Evidence map›Paper›PMID 40775282›Full record

ReviewBMC microbiology2025

Recent advances in the understanding, detection and therapeutic targeting of bacterial recalcitrance.

Elsa Roch, Jérémie Ducrocq, Nicolas Jacquier

Abstract readReview
In one paragraph

Review in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Current Insights into Antibiotic Resistance in UropathogenicAntibiotics (Basel, Switzerland) · 2025
    Review
  2. Review
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

3 authors.

Elsa Roch *School of Biology, University of Lausanne, Lausanne, 1015, Switzerland.
Jérémie Ducrocq *School of Biology, University of Lausanne, Lausanne, 1015, Switzerland.
Nicolas JacquierInstitute of Microbiology, University Hospital and University of Lausanne, Lausanne, 1011, Switzerland. nicolas.jacquier@chuv.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibiotic resistance is a growing threat for modern medicine, making treatment of infectious diseases increasingly tedious. However, even non-resistant bacteria can survive treatment and cause recurrent infections. This phenomenon is often due to non-proliferating bacteria able to survive the treatment and to resume infection afterwards, also called recalcitrant bacteria. Bacterial recalcitrance, which encompasses tolerance and persistence, is defined by increased survival of bacteria in the presence of antimicrobial agents. In contrast to resistance, the mechanisms underlying recalcitrance are only partially understood. In this review, we summarise the recent advances in the understanding of recalcitrance, its detection, as well as anti-recalcitrance therapies that have been developed. Recalcitrance is thought to be caused by a reduction of bacterial metabolism, mostly driven by stringent and SOS responses, leading to bacterial dormancy. These dormant bacteria escape the action of many antibiotics, preventing the complete resolution of infection. However, strategies have been proposed to tackle recalcitrance. Recalcitrant bacteria are susceptible to drugs whose action is independent of metabolic activity, such as membrane-targeting compounds. Inhibitors blocking the entry of bacteria into dormancy or locking bacteria in a permanent state of dormancy could help avoid recurrence of the infection. Dormant bacteria could also be forced to resume growth through supply of nutrients or signalling molecules. A phage specifically targeting dormant bacteria was recently described and may be an important tool to fight bacterial recalcitrance. Recalcitrance has been neglected for a long time, being in the shadow of resistance. However, both phenomena need to be further investigated in the future to develop a complete array of antibacterial agents that will allow to permanently eradicate all types of bacterial infections.

Indexed as

Bacterial InfectionsBacterial Physiological PhenomenaAnimalsBacteriaBiofilmsHumansAntibioticsAntimicrobial agentsBacterial persistenceBacterial toleranceBiofilmDormancyRecalcitranceSOS responseStringent response

Identifiers

PMID40775282
PMCPMC12333241

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.