Evidence map›Paper›PMID 29486796›Full record

Trial reportMicrobiome2018

Differential human gut microbiome assemblages during soil-transmitted helminth infections in Indonesia and Liberia.

Bruce A Rosa, Taniawati Supali, Lincoln Gankpala, Yenny Djuardi, Erliyani Sartono, Yanjiao Zhou, Kerstin Fischer, John Martin, Rahul Tyagi, Fatorma K Bolay and 3 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Microbiome, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 4 pooled it
7.1field-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

94 citing papers in PubMed, 4 syntheses or guidelines pooled it, 165 citations in OpenAlex.

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  16. AdultCurrent research in parasitology & vector-borne diseases · 2026
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34 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

13 authors at 6 institutions in 4 countries.

Bruce A RosaMcDonnell Genome Institute, Washington University, St. Louis, MO, 63108, USA.
Taniawati SupaliDepartment of Parasitology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Lincoln GankpalaPublic Health and Medical Research, National Public Health Institute of Liberia, Charlesville, Liberia.
Yenny DjuardiDepartment of Parasitology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Erliyani SartonoDepartment of Parasitology, Leiden University Medical Center, Leiden, The Netherlands.
Yanjiao ZhouMicrobial Genomics, The Jackson Laboratory for Genomic Medicine, Farmington, CT, USA.
Kerstin FischerDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
John MartinMcDonnell Genome Institute, Washington University, St. Louis, MO, 63108, USA.
Rahul TyagiMcDonnell Genome Institute, Washington University, St. Louis, MO, 63108, USA.
Fatorma K BolayPublic Health and Medical Research, National Public Health Institute of Liberia, Charlesville, Liberia.
Peter U FischerDepartment of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Maria YazdanbakhshDepartment of Parasitology, Leiden University Medical Center, Leiden, The Netherlands.
Makedonka MitrevaMcDonnell Genome Institute, Washington University, St. Louis, MO, 63108, USA. mmitreva@wustl.edu.
James S. McDonnell Foundation · USWashington University in St. Louis · USLeiden University Medical Center · NLNational Public Health Institute of Liberia · LRUniversity of Indonesia · IDJackson Laboratory · US

Funding

Large Scale Genome SequencingU54HG003079 · NHGRI · WASHINGTON UNIVERSITY · PI DUTCHER, SUSAN K · 2004 to 2016
$445.7M
COMPARATIVE GENOMICS OF PARASITIC NEMATODESR01AI081803 · NIAID · WASHINGTON UNIVERSITY · PI MITREVA, MAKEDONKA · 2009 to 2018
$3.1M
COMPARATIVE GENOMICS OF PARASITIC NEMATODESR56AI081803 · NIAID · WASHINGTON UNIVERSITY · PI MITREVA, MAKEDONKA · 2019 to 2019
$697k
NHGRI NIH HHS U54 HG003079NIAID NIH HHS R01 AI081803NIAID NIH HHS R56 AI081803
6 · The paper itself

Abstract

backgroundThe human intestine and its microbiota is the most common infection site for soil-transmitted helminths (STHs), which affect the well-being of ~ 1.5 billion people worldwide. The complex cross-kingdom interactions are not well understood.

resultsA cross-sectional analysis identified conserved microbial signatures positively or negatively associated with STH infections across Liberia and Indonesia, and longitudinal samples analysis from a double-blind randomized trial showed that the gut microbiota responds to deworming but does not transition closer to the uninfected state. The microbiomes of individuals able to self-clear the infection had more alike microbiome assemblages compared to individuals who remained infected. One bacterial taxon (Lachnospiracae) was negatively associated with infection in both countries, and 12 bacterial taxa were significantly associated with STH infection in both countries, including Olsenella (associated with reduced gut inflammation), which also significantly reduced in abundance following clearance of infection. Microbial community gene abundances were also affected by deworming. Functional categories identified as associated with STH infection included arachidonic acid metabolism; arachidonic acid is the precursor for pro-inflammatory leukotrienes that threaten helminth survival, and our findings suggest that some modulation of arachidonic acid activity in the STH-infected gut may occur through the increase of arachidonic acid metabolizing bacteria.

conclusionsFor the first time, we identify specific members of the gut microbiome that discriminate between moderately/heavily STH-infected and non-infected states across very diverse geographical regions using two different statistical methods. We also identify microbiome-encoded biological functions associated with the STH infections, which are associated potentially with STH survival strategies, and changes in the host environment. These results provide a novel insight of the cross-kingdom interactions in the human gut ecosystem by unlocking the microbiome assemblages at taxonomic, genetic, and functional levels so that advances towards key mechanistic studies can be made.

Indexed as

AdolescentAdultAnimalsArachidonic AcidChildCross-Sectional StudiesDouble-Blind MethodEubacterialesFecesFemaleGastrointestinal MicrobiomeHelminthiasisHelminthsHumansIndonesiaIntestinesArachidonic AcidRNA, Ribosomal, 16SSoil16S rRNA geneHelminthIntestineMetagenomeMicrobiotaNematodeParasite

Identifiers

PMID29486796
PMCPMC6389212
OpenAlexW2788177313

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.