Evidence map›Paper›PMID 27460800›Full record

ArticlemBio2016

Proteomics Analysis Reveals Previously Uncharacterized Virulence Factors in Vibrio proteolyticus.

Ann Ray, Lisa N Kinch, Marcela de Souza Santos, Nick V Grishin, Kim Orth, Dor Salomon

Open access · goldAbstract read
In one paragraph

Article in mBio, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

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  8. Emerging microbes & infections · 2020
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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

6 authors at 2 institutions in 1 country.

Ann RayDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas, USA Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Lisa N KinchHoward Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Marcela de Souza SantosDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Nick V GrishinHoward Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, USA Department of Biophysics, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Kim OrthDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas, USA Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas, USA kim.orth@utsouthwestern.edu dor.salomon@utsouthwestern.edu.ORCID 0000-0002-0678-7620
Dor SalomonDepartment of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas, USA kim.orth@utsouthwestern.edu dor.salomon@utsouthwestern.edu.ORCID 0000-0002-2009-9453
Howard Hughes Medical Institute · USThe University of Texas Southwestern Medical Center · US

Funding

UT GASTROENTEROLOGY/HEPATOLOGY RESEARCH TRAINING PROGRAMT32DK007745 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Rodney E Infante · 1997 to 2026
$6.8M
Biochemical Characterization of Yersinia Effector YopJ.R01AI056404 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI ORTH, KIM · 2003 to 2012
$2.8M
Computational methods for structural-functional studies of proteinsR01GM094575 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI GRISHIN, NICK V. · 2010 to 2017
$2.4M
Type VI Secretion System MIX-effectors and their use as anti-bacterial agentsK99AI116948 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI SALOMON, DOR SAMUEL · 2015 to 2015
$84k
NIAID NIH HHS K99 AI116948NIAID NIH HHS R01 AI056404NIDDK NIH HHS T32 DK007745NIGMS NIH HHS R01 GM094575
6 · The paper itself

Abstract

unlabelledMembers of the genus Vibrio include many pathogens of humans and marine animals that share genetic information via horizontal gene transfer. Hence, the Vibrio pan-genome carries the potential to establish new pathogenic strains by sharing virulence determinants, many of which have yet to be characterized. Here, we investigated the virulence properties of Vibrio proteolyticus, a Gram-negative marine bacterium previously identified as part of the Vibrio consortium isolated from diseased corals. We found that V. proteolyticus causes actin cytoskeleton rearrangements followed by cell lysis in HeLa cells in a contact-independent manner. In search of the responsible virulence factor involved, we determined the V. proteolyticus secretome. This proteomics approach revealed various putative virulence factors, including active type VI secretion systems and effectors with virulence toxin domains; however, these type VI secretion systems were not responsible for the observed cytotoxic effects. Further examination of the V. proteolyticus secretome led us to hypothesize and subsequently demonstrate that a secreted hemolysin, belonging to a previously uncharacterized clan of the leukocidin superfamily, was the toxin responsible for the V. proteolyticus-mediated cytotoxicity in both HeLa cells and macrophages. Clearly, there remains an armory of yet-to-be-discovered virulence factors in the Vibrio pan-genome that will undoubtedly provide a wealth of knowledge on how a pathogen can manipulate host cells. IMPORTANCE: The pan-genome of the genus Vibrio is a potential reservoir of unidentified toxins that can provide insight into how members of this genus have successfully risen as emerging pathogens worldwide. We focused on Vibrio proteolyticus, a marine bacterium that was previously implicated in virulence toward marine animals, and characterized its interaction with eukaryotic cells. We found that this bacterium causes actin cytoskeleton rearrangements and leads to cell death. Using a proteomics approach, we identified a previously unstudied member of the leukocidin family of pore-forming toxins as the virulence factor responsible for the observed cytotoxicity in eukaryotic cells, as well as a plethora of additional putative virulence factors secreted by this bacterium. Our findings reveal a functional new clan of the leukocidin toxin superfamily and establish this pathogen as a reservoir of potential toxins that can be used for biomedical applications.

Indexed as

ProteomicsAnimalsAquatic OrganismsCell SurvivalCytoskeletonEpithelial CellsHeLa CellsHemolysin ProteinsHumansMacrophagesMiceRAW 264.7 CellsVibrioVirulence FactorsHemolysin ProteinsVirulence Factors

Identifiers

PMID27460800
PMCPMC4981721
OpenAlexW2504274966

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.