Clinical manifestations and antimicrobial susceptibility of Nocardia species at a tertiary hospital in Taiwan, 2011-2020

J Formos Med Assoc. 2022 Oct;121(10):2109-2122. doi: 10.1016/j.jfma.2022.06.011. Epub 2022 Jul 8.

Abstract

Background: The study aimed to assess the clinical characteristics of patients with nocardiosis, to evaluate the in vitro susceptibility of antimicrobial agents against Nocardia species, and to explore changes in antimicrobial susceptibilities in this era of multidrug resistance.

Methods: Nocardia isolates were identified to the species level using matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) and 16S rRNA, hsp65, and secA1 gene sequencing, and minimum inhibitory concentrations (MICs) of 15 antimicrobial agents were assessed with the broth microdilution method.

Results: Eighty-nine isolates from 68 patients were identified to species level. The most common species were Nocardia brasiliensis (n = 28, 31.5%), followed by N. farcinica (n = 24, 27%) and N. cyriacigeorgica (n = 16, 18%). Skin and soft tissue were the most common sites of nocardiosis. In multivariate analysis, cutaneous infection (OR, 0.052; p = 0.009), immunosuppressant use (OR, 16.006; p = 0.013) and Charlson combidity index (OR, 1.522; p = 0.029) were significant predictors for death. In total, 98.9% isolates were susceptible to trimethoprim-sulfamethoxazole and linezolid. Further, the MIC range and resistance rate of all Nocardia species to ceftriaxone, imipenem, and amoxicillin-clavulanic acid were found to generally increase over time.

Conclusion: Considering that trimethoprim-sulfamethoxazole is effective against most Nocardia species, it is the antibiotic of choice in Taiwan. Besides, amikacin, tigecycline, and linezolid showed high activity against Nocardia species and are thus good alternatives or additional therapies to treat nocardiosis, depending on patient's underlying conditions and site of infection.

Keywords: Comorbidity; Drug resistance; Nocardia infections; Steroids; Sulfamethoxazole drug combination; Trimethoprim.

MeSH terms

  • Amikacin / pharmacology
  • Amikacin / therapeutic use
  • Amoxicillin-Potassium Clavulanate Combination / pharmacology
  • Amoxicillin-Potassium Clavulanate Combination / therapeutic use
  • Anti-Bacterial Agents / pharmacology
  • Anti-Bacterial Agents / therapeutic use
  • Anti-Infective Agents*
  • Ceftriaxone / therapeutic use
  • Humans
  • Imipenem / pharmacology
  • Imipenem / therapeutic use
  • Immunosuppressive Agents / therapeutic use
  • Linezolid
  • Microbial Sensitivity Tests
  • Nocardia Infections* / drug therapy
  • Nocardia* / genetics
  • RNA, Ribosomal, 16S / genetics
  • Taiwan
  • Tertiary Care Centers
  • Tigecycline / pharmacology
  • Tigecycline / therapeutic use
  • Trimethoprim, Sulfamethoxazole Drug Combination / pharmacology
  • Trimethoprim, Sulfamethoxazole Drug Combination / therapeutic use

Substances

  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Immunosuppressive Agents
  • RNA, Ribosomal, 16S
  • Tigecycline
  • Imipenem
  • Amoxicillin-Potassium Clavulanate Combination
  • Ceftriaxone
  • Trimethoprim, Sulfamethoxazole Drug Combination
  • Amikacin
  • Linezolid