Prokaryotic cells.
Highly diverse metabolism, cell envelopes and ecological roles.
Side 64
A study of microscopic life and infectious agents. Microbiology connects cellular structure, metabolism, growth, genetic exchange, microbial communities and host interaction across organisms too small to understand by naked-eye observation alone.
Bacteria, archaea, microscopic eukaryotes and viruses differ fundamentally in structure and replication.
Highly diverse metabolism, cell envelopes and ecological roles.
Share some cellular features with bacteria but differ deeply in membranes and molecular machinery.
Yeasts and molds obtain nutrients by absorption and can be decomposers, symbionts or pathogens.
Many are motile and occupy aquatic, soil or host-associated habitats.
Important primary producers in aquatic systems.
Viruses lack independent cellular metabolism and reproduce through host machinery.
Energy source, electron donor and carbon source can vary independently, producing many metabolic strategies.
CO₂ or organic compounds?
Autotrophs fix inorganic carbon; heterotrophs use organic carbon.
Phototroph or chemotroph.
Energy acquisition can be decoupled from carbon source.
Organic or inorganic donors.
Electron donors drive redox metabolism.
O₂, nitrate, sulfate, other?
Different terminal acceptors support different respiratory strategies.
CO₂, acids, gases, reduced compounds?
Microbial by-products reshape environments and host systems.
Cell division responds to nutrients, temperature, pH, oxygen and accumulated waste.
Cells adjust gene expression and metabolism to new conditions.
Under favorable conditions, abundance grows geometrically.
Nutrient limitation and waste accumulation balance division with death.
Environmental stress can exceed maintenance capacity.
Biofilms alter diffusion, gene expression and resistance to environmental stress.
Mutation and horizontal gene transfer can spread new traits rapidly through microbial populations.
Large populations generate many mutations even when per-cell rates are low.
Some microbes can incorporate DNA from the environment.
Bacteriophages can transfer genes between cells.
Plasmids can spread metabolic or resistance traits.
Transposons and related elements restructure genetic context.
Antibiotics, nutrients and host conditions can rapidly change population composition.
Competition, metabolic exchange and signaling create collective behavior.
| Interaction | Mechanism | Community effect |
|---|---|---|
| Competition | Shared resource limitation | Exclusion or niche separation |
| Cross-feeding | One species consumes another’s product | Metabolic interdependence |
| Quorum signaling | Population-density-dependent molecules | Coordinated gene expression |
| Biofilm formation | Attachment + extracellular matrix | Spatial structure and protection |
| Phage interaction | Viral infection of microbes | Population control and gene transfer |
Disease depends on entry, replication, tissue interaction, immune response and transmission—not microbe presence alone.
Reach a suitable host site through an exposure route.
Attach or colonize despite physical clearance mechanisms.
Obtain nutrients and conditions needed for replication.
Avoid or manipulate host defenses long enough to persist.
Direct microbial effects and host inflammation can both injure tissue.
Exit one host and reach another, completing the ecological cycle.