Evidence map›Paper›PMID 36527020›Full record

ArticleBMC biology2022

Construction and characterization of a genome-scale ordered mutant collection of Bacteroides thetaiotaomicron.

Heidi A Arjes, Jiawei Sun, Hualan Liu, Taylor H Nguyen, Rebecca N Culver, Arianna I Celis, Sophie Jean Walton, Kimberly S Vasquez, Feiqiao Brian Yu, Katherine S Xue and 6 more

Abstract read
In one paragraph

Article in BMC biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. CRISPR/Cas9-based nanodelivery systems for precision gene editing in neuroinflammation.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  2. Article
  3. Genomic instability and biofilm determinants inbioRxiv : the preprint server for biology · 2026
    Article
  4. Identification and characterization of the functional LolB ortholog inbioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Arylsulfamates inhibit colonic Bacteroidota growth through a sulfatase-independent mechanism.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
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

16 authors.

Heidi A Arjes *Department of Bioengineering, Stanford University, Stanford, CA, USA.
Jiawei Sun *Department of Bioengineering, Stanford University, Stanford, CA, USA.
Hualan LiuEnvironmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Taylor H NguyenDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Rebecca N CulverDepartment of Genetics, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Arianna I CelisDepartment of Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Sophie Jean WaltonBiophysics Training Program, Stanford University School of Medicine, Stanford, CA, USA.
Kimberly S VasquezDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Feiqiao Brian YuChan Zuckerberg Biohub, San Francisco, CA, 94158, USA.
Katherine S XueDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Daniel NewtonDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Ricardo ZermenoStanford Shared FACS Facility, Center for Molecular and Genetic Medicine, Stanford University, Stanford, CA, USA.
Meredith WeglarzStanford Shared FACS Facility, Center for Molecular and Genetic Medicine, Stanford University, Stanford, CA, USA.
Adam DeutschbauerEnvironmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.
Kerwyn Casey HuangDepartment of Bioengineering, Stanford University, Stanford, CA, USA. kchuang@stanford.edu.ORCID 0000-0002-8043-8138
Anthony L ShiverDepartment of Bioengineering, Stanford University, Stanford, CA, USA. ashiver@stanford.edu.

Funding

A universal pipeline for functional characterization of the human microbiota at a massive scaleRM1GM135102 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI BUIE, CULLEN RICHARD, DEUTSCHBAUER, ADAM M · 2020 to 2024
$7.6M
Antimicrobial Resistance and Horizontal Gene Transfer in the Human Gut Microbiome in Response to an AntibioticR01AI147023 · NIAID · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI RELMAN, DAVID A. · 2020 to 2024
$3.5M
NIAID NIH HHS R01 AI147023NIGMS NIH HHS RM1 GM135102
6 · The paper itself

Abstract

backgroundOrdered transposon-insertion collections, in which specific transposon-insertion mutants are stored as monocultures in a genome-scale collection, represent a promising tool for genetic dissection of human gut microbiota members. However, publicly available collections are scarce and the construction methodology remains in early stages of development.

resultsHere, we describe the assembly of a genome-scale ordered collection of transposon-insertion mutants in the model gut anaerobe Bacteroides thetaiotaomicron VPI-5482 that we created as a resource for the research community. We used flow cytometry to sort single cells from a pooled library, located mutants within this initial progenitor collection by applying a pooling strategy with barcode sequencing, and re-arrayed specific mutants to create a condensed collection with single-insertion strains covering >2500 genes. To demonstrate the potential of the condensed collection for phenotypic screening, we analyzed growth dynamics and cell morphology. We identified both growth defects and altered cell shape in mutants disrupting sphingolipid synthesis and thiamine scavenging. Finally, we analyzed the process of assembling the B. theta condensed collection to identify inefficiencies that limited coverage. We demonstrate as part of this analysis that the process of assembling an ordered collection can be accurately modeled using barcode sequencing data.

conclusionWe expect that utilization of this ordered collection will accelerate research into B. theta physiology and that lessons learned while assembling the collection will inform future efforts to assemble ordered mutant collections for an increasing number of gut microbiota members.

Indexed as

Bacteroides thetaiotaomicronDNA Transposable ElementsGene LibraryGenome, BacterialHumansMutagenesis, InsertionalDNA Transposable ElementsBarSeqB. thetaCell growthCell morphologyMicrobiomeMicrobiotaOrdered libraryRB-TnSeqSphingolipid synthesisThiamine scavengingTransposon mutagenesis

Identifiers

PMID36527020
PMCPMC9758874

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.