---
module: 095-01
language: en
chapter: 95
title: "Microbiome, Microbial Ecology, Evolution, and Host–Pathogen Co-adaptation"
module_title: "Colonisation, anatomical niches, community assembly, and host–microbiome ecology"
source_sha256: dec0ea0b0963b65f4b765498b18ecb67167115bb5110ecce5207c7f882ee4c1b
---
# Colonisation, niches, and host ecology

## Definitions and context dependence
### Microbiome: communities, genes, products, interactions
### Microbiota refers to the organisms themselves
### Most residents harmless or beneficial in usual niche
### Same organism causes disease after context change
#### Barrier breach
#### Immune change
#### Movement to a sterile compartment

## Site-specific burden and composition
### Skin: cool, dry, acidic, oxygenated, intermittent exposure
### Mouth: dense biofilms on teeth and mucosa
### Stomach: low biomass under acidity
### Colon: huge anaerobic community, slow transit, substrates
### Lower airway biomass low, shaped by aspiration and clearance

## Niche conditions and habitat construction
### Oxygen, pH, temperature, salt, water, nutrients, bile
### Microbes consume oxygen and shift pH
#### Community constructs part of its own habitat

## Early colonisation, succession, and low-biomass caveats
### Begins around birth, not a single event
### Delivery mode, gestational age, feeding, antibiotics
### Maternal microbes contribute but are not the sole source
### Unstable early, site-specific over years

### Placental microbiome claims remain controversial
### Reagent and environmental contamination dominate low biomass
### Microbial DNA does not prove living colonisation
### Need controls, culture, microscopy, localisation, plausibility

## Community assembly and diversity metrics
### Dispersal introduces organisms
### Selection favours traits fitting the niche
### Drift randomly changes low-abundance populations
### Mutation and gene transfer generate variation
### Priority effects: early colonisers alter later establishment
### Different taxa can perform overlapping functions

### Alpha diversity: richness and evenness within a sample
### Beta diversity: difference between samples
### Higher diversity not universally healthier
#### Low-diversity Lactobacillus vaginal states often healthy
### Metric choice and sequencing depth alter conclusions

## Spatial organisation and colonisation resistance
### Mucus separates luminal community from epithelium
#### Inner colonic mucus resists penetration
### Secretory IgA excludes, retains, or shapes without inflammation
### Peptides, epithelial oxygen use, immune cells keep structure
#### Loss of separation inflames without a new pathogen
### Colonisation resistance limits invaders
#### Nutrient competition and attachment-site occupancy
#### Bacteriocins, acidic metabolites, bile-acid transformation
#### Antibiotics let C. difficile or resistant organisms expand

## Relationships, pathobionts, and interpretation
### Commensalism, mutualism, parasitism shift with context
### S. aureus colonises nose yet causes invasive disease
### Pathogenicity is an interaction, not a fixed property
### Pathobiont harms under altered host or community
### Opportunistic infection needs a defence defect
### Positive nonsterile culture may be carriage

## Site ecologies: oral, skin, vaginal
### Plaque: pellicle, early adhesion, coaggregation
#### Frequent sugar selects acid-tolerant, demineralising communities
### Periodontitis: dysbiotic biofilm plus tissue destruction
### Skin differs by oily, moist, dry sites and follicles
#### Atopic dermatitis: barrier, type-two, staphylococcal expansion
### Vaginal ecology: oestrogen, glycogen, lactate, antibiotics
#### Bacterial vaginosis is polymicrobial, metabolite-altered
#### Avoid labelling normal diversity as disease

## Microbial functions for the host
### Fermentation to short-chain fatty acids, gases, biomass
### Transformation of bile acids, amino acids, polyphenols, drugs
### Function depends on substrate and strain
### Immune development: germ-free animals altered, extrapolate cautiously
### Gut-brain signalling via vagal, immune, endocrine, tryptophan
#### Human causal evidence limited and heterogeneous
### Virome: phages kill bacteria, move genes, alter competition

## Biofilms, exposures, and resilience
### Biofilm: surface community in self-produced matrix
#### Tolerance differs from inherited resistance
### Diet changes activity fast, composition slowly
#### Fibre supports saccharolytic fermentation
### Non-antibiotic drugs also reshape microbiota
#### Microbes activate or inactivate drugs
### Ageing and illness change diet, transit, immunity, drugs
#### Signature may be cause, consequence, or treatment effect
### Resilience is functional return; resistance is limited change
#### Recovery may be functional without taxonomic return
#### Repeated insults push alternative stable states
#### One post-treatment sample cannot prove recovery
### Health is a resilient, location-compatible configuration
