PXD053620 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Multi-omics approaches define novel aphid effector candidates associated with virulence and avirulence phenotypes |
Description | Compatibility between aphids and plant hosts is genetically determined by both interactingorganisms. For example, plants may carry resistance (R) genes or deploy chemical defences.Aphid saliva contains many proteins that are secreted into host tissues. Subsets of these proteins are predicted to act as effectors, either subverting or triggering host immunity. However, associating particular effectors with virulence or avirulence outcomes presents challenges due to the combinatorial complexity. Here we use defined aphid and host geneticsto test for co-segregation of expressed aphid transcripts and proteins with virulent or avirulent phenotypes. We compared virulent and avirulent pea aphid parental genotypes, and their bulk segregant F1 progeny on Medicago truncatula genotypes carrying or lacking the RAP1 resistance quantitative trait locus. Differential expression analysis based on RNA sequencing of whole bodyand head samples, in combination with proteomics of saliva and salivary glands, enabled us to pinpoint proteins associated with virulence/avirulence phenotypes. There was relatively little impact of host genotype, whereas large numbers of transcripts and proteins were differentially expressed between parental aphids, likely a reflection of their classification as divergent biotypes within the pea aphid species complex. Many fewer transcripts intersected with the equivalent differential expression patterns in the bulked F1F1 progeny, providing an effective filter for removing genomic background effects. Overall, there were more upregulated genes detected in the F1 avirulent dataset compared with the virulent one. Some of the differentially expressed transcripts were also found in the differentially expressed proteomes, with aminopeptidase N proteins being the most frequent differentiallyexpressed family. In addition, a substantial proportion (23%) of salivary proteins lack annotations, suggesting that many novel functions remain to be discovered. |
HostingRepository | PRIDE |
AnnounceDate | 2024-10-28 |
AnnouncementXML | Submission_2024-10-28_06:16:05.556.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | James Carolan |
SpeciesList | scientific name: Acyrthosiphon pisum (Pea aphid); NCBI TaxID: 7029; |
ModificationList | iodoacetamide derivatized residue |
Instrument | Q Exactive HF |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2024-07-03 16:40:30 | ID requested | |
⏵ 1 | 2024-10-28 06:16:05 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: biotypes, saliva, clones,Pea aphid, salivary glands |
Contact List
Dr Jim Carolan |
contact affiliation | Applied Proteomics Laboratory, Department of Biology, Maynooth University, Ireland. |
contact email | james.carolan@mu.ie |
lab head | |
James Carolan |
contact affiliation | Biology |
contact email | james.carolan@nuim.ie |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD053620
- Label: PRIDE project
- Name: Multi-omics approaches define novel aphid effector candidates associated with virulence and avirulence phenotypes