Evidence map›Paper›PMID 26330609›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

MavN is a Legionella pneumophila vacuole-associated protein required for efficient iron acquisition during intracellular growth.

Dervla T Isaac, Rita K Laguna, Nicole Valtz, Ralph R Isberg

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

56 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
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  5. Molecular evolution and adaptations ofFrontiers in cellular and infection microbiology · 2026
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  11. In vitro reconstitution of transition metal transporters.The Journal of biological chemistry · 2024
    Review
  12. Article
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  15. Article
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  17. The Sde phosphoribosyl-linked ubiquitin transferases protect theProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  18. Article
  19. Eat or Be Eaten: Strategies Used byInfection and immunity · 2023
    Review
  20. The Sde Phosphoribosyl-Linked Ubiquitin Transferases protect thebioRxiv : the preprint server for biology · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Dervla T IsaacDepartment of Microbiology and Molecular Biology, Tufts University School of Medicine, Boston, MA 02111; Howard Hughes Medical Institute, Tufts University School of Medicine, Boston, MA 02111.
Rita K LagunaDepartment of Microbiology and Molecular Biology, Tufts University School of Medicine, Boston, MA 02111;
Nicole ValtzDepartment of Microbiology and Molecular Biology, Tufts University School of Medicine, Boston, MA 02111;
Ralph R IsbergDepartment of Microbiology and Molecular Biology, Tufts University School of Medicine, Boston, MA 02111; Howard Hughes Medical Institute, Tufts University School of Medicine, Boston, MA 02111 ralph.isberg@tufts.edu.
Tufts University · USHoward Hughes Medical Institute · US

Funding

MOLECULAR ANALYSIS OF MICROBIAL PATHOGENST32AI007422 · NIAID · TUFTS UNIVERSITY BOSTON · PI Ralph R. Isberg · 1992 to 2026
$5.7M
Infectious Disease Training-Pathogenesis/Host ResponseT32AI007329 · NIAID · TUFTS MEDICAL CENTER · PI HU, LINDEN T · 1988 to 2018
$4.1M
Analysis of the interplay between cell adhesion and bacterial protein translocatiR21AI097728 · NIAID · TUFTS UNIVERSITY BOSTON · PI ISBERG, RALPH R. · 2012 to 2013
$454k
Mammalian cell modulation of iron availability for an intravacuolar pathogenR21AI115261 · NIAID · TUFTS UNIVERSITY BOSTON · PI ISBERG, RALPH R. · 2015 to 2016
$454k
Howard Hughes Medical InstituteNIAID NIH HHS 5 T32 AI07422NIAID NIH HHS R21 AI097728NIAID NIH HHS R21 AI115261NIAID NIH HHS T32 AI007329NIAID NIH HHS T32AI007329NIAID NIH HHS T32 AI007422
6 · The paper itself

Abstract

Iron is essential for the growth and virulence of most intravacuolar pathogens. The mechanisms by which microbes bypass host iron restriction to gain access to this metal across the host vacuolar membrane are poorly characterized. In this work, we identify a unique intracellular iron acquisition strategy used by Legionella pneumophila. The bacterial Icm/Dot (intracellular multiplication/defect in organelle trafficking) type IV secretion system targets the bacterial-derived MavN (more regions allowing vacuolar colocalization N) protein to the surface of the Legionella-containing vacuole where this putative transmembrane protein facilitates intravacuolar iron acquisition. The ΔmavN mutant exhibits a transcriptional iron-starvation signature before its growth is arrested during the very early stages of macrophage infection. This intracellular growth defect is rescued only by the addition of excess exogenous iron to the culture medium and not a variety of other metals. Consistent with MavN being a translocated substrate that plays an exclusive role during intracellular growth, the mutant shows no defect for growth in broth culture, even under severe iron-limiting conditions. Putative iron-binding residues within the MavN protein were identified, and point mutations in these residues resulted in defects specific for intracellular growth that are indistinguishable from the ΔmavN mutant. This model of a bacterial protein inserting into host membranes to mediate iron transport provides a paradigm for how intravacuolar pathogens can use virulence-associated secretion systems to manipulate and acquire host iron.

Indexed as

Amino Acid SequenceAnimalsBacterial ProteinsBase SequenceBiological TransportCation Transport ProteinsCell ProliferationCulture MediaCytoplasmDictyosteliumHost-Pathogen InteractionsHumansImmune SystemIronLegionella pneumophilaMacrophagesBacterial ProteinsCation Transport ProteinsCulture MediaIronIcm/DotironLegionellaMavNvacuole

Identifiers

PMID26330609
PMCPMC4577140
OpenAlexW1894024658

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.