In this video, we're going to talk about some other types of staining, specifically special staining. And so special staining, as its name implies, is going to use really special procedures to stain very specific structures, either on the inside or on the outside of cells. Now examples of special stains include the capsule stain, endospore stains, and flagella stains. And so if we take a look at our example down below, we can see today's special, special staining, which is going to be used to stain very specific cell structures. And so on the far left, we're showing you the example of the capsule stain, which is going to be staining the capsule of bacteria. And so here we're showing you the bacteria of the human eye, their capsules being stained here in white. So you can see that, you're able to actually visualize the capsules, this barrier that surrounds the cell, as these white borders, because of the particular stain that's being used here. Now, next what we're showing you here is the endospore stain. And the endospore stain, as its name implies, allows for the visualization of endospores. And so here in this image, we're staining the endospores of the bacteria Bacillus cereus. And the endospores are showing up as this bluish-greenish color. So all of these little blue dots that you see represent the endospores being formed by this particular bacteria. Now last but not least over here on the far right, we're showing you another example of a special stain called the flagella stain, which as its name implies allows for the visualization of flagella. And so here it's showing you the flagella of the same bacterium, Bacillus cereus. And so you can see all of the flagella branching off of this bacteria. Now notice over here on the left hand side, it's also showing you the same bacteria. Bacillus cereus is being shown in the left, the middle, and the right image. But notice that none of the flagella are actually being visualized over here on the left-hand side, but that is because the flagella stain is not being used over here. But as soon as the flagella stain is used, notice that where the scientists are able to visualize the flagella. And so this shows you the importance of using these special stains to be able to visualize the specific structures of interest a lot more easily. And so this here concludes our brief lesson on special staining 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
Other Types of Staining - Online Tutor, Practice Problems & Exam Prep
Special staining techniques, such as capsule, endospore, and flagella stains, are essential for visualizing specific bacterial structures. The capsule stain highlights the protective capsule, while the endospore stain reveals the bluish-green endospores of Bacillus cereus. The flagella stain allows for the observation of flagella, enhancing understanding of bacterial motility. Additionally, immunofluorescence utilizes fluorochrome dyes combined with antibodies to identify specific antigens, distinguishing living cells from dead ones based on cellular processes. These methods are crucial for microbiological studies and diagnostics.
Special Staining
Video transcript
Which of these is considered a special stain that correctly matches its description?
What is the major difference between special staining techniques and differential staining techniques?
Fluorescent Dyes
Video transcript
This video, we're going to talk a little bit more about fluorescent dyes. Recall from our previous lesson videos that fluorochrome dyes and immunofluorescence can be used to observe cells and or cell components. Recall that immunofluorescence is a very specific technique that combines a fluorochrome or a fluorescent dye with an antibody protein. This will allow for the tagging of very specific objects and very specific molecules. It's also worth noting that some fluorescent dyes can actually be changed by cellular processes. Therefore, some fluorescent dyes can be used to distinguish between living cells that contain those cellular processes and dead cells. Distinguish the living from the dead cells that the dead cells do not contain those cellular processes. If we take a look at our image down below, what we're showing you is an image of immunofluorescence, which is going to use a fluorochrome combined with an antibody. Over here on the far left, what we're showing you is the fluorochrome, which is in red. These red circles are these fluorochrome molecules or these fluorescent dyes that will fluoresce. In the bottom in green, we're showing you the antibodies, which are these Y-shaped proteins. These Y-shaped protein antibodies are capable of binding to very specific antigens. Antigens are going to be molecules that antibodies bind to. Over here, you can see that the antibodies and fluorochromes are combined together to create a single molecule. Over here, what we have is a string of bacteria, that all contain these antigens, these very specific antigens. The antibody, this Y-shaped protein, is going to be specific to binding to the antigen. The fluorochrome is only going to fluoresce when the antibody actually does bind to the antigen. If we take a look at this image over here on the right, notice that all of the Y-shaped antibodies are binding to the antigen on the surface of the bacteria. At that point, each of these fluorochromes is going to fluoresce, and that fluorescence can be detected. Ultimately, this is what we're seeing here in this image, is the fluorescence due to immunofluorescence, the use of the antibody here. This here concludes our brief introduction to fluorescent dyes and immunofluorescence. Once again, 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.
_______ is/are used to attach fluorochrome molecules to antigens on the surface of bacterial cells in immunofluorescence.
Do you want more practice?
Here’s what students ask on this topic:
What is the purpose of special staining techniques in microbiology?
Special staining techniques in microbiology are used to visualize specific structures within or on the surface of bacterial cells. These techniques include capsule stains, endospore stains, and flagella stains. For example, the capsule stain highlights the protective capsule surrounding some bacteria, the endospore stain reveals the resilient endospores formed by certain bacteria like Bacillus cereus, and the flagella stain allows for the observation of bacterial flagella, which are essential for motility. These methods are crucial for identifying and studying bacterial morphology, physiology, and pathogenicity, thereby aiding in diagnostics and research.
How does the capsule stain work and what does it reveal?
The capsule stain is a special staining technique used to visualize the capsule, a protective layer surrounding some bacterial cells. This stain typically involves a combination of a negative stain, which stains the background, and a positive stain, which stains the bacterial cell. The capsule itself remains unstained and appears as a clear halo around the cell. This method is particularly useful for identifying pathogenic bacteria, as the capsule often plays a role in virulence by protecting the bacteria from the host's immune system.
What are the steps involved in performing an endospore stain?
The endospore stain is a differential staining technique used to visualize bacterial endospores. The primary steps include: 1) Applying a primary stain, usually malachite green, to a heat-fixed bacterial smear. 2) Heating the slide to allow the stain to penetrate the endospores. 3) Rinsing the slide with water to remove the stain from the vegetative cells. 4) Counterstaining with safranin to stain the vegetative cells. Endospores will appear green, while vegetative cells will appear red. This technique is essential for identifying spore-forming bacteria like Bacillus and Clostridium species.
How does immunofluorescence work in identifying specific bacterial antigens?
Immunofluorescence is a technique that combines fluorochrome dyes with antibodies to identify specific bacterial antigens. The process involves: 1) Conjugating a fluorochrome dye to an antibody that specifically binds to the target antigen. 2) Applying this conjugated antibody to a sample containing the bacteria. 3) The antibody binds to the antigen on the bacterial surface. 4) When exposed to specific wavelengths of light, the fluorochrome emits fluorescence, which can be detected using a fluorescence microscope. This method allows for precise identification and localization of specific bacterial components, aiding in diagnostics and research.
What are the advantages of using fluorescent dyes in microbiological studies?
Fluorescent dyes offer several advantages in microbiological studies: 1) High specificity: When combined with antibodies, they can target specific antigens, allowing for precise identification of bacterial components. 2) Sensitivity: Fluorescence can be detected at very low concentrations, making it possible to observe minute details. 3) Distinguishing living from dead cells: Some fluorescent dyes can differentiate between living and dead cells based on cellular processes. 4) Versatility: They can be used in various applications, including studying cell structure, function, and interactions. These advantages make fluorescent dyes invaluable tools in microbiology research and diagnostics.