Cathepsin Z is a conserved susceptibility factor underlying tuberculosis severity

Tuberculosis (TB) outcomes vary widely, from asymptomatic infection to mortality, yet most animal models do not recapitulate human phenotypic and genotypic variation. The genetically diverse Collaborative Cross mouse panel models distinct facets of TB disease that occur in humans and allows identification of genomic loci underlying clinical outcomes. We previously mapped a TB susceptibility locus on mouse chromosome 2. Here, we identify cathepsin Z (Ctsz) as a lead candidate underlying this TB susceptibility and show that Ctsz ablation leads to increased bacterial burden, pulmonary inflammation and decreased survival in mice. Ctsz disturbance within murine macrophages enhances production of chemokine (C-X-C motif) ligand 1 (CXCL1), a known biomarker of TB severity. From a Ugandan household contact study, we identify significant associations between CTSZ variants and TB disease severity. Finally, we examine patient-derived TB granulomas and report CTSZ localization within granuloma-associated macrophages, placing human CTSZ at the host-pathogen interface. These findings implicate a conserved CTSZ-CXCL1 axis in humans and genetically diverse mice that mediates TB disease severity.

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Publication Details

Journal
PLoS Biology
Published
2025-09-09
DOI
https://doi.org/10.1371/journal.pbio.3003377
Citations
2
Primary Topic
interferon and immune responses
Type
article
Field-Weighted Citation Impact
1.59

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article

Cathepsin Z is a conserved susceptibility factor underlying tuberculosis severity

Erika J. Hughes, Penelope Benchek, Marco Túlio Pardini Gontijo, Charlie J. Pyle et al.
2 citations
PLoS Biology
interferon and immune responses
1.59
article

Cathepsin Z is a conserved susceptibility factor underlying tuberculosis severity

Erika J. Hughes, Penelope Benchek, Marco Túlio Pardini Gontijo, Charlie J. Pyle, Jason E. Stout, Rachel K. Meade, Oyindamola Adefisayo, Kaley M. Wilburn, Harriet Mayanja‐Kizza, Catherine M. Stein, David M. Tobin, Michael L. McHenry, S Harris, Jadee Neff, Clare M. Smith, Thomas R. Hawn, Dennis C. Ko, Joshua Ivie, Alwyn M. V. Ecker, Paloma D. Garcia
article en
2 citations

Abstract

Tuberculosis (TB) outcomes vary widely, from asymptomatic infection to mortality, yet most animal models do not recapitulate human phenotypic and genotypic variation. The genetically diverse Collaborative Cross mouse panel models distinct facets of TB disease that occur in humans and allows identification of genomic loci underlying clinical outcomes. We previously mapped a TB susceptibility locus on mouse chromosome 2. Here, we identify cathepsin Z (Ctsz) as a lead candidate underlying this TB susceptibility and show that Ctsz ablation leads to increased bacterial burden, pulmonary inflammation and decreased survival in mice. Ctsz disturbance within murine macrophages enhances production of chemokine (C-X-C motif) ligand 1 (CXCL1), a known biomarker of TB severity. From a Ugandan household contact study, we identify significant associations between CTSZ variants and TB disease severity. Finally, we examine patient-derived TB granulomas and report CTSZ localization within granuloma-associated macrophages, placing human CTSZ at the host-pathogen interface. These findings implicate a conserved CTSZ-CXCL1 axis in humans and genetically diverse mice that mediates TB disease severity.

PLoS BiologyVol. 23(9)
Duke University (US), University of Washington (US), Duke Medical Center (US), Case Western Reserve University (US), Makerere University (UG)
Case Western Reserve University, Steven G. Cancer Foundation
Openalex Percentile: Top 15%
interferon and immune responses
1.59
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