Strategies Used by Bacteria to Grow in Macrophages
Open accessAbstract
Intracellular bacteria are often clinically relevant pathogens that infect virtually every cell type found in host organisms. However, myeloid cells, especially macrophages, constitute the primary cells targeted by most species of intracellular bacteria. Paradoxically, macrophages possess an extensive antimicrobial arsenal and are efficient at killing microbes. In addition to their ability to detect and signal the presence of pathogens, macrophages sequester and digest microorganisms using the phagolysosomal and autophagy pathways or, ultimately, eliminate themselves through the induction of programmed cell death. Consequently, intracellular bacteria influence numerous host processes and deploy sophisticated strategies to replicate within these host cells. Although most intracellular bacteria have a unique intracellular life cycle, these pathogens are broadly categorized into intravacuolar and cytosolic bacteria. Following phagocytosis, intravacuolar bacteria reside in the host endomembrane system and, to some extent, are protected from the host cytosolic innate immune defenses. However, the intravacuolar lifestyle requires the generation and maintenance of unique specialized bacteria-containing vacuoles and involves a complex network of host-pathogen interactions. Conversely, cytosolic bacteria escape the phagolysosomal pathway and thrive in the nutrient-rich cytosol despite the presence of host cell-autonomous defenses. The understanding of host-pathogen interactions involved in the pathogenesis of intracellular bacteria will continue to provide mechanistic insights into basic cellular processes and may lead to the discovery of novel therapeutics targeting infectious and inflammatory diseases.
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Macrophages employ direct antimicrobial mechanisms including generation of RNS in the phagosome and delivery of cathepsins and other hydrolases into maturing phagosomes.
“Beyond the production of ROS, macrophages also employ an array of directly antimicrobial mechanisms, e.g., the generation of reactive nitrogen species (RNS) in the phagosome and the delivery of cathepsins and other hydrolases into maturing phagosomes [59,225,226,227,228,229,230].”
From Functions of ROS in Macrophages and Antimicrobial Immunity (2021) · cites this paper as [225]
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References 310 · Cited by 137
Research works printed but not linked: 1
- [155]Alix E Mukherjee S Roy CR 2011 Subversion of membrane transport pathways by vacuolar pathogens J Cell Biol 195 943 952 22123831 PMC3241728
- Authors
- Mitchell*, G., Chen*, C., & Portnoy, D. A.
- Affiliations
- Department of Molecular and Cell Biology
- University of California, Berkeley (US)
- ORCID
- Portnoy, Daniel A.
- Venue
- Microbiology Spectrum
- Publisher
- American Society for Microbiology
- Published
- 2016-05-06
- Volume
- 4
- Issue
- 3
- ISSN
- 2165-0497 (ISSN-L)
- PMC
- PMC4922531
- OpenAlex
- W2404703480
- Cited by
- 137
- References
- 310
- Citations by year
- 2026: 8 · 2025: 9 · 2024: 15 · 2023: 15 · 2022: 18 · 2021: 29 · 2020: 19 · 2019: 13 · 2018: 5 · 2017: 5 · 2016: 1
- FWCI
- 7.39
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Microbiology Spectrum (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institutes of Health
- Natural Sciences and Engineering Research Council of Canada
- National Institute of Allergy and Infectious Diseases (P01AI063302, R01AI027655, T32AI100829)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Tuberculosis Research and Epidemiology
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- intracellular bacteria, macrophages, host-pathogen interaction, phagolysosomes, autophagy, phagosome, cytosolic bacteria, bacterial vacuole, programmed cell death
- MeSH terms
- Animals, Bacteria, Cytosol, Humans, Macrophages, Vacuoles, Host-Pathogen Interactions, Immune Evasion
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