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Não fermentadores

Achromobacter xylosoxidans

Non-fermenting Gram-negative bacilli

Identification & Growth

Identification

  • Oxidase-positive, motile by peritrichous flagella, oxidizes xylose
  • Confirmation by MALDI-TOF

Growth Conditions

  • MacConkey agar-positive, blood agar 35 °C, 24–48 h; greyish colonies

Clinical Significance

  • Colonization in cystic fibrosis, catheter-related bacteremia, post-surgical infection

Intrinsic Resistance

  • Resistant to aztreonam, first- and second-generation cephalosporins and aminoglycosides

Bench Alerts

  • Piperacillin-tazobactam, meropenem and trimethoprim-sulfamethoxazole are the usual options
  • Do not extrapolate Pseudomonas breakpoints

Clinical Notes

Clinical presentations

  • Catheter-related bacteremia, ventilator-associated pneumonia and surgical-site infection in the hospital setting.
  • Chronic airway colonization in cystic fibrosis and bronchiectasis, associated with functional decline.
  • Peritonitis in peritoneal dialysis and post-procedure ocular infection, usually linked to a water source.

Specimens and collection

  • Blood culture, peritoneal fluid, sputum/tracheal aspirate or bronchoalveolar lavage according to the suspected site.
  • In cystic fibrosis, plate on selective media for non-fermenters to avoid overgrowth by P. aeruginosa.
  • Investigate water, solutions and diluted disinfectants when cases cluster.

Epidemiology and at-risk populations

  • It inhabits hospital water reservoirs and tolerates chlorhexidine and other disinfectants at inadequate concentrations.
  • Greater risk in cystic fibrosis, haematological malignancy, transplantation and prolonged device use.
  • Reported in common-source outbreaks, with documented cross-transmission between patients.

Resistance and therapeutic implications

  • Intrinsic resistance to aztreonam and to extended-spectrum cephalosporins (including ceftriaxone and cefotaxime), with reduced aminoglycoside susceptibility.
  • Piperacillin-tazobactam, ceftazidime, meropenem and trimethoprim-sulfamethoxazole are the usual active options, always confirmed by testing.
  • EUCAST/BrCAST criteria are limited: when absent, use MIC with non-species-related PK/PD criteria and state the method in the report.

Bench and reporting notes

  • Oxidase-positive, catalase-positive Gram-negative rod that oxidizes xylose and is motile by peritrichous flagella.
  • Frequently confused with Pseudomonas and Burkholderia on biochemical systems; confirm with MALDI-TOF.
  • Include the intrinsic-resistance alert in the report to prevent prescription of a third-generation cephalosporin.

Sources

Educational decision-support content. It does not replace laboratory validation, current guidelines or review by the responsible professional.

FAQ: Frequently Asked Questions

How to identify Achromobacter xylosoxidans in the lab?

Achromobacter xylosoxidans is identified through oxidase-positive, motile by peritrichous flagella, oxidizes xylose, confirmation by maldi-tof.

What are the intrinsic resistances of Achromobacter xylosoxidans?

This organism is naturally resistant to resistant to aztreonam, first- and second-generation cephalosporins and aminoglycosides. These drugs should not be reported as susceptible.

Where is Achromobacter xylosoxidans commonly found?

It is typically associated with colonization in cystic fibrosis, catheter-related bacteremia, post-surgical infection.

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