmission between host plants. Begomoviruses, the largest, most damaging and emerging group of plant viruses, infect hundreds of plant species, and new virus species of the group are discovered each year. Begomoviruses are transmitted by members of the whitefly Bemisia tabaci species complex in a persistent-circulative manner. Tomato yellow leaf curl virus (TYLCV) is one of the most devastating begomoviruses worldwide and causes major losses in tomato crops, as well as in many agriculturally important plant species. Different B. tabaci populations vary in their virus transmission abilities; however, the causes for these variations are attributed among others to genetic differences among vector populations, as well as to differences in the bacterial symbionts housed within B. tabaci. RESULTS: Here, we performed discovery proteomic analyses in 9 whitefly populations from both Middle East Asia Minor I (MEAM1, formerly known as B biotype) and Mediterranean (MED, formerly known as Q biotype) species. We analysed our proteomic results on the basis of the different TYLCV transmission abilities of the various populations included in the study. The results provide the first comprehensive list of candidate insect and bacterial symbiont (mainly Rickettsia) proteins associated with virus transmission. CONCLUSIONS: Our data demonstrate that the proteomic signatures of better vector populations differ considerably when compared with less efficient vector populations in the 2 whitefly species tested in this study. While MEAM1 efficient vector populations have a more lenient immune system, the Q efficient vector populations have higher abundance of proteins possibly implicated in virus passage through cells. Both species show a strong link of the facultative symbiont Rickettsia to virus transmission. Oxford University Press 2020-11-13 /pmc/articles/PMC7662926/ /pubmed/33185242 http://dx.doi.org/10.1093/gigascience/giaa124 Text en © The Author(s) 2020. Published by Oxford University Press GigaScience. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Data Note Kliot, Adi Johnson, Richard S MacCoss, Michael J Kontsedalov, Svetlana Lebedev, Galina Czosnek, Henryk Heck, Michelle Ghanim, Murad A proteomic approach reveals possible molecular mechanisms and roles for endosymbiotic bacteria in begomovirus transmission by whiteflies |
title | A proteomic approach reveals possible molecular mechanisms and roles for endosymbiotic bacteria in begomovirus transmission by whiteflies |
title_full | A proteomic approach reveals possible molecular mechanisms and roles for endosymbiotic bacteria in begomovirus transmission by whiteflies |
title_fullStr | A proteomic approach reveals possible molecular mechanisms and roles for endosymbiotic bacteria in begomovirus transmission by whiteflies |
title_full_unstemmed | A proteomic approach reveals possible molecular mechanisms and roles for endosymbiotic bacteria in begomovirus transmission by whiteflies |
title_short | A proteomic approach reveals possible molecular mechanisms and roles for endosymbiotic bacteria in begomovirus transmission by whiteflies |
title_sort | proteomic approach reveals possible molecular mechanisms and roles for endosymbiotic bacteria in begomovirus transmission by whiteflies |
topic | Data Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662926/ https://www.ncbi.nlm.nih.gov/pubmed/33185242 http://dx.doi.org/10.1093/gigascience/giaa124 |
work_keys_str_mv | AT kliotadi aproteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT johnsonrichards aproteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT maccossmichaelj aproteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT kontsedalovsvetlana aproteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT lebedevgalina aproteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT czosnekhenryk aproteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT heckmichelle aproteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT ghanimmurad aproteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT kliotadi proteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT johnsonrichards proteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT maccossmichaelj proteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT kontsedalovsvetlana proteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT lebedevgalina proteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT czosnekhenryk proteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT heckmichelle proteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies AT ghanimmurad proteomicapproachrevealspossiblemolecularmechanismsandrolesforendosymbioticbacteriainbegomovirustransmissionbywhiteflies |