Evidence map›Paper›PMID 42794758›Full record

ReviewInternational journal of molecular sciences2026

Antimicrobial Strategies in the Era of Resistance: It Is Too Early to Give Up Antibiotic Therapy.

Jennifer M Soares, Fernanda Alves, Koteswara Rao Yerra, Thalita H N Lima, Nadim Younes, Kate C Blanco, Vanderlei S Bagnato

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Jennifer M SoaresBiomedical Engineering, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0002-2978-7076
Fernanda AlvesBiomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Koteswara Rao YerraBiomedical Engineering, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0001-6063-904X
Thalita H N LimaBiomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Nadim YounesBiomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Kate C BlancoSão Carlos Institute of Physics, University of São Paulo, São Carlos 13566-590, SP, Brazil.
Vanderlei S BagnatoBiomedical Engineering, Texas A&M University, College Station, TX 77843, USA.ORCID 0000-0003-4833-239X

Funding

Brazilian Company for Research and Industrial InnovationBrazilian Federal Agency for Support and Evaluation of Graduate Education 001Cancer Prevention and Research Institute of Texas RR220054Chancellor's Research InitiativeGovernor's University Research InitiativeNational Council for Scientific and Technological Development 400468/2024-6São Paulo Research Foundation 2025/26084-6
6 · The paper itself

Abstract

The alarming rise of antimicrobial resistance constitutes a critical global health challenge, threatening the efficacy of conventional antibiotic therapies. Despite this crisis, abandoning antibiotics is premature; instead, a deliberate integration of traditional and emerging antimicrobial approaches is urgently required. The worldwide proliferation of resistant pathogens reflects decades of monotherapy, inadequate stewardship, and the persistent expectation that each new drug class would resolve resistance crises. This review provides a comprehensive overview of the fundamental mechanisms underlying antibiotic action and bacterial resistance, including reduced membrane permeability, efflux pump activity, target modification, and enzymatic inactivation. Building on this foundation, a broad spectrum of innovative antimicrobial strategies designed to complement or enhance antibiotic efficacy was critically examined. These approaches include natural products with intrinsic antimicrobial properties, immunotherapy to modulate host defenses, and antimicrobial photodynamic therapy (aPDT), which utilizes light-activated photosensitizers to generate reactive oxygen species and achieve localized microbial destruction. Notably, aPDT can overcome bacterial resistance, thereby restoring antibiotic effectiveness. Light delivery to infection sites is feasible across nearly all anatomical locations, whether by direct application, fiber optics, or endoscopic methods. Additional promising modalities, such as bacteriophage therapy, metallic and metal-oxide nanoparticles, and antimicrobial peptides (AMPs), are discussed with respect to their mechanisms, advantages, and translational potential. Collectively, these strategies represent a paradigm shift from antibiotic replacement to antibiotic revival and potentiation. By integrating multidisciplinary approaches, it is possible to extend the lifespan of current antibiotics while developing more robust, resistance-resilient therapies. The evidence presented confirms that antibiotic therapy remains an essential component of antimicrobial treatment, provided that it is supported by innovative, complementary technologies. Abandoning antibiotic therapy at this stage is unwarranted.

Indexed as

Anti-Bacterial AgentsBacteriaBacterial InfectionsDrug Resistance, BacterialAnimalsAntimicrobial PeptidesHumansPhotochemotherapyPhotosensitizing AgentsAnti-Bacterial AgentsAntimicrobial PeptidesPhotosensitizing Agentsalternative therapiesantibiotic resistancephotodynamic therapyphotosensitizers

Identifiers

PMID42794758
PMCPMC13607207

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.