Evidence map›Paper›PMID 40924186›Full record

ArticleArchives of microbiology2025

Escherichia coli strain O55 contains two cryptic plasmids that depend on each other to replicate.

José A Martínez-Álvarez, Sandra Ethelvina Coria-Alcaraz, Fátima Berenice Ramírez-Montiel, Ana Laura Medina-Nieto, Sairy Yarely Andrade-Guillen, Fátima Tornero- Gutiérrez, Ángeles Rangel-Serrano, Naurú Idalia Vargas-Maya, Rodolfo García-Contreras, Felipe Padilla-Vaca and 1 more

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Article in Archives of microbiology, 2025. 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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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

José A Martínez-ÁlvarezDivisión de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Sandra Ethelvina Coria-AlcarazDivisión de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Fátima Berenice Ramírez-MontielDivisión de Ciencias Naturales y Exactas, Departamento de Farmacia, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Ana Laura Medina-NietoDivisión de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Sairy Yarely Andrade-GuillenDivisión de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Fátima Tornero- GutiérrezDivisión de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Ángeles Rangel-SerranoDivisión de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Naurú Idalia Vargas-MayaDivisión de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico.
Rodolfo García-ContrerasDepartamento de Microbiología y Parasitología, Facultad de Medicina, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Felipe Padilla-VacaDivisión de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico. padillaf@ugto.mx.
Bernardo FrancoDivisión de Ciencias Naturales y Exactas, Departamento de Biología, Universidad de Guanajuato, Zip Code 36050, Guanajuato, Mexico. bfranco@ugto.mx.

Funding

Consejo Nacional de Humanidades, Ciencias y Tecnologías CF 2023-G-1274
6 · The paper itself

Abstract

Plasmids are fundamental to molecular biology and biotechnology, playing a crucial role in bacterial evolution. Some plasmids are linked to complex cellular dynamics, including pathogenicity islands, antibiotic resistance, and gene mobilization. This study reports the isolation and sequencing of two cryptic plasmids with different electrophoretic mobilities from the Escherichia coli clinical isolate O55. This strain was isolated based on its capacity to bind mannoses on the surface of yeast cells, a property that could be counteracted with methyl α-D-mannoside, a feature used to characterize yeast cell agglutination and, more recently, to assess virulence in Entamoeba histolytica. The strain exhibited no growth differences compared to the laboratory strain E. coli BW25113. Attempts to transform the plasmids independently were unsuccessful; however, they remained stable when the cells were co-transformed. Sequence analysis revealed that both plasmids have conserved counterparts in GenBank (over 100 sequences in Enterobacteriaceae) and can be classified into two distinct groups, regardless of host strain or species. Additionally, in E. coli and Klebsiella pneumoniae isolates, the smaller plasmid was identified as an integrated copy into the genome, aligning with the observation that the plasmids cannot be maintained separately. ORF content analysis identified only putative proteins except for two, one associated with the resistance to aminoglycosides (a functional aminoglycoside O-phosphotransferase), a putative sulfonamide resistance gene, and another associated with a replication protein, suggesting that one plasmid regulates the replication of the other based on AlphaFold3 DNA-protein models. Our findings underscore the importance of further analyzing plasmids in next-generation sequencing data from clinical samples to enhance our understanding of plasmid biology and their impact on the dissemination of pathogenesis-related traits in bacteria.

Indexed as

DNA ReplicationEscherichia coliPlasmidsEscherichia coli InfectionsHumansKlebsiella pneumoniaeCell growthClinical isolateEscherichia coliPhenotypePlasmidProtein modelling

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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.