Evidence map›Paper›PMID 24787713›Full record

ArticlePLoS pathogens2014

Malaria parasite infection compromises control of concurrent systemic non-typhoidal Salmonella infection via IL-10-mediated alteration of myeloid cell function.

Kristen L Lokken, Jason P Mooney, Brian P Butler, Mariana N Xavier, Jennifer Y Chau, Nicola Schaltenberg, Ramie H Begum, Werner Müller, Shirley Luckhart, Renée M Tsolis

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
15.6field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
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  6. Article
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  15. Article
  16. AlteredFrontiers in immunology · 2021
    Article
  17. Review
  18. Antibodies and Protection in SystemicInfection and immunity · 2020
    Review
  19. Clofazimine Reduces the Survival ofACS infectious diseases · 2020
    Article
  20. Frontiers in cellular and infection microbiology · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 4 countries.

Kristen L LokkenDepartment of Microbiology & Immunology, School of Medicine, University of California at Davis, Davis, California, United States of America.
Jason P MooneyDepartment of Microbiology & Immunology, School of Medicine, University of California at Davis, Davis, California, United States of America.
Brian P ButlerDepartment of Microbiology & Immunology, School of Medicine, University of California at Davis, Davis, California, United States of America.
Mariana N XavierDepartment of Microbiology & Immunology, School of Medicine, University of California at Davis, Davis, California, United States of America; Departamento de Clínica e Cirurgia Veterinária, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Jennifer Y ChauDepartment of Microbiology & Immunology, School of Medicine, University of California at Davis, Davis, California, United States of America.
Nicola SchaltenbergDepartment of Microbiology & Immunology, School of Medicine, University of California at Davis, Davis, California, United States of America.
Ramie H BegumDepartment of Microbiology & Immunology, School of Medicine, University of California at Davis, Davis, California, United States of America; Department of Life Sciences & Bioinformatics, Assam University, Diphu Campus, Karbi Anglong, Assam, India.
Werner MüllerFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
Shirley LuckhartDepartment of Microbiology & Immunology, School of Medicine, University of California at Davis, Davis, California, United States of America.
Renée M TsolisDepartment of Microbiology & Immunology, School of Medicine, University of California at Davis, Davis, California, United States of America.
University of California, Davis · USUniversidade Federal de Minas Gerais · BRUniversity of Manchester · GB

Funding

Comparative Medical Science Training ProgramT32OD011147 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI JEROEN SAEIJ, Sara Michelle Thomasy · 2012 to 2026
$5.5M
LABORATORY MEDICINE TRAINING PROGRAMT32RR007038 · NCRR · UNIVERSITY OF CALIFORNIA DAVIS · PI BARTHOLD, STEPHEN WILLIAM · 1988 to 2011
$4.0M
Animal Models of Infectious Diseases Training ProgramT32AI060555 · NIAID · UNIVERSITY OF CALIFORNIA DAVIS · PI MCSORLEY, STEPHEN J · 2004 to 2025
$3.3M
Pathogenesis of Salmonella bacteremiaR01AI098078 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI TSOLIS, RENEE M · 2012 to 2016
$1.8M
Mechanisms of Salmonella Bacteremia in Pediatric MalariaR21AI082320 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI TSOLIS, RENEE M · 2010 to 2011
$405k
Pathogenesis of Salmonella BacteremiaR56AI098078 · NIAID · UNIVERSITY OF CALIFORNIA AT DAVIS · PI TSOLIS, RENEE M · 2018 to 2018
$384k
NCRR NIH HHS T32 RR007038NCRR NIH HHS T32RR07038NIAID NIH HHS 2T32AI060555NIAID NIH HHS AI082320NIAID NIH HHS AI098078NIAID NIH HHS R01 AI098078NIAID NIH HHS R21 AI082320NIAID NIH HHS R56 AI098078NIAID NIH HHS T32 AI060555NIH HHS T32 OD011147Wellcome Trust
6 · The paper itself

Abstract

Non-typhoidal Salmonella serotypes (NTS) cause a self-limited gastroenteritis in immunocompetent individuals, while children with severe Plasmodium falciparum malaria can develop a life-threatening disseminated infection. This co-infection is a major source of child mortality in sub-Saharan Africa. However, the mechanisms by which malaria contributes to increased risk of NTS bacteremia are incompletely understood. Here, we report that in a mouse co-infection model, malaria parasite infection blunts inflammatory responses to NTS, leading to decreased inflammatory pathology and increased systemic bacterial colonization. Blunting of NTS-induced inflammatory responses required induction of IL-10 by the parasites. In the absence of malaria parasite infection, administration of recombinant IL-10 together with induction of anemia had an additive effect on systemic bacterial colonization. Mice that were conditionally deficient for either myeloid cell IL-10 production or myeloid cell expression of IL-10 receptor were better able to control systemic Salmonella infection, suggesting that phagocytic cells are both producers and targets of malaria parasite-induced IL-10. Thus, IL-10 produced during the immune response to malaria increases susceptibility to disseminated NTS infection by suppressing the ability of myeloid cells, most likely macrophages, to control bacterial infection.

Indexed as

CoinfectionAnimalsFemaleInflammationInterleukin-10Malaria, FalciparumMiceMice, Inbred C57BLMice, Inbred CBAMice, KnockoutMyeloid CellsPlasmodium falciparumSalmonella InfectionsSalmonella typhimuriumSepsisInterleukin-10

Identifiers

PMID24787713
PMCPMC4006898
OpenAlexW2039970602

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.