Evidence map›Paper›PMID 42388494›Full record

ReviewFrontiers in medicine2026

Bacterial mutation dynamics emerging insights into virulence evolution and drug resistance. A review study.

Sulaiman A Alsalamah

Abstract readReview
In one paragraph

Review in Frontiers in medicine, 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

1 author.

Sulaiman A AlsalamahDepartment of Biology, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Bacterial mutations are a fundamental driver of microbial evolution, enabling rapid adaptation to environmental stress and antimicrobial exposure. Genetic alterations may arise spontaneously or be induced by physical, chemical, or biological factors, generating phenotypic diversity that influences virulence, pathogenicity, and antimicrobial resistance. Understanding mutation dynamics is essential for predicting bacterial adaptation and addressing the growing threat of antimicrobial resistance. Methods: This review synthesizes current knowledge on the molecular mechanisms, evolutionary patterns, and biological consequences of bacterial mutations. Relevant literature was examined to evaluate the roles of spontaneous and induced mutations, mutational biases, virulence evolution, and antimicrobial resistance development. Emerging genomic technologies used to investigate mutation dynamics were also assessed. Results and Discussion: Evidence indicates that bacterial mutations contribute significantly to adaptive evolution by generating genetic variation upon which natural selection acts. Although mutations are undirected with respect to fitness, their distribution across genomes is influenced by mutational biases and DNA repair mechanisms. Mutation-driven genetic changes were found to play a critical role in enhancing virulence traits and promoting antimicrobial resistance. Furthermore, advanced genomic approaches, including CRISPR-based genome editing and single-cell sequencing, have expanded the ability to characterize mutation processes at high resolution. The findings highlight the importance of understanding both the mechanisms and biases of bacterial mutations in shaping evolutionary trajectories. The interplay between mutation-driven virulence evolution and antimicrobial resistance underscores the need for continued surveillance and molecular investigation. Emerging genomic technologies offer promising opportunities to predict bacterial adaptation and develop innovative strategies for controlling drug-resistant pathogens.

Indexed as

antimicrobial resistancebacterial mutationsmutationvirulencevirulence determinants

Identifiers

PMID42388494
PMCPMC13318777

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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.