The full extent of the clinical spectrum and optimal therapy of Anaerobiospirillum succiniciproducens infections remains to be determined. We describe the first case of bloodstream infection (BSI) due to A. succiniciproducens in an asymptomatic elderly male with poor dentition that was treated with levofloxacin.
CASE REPORTAn 81-year-old male presented to our institution for evaluation and treatment of worsening depression. His past medical history was significant for squamous cell carcinoma of the right cheek, for which he had undergone surgery and radiation therapy 15 years ago. He had a nonproductive cough for 3 months, but he denied fever, chills, nausea, vomiting, abdominal pain, or diarrhea. He had not seen a dentist for many years, and he denied any exposure to any pets, including cats or dogs. Physical examination revealed normal temperature, poor dentition, and rales at the right lung base but was otherwise unremarkable. His white blood cell count was 11,500 cells/mm 3 with 82% polymorphonuclear cells, and other laboratory data were normal. A chest X ray revealed an infiltrate at the right lung base, and the patient was started on oral levofloxacin, 500 mg daily for 10 days, for empirical treatment of community-acquired pneumonia. Blood cultures (the anaerobic bottles from 2 sets of blood cultures) obtained on admission due to his pneumonia subsequently grew a spiral Gram-negative rod after 4 days. This was ultimately identified as Anaerobiospirillum succiniciproducens.Bacterial growth was detected in two anaerobic bottles on day 4 of incubation using the BacT/Alert (bioMérieux, Marcy l'Etoile, France). Large Gram-negative spiral-shaped bacteria, measuring on average 6 m in length by 0.7 m in width, were detected on Gram stain (Fig. 1), and corkscrew motility was noted on wet mount. The organism was subcultured to blood agar, chocolate blood agar, and thioglycolate broth; incubated at 35°C in 5% CO 2 and brucella blood agar; and incubated at 35°C under anaerobic conditions. To rule out Campylobacter species, the organism was also subcultured to brucella blood agar and incubated at 35°C and 42°C in a microaerophilic environment. Anaerobic growth on brucella blood agar revealed translucent, nonhemolytic colonies; no growth was observed on blood agar or brucella blood agar in a microaerophilic atmosphere. The isolate was oxidase, catalase, and nitrate negative. RapID ANA II (Remel, Lenexa, KS) revealed positive ␣-glucosidase and N-acetylglucosaminidase reactions but was unable to successfully identify the organism. We further confirmed the identification of Anaerobiospirillum spp. by investigating the specific flagellar arrangement using a transmission electron microscope. Spiral bacteria with bipolar multitrichous flagella were evident in all grid fields examined (Fig. 2).Molecular identification of the bacterium was obtained by sequencing of the 16S rRNA gene. Whole-genomic DNA was extracted from a single colony of the bacterium using the NucliSENS easyMag system (bioMérieux, Durham, NC). The 5Ј 527 base...