Deck 31: Biofilms: Architects of Disease
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Deck 31: Biofilms: Architects of Disease
1
How do microorganisms that live in close proximity exchange DNA?
A) Frame-shift mutations and plasmid uptake
B) Transformation and conjugation
C) Conjugation and frame-shift mutations
D) All of the above
A) Frame-shift mutations and plasmid uptake
B) Transformation and conjugation
C) Conjugation and frame-shift mutations
D) All of the above
B
The biofilm is an optimal environment for the horizontal transfer for DNA.The microorganisms live in close proximity,which facilitates the uptake of DNA by transformation and conjugation.
The biofilm is an optimal environment for the horizontal transfer for DNA.The microorganisms live in close proximity,which facilitates the uptake of DNA by transformation and conjugation.
2
What are the metabolically inert microorganisms present in a biofilm called?
A) Spores
B) Pheromone cells
C) Quorum sensing cells
D) Persister cells
A) Spores
B) Pheromone cells
C) Quorum sensing cells
D) Persister cells
D
Persister cells,essentially metabolically inert microorganisms analogous to bacterial spores,are present in all biofilms and bacterial populations.Persister cells are hypothesized to have disabled programmed cell death or apoptosis.These cells have the greatest potential for maintenance of the gene pool and resistance to environmental stress including antimicrobial agents.
Persister cells,essentially metabolically inert microorganisms analogous to bacterial spores,are present in all biofilms and bacterial populations.Persister cells are hypothesized to have disabled programmed cell death or apoptosis.These cells have the greatest potential for maintenance of the gene pool and resistance to environmental stress including antimicrobial agents.
3
Cobiofilms of what two organisms are associated with serious lung infections in cystic fibrosis patients?
A) Pseudomonas aeruginosa and Moraxella
B) Pseudomonas aeruginosa and Burkholderia cepacia
C) Pseudomonas aeruginosa and Mycobacterium tuberculosis
D) Pseudomonas aeruginosa and Streptococcus pneumoniae
A) Pseudomonas aeruginosa and Moraxella
B) Pseudomonas aeruginosa and Burkholderia cepacia
C) Pseudomonas aeruginosa and Mycobacterium tuberculosis
D) Pseudomonas aeruginosa and Streptococcus pneumoniae
B
Cobiofilms of Pseudomonas aeruginosa and Burkholderia cepacia are associated with serious lung infections in patients with cystic fibrosis.
Cobiofilms of Pseudomonas aeruginosa and Burkholderia cepacia are associated with serious lung infections in patients with cystic fibrosis.
4
What is a sessile-type biofilm?
A) A biofilm made up of free-floating microorganisms
B) A multiple-species biofilm
C) A biofilm that is attached and made up of multiple species
D) A biofilm that is present in an aquatic environment
A) A biofilm made up of free-floating microorganisms
B) A multiple-species biofilm
C) A biofilm that is attached and made up of multiple species
D) A biofilm that is present in an aquatic environment
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5
Biofilms can protect its members from all of the following EXCEPT:
A) Antibodies
B) Oxygen-reactive molecules
C) Antimicrobial drugs
D) Phagocytosis
A) Antibodies
B) Oxygen-reactive molecules
C) Antimicrobial drugs
D) Phagocytosis
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6
What is stage IV of biofilm development?
A) Multiplication phase
B) Thickening phase
C) Cell dispersion
D) Planktonic stage
A) Multiplication phase
B) Thickening phase
C) Cell dispersion
D) Planktonic stage
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7
What do biofilms allow members of the microbial community to do?
A) Withstand the shear forces of blood and urine
B) Remain in a nutrient rich environment
C) Survive
D) All of the above
A) Withstand the shear forces of blood and urine
B) Remain in a nutrient rich environment
C) Survive
D) All of the above
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8
In which step of the infectious process could biofilms help bacteria when it comes to indwelling medical devices?
A) Downregulation
B) Phenotypic variation
C) Genotypic variation
D) Attachment
A) Downregulation
B) Phenotypic variation
C) Genotypic variation
D) Attachment
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9
What is stage II of biofilm development?
A) Irreversible binding phase
B) Multiplication phase
C) Attachment phase
D) Layering phase
A) Irreversible binding phase
B) Multiplication phase
C) Attachment phase
D) Layering phase
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10
In this level of the biofilm,the organisms downregulate very efficiently and are the least metabolically active.
A) Outer
B) Intermediate
C) Inner
D) Substrata
A) Outer
B) Intermediate
C) Inner
D) Substrata
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11
Biofilms are a universal strategy for:
A) Planktonic free-floating organisms
B) To increase plasmid transfer for antibiotic resistance
C) To battle sheer forces
D) Survival, horizontal gene transfer and growth
A) Planktonic free-floating organisms
B) To increase plasmid transfer for antibiotic resistance
C) To battle sheer forces
D) Survival, horizontal gene transfer and growth
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12
What is stage V of biofilm development?
A) Spreading phase
B) Multiplication phase
C) Cell dispersion
D) Layering phase
A) Spreading phase
B) Multiplication phase
C) Cell dispersion
D) Layering phase
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13
What process allows the bacteria of the biofilm to spread to other body sites?
A) Conjugation
B) Metastasis
C) Disaggregation
D) Planktonization
A) Conjugation
B) Metastasis
C) Disaggregation
D) Planktonization
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14
What is stage I of biofilm development?
A) Multiplication phase
B) Irreversible binding phase
C) Layering phase
D) Attachment phase
A) Multiplication phase
B) Irreversible binding phase
C) Layering phase
D) Attachment phase
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15
All of the following are considered some of the most efficient and upregulated prone microbes when stress hits EXCEPT:
A) Coagulase-negative staphylococci
B) Pseudomonas aeruginosa
C) Micrococcus luteus
D) Candida albicans
A) Coagulase-negative staphylococci
B) Pseudomonas aeruginosa
C) Micrococcus luteus
D) Candida albicans
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16
What is stage III of biofilm development?
A) Irreversible binding phase
B) Layering phase
C) Attachment phase
D) Multiplication phase
A) Irreversible binding phase
B) Layering phase
C) Attachment phase
D) Multiplication phase
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17
What is a biofilm?
A) Communities of organisms attached to a solid surface
B) The resulting thick, slimy mucous produced in cystic fibrosis
C) A slime factor that can be found in your gastrointestinal tract
D) The resulting film that is produced by necrotic tissue, bacteria, and immune cells
A) Communities of organisms attached to a solid surface
B) The resulting thick, slimy mucous produced in cystic fibrosis
C) A slime factor that can be found in your gastrointestinal tract
D) The resulting film that is produced by necrotic tissue, bacteria, and immune cells
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18
In this level of the biofilm,the organisms downregulate somewhat their metabolic activity,but they can still use nutrients and exchange genes.
A) Outer
B) Intermediate
C) Inner
D) Substrata
A) Outer
B) Intermediate
C) Inner
D) Substrata
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19
All of the following environmental and key cultural characteristics affect biofilms EXCEPT:
A) Movement of host
B) Genotypic factors
C) Nutritional resources
D) Mechanical factors and sheer forces
A) Movement of host
B) Genotypic factors
C) Nutritional resources
D) Mechanical factors and sheer forces
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20
This layer of a biofilm is exposed to the highest concentration of nutrients and oxygen,containing the most active organisms.What layer is this?
A) Outer
B) Inner
C) Middle
D) Substrata
A) Outer
B) Inner
C) Middle
D) Substrata
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21
All the following are laboratory-associated problems related to identifying biofilm-associated diseases EXCEPT:
A) False-positive cultures
B) False-negative cultures
C) Viable but noncultural organisms
D) Loss of or decreased antimicrobial susceptibility
A) False-positive cultures
B) False-negative cultures
C) Viable but noncultural organisms
D) Loss of or decreased antimicrobial susceptibility
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22
Treating infectious diseases has shifted from planktonic susceptibility profiles to:
A) Therapeutic modalities
B) Creative treatments
C) Multiple interventions
D) Degrading enzymes
A) Therapeutic modalities
B) Creative treatments
C) Multiple interventions
D) Degrading enzymes
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23
What is the common name for a dental biofilm?
A) Cavity
B) Gingivitis
C) Periodontitis
D) Plaque
A) Cavity
B) Gingivitis
C) Periodontitis
D) Plaque
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24
The late colonizers in the dental biofilm include all the following EXCEPT:
A) Capnocytophaga
B) Streptococcus salivarius
C) Selenomonas flueggei
D) Prevotella
A) Capnocytophaga
B) Streptococcus salivarius
C) Selenomonas flueggei
D) Prevotella
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25
What happens to dental plaque if it is allowed to remain undisturbed for several days?
A) The biofilm disaggregates.
B) The persister cells predominate the biofilm.
C) Pathogenic bacteria become the main bacterial constituents of the biofilm.
D) Nonpathogenic bacteria become the main bacterial constituents of the biofilm.
A) The biofilm disaggregates.
B) The persister cells predominate the biofilm.
C) Pathogenic bacteria become the main bacterial constituents of the biofilm.
D) Nonpathogenic bacteria become the main bacterial constituents of the biofilm.
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26
What disease,caused by biofilms,consumes more resources in the intensive care unit (ICU)than any other infectious disease?
A) Blood cultures positive with coagulase-negative staphylococci
B) Urinary tract infections due to gram-negative rods
C) Surgical site infections
D) Ventilator-associated pneumonia
A) Blood cultures positive with coagulase-negative staphylococci
B) Urinary tract infections due to gram-negative rods
C) Surgical site infections
D) Ventilator-associated pneumonia
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27
What types of cells in a biofilm are viable but nonculturable?
A) Phagocytes
B) Persister
C) Attachment cells
D) Layering cells
A) Phagocytes
B) Persister
C) Attachment cells
D) Layering cells
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