Do Pseudomonas bacteria produce New Delhi metallo-beta-lactamase (NDM) resistance?

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Pseudomonas Bacteria and NDM Resistance

Yes, Pseudomonas aeruginosa can produce New Delhi metallo-beta-lactamase (NDM) resistance, though it is not as common as in Enterobacterales. 1, 2

Prevalence and Significance of NDM in Pseudomonas

  • NDM-producing Pseudomonas aeruginosa has been detected in clinical isolates, though at lower rates compared to Enterobacterales 1
  • Studies from India have reported NDM-1 in 29.23% of carbapenem-resistant P. aeruginosa isolates 2
  • NDM-producing P. aeruginosa isolates are typically only susceptible to polymyxin B, making them extremely difficult to treat 1
  • The mortality rate for patients with NDM-producing P. aeruginosa infections is high, with most patients succumbing to infection despite treatment 1

Mechanism of NDM Resistance

  • NDM is a metallo-β-lactamase (MBL) enzyme that can hydrolyze virtually all β-lactam antibiotics, including carbapenems 3
  • NDM genes are typically encoded on plasmids (mobile genetic elements) that can be transmitted between different bacterial species 4
  • Currently, 40 NDM variants have been identified in different bacterial strains globally, with NDM-1 being the most common in P. aeruginosa 3, 2
  • Unlike in Acinetobacter baumannii where NDM-2 is common, P. aeruginosa predominantly harbors the NDM-1 variant 2

Treatment Options for NDM-Producing Pseudomonas

  • For infections caused by metallo-β-lactamase (MBL)-producing bacteria, including NDM-producing P. aeruginosa, ceftazidime/avibactam plus aztreonam should be preferred as first-line therapy 5, 6
  • This combination has shown significantly lower 30-day mortality (19.2% vs. 44%) compared to other treatment options 5, 6
  • Cefiderocol may also be considered as an alternative option with conditional recommendation (low certainty of evidence) 5
  • Novel β-lactam agents such as ceftolozane/tazobactam and ceftazidime/avibactam are currently the first-line options for targeted treatment of difficult-to-treat resistant P. aeruginosa, though their efficacy specifically against NDM-producers may be limited 5

Clinical Implications

  • NDM-producing P. aeruginosa isolates are typically only susceptible to polymyxin B and sometimes fosfomycin 7, 1
  • Patients with NDM-producing P. aeruginosa infections often have poor outcomes, with high mortality rates 1
  • Combination therapy may be considered on a case-by-case basis, especially upon consultation with infectious diseases specialists 5
  • Aggressive infection control measures are essential to prevent spread of NDM-producing organisms 8

Diagnostic Considerations

  • Molecular methods like PCR are the gold standard for detecting NDM genes in P. aeruginosa 7
  • Phenotypic methods such as the Meropenem-EDTA combined disk test have high sensitivity (96.43%) but lower specificity (55.15%) for NDM detection 7
  • The modified Hodge test has lower sensitivity (89.29%) and very low specificity (35.15%) for NDM detection 7

NDM-producing P. aeruginosa represents a significant clinical challenge with limited treatment options and high mortality rates. Early detection and appropriate antimicrobial therapy, preferably with ceftazidime/avibactam plus aztreonam or cefiderocol, are crucial for improving patient outcomes.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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