Intracellular survival of Shigella
Open accessAbstract
Bacterial invasion of eukaryotic cells and host recognition and killing of the invading bacteria are a key issue in determining the fate of bacterial infection. Once inside host cells, pathogenic bacteria often modify the phagosomal compartment or enter the host cytosol to escape from the lytic compartment and gain a replicative niche. Cytosolic invaders, however, are monitored by host innate immune systems, such as mediated by Nod/CARD family proteins, which induce inflammatory responses via activation of NF-kappaB. Furthermore, recent studies indicate that autophagy, a major cytoplasmic degradation system that eliminates cytosolic protein and organelles, also recognizes invading bacteria. Indeed, unless they are able to circumvent entrapping by autophagic membranes, bacteria targeted by autophagy ultimately undergo degradation by delivery into autolysosomes. In this article, we review recent advances in understanding of Shigella strategies to infect epithelial cells, and then focus on recent studies of an intriguing bacterial survival strategy against autophagic degradation.
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The autophagic machinery following pathogen entry into cells can target either bacteria-containing phagosomes or free cytosolic bacteria.
“The autophagic machinery following the entry of the pathogen into cells can target either bacteria-containing phagosomes, or free cytosolic bacteria [8,9,10,11].”
From LC3-Associated Phagocytosis (LAP): Connections with Host Autophagy (2012) · cites this paper as [8]
The Introduction says the autophagic pathway monitors bacteria that have escaped into the cytoplasm. The section ‘Shigella are trapped by the autophagic membrane unless they produce IcsB’ distinguishes the autophagic membranes around cytosolic Shigella from the phagocytic membrane present immediately after invasion. Our copy does not establish that autophagy also targets bacteria-containing phagosomes; page numbers are unavailable. (LLM, conf=0.85)
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Cites
Nod1, an Apaf-1-like Activator of Caspase-9 and Nuclear Factor-κB
Inohara, N., Koseki, T., del Peso, L., Hu, Y., Yee, C., Chen, S., Carrio, R., Merino, J., Liu, D., Ni, J., et al. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.21.14560 · Cited by 742 · see citing works
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- Yoshimori, T. (2004) Autophagy: a regulated bulk degradation process inside cells. Biochem Biophys Res Commun 313: 453-458. 14625822, 2006, 2, Downloaded from https://onlinelibrary.wiley.com/doi/10.1111/j.1462-5822.2005.00652.x, Wiley Online Library on [17/08/2026]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
Klionsky, D. J., Abdelmohsen, K., Abe, A., Abedin, M. J., Abeliovich, H., Acevedo Arozena, A., Adachi, H., Adams, C. M., Adams, P. D., Adeli, K., et al. (2016) · Autophagy · doi:10.1080/15548627.2015.1100356 · Cited by 5,894 · see citing works
Self-citationGuidelines for the use and interpretation of assays for monitoring autophagy
Klionsky, D. J., Abdalla, F. C., Abeliovich, H., Abraham, R. T., Acevedo-Arozena, A., Adeli, K., Agholme, L., Agnello, M., Agostinis, P., Aguirre-Ghiso, J. A., et al. (2012) · Autophagy · doi:10.4161/auto.19496 · Cited by 3,996 · see citing works
Self-citationLC3-Associated Phagocytosis (LAP): Connections with Host Autophagy
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“either bacteria-containing phagosomes, or free cytosolic bacteria [8 11].”
Background
- Authors
- Ogawa, M., & Sasakawa, C.
- Affiliations
- Institute of Medical Science, The University of Tokyo (JP)
- Japan Science and Technology Agency (JP)
- Corresponding author
- Sasakawa, Chihiro
- Venue
- Cellular Microbiology
- Publisher
- Hindawi Limited
- Published
- 2006-02
- Volume
- 8
- Issue
- 2
- Pages
- 177-184
- ISSN
- 1462-5814 (ISSN-L)
- 1462-5822
- OpenAlex
- W1985944042
- Cited by
- 89
- References
- 1
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 2 · 2023: 2 · 2022: 2 · 2021: 2 · 2020: 2 · 2018: 4 · 2017: 1 · 2016: 4 · 2015: 3 · 2014: 1 · 2013: 4 · 2012: 8
- FWCI
- 1.22
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cellular Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Science and Technology Agency
- Core Research for Evolutional Science and Technology
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Escherichia coli research studies
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- Shigella, intracellular survival, autophagy, autophagic degradation, epithelial cells, phagosome escape, NF-κB signaling, cytosolic bacteria
- MeSH terms
- Animals, Autophagy, Bacterial Proteins, Cytoplasm, Epithelial Cells, Humans, Immunity, Cellular, Immunity, Innate, Intestinal Mucosa, Intracellular Membranes, Macrophages, Shigella, NF-kappa B, Gram-Negative Bacterial Infections, Microbial Viability
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