Mycobacterium terrae infection can cause progressive debilitating disease. A case of a 63-year-old man with localized pulmonary infection characterized by extensive, thick-walled cavitary lesions is presented. A pneumonectomy was considered as definitive treatment, but the patient would not have tolerated the procedure given his severe deconditioning. Instead, he was placed on lifelong antibiotic treatment, but he continued to deteriorate and passed away. The slow-growing microorganism, Mycobacterium terrae, was isolated from bronchoalveolar lavage cultures seven weeks after specimen collection, five and a half weeks after the patient’s death. Clinical, microbiological and therapeutic data from this case and 16 other pulmonary cases from the literature are reviewed. Increased awareness of this microorganism will allow clinicians to consider Mycobacterium terrae in their differential diagnosis when dealing with nontuberculous mycobacteria infections.
Mycobacterium terrae was first isolated by Richmond and Cummings in 1950 from radish washings, which was originally simply called as the “radish bacillus”. This organism was described as a nonpathogenic saprophyte, as it did not cause any skin ulcerations or regional node involvement after being inoculated into guinea pigs . Wayne, in 1966, described it as being abundantly found in soil, for which it received its name M. terrae, for the Latin “Terra” . Mycobacterium terrae forms part of the Mycobacterium terrae complex, in conjunction with M. nonchromogenicum and M. triviale. These mycobacteria are described as slow-growing, nonchromogenic, acid-fast saprophytes, which exhibit high catalase activity, and β-galactosidase activity, which is not seen in other slow-growing mycobacteria .
Traditionally, M. terrae has been considered a contaminant. Despite being uncommon, there has been increasing evidence of infections caused by this microorganism. The most commonly affected areas are joints, tendon sheaths, bursae, and bones, with the tenosynovium of the hand and wrist being the most common site of infection . Additionally, there are cases of infection involving lungs, skin, gastrointestinal tract, genitourinary tract, lymph nodes, or disseminated disease . Here, we present a rare case of this challenging infectious disease affecting the lungs.
A 63-year-old man with a history of chronic obstructive pulmonary disease, former one pack per day cigarette smoker for 10 years, degenerative joint disease, and seizure disorder initially presented to another facility in September 2015 with chronic productive cough and an abnormal chest X-ray. His physician there performed a bronchoscopy with bronchoalveolar lavage (BAL), which confirmed M. terrae infection. The patient was started on an unknown treatment regimen. Sixteen months later, in February 2017, he presented to the hospital with complaints of shortness of breath, productive cough with green sputum, chills, night sweats, generalized muscle weakness, loss of appetite, and cachexia with a body mass index of 11.8 kg/m2 and albumin of 2.6 g/dL. He denied fevers. The patient stated he was not eating and decided to go to the emergency department because he became so weak that he was unable to get up from bed. A chest X-ray was taken (Figure 1) which showed left upper lobe and right basilar infiltration, with a cavitary process in the right upper lobe.
A pulmonologist was consulted, and a computerized tomography (CT) of the chest showed a large cavitary lesion occupying the right hemithorax (Figure 2). Due to the previous diagnosis of M. terrae and worsening symptoms, a bronchoscopy was performed and he was started on an empirical antibiotic regimen of clarithromycin, ethambutol, and rifampicin. A repeat CT chest taken a week later showed progression of disease (Figure 3). A pneumonectomy was considered as an option, but the patient was deemed a poor candidate for the procedure given his severe protein calorie malnutrition, generalized weakness, and overall deconditioning. Therefore, he was placed on lifelong treatment with the three-medication regimen for the treatment of M. terrae.
Despite therapy, the patient continued to deteriorate and requested comfort measures. A hospice consult was placed, and a meeting with the family was arranged. His code status was do not resuscitate (DNR). He became hypoxic overnight and passed away the following morning. Bronchoalveolar cultures of the right lower lobe confirmed infection by M. terrae seven weeks after specimen collection, five and a half weeks after the patient’s death.
The prevalence and incidence of lung disease by M. terrae has been increasing worldwide since the first reported case of pulmonary infection in 1983 [5,6]. Case reports from around the world were reviewed, including pulmonary and extra pulmonary M. terrae infections, in order to gain better clinical recognition and reach an understanding of this pathogen's behavior . Characteristics from 16 prior pulmonary cases and the one reported here are described in Table 1 [6-15].
In the 17 cases analyzed, the age range of patients was 13 to 74 years, with a median age of 50 years. There were five females and 12 males. The time from the first clinical symptom to definitive diagnosis ranged from two to eight months, with a median of five months. The cases were reported from various countries including Japan (eight), United States (five), Spain (two), Argentina (one), and Italy (one) [6-15].
Of the 17 patients, 12 (71%) had an underlying chronic medical condition [7-15]. Of these, two patients (11%) were immunosuppressed: one with acquired immunodeficiency syndrome and the other with active malignancy receiving bone marrow transplant treatments [11,13]. There were nine patients with predisposing lung conditions including history of tuberculosis infection (four), chronic smoking (four), and cystic fibrosis with bronchiectasis (one) [7,9,12,14,15].
There was a predominant pattern of cavitary lesions noted in imaging studies of the chest in 11 (65%) patients [6-10,14]. Miliary infiltrates in the lungs were reported in the two (11%) immunosuppressed patients [11,13]. Other patterns of pulmonary infection reported in the remaining patients were fibrocaseous lesions (one), bullous lesions (two), large lung mass (one), and bilateral infiltrates (one) [7,12,15]. There was no correlation identified between occupation and exposure to the mycobacteria.
A review of treatment regimens used in these 17 patients showed that 14 (82%) patients were on multidrug regimens during their course of treatment. The mean duration for their treatment was 12 months. Three of the 17 patients did not receive any treatment at all. Two patients who did not receive treatment reportedly died of cor pulmonale, and one died of respiratory failure before he could initiate treatment [6,13]. Treatment duration was adjusted based on negative culture findings as well as improved clinical and radiographic evidence of an ongoing disease.
There was no single combined antibiotic regimen that yielded a 100% cure rate. There was a tendency toward combined therapies including ethambutol and rifampicin noticed in eight (47%) cases [6-9,12,14]. Of the 13 cases in which in vitro susceptibility tests were performed, 12 cases (92%) were susceptible to ethambutol, five cases (38%) to rifampicin, three cases (23%) to streptomycin, and another three cases (23%) to ethoniamide. Other nonresistant drugs included cycloserine (one), rifabutin (one), ciprofloxacin (one), and clarithromycin (one) [6-10,13,14]. Consistent with the literature reviewed, in vitro drug susceptibility to ethambutol, rifampicin, and a macrolide antibiotic makes this the most reasonable empirical regimen to initiate in suspected M. terrae infections.
Reported outcomes showed that eight patients (47%) were completely cured from their condition with combined antibiotic therapy alone, two (12%) were cured from infection but structural lung lesions remained, one (6%) was cured after a lobectomy and combined antibiotic therapy, and six (35%) cases resulted in death [6-15]. Statistical analysis regarding treatment and outcome relation cannot be performed due to too few cases reported. Our analysis was based on all of the reported cases of pulmonary infection by M. terrae. We acknowledge that there may be unreported cases by this pathogen that could change the result of the data reviewed.
Patients who develop nontuberculous mycobacteria (NTM) lung disease usually have susceptibility factors, like structural lung damage, derived from conditions such as chronic obstructive pulmonary disease, bronchiectasis, prior history of tuberculosis, immunosuppression, primary ciliary dyskinesia, or cystic fibrosis, among others . Classically, microorganisms of the M. terrae complex are considered contaminants and nonpathogenic colonies, rather than true causative agents of NTM lung disease. When found in cultures, however, their presence should be carefully interpreted . After analyzing the literature, we found that this is the 17th case reported of pulmonary M. terrae infection worldwide.
In contrast with M. tuberculosis, isolation of M. terrae does not make the definitive diagnosis of NTM lung disease. According to the American Thoracic Society, criteria for diagnosis of pulmonary NTM disease, most recently updated in 2007, is based on integration of clinical, radiographic, and microbiological findings (Table 2) . This case met all the criteria, fitting with the nonspecific symptomatology of NTM lung disease, an extensive thick-walled cavitary lesion on the right hemithorax on the chest CT, and a positive BAL culture for M. terrae.
Isolation of acid-fast bacilli in a smear of sputum or BAL sample is usually the first sign that clinicians are dealing with a mycobacteria lung disease. Due to this, all the previously reported cases of pulmonary M. terrae infection were originally started on antituberculosis regimens, and after a slow three- to eight-week incubation period, microbiology services identified M. terrae and reported culture findings [6-15]. However, despite previous isolation in culture and diagnosis of pulmonary infection by M. terrae, there are no standard recommended treatment guidelines. The optimal antibiotic treatment is not established, but based on in vitro susceptibility, may include ethambutol, rifampicin, and a macrolide. After reviewing the literature, we found that the majority of cured cases followed a multi-antibiotic regimen for at least 12 months from the first negative culture [6,9,14,15]. In some cases, in which the microorganism persisted despite antibiotic therapy, amputation of the infected site, a partial or total pneumonectomy, was an alternative curative treatment . In our analysis, we found that the antibiotics with the highest in vitro susceptibility were ethambutol, followed by rifampicin, and streptomycin. We acknowledge that this susceptibility is based on the limited data reviewed of the few reported cases. Testing in vitro susceptibility may be useful to measure the growth response of this isolate to specific drugs to cover the possibility of variants and adjust therapy accordingly. Significant in our case, the patient had prior history of M. terrae infection; therefore, a chronic M. terrae infection was highly suspected. A confirmatory bronchoscopy was performed, and the patient was started on an empiric antibiotic regimen of clarithromycin, ethambutol, and rifampicin.
In the literature, only one case reports a lobectomy as the definitive treatment for chronic pulmonary M. terrae infection not eradicated by antibiotic therapy . We believe our patient could have benefited from a pneumonectomy of the affected area if he would not have been so deconditioned. Due to the severity of his disease, poor prognosis, and lack of standardized treatment guidelines, the patient was recommended lifelong antibiotic therapy, differing from prior cases where they only recommended therapy for 12 months to obtain complete eradication.
There have been reports hypothesizing that spontaneous resolution is part of the natural course of lung disease by M. terrae [11,14]. However, in the pulmonary cases reviewed, the absence of treatment correlated with death by respiratory insufficiency [7,13]. Our patient had a progressive course with fatal outcome, which raises concern of this inappropriately labeled “nonpathogenic” microorganism. Since the first pulmonary infection case by M. terrae, reported in 1983, there have been 17 cases reported [6-15]. Statistically, this is equivalent to one case reported every two years worldwide. For this reason, physicians should include this NTM in the differential diagnosis for atypical mycobacteria infections.
Mycobacterium terrae should be considered a human pathogenic microorganism. Although initial isolation of M. terrae is usually considered a contaminant rather than a diagnosis, it should not be clinically disregarded right away, and further microbiological testing is recommended. Increased awareness amongst clinicians and microbiologists may improve the recognition of this NTM, which can have a fatal outcome, as it did with the patient presented.
- Richmond L, Cummings MM: An evaluation of methods of testing the virulence of acid-fast bacilli. Am Rev Tuberc. 1950, 62:632-637.
- Wayne LG: Classification and identification of mycobacteria. 3. Species within group 3. Am Rev Respir Dis. 1966, 93:919-928. 10.1164/arrd.19188.8.131.529
- Wayne LG, Sramek HA: Agents of newly recognized or infrequently encountered mycobacterial diseases. Clin Microbiol Rev. 1992, 5:1-25. 10.1128/cmr.5.1.1
- Milne BW, Arnold MH, Hudson B, Coolican MR: Infectious arthritis of the knee caused by Mycobacterium terrae: a case report. J Orthop Surg (Hong Kong). 2009, 17:103-108. 10.1177/230949900901700123
- Smith DS, Lindholm-Levy P, Huitt GA, Heifets LB, Cook JL: Mycobacterium terrae: case reports, literature review, and in vitro antibiotic susceptibility testing. Clin Infect Dis. 2000, 30:444-453. 10.1086/313693
- Kuze F, Mitsuoka A, Chiba W, et al.: Chronic pulmonary infection caused by Mycobacterium terrae complex: a resected case. Am Rev Respir Dis. 1983, 128:561-565. 10.1164/arrd.19184.108.40.2061
- Tsukamura M, Kita N, Otsuka W, Shimoide H: A study of the taxonomy of the Mycobacterium nonchromogenicum complex and report of six cases of lung infection due to Mycobacterium nonchromogenicum. Microbiol Immunol. 1983, 27:219-236. 10.1111/j.1348-0421.1983.tb03585.x
- Krisher KK, Kallay MC, Nolte FS: Primary pulmonary infection caused by Mycobacterium terrae complex. Diagn Microbiol Infect Dis. 1988, 11:171-175. 10.1016/0732-8893(88)90020-x
- Tonner JA, Hammond MD: Pulmonary disease caused by Mycobacterium terrae complex. South Med J. 1989, 82:1279-1282. 10.1097/00007611-198910000-00021
- Palmero DJ, Teres RI, Eiguchi K: Pulmonary disease due to Mycobacterium terrae. Tubercle. 1989, 70:301-303. 10.1016/0041-3879(89)90026-3
- Peters EJ, Morice R: Miliary pulmonary infection caused by Mycobacterium terrae in an autologous bone marrow transplant patient. Chest. 1991, 100:1449-1450. 10.1378/chest.100.5.1449
- Spence TH, Ferris VM: Spontaneous resolution of a lung mass due to infection with Mycobacterium terrae. South Med J. 1996, 89:414-416. 10.1097/00007611-199604000-00013
- Carbonara S, Tortoli E, Costa D, et al.: Disseminated Mycobacterium terrae infection in a patient with advanced human immunodeficiency virus disease. Clin Infect Dis. 2000, 30:831-835. 10.1086/313773
- Diaz Ricoma N, Gonzalez Vargas F, Casado Moreno I, Galan Antonanza L, Rojas Sierra M, Alado Arboleda JC: Lung infection by Mycobacterium terrae. Arch Bronconeumol. 2001, 37:96-98. 10.1016/s0300-2896(01)75022-3
- Lopez-Rodriguez MJ, Herranz M, Disdier C, Vinuelas J: Infection by Mycobacterium terrae in a patient with cystic fibrosis. Med Clin (Barc). 2007, 128:798-789. 10.1157/13106335
- Cowman SA, Loebinger MR: Diagnosis of nontuberculous mycobacteria lung disease. Semin Respir Crit Care Med. 2018, 39:343-350. 10.1055/s-0038-1651493
- Koh WJ: Nontuberculous mycobacteria-overview. Microbiol Spectr. 2017, 5:10.1128/microbiolspec.TNMI7-0024-2016
- Griffith DE, Aksamit T, Brown-Elliott BA, et al.: An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases. Am J Respir Crit Care Med. 2007, 175:367-416. 10.1164/rccm.200604-571ST
Pulmonary Infection Caused by Mycobacterium terrae: A Case Report and Literature Review
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Cite this article as:
Duran M, Araiza A, Surani S R, et al. (November 25, 2019) Pulmonary Infection Caused by Mycobacterium terrae: A Case Report and Literature Review. Cureus 11(11): e6228. doi:10.7759/cureus.6228
Received by Cureus: November 15, 2019
Peer review began: November 19, 2019
Peer review concluded: November 20, 2019
Published: November 25, 2019
© Copyright 2019
Duran et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 3.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.