Research Article | | Peer-Reviewed

High Prevalence of Virulence Genes and in Vitro Biofilm Production in Clinical Multidrug-Resistant Escherichia coli in Dakar Senegal

Received: 28 September 2023    Accepted: 20 October 2023    Published: 31 October 2023
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Abstract

Bacterial virulence is a key factor determining the outcome of each bacterial infection, and virulent bacteria are often associated with high-risk infections. Thus, this study aimed to screen for virulence genes and evaluate the in vitro biofilm formation capacity of multidrug-resistant Escherichia coli isolated in Dakar. For the 16 virulence genes identified by standard polymerase chain reaction (PCR), all 78 ExPEC isolates carried at least four virulence genes. The prevalence of virulence genes was as follows: adhesin genes fimH (98.7%), mrkD (98.7%), papC (46.2%), afaC (9%), and sfa/focDE (1.3%); iron acquisition system genes entB (98.7%), fepA (98.7%), ybtS (93.6%), fyuA (91%), iucA (91%), iucB (91%), iutA (34.6), iroB (6.4%), iroN (6.4%), and toxin genes hlyA (10.3%) and cnf (1 & 2) (10.3%). Seventy-five of the 78 isolates (96.2%) carried at least two adhesin genes and two iron capture system genes. Evaluation of the biofilm formation capacity revealed that all (29/29) hospital-acquired isolates were biofilm producers with (6/29; 20.7%) strong biofilm producers, (15/29; 51.7%) moderate biofilm producers and (8/29; 27.6%) weak biofilm producers. Hospital-acquired isolates carrying papC had a greater biofilm formation capacity than those lacking papC (p < 0.001). The deepening of this type of study on bacterial virulence and hospital bacterial biofilms could lead to improvements in infection investigation, prevention, and therapeutic protocols.

Published in International Journal of Microbiology and Biotechnology (Volume 8, Issue 4)
DOI 10.11648/j.ijmb.20230804.11
Page(s) 69-81
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Virulence Genes, Virulence Factors, Extraintestinal Pathogenic Escherichia coli, Biofilms, Biofilm-Associated Infections

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Cite This Article
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    Komla Mawunyo Dossouvi, Bissoume Sambe Ba, Gora Lo, Issa Ndiaye, Awa Ba-Diallo, et al. (2023). High Prevalence of Virulence Genes and in Vitro Biofilm Production in Clinical Multidrug-Resistant Escherichia coli in Dakar Senegal. International Journal of Microbiology and Biotechnology, 8(4), 69-81. https://doi.org/10.11648/j.ijmb.20230804.11

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    Komla Mawunyo Dossouvi; Bissoume Sambe Ba; Gora Lo; Issa Ndiaye; Awa Ba-Diallo, et al. High Prevalence of Virulence Genes and in Vitro Biofilm Production in Clinical Multidrug-Resistant Escherichia coli in Dakar Senegal. Int. J. Microbiol. Biotechnol. 2023, 8(4), 69-81. doi: 10.11648/j.ijmb.20230804.11

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    AMA Style

    Komla Mawunyo Dossouvi, Bissoume Sambe Ba, Gora Lo, Issa Ndiaye, Awa Ba-Diallo, et al. High Prevalence of Virulence Genes and in Vitro Biofilm Production in Clinical Multidrug-Resistant Escherichia coli in Dakar Senegal. Int J Microbiol Biotechnol. 2023;8(4):69-81. doi: 10.11648/j.ijmb.20230804.11

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  • @article{10.11648/j.ijmb.20230804.11,
      author = {Komla Mawunyo Dossouvi and Bissoume Sambe Ba and Gora Lo and Issa Ndiaye and Awa Ba-Diallo and Ousmane Sow and Assane Dieng and Fatimata Talla and Abdoulaye Cissé and Serigne Mbaye Lo Ndiaye and Alioune Tine and Farba Karam and Habsa Diagne-Samb and Safietou Ngom-Cisse and Halimatou Diop-Ndiaye and Issaka Maman and Coumba Toure-Kane and Aïssatou Gaye-Diallo and Sika Dossim and Souleymane Mboup and Cheikh Saad Bouh Boye and Abdoulaye Seck and Makhtar Camara},
      title = {High Prevalence of Virulence Genes and in Vitro Biofilm Production in Clinical Multidrug-Resistant Escherichia coli in Dakar Senegal},
      journal = {International Journal of Microbiology and Biotechnology},
      volume = {8},
      number = {4},
      pages = {69-81},
      doi = {10.11648/j.ijmb.20230804.11},
      url = {https://doi.org/10.11648/j.ijmb.20230804.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijmb.20230804.11},
      abstract = {Bacterial virulence is a key factor determining the outcome of each bacterial infection, and virulent bacteria are often associated with high-risk infections. Thus, this study aimed to screen for virulence genes and evaluate the in vitro biofilm formation capacity of multidrug-resistant Escherichia coli isolated in Dakar. For the 16 virulence genes identified by standard polymerase chain reaction (PCR), all 78 ExPEC isolates carried at least four virulence genes. The prevalence of virulence genes was as follows: adhesin genes fimH (98.7%), mrkD (98.7%), papC (46.2%), afaC (9%), and sfa/focDE (1.3%); iron acquisition system genes entB (98.7%), fepA (98.7%), ybtS (93.6%), fyuA (91%), iucA (91%), iucB (91%), iutA (34.6), iroB (6.4%), iroN (6.4%), and toxin genes hlyA (10.3%) and cnf (1 & 2) (10.3%). Seventy-five of the 78 isolates (96.2%) carried at least two adhesin genes and two iron capture system genes. Evaluation of the biofilm formation capacity revealed that all (29/29) hospital-acquired isolates were biofilm producers with (6/29; 20.7%) strong biofilm producers, (15/29; 51.7%) moderate biofilm producers and (8/29; 27.6%) weak biofilm producers. Hospital-acquired isolates carrying papC had a greater biofilm formation capacity than those lacking papC (p < 0.001). The deepening of this type of study on bacterial virulence and hospital bacterial biofilms could lead to improvements in infection investigation, prevention, and therapeutic protocols.
    },
     year = {2023}
    }
    

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  • TY  - JOUR
    T1  - High Prevalence of Virulence Genes and in Vitro Biofilm Production in Clinical Multidrug-Resistant Escherichia coli in Dakar Senegal
    AU  - Komla Mawunyo Dossouvi
    AU  - Bissoume Sambe Ba
    AU  - Gora Lo
    AU  - Issa Ndiaye
    AU  - Awa Ba-Diallo
    AU  - Ousmane Sow
    AU  - Assane Dieng
    AU  - Fatimata Talla
    AU  - Abdoulaye Cissé
    AU  - Serigne Mbaye Lo Ndiaye
    AU  - Alioune Tine
    AU  - Farba Karam
    AU  - Habsa Diagne-Samb
    AU  - Safietou Ngom-Cisse
    AU  - Halimatou Diop-Ndiaye
    AU  - Issaka Maman
    AU  - Coumba Toure-Kane
    AU  - Aïssatou Gaye-Diallo
    AU  - Sika Dossim
    AU  - Souleymane Mboup
    AU  - Cheikh Saad Bouh Boye
    AU  - Abdoulaye Seck
    AU  - Makhtar Camara
    Y1  - 2023/10/31
    PY  - 2023
    N1  - https://doi.org/10.11648/j.ijmb.20230804.11
    DO  - 10.11648/j.ijmb.20230804.11
    T2  - International Journal of Microbiology and Biotechnology
    JF  - International Journal of Microbiology and Biotechnology
    JO  - International Journal of Microbiology and Biotechnology
    SP  - 69
    EP  - 81
    PB  - Science Publishing Group
    SN  - 2578-9686
    UR  - https://doi.org/10.11648/j.ijmb.20230804.11
    AB  - Bacterial virulence is a key factor determining the outcome of each bacterial infection, and virulent bacteria are often associated with high-risk infections. Thus, this study aimed to screen for virulence genes and evaluate the in vitro biofilm formation capacity of multidrug-resistant Escherichia coli isolated in Dakar. For the 16 virulence genes identified by standard polymerase chain reaction (PCR), all 78 ExPEC isolates carried at least four virulence genes. The prevalence of virulence genes was as follows: adhesin genes fimH (98.7%), mrkD (98.7%), papC (46.2%), afaC (9%), and sfa/focDE (1.3%); iron acquisition system genes entB (98.7%), fepA (98.7%), ybtS (93.6%), fyuA (91%), iucA (91%), iucB (91%), iutA (34.6), iroB (6.4%), iroN (6.4%), and toxin genes hlyA (10.3%) and cnf (1 & 2) (10.3%). Seventy-five of the 78 isolates (96.2%) carried at least two adhesin genes and two iron capture system genes. Evaluation of the biofilm formation capacity revealed that all (29/29) hospital-acquired isolates were biofilm producers with (6/29; 20.7%) strong biofilm producers, (15/29; 51.7%) moderate biofilm producers and (8/29; 27.6%) weak biofilm producers. Hospital-acquired isolates carrying papC had a greater biofilm formation capacity than those lacking papC (p < 0.001). The deepening of this type of study on bacterial virulence and hospital bacterial biofilms could lead to improvements in infection investigation, prevention, and therapeutic protocols.
    
    VL  - 8
    IS  - 4
    ER  - 

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Author Information
  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • West and Central Africa Regional Office, World Health Organization, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Pole of Microbiology, Pasteur Institute of Dakar, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Pole of Microbiology, Pasteur Institute of Dakar, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Pole of Microbiology, Pasteur Institute of Dakar, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Molecular Biology and Virology Laboratory, National Institute of Hygiene, Lomé, Togo

  • Institute for Health Research, Epidemiological Surveillance and Training (IRESSEF), Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Faculty of Health Sciences, University of Kara, Kara, Togo

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

  • Medical Analysis Laboratory, Pasteur Institute of Dakar, Dakar, Senegal

  • Bacteriology-Virology laboratory, National University Hospital Aristide le Dantec, Dakar, Senegal

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