Evidence map›Paper›PMID 36625642›Full record

ArticleAntimicrobial agents and chemotherapy2023

High-Resolution Bacterial Cytological Profiling Reveals Intrapopulation Morphological Variations upon Antibiotic Exposure.

Thanadon Samernate, Htut Htut Htoo, Joseph Sugie, Warinthorn Chavasiri, Joe Pogliano, Vorrapon Chaikeeratisak, Poochit Nonejuie

Open access · greenAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
5.4field-weighted citation impact, top 5% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Synthesis of Ag/TiOScientific reports · 2026
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  9. Sensing of Antibiotic-Bacteria Interactions.Antibiotics (Basel, Switzerland) · 2023
    Review
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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

7 authors at 3 institutions in 2 countries.

Thanadon SamernateInstitute of Molecular Biosciences, Mahidol University, Nakhon Pathom, Thailand.
Htut Htut HtooInstitute of Molecular Biosciences, Mahidol University, Nakhon Pathom, Thailand.
Joseph SugieDivision of Biological Sciences, University of California, San Diego, La Jolla, California, USA.
Warinthorn ChavasiriCenter of Excellence in Natural Products Chemistry, Department of Chemistry, Chulalongkorn University, Bangkok, Thailand.
Joe PoglianoDivision of Biological Sciences, University of California, San Diego, La Jolla, California, USA.
Vorrapon ChaikeeratisakDepartment of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.ORCID 0000-0003-2793-5394
Poochit NonejuieInstitute of Molecular Biosciences, Mahidol University, Nakhon Pathom, Thailand.ORCID 0000-0002-5130-1749
Mahidol University · THChulalongkorn University · THUniversity of California San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phenotypic heterogeneity is crucial to bacterial survival and could provide insights into the mechanism of action (MOA) of antibiotics, especially those with polypharmacological actions. Although phenotypic changes among individual cells could be detected by existing profiling methods, due to the data complexity, only population average data were commonly used, thereby overlooking the heterogeneity. In this study, we developed a high-resolution bacterial cytological profiling method that can capture morphological variations of bacteria upon antibiotic treatment. With an unprecedented single-cell resolution, this method classifies morphological changes of individual cells into known MOAs with an overall accuracy above 90%. We next showed that combinations of two antibiotics induce altered cell morphologies that are either unique or similar to that of an antibiotic in the combinations. With these combinatorial profiles, this method successfully revealed multiple cytological changes caused by a natural product-derived compound that, by itself, is inactive against Acinetobacter baumannii but synergistically exerts its multiple antibacterial activities in the presence of colistin. The findings have paved the way for future single-cell profiling in bacteria and have highlighted previously underappreciated intrapopulation variations caused by antibiotic perturbation.

Indexed as

Acinetobacter baumanniiAnti-Bacterial AgentsBacteriaColistinDrug Resistance, Multiple, BacterialMicrobial Sensitivity TestsAnti-Bacterial AgentsColistinantibiotic combinationshigh-content analysisphenotypic heterogeneitysingle-cell profiling

Identifiers

PMID36625642
PMCPMC9933734
OpenAlexW4315435716

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.