The final stage in the chain of infection is the colonization or establishment of a pathogen within or on a susceptible host. For a pathogen to successfully colonize, it typically must enter the host through specific portals of entry. These portals include natural body openings such as the eyes, ears, nose, mouth, genitourinary tract, as well as any open wounds or broken skin. The ability of a pathogen to cause infection largely depends on the particular entry point it uses to gain internal access. Understanding these portals of entry is crucial for comprehending how infections develop and spread within the body.
- 1. Introduction to Microbiology3h 22m
- Introduction to Microbiology18m
- 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 Design30m
- 2. Disproving Spontaneous Generation1h 18m
- 3. Chemical Principles of Microbiology3h 38m
- 4. Water1h 28m
- 5. Molecules of Microbiology2h 26m
- 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 37m
- 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 Growth31m
- 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 21m
- Introduction to Energy15m
- Laws of Thermodynamics15m
- Chemical Reactions9m
- ATP22m
- Enzymes14m
- Enzyme Activation Energy9m
- Enzyme Binding Factors9m
- Enzyme Inhibition10m
- Introduction to Metabolism8m
- Negative & Positive Feedback7m
- Redox Reactions22m
- Introduction to Aerobic Cellular Respiration25m
- Types of Phosphorylation14m
- 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 28m
- 15. Central Dogma & Gene Regulation7h 18m
- 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 Expression25m
- 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
- 25. Epidemiology2h 24m
- Introduction to Epidemiology37m
- Introduction to Chain of Infection5m
- Reservoirs of Infection12m
- Disease Transmission4m
- Horizontal Disease Transmission30m
- Colonization of Susceptible Host7m
- Factors Influencing Epidemiology11m
- Emerging Infectious Diseases12m
- Healthcare-Associated Infections13m
- Epidemiological Studies8m
- 26. Applications of the Immune Response2h 9m
- 28. Antimicrobial Drugs3h 35m
- Introduction to Antimicrobial Drugs8m
- How Antimicrobial Drugs Work10m
- Broad vs Narrow Spectrum Drugs9m
- Superinfections11m
- Drug Interactions: Synergism and Antagonism8m
- Therapeutic Window & Therapeutic Index6m
- Inhibitors of Cell Wall Synthesis: Beta-lactam & Penicillin36m
- Inhibitors of Cell Wall Synthesis: Polypeptide Antibiotics & Isoniazid6m
- Inhibitors of Protein Synthesis9m
- Disruptors of Cell Membranes11m
- Inhibitors of Nucleic Acid Synthesis9m
- Competitive Inhibitors of Metabolic Pathways12m
- Antifungal Drugs11m
- Antiviral Drugs10m
- Tests to Guide Antimicrobial Use21m
- Antimicrobial Resistance29m
Colonization of Susceptible Host: Videos & Practice Problems
Pathogens establish infection by colonizing susceptible hosts through specific portals of entry such as the respiratory tract, digestive system, or broken skin. Successful colonization depends on tissue specificity and environmental conditions like acidity. Respiratory pathogens typically cause disease when inhaled, while intestinal pathogens require ingestion. Fecal-oral transmission occurs when fecal pathogens are accidentally ingested, emphasizing the importance of hygiene. Understanding adherence, portals of entry, and tissue tropism is crucial for grasping pathogenesis and infection control in microbial diseases.
Colonization of Susceptible Host
Colonization of Susceptible Host Video Summary

Successful Colonization Depends on Entry Point
Successful Colonization Depends on Entry Point Video Summary
The success of pathogen colonization largely depends on the specific portal of entry through which the pathogen enters the host. Many pathogens are tissue-specific, meaning they can only attach, bind, and cause disease in particular tissues that provide the right environmental conditions for their survival. For instance, the stomach's highly acidic environment can inhibit certain pathogens, while other tissues like the respiratory tract offer different conditions that favor other types of pathogens.
Respiratory pathogens are typically airborne and most effective when inhaled through the nose or mouth, allowing them to colonize the lungs. If these pathogens are ingested instead, they are less likely to cause disease because the digestive system presents a hostile environment for them. Conversely, intestinal pathogens are adapted to survive the digestive tract and cause disease when swallowed with food or drink. They are less likely to cause infection if inhaled into the lungs.
Fecal-oral transmission is a common route for the spread of intestinal pathogens, occurring when fecal pathogens are unintentionally ingested, often due to poor hand hygiene. This mode of transmission highlights the importance of proper sanitation and handwashing to prevent gastrointestinal infections.
Understanding the relationship between a pathogen’s portal of entry and its tissue specificity is crucial for comprehending how infections develop and spread. This knowledge also informs preventive measures and treatment strategies by targeting the most vulnerable points of entry and the environmental conditions that support pathogen survival.
The following is a list of different:
- Respiratory tract.
- Gastrointestinal tract.
- Urinary tract.
- Skin wounds or lesions.
Modes of transmission.
Portals of entry or exit.
Regions of fomites.
Which of the following statements is true?
Most pathogens colonize the surface of a person’s skin & cause disease without a portal of entry.
Intestinal pathogens are usually inhaled via the nose.
Pores in the skin are a common portal of entry for respiratory pathogens.
If a pathogen is ingested but is unable to colonize within the host, it is unlikely to cause disease.
Do you want more practice?
Here’s what students ask on this topic:
Pathogens colonize susceptible hosts by entering through specific portals of entry, which are body openings or orifices. The main portals include the respiratory tract (nose and mouth), digestive tract (mouth and gastrointestinal system), genitourinary tract, eyes, ears, and any open wounds or broken skin. These entry points provide access for pathogens to internal tissues where they can establish infection. The choice of portal is crucial because pathogens are often tissue-specific and adapted to survive the environmental conditions of particular tissues. For example, respiratory pathogens thrive in the lungs, while intestinal pathogens are adapted to the acidic and enzymatic environment of the digestive system. Understanding these portals helps explain how infections start and spread within the body.
The portal of entry significantly influences the success of pathogen colonization because many pathogens are tissue-specific and require certain environmental conditions to survive and multiply. For instance, respiratory pathogens are adapted to the moist, less acidic environment of the lungs and are most successful when inhaled through the nose or mouth. If these pathogens enter through a different portal, like ingestion, they may not survive the acidic stomach environment and fail to cause disease. Conversely, intestinal pathogens are adapted to survive stomach acid and colonize the digestive tract but are less likely to cause disease if inhaled. Therefore, the portal of entry determines whether the pathogen can reach its preferred tissue and establish infection effectively.
Fecal-oral transmission is the process by which pathogens from fecal matter are accidentally ingested, often due to poor hygiene practices like not washing hands after using the restroom. This transmission route is important because it allows intestinal pathogens, which thrive in the digestive system, to enter a new host through the mouth. Once ingested, these pathogens can colonize the gastrointestinal tract and cause disease, such as diarrhea or stomach infections. Understanding fecal-oral transmission highlights the critical role of hygiene in preventing the spread of infections and controlling disease outbreaks, especially in environments where sanitation is compromised.
Pathogens are often tissue-specific because they have evolved to attach, bind, and survive in particular tissues that provide the right environmental conditions for their growth. Different tissues vary in factors like pH, temperature, oxygen levels, and immune defenses. For example, the stomach is highly acidic, which kills many pathogens, while the lungs provide a moist environment suitable for respiratory pathogens. This tissue tropism means that a pathogen’s ability to cause disease depends on reaching its preferred tissue via the correct portal of entry. If a pathogen enters through an inappropriate portal, it may not survive or establish infection, reducing its ability to cause disease. This specificity is key to understanding pathogenesis and designing targeted infection control strategies.
Adhesins are specialized molecules on the surface of pathogens that enable them to attach firmly to host tissues. This attachment is the first critical step in colonization because it prevents the pathogen from being washed away by bodily fluids like mucus or urine. Adhesins recognize and bind to specific receptors on the host’s cells, often determining the tissue specificity of the pathogen. For example, certain adhesins bind only to receptors found in the respiratory tract, facilitating colonization there. Without adhesins, pathogens would struggle to establish infection, as they could not maintain close contact with host cells to invade or produce toxins. Therefore, adhesins are essential for successful colonization and subsequent disease development.