PXD021221 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Proteomics analyses of immature (21 day post infection) Fasciola hepatica |
Description | The major pathogenesis associated with Fasciola hepatica infection results from the extensive tissue damage caused by the tunnelling and feeding activity of immature flukes during their migration, growth and development in the liver. This is compounded by the pathology caused by host innate and adaptive immune responses that struggle to repair this damage. Complementary transcriptomic and proteomic approaches defined the F. hepatica factors associated with their migration in the liver, and the resulting immune-pathogenesis. The liver-stage parasites display different secretome profiles, reflecting their distinct niche within the host, and supports the view that cathepsin peptidases, cathepsin peptidase inhibitors, saposins and leucine aminopeptidases play a central role in the parasite’s destructive migration, digest of host tissue and blood. Immature flukes are also primed for countering immune attack by secreting immunomodulating fatty acid binding proteins (FABP) and helminth defense molecules (FhHDM). The migration of immature F. hepatica parasites within the liver is associated with an increase in protein production, expression of signalling pathways and neoblast proliferation that drive their rapid growth and development. The secretion of a defined set of molecules, particularly cathepsin L peptidases, peptidase-inhibitors, saponins, immune-regulators and anti-oxidants allow the parasite to negotiate the liver micro-environment, immune attack and increasing levels of oxidative stress. This data contributes to the growing F. hepatica -omics information that can be exploited to understand parasite development more fully and for the design of novel control strategies to prevent host liver tissue destruction and pathology. |
HostingRepository | PRIDE |
AnnounceDate | 2021-09-09 |
AnnouncementXML | Submission_2021-09-09_09:19:17.671.xml |
DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD021221 |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | Krystyna Cwiklinski |
SpeciesList | scientific name: Fasciola hepatica; NCBI TaxID: 6192; |
ModificationList | No PTMs are included in the dataset |
Instrument | Orbitrap Fusion |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2020-08-31 04:04:13 | ID requested | |
⏵ 1 | 2021-09-09 09:19:18 | announced | |
Publication List
Cwiklinski K, Robinson MW, Donnelly S, Dalton JP, Complementary transcriptomic and proteomic analyses reveal the cellular and molecular processes that drive growth and development of Fasciola hepatica in the host liver. BMC Genomics, 22(1):46(2021) [pubmed] |
Keyword List
submitter keyword: Fasciola hepatica, somatic proteome, secretome, LC-MS-MS, liver, growth |
Contact List
John P Dalton |
contact affiliation | Molecular Parasitology Lab (MPL),Orbsen Building, School of Natural Sciences/Ryan Institute National University of Ireland, Galway, Ireland |
contact email | johnpius.dalton@nuigalway.ie |
lab head | |
Krystyna Cwiklinski |
contact affiliation | NUI Galway |
contact email | krystyna.cwiklinski@nuigalway.ie |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD021221
- Label: PRIDE project
- Name: Proteomics analyses of immature (21 day post infection) Fasciola hepatica