[Micro] pathogenesis
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Bacterial pathogenesis is a multi-step process involving the acquisition of virulence genes through bacterial conjugation, sensing environmental changes to regulate virulence genes, and damaging host tissues through various mechanisms. Key steps include sticking to host cells through adhesins, scavenging nutrients like iron, avoiding the immune system through stealth mechanisms, and spreading through host tissues and organs. Virulence is a spectrum, and linking a potential pathogen to disease can be difficult as most bacteria are normally non-pathogenic.
[Micro] pathogenesis
- 1. Principles of Pathogenesis Bacterial Infection
- 2. Microbes and humans Very few microbes are always pathogenic Many microbes are potentially pathogenic Most microbes are never pathogenic
- 3. Microbes and humans Disease can come about in several overlapping ways 1. PATHOGENS: Not normal flora subclinical infection (M tuberculosis) 2. Normal flora acquire extra virulence factors to be pathogenic, e.g. E. coli 3. Normal flora: Disease if they gain access to deep tissues by trauma, surgery, lines, especially if a foreign body, e.g. S. epidermidis 4. In immunocompromised patients free-living bacteria & normal flora can cause disease, especially if introduced into deep tissues, e.g. Acinetobacter
- 4. How do we know that a given pathogen causes a specific disease? • Koch's postulates – the pathogen must be present in every case of the disease – the pathogen must be isolated from the diseased host & grown in pure culture – the specific disease must be reproduced when a pure culture of the pathogen is inoculated into a healthy susceptible host – the pathogen must be recoverable from the experimentally infected host
- 5. Spectrum of virulence poliomyelitis in a child 0.1-1% of infections are clinically apparent rubella 50% of infections are clinically apparent rabies 100% of infections are clinically apparent The iceberg concept of infectious disease asymptomatic infection classical clinical disease less severe disease
- 6. potential pathogen isolated from or detected in clinical samples Recognised syndromes patient's clinical condition e.g. septicaemia, endocarditis, osteomyelitis meningitis, UTI, pneumonia pharyngitis How do we know that a given pathogen causes a specific disease? Diagnosis and effective treatment of infection depends not just on isolating an organism, but in establishing a plausible link between the laboratory findings, recognised syndromes and the patient's clinical condition
- 7. Microbes and humans • Evidence for a potential pathogen being clinical significant (particularly for bacteria) – Isolated in abundance – Isolated in pure culture – Isolated on more than one occasion – Isolated from deep tissues – Evidence of local inflammation – Evidence of immune response to pathogen – Fits with clinical picture
- 8. Normal flora • All body surfaces possess a rich normal bacterial flora, especially the mouth, nose, gingival crevice, large bowel, skin – This can be a nuisance in that • it can contaminate specimens • it can cause disease – This is beneficial in that • it can protect against infection by preventing pathogens colonising epithelial surfaces (colonisation resistance) • removal of the normal flora with antibiotics can cause superinfection, usually with resistant microbes • Endogenous viruses reside in the human genome – worries about similar pig viruses in xenografts
- 9. Bacterial Virulence A simplistic view • Some bacterial proteins (“exotoxins”) can elicit the features of a bacterial infection when injected as pure proteins, e.g. – tetanus toxin, botulinum toxin – diphtheria toxin, anthrax toxin • Vaccination with inactivated toxins (“toxoids”) led to a spectacular decline in the incidence of many bacterial infections. • Leading to the simplistic idea that all bacteria need to cause disease is a single toxin…
- 10. Bacterial Virulence A more sophisticated view • There are many different ways to define a “virulence factor”… • needed to colonise and/or damage tissues – “Molecular Koch’s postulates” • Delete gene, show loss of virulence in model system, add gene back (e.g. on plasmid), show restoration of virulence – Biochemical evidence of damaging potential • distinguishes pathogen from commensal • Comparative genomics • expressed or essential in vivo… …but not in the lab?
- 11. Bacterial Virulence A more sophisticated view • Virulence as a process is – MULTIFACTORIAL • A bacterial army, like a human army, needs more than just its firearms to enter and secure enemy territory… “An army marches on its stomach” Napoleon – MULTIDIMENSIONAL • A programme of events organised in time and space
- 12. Steps in successful infection • Sex comes before disease – acquire virulence genes • Sense environment – and Switch virulence genes on and off • Swim to site of infection • Stick to site of infection • Scavenge nutrients – especially iron • Survive stress • Stealth – avoid immune system • Strike-back – damage host tissues • Subvert – host cell cytoskeletal and signalling pathways • Spread – through cells and organs • Scatter
- 13. Bacterial Sex acquiring virulence genes • Bacteria have three ways of exchanging DNA – Transformation • cells take up naked DNA – Transduction • phages carry DNA – Conjugation • cells mate through specialised appendages
- 14. Bacterial Mobile genetic elements • Transposons – ST enterotoxin genes • Virulence Plasmids – e.g. TTSSs in Shigella, Yersinia; toxins in Salmonella, E. coli, anthrax • Phage-encoded virulence - botulinum toxin -diphtheria toxin, - shiga-like toxin(lysis), -staphylococcal toxins, TTSS substrates in Salmonella.
- 15. Bacterial Sex Pathogenicity Islands • Concept from study of uropathogenic Ecoli strains • Defining Features – Carriage of (many) virulence genes – Presence in pathogenic versus non-pathogenic strains – Different G+C content from host chromosome – Occupy large chromosomal regions (10-100 Kb) – Compact distinct genetic units, often flanked by DRs, tRNAs, ISs – Presence of (cryptic) mobility genes – Unstable, prone to deletion
- 16. Bacterial Sex Pathogenicity Islands • often encode secretion systems – LEE region in EPEC – Spi1, Spi2 in Salmonella – Cag in H. pylori • can also encode adhesins, siderophores, toxins – Uropathogenic E. coli (Pai I, II, IV, V) – Yersinia spp. (HPI) – V. cholerae (VPI or TCP-ACF element)
- 17. Sense environment • Bacteria can sense changes in environment – e.g. in temperature, nutrient availability, osmolarity, cell density (“quorum sensing”). • In simplest cases, change in intracellular concentration of ion linked directly to gene expression – e.g. fall in intra-cellular iron levels triggers de- repression of diphtheria toxin gene • In more complex cases, sophisticated signal transduction cascades allow bacteria to regulate gene expression in response to environmental cues – the pathogen as an information processor
- 18. Switch virulence factors on and off A multi-layered hierarchy • Changes in DNA sequence – Gene amplification – Genetic rearrangements • e.g. Hin flip-flop control of flagellar phase variation • Transcriptional Regulation – Activators and Repressors (helix-turn-helix motif) – mRNA folding and stability • Translational Regulation • Post-translational Regulation – Stability of protein, controlled cleavage – Covalent modifications • e.g. phosphorylation in two-component sensor-regulator systems
- 19. Swim • MOTILE bacterial pathogens – Enterics, Campylobacter, Helicobacter, spirochaetes • Motility crucial for virulence in some cases • Usual organelle of motility=flagellum • VariantTwitching motility – Swarming
- 20. Stick • To avoid physical and immunological removal, bacteria must adhere to – cell surfaces and extracellular matrix e.g. in respiratory, gastrointestinal and genitourinary tracts – solid surfaces e.g. teeth, heart valves, prosthetic material – other bacteria • Direct interaction • Molecular bridging via e.g. fibronectin • Adherence often combined with manipulation of host cell signalling and cytoskeleton – Invasion – Intimate adherence
- 21. Stick • COMMON ADHERENCE MECHANISMS: - CAPSULES/SLIME – BIOFILM FORMATION • GRAM POSITIVE ADHESINS – MSCRAMMs (microbial surface components recognizing adhesive matrix molecules), e.g. PROTEIN A – FIMBRIAE • GRAM NEGATIVE ADHESINS (CHO and protein receptors) – Fimbriae, Afimbrial adhesins (FHA, Pertactin etc.) – Outer Membrane Proteins – Types III-IV secretion
- 22. Stick
- 23. Scavenge nutrients e.g. iron • FREE IRON LEVELS: very low in body fluids – Acute phase response causes further drop – Iron overload increases susceptibility to infect • SCAVANGING IRON: – Siderophores chelate available iron & transport it into bacteria – Iron can be scavenged direct from host iron- binding proteins, e.g by lactoferrin-binding prot – Often co-ordinately regulated fur locus in Ecol cutting out need for iron, e.g. T pallidum • Iron used to regulate aggressive virulence factors – Diphtheria toxin (DtxR repressor)
- 24. Survive Stress • nutrient-limitation stress, other stresses – Acid stress within stomach – Heat shock during fever – Oxidative stress within phagocytes • Stress response proteins, such as chaperonins feature as immunodominant antigens • Detoxification proteins play a role in virulence, e.g. periplasmic Cu,Zn-superoxide dismutases • Infectious dose for enteric pathogens much lower in achlorhydria (no need to overcome acid stress)
- 25. Stealth avoid immune system • IgA proteases – metalloproteases active against IgA • Immunoglobulin-binding proteins – e.g. protein A of S. aureus • Resist complement, opsonisation – Capsule (usually polysaccharide) – Lipopolysaccharide – Surface proteins and OMPs • Antigenic mimicry – e.g. sialic acid capsule of group B meningococcus
- 26. Stealth avoid immune system .Antigenic or phase varia – Involves surface structures as LPS proteins, capsules – Variety of mechani . – slip-strand mispair • flip-flop • cassettes .Adopt cryptic niche in phagocytes in biofilm 67700 67710 67720 GAAGTGCATTTAACTT**GGGGGGGGGGGTAAT GAAGTGCATTTAACTT*GGGGGGGGGGGGTAAT GAAGTGCATTTAACTTGGGGGGGGGGGGGTAAT GAAGTGCATTTAACTT***GGGGGGGGGGTAAT GAAGTGCATTTAACTT**GGGGGGGGGGGTAAT GAAGTGCATTTAACTT****GGGGGGGGGTAAT GAAGTGCATTTAACTT*GGGGGGGGGGGGTAAT GAAGTGCATTTAACTT**GGGGGGGGGGGTAAT GAAGTGCATTTAACTT***GGGGGGGGGGTAAT GAAGTGCATTTAACTT***GGGGGGGGGGTAAT GAAGTGCATTTAACTT***GGGGGGGGGGTAAT GAAGTGCATTTAACTT**GGGGGGGGGGGTAAT GAAGTGCATTTAACTT*GGGGGGGGGGGGTAAT Homopolymeric tract in Campylobacter jejuni
- 27. Strike-back Damage host tissues • Endotoxin • Exotoxins – Toxins acting on cell membranes – Toxins active inside cells – Superantigens
- 28. Endotoxin of Gram-negatives cytopl. mem. peptidoglycan outer mem. Gram- negative cell Lipid A Core polysaccharide O sidechain The toxic part Helps solubilise Lipid A Somatic antigen Lipopolysaccharide (LPS)
- 29. Strike-back Endotoxin • ENDOTOXIN EFFECTS: – PYROGENICITY – LEUCOPENIA,THEN LEUCOCYTOSIS – HYPOTENSION • “Gram-negative Shock” • Life-threatening complication of septicaemia • e.g. in meningococcal infection, in ITU or oncology pts • Endotoxic shock seen with dirty intravenous equipmen Most effects of endotoxin mediated by tumour necrosis factor – THERAPY ATTEMPTS: ANTI-ENDOTOXIN – or ANTI TNF ANTIBODIES
- 30. Strike-back Membrane-Damaging Exotoxins TOXINS: 1.FORM PORES in eukaryotic cell membranes, producing oligomeric rings, -streptolysin O of S pyogenes -listeriolysin of L monocytogenes -alpha-toxin of S aureus 2. DEGRADE CM as phospholipases – e.g. Clostridium perfringens alpha toxin LYSIS!LYSIS!
- 31. Strike-back Toxins active inside cells • Toxins consist of: • 1 translocation and binding B subunit that delivers the active A subunit into the host cell cytoplasm • Example of AB toxin: diphtheria toxin an ADP- ribosyltransferase
- 32. AB5 Toxins
- 33. Subvert • Inject proteins into host cells to subvert the cytoskeleton and signal-transduction pathways -manipulating e.g. Rho GTPases and the cytoskeleton to induce membrane ruffling and bacterial invasion -preventing uptake by Phagocytes e.g. Yersinia & Pseudomonas -remaining within a vacuole by manipulating host cell vesicular transport & endocytosis
- 34. Spread …through CELLS & organs: • In Macrophages, e.g. in typhoid • Via BLOOD (need to be complement- resistant) • within cells – actin-based motility of L monocyogenes, depends on ActA protein.
- 35. Scatter Transmission, virulence and evolution • Established dogmas – balanced pathogenicity – being too virulent is no good – high virulence is a sign of recent emergence of a pathogen – pathogens evolve towards symbiosis • Counter-arguments Where pathogens rely on spread through biting arthopods, high bacteraemias advantageous Where pathogens rely on shedding into water, highest possible shedding rates good for pathogen Where pathogens cause incidenta disease (e.g. Legionella) no selective pressure towards low virulence – Virulence as a local adaptation (why meningitis?) – Bad vaccines and effect
- 36. Summary • Spectrum of virulence – Commensals – Potential pathogens – Obligate pathogens • Difficulties in linking pathogen to disease – Koch’s postulates • Multi-dimensional view of virulence • Sex • Sense • Switch • Swim • Stick • Scavenge • Survive stress • Stealth • Strike-back • Subvert • Spread • Scatter
- 37. Further Reading Bacterial Pathogenesis: A Molecular approach, Salyers and Whitt (2nd Ed if possible) Cellular Microbiology Cossart, Boquet, Normark, Rappuoli