A case of pleural effusion caused by Mycobacterium fortuitum and Mycobacterium mageritense coinfection

Non-tuberculous mycobacteria (NTM) are common organisms in the environment, and they can cause chronic pulmonary infection. As a group of NTM, rapid-growing mycobacteria (RGM) contain Mycobacterium chelonae, M. fortuitum and M. mageritense [1]. The most common sites of infection with these mycobacteria are pulmonary tissues, skin, bone, and soft tissue.

There are several reports of coinfection with different species of myobacteria. However, NTM infections rarely cause pleural effusion [1] and there are no reports of NTM coinfection associated with pleural effusion. Herein we report a case of pleural effusion caused by M. fortuitum and M. mageritense coinfection, which was identified from pleural effusion culture and bronchoalveolar lavage (BAL) fluid.

A 68-year-old woman with rheumatoid arthritis was admitted to our hospital complaining of fever, dry cough, and night sweats for the past 2 weeks. She had been diagnosed with rheumatoid arthritis 9 years prior. She had been taking 5 mg/day prednisone and azathioprine, and she had started taking certolizumab pegol from 6 months prior to the current admission.

She reported no malaise, hemoptysis, or weight loss. Other than the aforementioned factors she had no past medical history, including interstitial lung disease or tuberculosis, she was not taking any other medications, and she had no pets. She had never smoked, and she worked as a pharmacist.

On admission her body temperature was 38.2 °C but other vital signs were not remarkable. Chest x-ray revealed bilateral opacity that was more pronounced on her right side (Fig. 1). Her white blood cell count was 11,700 μL^− 1, hemoglobin was 10.0 g dL^− 1, and C-reactive protein was 17.12 mg/dL. An HIV assay for HIV-1 and HIV-2 was negative, as was an interferon gamma release assay.

Chest computed tomography (CT) depicted bilateral opacity on her lower lung and pleural effusion on her right thoracic cavity (Fig. 2). Thoracentesis was performed to obtain 150 mL of pleural effusion fluid from the right side. The white blood cell count of that fluid was 12,700/μL^− 1 (22.7% lymphocytes), and it contained 5.4 g protein/dL^− 1, 2.8 g albumin/dL^− 1, and 1503 U lactate dehydrogenase/L^− 1.

BAL fluid and pleural fluid culture were performed. Acid-fast bacilli were detected by Ziehl-Neelsen staining but the species could not identified using a DNA-DNA hybridization method or the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The drug susceptibility testing revealed resistance to amikacin (minimum inhibitory concentration > 32 μg/mL), but reexamination for microbial identification and the drug susceptibility testing suggested susceptibility to amikacin. To investigate contamination or mycobacterial coinfection, growth enhancement on Middlebrook 7H11C agar plate testing was performed. Two types of colonies were developed from both BAL and pleural fluid culture, and the causative microorganisms were identified as M. fortuitum and M. mageritense by MALDI-TOF MS—with each of the hsp65 and rpoB region sequences respectively exhibiting 100 and 99.0% matching with M. fortuitum, and 98.4 and 99.0% matching with M. mageritense.

Eight weeks of treatment with imipenem/cilastatin (500 mg every 6 h intravenously), minocycline (100 mg orally twice a day), and levofloxacin (500 mg orally once a day) were initiated, followed by 4 months maintenance therapy by minocycline and levofloxacin. After the maintenance therapy, Her symptoms and bilateral pulmonary opacity were improved (Figs. 3 and 4). Now we follow her for 2 years, her sputum culture is still negative and her chest x-ray is still clear.

This is the first report of pleural effusion caused by two species of RGM coinfection. There are several reports of pulmonary infection or pleural effusion caused by the coinfection of mycobacteria, which include NTM and Mycobacterium tuberculosis complex (MTC) coinfection or different subspecies of M. avium complex coinfection. In cases of pulmonary infection however, it is difficult to prove coinfection from sputum because it is easily colonized by NTM, and often it is difficult to isolate or identify the species involved. Aseptic collection of body fluid such as pleural effusion via needle aspiration is better for the verification of NTM coinfection [1], but NTM rarely causes pleural effusion than MTC. In the present case NTM coinfection was verified via pleural effusion and BAL. there are no previous reports of coinfection with nontuberculous mycobacteria in pleural effusions and this is the first report about it.

Neither DNA-DNA hybridization nor MALDI-TOF MS identified the species, and the aforementioned contradictory results of drug susceptibility testing were obtained twice. MALDI-TOF MS is one of the recommended molecular methods for identifying NTM [2], but the method is limited with regard to specificity in this respect (52.8–98.6%) [3, 4]. If the species cannot be identified, mycobacterial coinfection should be considered.

In conclusion, this report described a case of pleural effusion caused by M. fortuitum and M. mageritense coinfection. In cases of mycobacterial infection where microbiological testing cannot identify the species involved, coinfection should be considered and more extensive investigation to determine the species should be undertaken.