Evidence map›Paper›PMID 27302762›Full record

ArticlemBio2016

Functional Analysis of the Rhoptry Kinome during Chronic Toxoplasma gondii Infection.

Laura J Knoll

Open access · goldAbstract readComment
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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Therapeutic Antitoxoplasmosis Potential ofJournal of tropical medicine · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Laura J KnollDepartment of Medical Microbiology and Immunology, University of Wisconsin-Madison, Madison, Wisconsin, USA ljknoll@wisc.edu.
University of Wisconsin–Madison · US

Funding

Mechanisms of RNA regulation in the persistence of the AIDS pathogen ToxoplasmaR21AI114277 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI KNOLL, LAURA J · 2015 to 2016
$412k
Sexual development of Toxoplasma in feline intestinal organoids and cell cultureR21AI123289 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI KNOLL, LAURA J · 2016 to 2017
$408k
NIAID NIH HHS R21 AI114277NIAID NIH HHS R21 AI123289
6 · The paper itself

Abstract

Toxoplasma gondii is one of the most common parasitic infections of humans worldwide. Once exposed, humans remain infected with T. gondii for life, and there are no therapeutics capable of eliminating a chronic infection. In the search for novel drug targets, T. gondii is known to contain several unique secretory organelles, one of which is called the rhoptries. Rhoptry organelles contain and secrete numerous proteins with kinase domains, but the roles of most of these kinases during infection remain unknown. In a recent mBio article, B. A. Fox et al. [mBio 7(3):e00193-16, 2016, http://dx.doi.org/10.1128/mBio.00193-16] performed a tour de force deletion analysis of 31 rhoptry kinases and examined their roles in the development of chronic infection. While rhoptry kinase deletion strains that displayed an acute infection defect also showed a reduction in chronic infection cyst burden, two rhoptry kinase deletion strains had decreased cyst burden without any change in acute virulence. These results indicate the necessity of the rhoptry kinases for the establishment and perhaps maintenance of chronic infection. They also highlight the potential of these kinases as drug targets to clear chronic infection or as candidates to generate a nonpersisting vaccine.

Indexed as

Protozoan ProteinsHumansOrganellesToxoplasmaToxoplasmosisVirulenceProtozoan Proteins

Identifiers

PMID27302762
PMCPMC4916387
OpenAlexW2441996121

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.