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  <title>DSpace Coleção:</title>
  <link rel="alternate" href="https://repositorio.ufba.br/handle/ri/20013" />
  <subtitle />
  <id>https://repositorio.ufba.br/handle/ri/20013</id>
  <updated>2026-05-03T10:27:12Z</updated>
  <dc:date>2026-05-03T10:27:12Z</dc:date>
  <entry>
    <title>Sickle cell disease children’s gut colonization by extended-spectrum β-lactamase (ESBL)-producing Enterobacterales: an antibiotic prophylaxis effect?</title>
    <link rel="alternate" href="https://repositorio.ufba.br/handle/ri/34218" />
    <author>
      <name>Monteiro, Adriano de Souza Santos</name>
    </author>
    <author>
      <name>Oliveira, Eduardo Gomes de</name>
    </author>
    <author>
      <name>Santos, Djanilson Barbosa dos</name>
    </author>
    <author>
      <name>Cordeiro, Soraia Machado</name>
    </author>
    <author>
      <name>Couto, Ricardo David</name>
    </author>
    <author>
      <name>Couto, Fábio David</name>
    </author>
    <id>https://repositorio.ufba.br/handle/ri/34218</id>
    <updated>2022-10-22T22:09:15Z</updated>
    <published>2021-01-01T00:00:00Z</published>
    <summary type="text">Título: Sickle cell disease children’s gut colonization by extended-spectrum β-lactamase (ESBL)-producing Enterobacterales: an antibiotic prophylaxis effect?
Autor(es): Monteiro, Adriano de Souza Santos; Oliveira, Eduardo Gomes de; Santos, Djanilson Barbosa dos; Cordeiro, Soraia Machado; Couto, Ricardo David; Couto, Fábio David
Abstract: Introduction: Sickle cell disease (SCD) children have a high susceptibility to pneumococcal infection. For this reason, they are routinely immunized with pneumococcal vaccines and use antibiotic prophylaxis (AP). &#xD;
Hypothesis/Gap Statement: Yet, little is known about SCD children’s gut microbiota. If antibiotic-resistant Enterobacterales may colonize people on AP, we hypothesized that SCD children on AP are colonized by resistant enterobacteria species.&#xD;
Objective: To evaluate the effect of continuous AP on Enterobacterales gut colonization from children with SCD.&#xD;
Methodology: We analysed 30 faecal swabs from SCD children on AP and 21 swabs from children without the same condition. Enterobacterales was isolated on MacConkey agar plates and identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) (bioMérieux, Marcy l'Etoile, France). We performed the antibiogram by Vitek 2 system (bioMérieux, Marcy l'Etoile, France), and the resistance genes were identified by multiplex PCR. &#xD;
Results: We found four different species with resistance to one or more different antibiotic types in the AP-SCD children’s group: Escherichia coli, Klebsiella pneumoniae, Citrobacter freundii, and Citrobacter farmeri. Colonization by resistant E. coli was associated with AP (prevalence ratio 2.69, 95% confidence interval [CI], 1.98–3.67, P&lt;0.001). Strains producing extended-spectrum β-lactamases (ESBL) were identified only in SCD children, E. coli, 4/30 (13%), and K. pneumoniae, 2/30 (7%). The ESBL-producing Enterobacterales were associated with penicillin G benzathine use (95 % CI, 22.91–86.71, P&lt;0.001). CTX-M-1 was the most prevalent among ESBL-producers (3/6, 50%), followed by CTX-M-9 (2/6, 33%), and CTX-M-2 (1/6, 17%).&#xD;
Conclusion: Resistant enterobacteria colonize SCD children on AP, and this therapy raises the chance of ESBL-producing Enterobacterales colonization. Future studies should focus on prophylactic vaccines as exclusive therapy against pneumococcal infections.
Editora / Evento / Instituição: Journal of Medical Microbiology, Microbiology Society
Tipo: Artigo de Periódico</summary>
    <dc:date>2021-01-01T00:00:00Z</dc:date>
  </entry>
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