To the Editor: Actinomyces naeslundii is a gram-positive, rod-shaped, non–spore-forming, facultative anaerobe, which is present as a normal commensal of human oral cavity, intestines, vagina, and upper respiratory system.1 Bacteremia due to A. naeslundii is rare and poses an increased risk of subacute and chronic granulomatous inflammation, which can affect any organ system via hematogenous spread.1 Infections due to A. naeslundii has been mainly reported in cases of periodontitis and few others in endocarditis, septic arthritis, pelvic inflammatory disease, cholecystitis, liver abscess, cervical actinomycosis, mediastinitis, and pulmonary infection. We present the case of a 70-year-old woman who complained of a fall due to lower-limb weakness. She reported generalized fatigue, polyuria, and lower abdominal pain several days before the episode of falling. She had a history of recurrent urinary tract infection, diabetes mellitus type 2, hypertension, hysterectomy, and osteoarthritis. On admission, she was febrile (38°C), tachycardic (108 beats/min), and hypertensive (174/70 mm Hg). She was alert and oriented to person, place, and time with no focal or meningeal signs. She had multiple noninfected abrasions over her knees. Laboratory studies were significant for anemia (10.6 g/dL) and hyperglycemia (342 mg/dL). Urine examination showed pyuria (>1163 white blood cells), hematuria (15 red blood cells), and positive leukocyte esterase. Blood cultures were obtained, and she was empirically administered vancomycin and cefepime. Four days later, blood cultures grew gram-positive rods, which were further identified as A. naeslundii by matrix-assisted laser desorption ionization time of flight. As urine culture was taken after initiation of antibiotics, no growth was obtained. However, there was significant improvement in pyuria with resolution of her urinary symptoms. As part of the bacteremia workup, the patient underwent dental evaluation, which showed moderate to severe generalized chronic periodontitis and dental caries extending into the pulp. Abdominal and pelvic computed tomography and echocardiogram all did not show abnormalities. Her antibiotic treatment was switched from vancomycin and cefepime to piperacillin-tazobactam. Blood cultures cleared within 4 days of antibiotic therapy. After completing a week of intravenous piperacillin-tazobactam, the patient was discharged on oral amoxicillin-clavulanate for a duration of 1 month. In addition, she was scheduled for multiple dental extractions following discharge. Actinomyces naeslundii is the second most common cause of actinomycosis (median, 7.0%) after Actinomyces israelii (median, 72.7%). Distant infections are usually related to prior dental procedures or poor dental hygiene. It is well known that chronic hyperglycemia in diabetic patients is an element that increases the rates of infection due to structural changes in tissue and impaired wound healing.2 We believe that our patient developed Actinomyces bacteremia from chronic periodontitis precipitated by chronic hyperglycemia and poor oral hygiene. This species is usually susceptible to a great variety of antibiotics including penicillin, ceftriaxone, vancomycin, and linezolid.3 The duration of treatment has not been standardized and ranges from 2 weeks to 1 year.4,5 Although we could not obtain antimicrobial susceptibilities in our patient, we expected this strain to be sensitive to penicillin. However, we chose β-lactam/β-lactamase inhibitor antibiotics to cover potential anaerobes that might have been present in the oral cavity. Infection with A. naeslundii should be considered in every patient who presents with a mucosal barrier breach in oral cavity or gastrointestinal system where tissue healing might be impaired by age, chronic hyperglycemia, or trauma. Appropriate investigation is warranted to rule out causes or mucosal breach. Our case illustrates the pathogenic potential of A. naeslundii and highlights the importance of its treatment in elderly patients with diabetes mellitus. Keshav Bhandari, MBBS All India Institute of Medical Sciences New Delhi, IndiaJose Armando Gonzales Zamora, MD Division of Infectious Diseases Department of Medicine University of Miami Miller School of Medicine Miami, FL [email protected]
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