Evidence map›Paper›PMID 27849596›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Genome-wide screen identifies host colonization determinants in a bacterial gut symbiont.

J Elijah Powell, Sean P Leonard, Waldan K Kwong, Philipp Engel, Nancy A Moran

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
19.4field-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

93 citing papers in PubMed, 163 citations in OpenAlex.

  1. Article
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  7. Review
  8. Review
  9. Article
  10. The role of bacterial metabolism in human gut colonization.International microbiology : the official journal of the Spanish Society for Microbiology · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Type VI secretion systems promote intraspecific competition and host interactions in a bee gut symbiont.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

33 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

5 authors at 2 institutions in 1 country.

J Elijah PowellDepartment of Integrative Biology, University of Texas, Austin, TX 78712.
Sean P LeonardDepartment of Integrative Biology, University of Texas, Austin, TX 78712.
Waldan K KwongDepartment of Integrative Biology, University of Texas, Austin, TX 78712.
Philipp EngelDepartment of Ecology and Evolutionary Biology, Yale University, New Haven, CT 06520.
Nancy A MoranDepartment of Integrative Biology, University of Texas, Austin, TX 78712; nancy.moran@austin.utexas.edu.
The University of Texas at Austin · USYale University · US

Funding

Host and symbiont determinants of colonization by a co-evolved gut communityR01GM108477 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI MORAN, NANCY A. · 2014 to 2018
$1.4M
NIGMS NIH HHS R01 GM108477
6 · The paper itself

Abstract

Animal guts are often colonized by host-specialized bacterial species to the exclusion of other transient microorganisms, but the genetic basis of colonization ability is largely unknown. The bacterium Snodgrassella alvi is a dominant gut symbiont in honey bees, specialized in colonizing the hindgut epithelium. We developed methods for transposon-based mutagenesis in S. alvi and, using high-throughput DNA sequencing, screened genome-wide transposon insertion (Tn-seq) and transcriptome (RNA-seq) libraries to characterize both the essential genome and the genes facilitating host colonization. Comparison of Tn-seq results from laboratory cultures and from monoinoculated worker bees reveal that 519 of 2,226 protein-coding genes in S. alvi are essential in culture, whereas 399 are not essential but are beneficial for gut colonization. Genes facilitating colonization fall into three broad functional categories: extracellular interactions, metabolism, and stress responses. Extracellular components with strong fitness benefits in vivo include trimeric autotransporter adhesins, O antigens, and type IV pili (T4P). Experiments with T4P mutants establish that T4P in S. alvi likely function in attachment and biofilm formation, with knockouts experiencing a competitive disadvantage in vivo. Metabolic processes promoting colonization include essential amino acid biosynthesis and iron acquisition pathways, implying nutrient scarcity within the hindgut environment. Mechanisms to deal with various stressors, such as for the repair of double-stranded DNA breaks and protein quality control, are also critical in vivo. This genome-wide study identifies numerous genetic networks underlying colonization by a gut commensal in its native host environment, including some known from more targeted studies in other host-microbe symbioses.

Indexed as

AnimalsBeesBiofilmsDNA Breaks, Double-StrandedGammaproteobacteriaGastrointestinal MicrobiomeGastrointestinal TractGenome, InsectHigh-Throughput Nucleotide SequencingHost SpecificityMutagenesisPhylogenySymbiosisTranscriptomemicrobiotaNeisseriaceaesymbiosistransposon mutagenesistype IV pilus

Identifiers

PMID27849596
PMCPMC5137728
OpenAlexW2553306785

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.