Abstract

Pulmonary diseases due to mycobacteria cause significant morbidity and mortality to human health. In addition to tuberculosis (TB), caused by Mycobacterium tuberculosis (Mtb), recent epidemiological studies have shown the emergence of non-tuberculous mycobacteria (NTM) species in causing lung diseases in humans. Although more than 170 NTM species are present in various environmental niches, only a handful, primarily Mycobacterium avium complex and M. abscessus, have been implicated in pulmonary disease. While TB is transmitted through inhalation of aerosol droplets containing Mtb, generated by patients with symptomatic disease, NTM disease is mostly disseminated through aerosols originated from the environment. However, following inhalation, both Mtb and NTM are phagocytosed by alveolar macrophages in the lungs. Subsequently, various immune cells are recruited from the circulation to the site of infection, which leads to granuloma formation. Although the pathophysiology of TB and NTM diseases share several fundamental cellular and molecular events, the host-susceptibility to Mtb and NTM infections are different. Striking differences also exist in the disease presentation between TB and NTM cases. While NTM disease is primarily associated with bronchiectasis, this condition is rarely a predisposing factor for TB. Similarly, in Human Immunodeficiency Virus (HIV)-infected individuals, NTM disease presents as disseminated, extrapulmonary form rather than as a miliary, pulmonary disease, which is seen in Mtb infection. The diagnostic modalities for TB, including molecular diagnosis and drug-susceptibility testing (DST), are more advanced and possess a higher rate of sensitivity and specificity, compared to the tools available for NTM infections. In general, drug-sensitive TB is effectively treated with a standard multi-drug regimen containing well-defined first- and second-line antibiotics. However, the treatment of drug-resistant TB requires the additional, newer class of antibiotics in combination with or without the first and second-line drugs. In contrast, the NTM species display significant heterogeneity in their susceptibility to standard anti-TB drugs. Thus, the treatment for NTM diseases usually involves the use of macrolides and injectable aminoglycosides. Although well-established international guidelines are available, treatment of NTM disease is mostly empirical and not entirely successful. In general, the treatment duration is much longer for NTM diseases, compared to TB, and resection surgery of affected organ(s) is part of treatment for patients with NTM diseases that do not respond to the antibiotics treatment. Here, we discuss the epidemiology, diagnosis, and treatment modalities available for TB and NTM diseases of humans.

Highlights

  • Epidemiology and transmission of TB and non-tuberculous mycobacteria (NTM) Epidemiology of drug-sensitive and drug-resistant TB In 2018, about 1·5 million people died from TB, and nearly 10 million people fall ill with Mycobacterium tuberculosis (Mtb) infection worldwide, of which only 6·4 million were diagnosed and officially reported

  • We evaluate the progress made in the areas of Mtb and NTM infections of humans, assessing mainly on the epidemiology, diagnosis, and treatment (Table 1)

  • This study has revealed the recent emergence of dominant clones of M. abscessus that have spread between continents [74]

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Summary

Background

Tuberculosis (TB), caused by Mycobacterium tuberculosis (Mtb), is a leading killer among the infectious disease of humans that mainly affects the lungs [1]. Unlike TB, the treatment for NTM disease takes at least 18 months, with 12 months sputum-negative period [6] In both TB and NTM pulmonary diseases, the bacterial characteristics and the host factors influence the susceptibility and manifestations of infection as well as the outcome of treatment [11, 12]. Our understanding of the epidemiology, risk factors, and pathophysiology of pulmonary TB in humans has significantly improved over the past 50 years. These areas are underdeveloped for NTM diseases. We evaluate the progress made in the areas of Mtb and NTM infections of humans, assessing mainly on the epidemiology, diagnosis, and treatment (Table 1)

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