Evidence map›Paper›PMID 36823286›Full record

ArticleNature microbiology2023

Mycobacterial nucleoid-associated protein Lsr2 is required for productive mycobacteriophage infection.

Charles L Dulberger, Carlos A Guerrero-Bustamante, Siân V Owen, Sean Wilson, Michael G Wuo, Rebecca A Garlena, Lexi A Serpa, Daniel A Russell, Junhao Zhu, Ben J Braunecker and 6 more

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 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. Article
  2. Activity of a three-phage combination againstbioRxiv : the preprint server for biology · 2026
    Article
  3. Smooth-to-rough morphotype switching, a mechanism of phage resistance inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. The role of colony morphotype in shaping gene essentiality inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  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.

Charles L Dulberger *Department of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USA.ORCID 0000-0002-1334-5468
Carlos A Guerrero-Bustamante *Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0002-7256-5188
Siân V OwenDepartment of Biomedical Informatics and Laboratory of Systems Pharmacology, Harvard Medical School, Boston, MA, USA.
Sean WilsonDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.ORCID 0000-0002-7216-9804
Michael G WuoDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, USA.
Rebecca A GarlenaDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
Lexi A SerpaDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, PA, USA.
Daniel A RussellDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0001-6894-2748
Junhao ZhuDepartment of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USA.ORCID 0000-0002-3301-5677
Ben J BrauneckerDepartment of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
Georgia R SquyresDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.ORCID 0000-0002-8717-2897
Michael BaymDepartment of Biomedical Informatics and Laboratory of Systems Pharmacology, Harvard Medical School, Boston, MA, USA.ORCID 0000-0003-1303-5598
Laura L KiesslingDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID 0000-0001-6829-1500
Ethan C GarnerDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.ORCID 0000-0003-0141-3555
Eric J RubinDepartment of Immunology and Infectious Diseases, Harvard T. H. Chan School of Public Health, Boston, MA, USA. erubin@hsph.harvard.edu.ORCID 0000-0001-5120-962X
Graham F HatfullDepartment of Biological Sciences, University of Pittsburgh, Pittsburgh, PA, USA. gfh@pitt.edu.ORCID 0000-0002-6705-6821

Funding

The Chemistry and Biology of Galactofuranose-Containing GlycansR01AI126592 · NIAID · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Laura L Kiessling · 2017 to 2026
$5.2M
Bacteriophage diversity, dynamics, function, and exploitationR35GM131729 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Graham F. Hatfull · 2019 to 2026
$3.6M
Evolutionary Tradeoffs in Antibiotic ResistanceR35GM133700 · NIGMS · HARVARD MEDICAL SCHOOL · PI BAYM, MICHAEL · 2019 to 2023
$2.4M
Phage resistance in Mycobacterium tuberculosisR21AI156791 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HATFULL, GRAHAM F. · 2021 to 2022
$396k
Howard Hughes Medical Institute (HHMI) GT12053NIAID NIH HHS R01 AI126592NIAID NIH HHS R21 AI156791NIGMS NIH HHS R35 GM131729NIGMS NIH HHS R35 GM133700U.S. Department of Health & Human Services | National Institutes of Health (NIH) AI51264U.S. Department of Health & Human Services | National Institutes of Health (NIH) AI56772
6 · The paper itself

Abstract

Mycobacteriophages are a diverse group of viruses infecting Mycobacterium with substantial therapeutic potential. However, as this potential becomes realized, the molecular details of phage infection and mechanisms of resistance remain ill-defined. Here we use live-cell fluorescence microscopy to visualize the spatiotemporal dynamics of mycobacteriophage infection in single cells and populations, showing that infection is dependent on the host nucleoid-associated Lsr2 protein. Mycobacteriophages preferentially adsorb at Mycobacterium smegmatis sites of new cell wall synthesis and following DNA injection, Lsr2 reorganizes away from host replication foci to establish zones of phage DNA replication (ZOPR). Cells lacking Lsr2 proceed through to cell lysis when infected but fail to generate consecutive phage bursts that trigger epidemic spread of phage particles to neighbouring cells. Many mycobacteriophages code for their own Lsr2-related proteins, and although their roles are unknown, they do not rescue the loss of host Lsr2.

Indexed as

BacteriophagesMycobacteriophagesMycobacteriumMycobacterium smegmatis

Identifiers

PMID36823286
PMCPMC10066036

What OpenQuestion holds

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Registered trials

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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.