biofilms Flashcards

1
Q

biofilms

A

cause damage and disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what sort of sieges to biofilmscause

A

chronic infections on heart valves, implants, dental decay, catheters

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

biofilms act as

A

reservoirs of contimination/ infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

biofilms are difficult to control since

A

they require a higher dose of antibiotics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

biofilms are economically costly

A

e..g NHS costs/ steel pipers under the north sea which are corroded by sulphate reducing bacterial biofilsm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

cistern 2001

A

best that 65% of infections may be biofilm related

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

approx 60% of….

A

HAIs are biofilm related

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

biofilm

A

“matrix associated microbial populations adherent to each other and or to surfaces ir interfaces” Casterton et al

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

medical infections

A

implants/ contact lenses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

domestic

A

drains/ toilets

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

main infections causes by biofilms in tissues/ fluids are

A

Bacteremia (blood stream infection). UTIs, pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

biofilm microorganisms are

A

more successful than planktonic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

advantages of biofilms include

A
  • increased resistance to antimicrobial agents
  • increased resistance to host defences e.g TB, intracellular salmonella, reduced capacity for clearing by phagocytosis)
  • enhanced genetic interaction e.g. movement of resistance plasmids
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

when antimicrobials diffuse into the biofilm

A

reaction hiitions leads to tolerance: sub lethal cones lead to selection for resistance e.g. reaction eiwth EPS, chelation, enzymatic degradation, precipitation, volatilisation as alkylated metal compounds.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

uninhibited diffusion of antimicrobials

A

tolerance by slow growth e.g. VBNC and persisters. transfer of resistance genes- due to all being in close proximity.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

biofilms are destroyed using

A

biocides

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

which microflora was the first to be studied

A

the mouth

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

over…. species have been identified in the oral cavity

A

700

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

toothpaste and fluoride the fluoride in it

A

is used to control biofilm formation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

why is oral health so important

A

infections in the mouth can pass through the blood system and cause infection in organs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

how do plaques form

A

1) primar colonisers- on the surfaces of teeth and soft tissues
2) secondary colonisers- attach to primary colonisers
3) mutation of plaque- growth in situ and attachment and detachment to the existing biofilm
4) disease causation-pathogenic effect include release of toxins/acids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

which biofilm causes disease

A

the mature bioilms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

three main groups of plaque bacteria

A

aerobes, facultative anaerobes and obligate anaerobes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

aerobes

A

high proportion of young plaque. usually does not cause harm e.g. Neisseria subflaa

25
facultative naerobes
these are the majority of microbes in the mouth. able to survive and grow with high/ low oxygen concentration- usually gram positive e.g. Streptococcus mutants - usually gram neg
26
obligate anaerobes
high number in mature plaque- O2 is toxic or inhibitory to grothw. some of these species are harmful and associated with gum disease e.g.fusobacterium nucleotum
27
example of an aerobe
Neisseria subflave
28
example of a facultative anaerobe
Streptococcus mutans
29
example of an obligate anaerobe
Fusobacterium nucelotum.
30
examples of surfaces in healthcaree where pathogens survive
instruments, bed line, the floor
31
which pathogens survive well on healthcare surfaces
MRSA, salmonella, entrococci, Pseudomons aeruginosa, E.coli, Fusarium
32
% of UTIs caused by biofilms
95
33
% of bateremia cases
87%
34
86$ of pneumonia cases are
ventilator associated
35
prophylaxis
treatment to prevent disease
36
example of public prophylaxis
fluoride use in water- no consent, but very effective in reducing dental decay. only medical treatment give passively without consent
37
mode of action of fluoride
reduction in enzyme activity reduces acid production from carbohydrates. pathogens are outcompeted
38
biofilms cells in comparison to planktonic cells are generally much more
resistant to antibiotics and biocides
39
urinary catheters
quickly acquire organisms on the surge- 5-10% colonisation within 7 days (MRS may achieve a depth up to 5-6 ells in 2h) e.g. proteus spp
40
orthopaedic devices
external fixation from open fractures are out likely to be colonised. Often penetration of antibiotics into biofilms on stainless steel may fail to eradicate the infection
41
prosthetic joint infections
sometimes impossible to cure using antibiotics alone- this may lead to more surgery of even amputations.
42
basic stages of biofilm formation
attachment, growth ,detachment
43
attachment
free floating or planktonic bacteria encounter a submerged surface and within minutes become attached
44
Growth
Extracellular polymeric structure (EPS) production allows the emerging biofilm community to develop a complex, three dimensional structure
45
detachment
biofilms can propagate through detachment of small or large clumps of cells, or by a type of 'seeding dispersal' that releases individuals cells
46
biofilms can move in numerous ways
collectively by rippling or rolling across the surface, or by detachingin clubs or individuals by swarming and seeding
47
emergent properties fo biofilms and habitat formation
1) localised gradients- provide habitat diversity 2) sorption- resource capture 3) enzyme retention-external digestion system 4) cooperation- synergistic micro-consortia 5) competition- continous regeeration 6) tolerance and resistance- biofilm as a fortress
48
localised gradients
provide habitat diversity i.e. different bacteria will survive better at diff oxygen cones/ nutrients conc
49
a key resource of biofilms
calcium
50
cooperation
due to there being a variety of different bacteria which have different biochemical abilities, bacteria are able to use each others products to benefit themselves
51
competition
keeps all bacteria active
52
copiotrophs
an organism found in environments rich in nutrients particularly carbon. tend to grow iim high organise substrate conditions
53
oligotrophs
organisms that live in environments that offer very low levels of nutrients. characterised by slow growth, low rates of metabolism and generally low population density
54
copiotrophic biofilm
creates an oxygen gradient, producing niches for aerobes, fermenters and anaerobes
55
oligotrophic biofilm
nutrient gradients- some cell are more metabolically active, are starving, formation, VNBC, persister and dead cells.
56
communication
chemic and electrical communication
57
cooperation
nitrification- some cells are ammonia oxidisers and other nitrite oxidizers- syngerisist
58
competition
antibiotic, bacteriocins, killer vesicles, biosurfactants, inhibition of quorum sensing, nutrient depletion, cheating