Lecture - Cystic Fibrosis Infection Flashcards

1
Q

Cystic fibrosis intro

A
  • due to a defective transmembrane conductance regulator
  • the most common lethal genertic disorder of caucasians
  • 1/2500 caucasians
  • less prevalent in other racial groups
  • multisystem disease mainly manifested in lungs
  • lungs secrete thick mucus - prevents proper function in expelling foreign bodies such as microbes
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2
Q

CFTR mutation

A
  • caused by point mutations in the gene coding for CFTR
  • CFTR regulates chloride movement out of mucus-producing cells
  • most common point mutatin is a codon deletion in position 508 of the aa sequence - loss of phenylalanine
  • does not allow chloride ion out - leads to a mucus that is deficient, extremely dehydrated and static - not cleared and provides a good microbial habit
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3
Q

Microbes commonly infecting people with CG

  • bacteria
  • fungi
A
  • polymicrobial communities that can grow as mixed biofilms
  • may be inhaled directly through aerosols but also common oropharyngeal organisms
  • bacteria: staph aureaus, h. Influenzae, B. Cenocepacia, Stenotrophomonas maltophilia, Pseudomonas aeruginosa
  • Fungi: cryptosporidium sp, aspergillus fumigatus, Candida albicans
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4
Q

Changes in bacterial infection patterns with age

A
  • initially a mixed
  • S aureus most present early on but then drops
  • P. Aeruginosa most common in adults
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5
Q

Staph aureaus

A
  • common commensal
  • one of the earliest bacteria detected in infants and children with CF
  • peak prevalence between 11-15
  • its ability to form biofilms also decrease effectiveness of antibiotic treatment
  • antibiotic treatment has been made more difficult by the rise of MRSA in the last 10 yers
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6
Q

MRSA

A
  • resistance to b-lactam antibiotics and cephalosporins

- conflicting reports on wherther MRSA is associated with a significant decline in lung function

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7
Q

Small colony variants of S aureaus

A
  • smaller size on agar plates
  • less pigmentation
  • less hemolysis
  • increased intracellular persistence in in bitro studies
  • SCV continue to express SigB dependent genes encoding cell surface proteins such as adhesins - important in virulence
  • increased ability to adhere to host component, to form biofilms and to invade and persist
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8
Q

Treatment for staph aureus

A
  • primary prophylaxis
  • eradication
  • treatment of CF pulmonary exacerbations
  • treatment of MRSA
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9
Q
  • Treatment of staph aureus issues
A
  • may lead to a higher infection rate with P. Aeruginosa
  • no guidelines or recomendation for MRSA or SCV
  • lack of data
  • fear of increased MRSA resistance
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10
Q

H/ infleunzae

A
  • Gram - rod
  • also significant resp pathogen in non-CF patients
  • common infector early in childhood, decreasing in older. Present in encapsulated and non-encapsulated phenotypes
  • prevalence is increasing in children with CF
  • non-encapsulated H. Influenza is mostly associated with chronic lung infectin and acute exacerbation
  • presence of an adhesive gene and both persistence and long term cross-colonisation are significantly linked
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11
Q

Burkholderia cepacia

A
  • Bcc comprises 17 specied of catalase +ve, non-lactose fermenting, gfram - bacteria
  • opportunistic pathogen
  • most common in CF are B. Multivorans and B. Cenocepacia
  • not very prevalent but infection by some strains pose an immediate health risk
  • ET12 serovars of B cenopcepacia have the most serious health outcome - can be fatal
  • resistant to almost all antibiotics
  • patient to patient tranmission
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12
Q

B.cenopacia pathogenesis

A
  • intracellular parasite
  • intracellular survival in macrophage is associated with profound changes in metabolic activity and motility
  • cytotoxic toward macrophage host cell - killing it
  • virulence factors: quorum sensing, iron uptake, LPS, Exopolysaccharide, antimicrobial resistance, flagella
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13
Q

Treatment of B. Cenocepacia

A
  • resistant to many common antibiotics, including aminoglycosides and polymyxin B
  • treatment: ceftazidime, doxycline, piperacillin, meropenem, chloramphrenicol…
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14
Q

Stenotrophomonas maltophilia

A
  • gram -
  • agent of ventilator assisted pneumonia
  • MDR, persistent in 20% of cases
  • prevalence in CF is 10-15% in lige
  • ubiquituous
  • patients who acquire S maltophilia usually have more advanced disease and more exaggerated lung function decline
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15
Q

Pseudomonas aeroginosa

A
  • Gram - bacillus, non lactose fermenting, oxidase positive
  • ubiquituous in envt
  • adaptable
  • highly antibiotic resistant
  • prolific biofil former
  • acquired by susceptible persons from environment by inhalation
  • responsible for most adult CF patient deaths
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16
Q

REspiratory tract colonisation by P. Aeruginosa

A
  • requires fimbrial adherence
  • more virulent at acute infection but expression of virulence factor decrease with chronic infection
  • alkaline protease degrades epithelial fibronectin
  • opportunistic adherence to sites of injury
  • some strains produce invasins: pore-forming cytoxin and 2 hemolysins
17
Q

Treatment for P aeruoginosa

A
  • highly antibiotic resitance due to numerous multidrug efflux pumps with chromosomally encoded antiboitic resistance genes
  • antibiotics that may succeed: aminoglycosides, quinolones, cephalosporins, carbapenemes, polymixin, monubactam
18
Q

Genotypic characteristics of P aeruginosa

A
  • strains that infect more than one patient :FC
  • two australian FC: AES1 and AES2
  • two others identified in tasmania
  • FC not found in environment
  • person to person spread
  • FC represents 10-50% of isolates in CF clinics
  • FC are more persistent and cause more exacerbations and hospitalisation
  • AES1 is more virulent than PAO1
  • Chronic isolates are more persistent than early isolates
  • chronic infection leads to general downregulation of cirulence yet certain virulence factors were upregulated in AES1M
  • common function was enhanced biofilm formation
19
Q

What can we do about it

A
  • DNase I to disript e-DNA in CF patient works well initially but effectiveness falls off acter six months
  • if you combine it with GSH ( a natural antioxidant), the treatment had greater effectiveness
  • biofilm disruption enhances antibiotic effectiveness in vitro