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Vol. 30. Issue S1.
XXIV Brazilian Congress of Infectious Diseases 2025
(March 2026)
Vol. 30. Issue S1.
XXIV Brazilian Congress of Infectious Diseases 2025
(March 2026)
96
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OUTBREAK OF POLYMYXIN-RESISTANT ACINETOBACTER BAUMANNII CARRYING BLAOXA-23 CARBAPENEMASE IN A HOSPITAL IN RIO DE JANEIRO

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Bruna Ribeiro Sued-Karama,
Corresponding author
brunasued88@gmail.com

Corresponding author:
, Daiana Cristina Silva Rodriguesa, Gabriela Alves da Silvaa, Maria Eduarda Condea, Letícia da Silva Nascimentoa, Bruno Rocha Pribula, Diana Galvão Venturaa, Bibiana Nogueira Siqueirab, Melise Chaves Silveirac, Cláudio Marcos Rocha-de-Souzaa, Ana Paula D’Alincourt Carvalho-Assefa
a Laboratório de Bacteriologia Aplicada a Saúde Única e Resistência Antimicrobiana (LabSUR), Fundação Oswaldo Cruz, Fiocruz, Rio de Janeiro, RJ, Brazil
b Hospital Central Aristarcho Pessoa (CBMERJE), Rio de Janeiro, RJ, Brazil
c Laboratório Nacional de Computação Científica, Petrópolis, RJ, Brazil
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Vol. 30. Issue S1

XXIV Brazilian Congress of Infectious Diseases 2025

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Introduction/Objectives

Acinetobacter baumannii is a challenging pathogen and a major epidemiological threat responsible for healthcare-associated infections and increasing multidrug resistance, including to last-resort agents such as polymyxins. This study aimed to characterize carbapenem- and polymyxin-resistant A. baumannii clinical isolates from a state hospital in Rio de Janeiro.

Methods

Between September and December 2024, nine A. baumannii isolates resistant to carbapenems and polymyxin B were received at LabSUR from ICU patients of a state hospital. Carbapenemase genes were screened by multiplex PCR. Clonal relatedness was assessed by pulsed-field gel electrophoresis (PFGE). A representative isolate of the predominant clone underwent whole-genome sequencing (WGS), analyzed through the CABGen pipeline.

Results

All isolates were positive for blaOXA-23 and blaOXA-51 genes. The nine polymyxin-resistant isolates belonged to the same clonal group, six from tracheal secretions and three from surveillance swabs, originating from seven ICU patients (two patients with duplicate samples). Five patients occupied the same ICU beds at different times; two patients died. The sequenced representative strain belonged to sequence type 1 (ST1), a high-risk clone linked to outbreaks and global dissemination of resistance genes. The isolate also harbored aminoglycoside- and sulfonamide-resistance genes and mutations in pmrB and lpxC associated with polymyxin resistance.

Conclusion

The results suggest persistence and circulation of a clonal A. baumannii lineage resistant to carbapenems and polymyxin B within a hospital unit, belonging to a high-risk clone. These findings reinforce the importance of continuous monitoring, control of clonal dissemination, and targeted interventions to mitigate its impact on public health.

Keywords:
Acinetobacter baumannii
Polymyxin
Carbapenemase
Antimicrobials
Resistance
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