Applied Medical Science Exam 3 Flashcards

1
Q

What does the transesophogeal ridge develop into?

A

The Tracheoesophageal Ridge Forms a Septum to

Separate the Trachea and Esophagus

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2
Q

What does the respiratory diverticulum develop into?

A

The respiratory diverticulum lengthens to form the trachea and
then divides to form two lung buds

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3
Q

What do the long buds develop into?

A

These buds divide into three branches on the right and two on the left, reflecting the number of lobes of the respective lungs on those sides

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4
Q

Types of alveolar cells

A

Type 1
Type 2

16% of alveolar cells are present at birth; remainder develop for
10 years

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5
Q

Type 1 Alveolar cells

A

Gas Exchange

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6
Q

Type 2 Alveolar cells

A

(6.5-7 months) = secrete surfactant =
reduces surface tension in the alveoli so they can remain open
during breathing. If not for surfactant, alveoli would collapse.

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7
Q

Pleura of lungs

A

Visceral pleura covers the lungs directly

Parietal pleura forms the lung cavity

Both are formed from the lateral plate of the mesoderm

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8
Q

3 domains of life

A

Bacteria
archaea
Eukarya

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9
Q

Domian bacteria

A
Usually single‐celled.
Majority have cell wall with 
peptidoglycan.
Most lack a membrane‐bound 
nucleus.
Ubiquitous and some live in 
extreme environments.
Cyanobacteria produce 
significant amounts of oxygen.
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10
Q

Domain Eukarya

A

Protists—generally larger than Bacteria and Archaea.
• Algae—photosynthetic.
• Protozoa—may be motile, “hunters, grazers”.
• Slime molds—two life cycle stages.
• Water molds—devastating disease in plants.
Fungi.
• Yeast—unicellular.
• Molds and mushrooms—multicellular.

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11
Q

Domain Archaea

A
Distinguished from Bacteria by 
unique rRNA gene sequences.
Lack peptidoglycan in cell walls.
Have unique membrane lipids.
Some have unusual metabolic 
characteristics. 
Many live in extreme 
environments.
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12
Q

Spontaneous generation.

A

• Idea that living organisms can develop from nonliving or decomposing matter

Francesco Redi (1626 to 1697).
• Discredited spontaneous generation.

Louis Pasteur - swan neck flasks

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13
Q

Gram negative

A

Gram negative ‐ peptidoglycan cell wall, surrounded by
an outer membrane containing lipopolysaccharide.

Gram negative ‐ three principal layers in the envelope;
the outer membrane, the peptidoglycan cell wall, and
the cytoplasmic or inner membrane
.

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14
Q

Gram positive

A

Gram‐positive ‐ lack an outer membrane, surrounded by layers of peptidoglycan many times thicker than is found in the Gram‐negatives

In Gram positives ‐ threading through these layers of
peptidoglycan are long polymers called teichoic acids

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15
Q

Chemotaxis

A

• Move toward chemical attractants such as nutrients, away
from harmful substances.
• Move in response to temperature, light, oxygen, osmotic
pressure, and gravity.

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16
Q

Gram stain reactions in cell wall

A

Gram stain reaction due to nature of cell wall.
Shrinkage of the pores of peptidoglycan layer of Gram‐
positive cells.

• Constriction prevents loss of crystal violet during
decolorization step.

Thinner peptidoglycan layer and larger pores of Gram‐
negative bacteria do not prevent loss of crystal violet.

• Alcohol may also remove/extract some lipids from outer layer of Gram‐negative cell wall, making crystal violet dye removal easier.

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17
Q

Steps of gram stain

A

Add crystal violet stain over the fixed culture. Let stand for 10 to 60 seconds; Rinse

Add the iodine solution on the smear, . Let stand for 10 to 60 seconds. Rinse

Add a few drops of alcohol, Rinse it off with water after 5 seconds.

Counterstain with basic fuchsin solution for 40 to 60 seconds, Rinse

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18
Q

Flagellar Movement

A

Flagellum rotates like a

• Very rapid rotation up to
1100 revolutions/sec.

• In general, counterclockwise
(CCW) rotation causes
forward motion (run).

• In general, clockwise rotation
(CW) disrupts run causing
cell to stop and tumble.

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19
Q

Chlamydia

A

Elementary body (EB) attaches to host cell.

  • Reticulate body (RB) reproduction by binary fission.
  • Differentiate back into EB, lyses cell.

Releases EB’s

Cycle repeats

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20
Q

Chlamydia Metabolism information

A

Cannot catabolize carbohydrates.

Cannot synthesize ATP or NAD+
. • Import up from host.
• Do have genes for substrate-level phosphorylation, electrontransport, and oxidative phosphorylation.

RBs have biosynthetic capabilities when supplied
precursors from host; can synthesize some amino acids.

EBs seem to be dormant forms.

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21
Q

Spirochete diseases.

A

Lyme disease

syphilis

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22
Q

Mycobacterium cell walls

A

Outer membrane contains mycolic acids
linked to peptidoglycan by arabinogalactan, a
polysaccharide.

  • Cell walls very hydrophobic.
  • Impenetrable by antibiotics.

Basic fuchsin dye not removed by acid
alcohol treatment.

• non-acid-fast bacteria easily decolorize
on the addition of the acid-alcohol and
take up the counterstain dye of
methylene blue and appear blue.

This technique identifies Mycobacterium
tuberculosis and Mycobacterium leprae

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23
Q

Mycobacterium types

A

M. bovis. • Tuberculosis in cattle, other ruminants, and
primates.

M. tuberculosis. • Tuberculosis in humans.

M. leprae. • Leprosy.

M. avium complex (MAC).
• Various diseases.

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24
Q

Streptomycetales

A

Provide us with antibiotics

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25
Q

Bifidobacteriales

A

Pathogens and Probiotics

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26
Q

Bacillus

A

Produce the antibiotics bacitracin, gramicidin, and polymyxin.

B. cereus—food poisoning.

B. anthracis—anthrax.

B. thuringiensis and B. sphaericus—used as insecticide

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27
Q

Three Groups of Streptococci

A

Pyogenic (pus producing) streptococci.
• For example, S. pyogenes—streptococcal sore
throat, acute glomerulonephritis, and rheumatic
fever.

Oral streptococci.
• For example, S. mutans—dental caries.

Other streptococci.
• For example, S. pneumoniae—pneumonia and otitis
media.

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28
Q

Prion diseases

A

TSE
Bovine spongeform
Kuru
Creutzfeld Jakob

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29
Q

Prions

A

Abnormaly folded proteins

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30
Q

Protists

A

Flagellated
lack mitochondria
some have mitosomes

Protozoa—wide
distribution in nature;
single-celled eukaryotic
chemoorganotrophs.

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31
Q

Naegleria fowleri

A

Protozoan
Amebic Meningoencephalitis

Muscosal Membranes: Ears,
Eyes, Nose, Genitals

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32
Q

Acanthamoeba spp.

A

Protozoan
Amebic Meningoencephalitis

Muscosal Membranes: Ears,
Eyes, Nose, Genitals

33
Q

Entamoeba histolytica

A

Protozoan
Amebiasis

Intestinal tract

34
Q

Trypanosoma brucei

A

Protozoan
African sleeping sickness

Blood

35
Q

Plasmodium spp.

A

Protozoan
Malaria

Blood

36
Q

Baltimore classification

A

7 groups

Double DNA
Single DNA
Double RNA
Single RNA +
Single RNA -
Single RNA Reverse transcriptase (Retrovirus)
Double DNA Reverse transcriptase
37
Q

Double DNA

A

Baltimore classification Group

Mode of production:
mRNA is transcribed directly from the DNA template

Example:
T4 bacteriophage
Herpes simplex

Largest group of known viruses.
Most bacteriophages and archaeal viruses.

38
Q

Single DNA

A

Baltimore classification Group

Single-Stranded DNA Viruses Use a Double-Stranded Intermediate in Their Life Cycles

Bacteriophage oX174

39
Q

Double RNA

A

Baltimore classification Group

RNA-Dependent RNA Polymerase Replicates
the Genome and Synthesizes mRNA

Rotavirus

40
Q

Single RNA +

A

Baltimore classification Group

Mode of production:
plus stranded

Example:
Polio
Zika
Hep A
Eastern Quine Encephalitis
41
Q

Single RNA -

A

Baltimore classification Group

Mode of production:
Cannot serve as mRNA to form viral proteins
Must bring pre-formed RNA-dependent RNA polymerase into cell

Example:
RSV
Influenza
Ebola
Rabies
42
Q

Single RNA Reverse transcriptase

Retrovirus

A

Baltimore classification Group

Mode of production:
Plus-Strand Viruses That Use Reverse Transcriptase in Their Life Cycles

Example:
HIV

43
Q

Double DNA Reverse transcriptase

A

Baltimore classification Group

Mode of production:
Production of new virions takes place largely inside of liver cells (hepatocytes)

Example:
Hep B

44
Q

Other protists and fungi

A

Fornicata Microaerophilic protist

Pathogenic Trichomonads

Trypanosomes—Pathogenic Euglenozoa

Entamoebida

Apicomlexans

45
Q

Main types of mutations

A

Frameshift mutations

Chromosomal Mutations

46
Q

Frameshift mutations

A

Addition or deletion

much more profound consequences

alter reading downstream frames

Huntingtons

47
Q

Chromosomal mutations

A

Deletions (part of chromosome is lost)

Duplication (part is copied)

Inversion (part is reversed)

Translocation (part is moved)

48
Q

Gram positive

A

Agar
Catalase test

C diff, MRSA, VRE (most common resistant)

49
Q

Gram Negative

A

Oxidase
Agar
Broth

Campylobacter
Cholera
E coli
influenza
legionaires
pertussis
salmonella
typhoid
psuedomonas
plague
50
Q

Point mutation

A

Mutation of single base

sickle cell

51
Q

Base substitution

A
Silent mutation (same AA is inserted) 
doesn't change function
AAG - AAA
Nonsense mutation (codon changed to "stop" codon)
AAG - UAG
Missense mutation (changes amino acid)
differnet protein codon
AAG - AGG
Purine to Purine (Transistion)
Purine to pyrimidine (transversion)
52
Q

Haploid

A

1 set of chromosomes

53
Q

Diploid

A

2 complete sets of chromosomes
Humans are diploid and have 46 total chromosomes
23 pairs

54
Q

Dominant

A

The phenotype can be seen whe either homo or heterozygous

55
Q

Recessive

A

The phenotype can only be seen if homozygous

56
Q

Chargoff rules

A

A is equal to T
C is equal to G

Purines and pyrimidine are proportional

Purines are A & G
Pyrimidines are C & T

57
Q

Rosalind franklin

A

Performed xray diffraction studies to ID 3D structures

Discoverd that DNA is Helical

Determined that the molecule has a uniform diameter

58
Q

Blood Type

A+

A

A+ can receive from:
A+, A-, O+, O-

A+ can donate to:
A+, AB+

59
Q

Blood Type

O+

A

O+ can receive from:
O+, O-

O+ can donate to:
O+, A+, B+, AB+

60
Q

Blood Type

B+

A

B+ can receive from:
B+, B-, O+, O-

B+ can donate to:
B+, AB+

61
Q

Blood Type

AB+

A

AB+ can receive from:
ALL (universal recipient)

AB+ can donate to:
AB+

62
Q

Blood Type

A-

A

A- can receive from:
A-, O-

A- can donate to:
A+, A-, AB+, AB-

63
Q

Blood Type

O-

A

O- can receive from:
O-

O- can donate to:
ALL (Universal Donor)

64
Q

Blood Type

B-

A

B- can receive from:
B-, O-

B- can donate to:
B+, B-, AB+, AB-

65
Q

Blood Type

AB-

A

AB- can receive from:
AB-, A-, B-, O-

AB- can donate to:
AB+, AB-

66
Q

Blood type antibodies

A

Blood type has the antibody of the letter that is mssing

Examples
Type A has B antibodies
Type B has A antibodies
Type O has A & B antibodies
Type AB has no antibodies
67
Q

DNA structure make up

A

5 carbon sugar
with a phosphate group attached
then 1 of 4 nitrogenous bases attached A,C,G,T

Hydrogen bonds hold the 2 starnds together lightly so they can be pulled apart in transcription

phosphodiester bonds join adjacent nucleotides

covalent bonds

DNA strand is coiled arounf 8 Histone proteins every 200 nucleotides

68
Q

Polygenic traits

A

controlled by many genes

69
Q

Pleiotrophy

A

the ability of a single gene to have multiple effects on phenotypes

Examples:
Hemophilia
Factor VIII deficiency

70
Q

Lysogenic vs Lytic

A

Lysogenic=
Infected cell replicates creating new cells that are already infected

Lytic=
infected cell ruptures releasing infection to spread and infect new cells

71
Q

Lysogenic cycle

A

Phage infects cell

Phage inserts self into Cells DNA

Cell replicates with New DNA in it

New replicated cells are already infected with modified phage DNA

72
Q

Lytic cycle

A

Phage infects cell

Phage DNA circularizes

Host cell is used to make new phage DNA and Phage proteins

Phage eventually bursts and spreads new phages

(Primary way Phages replicate)

73
Q

Proteobacteria

A

Gram negative

The largest phylogenetically coherent bacterial
group with more than 500 genera.

Class Alphaproteobacteria

Class Betaproteobacteria

Class Gammaproteobacteria

CLass Epsilonproteobacteria

74
Q

Proteobacteria

Class Alphaproteobacteria

A

Gram negative

Most are oligotrophs.
Rickettsiales– Rocky Mountain Spotted Fever

Metabolically diverse.
• Methylotrophy, chemolithotrophs, nitrogen fixers

75
Q

Proteobacteria

Class Betaproteobacteria

A

Gram negative

Considerable metabolic diversity.

Chemoorganotrophs, photolithotrophs, and
chemolithotrophs.

Neisseria gonorrhoeae—gonorrhea.
Neisseria meningitidis—some cases of bacterial meningitis.

Burkholderiales
Genus Bordetella

76
Q

Proteobacteria

Class Gammaproteobacteria

A

Gram negative

Largest subgroup of proteobacteria.
• Contains 14 orders and 27 families

Very diverse physiological types.
• Chemoorganotrophs, photolithotrophs,
chemolithotrophs, methylotrophs
• Aerobic and anaerobic.

Genus Thiomicrospira
Genus Coxiella
Genus Legionella
Genus Pseudomonas

Escherichia coli

Order Vibrionales
Order Pasteurellales

Order Enterobacteriales
Salmonella—typhoid fever and gastroenteritis.
Shigella—bacillary dysentery.
Klebsiella—pneumonia.
Family Yersiniaceae
Yersinia—plague.
77
Q

Proteobacteria

Class Epsilonproteobacteria

A

Gram Negative

Smallest of proteobacterial classes.

Genus Campylobacter
Genus Helicobacter

78
Q

Gram Positive bacteria

A
Actinobacteria
Corynebacterium (diphtheria)
Mycobacterium (tuberculosis, bovis, leprosy)
Nocardia.
Propionibacteriales (Acne)
Streptomycetales: (scabies)
Bifidobacteriales
Bacillales
Thermoactinomyces
Staphylococcaceae
Listeria
Lactobacillales