In this video, we're going to talk about yet another method that some pathogens can use to evade or avoid the immune system, and that is through surviving inside of phagocytic cells. So recall from some of our previous lesson videos that we describe the process of phagocytosis in a stepwise manner. And so recall from those videos that when a pathogen is engulfed by a phagocyte, that pathogen will enter the phagocyte within a phagosome. And the phagosome will generally fuse with a lysosome, which will allow for the pathogen to be digested and eliminated. Now some bacteria have evolved mechanisms to be able to survive inside of a phagocytic cell even after they have been engulfed. And they can do this in 3 different ways that we have down below in our image. And so notice in this image on the outside right here what we have is our pathogen. And of course, our phagocytic cell is going to be this big blue cell that you see here. This is going to be our macrophage. And so notice that the pathogen, here has opsonins on its surface and those opsonins allow for the process of opsonization that makes the pathogen easier to be engulfed through the process of phagocytosis. And so when the pathogen is engulfed, notice that it is brought into the cell, within a phagosome. Okay? Now the first mechanism that some bacteria have evolved to survive inside of phagocytes is, they have evolved mechanisms to escape from the phagosome before the phagosome fuses with the lysosome. And so what you'll notice here in this image, right here in this region, we are showing you how some bacteria have evolved the mechanism to escape the phagosome. And when they escape the phagosome, they escape their destiny to be degraded and destroyed. And so when they escape, they are able to survive within the macrophage. Now another mechanism that some bacteria have been able to evolve over time to survive in phagocytes is that they can avoid or block the fusion of the phagosome with the lysosome by producing inhibitory proteins. And so notice here that, sometimes right here, step number 2, where the phagosome would usually fuse with lysosomes, this step can be blocked and prevented. And so that will allow the pathogen to survive within the phagosome and not have to worry about the digestive enzymes from the lysosome. Now the third possibility here that some bacteria have evolved is the amazing ability to be able to survive inside of the phagolysosome even after the lysosomes have fused with the phagosome. And so, even when the lysosomes fuse with the phagosome and all of these digestive hydrolytic enzymes are there, trying to degrade the pathogen. In some cases, the pathogens have been able to survive those conditions and avoid being destroyed by the contents of the lysosome. And so notice this pathogen here is saying 'can't kill me' because they are able to survive even inside microbes that are able to survive inside of phagocytes by using each of these 3 different methods. And so this here concludes our brief lesson on how some pathogens can survive inside of phagocytic cells, and we'll be able to get some practice applying these concepts as we move forward. So I'll see you all in our next video.
- 1. Introduction to Microbiology3h 21m
- Introduction to Microbiology16m
- Introduction to Taxonomy26m
- Scientific Naming of Organisms9m
- Members of the Bacterial World10m
- Introduction to Bacteria9m
- Introduction to Archaea10m
- Introduction to Eukarya20m
- Acellular Infectious Agents: Viruses, Viroids & Prions19m
- Importance of Microorganisms20m
- Scientific Method27m
- Experimental DesignÂ30m
- 2. Disproving Spontaneous Generation1h 18m
- 3. Chemical Principles of Microbiology3h 38m
- 4. Water1h 28m
- 5. Molecules of Microbiology2h 23m
- 6. Cell Membrane & Transport3h 28m
- Cell Envelope & Biological Membranes12m
- Bacterial & Eukaryotic Cell Membranes8m
- Archaeal Cell Membranes18m
- Types of Membrane Proteins8m
- Concentration Gradients and Diffusion9m
- Introduction to Membrane Transport14m
- Passive vs. Active Transport13m
- Osmosis33m
- Simple and Facilitated Diffusion17m
- Active Transport30m
- ABC Transporters11m
- Group Translocation7m
- Types of Small Molecule Transport Review9m
- Endocytosis and Exocytosis15m
- 7. Prokaryotic Cell Structures & Functions5h 52m
- Prokaryotic & Eukaryotic Cells26m
- Binary Fission11m
- Generation Times16m
- Bacterial Cell Morphology & Arrangements35m
- Overview of Prokaryotic Cell Structure10m
- Introduction to Bacterial Cell Walls26m
- Gram-Positive Cell Walls11m
- Gram-Negative Cell Walls20m
- Gram-Positive vs. Gram-Negative Cell Walls11m
- The Glycocalyx: Capsules & Slime Layers12m
- Introduction to Biofilms6m
- Pili18m
- Fimbriae & Hami7m
- Introduction to Prokaryotic Flagella12m
- Prokaryotic Flagellar Structure18m
- Prokaryotic Flagellar Movement11m
- Proton Motive Force Drives Flagellar Motility5m
- Chemotaxis14m
- Review of Prokaryotic Surface Structures8m
- Prokaryotic Ribosomes16m
- Introduction to Bacterial Plasmids13m
- Cell Inclusions9m
- Endospores16m
- Sporulation5m
- Germination5m
- 8. Eukaryotic Cell Structures & Functions2h 18m
- 9. Microscopes2h 46m
- Introduction to Microscopes8m
- Magnification, Resolution, & Contrast10m
- Introduction to Light Microscopy5m
- Light Microscopy: Bright-Field Microscopes23m
- Light Microscopes that Increase Contrast16m
- Light Microscopes that Detect Fluorescence16m
- Electron Microscopes14m
- Reviewing the Different Types of Microscopes10m
- Introduction to Staining5m
- Simple Staining14m
- Differential Staining6m
- Other Types of Staining11m
- Reviewing the Types of Staining8m
- Gram Stain13m
- 10. Dynamics of Microbial Growth4h 36m
- Biofilms16m
- Growing a Pure Culture5m
- Microbial Growth Curves in a Closed System21m
- Temperature Requirements for Microbial Growth18m
- Oxygen Requirements for Microbial Growth22m
- pH Requirements for Microbial Growth8m
- Osmolarity Factors for Microbial Growth14m
- Reviewing the Environmental Factors of Microbial Growth12m
- Nutritional Factors of Microbial Growth30m
- Growth Factors4m
- Introduction to Cultivating Microbial Growth5m
- Types of Solid Culture Media4m
- Plating Methods16m
- Measuring Growth by Direct Cell Counts9m
- Measuring Growth by Plate Counts14m
- Measuring Growth by Membrane Filtration6m
- Measuring Growth by Biomass15m
- Introduction to the Types of Culture Media5m
- Chemically Defined Media3m
- Complex Media4m
- Selective Media5m
- Differential Media9m
- Reducing Media4m
- Enrichment Media7m
- Reviewing the Types of Culture Media8m
- 11. Controlling Microbial Growth4h 10m
- Introduction to Controlling Microbial Growth29m
- Selecting a Method to Control Microbial Growth44m
- Physical Methods to Control Microbial Growth49m
- Review of Physical Methods to Control Microbial Growth7m
- Chemical Methods to Control Microbial Growth16m
- Chemicals Used to Control Microbial Growth6m
- Liquid Chemicals: Alcohols, Aldehydes, & Biguanides15m
- Liquid Chemicals: Halogens12m
- Liquid Chemicals: Surface-Active Agents17m
- Other Types of Liquid Chemicals14m
- Chemical Gases: Ethylene Oxide, Ozone, & Formaldehyde13m
- Review of Chemicals Used to Control Microbial Growth11m
- Chemical Preservation of Perishable Products10m
- 12. Microbial Metabolism5h 16m
- Introduction to Energy15m
- Laws of Thermodynamics15m
- Chemical Reactions9m
- ATP20m
- Enzymes14m
- Enzyme Activation Energy9m
- Enzyme Binding Factors9m
- Enzyme Inhibition10m
- Introduction to Metabolism8m
- Negative & Positive Feedback7m
- Redox Reactions22m
- Introduction to Aerobic Cellular Respiration25m
- Types of Phosphorylation12m
- Glycolysis19m
- Entner-Doudoroff Pathway11m
- Pentose-Phosphate Pathway10m
- Pyruvate Oxidation8m
- Krebs Cycle16m
- Electron Transport Chain19m
- Chemiosmosis7m
- Review of Aerobic Cellular Respiration19m
- Fermentation & Anaerobic Respiration23m
- 13. Photosynthesis2h 31m
- 14. DNA Replication2h 25m
- 15. Central Dogma & Gene Regulation7h 14m
- Central Dogma7m
- Introduction to Transcription20m
- Steps of Transcription22m
- Transcription Termination in Prokaryotes7m
- Eukaryotic RNA Processing and Splicing20m
- Introduction to Types of RNA9m
- Genetic Code25m
- Introduction to Translation30m
- Steps of Translation23m
- Review of Transcription vs. Translation12m
- Prokaryotic Gene Expression21m
- Review of Prokaryotic vs. Eukaryotic Gene Expression13m
- Introduction to Regulation of Gene Expression13m
- Prokaryotic Gene Regulation via Operons27m
- The Lac Operon21m
- Glucose's Impact on Lac Operon25m
- The Trp Operon20m
- Review of the Lac Operon & Trp Operon11m
- Introduction to Eukaryotic Gene Regulation9m
- Eukaryotic Chromatin Modifications16m
- Eukaryotic Transcriptional Control22m
- Eukaryotic Post-Transcriptional Regulation28m
- Post-Translational Modification6m
- Eukaryotic Post-Translational Regulation13m
- 16. Microbial Genetics4h 44m
- Introduction to Microbial Genetics11m
- Introduction to Mutations20m
- Methods of Inducing Mutations15m
- Prototrophs vs. Auxotrophs13m
- Mutant Detection25m
- The Ames Test14m
- Introduction to DNA Repair5m
- DNA Repair Mechanisms37m
- Horizontal Gene Transfer18m
- Bacterial Transformation11m
- Transduction32m
- Introduction to Conjugation6m
- Conjugation: F Plasmids18m
- Conjugation: Hfr & F' Cells19m
- Genome Variability21m
- CRISPR CAS11m
- 17. Biotechnology3h 0m
- 18. Viruses, Viroids, & Prions4h 56m
- Introduction to Viruses20m
- Introduction to Bacteriophage Infections14m
- Bacteriophage: Lytic Phage Infections12m
- Bacteriophage: Lysogenic Phage Infections17m
- Bacteriophage: Filamentous Phage Infections8m
- Plaque Assays9m
- Introduction to Animal Virus Infections10m
- Animal Viruses: 1. Attachment to the Host Cell7m
- Animal Viruses: 2. Entry & Uncoating in the Host Cell19m
- Animal Viruses: 3. Synthesis & Replication22m
- Animal Viruses: DNA Virus Synthesis & Replication14m
- Animal Viruses: RNA Virus Synthesis & Replication22m
- Animal Viruses: Antigenic Drift vs. Antigenic Shift9m
- Animal Viruses: Reverse-Transcribing Virus Synthesis & Replication9m
- Animal Viruses: 4. Assembly Inside Host Cell8m
- Animal Viruses: 5. Release from Host Cell15m
- Acute vs. Persistent Viral Infections25m
- COVID-19 (SARS-CoV-2)14m
- Plant Viruses12m
- Viroids6m
- Prions13m
- 19. Innate Immunity7h 15m
- Introduction to Immunity8m
- Introduction to Innate Immunity17m
- Introduction to First-Line Defenses5m
- Physical Barriers in First-Line Defenses: Skin13m
- Physical Barriers in First-Line Defenses: Mucous Membrane9m
- First-Line Defenses: Chemical Barriers24m
- First-Line Defenses: Normal Microflora5m
- Introduction to Cells of the Immune System15m
- Cells of the Immune System: Granulocytes29m
- Cells of the Immune System: Agranulocytes25m
- Introduction to Cell Communication5m
- Cell Communication: Surface Receptors & Adhesion Molecules16m
- Cell Communication: Cytokines27m
- Pattern Recognition Receptors (PRRs)45m
- Introduction to the Complement System24m
- Activation Pathways of the Complement System23m
- Effects of the Complement System23m
- Review of the Complement System12m
- Phagoctytosis21m
- Introduction to Inflammation18m
- Steps of the Inflammatory Response26m
- Fever8m
- Interferon Response25m
- 20. Adaptive Immunity7h 14m
- Introduction to Adaptive Immunity32m
- Antigens12m
- Introduction to T Lymphocytes38m
- Major Histocompatibility Complex Molecules20m
- Activation of T Lymphocytes21m
- Functions of T Lymphocytes25m
- Review of Cytotoxic vs Helper T Cells13m
- Introduction to B Lymphocytes27m
- Antibodies14m
- Classes of Antibodies35m
- Outcomes of Antibody Binding to Antigen15m
- T Dependent & T Independent Antigens21m
- Clonal Selection20m
- Antibody Class Switching17m
- Affinity Maturation14m
- Primary and Secondary Response of Adaptive Immunity21m
- Immune Tolerance28m
- Regulatory T Cells10m
- Natural Killer Cells16m
- Review of Adaptive Immunity25m
- 21. Principles of Disease6h 57m
- Symbiotic Relationships12m
- The Human Microbiome46m
- Characteristics of Infectious Disease47m
- Stages of Infectious Disease Progression26m
- Koch's Postulates26m
- Molecular Koch's Postulates11m
- Bacterial Pathogenesis36m
- Introduction to Pathogenic Toxins6m
- Exotoxins Cause Damage to the Host40m
- Endotoxin Causes Damage to the Host13m
- Exotoxins vs. Endotoxin Review13m
- Immune Response Damage to the Host15m
- Introduction to Avoiding Host Defense Mechanisms8m
- 1) Hide Within Host Cells5m
- 2) Avoiding Phagocytosis31m
- 3) Surviving Inside Phagocytic Cells10m
- 4) Avoiding Complement System9m
- 5) Avoiding Antibodies25m
- Viruses Evade the Immune Response27m
3) Surviving Inside Phagocytic Cells - Online Tutor, Practice Problems & Exam Prep
Pathogens can evade the immune system by surviving within phagocytic cells through three mechanisms. First, some bacteria escape the phagosome before it fuses with the lysosome, avoiding degradation. Second, they can inhibit the fusion of the phagosome and lysosome using specific proteins. Lastly, certain pathogens endure even within the phagolysosome, resisting the lysosomal enzymes. Understanding these survival strategies is crucial for developing effective treatments against infections caused by these resilient pathogens.
Surviving Inside Phagocytic Cells
Video transcript
Which of the following answers is not a mechanism pathogen use to survive within a phagocytic host cell?
Some encapsulated bacterial pathogens are said to be serum-resistant. Serum resistant pathogens avoid the effects of the complement system proteins. How are encapsulated bacteria able to be serum-resistant and avoid phagocytosis?
Do you want more practice?
Here’s what students ask on this topic:
What are the mechanisms by which bacteria can survive inside phagocytic cells?
Bacteria can survive inside phagocytic cells through three main mechanisms. First, some bacteria escape the phagosome before it fuses with the lysosome, thus avoiding degradation. Second, they can inhibit the fusion of the phagosome and lysosome by producing specific inhibitory proteins. Lastly, certain pathogens can endure even within the phagolysosome, resisting the lysosomal enzymes. These survival strategies allow bacteria to evade the immune system and persist within the host, making infections more difficult to treat.
How do bacteria escape from the phagosome before it fuses with the lysosome?
Bacteria escape from the phagosome before it fuses with the lysosome by employing various mechanisms. Some bacteria produce enzymes that degrade the phagosomal membrane, allowing them to escape into the cytoplasm. Others may use specialized secretion systems to inject proteins that disrupt the phagosomal membrane. By escaping the phagosome, these bacteria avoid the degradative environment of the lysosome, allowing them to survive and replicate within the host cell.
What role do inhibitory proteins play in bacterial survival within phagocytic cells?
Inhibitory proteins play a crucial role in bacterial survival within phagocytic cells by preventing the fusion of the phagosome with the lysosome. These proteins interfere with the normal cellular processes that facilitate this fusion, thereby creating a safe environment for the bacteria within the phagosome. By blocking this fusion, the bacteria avoid exposure to the lysosomal enzymes that would otherwise degrade them, allowing them to persist and potentially cause chronic infections.
How do some bacteria survive within the phagolysosome despite the presence of lysosomal enzymes?
Some bacteria have evolved mechanisms to survive within the phagolysosome despite the presence of lysosomal enzymes. These bacteria can resist the harsh conditions by producing protective proteins or enzymes that neutralize the lysosomal enzymes. Additionally, they may alter the pH of the phagolysosome to create a less hostile environment. These adaptations enable the bacteria to withstand the degradative processes and continue to live and replicate within the phagocytic cell.
Why is understanding bacterial survival mechanisms inside phagocytic cells important for developing treatments?
Understanding bacterial survival mechanisms inside phagocytic cells is crucial for developing effective treatments because these mechanisms allow bacteria to evade the immune system and persist within the host. By identifying and targeting these survival strategies, researchers can develop new therapeutic approaches to combat infections. For example, drugs that inhibit bacterial escape from the phagosome or block the production of inhibitory proteins could enhance the effectiveness of the immune response, leading to better outcomes for patients with bacterial infections.