Engineered Mycobacterium tuberculosis triple-kill-switch strain provides controlled tuberculosis infection in animal models

Human challenge experiments could accelerate tuberculosis vaccine development. This requires a safe Mycobacterium tuberculosis (Mtb) strain that can both replicate in the host and be reliably cleared. Here we genetically engineered Mtb strains encoding up to three kill switches: two mycobacteriophage lysin operons negatively regulated by tetracycline and a degron domain-NadE fusion, which induces ClpC1-dependent degradation of the essential enzyme NadE, negatively regulated by trimethoprim. The triple-kill-switch (TKS) strain showed similar growth kinetics and antibiotic susceptibilities to wild-type Mtb under permissive conditions but was rapidly killed in vitro without trimethoprim and doxycycline. It established infection in mice receiving antibiotics but was rapidly cleared upon cessation of treatment, and no relapse was observed in infected severe combined immunodeficiency mice or Rag<sup>-/-</sup> mice. The TKS strain had an escape mutation rate of less than 10<sup>-10</sup> per genome per generation. These findings suggest that the TKS strain could be a safe, effective candidate for a human challenge model.

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Publication Details

Journal
Nature Microbiology
Published
2025-01-10
DOI
https://doi.org/10.1038/s41564-024-01913-5
Citations
14
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
19.55

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article

Engineered Mycobacterium tuberculosis triple-kill-switch strain provides controlled tuberculosis infection in animal models

Michelle Gardner, Véronique Dartois, Joshua B. Wallach, Eric J. Rubin et al.
14 citations
Nature Microbiology
Tuberculosis Research and Epidemiology
19.55
article

Engineered Mycobacterium tuberculosis triple-kill-switch strain provides controlled tuberculosis infection in animal models

Michelle Gardner, Véronique Dartois, Joshua B. Wallach, Eric J. Rubin, Sabine Ehrt, Yue J. Liu, Philana Ling Lin, Dirk Schnappinger, Junhao Zhu, Matthew Zimmerman, Xin Wang, Mark A. Rodgers, Kristine M. Guinn, Thaís Klevorn, Shoko Wakabayashi, Douaa Mugahid, Jaimie Sixsmith, JoAnne L. Flynn, Sarah M. Fortune, Nicole C. Howard, Benjamin J. Braunecker, Yao Liu, Jeffrey C. Wagner, Hong-Wei Su, Kan Lin
article en
14 citations

Abstract

Human challenge experiments could accelerate tuberculosis vaccine development. This requires a safe Mycobacterium tuberculosis (Mtb) strain that can both replicate in the host and be reliably cleared. Here we genetically engineered Mtb strains encoding up to three kill switches: two mycobacteriophage lysin operons negatively regulated by tetracycline and a degron domain-NadE fusion, which induces ClpC1-dependent degradation of the essential enzyme NadE, negatively regulated by trimethoprim. The triple-kill-switch (TKS) strain showed similar growth kinetics and antibiotic susceptibilities to wild-type Mtb under permissive conditions but was rapidly killed in vitro without trimethoprim and doxycycline. It established infection in mice receiving antibiotics but was rapidly cleared upon cessation of treatment, and no relapse was observed in infected severe combined immunodeficiency mice or Rag<sup>-/-</sup> mice. The TKS strain had an escape mutation rate of less than 10<sup>-10</sup> per genome per generation. These findings suggest that the TKS strain could be a safe, effective candidate for a human challenge model.

Nature MicrobiologyVol. 10(2)
Harvard University (US), University of Pittsburgh (US), Cornell University (US), Ragon Institute of MGH, MIT and Harvard (US), Children's Hospital of Pittsburgh (US), University of Pittsburgh Medical Center (US), Hackensack Meridian Health (US), Center for Discovery (US), Zhejiang University (CN)
Bill and Melinda Gates Foundation, University of Pittsburgh, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 0%
Tuberculosis Research and Epidemiology
19.55
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