Term
Trisomy 13 (Patau syndrome) |
|
Definition
Extra chromosome 13
Cause: Variable, but usually NDJ during Meiosis or Mitosis
Signs: Cleft palate and rocker-bottom feet |
|
|
Term
Trisomy 18 (Edward syndrome) |
|
Definition
Extra chromosome 18
Cause: Variable, but usually NDJ during Meiosis or Mitosis
Signs: Clenched fist and rocker-bottom feet |
|
|
Term
Trisomy 21 (Down syndrome) |
|
Definition
Extra chromosome 21 (most common aneuploidy)
Cause: Variable, but usually NDJ during Meiosis or Mitosis
Signs: Slanted eyes, heart defects |
|
|
Term
Monosomy X (Turner syndrome) |
|
Definition
Missing sex chromsome (only known viable monosomy)
Cause: Usually paternal NDJ or Anaphase lag (thus can be mosaic)
Signs: Short stature, sterile female |
|
|
Term
|
Definition
Extra X-chromosome 47, XXY (more X's possible, with worse phenotype)
Cause: Variable, NDJ in Mitosis or Meiosis
Signs: Tall, elongated, normal life expectancy |
|
|
Term
|
Definition
Extra Y-chromosome
Cause: Paternal NDJ
Signs: Tall, normal fertility |
|
|
Term
|
Definition
Multiple X-chromosomes
Cause: Usually maternal (95%) NDJ
Signs: Tall, sometimes infertile |
|
|
Term
|
Definition
Deletion of p-arm of chromosome 5
Signs: High-pitched crying |
|
|
Term
|
Definition
Partial monosomy ring chromosome
Cause: De-novo breaks and fusion of ends
Signs: Growth and mental retardation |
|
|
Term
|
Definition
Insoluble, sickle-shaped fiber formation from hemoglobin molecules
Cause: Genetic point mutation (Val for Glu)
Signs: Sickle-shaped cells obvious under microscope |
|
|
Term
|
Definition
Abnormal bone formation
Cause: Mutation that replaces Gly in collagen, disrupting alpha-chain structure. Alpha-1 more severe than alpha-2.
Signs: Abnormal collagen, poor bone mineralization |
|
|
Term
|
Definition
Abnormally folded prion protein in brain leads to progressive aggregation
Cause: PrP occurs in altered conformation with more beta-sheet character, aggregates and affects other normal protein
Signs: Variable, loss of neuronal function most common |
|
|
Term
|
Definition
Obstruction of GI and respiratory tracts caused by improper cellular transport of chloride and water
Cause: Mutation in CFTR-encoding gene, leading to mis-folding and degradation of CFTR (a Cl- channel)
Signs: Excess chloride in sweat, difficulty breathing/swallowing |
|
|
Term
X-linked adrenoleukodystrophy (X-ALD) |
|
Definition
Build-up of cellular components in brain and adrenal cortex
Cause: Mutation to peroxisomal transport protein
Signs: Variable, neuronal dysfunction |
|
|
Term
|
Definition
Build-up of inclusion bodies containing various cellular components
Cause: Mutation in lysosomal transport protein |
|
|
Term
|
Definition
Autosomal recessive, "cherry-red" spot on macula and progressive neurodegeneration
Cause: Lysosomal storage disease linked to a deficiency in lysosomal enzyme hexosaminidase A, causing accumulation of GM2 ganglioside |
|
|
Term
|
Definition
Accumulation of phenylalanine, leading to excess phenylpyruvate
Cause: Deficiency in enzyme phenylalanine hydroxylase, which converts Phe to Tyr |
|
|
Term
21-hydroxylase deficiency |
|
Definition
Ambiguous genitalia (pseudohermaphroditism) development in women
Cause: 21-hydroxylase deficieny, enzyme which catalyzes rxn in corticoid biosynthetic pathway, resulting in buildup of androgen and other precursors |
|
|
Term
11beta-hydroxylase deficiency |
|
Definition
Ambiguous genitalia (pseudohermaphroditism) development in women and abnormal salt retention
Cause: 11beta-hydroxylase deficiency, enzyme which catalyzes rxn in corticoid biosynthetic pathway, resulting in buildup of deoxycortisol and other precursors |
|
|
Term
Pyruvate kinase deficiency |
|
Definition
Hemolytic anemia caused by insufficient or abnormal supply of pyruvate kinase
Cause: Pyruvate kinase isozyme in erythrocytes is either mutated or deficient, leading to upsets in glycolysis |
|
|
Term
|
Definition
Build up of lactate accompanied by overall energy loss
Cause: Variable, including pyruvate dehydrogenase (PDH) deficiency and any other enzyme involved in aerobic respiration |
|
|
Term
|
Definition
Insufficient bodily iron levels leading to decreased energy levels
Cause: Variable, but Fe plays crucial role in Fe-S centers and cytochromes needed for ATP production via ETC |
|
|
Term
Chronic progressive external opthalmoplegia (CPEO) |
|
Definition
mtDNA disorder; Progressive atrophy of extraocular muscles
Cause: tRNA mutation and large deletions in mitochondrial DNA |
|
|
Term
Kearns-Sayre syndrome (KSS) |
|
Definition
mtDNA disorder; Large deletion in mitochondrial DNA leading to progressive myopathy, PEO, heart problems, etc. |
|
|
Term
Pearson marrow/pancreas syndrome |
|
Definition
mtDNA disorder; Pancytopenia caused by rearrangement mutation in mitochondrial DNA |
|
|
Term
Leber hereditary optic neuropathy (LHON) |
|
Definition
mtDNA disorder; Blindness caused by mitochondrial DNA mutation. Only known homoplasmic mtDNA mutation, i.e. affects all mitochondria in given cells. |
|
|
Term
Mitochondrial encephalomyopathy and lactic acidosis (MELAS) |
|
Definition
mtDNA disorder; tRNA mitochondrial mutation affecting a variety of systems, including a disruption of ETC. |
|
|
Term
Myoclonic epilepsy with red-ragged muscle fibers (MERRF) |
|
Definition
mtDNA disorder; tRNA mitochondrial mutation affecting a variety of systems, including odd musculature. |
|
|
Term
|
Definition
Glycogen storage disease; disruption in gluconeogenesis resulting in hypoglycemia and glycogen accumulation. Only glycogen storage disease that increases blood lactate levels.
Cause: Glucose-6-phosphatase deficiency, the enzyme which catalyzes G6P conversion to glucose in gluconeogenesis. |
|
|
Term
|
Definition
Glycogen storage disease; lysosomal storage disease involving accumulation of glycogen.
Cause: Genetic defect in lysosomal glucosidase (debranching enzyme), disrupting glycogen degradation. |
|
|
Term
|
Definition
Glycogen storage disease caused by defect in glucosidase (debranching enzyme). Similar to Pompe's disease, but NOT located in lysosome. |
|
|
Term
|
Definition
Glycogen storage disease; exercise-induced muscular pain caused by disruption in muscular glycogen phosphorylase. |
|
|
Term
|
Definition
Glycogen storage disease; defective glycogen phosphorylase in hepatocytes. |
|
|
Term
|
Definition
Glycogen storage disease; branching enzyme deficiency in hepatocytes. |
|
|
Term
|
Definition
First step in the immune system response:
- always "on"
- soluble factors followed by cellular response
- soluble:
- complements pathway
- protease cascade (C3 is critical!!)
- inflammatory (esp. C5a!!)
- defensins
- interferons
- cytokines & chemokines
- TNFalpha major inflammatory!!
- cellular:
- neutrophils (always on)
- macrophages (need activation)
- dendritic (DC) cells (shift to immune)
- langerhans cells
|
|
|
Term
|
Definition
Second step to the immune system response:
- directed by innate dendritic cells (DC)
- activate CD4 & CD8 T cells
- CD4 activates other cells
- B cells make antibodies
- macrophages at infection site
- T cells mature in Thymus
- B cells mature in Bone marrow
- memory cells are mature T & B cells
- plasma cells are pure antibody factories (lotta ER)
|
|
|
Term
|
Definition
Innate reponse immunity cell
- predominant, short-lived phagocytic WBC
- filled w/ granules = "granulocyte"
- inflammatory
- always "on"
|
|
|
Term
|
Definition
Innate reponse immunity cell
- also called "monocyte"
- phagocytic, but must be activated
- tissue-specific
- e.g. Kupher cell, osteoclast, etc...
|
|
|
Term
|
Definition
Innate reponse immunity cell
- coordinates shift from innate ---> immune
- different types:
- myeloid
- Langerhans - in the skin
- plasmacytoid - make cytokines
- follicular - "sticky" cell w/ no myeloid origin
- CANNOT issue immune response
|
|
|
Term
|
Definition
Innate reponse immunity cells
- NK cell
- no T cell receptors
- kills infected, antibody-covered cells
- makes interferon gamma
- NKT & Gamma delta T
- T cell & NK cell receptors
- respond to bacterial products/secretions
|
|
|
Term
|
Definition
Immune reponse cell
- mature in Thymus
- CD2, CD3 receptors
- release cytokines
- recognizes T cell receptors (TCR):
- two important types:
- CD4 - activatory & phagocytic
- CD8 - phagocytic
|
|
|
Term
|
Definition
Immune reponse cell
- mature in bone marrow
- have surface Ig & MHC II
- make antibodies
|
|
|
Term
|
Definition
Component of the innate response
- protease cascade ---> activate C3
- "A is for Activity, B is for Binding"
- classified by way of activation:
- alternate ---> bacterial cell surface
- lectin ---> bacterial carbohydrates
- classical ---> IgG or IgM
- C1 unique to this pathway
- activates inflammatory processes:
- anaphylaxis
- chemotaxis
- C5a = potent inflammatory product
- Membrane Attack Complex (MAC)
|
|
|
Term
|
Definition
- gram (+) cocci
- catalase (+)
- coagulase (+)
- naturally found on skin, nose
- food poisoning, hospitals!!
- virulence factors:
- capsule
- peptidoglycan w/ teichoic acid
- TSS toxin, enterotoxin
- causes:
- skin infection (impetigo, foliculitis, furuncle)
- Toxic shock syndrome (TSS)
- Pyogenic
|
|
|
Term
Staphylococcus epidermidis |
|
Definition
- gram (+) cocci
- catalase (+)
- coagulase (-)
- naturally found on skin (hospitals!!)
- virulence factors:
- capsule
- peptidoglycan w/ teichoic acid
- causes:
- skin infection (impetigo, foliculitis, furuncle)
- UTI
- Pyogenic
|
|
|
Term
|
Definition
- gram (+) cocci
- alpha hemolytic - incomplete hemolysis
- catalase (-)
- virulence factors:
- capsule
- peptidoglycan w/ teichoic acid
- M protein (superantigen)
- causes:
- pneumonia
- meningitis
- Pyogenic
|
|
|
Term
|
Definition
- gram (+) cocci
- beta hemolytic - complete hemolysis
- catalase (-)
- Group A (bacitracin sensitive)
- ubiquitous, mouth & throat
- give Penicillin
- virulence factors:
- capsule
- peptidoglycan w/ teichoic acid
- M protein (superantigen)
- causes: (most pathogenic)
- Scarlet fever
- Strep throat
- Glomerulonephritis
- Puerperal fever
- Rheumatic fever (later heart disease)
- Pyogenic
|
|
|
Term
|
Definition
- gram (+) rods
- ubiquitous anaerobe
- endospores
- virulence factors:
- Tetanospasmin (A-B toxin)
- neuro-exotoxin => block NT release
- Tetanolysin
- peptidoglycan (w/ teichoic acid)
- causes:
- Tetanus (spastic paralysis)
- respiratory failure
|
|
|
Term
|
Definition
- gram (+) bacillus
- ubiquitous anaerobe (soil, food)
- endospores
- virulence factors:
- 7 types of A-B toxin (A-G)
- affect NMJ => block ACh release
- peptidoglycan (w/ teichoic acid)
- causes:
- Botulism
- descending motor loss, flaccid paralysis
|
|
|
Term
|
Definition
- gram (+) bacillus
- ubiquitous anaerobe (soil)
- endospores
- virulence factors:
- lethal toxins (a,b,e,I)
- degradative enzymes
- peptidoglycan (w/ teichoic acid)
- causes:
- Myonecrosis (gas gangrene)
- life-threatening!
- rapidly spreading edema, necrosis, CO2
- cellulitis
- fascitis/myositis
|
|
|
Term
|
Definition
- gram (+) bacillus
- normal gut flora, anaerobic, common to hospitals
- pathology when it overpopulates => too much antibiotics
- give vancomycin
- endospores
- virulence factors:
- peptidoglycan (w/ teichoic acid)
- causes:
- diarrhea
- intestinal infections
|
|
|
Term
|
Definition
- gram (+) bacillus, very large
- always pathogenic
- endospores, aerobic & anaerobic
- virulence factors:
- Anthrax toxin
- factor I - edema factor (EF)
- factor II - protective antigen (PA)
- factor III - lethal factor (LF)
- capsule
- peptidoglycan (w/ teichoic acid)
- S-layer => unique protein coat
- causes:
- Anthrax
- cutaneous easily resolved
- GI & pulmonary extremely fatal
|
|
|
Term
|
Definition
- Gram (-)
- oxidase (-)
- variable O-antigen
- Lactose fermenting:
- (+) E. coli, Enterobacter, Klebsiella, Citrobacter, Serratia
- (-) Salmonella, Shigella, Proteus
- ubiquitous to gut => pathogenic elsewhere
- EXCEPT Salmonella (never natural)
- virulence:
- LPS (endotoxin)
- cytotoxins, enterotoxins
- O-antigen
- siderophores
- causes:
- gastroenteritis
- UTI
- sepsis
- pneumonia
- meningitis
|
|
|
Term
Enteropathogenic E. coli (EPEC) |
|
Definition
- Gram (-)
- oxidase (-)
- O-127 antigen
- Lactose fermenting (+)
- ubiquitous to gut => pathogenic elsewhere
- attach and disrupt microvilli
- virulence:
- LPS (endotoxin)
- cytotoxins, enterotoxins
- O-antigen
- siderophores
- causes:
- diarrhea (infantile & watery)
|
|
|
Term
Enterotoxigenic E. coli (ETEC) |
|
Definition
- Gram (-)
- oxidase (-)
- O-127 antigen
- Lactose fermenting (+)
- ubiquitous to gut => pathogenic elsewhere
- attach and disrupt microvilli
- virulence:
- LPS (endotoxin)
- enterotoxins, heat labile/stabile (LT-1 & Sta)
- LT activates adenylate cyclase (cAMP)
- Sta binds guanylate cyclase (cGMP)
- O-antigen
- siderophores
- causes:
|
|
|
Term
Enteroinvasive E. coli (EIEC) |
|
Definition
- Gram (-)
- oxidase (-)
- O-127 antigen
- Lactose fermenting (+)
- ubiquitous to gut => pathogenic elsewhere
- similar to Shigella (not as bad)
- virulence:
- LPS (endotoxin)
- cytotoxins, enterotoxins
- O-antigen
- siderophores
- causes:
|
|
|
Term
Enterohemorrhagic E. coli (EHEC) |
|
Definition
- aka Shigatoxin E. coli (STEC)
- Gram (-)
- oxidase (-)
- O157:H7 antigen => can't ferment sorbitol
- Lactose fermenting (+)
- invades macrophages => initiates inflammation
- spread aided by host cell actin
- virulence:
- LPS (endotoxin)
- Shiga toxin (Stx I & II)
- A-B toxin
- inhibits protein synthesis
- O157:H7
- siderophores
- causes:
- bloody diarrhea
- hemolytic uremic syndrome (HUS)
- dysentery
|
|
|
Term
|
Definition
- Gram (-)
- oxidase (-)
- Lactose fermenting (-)
- NOT normal flora
- immediately leaves the gut upon ingestion
- invade lamina propria --> peripheral immune system
- intracellular growth (immune-evading)
- virulence:
- LPS (endotoxin)
- Salmonella pathogenecity island (SPI)
- Salmonella plasmid virulence (spv) genes
- antigen switch (immune-evading)
- causes:
- Typhoid fever
- primary bacteremia --> septicemia
- GI symptoms, headache, myalgia, etc..
|
|
|
Term
|
Definition
Lactose fermentor test
- active fermenting => pink or red
- E. coli releases bile as well
- use to differentiate gram (-) bacteria
- Recall,
- (+) E. coli, enterobacter, klebsilla, etc...
- (-) Salmonella, shigella, proteus
|
|
|
Term
|
Definition
Lactose/sucrose fermentor test
- lactose/sucrose fermentors = yellow/orange
- H2S producers = black
- good for gram (+) differentiation
|
|
|
Term
|
Definition
Mannitol fermentor test
- only Staphylococci survive high [salt]
- S. aureus = yellow
|
|
|
Term
|
Definition
Mycobacteria test
similar to Middlebrook agar |
|
|
Term
|
Definition
Mycobacteria test
similar to LJ medium |
|
|
Term
|
Definition
|
|
Term
Buffered charcoal yeast extract |
|
Definition
|
|
Term
|
Definition
- Gram (-), pleomorphic coccobacillus
- needs low temp, Cys for growth
- virulence:
- LPS (endotoxin)
- grows intracellular (ameoba, macrophages)
- immune response requires T cells
- causes:
- pneumonia
- fatigue, diarrhea, confusion
|
|
|
Term
|
Definition
- Gram (-) bacilli
- Oxidase (+)
- grape-like, corn tortilla odor
- ubiquitous; soil, water, hospitals
- biofilm => blue/green slime
- resistant to most antimicrobials
- virulence:
- capsule
- pili
- LPS (endotoxin)
- cytotoxins & exotoxins
- elastase
- Alginate - hallmark of chronic infection
- biofilm
- causes:
- respiratory disease (e.g. pneumonia)
- immunocomprised/hospitalized
- septic shock
- UTI
- endocarditis
- osteochondritis
|
|
|
Term
|
Definition
- Gram (-) diplococci
- "coffee bean" morphology
- Oxidase (+)
- Catalase (+)
- Maltose & Glucose fermentor
- Lipooligosaccharide (LOS)
- normal oral flora
- virulence:
- capsule (need spleen)
- LOS (endotoxic)
- intracellular growth
- causes:
- meningitis
- fever, arthritis, lesions
- Waterhouse-Friedrichson syndrome
- septic shock
|
|
|
Term
|
Definition
- Gram (-) diplococci
- "coffee bean" morphology
- Oxidase (+)
- Catalase (+)
- Glucose fermentor only
- likes chocolate agar
- Lipooligosaccharide (LOS)
- normal oral flora
- virulence:
- capsule (need spleen)
- pili => adherence
- beta-lactamase
- LOS (endotoxic)
- intracellular growth
- causes:
- gonorrhea => discharge
- skin lesions
|
|
|
Term
|
Definition
- Gram (-) comma-shaped rods
- Oxidase (+)
- facultative anaerobe
- lives in water
- virulence:
- cholera toxin (A-B toxin)
- pili
- chemotaxis, zona occludens toxins
- LPS (endotoxin)
- causes:
- cholera => watery diarrhea, cramps, N&V
- dehydration
|
|
|
Term
|
Definition
- Gram (-) spirochetes
- stain w/ aniline dyes (Giemsa or Wright)
- obligate anaerobe
- grows in ticks
- virulence:
- flagella
- LPS (endotoxin)
- gene heterogeneity for protein C
- antigenic shift => immune evasive
- causes:
- Lyme disease ("bulls-eye" bite mark)
- chronic, recurrent fever
|
|
|
Term
|
Definition
Immunoglobin G
- H chain = γ
- most functional/useful Ig
- most prevalent, longest half-life
- early neonatal protection => babies get from Mom
- antigen clearance (agglutination, opsonization)
- T-cell dependent
- slow immune response
- associated w/ immune memory
- levels MUCH higher upon 2nd infection
|
|
|
Term
|
Definition
Immunoglobin M
- H chain = μ
- first class made by neonates
- early defense, primary response
- antigen clearance (agglutination, opsonization)
- T-cell independent
- fast immune response
|
|
|
Term
|
Definition
Immunoglobin A
- H chain = α
- actively secreted
- antigen clearance (agglutination, opsonization)
- T-cell depedent
- slow immune response
- associated w/ immune memory
|
|
|
Term
|
Definition
Immunoglobin D
- H chain = δ
- B-cell activation
- early defense, primary response
- T-cell independent
- fast immune response
|
|
|
Term
|
Definition
Immunoglobin E
- H chain = ε
- anti-parasitic
- activates Mast cells
- T-cell dependent
- slow immune response
- associated w/ immune memory
|
|
|
Term
|
Definition
- Class switch requires T cell help
- T interacts w/ B cell, directs expression via cytokines
- does NOT change VDJ (antigen-binding)
- combines VDJ w/ new heavy chain region
|
|
|
Term
|
Definition
Deficiency in any one complement can result in a susceptibility to bacterial infections:
- C3 = worse, all bacterial infections
- C1-C4 = pyogenic infections
- C5-C9 = Neisserial infections (meningitis, gonorrhea)
|
|
|
Term
|
Definition
- Clostridium perfringens
- Clostridium tetani
- Clostridium botulinum
- C. difficile
- Bacillus anthracis
- Bacillus cereus
|
|
|
Term
|
Definition
- enterobacteriaceae
- ETEC, EHEC, EIEC, EAEC
- bacteremia, UTI, neonatal meningitis
- Salmonella typhi (human -> human)
- Salmonella typhimurium (animal -> human)
- Shigella
- Vibrio cholera
- Pseudomonas
|
|
|
Term
|
Definition
- Neisseria meningitidis
- Neisseria gonorrhoeae
- Borrelia burgdorferi
- Treponema pallidum
|
|
|
Term
|
Definition
- Mycoplasma pneumoniae
- Mycoplasma (other)
- Rickettsia rickettsi
- Rickettsia prowazecki
- Chlamydia trachomatis
- Chlamydophila pneumoniae
- Chlamydophila psittaci
|
|
|
Term
|
Definition
- tiny, tiny, tiny => cannot stain
- NO cell wall => resistant to cell wall antibiotics
- slow growing aerobe, require sterols
- human reservoir
- virulence:
- P1 adhesion protein
- NO cell wall => antibiotic resistant
- intracellular growth
- causes pneumonia
- primary in respiratory tract
- fever, chills, malaise
|
|
|
Term
|
Definition
- Gram (-) weak, coccobacillus
- half-breed => some LPS, some peptidoglycan
- tiny => intracellular growth (endothelial cells)
- ticks are main reservoir
- virulence:
- peptidoglycan, some LPS
- intracellular growth (endothelial cells)
- causes Rocky Mountain spotted fever
- fever, headache, chills, myalgia, rash
|
|
|
Term
|
Definition
- Gram (-) weak, coccobacillus
- part bact, part virus (energy parasite)
- tiny => intracellular growth
- little LPS, peptidoglycan
- human reservoir => most common STD
- two forms = elementary & reticulate
- elementary is infective, spore-like
- virulence:
- intracellular growth (epithelial cells)
- inhibits phagosome/lysosome fusion
- variation of outer membrane proteins
- causes Chlamydia
- UTI, conjunctivitis, trachoma (eye)
|
|
|
Term
|
Definition
- NR to Gram stain!
- too small, use dark field microscopy
- clinically => use serology (cannot culture)
- small, coiled spirochete
- humans only => STD
- virulence:
- small
- adherence proteins
- hyaluronidase
- causes syphilis
- painless lesions (remissions possible)
- can spread to other systems
|
|
|
Term
Mycobacterium tuberculosis |
|
Definition
- Gram (+) - weak, rods, non-spore, acid fast
- lipid coat reduces Gram stain
- complex, thick cell wall
- slow growing, antibiotic resistant
- human reservoir (immunocompromised)
- most infected asymptomatic
- virulence:
- thick cell wall => antibiotic resistant
- intracellular growth
- inhibit phagosome fusion w/ lysosome
- granulomas
- causes Tuberculosis (no vaccine)
- primary in respiratory tract
- only affects 5% infected
- malaise, weight loss, night sweats
- tissue degeneration, can spread (hip, knee, spine)
|
|
|