Volume 22, Number 3—March 2016
Leveraging Advances in Tuberculosis Diagnosis and Treatment to Address Nontuberculous Mycobacterial Disease
In recent years, major investments in basic research related to Mycobaterium tuberculosis have culminated in the large-scale rollout of the GeneXpert (Cepheid, Sunnyvale, CA, USA) diagnostic platform, the approval of bedaquiline for treatment of patients with drug-resistant tuberculosis (TB), and a deeper fundamental understanding of how the bacteria causes disease. These advancements stand in stark contrast to the poor understanding of the nontuberculous mycobacteria (NTMs). The NTMs are a group of organisms within the genus Mycobacterium (excluding M. tuberculosis and M. leprae) that cause a spectrum of diseases that include TB-like lung disease; localized infections of the lymphatic system, skin, soft tissue, or bone; and systemic disease (1). Previous studies have helped uncover NTM prevalence in industrialized countries in which differentiating between TB and NTM infections is much less challenging because of the availability of molecular techniques for detecting and identifying microorganisms. However, recent studies that have been done to examine the NTM burden of illness in industrialized settings have consistently uncovered an unexpectedly large prevalence (Figure).
Major obstacles to adequately addressing NTM disease include the challenges of diagnosis and treatment as well as the lack of active research to understand the pathogenesis of these organisms. In each of these arenas, it is critical that we address gaps in the knowledge and capacity to deal with NTM-associated illness. By increasing funding to programs that seek to expand basic knowledge of NTMs and leveraging advancements in TB diagnostics and therapeutics, we can begin to form a deeper understanding of these pathogens and develop appropriate measures to address them. Here, we outline some of the challenges surrounding the diagnosis and treatment of NTMs and research of these organisms and propose avenues for how the road paved by the fight against TB can serve as a scaffold for advancing our understanding of these related, neglected pathogens.
NTMs share many characteristics with M. tuberculosis that make the bacteria difficult to differentiate in resource-poor settings. The standard method for diagnosing TB is through microscopic examination of sputum smears, but when this approach is used, NTMs appear identical to M. tuberculosis. Without molecular methods, which are unavailable in much of the developing world, these organisms are difficult to distinguish. Furthermore, in resource-limited settings, patients are often assumed to have M. tuberculosis infections because the clinical manifestations of many NTMs can mimic those of TB. In a study in Nigeria, Pokam et al. found that 16.5% of culture and sputum isolates thought to be M. tuberculosis were bacteria other than M. tuberculosis upon molecular typing; 25% of these misdiagnosed cases (4% overall) were found to be caused by NTMs (2). In another study in Nigeria, Aliyu et al. found that of 1,603 suspected TB cases, 15% were found to be NTM infections (3). Recent evidence has suggested that the rate of confusion between M. tuberculosisand NTMs may be even larger. Turnbull et al. discovered that inmates in a prison in Zambia who had symptoms of cough and an abnormal chest radiograph image showed an NTM prevalence of 5.4% compared with a 3.8% rate for M. tuberculosis (4).
These findings have substantial implications for global health approaches to TB. Given that traditional treatments for M. tuberculosis infection are ineffective against most NTMs, the unexpectedly high rate of NTMs is likely a contributing factor to perceived TB treatment failure. In Brazil, a national mycobacterial referral center found that of 174 patients with pulmonary NTM, 79% had undergone TB treatment for up to 6 months before NTM infection was diagnosed (5). Studies conducted in Burkino Faso and Mali found that 18%–20% of patients suspected of having chronic TB were found to have NTM in their sputum (6). Similarly, a study in Iran showed that as many as 30% of suspected cases of multidrug-resistant TB were in fact NTMs, further suggesting the generalization of this phenomenon (7). Understanding the true prevalence of NTMs in the developing world is especially valuable considering that evidence suggests that NTM infection may interfere with the Bacille Calmette-Guérin vaccine, a widely used tool in preventing TB infections in the developing world (8).
These studies must be taken with some caution, as it is often difficult to distinguish whether the NTMs are a true source of infection or a contaminant in biological specimens or laboratory equipment. To account for this, the American Thoracic Society and the Infectious Disease Society of America guidelines for NTM diagnosis require isolation and growth of the pathogen on >2 separate occasions from the same patient to diagnose a pulmonary NTM infection (9). Because clinicians in most countries in the developing world often make diagnosis of TB on the basis of clinical symptoms, these guidelines may place a tremendous burden on laboratories in resource-poor settings. Any new diagnostic platform for the NTMs must account for the issues behind species differentiation and contamination and do so in a way that is feasible for application globally.
The difficulty of diagnosing NTMs and the frequent confusion of these pathogens with TB is compounded by the fact that standard TB treatments are often ineffective against NTM infections. Anti-TB medications produce a disappointing ≈50% response rate (10) in NTM-associated disease. As a result, misdiagnosis and mistreatment have huge implications on patient outcomes. Even within the NTM class, there is a substantial difference between the various species, which defies a one-size-fits-all treatment approach. This group encompasses pathogens with huge varieties of growth rates, host preferences, and inherent resistance to antibacterial drugs.
The introduction of macrolides, such as clarithromycin, for treatment for NTMs did improve cure rates for certain species, but in a retrospective study by Huang et al., many patients treated with these drugs for at least 12 months continued to have symptoms, and chronic illness was documented among patients who were successfully treated (11). Moreover, macrolide resistance is now well documented (12). The recommendation of multidrug regimens to counter such resistance is a logical next step, but often these regimens are minimally studied, and few if any have been investigated in a rigorous clinical trial. Therefore, while many clinicians rely on multidrug regimens for the treatment for NTM disease, the ideal combination of agents, duration of therapy, and true efficacy remain unvalidated and unknown.
Fundamentally, poor understanding of the NTMs arises from a lack of investment. There have been few clinical studies of treatment for NTM-associated disease; most date from a time when advanced HIV infection was common in industrialized countries and opportunistic NTM infections were seen at an alarming frequency among HIV/AIDS patients. We conducted a search using the RePORTER tool (http://projectreporter.nih.gov/reporter.cfm) to find currently active grants from the US National Institutes of Health for this topic and found 228 grants related specifically to research on mycobacterial pathogens. Of these, only 5 (2.2%) were awarded to study specific aspects of the NTMs. These 5 grants cover a wide range of unmet needs, from understanding NTM susceptibility to novel drug discovery. However, this level of attention is clearly insufficient to address the many gaps that exist.
As prevalent as they are, many basic facts about the NTMs remain unknown. For example, it was largely thought that environmental exposure was the sole method of infection. However, a recent report that described whole genome sequencing as a molecular epidemiologic tool suggested that, in the context of cystic fibrosis patients, which is a population exceptionally susceptible to these pathogens, there may be a possibility of person-to-person transmission ofM. abscessus (13). If true, control measures similar to those used for TB transmission might be effective, at least for highly susceptible persons. Although this study suggests that alternate modes of transmission may exist, it is still widely believed that environmental transmission is the major source of NTM infection, and numerous reservoirs such as household water sources have been identified (14). However, it can often be difficult to trace infections to a specific environmental source, which is a problem that is compounded by delayed and often incorrect diagnoses.
Additionally, it remains unclear why anti-TB medications are not effective treatment options. NTMs have complex cell walls, systems that modify both antibacterial drugs and their targets, and an extensive array of drug efflux pumps, but all these mechanisms also exist in M. tuberculosis. It may be that in NTMs, differing synergy of these and other mechanisms might conspire to produce a poor response to therapy. However, these differences must be studied to determine their significance. Such questions highlight the numerous areas in which our ability to address these pathogens would benefit from a better fundamental understanding.
Although there are no simple solutions to the challenges of effectively addressing the NTMs, recent advancements in the TB field have potential for synergistic effects. One of the major breakthroughs in TB diagnostics over the past decade was the move toward using molecular methods such as the GeneXpert system. Although GeneXpert testing distinguishes fairly well between NTMs and M. tuberculosis, it does not distinguish within the broad category of NTMs, which is a necessary prerequisite to effective treatment. However, this advancement provides an opportunity to reconfigure molecular diagnostic platforms to include at least common NTM pathogens, providing a rapid and specific detection method. Even so, this method would not be a panacea. Because NTMs can colonize humans without causing disease and can contaminate biologic samples and laboratory equipment, simply finding the organism does not provide a definitive diagnosis. However, even raising the possibility can alert a clinician to consider the diagnosis of NTM-associated illness, limiting misdiagnosis and, as a result, incorrect treatment. These systems would also provide researchers with a tool to uncover the true burden of illness from NTMs.
Substantial efforts have been invested in anti-TB drug development. These have yielded 2 new approved antibiotics, bedaquiline and delamanid; several others are in clinical development. These drug discovery platforms could easily be transferred to screening for NTM-active compounds, and some of the new agents have already been shown to have activity against NTMs. For example, bedaquiline is more effective than currently existing antimycobacterial agents in treating M. ulcerans in a mouse model of infection and has shown promise as a salvage therapy for M. avium and M. abscessus (15,16). Moreover, new oxazolidinones, a class of drug effective against many NTMs, are currently being developed for TB and might prove clinically useful (17). Although many antitubercular compounds have poor activity against NTMs, new agents could serve as starting points that could be optimized; for example, bedaquiline derivatives have been found to have broad-spectrum activity (18).
While building on discoveries in the TB field, developing new interventions to diagnose, treat and prevent NTM-associated illness will likely require a better basic understanding of these organisms. Mycobacteria are extremely diverse; >150 species have been identified to date and vary in pathogenicity, virulence, mode of transmission, and antibiotic susceptibility. Here, too, the path paved by TB biologists could afford some insight into NTM physiology. The sequencing of the M. tuberculosis genome and the development of genetic tools to probe the bacterium’s physiology afforded novel insights into how this pathogen causes disease. Similarly, the sequencing of many NTM species, now being completed, could lead to novel discoveries that highlight why these organisms have been so difficult to treat in the past and why exactly they diverge from M. tuberculosis (19).
None of these measures will be taken without increased funding. The prevalence of NTMs not only in developing countries but also in the United States and many parts of Asia suggests that many public agencies should be willing to support NTM research. However, public funding is not the only avenue for increasing investment. Considering the prevalence and chronicity of these organisms in the industrialized world, a potentially substantial market of affected entities may exist. Resources from private interests and pharmaceutical companies could be leveraged to develop novel diagnostics and therapeutics if encouraged by advancements in the academic setting in our basic understanding of these pathogens.
The evidence that has been uncovered to date points to the NTMs as a source of substantial and growing burden of illness. NTM infections not only effect thousands of people, requiring lengthy and taxing treatments that are often not available in resource-poor settings; they also muddy the waters in the global fight against TB by draining resources resulting from misdiagnosis and mistreatment. Only through a concerted effort by researchers, clinicians, industry, and global health policy stakeholders to understand and address these issues can we respond to this large and neglected threat.
Dr. Raju is a physician and scientist and is currently a pediatric resident at Children’s Hospital Boston, Boston, Massachusetts, in the Urban Health and Advocacy Track. His professional and research interests are in the biology of essential physiologic processes in M. tuberculosis and nontuberculous mycobacteria, with the overall goal of developing novel therapeutics for these neglected diseases.
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Suggested citation for this article: Raju RM, Raju SM, Zhao Y, Rubin EJ. Leveraging advances in tuberculosis diagnosis and treatment to address nontuberculous mycobacterial disease. Emerg Infect Dis. 2016 Mar [date cited]. http://dx.doi.org/10.3201/eid2203.151643
1These authors contributed equally to this article.
The footnote "1 " is not cited in the text. Please add an in-text citation or delete the footnote.
Medline reports that reference 9 "Griffith, Aksamit, Brown-Elliott, Catanzaro, Daley, Gordin, et al., 2007" was corrected in "Am J Respir Crit Care Med. 2007 Apr 1;175(7):744-5" (Note: Dosage error in article text).
Reference has only first page number. Please provide the last page number if article is longer than one page. (in reference 19 "Tateishi, Kitada, Miki, Maekura, Ogura, Ozeki, et al., 2012").