Evidence map›Paper›PMID 27821741›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Siderophore-based immunization strategy to inhibit growth of enteric pathogens.

Martina Sassone-Corsi, Phoom Chairatana, Tengfei Zheng, Araceli Perez-Lopez, Robert A Edwards, Michael D George, Elizabeth M Nolan, Manuela Raffatellu

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
17.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 73 citations in OpenAlex.

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  13. Effects of deferoxamine on intrinsic colistin resistance ofExperimental and therapeutic medicine · 2023
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  17. Comparative Pathogenomics ofInfection and immunity · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Martina Sassone-CorsiDepartment of Microbiology and Molecular Genetics, School of Medicine, University of California, Irvine, CA 92697.
Phoom ChairatanaDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139.
Tengfei ZhengDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139.
Araceli Perez-LopezDepartment of Microbiology and Molecular Genetics, School of Medicine, University of California, Irvine, CA 92697.
Robert A EdwardsDepartment of Pathology and Laboratory Medicine, University of California, Irvine, CA 92697.
Michael D GeorgeDepartment of Medical Microbiology and Immunology, School of Medicine, University of California, Davis, CA 95616.
Elizabeth M NolanDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139; lnolan@mit.edu manuelar@uci.edu.
Manuela RaffatelluDepartment of Microbiology and Molecular Genetics, School of Medicine, University of California, Irvine, CA 92697; lnolan@mit.edu manuelar@uci.edu.
University of California, Irvine · USMassachusetts Institute of Technology · USUniversity of California, Davis · US

Funding

Vaccines and Diagnostics TrialsU54AI065359 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI BARBOUR, ALAN G. · 2005 to 2013
$88.8M
INTESTINAL VITAMIN H UPTAKE--MOLECULAR/CELL REGULATIONR01DK058057 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI SAID, HAMID M · 2000 to 2019
$6.8M
Nutritional immunity during Salmonella infectionR01AI126277 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RAFFATELLU, MANUELA · 2016 to 2020
$1.9M
Development of siderophore-based vaccines against non-typhoidal Salmonella infectionR01AI114625 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NOLAN, ELIZABETH M, RAFFATELLU, MANUELA · 2015 to 2019
$1.9M
Nutritional immunity during Salmonella infectionR37AI126277 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Manuela Raffatellu · 2023 to 2026
$1.8M
The new chemokine CCL28 and its role during Salmonella infectionR21AI121928 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RAFFATELLU, MANUELA, ZLOTNIK, ALBERT · 2016 to 2017
$425k
The role of the circadian clock during Salmonella infectionR21AI105374 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI RAFFATELLU, MANUELA, SASSONE-CORSI, PAOLO · 2014 to 2015
$424k
Targeting iron acquisition in Salmonella with siderophore-based immunizationR21AI101784 · NIAID · UNIVERSITY OF CALIFORNIA-IRVINE · PI NOLAN, ELIZABETH M, RAFFATELLU, MANUELA · 2014 to 2015
$418k
Harnessing iron acquisition to hinder enterobacterial pathogenesisR56AI114625 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI NOLAN, ELIZABETH M, RAFFATELLU, MANUELA · 2022 to 2022
$400k
NIAID NIH HHS R01 AI114625NIAID NIH HHS R01 AI126277NIAID NIH HHS R21 AI101784NIAID NIH HHS R21 AI105374NIAID NIH HHS R21 AI121928NIAID NIH HHS R37 AI126277NIAID NIH HHS R56 AI114625NIAID NIH HHS U54 AI065359NIDDK NIH HHS R01 DK058057
6 · The paper itself

Abstract

Infections with Gram-negative pathogens pose a serious threat to public health. This scenario is exacerbated by increases in antibiotic resistance and the limited availability of vaccines and therapeutic tools to combat these infections. Here, we report an immunization approach that targets siderophores, which are small molecules exported by enteric Gram-negative pathogens to acquire iron, an essential nutrient, in the host. Because siderophores are nonimmunogenic, we designed and synthesized conjugates of a native siderophore and the immunogenic carrier protein cholera toxin subunit B (CTB). Mice immunized with the CTB-siderophore conjugate developed anti-siderophore antibodies in the gut mucosa, and when mice were infected with the enteric pathogen Salmonella, they exhibited reduced intestinal colonization and reduced systemic dissemination of the pathogen. Moreover, analysis of the gut microbiota revealed that reduction of Salmonella colonization in the inflamed gut was accompanied by expansion of Lactobacillus spp., which are beneficial commensal organisms that thrive in similar locales as Enterobacteriaceae. Collectively, our results demonstrate that anti-siderophore antibodies inhibit Salmonella colonization. Because siderophore-mediated iron acquisition is a virulence trait shared by many bacterial and fungal pathogens, blocking microbial iron acquisition by siderophore-based immunization or other siderophore-targeted approaches may represent a novel strategy to prevent and ameliorate a broad range of infections.

Indexed as

ImmunizationAnimalsAntibody FormationColony Count, MicrobialEnterobacteriaceaeFemaleGastrointestinal MicrobiomeImmunity, MucosalInflammationMice, Inbred C57BLSiderophoresSiderophoresimmunizationironmicrobiotaSalmonellasiderophore

Identifiers

PMID27821741
PMCPMC5127304
OpenAlexW2556896730

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.