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Volume 32, Number 9—September 2026

Letter

Recent Mycobacterium tuberculosis Transmission, United States, 2018–2022

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In Response: We thank Dr. Zubairi for raising the points in his letter (1). We view those methodological considerations as valid questions within the context of applying our results to tuberculosis (TB) prevention and control.

We agree that transmission networks can be more complex than are represented by our plausible source case algorithm and use of whole-genome single nucleotide polymorphism distances to assess genomic similarity. However, our integration of spatial and temporal proximity with genomic similarity represents our best estimates of recent transmission, which were validated with locally provided contact investigation data from multiple sites in the United States. In addition, we accept that those estimates can misclassify cases as false-positive or false-negative transmission events. Validation of the algorithm demonstrated an accuracy of 95.8% compared with on-the-ground epidemiologic data, with sensitivity of 79.1% and specificity of 97.7% (S. Kammerer, unpub. data)

Regarding external validation of the adaptive boosting machine learning model, our study examined the epidemiology of TB transmission in the United States. Generalization to other settings with different transmission dynamics, demographics, genomic diversity, healthcare utilization, and public health infrastructure, including settings that do not genotype nearly all isolates from culture-confirmed cases, would not be appropriate. Our findings are appropriate to consider for prioritizing interventions in the United States. The methodological approach could also be a starting place for a similar analysis in other settings with similar epidemiology and genotyping coverage.

We agree that diagnostic delay is a major driver of TB transmission; however, we did not have reliable data regarding symptom onset to assess in our study. Accurate data regarding symptom onset are challenging to obtain in clinical settings. However, we did consider objective clinical findings associated with diagnostic delay and advanced disease (e.g., sputum smear positivity), and those findings were associated with plausible source cases in our analysis.

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Steve Kammerer
Author affiliation: Centers for Disease Control and Prevention, Atlanta, Georgia, USA

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References

  1. Kammerer  S, Flanagan  D, Raz  K, Shaw  T, Wortham  J, Talarico  S. Mycobacterium tuberculosis transmission, United States, 2018–2022. Emerg Infect Dis. 2026;32:88093.DOIPubMedGoogle Scholar

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Suggested citation for this article: Kammerer S. Recent Mycobacterium tuberculosis transmission, United States, 2018–2022. Emerg Infect Dis. 2026 Sep [date cited]. https://doi.org/10.3201/eid3209.261478

DOI: 10.3201/eid3209.261478

Original Publication Date: August 19, 2026

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Table of Contents – Volume 32, Number 9—September 2026

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Page created: August 10, 2026
Page updated: August 19, 2026
Page reviewed: August 19, 2026
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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