Evidence map›Paper›PMID 42611360›Full record

ReviewBrazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]2026

Genetic architecture and functional dynamics of integrons in Staphylococcus aureus resistance.

Anjaneyulu Musini, Madeeha Owais, Rerelly Joshika

Abstract readReview
In one paragraph

Review in Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology], 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

3 authors.

Anjaneyulu MusiniCentre for Biotechnology, University College of Engineering, Science and Technology Hyderabad (UCESTH), Jawaharlal Nehru Technological University Hyderabad, Hyderabad, Telangana, 500085, India. manjaneyulu@jntuh.ac.in.ORCID http://orcid.org/0000-0002-2205-2616
Madeeha OwaisCentre for Biotechnology, University College of Engineering, Science and Technology Hyderabad (UCESTH), Jawaharlal Nehru Technological University Hyderabad, Hyderabad, Telangana, 500085, India.
Rerelly JoshikaCentre for Biotechnology, University College of Engineering, Science and Technology Hyderabad (UCESTH), Jawaharlal Nehru Technological University Hyderabad, Hyderabad, Telangana, 500085, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Staphylococcus aureus is a major opportunistic pathogen and a leading cause of community and hospital-acquired infections worldwide, with a growing capacity to develop multidrug resistance (MDR). Among the genetic mechanisms driving this resistance, integrons play a critical role by capturing, rearranging, and expressing antimicrobial resistance gene cassettes through site-specific recombination. Although integrons are traditionally associated with Gram-negative bacteria, increasing evidence highlights their significant contribution to resistance dissemination in S. aureus, particularly in methicillin-resistant S. aureus (MRSA) strains. This review focuses on current knowledge on the structure, function, and types of integrons, and their role in prevalence and mechanistic role in S. aureus. Integrons interact with other mobile genetic elements like transposons and plasmids to enable horizontal gene transfer across strains and species. Among the four recognized classes of integrons, class 1 is the most prevalent in S. aureus frequently associated with plasmids and transposons and show resistance to β-lactams, aminoglycosides, fluoroquinolones, and tetracyclines. Class 2 integrons occur less commonly and exhibit limited cassette diversity, while class 3 integrons remain rare. Epidemiological studies report class 1 integron prevalence ranging from 40 to 70% in clinical isolates across different regions, often correlating with resistance to β-lactams, aminoglycosides, fluoroquinolones, tetracyclines, and rifampicin, and co-occurring with SCCmec elements in MRSA. Integron-mediated resistance is further enhanced by stress-induced integrase activity and biofilm formation, promoting persistence in healthcare settings. Molecular detection methods, particularly multiplex PCR targeting integrase genes, are essential for surveillance. Understanding integron dynamics in S. aureus is crucial for informing antimicrobial stewardship, infection control strategies, and future interventions aimed at limiting the spread of MDR pathogens.

Indexed as

Drug Resistance, Multiple, BacterialIntegronsStaphylococcal InfectionsStaphylococcus aureusAnti-Bacterial AgentsGene Transfer, HorizontalHumansAnti-Bacterial AgentsGene cassettesHorizontal gene transferMethicillin-resistant Staphylococcus aureus (MRSA)Mobile genetic elementsMulti-drug resistance

Identifiers

PMID42611360
PMCPMC13486446

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.