# Severe pneumonia due to Cupriavidus gilardii in a critically ill patient: a case report highlighting therapeutic dilemmas and the imperative for standardized antimicrobial guidance

**Authors:** Gengchen Huang, Shuxin Li, Yitong Zhang, Binbin Wang, Lihuan Zhang, Yutao Ma, Zihan Gao, Wei Wei

PMC · DOI: 10.3389/fmed.2025.1732674 · Frontiers in Medicine · 2026-02-19

## TL;DR

A rare bacteria, Cupriavidus gilardii, caused severe pneumonia in a critically ill patient, highlighting the need for standardized treatment guidelines.

## Contribution

This case report emphasizes the clinical challenges and therapeutic dilemmas in treating C. gilardii infections due to lack of standardized antimicrobial guidance.

## Key findings

- C. gilardii can cause life-threatening pneumonia in critically ill patients.
- Empirical and later adjusted antibiotic regimens led to clinical improvement.
- Standardized antimicrobial susceptibility testing protocols are urgently needed for this pathogen.

## Abstract

Cupriavidus gilardii is a rare environmental Gram-negative bacillus that has increasingly been recognized as an opportunistic pathogen in recent years. Clinical management of infections caused by this microorganism remains challenging due to difficulties in identification and the lack of standardized guidelines for antimicrobial susceptibility testing (AST). This article reports the case of a 75-year-old male with severe pneumonia and multiple comorbidities. Cupriavidus gilardii meeting the quality standards was identified in both bronchoalveolar lavage fluid (BALF) and sputum cultures. However, conventional AST could not be performed on this rare isolation. In the absence of susceptibility data, initial empirical therapy consisted of meropenem combined with amphotericin B cholesteryl sulfate complex. Based on literature review and microbiological findings, the regimen was later adjusted to cefoperazone–sulbactam (Sulperazon) combined with minocycline. Targeted treatment led to marked improvement in inflammatory markers and chest imaging. However, therapy was discontinued prematurely at the family’s request due to financial constraints, and the patient was transferred to a local hospital before full recovery could be achieved. This case demonstrates that C. gilardii can cause severe, life-threatening pneumonia in critically ill patients with multiple comorbidities, challenging its perception as a low-virulence opportunist. The absence of standardized antimicrobial susceptibility testing for this pathogen necessitated a literature-guided, multidisciplinary therapeutic approach, which ultimately led to clinical improvement. Our experience underscores the urgency of establishing standardized testing protocols and fostering multidisciplinary collaboration to guide the management of emerging, multidrug-resistant environmental pathogens like C. gilardii.

## Linked entities

- **Chemicals:** meropenem (PubChem CID 441130), minocycline (PubChem CID 54675783)
- **Diseases:** pneumonia (MONDO:0005249)
- **Species:** Cupriavidus gilardii (taxon 82541)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** arteriovenous fistula (MESH:D001164), lethargic (MESH:D004674), post-COVID-19 (MESH:D000094024), bloodstream infections (MESH:D018805), hypoxemia (MESH:D000860), hematologic malignancies (MESH:D019337), aplastic anemia (MESH:D000741), AST (MESH:D013736), hypoalbuminemia (MESH:D034141), pneumonia (MESH:D011014), opacities (MESH:D003318), bacterial (MESH:D001424), acquired immunodeficiency (MESH:D000163), pulmonary infiltrates (MESH:D017254), aspiration pneumonia (MESH:D011015), cough (MESH:D003371), anuria (MESH:D001002), Chronic renal insufficiency (MESH:D051436), anorexia (MESH:D000855), lung injury (MESH:D055370), dyspnea (MESH:D004417), C. gilardii infection (MESH:D007239), chronic renal failure (MESH:D007676), immune dysfunction (MESH:D007154), opportunistic infections (MESH:D009894), impaired consciousness (MESH:D003244), physical disability (MESH:D059445), hypertension (MESH:D006973), malnutrition (MESH:D044342), S. maltophilia (MESH:C531821), inflammatory (MESH:D007249), atelectasis (MESH:D001261), critically ill (MESH:D016638)
- **Chemicals:** glucose (MESH:D005947), heavy-metal (MESH:D019216), beta-lactam (MESH:D047090), Sulperazon (MESH:C057923), carbapenem (MESH:D015780), minocycline (MESH:D008911), trimethoprim-sulfamethoxazole (MESH:D015662), tetracyclines (MESH:D013754), meropenem (MESH:D000077731), fluoroquinolones (MESH:D024841), amphotericin B (MESH:D000666), oxygen (MESH:D010100), AST (-)
- **Species:** Cupriavidus nantongensis (species) [taxon 1796606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Cupriavidus pauculus (species) [taxon 82633], Cupriavidus gilardii (species) [taxon 82541], Homo sapiens (human, species) [taxon 9606], Nakaseomyces glabratus (species) [taxon 5478], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Stenotrophomonas maltophilia (species) [taxon 40324], Candida albicans (species) [taxon 5476]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960503/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960503/full.md

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Source: https://tomesphere.com/paper/PMC12960503