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<p><i>Pseudomonas aeruginosa</i> is an opportunistic pathogen frequently associated with hospital-acquired infections, particularly in intensive care units. This study aimed to evaluate the virulence of the clinical strain <i>P. aeruginosa</i> VAP112, isolated from a patient with ventilator-associated pneumonia (VAP), using a murine model of pulmonary infection. Antimicrobial susceptibility testing was performed using the VITEK<sup>®</sup> 2 system and disk diffusion method. Experiments were conducted to evaluate biofilm formation by VAP112, as well as the survival of <i>Tenebrio molitor</i> larvae and C57BL/6 mice. Animals were instilled with VAP112 via tracheal to evaluate the bacterial load in the organs, inflammatory markers, cell quantification, and histology of organs. Polymerase chain reaction (PCR) identified the presence of virulence and resistance genes, including <i>exoU</i>,<i> exoT</i>,<i> exoS</i>,<i> phzI</i>,<i> phzM</i>,<i> oprI</i>, <i>bla</i><sub>OXA− 23</sub>, and <i>bla</i><sub>OXA− 51</sub>. The strain demonstrated the ability to form biofilms and caused mortality in <i>T. molitor</i> larvae. In mice, tracheal instillation of VAP112 led to pneumonia with rapid progression to lethal sepsis within 48&#xa0;h. This was associated with bacterial dissemination to various organs, significant increase in nitric oxide and IL-6 levels, and elevated cell counts in bone marrow and bronchoalveolar fluid. Histological analysis revealed inflammatory infiltrates, edema, and congestion in the affected organs. Taken together, these findings showed the virulence potential of <i>P. aeruginosa</i> VAP112 to induce severe pneumonia in animals with rapid progression to lethal sepsis. Given its great importance in the clinical context, this study underscores the urgent need for the development of novel therapeutic strategies to combat infections caused by virulent strains of <i>P. aeruginosa</i>.</p>

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Genotypic and phenotypic characterization of Pseudomonas aeruginosa PAV112: a virulent clinical strain causing severe pneumonia and lethal sepsis in a murine infection model

  • 期刊论文

  • 发表日期：

    2026年1月16日

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  • Raissa Guará Assunção,
  • Beatriz Gomes Vila Nova,
  • Lully Gabrielly Silva Alves,
  • Leticia Cely Tavares da Silva,
  • Gabrielle Chaves Sá,
  • Lucas dos Santos Silva,
  • Marcos Andrade-Silva,
  • Amanda Vitória Sevidanes de Santana,
  • Ivana Fiquene Zafred,
  • Sarah Rackel Silva Soares,
  • Francisco Jonathas Rodrigues Nogueira,
  • Maria Rosa Quaresma Bomfim,
  • Johnny Ramos do Nascimento,
  • Rafael Cardoso Carvalho,
  • Joicy Cortez de Sá Sousa,
  • Marliete Carvalho da Costa,
  • Afonso Gomes Abreu

摘要

Pseudomonas aeruginosa is an opportunistic pathogen frequently associated with hospital-acquired infections, particularly in intensive care units. This study aimed to evaluate the virulence of the clinical strain P. aeruginosa VAP112, isolated from a patient with ventilator-associated pneumonia (VAP), using a murine model of pulmonary infection. Antimicrobial susceptibility testing was performed using the VITEK® 2 system and disk diffusion method. Experiments were conducted to evaluate biofilm formation by VAP112, as well as the survival of Tenebrio molitor larvae and C57BL/6 mice. Animals were instilled with VAP112 via tracheal to evaluate the bacterial load in the organs, inflammatory markers, cell quantification, and histology of organs. Polymerase chain reaction (PCR) identified the presence of virulence and resistance genes, including exoU, exoT, exoS, phzI, phzM, oprI, blaOXA− 23, and blaOXA− 51. The strain demonstrated the ability to form biofilms and caused mortality in T. molitor larvae. In mice, tracheal instillation of VAP112 led to pneumonia with rapid progression to lethal sepsis within 48 h. This was associated with bacterial dissemination to various organs, significant increase in nitric oxide and IL-6 levels, and elevated cell counts in bone marrow and bronchoalveolar fluid. Histological analysis revealed inflammatory infiltrates, edema, and congestion in the affected organs. Taken together, these findings showed the virulence potential of P. aeruginosa VAP112 to induce severe pneumonia in animals with rapid progression to lethal sepsis. Given its great importance in the clinical context, this study underscores the urgent need for the development of novel therapeutic strategies to combat infections caused by virulent strains of P. aeruginosa.