Evidence map›Paper›PMID 41838180›Full record

ArticleCurrent microbiology2026

Multi-replicon Architecture Drives the Global Accumulation of Resistance to Antimicrobials, Biocides, and Metals in IncF and IncH Plasmids.

Hannay Crystynah Almeida de Souza, Arlen Carvalho de Oliveira Almeida, Carlos Adam ConteJunior, Pedro Panzenhagen

Abstract read
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Article in Current 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.

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0citing papers in PubMed
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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

4 authors.

Hannay Crystynah Almeida de SouzaCenter for Food Analysis (NAL), Technological Development Support Laboratory (LADETEC), Federal University of Rio de Janeiro (UFRJ), Cidade Universitária, Rio de Janeiro, 21941-598, Brazil.
Arlen Carvalho de Oliveira AlmeidaCenter for Food Analysis (NAL), Technological Development Support Laboratory (LADETEC), Federal University of Rio de Janeiro (UFRJ), Cidade Universitária, Rio de Janeiro, 21941-598, Brazil.
Carlos Adam ConteJuniorCenter for Food Analysis (NAL), Technological Development Support Laboratory (LADETEC), Federal University of Rio de Janeiro (UFRJ), Cidade Universitária, Rio de Janeiro, 21941-598, Brazil.
Pedro PanzenhagenGraduate Program in Biochemistry (PPGBq), Institute of Chemistry (IQ), Federal University of Rio de Janeiro (UFRJ), Cidade Universitária, Rio de Janeiro, 21941-909, RJ, Brazil. pedropanzen@iq.ufrj.br.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmids are major vectors driving the environmental dissemination of antimicrobial resistance (AMR) and other stress-resistance traits. The convergence between AMR and tolerance to multiple environmental stressors has become increasingly concerning, as these interactions intensify horizontal gene transfer and enhance plasmid conjugation. In this study, we investigated whether the co-occurrence of resistance determinants against different stressors results from random aggregation or statistically meaningful associations. We analyzed 25,116 complete plasmids from PLSDB and applied multivariate correspondence analysis to examine relationships between incompatibility groups and resistance categories. Pairwise co-occurrence patterns among resistance genes were assessed using Fisher's exact test to determine whether their distribution deviated from randomness. IncF and IncH plasmids emerged as the incompatibility groups most strongly enriched in multidrug resistance, showing a marked tendency to co-carry genes conferring tolerance to antimicrobials, biocides, and metals-traits highly relevant under environmental co-selection. While pairwise tests did not reveal significant associations between specific gene pairs, the broader patterns of resistance accumulation highlight the structural evolution of plasmids via multireplicon cointegration as a primary mechanism for multi-stressor resistance. Our findings underscore the ecological importance of multireplicon plasmids, particularly those involving IncF and IncH, as high-risk vectors that sustain multi-stressor resistance in microbial communities.

Indexed as

Anti-Bacterial AgentsAnti-Infective AgentsBacteriaDisinfectantsDrug Resistance, BacterialDrug Resistance, Multiple, BacterialMetalsPlasmidsRepliconGene Transfer, HorizontalAnti-Bacterial AgentsAnti-Infective AgentsDisinfectantsMetals

Identifiers

PMID41838180
PMCPMC12992427

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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.