o Colonisation: microorganism presence without tissue invasion
o Invasion: entry and multiplication within host tissues
o Evasion: avoiding host immune responses
o Dissemination: local spread or haematogenous dissemination
o Toxins:
Exotoxins (e.g., tetanus, diphtheria)
Endotoxins (LPS in Gram-negative bacteria → sepsis)
o Adhesion proteins:
Pili, fimbriae (e.g., E. coli UTI)
o Capsules:
Avoid phagocytosis (e.g., S. pneumoniae, Neisseria meningitidis)
o Biofilm formation:
E.g., Staphylococcus epidermidis on catheters, prosthetic devices
Direct contact
Herpes simplex virus (HSV), HIV, MRSA
Droplet
Influenza, SARS-CoV-2, Neisseria meningitidis
Airborne
Tuberculosis, measles, varicella-zoster
Faeco-oral
Cholera, hepatitis A, norovirus, poliovirus
Vector-borne
Malaria (Anopheles), dengue, Zika, Lyme disease (ticks), leishmaniasis (sandflies)
Zoonotic
Leptospirosis (rats), brucellosis (unpasteurised dairy), rabies (dogs, bats), Q fever (Coxiella burnetii, livestock)
• Fomite transmission: indirect via contaminated surfaces (e.g., RSV, norovirus)
o Average number of secondary cases from one index case in a fully susceptible population
• Interpretation:
o R₀ >1: infection can spread in the population
o R₀ <1: infection likely to die out
o Formula: 1 – (1/R₀)
o Examples:
Measles: R₀ ≈ 12–18 → ~95% needed for herd immunity
COVID-19 original strain: R₀ ≈ 2–3 → ~60–70% threshold
o MRSA: surgical site, bloodstream infections
o Clostridioides difficile: antibiotic-associated colitis
o Catheter-associated urinary tract infections (CAUTI)
o Central line–associated bloodstream infections (CLABSI)
o Ventilator-associated pneumonia (VAP)
• Key control measures:
o Strict hand hygiene (alcohol-based rub or soap and water for C. difficile)
o Barrier precautions (gloves, gowns)
o Environmental cleaning
o Judicious catheter/device use; early removal when possible
• Antimicrobial stewardship:
o Reduces selective pressure and multi-drug resistant organisms (MDROs)
o Examples: MMR (measles, mumps, rubella), yellow fever, varicella, intranasal influenza, BCG
o Contraindicated in severe immunosuppression (e.g., HIV with CD4 <200, chemotherapy, high-dose steroids)
o Examples: injectable influenza, hepatitis A, rabies, HPV
o Safe in immunocompromised patients but may be less immunogenic
o Examples: tetanus, diphtheria
o Examples: pneumococcal (PCV13, PPV23), meningococcal, Hib
o Given at birth in high-risk groups in UK
o Protects against severe TB forms (e.g., TB meningitis)
o HIV: antiretrovirals within 72 hours
o Hepatitis B: HBV vaccine ± HBIG
o Rabies: vaccine + rabies immunoglobulin
o Immediate washing
o Baseline serology (HIV, HBV, HCV)
o Consider PEP
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Author & Educational Disclaimer
Author:
Dr Phillip Cockrell BM FRCP DipClinEd
Dr Phillip Cockrell is a UK Consultant Physician in Internal Medicine, currently working at Queen Alexandra Hospital, Portsmouth University Hospitals NHS Trust. He has previously worked as a registrar across Intensive Care Medicine, Gastroenterology, Cardiology, Stroke Medicine, Acute Medicine, and Respiratory Medicine.
He has held senior leadership roles including Associate Clinical Director of the Acute Medical Unit, Clinical Director of Internal Medicine, and Chief of Medicine. Dr Cockrell has over 15 years’ experience in postgraduate medical education, having lectured extensively across the MRCP syllabus and contributed to MRCP revision teaching and course development.
Dr Cockrell holds a Bachelor of Medicine (BM), Fellowship of the Royal College of Physicians (FRCP), and a Diploma in Clinical Education (DipClinEd). His teaching approach is based on structured consolidation of complex medical topics to support efficient and effective revision for postgraduate examinations.
Purpose of this content:
The material on this page is intended solely for educational purposes to support revision for the MRCP (UK) Part 1 examination. It reflects examination-relevant principles of internal medicine and is designed to aid learning and pattern recognition.
Medical disclaimer:
This content is designed for postgraduate medical examination revision and does not constitute medical advice, diagnosis, or treatment guidance and must not be used as a substitute for professional clinical judgement, local guidelines, or specialist consultation. Clinical decisions should always be made in the context of individual patient circumstances and current national guidance.