Evidence map›Paper›PMID 37653008›Full record

ArticleNature microbiology2023

Single-cell massively-parallel multiplexed microbial sequencing (M3-seq) identifies rare bacterial populations and profiles phage infection.

Bruce Wang, Aaron E Lin, Jiayi Yuan, Katherine E Novak, Matthias D Koch, Ned S Wingreen, Britt Adamson, Zemer Gitai

Abstract read
In one paragraph

Article in Nature microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
–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

68 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  20. CBASS limits bacteriophage production while maintaining cell viability inbioRxiv : the preprint server for biology · 2026
    Article

8 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

8 authors.

Bruce WangLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0000-0003-4930-0998
Aaron E LinLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0000-0001-7400-4125
Jiayi YuanDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0009-0007-0121-4990
Katherine E NovakDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0009-0001-3564-9841
Matthias D KochLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA.ORCID http://orcid.org/0000-0003-4408-9900
Ned S WingreenLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA. wingreen@princeton.edu.ORCID http://orcid.org/0000-0001-7384-2821
Britt AdamsonLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA. badamson@princeton.edu.ORCID http://orcid.org/0000-0002-9451-5819
Zemer GitaiDepartment of Molecular Biology, Princeton University, Princeton, NJ, USA. zgitai@princeton.edu.ORCID http://orcid.org/0000-0002-3280-6178

Funding

Quantitavie and Computational Biology Graduate ProgramT32HG003284 · NHGRI · PRINCETON UNIVERSITY · PI Joshua Michael Akey, Stanislav Y. Shvartsman · 2004 to 2026
$9.9M
Small RNAs as Novel Modulators of Microbe-Host InteractionsR01AT011963 · NCCIH · PRINCETON UNIVERSITY · PI ABOU DONIA, MOHAMED, GITAI, ZEMER · 2021 to 2025
$7.5M
Thermally robust chemotaxis and thermotaxis in Escherichia coliR01GM082938 · NIGMS · PRINCETON UNIVERSITY · PI WINGREEN, NED S · 2008 to 2025
$5.5M
Mechano-microbiology: how physical forces control bacterial-host interactionsDP1AI124669 · NIAID · PRINCETON UNIVERSITY · PI GITAI, ZEMER · 2015 to 2019
$4.0M
Methods and Logic in Molecular Biology Training ProgramT32GM148739 · NIGMS · PRINCETON UNIVERSITY · PI Ileana M. Cristea · 2023 to 2026
$3.6M
NCCIH NIH HHS R01 AT011963NHGRI NIH HHS T32 HG003284NIAID NIH HHS DP1 AI124669NIGMS NIH HHS R01 GM082938NIGMS NIH HHS T32 GM148739
6 · The paper itself

Abstract

Bacterial populations are highly adaptive. They can respond to stress and survive in shifting environments. How the behaviours of individual bacteria vary during stress, however, is poorly understood. To identify and characterize rare bacterial subpopulations, technologies for single-cell transcriptional profiling have been developed. Existing approaches show some degree of limitation, for example, in terms of number of cells or transcripts that can be profiled. Due in part to these limitations, few conditions have been studied with these tools. Here we develop massively-parallel, multiplexed, microbial sequencing (M3-seq)-a single-cell RNA-sequencing platform for bacteria that pairs combinatorial cell indexing with post hoc rRNA depletion. We show that M3-seq can profile bacterial cells from different species under a range of conditions in single experiments. We then apply M3-seq to hundreds of thousands of cells, revealing rare populations and insights into bet-hedging associated with stress responses and characterizing phage infection.

Indexed as

BacteriophagesBacteriaHigh-Throughput Nucleotide SequencingRNA, RibosomalRNA, Ribosomal

Identifiers

PMID37653008
PMCPMC10522482

What OpenQuestion holds

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LicenceCC BY
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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.