⮝ Full datasets listing

PXD047879-1

PXD047879 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleLC-MS/MS of excreted-secreted proteins of adult Ancylostoma ceylanicum hookworms, collection E20201108-07
DescriptionHookworms are parasitic nematodes that chronically infect 170-440 million people, despite healthy human immune systems ending most infections quickly. How hookworms successfully overcome host resistance is unclear, but is thought to involve hookworm proteins that either digest host tissues or dampen the host's immune system. To find such proteins in the model hookworm Ancylostoma ceylanicum, we identified hookworm genes encoding proteins excreted into the environment, genes expressed in the intestine, and genes transcriptionally upregulated in response to a normal host immune system. To maximize our accuracy, we repredicted 33,190 protein-coding genes in A. ceylanicum with a BUSCO completeness of 95.3%. We collected excreted-secreted (ES) proteins from two sets of adult hookworms in vitro, and used mass spectrometry to identify 565 A. ceylanicum genes encoding ES proteins; we also used RNA-seq to identify A. ceylanicum genes expressed both in young adults (12 days post-infection) and in intestines and non-intestinal tissues dissected from mature adults (19 days post-infection), with hamster hosts that either had normal immune systems or were immunosuppressed by dexamethasone. In adult A. ceylanicum, we observed 2,145 and 1,694 genes with intestine- and non-intestine-biased expression, respectively. Comparing hookworm gene activity in normal versus immunosuppressed hosts, we observed essentially no changes of gene activity in non-blood-feeding 12-day young adults or non-intestinal 19-day adult tissues. However, in intestinal 19-day adult tissues, we observed 671 genes upregulated at least two-fold in normal hosts versus immunosuppressed hosts (positively immunoregulated), and 75 genes that were negatively immunoregulated; thus, immunoregulation was observed only in mature adult hookworm intestine, directly exposed to host blood. Of the positively immunoregulated intestinal genes, 590 (87.9%) showed male-biased gene expression (9.8-fold greater overlap than chance), suggesting that male and female hookworms have different responses to host immune systems; of the other 81 non-male-biased genes, 53 encoded ES proteins, a 38-fold greater overlap than expected by chance. Of these 53 immunoregulated ES genes, 26 had ES gene homologs in the closely related hookworm Ancylostoma caninum, five in the human hookworm Necator americanus, and four in the more distantly related strongylid parasite Haemonchus contortus. Such a mixture of rapidly evolving and conserved genes could serve as virulence factors enabling infection.
HostingRepositoryPRIDE
AnnounceDate2025-10-30
AnnouncementXMLSubmission_2025-10-30_13:32:01.757.xml
DigitalObjectIdentifierhttps://dx.doi.org/10.6019/PXD047879
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportSupported dataset by repository
PrimarySubmitterErich Schwarz
SpeciesList scientific name: Ancylostoma ceylanicum; NCBI TaxID: NEWT:53326;
ModificationListacetylated residue; monohydroxylated residue; iodoacetamide derivatized residue
InstrumentOrbitrap Exploris 480
Dataset History
RevisionDatetimeStatusChangeLog Entry
02023-12-17 17:46:53ID requested
12025-10-30 13:32:02announced
Publication List
10.6019/PXD047879;
10.1101/2025.02.01.636063;
Schwarz EM, Noon JB, Chicca JD, Garceau C, Li H, Antoshechkin I, Il, í, k V, Paf, č, o B, Weeks AM, Homan EJ, Ostroff GR, Aroian RV, Hookworm genes encoding intestinal excreted-secreted proteins are transcriptionally upregulated in response to the host's immune system. bioRxiv, ():(2025) [pubmed]
Keyword List
submitter keyword: Ancylostoma ceylanicum,Hookworm, excreted/secreted proteins, ES proteins
Contact List
Raffi Van Aroian
contact affiliationProgram in Molecular Medicine, University of Massachusetts Chan Medical School, Worcester, MA, 01605-2377, USA
contact emailraffi.aroian@umassmed.edu
lab head
Erich Schwarz
contact affiliationDepartment of Molecular Biology and Genetics, Cornell University
contact emailems394@cornell.edu
dataset submitter
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2025/10/PXD047879
PRIDE project URI
Repository Record List
[ + ]