pathology

    Cards (84)

    • Less than 100 human pathogenic species identified and >5000 bacterial species identified to date (estimated many times more than this on Earth). Therefore < than 0.02%, but probably <0.0001% of bacterial species are human pathogens.
    • Why do bacteria cause infections?
      Body provides favourable niche in which to reproduce; human tissues provide nutrients and reduced competition for resources
    • Why don't all bacteria cause infections?
      • Not favourable environment for all species
      • Immune system prevents vast majority of bacteria from colonizing, pathogens need adaptations to avoid or overcome immune response
    • Where can bacteria infect?
      • Gastrointestinal tract
      • Central nervous system
      • Respiratory tract
      • Urogenital tract
      • Skin and muscle
      • Multisystem
    • Gastrointestinal tract
      • Escherichia coli
      • Shigella
      • Salmonella
      • Campylobacter jejuni
      • Vibrio cholerae
      • Clostridium difficile
    • Central nervous system
      • Neisseria meningitidis
      • Haemophilus influenzae
      • Streptococcus pneumoniae
      • Clostridium tetani
      • Clostridium botulinum
    • Respiratory tract
      • Streptococcus pyogenes
      • Streptococcus pneumoniae
      • Bordetella pertussis
      • Mycobacterium tuberculosis
      • Legionella pneumophila
      • Pseudomonas aeruginosa
      • Haemophilus influenzae
      • Corynebacterium diphtheriae
    • Urogenital tract
      • Escherichia coli
      • Proteus mirabilis
      • Chlamydia trachomatis
      • Treponema pallidum
      • Neisseria gonorrhoeae
    • Skin and muscle
      • Staphylococcus aureus
      • Streptococcus pyogenes
      • Rickettsia prowazekii
    • Multisystem
      • Borrelia burgdorferi
      • Yersinia pestis
      • Franciscella tularensis
      • Coxiella burnetii
      • Leptospira spp.
    • Ingestion (faecal-oral)

      • Infection - Pathogen reaches gastrointestinal tract and rapidly multiplies e.g Campylobacter jejuni, Salmonella species (S. enterica s. Typhimurium - typhoid), certain strains of Escherichia coli
      • Intoxication - Ingestion of toxins produced by bacteria. Typically results in acute vomiting 1-6 h post ingestion e.g. Clostridium botulinum
    • Vector-borne
      • Ticks - Lone Star tick - Ehrlichia chaffeensis - Ehrlichiosis
      • Ticks - Ixodes tick - Borrelia burgdorferi - Lyme disease
      • Ticks - Many ticks - Coxiella burnetii - Q fever
      • Ticks - Wood tick/Dog tick – Rickettsia rickettsii – Rocky Mountain Spotted Fever
      • Lice - Body louseRickettsia prowazekii – Epidemic typhus
      • Fleas - Rat fleas – Rickettsia typhi – Endemic typhus
      • Fleas - Rat fleas – Yersinia pestis – Bubonic plague (pneumonic is airborne)
    • Zeihl-Neelsen stain of skin biopsy reveals Mycobacterium leprae - bacteria are stained red/pink
    • Pathophysiology
      • Virulence factors enable pathogenic bacteria to colonise, invade and replicate within host organism
      • E.g. adhesins and fimbriae, capsule, exoenzymes, toxins
      • Some of these enable the bacteria to avoid or overcome the immune response
      • Some bacteria produce toxins that help to overcome immune response and enable them to invade cells / access nutrients cause direct damage to host human cells / tissues / organs
      • In many cases damage caused during bacterial infection is the result of immune responses to the pathogen and not directly due to the pathogen itself
    • Prevention of bacterial infections
      • Hygiene & sanitation - Personal, Food, Environment (e.g. water treatment)
      • Vaccines: Inactivated, attenuated, subunit, toxoid - DTaP (Diptheria, Tetanus, Pertussis), Hib/MenC & MenACWY (Meningitis)
      • Prophylaxis (antibiotics, immunotherapy, antimicrobial coatings) - Post surgery, In pregnancy if GBS carriage detected, Immunocompromised e.g. Sickle cell anaemia, Antimicrobial coatings on medical devices
      • Safe sex
      • Insecticides (vector control)
      • Quarantine and contact tracing
    • Detection
      How do you diagnose a bacterial infection?
    • Detection of bacterial infections
      • Patient presentation (signs and symptoms) - E.g. fever, diarrhoea, vomiting, cough, pus/exudate, rash
      • Identify most likely causative agents
      • Samples taken from sputum, blood, urine, stools
      • Urine dip-stick test
      • Microbial culture - Colony morphology, selective media
      • Microscopy - Cellular morphology, Differential stain
      • Biochemical tests
      • Molecular diagnostics e.g. PCR
      • Serological diagnostics e.g. ELISA
    • Treatment
      How do you cure bacterial infections?
    • Treatment of bacterial infections
      • Topical disinfectants - Chlorhexidine
      • Surgery / Debridement
      • Antimicrobial coatings - Silver nanoparticles used in wound dressings
      • Antibiotics - Target specific components of bacterial cellular machinery, Inhibit growth = bacteriostatic, Cause bacterial death = bactericidal, Oral / intravenous / intramuscular / topical, Usually prescribed a course of treatment
    • How do antibiotics work?
      • Combination of antibiotics may help prevent evolution of resistance and treat infections caused by MDR bacteria
      • Clavulanic acid given in combination with penicillin to inactivate B-lactamases
    • Concern: Antibiotic resistance
    • Fix the antibiotics pipeline M. A. Cooper & D. Shlaes Nature 472, 32 (2011)
    • Case study 1: Airborne
      Mycobacterium tuberculosis - Causative agent of Tuberculosis
    • Mycobacterium tuberculosis
      • Weak Gram positive rod, discovered by Robert Koch (1882)
      • Determined that this is causative agent of the disease tuberculosis (Koch's postulates)
      • Mycobacteria have a unique cell wall structure with high concentration of mycolic acid
      • Slow growing (generation time approx. 16 hr) – takes 10 – 14 days to culture in lab
    • Tuberculosis: infection vs. disease

      • Tuberculosis (TB) is an ancient human disease
      • Clear cut distinction between infection & disease
      • only 5% of infections lead to disease, 95% latent infections
      • If untreated 50% active infections are fatal
      • M. tuberculosis survives and multiplies in macrophages
    • Rook et al. (2005) Nature Reviews Immunology 5, 661-667
    • Tuberculosis: Latent infection
      • Immune response involves formation of granulomas ("tubercles") consisting of macrophages, lymphocytes and epithelioid cells which trap the bacteria
      • Mtb survive inside granulomas and become dormant, but can be reactivated to cause active infection if untreated
    • Tuberculosis: Active disease
      • Fever
      • Night Sweats
      • Weight loss
      • Cough
      • Cavities in lung
      • 85% of cases in the lungs (pulmonary TB) but other organs can be affected (extrapulmonary TB) e.g. lymphatics, kidneys, urogenital tract, CNS, bones, blood vessels (death by hemorrhage)
      • Fatality in 50% untreated cases - occurs due to aggravated immune response
    • Tuberculosis: Detection
      • Use Ziehl Neelsen stain to differentiate acid-fast bacteria
      • Sample stained with carbolfuschin stain and heated – all cells stain red/pink
      • After washing with alcohol….Acid fast bacteria retain the carbolfuschin stain due to high concentration of mycolic acids in cell wall and they remain red/pink
      • Non-acid fast bacteria are decolourised as alcohol can penetrate the cell wall due to lower lipid concentration and they are then counterstained with methylene blue
    • Tuberculosis: Detection
      • Mantoux test - 0.1 ml of PPD injected into the forearm to produce a small bleb, Localised hardening ("induration") indicates hypersensitivity +ve test indicates infection or previous infection/vaccination
      • X-Ray test - Cavities seen as radio-opaque patches in lower parts of lung
    • Tuberculosis: Treatment/Prevention
      • Triple therapy over 6 months of:
      • Isoniazid - interferes with mycolic acid cell wall synthesis
      • Pyrazinamide - action unknown, but converted to active form in the liver, pyrazinoic acid
      • Rifampicin / Rifampin - inhibits transcription by binding to β-subunit of RNA polymerase
      • Alarming increase in rifampicin resistant (RR) and multi-drug resistant (MDR) strains
      • Prophylaxis for 1 year with Isoniazid recommended for people in close contact
      • BCG (Bacille Calmette-Guérin) vaccine - live attenuated strain of M. bovis; 20-80% efficacy
    • Tuberculosis: Epidemiology

      • TB is in the TOP 10 leading causes of death globally
      • It is the leading cause of death
    • Non-acid fast bacteria
      Decolourised as alcohol can penetrate the cell wall due to lower lipid concentration and they are then counterstained with methylene blue
    • Acid fast bacteria
      Have a high concentration of mycolic acids in cell wall and they remain red/pink
    • Tuberculosis: Detection
      1. Mantoux test - 0.1 ml of PPD injected into the forearm to produce a small bleb
      2. Localised hardening ("induration") indicates hypersensitivity
      3. +ve test indicates infection or previous infection/vaccination
      4. X-Ray test - Cavities seen as radio-opaque patches in lower parts of lung
    • Tuberculosis: Treatment/Prevention
      1. Triple therapy over 6 months of:
      2. Isoniazid - interferes with mycolic acid cell wall synthesis
      3. Pyrazinamide - action unknown, but converted to active form in the liver, pyrazinoic acid
      4. Rifampicin / Rifampin - inhibits transcription by binding to β-subunit of RNA polymerase
      5. Prophylaxis for 1 year with Isoniazid recommended for people in close contact
      6. BCG (Bacille Calmette-Guérin) vaccine - live attenuated strain of M. bovis; 20-80% efficacy
    • Alarming increase in rifampicin resistant (RR) and multi-drug resistant (MDR) strains
    • Tuberculosis is in the TOP 10 leading causes of death globally
    • It is the leading cause of death from a single infectious agent
    • 2 billion people currently infected globally (latent TB, do not transmit)
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