Ewingella Americana: An Emerging True Pathogen

Infections caused by Ewingella americana have been rarely reported in the literature. Most of the cases that have been reported were among the immunocompromised patients. We report a case of E. americana causing osteomyelitis and septic arthritis of the shoulder joint in a previous intravenous drug abuser. The causative pathogen was identified by synovial fluid analysis and culture.

This case report is the first clinical description of E. americana causing osteomyelitis and septic arthritis of the shoulder joint.

Case Report
A 50-year-old male was admitted to the hospital, with gradual onset of pain and swelling in the right shoulder since 4 days. He denied fever, chills, or rigors. His past medical history was significant for hypertension and intravenous drug abuse. His last use of heroin was 2 months ago with an unsterilized needle contaminated by saliva, in the right arm. Physical examination revealed limited range of motion of right shoulder secondary to pain. Radiograph of the right shoulder was suggestive of osteomyelitis. A computed topographic scan of the shoulder revealed multifocal, intraarticular abscess formation involving the right upper extremity.
It also showed erosion of the humeral head and the glenohumeral joint, consistent with septic arthritis (Figure 1). Arthrocentesis was done, and the cell count of the synovial fluid showed white blood cell count of 9.4 × 10 9 /L (90% neutrophils, 1% bands). Cultures of the synovial fluid grew Ewingella americana. The antimicrobial susceptibility test carried out by disk diffusion method showed susceptibility to amikacin, ampicillin, cefazolin, gentamicin, piperacillin tazobactam, tobramycin, and trimethoprim sulfamethoxazole while was resistant to ciprofloxacin.
The patient was started on ceftriaxone 2 gm intravenous every 24 hours. He continued to improve and was discharged home to complete 6 weeks of intravenous antibiotic therapy. He was followed 4 weeks later in the outpatient clinic and showed resolution of infection which was confirmed both clinically and by imaging. The antibiotic course was completed with no complications.
E. Americana is seen in patients who were immunosuppressed due to diabetes mellitus [5], bone marrow transplantation, chemotherapy [7], end stage renal disease [10], 2 Case Reports in Infectious Diseases and use of mercaptopurine [15]. Although, a few cases of E. americana have been reported earlier causing conjunctivitis [3,4] and Waterhouse-Friderichsen syndrome [16] in previously healthy individuals, this is the first case of osteomyelitis involving the joint due to intravenous drug abuse. Based on this observation, clinicians may want to consider Ewingella Americana as an emerging true pathogen.
Since little information exists on the ecological niche of this organism, in our case we speculate on the source of contamination as saliva from the patient's mouth. Kati et al. [10] proposed domestic water to be a source of infection in peritonitis of a patient undergoing peritoneal dialysis. A contaminated ice bath was identified as the probable source in an outbreak of E. americana bacteremia, in patients who had undergone cardiovascular or peripheral vascular surgery [8]. Maertens et al. [7] speculated on inadequate hand hygiene as the source of infection. E. americana is an organism without nutritional needs that can survive in water and citrate solution and preferably grows at 4 • C.
The only risk factor in our patient was that he was an intravenous drug abuser while using unsterilized needles for his heroin injections; he might have inoculated the pathogen into his blood causing transient blood stream infection which ultimately seeded into his shoulder joint.
To our knowledge, this case is the first report of osteomyelitis and septic arthritis caused by E. americana infection. Earlier reports suggested E. americana causing infections in immunocompetent host; however, in our case the infections were certainly favored by intravenous injections with contaminated material.

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Informed consent is obtained from the patient for publication of this paper.