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EDITORIAL article

Front. Microbiol., 15 April 2021 | https://doi.org/10.3389/fmicb.2021.681420

Editorial: New Approaches Against Drug-Resistant M. tuberculosis

Yossef Av-Gay1*, Giorgia Mori2* and Maria Rosalia Pasca3*
  • 1Departments of Medicine and Microbiology & Immunology, The University of British Columbia, Vancouver, BC, Canada
  • 2The University of Queensland Diamantina Institute, The University of Queensland, Woolloongabba, QLD, Australia
  • 3Department of Biology and Biotechnology “Lazzaro Spallanzani”, University of Pavia, Pavia, Italy

Tuberculosis (TB) is the most devastating infectious disease worldwide, killing 1.4 million people each year (World Health Organization [WHO], 2020). Treatment regimens are lengthy and cause considerable adverse effects, leading to poor patient compliance, as well as high costs and economic burden worldwide. Moreover, resistance to newly approved antimicrobials for TB develops quickly (Bloemberg et al., 2015; Zimenkov et al., 2017). This, together with the widespread occurrence of Mycobacterium tuberculosis (Mtb) drug-resistant strains, necessitates discovery of novel and innovative drugs that will shorten the duration of TB treatments and/or be less toxic to the human host.

Our Research Topic entitled “New approaches against drug-resistant Mtb” called for original research papers and reviews describing novel approaches for drug discovery, target identification and mechanisms of drug resistance. The response we have received was exciting resulting in 13 articles with more than 30,000 views.

Our collection includes an exciting review describing drug development in our era where modern -omic technologies, such as DNA and RNA sequencing, proteomics, and genetic manipulation of organisms, facilitate the drug discovery process for TB treatment. These methods enable us to better understand mechanisms of action of antibiotics and allow the evaluation of new drug candidates using mathematical modeling and modern computational analysis for the drug discovery process.

Mtb, the causative agent of TB, infects, survives, and replicates intracellularly within alveolar macrophages. Mtb utilizes numerous strategies to avoid host defense mechanisms and preys on the host cell response to establish infection (Hmama et al., 2015). A novel drug discovery approach termed Host Directed Therapy (HDT), was proposed recently to overcome drug resistance (Zumla et al., 2016; Parish, 2020). Since HDTs do not target Mtb directly but rather assist the host in fighting infection, they would have reduced chances of generating resistance.

A series of publications within our Collection explore this new and exciting approach to TB drug development.

Shapira et al. screened a library of human kinase inhibitors and identified several compounds that are active in an intracellular model of TB infection. A specific checkpoint inhibitor showed promising activity and CHK2 inhibition by RNAi phenocopied the intracellular inhibitory effect of the drug.

Smyth et al. showed that Protein Kinase R (PKR) is a human host cell sensor that function in the cellular response to mycobacterial infection. They demonstrated that the over-expression of PKR enhanced anti-mycobacterial activity of macrophages and it is mediated by selective autophagy and by the inhibition of autophagolysosome maturation which limit Mtb replication, suggesting that PKR can be considered for HDT development.

Screening of compound libraries is a valuable tool in drug discovery; Pollo et al. tested a library of 52 natural and synthetic compounds for activity against Mtb growth and identified the natural products isobavachalcone and isoneorautenol, and a synthetic chromene as active at low micromolar concentrations.

Noschka et al., screened a library of antimicrobial peptides generated from hemo-filtrate identifying Angiogenin as the only active compound against Mtb growth. They confirmed its activity using the synthetic Angiogenin. They derived the small peptide fragment Angie1, which is active against intracellular and extracellular Mtb growth, as well as they tested that it is not toxic for zebrafish embryos.

Khara et al. assessed the anti-mycobacterial potency of three novel synthetic anti-microbial peptoides against Mtb growth and showed that BM2 peptoid kills mycobacteria both in vitro and intracellularly. More importantly, it significantly reduced bacterial load in the lungs of infected mice.

The effect of novel and alternative compounds was also described in our collection; selenium nanoparticles (by Estevez et al.) and epidioxy-sterol analogs (Baena et al. In particular, Estevez et al. demonstrated that the selenium nanoparticles are active against both Mtb and Mycobacterium smegmatis growth by targeting their cell envelope. This finding opens new perspectives because this type of nanoparticles is characterized by a low toxicity.

Baena et al. tested the activity of 15 epidioxy-sterol analogs against Mtb both in vitro and ex vivo. T5 epidioxy-sterol-ANB was effective against Mtb in vitro only inside macrophages. Furthermore, it was showed that it is active also in a Mtb infected murine model. By transcriptomics analysis of Mtb infected macrophages after T5 epidioxy-sterol-ANB treatment, a significant down-regulation of enzymes involved in the cholesterol and folic acid pathways was discovered.

Study of the mechanism of resistance and mode of action of drugs used in TB treatment as well as identification of novel resistance mutations are extremely important for our understanding of this topic and for the development of novel approaches to fight these emerging Mtb drug-resistant strains.

Isoniazid (INH) and rifampicin (RIF) are two first-line drugs which are extensively used in TB therapy (Lange et al., 2019). Several SNPs conferring drug resistance have already known for both compounds, but it is mandatory to continue to search for new ones.

Hsu et al. identified two novel mutations (W341R and L398P) in the known drug activator KatG conferring INH resistance. Interestingly, they showed that these two polymorphisms are responsible for INH resistance by complementation and by the construction of two mutants harboring the same mutations.

Lai et al. demonstrated that a specific insertion in the rpoB gene confers RIF resistance, by the construction of a Mtb mutant harboring the same mutation.

Unfortunately, several Mtb clinical isolates resistant to new compounds used in TB therapy, such as bedaquiline (BDQ), have already spreaded worldwide (Bloemberg et al., 2015; Zimenkov et al., 2017). To better understand this phenomenon, Degiacomi et al. generated Mtb mutants resistant to BDQ starting from two MDR clinical isolates, miming what happens in clinical setting. These new BDQ resistant mutants harbored mutations in both atpE gene, coding for the target, and Rv0678, which encodes the repressor of MmpL5 efflux pump. The growth curves of BDQ resistant mutants were also evaluated. It was shown that Rv0678 mutations could give an advantage in the growth rate, explaining the spread of BDQ resistance among Mtb clinical isolates also prior to BDQ treatment.

Further findings in the study of new TB drug targets and in the characterization of the existing ones are present in our collection.

In order to characterize GreA as new drug target, Feng et al. isolated Mycobacterium smegmatis and Mtb mutants and showed that knock-down greA mutant resulted in growth retardation in Mtb and it is essential for its survival under heat shock stress. Furthermore, these mutants are more susceptible to vancomycin and RIF. By RNA-seq, they showed the role of GreA in the metabolic regulation of mycobacteria.

Rohde and Sorci evaluated the possible synergy of NAD biosynthesis inhibitors with some antitubercular drugs for drug combination. In fact, several prodrugs require a NAD biosynthesis enzyme to be activated, such as INH, ethionamide, and delamanid.

This unique collection of articles in our Research Topic gives new insights into the characterization drug resistance mechanisms in Mtb as well as provides novel strategies to fight this notorious pathogen.

We would like to thank the reviewers for their comments that improved our manuscripts, and the authors for their excellent contributions.

Finally, we hope that this Collection would stimulate open discussions about this topic and new researches which will assist the scientific and pharmaceutical communities in finding promising weapons against TB.

Author Contributions

All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.

Funding

This research was supported by the Italian Ministry of Education, University and Research (MIUR): Dipartimenti di Eccellenza Program (2018–2022)—Department of Biology and Biotechnology Lazzaro Spallanzani, University of Pavia to MP, and the TB Veterans Association to YA-G.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We are grateful to all the authors and reviewers for their contributions to this Research Topic.

References

Bloemberg, G. V., Keller, P. M., Stucki, D., Trauner, A., Borrell, S., Latshang, T., et al. (2015). Acquired resistance to bedaquiline and delamanid in therapy for tuberculosis. N. Engl. J. Med. 373, 1986–1988. doi: 10.1056/NEJMc1505196

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Keywords: tuberculosis, host directed therapy, drug discovery, antimicrobial resistance, drug targets, anti-tubercular drugs

Citation: Av-Gay Y, Mori G and Pasca MR (2021) Editorial: New Approaches Against Drug-Resistant M. tuberculosis. Front. Microbiol. 12:681420. doi: 10.3389/fmicb.2021.681420

Received: 16 March 2021; Accepted: 24 March 2021;
Published: 15 April 2021.

Edited by:

Thomas Dick, Center for Discovery and Innovation, Hackensack Meridian Health, United States

Reviewed by:

Marco Pieroni, University of Parma, Italy

Copyright © 2021 Av-Gay, Mori and Pasca. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yossef Av-Gay, yossi@mail.ubc.ca; Giorgia Mori, g.mori@uq.edu.au; Maria Rosalia Pasca, mariarosalia.pasca@unipv.it