Listeria monocytogenes favors the vacuolar compartment during ex vivo human placental infections
- 1Department of Biological Sciences, Centre for Cell Biology, Development, and Disease (C2D2), Simon Fraser University
- 2Division of General Obstetrics & Gynaecology, Royal Columbian Hospital
- 3Life Sciences Institute and Department of Cellular and Physiological Sciences, Faculty of Medicine, University of British Columbia
Abstract
Listeria monocytogenes poses a serious concern during pregnancy, as these microbes can cross the placental barrier to infect the developing fetus. The pathogen’s intracellular lifecycle has been well characterized in cultured cells, where the internalized bacteria escape short-lived Listeria -containing vacuoles (LCVs), replicate in the cytoplasm, and recruit host actin to generate comet tails that enable their intra- and inter-cellular movement. Whether these events occur during intact human placental infections remains unknown. Through ex vivo placental infections, we characterized the spatiotemporal progression of L. monocytogenes in a physiologically relevant system. We found that the actin-rich structures, which are hallmarks of cultured cell infections, were essentially absent (<1% of L. monocytogenes were associated with actin-rich structures). Instead, the bacteria remained predominantly restricted within LCVs, where they also replicated. Quantitative histological and immunofluorescence analyses showed that 39% of wild-type L. monocytogenes remained within Rab5-positive vacuoles and 44% in Lamp1-positive vacuoles, whereas only 1%–4% were observed in cultured placental cells. Most vacuoles lacked the vATPase and cathepsin B, indicating that placental LCV vacuoles were non-acidified, non-degradative endosomal niches. These results closely phenocopied infections using Δ hly-L. monocytogenes , which do not generate listeriolysin O (LLO), a bacterial toxin crucial for LCV escape. Together, our findings reveal that L. monocytogenes primarily reside within LCVs during ex vivo human placental infections, contrasting the classical in vitro models and emphasizing the importance of studying bacterial pathogenesis in intact human tissues.
IMPORTANCE: L. monocytogenes infection during pregnancy can result in miscarriage, stillbirth, or severe neonatal disease because the bacterium can cross the placental barrier. Current understanding of L. monocytogenes pathogenesis is largely based on cultured cell models, where bacteria rapidly escape vacuoles, replicate in the cytoplasm, and spread using host actin. By examining infections in intact ex vivo human placental tissue, we show that this paradigm does not accurately reflect a placental infection. Instead, L. monocytogenes remains predominantly within vacuoles that may support bacterial replication, while actin-based motility is rare. Our work provides new insight into placental listeriosis and highlights the importance of studying host-pathogen interactions in physiologically relevant models.
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BibTeX
@article{mcleod2026listeria,
title = {{Listeria monocytogenes favors the vacuolar compartment during ex vivo human placental infections}},
author = {Petra A. McLeod and Jagdeep S. Ubhi and A. Wayne Vogl and Julian A. Guttman},
journal = {mBio},
year = {2026},
month = oct,
doi = {10.1128/mbio.01704-26},
url = {https://journals.asm.org/doi/10.1128/mbio.01704-26},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Listeria monocytogenes favors the vacuolar compartment during ex vivo human placental infections
AU - Petra A. McLeod
AU - Jagdeep S. Ubhi
AU - A. Wayne Vogl
AU - Julian A. Guttman
PY - 2026
DA - 2026/10/28
JO - mBio
DO - 10.1128/mbio.01704-26
UR - https://journals.asm.org/doi/10.1128/mbio.01704-26
AB - Listeria monocytogenes poses a serious concern during pregnancy, as these microbes can cross the placental barrier to infect the developing fetus. The pathogen’s intracellular lifecycle has been well characterized in cultured cells, where the internalized bacteria escape short-lived Listeria -containing vacuoles (LCVs), replicate in the cytoplasm, and recruit host actin to generate comet tails that enable their intra- and inter-cellular movement. Whether these events occur during intact human placental infections remains unknown. Through ex vivo placental infections, we characterized the spatiotemporal progression of L. monocytogenes in a physiologically relevant system. We found that the actin-rich structures, which are hallmarks of cultured cell infections, were essentially absent (<1% of L. monocytogenes were associated with actin-rich structures). Instead, the bacteria remained predominantly restricted within LCVs, where they also replicated. Quantitative histological and immunofluorescence analyses showed that 39% of wild-type L. monocytogenes remained within Rab5-positive vacuoles and 44% in Lamp1-positive vacuoles, whereas only 1%–4% were observed in cultured placental cells. Most vacuoles lacked the vATPase and cathepsin B, indicating that placental LCV vacuoles were non-acidified, non-degradative endosomal niches. These results closely phenocopied infections using Δ hly-L. monocytogenes , which do not generate listeriolysin O (LLO), a bacterial toxin crucial for LCV escape. Together, our findings reveal that L. monocytogenes primarily reside within LCVs during ex vivo human placental infections, contrasting the classical in vitro models and emphasizing the importance of studying bacterial pathogenesis in intact human tissues. IMPORTANCE: L. monocytogenes infection during pregnancy can result in miscarriage, stillbirth, or severe neonatal disease because the bacterium can cross the placental barrier. Current understanding of L. monocytogenes pathogenesis is largely based on cultured cell models, where bacteria rapidly escape vacuoles, replicate in the cytoplasm, and spread using host actin. By examining infections in intact ex vivo human placental tissue, we show that this paradigm does not accurately reflect a placental infection. Instead, L. monocytogenes remains predominantly within vacuoles that may support bacterial replication, while actin-based motility is rare. Our work provides new insight into placental listeriosis and highlights the importance of studying host-pathogen interactions in physiologically relevant models.
SN - 2150-7511
ER -