Infections On Surfaces Flashcards

1
Q

What is a surface?

A

Interface between a solid and either a liquid

or gas.

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2
Q

Name some skin micro organisms

A

Viruses
– Papilloma (can be carcinogenic)
– Herpes simplex

Bacteria
Gram positive
– Staph aureus
– Coagulase negative staphylococci - All staphylococci except staph aureus
– Corynebacterium - Never cause significant disease outside a healthcare setting
Gram negative
– Enterobacteriaceae

Fungi
– Yeasts - All have small numbers of candida species,
– Dermatophytes - Multicellular fungi, live on skin, some infect hair and nails, cause athletes foot,

Parasites
– mites

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3
Q

Name mucosal flora of the eye

A

Coagulase negative staphylococci, diphtheroids, saprophytic Neisseria species, viridans group streptococci

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4
Q

Name mucosal flora of the nares

A

Staph aureus

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5
Q

Name mucosal flora of the nasopharyngeal

A
Neisseria meningitidis (a lot of people have this but not have disease), Streptococcus pneumoniae, Haemophilus
influenzae,
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6
Q

Name mucosal flora of the mouth

A

Viridans Streptococci (can get to heart), Neisseria, Veillonella, Lactobacillus, Actinomyces, Bacteroides, Capnocytophaga, Eikenella, Prevotella, fusobacteria, clostridia, propionibacteria, Candida, Geotrichum species

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7
Q

NAME MUCOSAL FLORA OF THE STOMACH

A

Helicobacter - can cause peptic ulceration - treated with a week/2 of antibiotics - they are a precursor for gastric cancer or lymphoma , streptococci, staphylococci, lactobacilli,

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8
Q

Name mucosal flora of the intestine

A

Bacteroides, Bifidobacterium, Eubacterium, Lactobacillus, coliforms,
aerobic and anaerobic streptococci, Clostridium, yeasts
Anaerobes in the large bowel

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9
Q

NAME mucosal flora of the urethra

A

Enterobacteriaceae - gram negs, lactobacilli, diphtheroids, alpha and non-haemolytic streptococci, enterococci,
Can causeuti

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10
Q

Name mucosal flora o the vagina

A

Lactobacilli - most are these. These produce lactic acid to reduce candida (which cause thrush), diphtheroids, micrococci, coagulase-negative staphylococci, Enterococcus faecalis, microaerophilic and anaerobic streptococci, mycoplasmas, ureaplasmas, yeasts

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11
Q

Describe the distribution of bacteria in the human body

A

See slide for diagram

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12
Q

What is the most common way of infection

A

From own microbiota - when you acquire a new strain of myth ur not immune to
• Microbiota = “commensals”
– micro-organisms carried on skin and mucosal surfaces
– normally harmless or even beneficial
– transfer to other sites can be harmful

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13
Q

Name methods of transfer

A
– Invasion
• e.g. Strep pyogenes pharyngitis 
– Migration
• e.g. Escherichia coli urinary tract
infection
– Innoculation
• e.g. Coagulase negative
staphylococcus prosthetic joint
infection eg after surgery 
– Haematogenous
• e.g. viridans Strep endocarditis -
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14
Q

How can viridans strep cause endocarditis

A

Viridans need to be anchored down in the mouth, some people e have congenital abnormalities of valves eg bicuspid aorti valve - significant risk of endocarditis - turbulent blood flow over the valves - that erodes the epithelial surface, any bacteria that get from mouth into blood stream (usually taken up by macrophages or in spleen), but bacteria can attach to fibronectin - grow in the heart, body causes inflammatory processes, growth of bacteria and host response

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15
Q

Name extranal natural surface infections

A
– Cellulitis
– Pharyngitis
– Conjunctivitis
– Gastroenteritis
– Urinary tract
infection – Pneumonia
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16
Q

Name internal natural surface infections

A

Endovascualer - endocarditis, vasculitis

  • septic arthritis
  • osteomyelitis
  • empyema
17
Q

What are example s of prosthetic surfaces that can become infected

A
  • Intravascular lines
  • Peritoneal dialysis catheters
  • Prosthetic joints
  • Cardiac valves - artificial or derived from animals - put in when patients valves damage
  • Pacing wires
  • Endovascular grafts
  • Ventriculo-peritoneal shunts
18
Q

What causes native alve endocarditis and prosthetic valve endocarditis >1 year post op

A

viridans Streptococci Enterococcus faecalis Staph aureus
HACEK group
Candida

19
Q

What causes prosthetic valve endocarditis <1year post op?

A

coagulase negative staphylococci

20
Q

What are ventricular-peritoneal shunts

A

A ventriculoperitoneal (VP) shunt is a medical device that relieves pressure on the brain caused by fluid accumulation.

VP shunting is a surgical procedure that primarily treats a condition called hydrocephalus. This condition occurs when excess cerebrospinal fluid (CSF) collects in the brain’s ventricles.

Drains liquid into peritoneum

21
Q

What are causative organisms of prosthetic joint infections

A

coagulase negative staphylococci - mostly this

Staphylococcus aureus

22
Q

What is cardia pacing wire endocarditis and what are the causative organisms

A

Infection of the pace maker wires

coagulase negative staphylococci Staphylococcus aureus

23
Q

What are the processes n the pathogenesis of infection a surfaces

A

• Adherence to host cells or prosthetic surface
• Biofilm formation
• Invasion and multiplication
• Host response
– Pyogenic (neutrophils -> pus)
– Granulomatous (fibroblasts, lymphocytes, macrophages -> nodular inflammatory lesions)

24
Q

What are pili/l

A

Fimbriae and pili are interchangeable terms used to designate short, hair-like structures on the surfaces of procaryotic cells. Like flagella, they are composed of protein
Bind to surface of host

25
Q

What is a biofilm

A

A biofilm is an assemblage of surface-associated microbial cells that is enclosed in an extracellular polymeric substance matrix
If we can make prosthetics that biofilms cannot get a foothold on - reduce infections on them

26
Q

What is quorum sensing

A

Quorum sensing is the regulation of gene expression in response to fluctuations in cell-population density. Quorum sensing bacteria produce and release chemical signal molecules called autoinducers that increase in concentration as a function of cell density

27
Q

What does quorum sensing control and what are the 3 principles

A
• Controls
– Sporulation 
– Biofilm formation 
– Virulence factor secretion….
• Three principles
– Signalling molecules 
– autoinducers (AI) 
– Cell surface or cytoplasmic receptors – Gene expression ->co-operative behaviours and more AI production.
28
Q

How are surface infections managed

A

Diagnosis
• Aim is to identify infecting organism and its
antimicrobial susceptibilities.
• Challenges
– Adherent organisms - difficult to get samples
– Low metabolic state/small colony variants
• Blood cultures
• Tissue/prosthetic material sonication and culture

29
Q

What is teh differential time to positivity

A

The differential time to positivity was defined as the difference in the time it took for a blood culture drawn through the central venous catheter and a culture drawn from a peripheral vein to become positive
- (from central line and peripheral. If central line bacteria grow faster, central line infection as more bacteria there - Differential time to positivity)

30
Q

How is surface infection managed in terms of treatment

A

• Treatment
• Aim:
– sterilise tissue
– reduce bioburden
• Antibacterials - only work bile bacteria is dividing - bacteria resistant if they are not going through right element of growth
• Remove prosthetic material - If a patient is frail/old and infected prostetic cannot be removed, keep them comfortable
• Surgery – resect infected material
• Challenges
– poor antibacterial penetration into biofilm
– low metabolic activity of biofilm micro-organisms
– dangers/difficulties of surgery

31
Q

How are surface infections managed in terms of prevention

A
Natural surface 
• Maintain surface integrity 
• Prevent bacterial surface
colonisation 
• Remove colonising bacteria 

Prosthetic surfaces
• Prevent contamination
• Inhibit surface colonisation
• Remove colonising bacteria