# Understanding Daptomycin Resistance Mechanisms and Treatment Challenges in Enterococcus faecium Infection: A Case Series

**Authors:** Sangeeta Nair-Collins, Gabriel Godart, Nipakumari Patel, Vidit Yadav, Kelly Larimore, Jordan D. LeGout, Rohit Chitale, Ravi Durvasula, Justin Oring

PMC · DOI: 10.3390/antibiotics15030243 · Antibiotics · 2026-02-26

## TL;DR

This paper presents three cases of daptomycin-resistant Enterococcus faecium infections in liver disease patients, highlighting treatment challenges and successful management strategies.

## Contribution

The study contributes new clinical insights into managing daptomycin-resistant E. faecium through combination therapy and source control.

## Key findings

- Three patients with advanced liver disease developed daptomycin-resistant E. faecium infections.
- Combination therapy with high-dose daptomycin and ceftaroline, along with source control, successfully managed the infections.
- Periodic reassessment of antimicrobial susceptibility is emphasized to address evolving resistance during treatment.

## Abstract

Daptomycin-resistant Enterococcus faecium (DRE) poses an increasing therapeutic challenge, particularly in immunocompromised patients and solid organ transplant recipients. Surveillance data from the Centers for Disease Control and Prevention indicate that approximately 6.5% of E. faecium isolates are daptomycin-resistant, underscoring the need for heightened clinical vigilance, particularly for prompt identification and treatment. In this case series, three patients with advanced liver disease, including two status post orthotopic liver transplantation, are described who developed DRE during treatment for bloodstream infection. These cases illustrate the dynamic nature of antimicrobial susceptibility under daptomycin exposure and highlight the contributions of persistent source control issues, intravascular infection, and altered host factors to treatment failure. All patients were successfully managed by escalating to combination therapy with high-dose daptomycin and ceftaroline, alongside appropriate source control. This series emphasizes the importance of periodic susceptibility reassessment during daptomycin therapy and cautions clinicians against assuming sustained susceptibility in patients with prolonged bacteremia or complex infections. Early recognition of evolving resistance and timely therapeutic adjustment may improve outcomes in this high-risk population.

## Linked entities

- **Chemicals:** daptomycin (PubChem CID 21585658), ceftaroline (PubChem CID 9852981)
- **Species:** Enterococcus faecium (taxon 1352)

## Full-text entities

- **Genes:** VanB [NCBI Gene 6779647], VanA [NCBI Gene 13874695], ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, pdr [NCBI Gene 5171]
- **Diseases:** protein malnutrition (MESH:D044342), bacterial peritonitis (MESH:D010538), renal dysfunction (MESH:D007674), thrombophlebitis (MESH:D013924), bacterial infections (MESH:D001424), abscess (MESH:D000038), hypotension (MESH:D007022), enterococcal disease (MESH:D004194), peripheral neuropathy (MESH:D010523), Clostridium difficile infections (MESH:D003015), end-stage liver disease (MESH:D058625), cholangitis (MESH:D002761), VRE bacteremia (MESH:D016470), leukocytosis (MESH:D007964), syncopal episode (MESH:D013575), CVID (MESH:D017074), injury to (MESH:D014947), nausea (MESH:D009325), Enterococcus infections (MESH:D007239), Metamycoplasma hominis (MESH:D016776), abdominal pain (MESH:D015746), cholangiocarcinoma (MESH:D018281), serotonin syndrome (MESH:D020230), DRE (MESH:D060467), CMV (MESH:D003586), purulence (MESH:D003234), enterocaval fistula (MESH:D005402), diabetes (MESH:D003920), tachycardia (MESH:D013610), abdominal distension (MESH:D000007), HCC (MESH:D006528), choledocholithiasis (MESH:D042883), body aches (MESH:D010146), septic (MESH:D001170), cardiovascular disease (MESH:D002318), toxicity (MESH:D064420), candidemia (MESH:D058387), cancer (MESH:D009369), Crohn's disease (MESH:D003424), duodenal defect (MESH:D004382), ITP (MESH:D011696), bloodstream infection (MESH:D018805), lactic acidosis (MESH:D000140), systemic lupus erythematosus (MESH:D008180), cellulitis (MESH:D002481), ischemic cholangiopathy (MESH:D002545), acute renal failure (MESH:D058186), urinary tract infections (MESH:D014552), ascites (MESH:D001201), tachypnea (MESH:D059246), hepatic abscess (MESH:D008100), vomiting (MESH:D014839), skin (MESH:D012871), rhabdomyolysis (MESH:D012206), thrombus (MESH:D013927), autoimmune hepatitis (MESH:D019693), intra-abdominal infection (MESH:D059413), liver cirrhosis (MESH:D008103), cholestasis (MESH:D002779), endocarditis (MESH:D004696)
- **Chemicals:** amoxicillin (MESH:D000658), beta-lactam antibiotics (MESH:D008997), rifampicin (MESH:D012293), lactate (MESH:D019344), meropenem (MESH:D000077731), Ca2+ (-), Eravacycline (MESH:C571179), tedizolid (MESH:C546016), clindamycin (MESH:D002981), rifamycin (MESH:C023808), beta-lactam (MESH:D047090), caspofungin (MESH:D000077336), polysaccharide (MESH:D011134), cefepime (MESH:D000077723), Oritavancin (MESH:C100708), ceftolozane-tazobactam (MESH:C000594038), ceftaroline (MESH:C490727), lipoglycopeptide (MESH:D000077427), ceftriaxone (MESH:D002443), oxazolidinones (MESH:D023303), Ampicillin (MESH:D000667), bile acids (MESH:D001647), imipenem (MESH:D015378), Rifaximin (MESH:D000078262), phospholipid (MESH:D010743), piperacillin/tazobactam (MESH:D000077725), Vancomycin (MESH:D014640), quinupristin (MESH:C113825), penicillin (MESH:D010406), Daptomycin (MESH:D017576), cephalosporin (MESH:D002511), doxycycline (MESH:D004318), creatinine (MESH:D003404), ertapenem (MESH:D000077727), ceftobiprole (MESH:C443755), levofloxacin (MESH:D064704), Linezolid (MESH:D000069349), Tigecycline (MESH:D000078304), voriconazole (MESH:D065819), Trimethoprim-Sulfamethoxazole (MESH:D015662), Gentamicin (MESH:D005839), dalfopristin (MESH:C113826), tetracycline (MESH:D013752), fluconazole (MESH:D015725)
- **Species:** Enterobacter cloacae (species) [taxon 550], Staphylococcus aureus (species) [taxon 1280], Mus musculus (house mouse, species) [taxon 10090], Citrobacter freundii complex (species group) [taxon 1344959], Enterococcus faecium (species) [taxon 1352], Homo sapiens (human, species) [taxon 9606], Nakaseomyces glabratus (species) [taxon 5478], Staphylococcus lugdunensis (species) [taxon 28035], Candida tropicalis (species) [taxon 5482], Citrobacter freundii (species) [taxon 546], Pseudomonas aeruginosa (species) [taxon 287], Enterococcus faecalis (species) [taxon 1351], Klebsiella pneumoniae (species) [taxon 573], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

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## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023491/full.md

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Source: https://tomesphere.com/paper/PMC13023491