Rapid and efficient labeling by a selective organic fluorophore probe highlights heterogeneity of mycobacterial populations and persister resuscitation

Priyanka Chauhan, Sander van Otterdijk, Susanna Commandeur, Dirk Bald*, Frank J. Bruggeman*

*Corresponding author for this work

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Stress tolerant slow- or non-growing bacterial subpopulations represent a key factor for chronic, recurrent, antibiotic-tolerant infections and necessitate prolonged antibiotic therapy. Consequently, new tools that facilitate investigation of these small subpopulations are highly needed. To characterize slow-/non-growing populations of mycobacteria, we here utilized Vybrant DiD, a lipophilic, fluorescent organic probe that detected pathogenic and non-pathogenic species in a rapid, specific and noninvasive manner. It enabled accurate, direct quantification of mycobacterial replication rate in vitro and in murine macrophages at the population and single-cell level, providing insight into population heterogeneity. We determined the preexisting slow-/ non-growing fraction of mycobacteria during exponential growth, which increased upon stress. Monitoring mycobacterial resuscitation after antibacterial treatment and after low-oxygen-induced dormancy revealed the stochastic and heterogeneous nature of the resuscitation process. We anticipate that this method will be widely utilized in basic research on bacterial persistence and may also be included in applied settings, e.g., high-throughput drug characterization.

Original languageEnglish
Article numbere0338563
Pages (from-to)1-23
Number of pages23
JournalPLoS ONE
Volume20
Issue number12
Early online date18 Dec 2025
DOIs
Publication statusPublished - Dec 2025

Bibliographical note

Publisher Copyright:
© 2025 Chauhan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Funding

This project has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement no. 713669. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors wish to thank Prof. Holger Lill and Prof. Wilbert Bitter for insightful discussions, Dr. Sieze Douwenga for helping with the initial screening of suitable probe for study, Alicia Berkvens for helping with data analysis, Dr. Evelina Tutucci for helping with microscopy and related data analysis, and Emile Zwering for technical assistance.

FundersFunder number
Horizon 2020 Framework Programme713669

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