The transcriptional response of Yersinia pseudotuberculosis to macrophage-released metabolites during growth within synthetic microcolonies
5 affiliations
- 1Department of Molecular Biology and Microbiology, Tufts University Graduate School of Biomedical Sciences, Boston, Massachusetts, USA
- 2Graduate Program in Molecular Microbiology, Tufts University Graduate School of Biomedical Sciences, Boston, Massachusetts, USA
- 3Tufts University School of Medicine, Boston, Massachusetts, USA
- 4W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA
- 5Boston Children’s Hospital, Division of Infectious Diseases, Harvard Medical School, Boston, Massachusetts, USA
Abstract
Yersinia pseudotuberculosis (Yptb) replicates in immune cell-encompassed microcolonies within tissues. Bacterial replication is controlled by protection against neutrophil attack and by macrophage-released antimicrobial factors, such as nitric oxide (NO). During these attacks, bacteria located on the microcolony periphery encounter extracellular signals that differ from those in the interior. To dissect individual microbial populations, γ interferon-activated macrophages were used to challenge microdroplet-grown Yptb harboring an NO-responsive mCherry reporter. Subsequently, bacterial subpopulations that hyperactivated the reporter were isolated from droplets composed of a reversible polymer matrix. RNA-seq analysis indicated that induction of nitrosative stress-associated genes was the primary determinant distinguishing peripheral bacteria from the remaining population. In addition, a secondary stress response that induced prophage-associated genes was detected, which could not be traced to either DNA damage or nitrosative stress responses. Activated macrophages also induced the expression of the Yptb itaconate degradation enzyme-encoding transcript throughout the entire colony. To determine if itaconate production by the interferon-activated Irg1 protein played a role in restricting Yptb, bacteria harboring an itaconate-responsive reporter and Yptb mutants defective for itaconate degradation were analyzed during bacterial colonization of the murine spleen. Only a subset of colonies appeared to be exposed to itaconate, which may explain the very small defects exhibited by mutants unable to degrade the interferon-induced macrophage product. These results indicate that the primary response of bacteria to macrophage-elicited factors is likely associated with protection against NO-derived metabolites.
IMPORTANCE: Bacterial microcolonies are often linked to invasive infectious diseases. Once established, organisms as diverse as Staphylococcus aureus and enteropathogenic Yersinia recruit activated macrophages that surround these sites. For Yersinia pseudotuberculosis, the layer of distant macrophages induces a nitric oxide (NO)-inactivating enzyme in the outermost bacteria, enabling bacteria in the core to survive. This study shows that the cellular states of bacteria in the periphery and the core can be examined by recreating tissue infection in an in vitro system, in which microcolonies form within droplets of a degradable solid matrix, surrounded by interferon-activated macrophages. Transcriptomic analysis revealed that the peripheral bacteria primarily differ from the core in their response to NO. Surprisingly, the entire colony is bathed in itaconate, an immune-modulating chemical produced by activated macrophages. The ability to respond to itaconate may help rare bacteria engulfed by macrophages to survive phagocytic attack.
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BibTeX
@article{clark2026transcriptional,
title = {{The transcriptional response of Yersinia pseudotuberculosis to macrophage-released metabolites during growth within synthetic microcolonies}},
author = {Stacie A. Clark and Alexander Palmer and Wenwen Huo and Alexander C. Joyce and Kimberly M. Davis and Juan Ortiz-Marquez and Tim van Opijnen and Ralph R. Isberg},
journal = {mBio},
year = {2026},
month = sep,
doi = {10.1128/mbio.00691-26},
url = {https://doi.org/10.1128/mbio.00691-26},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - The transcriptional response of Yersinia pseudotuberculosis to macrophage-released metabolites during growth within synthetic microcolonies
AU - Stacie A. Clark
AU - Alexander Palmer
AU - Wenwen Huo
AU - Alexander C. Joyce
AU - Kimberly M. Davis
AU - Juan Ortiz-Marquez
AU - Tim van Opijnen
AU - Ralph R. Isberg
PY - 2026
DA - 2026/09/21
JO - mBio
DO - 10.1128/mbio.00691-26
UR - https://doi.org/10.1128/mbio.00691-26
AB - Yersinia pseudotuberculosis (Yptb) replicates in immune cell-encompassed microcolonies within tissues. Bacterial replication is controlled by protection against neutrophil attack and by macrophage-released antimicrobial factors, such as nitric oxide (NO). During these attacks, bacteria located on the microcolony periphery encounter extracellular signals that differ from those in the interior. To dissect individual microbial populations, γ interferon-activated macrophages were used to challenge microdroplet-grown Yptb harboring an NO-responsive mCherry reporter. Subsequently, bacterial subpopulations that hyperactivated the reporter were isolated from droplets composed of a reversible polymer matrix. RNA-seq analysis indicated that induction of nitrosative stress-associated genes was the primary determinant distinguishing peripheral bacteria from the remaining population. In addition, a secondary stress response that induced prophage-associated genes was detected, which could not be traced to either DNA damage or nitrosative stress responses. Activated macrophages also induced the expression of the Yptb itaconate degradation enzyme-encoding transcript throughout the entire colony. To determine if itaconate production by the interferon-activated Irg1 protein played a role in restricting Yptb, bacteria harboring an itaconate-responsive reporter and Yptb mutants defective for itaconate degradation were analyzed during bacterial colonization of the murine spleen. Only a subset of colonies appeared to be exposed to itaconate, which may explain the very small defects exhibited by mutants unable to degrade the interferon-induced macrophage product. These results indicate that the primary response of bacteria to macrophage-elicited factors is likely associated with protection against NO-derived metabolites. IMPORTANCE: Bacterial microcolonies are often linked to invasive infectious diseases. Once established, organisms as diverse as Staphylococcus aureus and enteropathogenic Yersinia recruit activated macrophages that surround these sites. For Yersinia pseudotuberculosis, the layer of distant macrophages induces a nitric oxide (NO)-inactivating enzyme in the outermost bacteria, enabling bacteria in the core to survive. This study shows that the cellular states of bacteria in the periphery and the core can be examined by recreating tissue infection in an in vitro system, in which microcolonies form within droplets of a degradable solid matrix, surrounded by interferon-activated macrophages. Transcriptomic analysis revealed that the peripheral bacteria primarily differ from the core in their response to NO. Surprisingly, the entire colony is bathed in itaconate, an immune-modulating chemical produced by activated macrophages. The ability to respond to itaconate may help rare bacteria engulfed by macrophages to survive phagocytic attack.
SN - 2150-7511
ER -