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ORIGINAL RESEARCH article

Front. Cell. Infect. Microbiol.
Sec. Clinical Microbiology
Volume 14 - 2024 | doi: 10.3389/fcimb.2024.1412007
This article is part of the Research Topic Global Excellence in Clinical + Immune Microbiology: North America View all articles

Analysis of in vitro expression of virulence genes related to antibiotic and disinfectant resistance in Escherichia coli as an emerging periodontal pathogen

Provisionally accepted
Eric Monroy-Pérez Eric Monroy-Pérez 1*Tania Hernández-Jaimes Tania Hernández-Jaimes 1*Rosario Morales-Espinosa Rosario Morales-Espinosa 1Gabriela Delgado Gabriela Delgado 1Hector Martínez-Gregorio Hector Martínez-Gregorio 1*Luis Rey García-Cortés Luis Rey García-Cortés 2*Jennefer Paloma Herrera-Gabriel Jennefer Paloma Herrera-Gabriel 1*Andrea De Lira-Silva Andrea De Lira-Silva 1*Felipe V. Paniagua Felipe V. Paniagua 1Gloria Luz Paniagua-Contreras Gloria Luz Paniagua-Contreras 1*
  • 1 National Autonomous University of Mexico, México City, Mexico
  • 2 Mexican Social Security Institute, Mexico City, México, Mexico

The final, formatted version of the article will be published soon.

    The collective involvement of virulence markers of Escherichia coli as an emerging pathogen associated with periodontitis remains unexplained. This study aimed to implement an in vitro model of infection using a human epithelial cell line to determine the virulome expression related to the antibiotic and disinfectant resistance genotype and pulse field gel electrophoresis (PFGE) type in E. coli strains isolated from patients with periodontal diseases. We studied 100 strains of E. coli isolated from patients with gingivitis (n = 12), moderate periodontitis (n = 59), and chronic periodontitis (n = 29). The identification of E. coli and antibiotic and disinfectant resistance genes was performed through PCR. To promote the expression of virulence genes in the strains, an in vitro infection model was used in the human epithelial cell line A549. RNA was extracted using the QIAcube robotic equipment and reverse transcription to cDNA was performed using the QuantiTect reverse transcription kit (Qiagen). The determination of virulence gene expression was performed through real-time PCR. Overall, the most frequently expressed adhesion genes among the isolated strains of gingivitis, moderate periodontitis, and chronic periodontitis were fimH (48%), iha (37%), and papA (18%); those for toxins were usp (33%); those for iron acquisition were feoB (84%), fyuA (62%), irp-2 (61%), and iroN (35%); those for protectins were traT (50%), KpsMT (35%), and ompT (28%); and those for pathogenicity islands were malX (45%). The most common antibiotic and disinfectant resistance genes among gingivitis, moderate periodontitis, and chronic periodontitis strains were sul-2 (43%), blaSHV (47%), blaTEM (45%), tet(A) (41%), dfrA1 (32%), marR-marO (57%), and qacEA1 (79%). The findings revealed the existence of a wide distribution of virulome expression profiles related to the antibiotic and disinfectant resistance genotype and PFGE type in periodontal strains of E. coli. These findings may contribute toward improving the prevention and treatment measures for periodontal diseases associated with E. coli.

    Keywords: Periodontitis, Escherichia coli, Expression of virulence genes, antibiotic and disinfectant resistance genes, real-time PCR were statistically significant 963 964 965

    Received: 04 Apr 2024; Accepted: 25 Jul 2024.

    Copyright: © 2024 Monroy-Pérez, Hernández-Jaimes, Morales-Espinosa, Delgado, Martínez-Gregorio, García-Cortés, Herrera-Gabriel, De Lira-Silva, Paniagua and Paniagua-Contreras. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Eric Monroy-Pérez, National Autonomous University of Mexico, México City, Mexico
    Tania Hernández-Jaimes, National Autonomous University of Mexico, México City, Mexico
    Hector Martínez-Gregorio, National Autonomous University of Mexico, México City, Mexico
    Luis Rey García-Cortés, Mexican Social Security Institute, Mexico City, 06600, México, Mexico
    Jennefer Paloma Herrera-Gabriel, National Autonomous University of Mexico, México City, Mexico
    Andrea De Lira-Silva, National Autonomous University of Mexico, México City, Mexico
    Gloria Luz Paniagua-Contreras, National Autonomous University of Mexico, México City, Mexico

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