Evidence map›Paper›PMID 42060825›Full record

ArticleJournal of extracellular vesicles2026

Outer Membrane Vesicles Mediate the Secretion and Nuclear Trafficking of a Bacterial Nucleomodulin.

Jack K Emery, Variya Nemidkanam, Nina Colon, Kate R J Friesen, Lena H M Le, Angus R Cramond, Maxine Yap, Mônica S Barbosa, Georgie Wray-McCann, David J McGee and 5 more

Abstract read
In one paragraph

Article in Journal of extracellular vesicles, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Jack K EmeryCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0009-0003-8191-8381
Variya NemidkanamCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0000-0001-9426-5568
Nina ColonCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0000-0002-0112-975X
Kate R J FriesenCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0009-0004-9858-520X
Lena H M LeCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0009-0009-9215-5416
Angus R CramondCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0009-0005-2922-562X
Maxine YapCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0009-0006-9544-5441
Mônica S BarbosaCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0000-0001-6964-5219
Georgie Wray-McCannCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.
David J McGeeDepartment of Microbiology and Immunology, Louisiana State University Health Sciences Center Shreveport, Shreveport, Louisiana, USA.
Natalia Castaño-RodríguezSchool of Biotechnology and Biomolecular Science, University of New South Wales, Sydney, Australia.ORCID https://orcid.org/0000-0001-8819-8872
Dongmei TongCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0000-0002-3468-5293
Caroline SkeneCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.
Laurent TerradotLaboratory of Molecular Microbiology and Structural Biochemistry, Centre National de la Recherche Scientifique UMR5086, Université de Lyon, Lyon, France.ORCID https://orcid.org/0000-0003-4279-9167
Richard L FerreroCentre for Innate Immunity and Infectious Diseases, Hudson Institute of Medical Research, Melbourne, Australia.ORCID https://orcid.org/0000-0001-6817-6211

Funding

Australian Research Council DP210103881Canadian Queen Elizabeth II Diamond Jubilee ScholarshipCancer Australia/Pancare Foundation PdCCRS Early Career Researcher Grant 2012944Mitacs Globalink Research AwardNational Health and Medical Research Council APP2012620National Health and Medical Research Council APP2021710Research Training Program, Australian Department of EducationRoyal Golden Jubilee Funding SchemeUNSW Scientia FellowshipU.S. Department of Defense Award no. CA200760U.S. Department of Defense contract no. W81XWH2110953Victorian Government's Operational Infrastructure Support Program
6 · The paper itself

Abstract

Nucleomodulins are a family of bacterial virulence proteins that traffic to the nucleus of host cells to disrupt nuclear processes and, in some cases, promote carcinogenesis. The mechanisms by which nucleomodulins are secreted and injected into host cells are not entirely clear. We hypothesised that bacterial extracellular vesicles (EVs), also known as outer membrane vesicles, may represent a novel mechanism for nucleomodulin delivery to host cells. To address this, we studied the role of EVs in the secretion of Helicobacter pylori tumour necrosis factor-α-inducing protein (Tipα), a protein that was reported to undergo nuclear trafficking and to promote carcinogenesis. Importantly, we showed that most Tipα present in H. pylori culture supernatants is associated with EVs and, moreover, is encapsulated within these particles in its biologically active dimeric form. Confocal microscopy and cell fractionation studies demonstrated that EVs carry Tipα to the nuclear compartment of host cells and can bind host DNA. EVs from isogenic tipA mutants induced greater pro-inflammatory cytokine responses in host cells than EVs from wild-type bacteria; however, this effect was dependent on the EV isolation method. We propose that EVs represent a new mechanism by which bacteria secrete and deliver nucleomodulins to their target cells, resulting in altered immune responses and possibly carcinogenesis.

Indexed as

Bacterial ProteinsCell NucleusExtracellular VesiclesHelicobacter pyloriHumansProtein TransportBacterial ProteinsTipalpha protein, Helicobacter pyloriextracellular vesiclesHelicobacter pylorinucleomodulinOMVsouter membrane vesiclesTipαtumour necrosis factor‐α‐inducing protein

Identifiers

PMID42060825
PMCPMC13132344

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Registered trials

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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.