Evidence map›Paper›PMID 23813730›Full record

ArticleJournal of bacteriology2013

Identification of Coxiella burnetii type IV secretion substrates required for intracellular replication and Coxiella-containing vacuole formation.

Mary M Weber, Chen Chen, Kristina Rowin, Katja Mertens, Gloria Galvan, Hui Zhi, Christopher M Dealing, Victor A Roman, Simran Banga, Yunhao Tan and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

87 citing papers in PubMed, 119 citations in OpenAlex.

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27 more citing papers are in PubMed but not listed here.

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

12 authors at 2 institutions in 1 country.

Mary M WeberDepartment of Microbial and Molecular Pathogenesis, Texas A&M Health Science Center, College of Medicine, Bryan, Texas, USA.
Chen Chen
Kristina Rowin
Katja Mertens
Gloria Galvan
Hui Zhi
Christopher M Dealing
Victor A Roman
Simran Banga
Yunhao Tan
Zhao-Qing Luo
James E Samuel
Texas A&M Health Science Center · USPurdue University West Lafayette · US

Funding

Identification and Role of Type IV Secretion Effector Proteins in Coxiella burnetiiR01AI090142 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI SAMUEL, JAMES EVANS · 2012 to 2024
$3.4M
Modulation of Host Vesicle Trafficking by Legionella pneumophilaK02AI085403 · NIAID · PURDUE UNIVERSITY · PI LUO, ZHAO-QING · 2010 to 2014
$556k
Identification of Coxiella burnetii Virulence Factors by Transposon MutagenesisR21AI088430 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI SAMUEL, JAMES EVANS · 2010 to 2011
$401k
Identification and Role of Type IV Effector Proteins in Coxiella burnetiiR56AI090142 · NIAID · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI SAMUEL, JAMES EVANS · 2010 to 2010
$379k
NIAID NIH HHS AI088430NIAID NIH HHS AI090142NIAID NIH HHS K02 AI085403NIAID NIH HHS K02AI085403NIAID NIH HHS R01 AI090142NIAID NIH HHS R21 AI088430NIAID NIH HHS R56 AI090142
6 · The paper itself

Abstract

Coxiella burnetii, the etiological agent of acute and chronic Q fever in humans, is a naturally intracellular pathogen that directs the formation of an acidic Coxiella-containing vacuole (CCV) derived from the host lysosomal network. Central to its pathogenesis is a specialized type IVB secretion system (T4SS) that delivers effectors essential for intracellular replication and CCV formation. Using a bioinformatics-guided approach, 234 T4SS candidate substrates were identified. Expression of each candidate as a TEM-1 β-lactamase fusion protein led to the identification of 53 substrates that were translocated in a Dot/Icm-dependent manner. Ectopic expression in HeLa cells revealed that these substrates trafficked to distinct subcellular sites, including the endoplasmic reticulum, mitochondrion, and nucleus. Expression in Saccharomyces cerevisiae identified several substrates that were capable of interfering with yeast growth, suggesting that these substrates target crucial host processes. To determine if any of these T4SS substrates are necessary for intracellular replication, we isolated 20 clonal T4SS substrate mutants using the Himar1 transposon and transposase. Among these, 10 mutants exhibited defects in intracellular growth and CCV formation in HeLa and J774A.1 cells but displayed normal growth in bacteriological medium. Collectively, these results indicate that C. burnetii encodes a large repertoire of T4SS substrates that play integral roles in host cell subversion and CCV formation and suggest less redundancy in effector function than has been found in the comparative Legionella Dot/Icm model.

Indexed as

AnimalsBacterial ProteinsCell LineComputational BiologyCoxiella burnetiiDNA, BacterialEpithelial CellsHumansMacrophagesMiceMutagenesis, InsertionalProtein TransportSaccharomyces cerevisiaeVacuolesVirulence FactorsBacterial ProteinsDNA, BacterialVirulence Factors

Identifiers

PMID23813730
PMCPMC3754607
OpenAlexW2103394301

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.