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Side 64

Microbiology

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.

cell→metabolism→growth→interaction→ecology / pathogenesis
06microbial lenses
05growth controls
05interaction modes
64Side

“Microbe” describes scale more than one lineage.

Bacteria, archaea, microscopic eukaryotes and viruses differ fundamentally in structure and replication.

Bacteria

Prokaryotic cells.

Highly diverse metabolism, cell envelopes and ecological roles.

Archaea

Distinct prokaryotic lineage.

Share some cellular features with bacteria but differ deeply in membranes and molecular machinery.

Fungi

Eukaryotic microbes.

Yeasts and molds obtain nutrients by absorption and can be decomposers, symbionts or pathogens.

Protozoa

Diverse unicellular eukaryotes.

Many are motile and occupy aquatic, soil or host-associated habitats.

Algae

Photosynthetic microbial eukaryotes.

Important primary producers in aquatic systems.

Viruses

Replicating genetic entities dependent on host cells.

Viruses lack independent cellular metabolism and reproduce through host machinery.

Microbes exploit extraordinary chemical possibilities.

Energy source, electron donor and carbon source can vary independently, producing many metabolic strategies.

01 · Carbon

Where does biomass carbon come from?

CO₂ or organic compounds?

Autotrophs fix inorganic carbon; heterotrophs use organic carbon.

02 · Energy

Light or chemical reactions?

Phototroph or chemotroph.

Energy acquisition can be decoupled from carbon source.

03 · Electrons

What supplies reducing power?

Organic or inorganic donors.

Electron donors drive redox metabolism.

04 · Acceptor

Where do electrons end?

O₂, nitrate, sulfate, other?

Different terminal acceptors support different respiratory strategies.

05 · Product

What is released?

CO₂, acids, gases, reduced compounds?

Microbial by-products reshape environments and host systems.

Microbial growth is population growth.

Cell division responds to nutrients, temperature, pH, oxygen and accumulated waste.

Lag

Adapt before rapid division.

Cells adjust gene expression and metabolism to new conditions.

Exponential

Population doubles repeatedly.

Under favorable conditions, abundance grows geometrically.

Stationary

Net growth slows.

Nutrient limitation and waste accumulation balance division with death.

Death

Viable cells decline.

Environmental stress can exceed maintenance capacity.

Biofilm

Surface-associated community state.

Biofilms alter diffusion, gene expression and resistance to environmental stress.

Microbes exchange genes as well as inherit them.

Mutation and horizontal gene transfer can spread new traits rapidly through microbial populations.

Mutation

Create new sequence variants.

Large populations generate many mutations even when per-cell rates are low.

Transformation

Take up free DNA.

Some microbes can incorporate DNA from the environment.

Transduction

Viruses move bacterial DNA.

Bacteriophages can transfer genes between cells.

Conjugation

Direct cell-to-cell DNA transfer.

Plasmids can spread metabolic or resistance traits.

Mobile elements

DNA can move within genomes.

Transposons and related elements restructure genetic context.

Selection

Environment filters variants.

Antibiotics, nutrients and host conditions can rapidly change population composition.

Most microbes live in communities, not isolation.

Competition, metabolic exchange and signaling create collective behavior.

InteractionMechanismCommunity effect
CompetitionShared resource limitationExclusion or niche separation
Cross-feedingOne species consumes another’s productMetabolic interdependence
Quorum signalingPopulation-density-dependent moleculesCoordinated gene expression
Biofilm formationAttachment + extracellular matrixSpatial structure and protection
Phage interactionViral infection of microbesPopulation control and gene transfer

Pathogenesis is an interaction between microbe and host.

Disease depends on entry, replication, tissue interaction, immune response and transmission—not microbe presence alone.

Entry

Reach a suitable host site through an exposure route.

Adhere

Attach or colonize despite physical clearance mechanisms.

Acquire

Obtain nutrients and conditions needed for replication.

Evade

Avoid or manipulate host defenses long enough to persist.

Damage

Direct microbial effects and host inflammation can both injure tissue.

Transmit

Exit one host and reach another, completing the ecological cycle.

Brock Biology of Microorganismsmicrobiology foundation
Prescott’s Microbiologymicrobial diversity and metabolism
Medical Microbiologyhost–microbe interaction
Microbial Ecologycommunities and environmental microbiology