Midterm 1 Flashcards

1
Q

Goals of molecular typing

A
  • identify the MICROBIAL CAUSE of disease
  • identify RELATIONSHIPS between Bacteria
  • identify how population of bacteria change with changing conditions
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2
Q

Uses of 16S rDNA Sequencing

A

❤types of microbes present( single or multiple species)

❤compare strains of bacteria-in an outbreak can be used to determine how isolated relate to one another

❤study complex microbial populations-in a microbial community can determine what species are present and how they change under certain conditions.

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3
Q

Infection

A

Colonization of the body by a bacterium CAPABLE of causing ⚡️⚡️DISEASE⚡️⚡️⚡️

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4
Q

Disease

A

Infection that produces 💥💥💥💥💥💥SYMPTOMES💥💥💥

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5
Q

Colonization

A

Bacterium OCCUPIES and MULTIPLIES in a particular area of the body.

This is our microbiota

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6
Q

A symptomatic carrier

A

An INFECTED person who does not have symptoms

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7
Q

Symptoms

A

Effects of bacterial infection apparent in an infected individual

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8
Q

Virulence/pathogenicity

A

Ability of a bacterium to cause disease

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9
Q

Virulence factors

A

Bacterial PRODUCTS or STRATEGIES that contribute to virulence/pathogenicity

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10
Q

Opportunist

A

Bacteria that normally do not cause disease in healthy people but can cause disease in people with impaired defences

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11
Q

Pathogen

A

An ORGANISM with a reputation of causing infectious disease

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12
Q

New disease caused by newly identified bacterial species

A

Legionnaire’s disease

Lyme disease

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13
Q

Old disease that were thought to be under control

A

Tuberculosis

MRSA

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14
Q

Old disease that are now know to have bacterial causes

A

Gastric ulcers and

Helicobacter pylori

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15
Q

Old disease with known causes that are getting more attention from the public and media

A

Gonorrhea

Chlamydia trachomatis

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16
Q

Periodontal disease

A

Porphyromonas gingivalis

17
Q

Atherosclerosis

A

Chlamydophila pneumonia

18
Q

An example of a bacteria that uses INVASION as a way to evade the host immune response
AND

Can escape the phagosome and live in the cytoplasm of phagocytic cells

A

Listeria Monocytogenes

19
Q

2 bacteria that inhibit phagosome-lysosome fusion

A

Legionella

M. tuberculosis

20
Q

Some bacteria change their surface antigens to keep one step ahead of the antibody response

21
Q

Cause of Buruli ulcer

A

Mycobacterium ulcerans

—-passed by plasmid

22
Q

An exotoxin not part of the bacterial genome passed by bacteriophage

A

Diphtheria toxin

23
Q

An exotoxin not part of the bacterial genome passed by plasmid

A

Type G botulinum toxin

24
Q

Who releases lecithinase

Which is a phospholipase that hydrolyzes the lipid lecithin in cell membrane

A

Clostridium perfringens

25
Who releases botulinum toxin
Clostridium botulinum
26
Toxic shock shock syndrome toxin-1
Staphylococcus aureus This bacteria also has an alpha toxin which is a pore forming toxin
27
Streptococcal superantigen
Streptococcus pyrogens
28
Causes Lyme disease
Borrelia burdorferi This one used manganese instead of iron
29
Gonocci
❤❤Adds sialic acid to its LPS to prevent C3 convertase formation ❤❤ some bacteria change their surface antigens to keep one step ahead of the antibody response
30
What bacteria inhibit phagosome-lysosome fusion
Legionella M. Tuberculosis
31
What bacteria escapes the phagosome and lived in the cytoplasm of phagocytic cells
Listeria monocytogenes
32
Whah bacteria cannot be cultivated? It is the causative agent of syphilis
Treponema pallidum
33
Kochs #1 postulate
Bacteria must be associated with symptomes and present at the site of infection
34
Limitations of organ culture
❤They don't last very long in vitro, they cannot be split & maintained ❤they don't have intact circulation & lymphatic supply to take the immune response into account
35
Molecular kochs Postulate
#1: the gene or its product should only be found in strains of bacteria that cause disease. #2: gene should be isolated by cloning #3: adding the isolated gene to a non-virulent strain should make it virulent. #4: the gene is expressed by the bacterium during infection in humans(or animals) Limitation: virulence is multifactorial
36
Steps in IVET
#1) creat plasmids in E.coli that have Salmonella sequences upstream of promoterless purA/lacZ genes #2) introduce plasmid into purA- salmonella by conjugation #3) inject mice with engineered SALMONELLA, recover surving bacteria
37
Septic shock symptoms Vs Toxic shock
``` Septic shock 💥hypotension 💥DIC 💥internal hemorrhages Causes by too much bacteria in our system --------------------------------------------- Toxic shock 💥 fever 💥 malaise 💥nausea 💥 vomiting ```