Pseudomonas aeruginosa · Pseudomonas aeruginosa gram-negative non-sporing bacteria Obligate...
Transcript of Pseudomonas aeruginosa · Pseudomonas aeruginosa gram-negative non-sporing bacteria Obligate...
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Pseudomonas aeruginosa
Ιωαννης Γ. Ρούτσιας, Επικ. Καθηγητης Ανοσολογιας/Μικροβιολογιας
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Pseudomonas aeruginosa gram-negative non-sporing bacteria Obligate Aerobe, mostly saprophytic Motile
Commonly found in the environment(water, air, soil) At any moist location
Common cause of nosocomial infections
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P. aeruginosa (ευκαιριακό παθογόνο) Extremely broad host spectrum Hardly any infections in the normal human host Severe immunodeficiencies and medical devices
predispose the patients to P. aeruginosa infections Broad spectrum of clinical symptoms Urinary tract infections Pulmonary infections Soft tissue infections Sepsis Bone and joint infections Endocarditis
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Community Suppurative (πυωδης) Otitis
Hospital
Eye Keratitis and Endophthalmitis
Ear Otitis externa and Otitis media
Skin Burns infection, wound sepsis
UTI Cystitis (catheterized)
RTI Pneumonia (ventilation / tracheostomy)
GIT Infantile (βρεφική) diarrhea
CNS Meningitis brain abscess (iatrogenic)
Diseases (Pathogenicity)
Nosocomial infection
Ecthyma gangrenosum
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P. aeruginosa & λοιμώξεις P. aeruginosa infections are of particular concern for Cystic
fibrosis patients
Burn patients
Cancer – cytotoxic drugs
Hospitalised patients Case mortality rate for patients infected with P. aeruginosa
approaches 50%
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Νοσοκομειακές λοιμώξεις Fourth most common isolated nosocomial pathogen
accounting for approx. 10 % of all hospital acquired infections. Patient-to-patient spread and direct patient contact with
environmental reservoirs respiratory equipment, food, sinks, taps
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Διάγνωση λοίμωξης από P. aeruginosa
Isolation and lab identification of the pathogen P. aeruginosa grows well on most laboratory media Identified on the basis of its: Gram morphology, inability to ferment lactose, a positive oxidase reaction, its characteristic odor(οσμή), Green pigments (Pyocyanin, Flurescein) its ability to grow at 42° C.
Fluorescence is helpful in early identification of P. aeruginosa colonies and may also help identify its presence in wounds.
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–Pyocyanin (blue-green) – Fluorescein (green-yellow, fluorescent)
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Δοκιμασία κινητικότητας
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Θεραπεία των λοιμώξεων από P. aeruginosa
P. aeruginosa is frequently resistant to many commonly used antibiotics.
Antipseudomonad beta lactam Aminoglycoside Fluoroquinolone
To archive synergy a combination of e.g. gentamicin and carbenicillin is frequently used.
No vaccines so far
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Μηχανισμοί παθογονικότητας
Adhesion(Προσκόληση) Pili(κροσσοι), flagella(μαστίγια) and fimbriae(φιμπριες)
Invasion(Διείσδυση) Extracellular enzymes and toxins (proteases, elastase, phospholipases,
rhamnolipids, Exotoxin A) rhamnolipids: glycolipids that kill epithelial cells, kill polymorphonuclear
leukocytes and macrophages and inhibit phagocytosis Exotoxin A blocks protein synthesis by ADP ribosylation of elongation factor
2, thereby triggering cell death
Dissemination (Διασπορά) Leukocidin inhibits neutrophils und leukocytes LPS (Endotoxin)
Protection Capsule (έλυτρο)
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Interbacterial Communication
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McKnight et al, 2000
Quorum Sensing (Διακυτταρική επικοινωνία βακτηρίων) in P. aeruginosa
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Cooperative traits and coordinated behavior of bacteria
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Adaptation and survival is facilitated by diversity
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„Small colony variants“ (SCV)
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SCVs of P. aeruginosa in CF
• Slow growing subpopulations (3% of the P. aeruginosa positive sputum specimens)
• SCVs exhibit an increased resistance towards a broad spectrum of antimicrobial agents
• The recovery of SCV correlates with parameters revealing poor lung function and an inhalative antimicrobial therapy
• Fast growing revertants REV can be isolated from the SCV population
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Auto-aggregation in liquid cultures
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M. Rohde, GBF Braunschweig
CupA encoded fimbria expression in P. aeruginosa
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Molecular Mechanisms controlling the conversion to a SCV biofilm phenotype
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Bacterial Biofilms
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Biofilms in the environment
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Catheter associated biofilms
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Chronic biofilm infections
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Despite even intensified antibiotic therapy,
no eradication of chronic P. aeruginosa infections of the cystic fibrosis lung
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Cystic fibrosis (Κυστική ίνωση) Most common life-threatening inherited genetic disorder in the
Caucasian population Mutation in the cystic fibrosis transmembrane conductance
regulator (CFTR) gene CFTR: ρυθμιστικήπρωτεΐνη πουελέγχειτηνδιέλευσηχλωρίουδιαμέσουτωνμεμβρανώντωνεπιθηλιακώνκυττάρωνδιαφόρωνοργάνωντουσώματοςόπωςτωνπνευμόνων,τουπαγκρέατος,τωνιδρωτοποιώναδένωνκαιτουεντέρου
Περίπου1στα2000‐2500παιδιάεκτιμάταιότιγεννιούνταικάθεχρόνοστηνΕλλάδαμεκυστικήίνωση,ενώτο4‐5%τουπληθυσμούθεωρείταιότιείναιφορείς.
Life expectancy: Until the 1930s: the life expectancy of a baby with CF was only a few months, in the 1980s, most deaths from CF occurred in children and teenagers. Today with improved treatments,
nearly 40 percent of the CF population is aged 18 and older, for a person with CF the median age of survival is nearly 37 years.
Cystic Fibrosis affects a number of organs in the body, cycles of infection and inflammation lead to a progressive deterioration of lung function.
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Cystic fibrosis (Κυστική ίνωση) ΜεταλλάξειςστογονίδιοCHTFR προκαλούνμειωμένηπαραγωγήήλειτουργικότητατηςπρωτεΐνηςμεαποτέλεσμαστοεπιθήλιοτωνπροσβαλλομένωνοργάνωνναπαράγεταιπαχύρρευστηκολλώδηςβλένναηοποίααποφράσσειτουςπόρουςτωναδένωνμεσυνέπειατηνπροοδευτικήκαταστροφήτουιστούτωνοργάνων(ίνωση)καιτηντελικήανεπάρκειατους.
Ταάτομαμεκυστικήίνωσηέχουναφύσικαυψηλάεπίπεδαάλατοςστονιδρώτα
Υψηλάεπίπεδαάλατοςεμποδίζουνναδράσουνταφυσικάαντιμικροβιακάπεπτίδια(defensins)ευνοείταιηανάπτυξητηςΨευδομονάδας
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Chronic infection of the Cystic Fibrosis lung
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Why is traditional antimicrobial therapy ineffective against biofilm bacteria?
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The end