iHere we report in a human, a renal transplant patient, the first disseminated infection with Nocardia cerradoensis, isolated after a brain biopsy. Species identification was based on 16S rRNA, gyrB, and hsp65 gene analyses. Antibiotic treatment was successful by combining carbapenems and aminoglycosides and then switching to oral trimethoprim-sulfamethoxazole.
CASE REPORTA 59-year-old woman with a history of end-stage renal disease, secondary to autosomal-dominant polycystic kidney disease, received a renal transplant in 2010. Her immunosupressive regimen included tacrolimus at 12 mg/day and prednisolone at 7.5 mg/day. Prophylaxis with trimethoprim-sulfamethoxazole (SXT) was given for 6 months after the transplantation and then stopped due to intolerance symptoms. The patient had no history of recent travel. Two weeks before admission, she had had a mild headache with fever and chills and she was empirically treated with amoxicillin and prednisone for 7 days. After a brief improvement, she developed a nonproductive cough with dyspnea. Based on the hypothesis of pneumonia, antibiotic treatment was switched to ceftriaxone combined with aerosol bronchodilators. The patient's pulmonary symptoms rapidly worsened, and in September 2013, she was admitted to the hospital for further investigation.On examination, the patient was awake and complained of inspiratory dyspnea. Diarrhea was noted a few days after the initiation of antibiotic treatment and resolved spontaneously. The patient's temperature was measured at 37.8°C, blood pressure was 150/90 mm Hg, pulse was 97 beats/min, respiratory rate was 36/ min, and oxygen saturation was 97% while she was breathing ambient air. The auscultation evidenced bilateral basal crepitus and no other abnormal sounds. Heart sounds were normal, abdomen was soft, without tenderness, distention, or organomegaly, and neurologic examination was normal. No peripheral lymph nodes were detected. Subcutaneous nodules of the lower extremities appeared a few days after the patient was admitted (Fig. 1A). The white cell count was 18.6 ϫ 10 9 /liter, with 95% neutrophils, and the blood level of C-reactive protein was 159 mg/liter. A chest X-ray and a computed tomography (CT) scan showed wall thickening of the right main bronchus, moderate ground-glass opacities of the right upper lobe, a right hilar lymph node, a small right parenchymal nodule (Ͻ10 mm), and moderate homolateral pleural effusion (Fig. 1B). An abdominal CT scan revealed diffuse peritoneal and right retroperitoneal nodules (Fig. 1C) and a thickening of the cecal wall. Bronchoalveolar lavage (BAL) fluid, bronchial, and subcutaneous biopsy specimens were collected, and examination of stained smears (using Gram, Ziehl-Neelsen, May-Grünwald-Giemsa, Papanicolaou, Perls, and hematoxylin-safranin stains) showed no bacteria or abnormal cells. Cultures for bacteria, fungi, and mycobacteria were all negative. Histological examination of the subcutaneous nodule identified an erythema nodosum. Amplification of bacterial 16S rRNA gene from the c...