cWe report a multidrug-resistant strain of Leclercia adecarboxylata responsible for catheter-related bacteremia in a 47-year-old female with breast cancer. The isolated strain was resistant to several -lactams, aminoglycosides, and folate pathway inhibitors and harbored bla TEM-1 and bla CTX-M group 1 and intl1 genes (dfrA12-orfF-aadA2) as genetic determinants for resistance. Based on a review of the L. adecarboxylata literature, there have been only 4 reports of antibiotic-resistant strains. To our knowledge, this is the first report of an L. adecarboxylata strain with simultaneous resistance to -lactams, aminoglycosides, and sulfonamides.
CASE REPORTA 47-year-old female was diagnosed with cancer of the right breast. Chemotherapy was administered through a peripherally inserted central catheter (PICC) inserted in the left basilic vein. Twenty days after PICC insertion, the patient developed a high fever and general myalgia. Due to her symptoms, she visited the emergency room at Chonbuk National University hospital on 29 August 2011. On admission, her blood pressure was 120/86 mmHg, pulse was 78/min, respiration rate was 20/min, and temperature was 38.4°C. Laboratory studies revealed a white blood cell (WBC) count of 2,700/ml, hemoglobin level of 11.7 g/dl, platelet count of 310,000/ml, serum creatinine of 0.67 mg/dl, aspartate aminotransferase level of 20 IU/liter, alanine aminotransferase level of 13 IU/liter, and total bilirubin level of 0.47 mg/dl. Plain abdominal erect imaging and chest computed tomography were unremarkable. The initial antibiotic therapy included cefminox sodium and isepamicin for 3 days. Her fever persisted, however, and her WBC count increased abruptly to 17,020/ml 2 days following admission. The treatment regimen was changed to cefepime, based on antibiotic susceptibility tests (AST) from blood cultures. This guided antibiotic therapy was successful and the patient became afebrile.Initial cultures from venous and catheter blood were sampled separately, and the causative microorganism was identified as a Gram-negative bacillus. One day following admission, the catheter tip (PICC) was cultured and yielded bacteria similar to those in the blood culture by microscopic examination. The blood culture was subcultured on sheep blood agar to generate a pure colony. The isolate was identified as Leclercia adecarboxylata by a Vitek2 automatic identification system using a GN card (bioMérieux, Marcy l' Etoile, France). The bacteria were further identified by partially sequencing the 16S rRNA gene from genomic DNA. DNA was amplified and sequenced by Genotech (Korea). The partial 16S rRNA sequences of the isolate had 99.8% identity with L. adecarboxylata GTC1267 (accession no. AB273740) in the NCBI genomic database. The isolate was maintained in the Chonbuk National University Hospital Culture Collection for pathogens as KBN0601918.The AST of L. adecarboxylata was investigated using the Vitek2 automatic system with the AST-N131 card and the disk diffusion method. The results are summarized in Table...