# Emerging Threat of Acinetobacter radioresistens Infection in Immunocompromised Patients

**Authors:** Jyotsna Mary George, Guiseppe Calandrino, Rushdah Malik

PMC · DOI: 10.1155/crdi/2388640 · Case Reports in Infectious Diseases · 2026-02-20

## TL;DR

A rare Acinetobacter species, A. radioresistens, caused infection in an immunocompromised patient, highlighting the need for accurate diagnostics and antimicrobial stewardship.

## Contribution

This case report highlights A. radioresistens as an emerging opportunistic pathogen in immunocompromised patients.

## Key findings

- A. radioresistens was identified as pan-susceptible using MALDI-TOF mass spectrometry.
- Rapid molecular diagnostics and confirmatory methods are critical for accurate identification and treatment.
- The case emphasizes the importance of vigilance for uncommon Acinetobacter species in high-risk patients.

## Abstract

Acinetobacter radioresistens is an uncommon human pathogen rarely reported to cause bacteremia. Its accurate identification is crucial yet challenging, with implications for antimicrobial stewardship due to its potential to harbor carbapenem resistance genes. We present the case of a 77‐year‐old male with metastatic lung adenocarcinoma, COPD, and dementia who presented with acute hypoxic respiratory failure and septic shock. Initial empiric antibiotics were vancomycin and cefepime. Gram stain of positive blood cultures revealed Gram‐negative coccobacilli. The VERIGENE BC‐GN microarray system identified an Acinetobacter species, negative for common resistance markers, which was subsequently confirmed as pan‐susceptible Acinetobacter radioresistens by MALDI‐TOF mass spectrometry. The patient’s antibiotic regimen was de‐escalated to intravenous ampicillin‐sulbactam, to which he initially responded. His course was later complicated by recurrent respiratory failure, and his family transitioned him to comfort care. He expired shortly after withdrawal of life support. This case underscores the emerging clinical significance of A. radioresistens as an opportunistic pathogen in immunocompromised hosts. It highlights the utility of rapid molecular diagnostics for precise pathogen identification and antimicrobial stewardship, while also illustrating the critical role of confirmatory methods like MALDI‐TOF. Vigilance for less common Acinetobacter species is warranted in patients with significant comorbidities.

## Linked entities

- **Chemicals:** vancomycin (PubChem CID 14969), cefepime (PubChem CID 5479537), ampicillin-sulbactam (PubChem CID 119561)
- **Diseases:** COPD (MONDO:0005002), dementia (MONDO:0001627), respiratory failure (MONDO:0021113)
- **Species:** Acinetobacter radioresistens (taxon 40216)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** septic shock (MESH:D012772), infectious (MESH:D003141), bloodstream infection (MESH:D018805), aspiration (MESH:D011015), dementia (MESH:D003704), hypoglycemia (MESH:D007003), Infection (MESH:D007239), colitis (MESH:D003092), bacteremia (MESH:D016470), metabolic acidosis (MESH:D000138), leukocytosis (MESH:D007964), atelectasis (MESH:D001261), metastasis (MESH:D009362), death (MESH:D003643), hypotension (MESH:D007022), hypernatremia (MESH:D006955), Acinetobacter infection (MESH:D000151), respiratory failure (MESH:D012131), adenocarcinoma of the lung (MESH:D000077192), hypoxic (MESH:D002534), multiorgan dysfunction (MESH:D009102), fatigue (MESH:D005221), COPD (MESH:D029424), pneumonia (MESH:D011014), cholangiocarcinoma (MESH:D018281), acute kidney injury (MESH:D058186), bacterial pneumonia (MESH:D018410), shortness of breath (MESH:D004417), Alzheimer's/ (MESH:D000544), cancer (MESH:D009369), neutropenic (MESH:D044504), liver lesions (MESH:D008107), disease (MESH:D004194), critically ill (MESH:D016638), hyperkalemia (MESH:D006947), Parkinson's (MESH:D010300), alcohol abuse (MESH:D000437)
- **Chemicals:** creatinine (MESH:D003404), ampicillin-sulbactam (MESH:C035444), ampicillin (MESH:D000667), trimethoprim/sulfamethoxazole (MESH:D015662), cephalosporins (MESH:D002511), NDM (MESH:C052821), piperacillin/tazobactam (MESH:D000077725), CTX-M (-), bicarb (MESH:D017693), aztreonam (MESH:D001398), tobramycin (MESH:D014031), gentamicin (MESH:D005839), ertapenem (MESH:D000077727), ceftazidime (MESH:D002442), carbapenem (MESH:D015780), Vancomycin (MESH:D014640), Cefepime (MESH:D000077723), lactic acid (MESH:D019344), IMP (MESH:D007291), ciprofloxacin (MESH:D002939), metronidazole (MESH:D008795), oxygen (MESH:D010100)
- **Species:** Acinetobacter baumannii (species) [taxon 470], Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097], Acinetobacter radioresistens (species) [taxon 40216], Acinetobacter (genus) [taxon 469], Klebsiella pneumoniae (species) [taxon 573]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12921414/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921414/full.md

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Source: https://tomesphere.com/paper/PMC12921414