PXD027638 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | The human innate immune protein calprotectin elicits a multi-metal starvation response in Pseudomonas aeruginosa |
Description | To combat infections, the mammalian host limits availability of essential transition metals such as iron (Fe), zinc (Zn), and manganese (Mn) in a strategy termed “nutritional immunity”. The innate immune protein calprotectin (CP) contributes to nutritional immunity by sequestering these metals to exert antimicrobial activity against a broad range of microbial pathogens. One such pathogen is Pseudomonas aeruginosa, which causes opportunistic infections in vulnerable populations including individuals with cystic fibrosis. CP was previously shown to withhold Fe(II) and Zn(II) from P. aeruginosa and induce Fe- and Zn-starvation responses in this pathogen. In this work, we performed quantitative, label-free proteomics to further elucidate how CP impacts metal homeostasis pathways in P. aeruginosa. We report that CP induces an incomplete Fe-starvation response, as many Fe-containing proteins that are repressed by Fe limitation are not affected by CP treatment. The Zn-starvation response elicited by CP seems to be more complete than the Fe-starvation response and includes increases in Zn transporters and Zn-independent proteins. CP also induces the expression of membrane-modifying enzymes, and metal-depletion studies indicate this response results from the sequestration of multiple metals. Moreover, the increased expression of membrane-modifying enzymes upon CP treatment correlates with increased tolorance to polymyxin B. Thus, response of P. aeruginosa to CP treatment includes both single and multi-metal starvation responses and includes many factors related to virulence potential, broadening our understanding of this pathogen’s interaction with the host. |
HostingRepository | PRIDE |
AnnounceDate | 2021-07-29 |
AnnouncementXML | Submission_2021-07-29_10:58:13.525.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Weiliang Huang |
SpeciesList | scientific name: Pseudomonas aeruginosa PA14; NCBI TaxID: 652611; |
ModificationList | iodoacetamide derivatized residue |
Instrument | Orbitrap Fusion Lumos |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2021-07-29 02:00:46 | ID requested | |
⏵ 1 | 2021-07-29 10:58:13 | announced | |
2 | 2024-10-22 05:24:22 | announced | 2024-10-22: Updated project metadata. |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: innate immune, calprotectin, multi-metal starvation, Pseudomonas aeruginosa |
Contact List
Maureen Kane |
contact affiliation | Mass spectrometry research center, School of pharmacy University of Maryland, Baltimore |
contact email | mkane@rx.umaryland.edu |
lab head | |
Weiliang Huang |
contact affiliation | University of Maryland, Baltimore |
contact email | whuang@rx.umaryland.edu |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD027638
- Label: PRIDE project
- Name: The human innate immune protein calprotectin elicits a multi-metal starvation response in Pseudomonas aeruginosa