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457 Cards in this Set
- Front
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What is periplasm?
significance? |
space b/t the cytoplasmic membrane and outer membrane in gram negative bacteria
contains hydrolytic enzymes including B-lactamses |
|
What is the composition of histone octamer?
Where does H1 histone protein belong? |
4 pairs to form a nucleosome, which bind to negatively charged DNA
H1 is not part of the octamer; it binds nucleosome octomers in a string. |
|
What is the composition of bacterial capsule?
exception? |
polysaccharide
exception: Bacillus anthracis: contains D-glutamate |
|
Euchromatin vs heterochromatin
|
Heterochromatin: not accessible for transcription ("Highly Condensed)
Euchromatin: accesible for transcription |
|
What do pilus/fimbria adhere to?
exception? |
adhere to cell surface
Strep mutans (viridan) attaches to fibrin |
|
Acetylation vs hypermethylation of histone.
|
acetylation: weakens DNA-Histone bond --> more transcription
hypermethylation: prevent transcription |
|
Elaborate on the following bacteria's cell membrane/walls:
mycoplasma mycobacteria |
mycoplasma: contains sterol and no cell wall
mycobacteria: contains mycolic acid. high lipid content in the cell wall |
|
Required components for:
1. Purine 2. Pyridmidine |
1. Purine: glycine, aspartate, glutamate ("GAG")
2. pyrimidine: Carbamoyl phosphate and Aspartate |
|
gram positive cocci in clusters?
gram positive cocci in chains? spirochtes? (3) |
clusters: staph
chains: strep spirochetes: Borrelia, Leptospira, Treponema (BLT) |
|
Carbamoyl phosphate
What 2 metabolic pathways is this involved in? |
Urea cycle
De novo pyrimidine synthesis |
|
6 bacteria that don't gram stain.
|
These Rascals May Microscopically Lack Color
Treponema Rickettsia Mycoplasma Mycobacteria Legionella Chlamydia |
|
Increased orotic acid, Megaloblastic anemia (does not improve with vit B12 or folate).
disease? inheritance pattern? |
Orotic aciduria: defect in either ortic acid phosphoribosyl transferase or orotidine 5-phosphate decarboxylase
Autosomal recessive |
|
What organisms are stained with following dyes?
1. Giema 2. PAS 3. Carbol-fulschin 4. Silver |
1. Giema: Borrelia, Plasmodium, trypanosomes, Chlamydia
2. PAS: Whipple's disease (Tropheryma whippelii) 3. Carbol-fulschin: acid-fast organisms 4. Silver: fungi and Legionella |
|
Orotic acid + hyperammonemia.
Disease? inheritance pattern? |
OTC (ornithin transcarbamoylase) deficiency
X-linked recessive |
|
Thayer-Martin or VPN media
What organism? |
N. gonorrhea
|
|
Hydroxyurea
MOA? indication? |
inhibits ribonucleotide reductase --> inhibits de novo pyrimidine synthesis
for sickle cell anemia (increase HbF) |
|
Lactose-fermenting enterics.
What special culture is used? |
"CEEKS"
Citrobacteria E.Coli Enterobacter Klebsiella Serratia cultured in MacConkey Agar |
|
Methotrexate and Trimethprime
MOA? difference? |
inhibits dihydrofolate reductase
MTX: eukaryotic cells TMP: prokaryotic cells |
|
4 Obligate aerobes?
3 obligate anaerobes? |
aerobes: Nocardia, Pseudomonas aeurignosa, Mycobacterium tuberculosis, and Bacillus
Anaerobes: Clostridium, Bacteriodes, and Actinomyces |
|
Adenosine deaminase deficiency
defective pathway? pathogenesis? associated disorder? |
Purine salvage pathway
Excess ATP and dATP imbalances nucleotide pool via feedback inhibition of ribonucleotide reductase -> prevents DNA synthesis and thus lower lymphocyte count. One of the major causes of SCID (severe combined immunodefieciency disease) |
|
2 obligate intracellular bugs
|
"stay inside when it is Really Cold"
Rickettisa and Chlamydia |
|
Lesch-Nyhan syndrome
defect? inheritance pattern? sxs? |
deficiency in HGPRT (used in purine salvage pathway) --> increased uric acid
X-linked recessive retardation, self-mutilation, aggression, hyperuricemia, gout, choreoathetosis |
|
urease positive bugs
|
"Particular Kinds Have Urease"
Proteus Klebsiella H. Pylori Ureaplasma |
|
DNA topoisomerase
fxn? what antimicrobial blocks this enzyme? |
uncoils DNA
flouroquinolone |
|
Yellow sulfur granule, what bacteria?
red pigment, what bacteria? |
yellow sulfur: Actinomyces israelii
red: Serratia marcescens |
|
DNA polymerase I vs DNA polymerase III
|
DNA pol I: 5 --> 3 DNA exonuclease activity; degrades RNA primers
DNA pol III: 3 --> 5 DNA exonuclease activity; elongates both leading and lagging strands both are only in prokaryotes |
|
Quellung bacteria (6)
|
K S SHiN: encapsulated --> avoid phagocytosis
Klebsiella Salmonella Strep pneumoniae Haemophilus influenza B Neisseria meningitidis |
|
Xeroderma pigmentosum
defect? |
defective endonuclease that removed damaged base (or thymidine dimers in this case)
|
|
"SHiN" Bacteria
|
Strep pneumoniae
Haemophilus influenza B Neisseria meningitidis IgA protease transformation encapsulated |
|
Lynch syndrome
defect? |
HNPCC (hereditary nonpolyposis colorectal cancer)
defective mismatch repair gene |
|
Protein A
what bacteria? fxn? |
Staph aureus
binds Fc region of Ig --> prevent opsonization and phagocytosis |
|
How does radiation damage DNA?
|
breaks DNA double strands and forms O2 free radicals, which further damages it
|
|
M protein
what bacteria? fxn? |
Group A strep (pyogene)
prevent phagocytosis |
|
3 main types of RNA and feature of each
|
RMT (Rampant, Massive, Tiny)
rRNA: most abundant mRNA: longest tRNA: smallest |
|
what is the only gram + bacteria with endotoxin?
|
Listeria
|
|
What is added at the 3 end of mRNA post trascriptionally? its fxns?
|
poly A tails
prevent degradation signal to exit nucleus |
|
superantigens (exotoxin)
2 associated bacteria and the toxins |
S aureus: TSST-1 (toxic shock syndrome), enterotoxin, exfoliatin (SSSS)
S. pyogene: Erythrogenic toxin causes toxic-shock like syndrome |
|
TATA or CAAT box
what is it? |
promoter region on DNA
|
|
ADP ribosylating AB toxins.
components of toxin? 4 associated bacteria? |
A: active compound --> alter host's protein fxn
B: binding component Corynebacterium diphtheria Vibrio cholerae E coli Bordetella pertusis |
|
RNA polymerase I, II, III
fxn? |
I: rRNA
II: mRNA III: tRNA in order of products produced |
|
Inactivation of EF2
what bacteria? sxs? |
Corynebacterium diphtheriae
pharyngitis and pseudomembrane in throat |
|
alpha-amanitin
|
found in death cap mushrooms
inhibit RNA polymerase II causes liver failure |
|
2 types of toxins in E coli (ETEC)?
|
Heat-labile stimulates Adenylate cyclase
Heat-stable toxins stimulate Guanylate cyclase both cause watery diarrhea |
|
hnRNA
what is it? fxn? |
hetergenous nuclear RNA
mRNA before post-transcription |
|
how does pertussis toxin increase cAMP?
|
increases cAMP by inhibiting Gi
|
|
snRNP
what is it? fxn? related diseases? |
snRNPs and other proteins form spicesome, which splice out intron and spice in exons.
mixed connective disorder and lupus pts make antibodies aginst snRNPs. |
|
what toxin causes HUS?
|
shiga toxin from Shigella
shiga-like toxin from E coli O157:H7 |
|
Mischarged tRNA
defect? |
reads the usual codon but carries a wrong AA
|
|
4 cAMP inducers?
|
Vibrio cholerae
Pertussis E. Coli (ETEC) - heat labile toxin Bacillus anthracis |
|
enzyme responsible for adding amino acid to tRNA?
where on tRNA? what is the common code at the site? |
aminoacy-tRNA synthase
AA added on the 3 end and has CCA code on it |
|
what 3 immune components are activated by the endotoxin (especially lipid A)?
|
1. activated macrophages: IL-1, TNF, NO
2. complement (alternative pathway): C3a and C5a --> anaphylaxis 3. Hageman factor: DIC |
|
3 sites of ribosome complex and their fxns?
|
A site: incoming Aminoacyl tRNA
P site: accomodates growing Peptide E site: holds Empty tRNA as it exits |
|
5 bacterial toxins encoded in a lysogenic phage?
|
ABCDE
ShigA-like toxin Botulinum toxin Cholera toxin Diphtheria toxin Erythrogenic toxin from Strep pyogene (due to specialized transduction) |
|
energy requirement for translation of each amino acid.
|
tRNA aminoacylation: ATP --> AMP
Loading tRNA onto ribosome: GTP --> GDP translocation: GTP --> GDP total 4 high energy Pi |
|
Identify gram + cocci by the following categories:
1. Novobiocin 2. Optochin 3. Bile acid solubility 4. Bacitracin |
1. Novobiocin: "NO StRES"
Staph saprophyticus: resistant Staph epidermis: sensitive 2. Optochin: "OVRPS" Strep viridan group: resistant Strep pneumoniae: sensitive 3. Bile acid Strep pneumoniae: soluble Strep vidian group: insoluble 4. Bacitracin: "B-BRAS" group B (S. agalactiae): resistant Group A (S. pyogene): sensitive |
|
ubiquitin
what is it? fxn? |
attached to defective protein for degradation
|
|
4 beta hemolytic bacteria?
|
Strep pyogene (group A)
Strep agalactiae (group B) Staph aureus Listeria monocytogenes |
|
telomerase
what is it? fxn? |
reverse transcriptase that adds TTAGGG repeats to the 3 end of DNA
a RNA-dependent DNA polymerase |
|
chronic granulomatous disease pts are more prone to what bacteria? why?
|
Staph aureus b/c catalase positive
CGD: NADPH oxidase deficiency --> little H2O2 |
|
cyclin-CDK complex
fxn? |
both must be activated or inactivated for the cell cycle to progress
|
|
List 3 toxin mediated diseases of S aurues.
|
TSST-1: toxic shock syndrome
exfoliative toxin: SSSS enterotoxin: food poisoning (mayonnaise) |
|
Rb or P53
what are they? |
tumor suppressor genes
inhibits G1 to S progression |
|
infection of prosthetic devices and IV catherer.
organism? |
staph epidermidis
|
|
Permanent, stable or labile?
Lymphocyte |
stable
|
|
Strep pneumoniae is the most common cause what 4 disorders?
|
MOPS
Meningitis in adults Otitis media in children Pneumonia Sinusitis |
|
Permanent, stable or labile?
RBC |
permanent
|
|
rusty sputum, sepsis in sickle cel anemia and splenctomy.
organism? |
strep pneumoniae
|
|
Nissl bodies
what are they? fxn? |
RER in neurons
produces peptide neurotransmitters |
|
what organism causes dental caries?
subacute bacterial endocarditis? |
Viridan group strep: normal flora of the mouth
dental caries: Strep mutans subacute endocarditis: Strep sanguis |
|
Give 2 examples of cells that are rich in RER.
rich in smooth ER? |
rich in RER: mucous-secreting goblet cells, plasma cells
rich in smooth ER: hepatocytes and adrenal cortical cells |
|
Pathogenesis of rheumatic fever?
sxs? |
antibodies to M protein of Strep pyogene (group A)
No "rheum" for SPECCulation SubQ plaques Polyarthritis Erythema marginatum Chorea Carditis |
|
I cell disease
defect? sxs? |
failure of addition of mannose-6-phsphate to lysosome protein
lysosomal proteins are secreted coarse facial features, clouded corneas, restricted joint movement, and high plasma levels of lysosomal enzymes |
|
list 3 pyogenic disease caused by group A strep.
|
pharyngitis
cellulitis impetigo |
|
Clathrin protein
fxn? |
trafficking protein:
trans-golgi --> lysosomes plasma membrane --> endosomes (receptor-mediated endocytosis) |
|
causes pneumonia, meninigitis, and sepsis mainly babies.
what bacteria? tx? |
strep agalactiae (group B)
prophylactic tx with intrapartum penicillin or ampicillin |
|
List 2 drugs that inhibit microtubule polymerization.
List 1 drug that hyperstabilize microtubule. |
inhibit polymerization: vincristine/vinblastine, colchicine
hyperstabilization; Paclitaxel/taxols |
|
group D strep
name? location? |
Enterococci: normal colonic flora
Strep bovis: can cause bacteremia and subacute endocarditis in colon cancer pts |
|
Chediak-Higashi syndrome
defect? sxs? |
microtubule polymerization defect --> decreased phagocytosis
recurrent pyogenic infections (staph, strep) partial albinism peripheral neuropathy |
|
pseudomembranous pharyngitis
causative bacteria? pathogenesis? |
Corynebacterium diptheria
via exotoxin encoded by beta-prophage --> inhibit protein synthesis via ADP ribosylation of EF-2 |
|
Cilia structure
what protein is incorporated? |
9+2 microtubule arrangement
dynein |
|
List spore forming bacteria. (5)
which ones are found in soil |
gram positive rods
soil: Bacillus anthracis, Clostridium perfirngens, C. tetani others: B. cereus and C botulinum |
|
Kartagener's syndrome
defect? sxs? |
immotile cilia due to a dynein arm defect
male/female infertility bronchietasis recurrent sinusitis situs inversus |
|
which bacteria?
1. spastic paralysis, trismus, risus sardonicus 2. floppy baby syndrome 3. gas gangrene and hemolysis 4. pseudomembranous colitis |
1. C tetani
2. C botulinum 3. C perfrigens 4. C difficile |
|
What tissue is associated following IHC markers?
Vimetin Desmin |
Vimetin: connective tissue
Desmin: muscle |
|
Bacterium with polypeptide capsule
|
Bacillus anthracis
contains D-glutamate |
|
2 drugs that disrupt Na/K pump.
|
Ouabain
Cardiac glycosides (digoxin, and digitoxin): blocks Na/K --> increase Ca/Na antiport action --> increase intracellular Ca |
|
Woolsorter's disease
bacteria? sxs? |
Bacillus anthracis
black eschar (painless ulcer) --> bacteremia and death pulmonary sxs: flulike sxs --> fever, pulmonary hemorrhage, mediastinitis, and shock |
|
List 4 types of collagen and associated tissues.
|
Be (So Totally) Cool, Read Books
Type I: bone, skin, tendon type II: cartilage type III: reticullin (skin, blood vessels, uterus, fetal tissue, granulation tissue) type IV: Basement membrnae |
|
tumbling motility and endotoxin
bacteria? modes of transmission? (2) |
Listeria monocytogenes
unpasteurized milk/cheese and deli meats vaginal transmission during birth |
|
What disease(s) is associated following deficiency?
type I collagen type III collagen type IV collagen fibrillin |
type I collagen: Osteogenesis imperfecta
type III collagen: Ehlers-Danlos syndrome type IV collagen: Goodpasture's, Alport's fibrillin-1: Marfan's |
|
aminionitis, speticemia and spontaneous abortion in pregnant women
granulomatosis infantiseptica, neonatal meningitis bacteria? |
Listeria monocytogenes
|
|
What 3 AAs are most abundant in collagen chains?
What vitamin is needed for collagen synthesis? if deficient? |
Glycine-proline-lysine
Vitamin C; Scurvy if deficient |
|
List 2 bacteria with long branching filaments.
tx for each? |
Actinomyces israelii
Nocardia asteroides SNAP: Sulfa for Nocardia Actinomyces use Penicillin |
|
What enzyme cross-links tropocollagen to make collage fibrils? What does it link?
|
links lysine and hydroxylysine by lysyl oxidase
|
|
Ghon complex? its significance?
|
Ghon complex = TB granulomas (Ghon focus) + hilar node involvement
reflects primary infection or exposure |
|
What accounts for elastin's ability to recoil?
What enzyme is responsible for making this property? |
due to desmosine cross-linking b/t lysyl residues with elastin chains
lysyl hydroxylase cross-links the elastin |
|
PPD+ in what group?
PPD- in what group? |
PPD+: current infection, past exposure, BCG vaccinated
PPD-: no infection or anergic (steroids, malnutration, immunocompromised, sarcodosis) |
|
Ehlers-Danlos syndrome
defect? sxs? |
type III collagen deficiency
hyperextensible skin, easy bruising, hypermobile joint, berry aneurysm |
|
fibrocaseous cavitary lesion in the upper lobes.
In terms of TB infection, what is the clinical significance? |
secondary TB by either reinfection or reactivation
|
|
Osteogenesis imperfecta
defect? sxs? genetic pattern? |
type I collagen deficiency
Multiple fractures with minimal trauma blue sclerae hearing loss dental imperfection autosomal dominant (most common) |
|
M. Avium-intracellulares
affected group? prophylactic tx? |
presents in AIDS pts with CD4 < 50
prophylactic tx with Azithromycin |
|
Alport's syndrome
defect? sxs? genetic pattern? |
type IV collagen
deafness, nephritis X-linked recessive |
|
2 forms of Hansen's disease?
why are they different? |
Lepromatous: diffusely over skin and communicable; can be lethal; due to defective Th1 activation
Tuberculoid: limited to a few hypoesthetic nodules |
|
Microarrays
What is this used for? |
used to detect single nucleotide polymorphism or to profile gene expression levels
|
|
tx of Hansen's disease?
its toxicity? |
Dapsone
can cause hemolysis and methemoglobinemia |
|
RNAi
What is it? used for? |
dsRNA complementary to mRNA.
when transfected into human cells, dsRNA separates and promotes degradation of target mRNA, knocking down gene expression |
|
What 2 antibiotics do most gram negative bacillis are resistant to?
|
penicillin G
Vancomycin |
|
Pleiotropy
|
one gene, multiple phenotypes
|
|
What correlates with mortality and morbidity when infected with N. Menigococcus?
|
lipooligosacharrides (LOS)
|
|
Imprinting
|
differences in phenotype depend on whether the mutation is maternal or paternal origin
|
|
List 3 diseases associated with N. menigococcus.
affected group? |
meningococcemia
meningitis Waterhouse-Friderischsen syndrome occurs in close quarters such as college dorms and military barracks. |
|
loss of heterozygosity
|
If a pt inherits or develops a mutation in a tumor suppressor gene, the complementary allele must be deleted/mutated before cancer develops.
not true of oncogenes |
|
List 5 diseases associated with N. gonorrhea.
|
gonorrhea
septic arthritis neonatal conjunctivitis PID Fitz-Hugh-Curtis syndrome |
|
Heteroplasmy
|
presence of both normal and mutated mtDNA, resulting in variable expression of mitochondria inherited disease
|
|
List 4 diseases associated with haemophilus influenzae.
|
haEMOPhilus
Epiglottitis ("cherry red" in children) Meningitis Otitis media Pneumonia |
|
Hardy-Weinberg equation
how do you calculate prevalence of X-linked recessive diseases? |
p^2 +2pq + q^2 = 1
p + q =1 in X-linked recessive disease p = disease prevalence in male q^2 = disease prevalence in female |
|
Chocolate agar with factors V and X are needed for culture of what organism?
|
Haemophilus influenza
|
|
Prader-Willi syndrome
defect? sxs? |
delection of normally active Paternal allele on chrom 15
MR, hyperphagia, obesity, hypogonadism, hypotonia |
|
type B Haemophilus influeza vaccine is conjugated with what?
|
diptheria toxoid to improve immune system recognition of polysacchride and promote class switching
|
|
Angelman's syndrome
defect? sxs? |
deletion of normally active maternal allele on chrom 15
MR, seizures, ataxia, inappropriate laughter |
|
Rimfapin monotherapy is used for? (2)
|
prophylactic tx for haemophilus influenza and meningococcal infection
also used with Dapsone in Hansen's disease to slow resistance to Dapsone |
|
List 3 examples of mitochondral inheritance pattern diseases.
|
Myoclonic epilepsy with ragged red fibers (MERRF)
Leber's hereditary optic neuropathy Mitochondrial encephalopathy with stroke-like episodes and lactic acidosis (MELAS) |
|
Culture for Legionella pneumophilia?
habitat? |
charcola yeast extract culture with iron and cysteine
water source habitat |
|
Hypophosphatemic rickets
inhertiance pattern? presenation? |
x-linked dominant
rickets-like presentation due to increased PO4 wasting |
|
Pseudomonas aeruginosa is associated with?
|
"PSEUDOmonas"
wound and burn infection Pneumonia (in CF pts) Sepsis External otitis (Swimmer's ear) UTI Drug use and Diabetic Osteomyelitis hot tub folliculitis Malignant otitis externa in diabetics |
|
What inheritance pattern is associated with the following:
defective structural genes enzyme deficiencies |
defective structural genes: autosomal dominant
enzyme deficiencies: autosomal recessive |
|
pyocyanin
what is it? what organism produces it? |
blue-green pigment by Pseudomonas
|
|
Marfan's syndrome
defect? sxs? complications? |
fibrillin gene mutation
tall with long extremities, pectus excavatum, hyperextensive joints, and long, tapering fingers/toes (arachnodactyly) dissecting aneurysm (due to cystic medial necrosis of aorta) floppy mitral valve subluxation of lenses |
|
Feature of Enterobacteriaceae
|
COFFEe
Capsular O antigen Flagellar antigen Ferment glucose Enterobacteriaceae |
|
Neurofibromatosis 2
genetic defect? associated diseases? |
NF2 gene mutation on chrom 22
bilateral Schwanomma, juvenile cataracts |
|
What type of E coli causes...
1. dysentery? 2. Traveler's diarrhea? 3. diarrhea? |
1. EIEC and EHEC
2. ETEC 3. EPEC |
|
Cystic fibrosis
genetic defect? cellular changes in the lung and sweat glands? how you so dx? |
AR, CFTR gene defect on chrom 7 (deletion of Phe) --> defective chlorine channels
Lungs (epithelial tissues): decreased Cl secretion --> increased Na/H20 reabsorption --> dry Sweat glands: decreased Cl- reabsorption and Na reabsorption dx via sweat test |
|
HUS is caused by what organism?
triad? pathogenesis? |
by EHEC producing Shiga-like toxin
triad of hemolytic anemia, thrombocytopenia and acute renal failure Endothelium swells due to toxins --> narrows the lumen --> mechanical hemolysis and reduced renal blood flow; damaged endothelium consumes platelets |
|
Pseudohypertrophy of calf muscles, Gower's maneuever
dx? defective gene? inheritance? |
Duchenne's muscular dystrophy
deletion of dystrophin gene X-linked recessive |
|
4 disorders associated with Klebsiella
|
4 A's
Aspiration pneumonia Abscess in lungs Alcoholics di-A-betics |
|
List X-linked recessive disorders.
|
Be Wise, Fool's GOLD Heeds Silly Hope
Bruton's agammaglobulinemia Wiskott-Aldrich Fabry's disease G6PD deficiency Ocular albinism, ornithine transcarbamolyase deficiency Lesch-Nyhan syndrome Duchenne's (Becker's) Hunter's Syndrome Hemophilia A and B also, Alport's syndrome |
|
fever, diarrhea, headache, rose spots on abdomen, and can remain in gallbladder chronically.
organism? |
Salmonella typhi
|
|
Fragile X syndrome
defective gene? genetic findings? findings? |
defective FMR1 gene
CGG trinucleotide repeat disorder 2nd most common cause of MR (after Down's) macro-orchidim, long face with a large jaw, large everted ears, autism, mitral valve prolpase |
|
Salmonella and Shigella
common sxs? virulence? |
both invade intestinal mucosa and cause bloody diarrhea
shigella is more virulent than salmonella |
|
List 4 trinucleotide repeat expansion diseases.
What genetic feature do they all share? |
Try hunting for my friend eggs (X)
Huntington's (CAG) myoTonic dystrophy (CTG) Fragile X syndome (CGG) Freidreich ataxia (GAA) genetic anticipation |
|
causes gastritis and duodenal ulcers.
organism? tx? |
Helicobacter pylori
triple therapy 1: metronidazole, bismuth, either tetracycline or amoxicillin triple therapy 2: metronidazole, omeprazole, and clarithroycin |
|
Down's syndome
genetic defects? causes of genetic defects (3)? findings? |
trisomy 21 due to meiotoic nondisjuction (95%), robertosonian translocation (4%), Down mosaicism (1%)
MR (most common cause), epicanthal folds, simian crease, duodenal atresia, congenital heart disease (most commonly septum primum ASD) Decreased AFP, estriol and increased beta-hCG and inhibin A in amniocentesis |
|
visualized by dark-field microscopy?
|
Treponema
|
|
Edward's
genetic defect? findings? |
trisomy 18
severe MR, rocker-bottom feet, micrognathia, clenched hands usually die within 1 year of birth |
|
Weil's disease
organism? sxs? |
Leptospira interrogans (a spiorchetes
sxs: severe form with jaundice and azotemia from liver and kidney dysfxn; fever, hemorrhage and anemia |
|
Patau's
genetic defect? findings? |
trisomy 13
severe MR, rocker-bottom feet, cleft lip/palate, holoProsecephaly, Polydactyly usually die within 1 yr of birth |
|
Bell's palsy, Arthritis, Cardiac block, Erythema migrans
dx? causative organism? vector? |
Lyme disease
("BAKE a key Lyme pie) Borrelia burgdorferi tick Ixodes |
|
Robertsonian translocation
what is it? affected chromosomes? |
occurs when the long arms of 2 acrocentric chromosomes fuse at the centromere and the 2 short arms are lost
13, 14, 15, 21, and 22 |
|
sxs of stage 2 lyme disease?
|
Bell's palsy
AV nodal block (third degree) |
|
Cri-cu-chat syndrome
genetic defects? findings? |
congenital microdeletion of 5p
microcephaly, MR, high-pitched crying/mewing, epicanthal folds, cardiac abnormalities |
|
Gummas, aortitis, broad-based ataxia, positive Romberg, Charcot joint.
dx? causative organism? |
tertiary syphilis caused by Treponema pallidum
|
|
Williams syndrome
genetic defects? findings? |
congenital microdeletion of 7q
"elfin" facies, MR, hypercalcemia, well-developed verbal skills, extreme freindliness with strangers, cardiovascular problems |
|
Saber shins, saddle nose, CN VIII deafness, Hutchinson's teeth, mulberry molars.
dx? causative organism? |
congenital syphilis caused by Treponema pallidum.
|
|
2 syndromes associated with 22q11 deletion?
defects for each? |
DiGeorge syndrome: thymic, parathyroid, and cardiac defects (truncus arteroisus, tet of Fallots)
Velocardiofacial syndrome: palate, facial, cardiac defects |
|
Most specific test for syphillis?
|
FTA-ABS
|
|
List water soluble vitamins.
Which ones stay in the system for a while? (2) |
B1 (Thiamine: TPP)
B2 (riboflavin: FAD, FMN) B3 (niacin: NAD+) B5 (panthothenic acid: CoA) B6 (pyridoxine: PLP) B7 (biotin) B12 (cobalamin) C (ascorbic acid) folate B12 and folate stay in the system b/c they are stored in the liver |
|
List factors that can cause false positives in VDRL test for detecting syphillis.
|
VDRL
Viruses (mono, hepatitis) Drugs Rhematic fever Lupus and leprosy |
|
List common sxs of vitamin B complex deficiency.
|
dermatitis, glossitis, and diarrhea
|
|
causes bacillary angiomatosis and from cat scratch.
causative organism? |
Bartonella spp.
|
|
Isoretinoin
indication? requirement before using it? why? |
indicated for acne
pregnancy test before using it b/c it is a form of Vit A, which is teratogenic |
|
Brucella spp.
causes what? transmission? |
causes undulant fever
transmission via dairy products, contact with animals |
|
TPP
what vitamin? cofactor what enzymes? (4) |
B1 (thiamine)
Pyruvate dehydrogenase (glycolysis) alpha-ketoglutarate (TCA cycle) Transketolase (HMP shunt) branched-chain AA dehydrogenase |
|
Yersinia pestis
disease? transmission and source? |
Plague
fleabite, rodents, especially prairie dogs |
|
Wernicke-Korsakoff syndrome
what causes it? sxs? irreversible sxs? |
due to thiamine (B1) deficiency; usually associated with chronic alcoholism and malnutrition
Wernicke: confusion, opthalmoplegia, ataxia Korsakoff: memory loss, confabulation, personality change Korsakoff sxs are irreversible b/c the damage to medial dorsal nucleus of thalamus is permanent |
|
what are Clue cells?
associated disease? |
clue cells are vaginal epithelial cells covered with bacteria
associated with bacterial vaginosis |
|
Niacin
what vitamin? what AA is it made from? cofactor for what type of reaction? |
vitamin B3
made from tryptophan constituent of NAD+, NADP+, which are used in redox rxns |
|
headache, fever, rash on palms and soles, which migrate to the trunk.
dx? causative organism? |
Rocky mountain spotted fever caused by Rickettsia rickettsii infection
|
|
vitamin B3 deficiency
List 3 causes. sxs? |
1. Hartup disease (decreased tryptophan reabsorption in the proximal tubule)
2. carcinoid syndrome (increased tryptophan metabolism; used as serotonin) 3. INH (decrease vit B6, which is required to make B3) sxs: Pellagra (diarrhea, dementia, dermatitis) and glossitis |
|
pneumonia, negative Weil-Felix reaction, no rash, due to inhaled aerosole.
dx? causative organism? |
Q fever by Coxiella burnetii
|
|
Pyridoxine
what vitamin? fxns? (6) |
vitamin B6
used as a cofactor for: 1. transmination 2. decarboxylation 3. glycongen phosphorylase 4. cystathione synthesis 5. heme synthesis 6. synthesis of niacin from tryptophan |
|
Chlaymydia trachomatis types L1-3
causes? |
lymphogranuloma venereum
|
|
Drugs that decrease pyridoxine (2)
|
INH
oral contraceptives |
|
This bacteria has choleterol in the membrane.
which bacteria? associated disease? infected group? |
Mycoplasma pneumonia
atypical "walking" pneumonia frequent outbreaks in military recruits and prisons |
|
Which one has a larger reserve pool: cobalamin or folate?
clinical significance of having a small or large reserve pool? |
cobalamin: very large reserve pool in the liver
folate: small reserve pool in the liver; most common vitamin deficiency in US (remember, small reserve pool) |
|
What is the function of following forms of Chlamydiae?
1. Elementary body 2. Reticulate body |
elementary body: infectious and enters cell via endocytosis
reticulate body: replicates in cell by fission |
|
What parasite can cause vitamin B12 deficiency?
What are 2 elevated serum markers for B12 deficiency? |
Diphyllobothrium latum --> Vit B12 deficiency
Elevated homocysteine, and methymalonylic acid |
|
Histoplasmosis
endemic location? pathological features? |
Mississipi and Ohio river valleys
Causes pneumonia Macrophage filled with Histoplasma (smaller than RBC) |
|
increased anion gap acidosis, hypoglycemia, ketosis, increased methymalonylic acid.
suspect? |
Methylmalnonylic acidemia due to deficiency in Isomerase
Isomerase: methylmalony-Coa --> succinyl-CoA |
|
Blastomycosis
endemic location? pathological features? |
Southeast and Central America
Broad-base budding (same size as RBC) inflammatory lung disease and can disseminate to skin and bone. forms granulmatous nodules |
|
S-adenosyl-methinoine (SAM)
fxn? regeneration of SAM requires? |
SAM transfers methylunit; required for NE --> E nad methionine to homocysteine
regeneration requires Vit B12 and folate |
|
Coccidioiodomycosis
endemic location? pathological features? |
Southwestern US, California; increased rate after earthquakes
pneumonia and meningitis can disseminate to bone and skin Spherule filled with endospores |
|
What general reaction uses biotin as a cofactor?
What 3 pathways utilize biotin? |
cofactor carboxylation enzymes (add 1 carbon goup)
1. generation of oxaloacetate (for TCA or gluconeogenesis) 2. synthesis of FA chain 3. odd # FA beta oxidation |
|
Paracoccidioidomycosis
endemic location? pathological features? |
latin America
Budding yeast with "captain's wheel" formation (much large than RBC) |
|
List 4 functions of ascorbic acid.
|
ascorbic acid = vitamin C
1. antioxidant 2. facilitate Fe absorption by keeping it at reduced state (Fe2+) 3. for hydroxylation of proline and lysine in collagen synthesis 4. for dopamine Beta-hydroxylase, which converts dopamine to NE |
|
list 4 dimorphic fungi.
how is the morphology determined? |
Histoplasmosis
Blastomycosis Cocciciomycosis paracoccidioidomycosis Cold = mold Heat = yeast; exception is coccidioidomyocosis, which is a spherule (not yeast) in tissue |
|
Vitamin K
Biochemical action? necessary for synthesis of what substances? |
catalyzes gamma-carboxylation of glutamine acid residues on various proteins concerned with blood clotting
coagulation factors II, VII, XI, X, proteins C and S |
|
Malassezia furfur
presentation? histology? |
Tinea Vesicolor
degradation of lipids produces acids that damage melanocytes and cause hypopigmented patches. Occurs in hot, humid weather. "Spaghetti and meatball" looking |
|
What is the pathogenesis of hepatocellular steatosis seen in chronic alcoholics?
|
ethanol metabolism --> increased NADH/NAD+ in liver
not enough NAD+ to drive TCA cycle and beta oxidation -> TG accumulation |
|
List 3 fungi that are dermatophytes.
morphology? |
Microsporum, Trichophyton, Epidermophyton
mold hyphae in KOH prep, not dimorphic |
|
Kwashiorkor
cause? sxs? |
protein malnutrtion
MEAL Malnutrition (protien) Edema (swollen belly) Anemia Liver (fatty) due to decreased apolipoprotein synthesis |
|
List 5 opportunistic fungal infections.
|
Candida albicans
Aspergillus fumigatus Cryptococcus neoformans Mucor and Rhizopus spp Pneumocystis jiroveci |
|
Marasmus
cause? sxs? |
overall energy malnutrtion
tissue and muscle wastign loss of subQ fat variable edema |
|
Candida albicans
morphology? tx? |
pseudohyphae + budding yeast at 20C
germ tubes at 37 C nystatin for superficial infection amphotericin B for serious systemic infection |
|
List 3 metabolic pathways that take place in both mitochondria and cytoplasm
|
HUG
Heme synthesis Urea cycle Gluconeogenesis |
|
Aspergillus fumigatus
morphology? |
mold with septate hyphae with acute branching (<45 degrees) + rare fruiting bodies
not dimorphic |
|
Metabolism of one glucose molecule results in how many ATPs?
|
30 ATPs in muscle (via glycerol-3-phosphate shuttle)
32 ATPs in heart and liver (via malate-aspartate shuttle) |
|
Cryptococcus neoformans
morphology? found in? |
yeasts with wide capsular halo, narrow-based unequal budding (seen with India Ink stain)
found in soil, PIGEON droppings |
|
List 4 processes that utilize NADPH.
|
1. anabolic process
2. respiratory burst 3. P450 4. glutatione reductase |
|
Mucor and Rhizopus spp
morphology? affected goup? |
irregular board nonseptate hyphae, wide-angle branching mold
in ketoacidotic diabetic and leukemic patients |
|
Hexokinase vs Glucokinase in terms of:
1. fxn 2. location 3. Km, Vmax 4. action of insulin |
1. both add Pi to glucose
2. Hexokinase is ubiquitous, glucokinase is in liver and beta cells of pancreas 3. Hexokinase: low Km, low Vmax Glucokinase: high Km, High Vmax 4. only glucokinase is induced by insulin |
|
Soup Bubble lesions in brain
what fungus? |
Cryptococcus neoformans
|
|
What is the fxn of:
1. Hexokinase 2. glucokinase |
Hexokinase: trap glucose in the tissue
glucokinase: to sequester excess glucose in the liver (glucose "buffer"); induced by insulin |
|
Pneumocystis jiroveci
affected group? associated disorder? when do you start prophylactic tx? |
immunocompromised (e.g. AIDS)
start prophylaxis when CD4 < 200 diffuse interstitial pneumonia |
|
List 5 cofactors for pyruvate dehydrogenase.
What 2 other enzyme complexes use the same set cofactors? |
1. pyrophosphate (B1, thiamine; TPP)
2. FAD (B2) 3. NAD (B3) 4. CoA (B5) 5. Lipoic acid alpha-ketoglutarate dehydrogenase complex alpha-ketoacid dehydrogenase |
|
rose gardener's disease?
sxs? |
Sporothrix schenckii (yeast form)
local pustule or ulcer with nodules along draining lymphatics |
|
What is the rate-limiting enzyme for glycolysis?
list 2 inducers and 2 inhibitors |
Phosphofructokinase-1
Inducers: F-2,6-P, AMP Inhibitors: ATP, citrate |
|
Giardia lamblia
causes? often seen in? |
bloating, flatulence, foul-smelling fatty diarrhea
NOT INVASIVE seen in campers/hikers |
|
Describe how F-2,6-BP is regulated.
|
F-2,6-BP induces PFK-1, which is the rate-limiting enzyme for glycolysis.
Fed state: insulin -> high PFK-2 activity, low FBP-2 activity -> more F-2,6-P -> glycolysis fasting state: glucagon -> high FBpase-2 activity, low PFK-2 activity --> less F-2,6-P --> gluconeogenesis |
|
Entamoeba histolyica
sxs? histology? dx? |
dysentery, liver abscess (reddish brown), RUQ pain
flash-shaped ulcer in the colon if the submucosal abscess ruptures serology and/or trophozoites or cysts in stool; RBCs in cytoplasm of enamoeba |
|
Pyruvate kinase deficiency
sxs? |
Pyruvate kinase is used for making pyruvate
hemolytic anemia due to inability to maintain Na/K pump |
|
Toxoplasma gondii
affected population? causes? transmission? |
HIV: brain abscess (ring-enhancing lesions on CT/MRI)
congenital toxo: chorioretinitis, hydrocephalus, and intracranial calcification cysts in meat or CAT feces |
|
What inhibits lipoic acid, presents with vomiting, rice water stools, garlic breath?
|
Arsenic poisoning
|
|
African sleeping sickness
organism? sxs? transmission? |
Trypanosoma gambiense or T. rhodesiense
enlarged lymph nodes, recurring fever, somnolence, coma Tsetes fly, a painful bite |
|
Pyruvate dehydrogenase deficiency
what is increased in the serum? findings? tx? |
increased lactic acid
neurologic defects tx with high ketogenic nutrients (Lys, Leu, high fat diet) |
|
Chaga's disease
organism? sxs? transmission? |
Trypanosoma cruzi
dilated cardiomyopathy, megacolon, achalasia Reduviid bug ("kissing bug") a painless bite |
|
Cori cycle
fxn? energy cost? |
Transfers Lactate from muscle, RBC to the liver for gluconeogenesis. Glucose produced is moved back the tissue for glycolysis.
costs 4 ATPs |
|
Visceral leishmaniasis
organism? sxs? transmission? |
Leishmania donovani
spiking fevers, hepatosplenomegaly, pancytopenia sandfly |
|
TCA cycle
how many ATPs are generated per cycle? list 2 irreversible enzymes |
3 NADH, 1 FADH, 1 GTP = 12 ATPs per cycle
alpha-ketoglutarate dehydrogenase Isocictrate dehydrogenase |
|
Most severe form of plasmodium infection? why?
2 forms that are dormant in the liver? tx? |
P. falciparum: most severe b/c parasitized RBCs occlude capillaries of brain, kidney and lungs
P. Vivax and P. ovale: dormant form in the liver; tx with primaquine |
|
How is the NADH made from glycolysis is transferred for electron transport chain?
|
Muscle: glycerol-3p shuttle
Heart, liver: malate-aspartate shuttle |
|
fever, hemolytic anemia, blood smear shows Maltese cross and ring forms.
causative organism? |
Babesia
|
|
Oligomycin
what is it? what metabolic process is halted? |
mitochondrial ATPase inhibitor
halts oxidative phosphorylation; increased proton gradient but no ATP is produced |
|
protozoa that causes foul-smelling vaginitis?
|
Trichomonas vaginalis
|
|
CN-, CO poisoning
How do they affect oxidative phosphorylation? |
direct electron transport inhibitors
a decrease in proton gradient and block ATP synthesis |
|
Transmitted by female blackflies
causes hyperpigmented skin and river blindness. causative organism? |
Onchocerca volvulus (a nematode)
|
|
2,4 DNP
how does it affect oxidative phosphorylation? what endogenous substance has a similar property? |
uncoupling agent
increased permeability of membrane --> decreased proton gradient but increased O2 consumption. ATP synthesis stops but electron transport chain continues --> generates heat thermogenin in brown fat |
|
causes elephantiasis, transmission via female mosquito
causative organism? |
Wuchereria bancrofti (a nematode)
|
|
List 3 potential substrates for gluconeogenesis.
|
Propyl-CoA (from odd-chain FA)
Oxaloacetate Alanine |
|
3 nematode infections via ingetion?
|
EAT
Enterobius Ascaris Trichinella |
|
List 4 Irreversible enzymes for gluconeogenesis.
|
Pathway Produces Fresh Glucose
Pyruvate carboxylase (biotin) PEP carboxylase Fructose-1,6-bisphosphatase Glucose-6-phosphatase |
|
3 nematode infections via cutaneous lesions (skin of feet)?
|
SANd
Strogyloides Ancylostoma Necator |
|
What type of FA can enter gluconeogenesis? why
|
Odd-chain FA b/c it produces propyl-CoA, which can enter TCA and converted to oxaloacetate.
even-chain FA produces acetyl-CoA, which can't enter gluconeogenesis |
|
What parasite?
1. brain cysts, seizures 2. Liver cysts 3. B12 deficiency, anemia |
1. brain cysts, seizures: Taenia solium (cysticercosis)
2. Liver cysts: Echinococcus granulosus 3. B12 deficiency, anemia: Diphyllobothrium latum |
|
What is the purpose of HMP shunt
Energy cost? |
aka Pentose phosphate pathway
to generate NADPH for various reactions and F6P, G3P for glycolysis zero ATP used |
|
what parasite?
1. biliary tract disease, cholangiosarcoma 2. hemoptysis 3. portal HTN |
1. biliary tract disease, cholangiocarcinoma: Clonorchis sinesis (also causes pigmented gallstones)
2. hemoptysis: Paragonimus westermani (due to secondary bacterial infection in the lung) 3. portal HTN: Schistosoma mansoni (Snails as hosts) |
|
List 2 main enzymes for HMP shunt?
Rate limiting step? cofactor used? |
Glucose-6-phosphate dehydrogenase (G6PD): rate-limiting
transketolase: requires B1 |
|
What parasite?
1. Hematuria, bladder SCC? 2. microcytic anemia? 3. Perianal pruirits, scotch tape test for dx? |
1. Hematuria, bladder SCC? Shcistosoma haematobium
2. microcytic anemia? Ancyclostoma and necator (by sucking blood) 3. Perianal pruirits, scotch tape test for dx? Enterobius |
|
Glucose-6-phosphate dehydrogenase (G6PD) is used for what 2 processes?
|
pentose phosphate pathway (HMP shunt)
detoxification of oxidative free radicals (esp in macrophages) |
|
Hydatid disease
causative organism? transmission? complication? |
Echinococcus granulosus
eggs in dog feces causes anaphylaxis if echinococcal antigens are released from cysts in the liver |
|
NADPH deficiency
what disease? findings? |
chronic granulomatous disease
recurrent infection with catalase + organisms (Staph aureus, E coli, aspergeillus etc) |
|
List Live attenuated viral vaccines.
What immune response is induced? |
small pox, yellow fever, chickenpox (VZV), Sabin's polio virus (oral), MMR (measles, mumps, and rubella)
Induces cell-mediated and humoral responses |
|
G6PD defiency
findings? inheritance pattern? |
Intrinsic hemolytic anemia (normocytic), bite cells, Heinz bodies
due to inability to detoxify free radicals X-linked recessive |
|
List killed viral vaccines
What immune response is induced? |
RIP Always
Rabies, Influenza, Salk's Polio (IV), HAV Only humoral response is induced. |
|
Aldolase B deficiency
accumulated substance? sxs? milder form? |
Fructose-1-p
hypoglycemia, jaundice, cirrhosis, vomiting Milder form: defect in fructokinase; frutose in urine and blood |
|
List recombinant viral vaccines.
|
HBV (HBsAg antigen), HPV (types 6, 11, 16, and 18)
|
|
Infantile cataracts, jaundice, hepatomegaly, Mental retardation
dx? defect? milder form? |
Galatosemia due to galactose-1p uridyl transferase defiency
galatokinase deficiency: milder form |
|
What DNA virus is single stranded?
|
Parvovirus (ssDNA, (-) strand)
|
|
solbitol dehydrogenase
accumulated substance? affected tissues? unaffected tissues? affected group? |
Sorbitol accumulation (glucose -> sorbitol by aldolase reductase)
affected tissues: kidney, peripheral nerves, retina, lens unaffected tissue: liver, ovaries, seminal vesicles common in chronic DM pts |
|
What RNA virus is double stranded?
|
Reoviridae (Reovirus and Rotavirus)
all RNA viruses are ssRNA excepto Reoviridae |
|
why are liver, ovaries, and seminal vesicles unaffected by sorbitol accumulation?
|
due to sorbitol dehydrogenase, which converts sorbitol to fructose
|
|
What viruses replicate in the nucleus?
|
all DNA viruses except poxvirus
RNA: Retrovirus and influenza (orthomyxo) |
|
lactase deficiency
sxs? where is the enzyme located? |
lactase is a brush-border enzyme in the small intestine
bloating, cramps, osmotic diarrhea |
|
what viruses replicate in the cytoplasm?
|
all RNA viruses except for retrovirus and influenza virus (orthomyxo)
|
|
List 4 glucogenic amino acids.
|
MAV H
Met Arg Val His |
|
What viruses are not enveloped?
|
Naked CPR and PAPP smear
CPR = RNA viruses Calicivirus Picornavirus Reovirus PAPP: DNA virus Parvovirus Adenovirus Papilloma Polyoma |
|
List 4 amino acids that are both glucogenic and ketogenic.
|
PITT
Phe Ile Thr Trp |
|
Where do viruses retain their envelop?
|
from plasma membrane except herpesviruses, which aqcuire envelopes form nuclear membrane.
|
|
List 2 amino acids that are ketogenic
|
Lysine, Leucine
|
|
List all DNA viruses.
|
HHAPPPPy viruses
Herpes Hepadna Adeno Parvo Papilloma Polyoma Pox |
|
What 2 amino acids are needed for growth?
|
Arg and His
|
|
DNA virus with reverse transcriptase?
|
Hepadnavirus B
|
|
List 2 amino acids that are major components of histone.
|
Arg and Lys (+ molecules)
|
|
DNA virus, causes: febrile pharyngitis, pneumonia, conjunctivits ("pink eye")
|
Adenovirus
|
|
List 2 sources of nitrogen groups on urea.
|
Ammonium (NH4+)
Aspartate |
|
Causes aplstic crises in sickle cell disease
what virus? |
Parvovirus
|
|
NAG synthase defiency.
What metabolic pathway is affected? how? |
urea cycle
NAG activates carbamoyl phosphate synthetase I, which is the rate-limiting enzyme for the urea cycle |
|
Molluscum contagiousm
|
Poxvirus
|
|
what 2 urea cycle enzymes are in the mitochondria?
|
Carbamoyl phosphate synthetase I
Ornithine transcarbamoylase |
|
Most common cause of sporadic encephalitis (temporal lobe) in the US
what virus? |
HSV-1
|
|
What transports NH3 from peripheral tissue to liver for eventual metabolism and excretion?
|
alanine
|
|
Herpes genitalis, neonatal herpes?
virus? |
HSV-2
|
|
what amino acid acts as an NH3 carrier inside the cell?
|
glutamate
|
|
causes roseola.
organism? sxs? |
HHV-6
high fevers for several days that cause seizures, followed by a diffuse macular rash |
|
Hyperammonemia
What metabolic pathway is inhibited as a result of increased NH3? why? |
TCA cycle is inhibited b/c excess NH4+ depletes alpha-ketoglutarate
|
|
Tzanck test
used for? finding? |
used to assay for HSV-1, HSV-2, VZV.
a smear of an opened skin vesicle to detect multinucleated giant cells. can also have intranuclear Cowdry A inclusions |
|
2 drugs used to tx hyperammonemia.
|
Benzoate
Phenybutyrate both bind to AA and lead to excretion |
|
EBV
infected cells? causes? dx? |
infects B cells
causes mononucleosis: fever, hepatosplenomagly, pharyngitis, and lymphadenopathy positive Monospot test |
|
Increased orotic acid
list 2 ddx. |
defect in orotic acid -> IMP in de novo pyrimidine synthesis
ornithine transcarbamoylase deficiency (OTC) |
|
What virus can replicate in both nucleus and cytoplasm?
|
Influenza virus (Orthomyxovirus)
|
|
Ornithing transcarbamoylase deficiency (OTC)
inhibited metabolic process? findings? |
urea cycle is inhibited
increased orotic acid, hyperammonemia, decreased BUN |
|
List Inclusion bodies associated viruses (4)
|
Rabies – Negri bodies – intracytoplasmic
Pox virus – Guarnieri – intracytoplasmic & acidophilic CMV – Owl’s eyes – intracytoplasmic & intranuclear HSV/VZV – Cowdry bodies – intranuclear |
|
4 amino acid derivatives that require B6 as a cofactor?
|
Niacin
Histamine Porphyrin --> heme GABA |
|
Nonenveloped, +ssRNA viruses.
dsRNA virus? |
Picorna
Hepevirus (HEV) Calici dsRNA: reo/rota |
|
What AA is the precursor to following AA derivatives?
1. Heme 2. melatonin 3. GABA 4. NO |
1. Heme: glycine
2. melatonin: tryptophan 3. GABA: glutamate 4. NO: arginine |
|
Enveloped, +ssRNA viruses
|
Flavi
Toga Retro (HIV, HTLV) Corona |
|
What are the enzyme and cofactor used for the following synthesis?
1. Dopamine -> NE 2. NE -> epinephrine |
1. Dopamine -> NE: dopamine beta hydroxylase; requires vit C
2. NE -> epinephrine: PNMT, requires SAM |
|
enveloped, -ssRNA viruses
|
Paramyxo
Rhado Filo Arena Bunya Delta |
|
Mental retardation, growth retardation, fair skin, eczema, musty body odor
dx? tx? |
Phenyketouria
decreased phenylalanine and increased tyrosine in the diet |
|
Segmented viruses
significance? |
BOAR
Bunya (3 segments) Orthomyxo (8 segments) Arena (2 segments) Reo/Rota (10-12 segments) can undergo reassortment, causing antigenic shifts that lead to worldwide pandemics of the flue |
|
List 2 causes of phenylketouria.
|
decreased phenylalanine hydroxylase
decreased BH4 (a cofactor for Phe hydroxylase) |
|
Piconarvirus
|
PERCH
Poliovirus Echovirus Rhinovirus Coxsackivirus A/B HAV |
|
Alkaptouria
deficiency? what pathway is affected? |
congenital deficiency in homogenistic acid oxidase in the degradative pathway of tyrosine
|
|
aseptic viral meningitis
causative organisms? |
Echovirus
Coxackievirus |
|
List 3 causes of albinism.
associated complication? |
1. tyrosinase deficiency
2. defective tyrosine transporter 3. lack of migration of neural crest cells associated with increased risk of skin cancer due to no melanin |
|
common cold
causative organism? |
Rhinovirus (a picornavirus)
|
|
what special genetic feature does albinism have?
|
variable inheritance due to locus heterogeneity
|
|
yellow fever
cause? sxs? |
a flavivirus
high fever, black vomitus, and jaundice. Councilman bodies may be seen in liver |
|
Congenital disease with MR, increased homocystine in urine, osteoporosis, tall stature, kyphosis, lens subluxation, and atherosclerosis
dx? defects? |
Homocytinuria due to:
Cystathionine synthase deficiency decreased affinity cystathione synthase for B6 OR homocysteine methylase transferase deficiency |
|
Major cause of acute diarrhea in the US during winter, especially in day-care centers, kindergartens.
organism? |
Rotavirus (a reovirus)
|
|
Cystic kidney stone
common cause? tx? |
hereditary defect of renal tubular AA transporters for cysteine, ornithine, lysine, and arginine in the PCT
tx: acetazolamide to alkaline the urine |
|
2 antigens of influenza viruses and their fxns?
|
Hemagglutinin: promote viral entry
neuraminidase: promotes progeny virion release |
|
Maple syrup disease
defect? findings? |
blocked degradation of branched AA (Ile, Leu, Val) due to decreased alpha-ketoacid dehydrogenase
Urine smells like maple syrup ("burned sugar" smell) severe CNS defects, MR and death |
|
Reassortment of viral genome is called?
|
genetic shift
|
|
Hartnup disease
defect? findings? |
defective neutral AA transporter on renal and intestinal epithelial cells
pellagra (diarrhea, dementia, dermatitis) |
|
Rubella virus as congenital infection.
sxs? |
A togavirus
Encephalopathy, deafness, blindness, PDA Maculopapular rash: from head to toe postauricular/occipital lymphadenpathy |
|
What is the rate-limiting enzyme for glycogenolysis.
List inducers (3) and an inhibitor (1). |
Glycogen phophorylase
Inducers: Glucagon (liver), Epi (liver/muscle), Ca++/calmodulin (muscle); all phosphorylate the enzyme inhibitor: insulin (dephosphorylates the enzyme) |
|
List 4 paramyxoviruse
|
Parainfluenza
measles mumps respiratory syncytial virus (RSV) |
|
What is the first step of glycogenolysis? main product?
2nd step? |
1st step: glycogen phosphorylase to cleave 1,4 bonds until 4 glucose residues are left (limit dextran)
2nd step: debranching enzyme |
|
Palivizumab
indication? MOA? |
blocks surface F (fusion) protein of RSV (a paramyxovirus)
|
|
List 4 important glycogen storage diseases.
|
Very Poor Carb Metabolism
Von Gierke's (type I) Pompe's disease (type II) Cori's disease (type III) McArdle's disease (type V) |
|
measles
sxs? |
3 C's + K
cough coryza conjunctivitis Koplik spots |
|
What enzyme is alternatively used to cleaven glycogen to glucose molecules (minor pathway)?
associated disease if deficient? |
Lysosomal alpha1,4 glucosidase (acid maltase)
Pompe's disease (type II) |
|
mumps
sxs? |
POM
parotitis orchitis aseptic meningitis |
|
Von Gierke's disease
defect? findings? |
glucose-6-phosphatase deficiency
type II severe fasting hypoglycemia, increased glycogen in liver, high blood lactate, hepatomegaly |
|
Rabies
mode of transmission? morphology? affected cells? |
bites from bat, raccoon and skunk in the US (dogs also)
bullet-shaped capsid negri bodies travel to the CNS by migrating in a retrograde fashion up nerve axons |
|
congenital, increased glycogen in liver, cardiomegaly
dx? defect? |
Pompe's disease
defective lysosomal alpha 1,4 glucosidase (acid maltase) |
|
HAV
transmission? class? |
fecal-oral route of transmission
a RNA picornavirus |
|
congenital, increased, glycogen in muscle, painful muscle cramping and myogloburia with exercise
dx? defect? |
McArdle's disease
skeletal muscle glycogen phosphorylase deficiency |
|
Which hepatic virus integrates into host's genome?
|
hep B (a DNA virus)
|
|
List X-linked recessive lysosomal storage disorders (2)
|
Fabry's disease
Hunter's syndrome |
|
which hepatic virus requires coinfection with other virus? What does it require?
|
hep D requires coinfection with hep B virus.
requires HBsAg as its envelope |
|
List 3 lysosomal storage diseases common in Ashkenazi jews.
|
Niemann-Pick
Tay-Sachs Gaucher's disease |
|
which hep virus causes high mortality in pregnant women but usually asymptomatic in healthy individuals?
|
hep E
|
|
Peripheral neuropathy of hands/feet, angiokeratomas, CV and renal disease
increased ceramide trihexoside in blood dx? defect? |
Fabry's disease
alpha-galactosidase A deficiency |
|
Interpret the following 3 separate results:
1. HBsAb 2. IgM HBcAb 3. IgG HBcAb |
1. HBsAb: immunized or cured
2. IgM HBcAb: positive during window period, recent disease 3. IgG HBcAb: positive during wndow period, chornic disease |
|
Hepatosplenomegaly, aspectic necrosis of femur, bone crises, increases glucocerebroside.
dx? defect? hallmark cell? |
Goucher's disease
defective Beta-glucocerebrosidase Gaucher's cells (macrophages that look like crumpled tissue paper) |
|
What serum marker indicates high transmissiblity in hep B infection? how about low transmissibility?
|
high: HBeAg
low: HBeAb |
|
Niemann-Pick disease vs Tay-Sachs disease
common findings? difference? defect and accumulated substance? |
common findings: progressive neurodegeneration, developmental delay, cherry-red spot on macula
difference: hepatosplenomegaly ONLY IN Niemann-Pick Niemann-Pick: deficiency in sphongomyelinase and accumulated sphingomyelin Tay-Sachs("SaX): deficiency in HeXosaminidase A and accumulated GM2 ganglioside |
|
ALT > AST vs AST>ALT
|
ALT > AST: viral hepatitis
AST>ALT: alcoholic hepatitis |
|
2 diseases with heparin sulfate, dermatan sulfate accumulation?
|
Mucopolysaccharidoses
Hurler's syndrome Hunter's syndrome |
|
What proteins are associated with the following HIV genes?
1. env 2. gag 3. pol |
1. env: gp42, gp 120 (envelop proteins involved in fusion of virus)
2. gag: p24 (capsid protein) 3. pol: reverse transcriptase |
|
Hurler's syndrome
defect? findings? accumulated substance? |
alpha-L-iduronidase deficiency
accmuluated heparan sulfate and dermatan sulfate developmental delay, gargoylism, airway obstruction, corneal clouding, hepatosplenomegaly |
|
what surface antigens do HIV bind to on host cells?
|
CXCR4 and CD4 on T cells
CCR5 and CD4 on macrophages |
|
What shuttle is used to transport FA for FA synthesis? Where is it transported to?
for beta-oxidation? |
FA synthesis: citrate shuttle; out of mitochondria to cytoplasm
Beta oxidation: Carnitine shuttle: into the mitochondria |
|
How do you dx HIV infection?
|
ELISA/Western blot tests to look for antibodies to viral proteins
ELISA to rule out first (highly sensitive) Western blot to rule in (highly specific) |
|
Carnitine deficiency
What process is halted? findings? |
beta oxidation due to lack of carnitine shuttle, which transport FA into mitochondria
hypoketotic hypoglycemia weakness, hypotonia |
|
how do you dx AIDS?
|
CD4+ < 200 (normal 500-1500) or
CD4/CD8 ratio < 1.5 |
|
Acyl-CoA dehydrogenase deficiency
findings? |
decreased ability to oxidize fatty acid
increased dicarboxylic acids hypoglycemia after fasting with decreased ketones |
|
When do HIV dx tests result in high false positives?
how about high false negatives? |
high false positives: in babies born to infected mothers due to anti-gp120 crossing the placenta
high false negatives: first 1-2 months of HIV infection |
|
List 2 examples of ketone bodies.
How and where are they formed? where are they used primarily? |
acetoacetate and beta-hydroxybutyrate
in the liver, fatty acids and amino acids are metabolized to be used in muscle and brain |
|
List 4 neoplasms associated with HIV.
|
Kaposi's sarcoma (HHV-8)
invasive cervica carcinoma (HPV) primary CNS lymphoma (EBV associated) non-Hodgkin's lymphoma |
|
List 3 states that causes high ketone levels.
Why do ketones form in each state? |
starvation: depletion of oxaloacetate
diabetic keoacidosis: depletion of oxaloacetate chronic alcoholism: NADH shunts oxaloacetate to malate all stall TCA cycle --> ketone generation |
|
What infections are associated with the following scenarios:
1. CD < 400 2. CD < 50 |
1. CD < 400: oral thrush, tinea pedis, reactivation of TB, VZV, other bacterial infections
2. CD < 50: CMV retinitis, disseminated M. avium-intracellulare, cryptococcal meningoencephalitis |
|
List 4 sources of hepatic gluconeogenesis when starving for 2 days.
|
1. glycerol (as glycerol phosphate but has to be delivered to the liver b/c adipocytes cannot convert glycerol to glycerol-p)
2. lactate (via Cori cycle) 3. Amino acids (as oxaloacetate and a-ketoglutarate) 4. propionyl-CoA (from odd # FA) |
|
What determines increased risks of following infections in HIV pts?
1. Pneumocytisi pneumonia 2. toxoplamosis 3. histoplasmosis |
1. Pneumocystis pneumonia: CD < 200
2. toxoplamosis: CD < 100 3. histoplasmosis: CD < 100 |
|
Apolipoprotein A-I
associated lipoprotein? fxn? |
associated with HDL
activates LCAT, which esterifies the trapped cholesterol in the HDL |
|
What is the diseased form of prion proteins?
|
beta-pleated form: PrPsc
|
|
Apolipoprotein B-100
associated lipoproteins? fxn? |
VLDL, IDL, LDL
binds to LDL receptor, mediates VLDL secretion |
|
What is the normal flora of the following sites?
1. skin 2. nose 3. oropharynx 4. colon 5. vagina |
1. skin: staph epidermidis
2. nose: staph epidermidis and colonized by staph aureus 3. oropharynx: viridans group strep 4. colon: Bacteriodes fragilis > E coli 5. vagina: lactobacillus, colonized by E coli and group B strep |
|
Apolipoprotein E
associated lipoproteins? fxn? |
chylomicron, chylomicon remnant, VLDL, IDL
mediates Extra (remnant) uptake; delivers chylomicron remnant, IDL back to liver after distributing TGs in the peripheral tissue |
|
What bug causes food poisoning in following scenarios?
1. contaminated seafood 2. reheated rice 3. Mayonnaise, custard |
1. contaminated seafood: Vibrio parahaemolyticus and V. vulnificus
2. reheated rice: Bacillus cereus 3. Mayonnaise, custard: Staph aureus |
|
Apolipoprotein CII
associated lipoproteins? fxn? what protein has the opposite fxn? |
chylomicron, chylomicron remnant, VLDL
increases lipoprotein lipase activity apo C-III has the opposite fxn |
|
What bug causes food poisoning in following scenarios?
1. undercooked meat (beef) 2. poultry, meat and eggs |
1. undercooked meat (beef): EHEC (O157:H7)
2. poultry, meat and eggs: salmonella |
|
HDL
fxn and route? |
mediates reverse cholesterol transport form periphery to liver.
act as a repository for apoC and apoE, which are needed for chylomicron and VLDL metabolism secreted from both liver and intestine |
|
What bug causes dysentery and pseudoappendicitis that is usually due to Day-care outbreaks?
|
Yersinia enterocolitica
|
|
LDL
fxn and route? |
delivers hepatic cholesterol to peripheral tissues.
formed by lipoprotein lipase modifacation of VLDL in the peripheral tissue taken up by target cells via receptor-mediated endocytosis |
|
Dysentery, causes flask-shaped ulcer in the colon submucosally.
causative bug? |
Entamoeba histolytica
|
|
LCAT and CETP
fxn? |
LCAT: catalyzes esterification of cholesterol
CETP: mediates transfer of cholesterol esters to other lipoprotein particles (VLDL, LDL, IDL) |
|
Aspiration pneumonia + lung abscess
causative bugs? |
anaerobe organisms
|
|
Increased chylomicron, TG, and choleterol?
what type of dyslipidemia? defect? |
hyerpchylomicronemia (type I)
lipoprotein lipase deficiency or altered apolipoprotein C-II |
|
pneumonia in alcoholics and IV drug users
causative bugs? |
S pneumoniae
Klebsiella Staph |
|
Absent or LDL receptor
dx? findings? |
familial hypercholeterolemia (type IIa)
accelerated atherlsclerosis, tendon xanthomas, corneal arcus |
|
Most common cause of atypical pneumonia? 2nd most common?
|
most common: Mycoplasma
2nd: Chlamydia pneumoniae |
|
type IV dyslipidemia
cause? findings? |
hepatic overproduction of VLDL
causes pancreatitis increased VLDL and TG |
|
Postviral pneumonia
causative bugs? affected population? |
in the elderly
Staph, H. influenza, Strep pneumoniae |
|
Abetalipoproteinemia
deficiencies? findings? |
inability to synthesize lipoproteins due to deficiencies in apoB-100 and apoB-48
failure to thrive, steatorrhea, acanthocytosis, ataxia, nightblidness |
|
Most common cause of meningitis in the newborn?
2nd most common? |
most common: group B strep
2nd: E coli |
|
HMG-CoA reductase
3 side effects |
hepatotoxicity (increased LFTs)
rhabdomyolysis teratogenic |
|
Most common cause of meningitis in adults?
|
Strep pneumoniae
|
|
Niacin
MOA? 4 side effects? |
MOA:
inhibit lipolysis in adipose tissue reduces hepatic VLDL secretion into circulation side effects 1. red, flushed face, which is decreased by aspirin or long-term use 2. hyperglycemia (acanthosis nigricans) 3. hyperuricemia (exacerbates gout) 4. hepatitis |
|
Most common causative organism of osteomyelitis?
how about in diabetics and drug addicts? Sickle cell pts? |
Most people: staph aureus
diabetics/ drug addicts: Pseudomonas aeruginosa Sickle cell: Salmonella |
|
2 lipid lowering agents that increase the risk of cholesterol gallstones
|
bile acid resins (cholestyramine, colestipol, colesevelam)
Fibrates (gemfibrozil, clofibrate, bezafibrate, fenofibrate) |
|
osteomyelitis after cat/dog bites or scratch?
what bug? |
Pasteurella multocida
|
|
what lipid lowering agent is best at lowering TG?
|
Fibrates (gemfibrozil, clofibrate, bezafibrate, fenofibrate)
|
|
Risk factor for UTI in:
1. male newborns 2. male elderly |
1. male newborns: congenital defects (hypospadias), vesicoureteral reflux
2. male elderly: enlarged prostate |
|
Positive urine leukocyte test indicates?
positive nitrate test indicates? |
leukocyte: bacterial UTI
nitrate: gram negative bacterial UTI |
|
List UTI causing bugs.
most common? 2nd most common? |
SSEEK PP
Serratia marcescens Staph saprophyticus: 2nd most common E coli: most common Enterobacter cloacae Klebsiella pneumoniae Proteus mirabilis Pseudomonas aeruginosa |
|
UTI, struvite stones
what bug? |
proteus mirabilis
|
|
TORCH infection?
|
Toxoplasmosis
Rubella CMV HIV HSV-2 Syphilis |
|
Toxo triad in infants?
|
CHI
chorioretinitis hydrocephalus Intracranial calcification |
|
Classic triad of Rubella
|
PDA (or pulmonary artery hypoplasia)
cataracts deafness +/- blueberry muffin rash |
|
What TORCH infection presents with hearing loss and seizures?
|
CMV
|
|
Erythema infectiosum
cause? sxs? |
Parvovirus B19
"Slapped cheek" rash on face later appears over body in reticular, "lace-like" pattern can cause hydrops fetalis in pregnant women |
|
Scarlet fever
cause? sxs? |
Strep pyogenes
erythematous, sandpaper-like rash with fever and sore throat |
|
Hand-foot-mouth disease in newborns
cause? sxs? |
Coxsackievirus type A
vescicular rash on palms and soles; ulcers in oral mucosa |
|
Chancroid
cause? sxs? |
Haemophilus ducreyi
painful genital ulcer, inguinal adenopathy |
|
Lymphogranuloma venereum
cause? sxs? |
Chlamydia trachomatis (L1-L3)
ulcers, lymphadenoapthy, rectal strictures |
|
condylomata acuminanta
cause? sxs? |
genital warts, koilocytes
HPV 6, 11 |
|
PID
2 most common cause? sxs? complications? |
Chlamydia trachomatis (D-K), N. gonorrhea
chandelier sign (cervical motion tenderness), purulent cervical discharge. can lead to Fitz-Hugh-Curtis syndrome ("violin string" adhesions of parietal peritoneum to liver), ectopic pregnancy, infertility, and chronic pelvic pain |
|
urinary catherization prediposes to infection caused by what organism?
|
E coli (most common)
Proteus mirabilis |
|
Respiratory therapy unit predisposes to infection caused by what organism?
|
Pseudomonas aeurginosa
|
|
Newborn nursery prediposes to infection caused by what 2 organisms?
|
CMV
RSV |
|
What 2 dermatological complications are often confused in advanced AIDS pts?
how do you differentiate the two? |
Bacillary angiomatosis caused by Bartonella henselae
Kaposi's sarcoma caused by HHV-8 Biopsy results Bacillary angiomatosis: neutrophilic inflammation Kaposi: lymphocytic inflammation |
|
Cotton-wool spots on funduscopic exam in AIDS pts with CD4 <50.
dx? |
retinitis due to CMV
|
|
What 2 bugs cause Rash in unimmunized children beginning at head and moving down?
How do you differentiate the two? |
Rubella virus (German Measle, togavirus): with postauricular lymphadenopathy
Measles virus (Rubeola): with Koplik spots on buccal mucosa, cough, conjunctivitis, and coryza |
|
Bug hints (if all else fails):
Pus, empyema, abscess |
Staph aureus
|
|
Bug hints (if all else fails):
traumatic open wound |
Clostridium perfringens
|
|
Bug hints (if all else fails):
Surgical wound |
Staph aureus
|
|
Bug hints (if all else fails):
currant jelly sputum |
Klebsiella
|
|
Bug hints (if all else fails):
healthcare provider |
HBV from needle stick
|
|
Bug hints (if all else fails):
fungal infection in diabetic |
Mucor or Rhizopus spp.
|
|
Bug hints (if all else fails):
Asplenic pts |
encapsulated bacteria, esp SHiN
Strep pneumoniae Haemophilus influeza type B N. meningitidis |
|
Bug hints (if all else fails):
chronic granulomatous disease |
catalase-positive microbes
Staph aureus Nocardia spp Serratia marcescens Pseudomonas cepacia Aspergillus spp E coli |
|
Bug hints (if all else fails):
Bilateral Bell's palsy |
Borrelia burgodorferi (Lyme disease)
|
|
Bug hints (if all else fails):
pediatric infection |
Haemophilus influenzae (including epiglottitis)
|
|
List beta lactams.
MOA? |
Penicillin
Methicillin Ampicillin Ticarcilln, pipercillin Cephalosporins Aztreonam Imipenem blocks peptidoglycan cross-linking |
|
List 30S inhibitors
|
AT
Aminoglcosides: Gentamicin, Neomycin, Amikacin, Tobramycin, Streptomycin ("GNATS") Tetracycline (all the"-cyclines") |
|
List 50S inhibitors.
What is the common feature? |
Macrolides: Erythromycin, azithromycin, clrithrymycin
Chloramphenicol Clindamycin all are bacteriostatic |
|
What antibiotic blocks DNA topoisomerases?
blocks mRNA synthesis? |
Flouroquinolones: blocks topoisomerase
Rifampin: blocks mRNA synthesis |
|
Methicillin, nafcillin
spectrum? toxicity? |
a beta lactamase resistant
Staph aureus except MRSA toxicity: interstitial nephritis |
|
Ampicillin
adjunctive therapy? indication? |
combine with clavulanic acid (penicillinase inhibitor) to enhance spectrum
Gram positives + gram negative rods (HELPS) Haemophilus influezae E coli Listeria Proteus Salmonella Enterococci |
|
list 3 antipseudomonals
adjunctive therapy? |
Take Care of Pseudomonas
Ticarcillin Carbenicillin Piperacillin adjunct with clavulanic acid (penicillinase inhibitor) |
|
1st generation cephalosporin
2 prototypes? specturm? |
Cefazolin, cephalexin
gram+ and "PEcK" Proteus E coli Klebsiella |
|
2nd generation cephalosporin
3 prototypes? spectrum? |
cefoxitin, cefaclor, cefuroxime
gram + and "HEN PEcKS" Haemophilus Enterobacter aerogenes Neisseria spp. Proteus E coli Klebsiella Serratia marcescens |
|
3rd generaiton cephalosporin
3 prototypes? spectrum? |
ceftriaxone, cefotaxime, ceftazidime
serious gram-negative infections resistant to other beta-lactams; meningitis (most penetrate BBB) |
|
Aztreonam
spectrum? indication? |
gram negative rods: Klebsiella, Pseudomonas, Serratia
NO activity against gram positives or anaerobes for penicillin-allergic pts and those with renal insufficiency who cannot tolerate aminoglycosides |
|
Imipenem
MOA? adjunctive therapy? |
B-lactamse resistant carbapenem
always administered with cilastatin (inhibitor of renal dihydropeptidase I) to decrease inactivation in renal tubules |
|
Imipenem
indication? side effects? better alternative? |
drug of choice for Enterobacter
causes seizures, GI stress, skin rash Meropenum has a reduced risk of seizures and is stable for dihydropeptidase I |
|
Vancomycin
MOA? toxicity? resistance? |
blocks D-ala D-ala cell wall mucopeptide formation
NOT Nephrotoxicity Ototoxicity Thrombophlebitis diffusing flushing (red man syndrome) resistance develops when mucopeptide changes to D-ala D-lac |
|
Aminoglycosides
requirement? indication? toxicity? |
require O2 uptake (ineffective against anaerobes)
severe gram negative rod infections NOT Nephrotoxicity Ototoxicity Teratogen (CN VIII toxicity) |
|
Tetracycline
special direction for administration? toxicity? |
must NOT take with milk, antacids, or Fe-containing preps b/c divalent cations inhibit its absorption in the gut
discoloration of teeth and inhibition of bone growth in children photosensitivity contraindicated in pregnancy |
|
Doxycycline
class? indicaiton? |
a tetracycline (30s inhibitor)
fecally eliminated so indicated for pts with renal failure |
|
Erythromycin
MOA? toxicity? |
blocking translocation by binding to 23S rRNA of the 50S ribosomal subunit.
prolonged QT interval |
|
Chloramphenicol
indication? toxicities? |
menigitis
Anemia, aplastic anemia Gray baby syndrome (in premature infants b/c lack live UDP-glucoronyl transferase) |
|
Clindamycin
indication? toxicity? |
treat anaerobic infections
pseudomembranous colitis (C. difficile overgorwth) |
|
Sulfamethoxazole
MOA? toxicity? |
PABA antimetabolites inhibit dihydropterate synthase --> decreased THF
hemolysis in G6PD deficient kernicterus in infants displace other drugs from albumin |
|
Trimethoprim
MOA? toxicity? |
inhibit bacterial dihydrofolate reductase
megaloblastic anemia, leukopenia, granulocytopenia |
|
Ciprofloxacin
class and MOA? toxicity? |
a flouroquinolone
inhibit DNA gyrase (topoisomerase II) damage cartilage (contraindicated in pregnant women and children) tendonitis and tendon rupture in adults |
|
Metronidazole
MOA? indication? toxicity? |
toxic metabolites in bacterial cell that damage DNA
GET CAP on the Metro Giardia Entamoeba Trichomonas Gardnerella vaginalis Anaerobes (bacteroides, Clostridium) h Pylori |
|
polymyxins
MOA? clinical use? |
disrupts cell membrnae
for resistant gram-negative infections |
|
List 5 anti-TB drugs and their toxicity.
|
INH-SPiRE
INH (Isoniazid) Streptomycin Pyrazinamide Rifampin Ethambutol: red-green color blindness all others cause hepatotoxicity |
|
prophylactic tx for M. tuberculosis
prophylactic tx for M avium-intracellulare? |
MTb: Isoniazid
M. Avium-intracellulare: Azithromycin |
|
INH (Isoniazid)
MOA? toxicity? metabolism? |
decreased synthesis of mycolic acid
neurotoxicity (prevent with vit B6) and hepatotoxicty Bimodal distribution of metabolism due to different INH half-lives in fast vs slow acetylators |
|
Rifampin
MOA? Toxicity? |
4 R's
RNA polymerase inhibitor Revs up microsomal p450 Red/orange body fluids Rapid resistance if used alone |
|
prophylactic tx for menigococcal infection?
|
Rifampin
|
|
Prophylactic tx for Pneumocystis jiroveci pneumonia?
|
TMP-SMX
|
|
Treament for MRSA?
Treament for VRE? |
MRSA: vancomycin
VRE: linezolid and streptogramins |
|
Amphotericin B
MOA? toxicity? |
binds ergosterol --> pore formation
Nephrotoxicity (reduced with hydration) arrhythmias due to hypokalemia and hypomagnesia |
|
Nystatin
MOA? clinical use? |
binds to ergosterol
for oral candidiasis (thrush) topical for diaper rash or vaginal candidiasis |
|
Azoles
MOA? toxicity? |
inhibit fungal ergosterol synthesis
hormone synthesis inhibition (gynecomastia), liver dysfxn |
|
what drug is used to tx cryptococcal meningitis in AIDS pts?
|
Fluconazole
can cross BBB |
|
Caspofungin
MOA? clinical use? |
inhibit beta-glucan --> inhibit cell wall synthesis of fungus
invasive aspergillosis |
|
Terbinafine
MOA? clinical use? |
inhibit fungal enzyme squalene epoxidase
used to tx dermatophytoses (especially onychomycosis) |
|
Amantadine
MOA? clincal use? |
blocks viral penetration/uncoating (M2 protein)
also causes the release of DA from intact nerve terminals prophylactic tx for influenza A Parkinson's disease |
|
Amatadine vs Rimantidine
compare |
both block viral uncoating (M2 protein)
Rimantidine does not cross BBB, so fewer CNS side effects Amatadine causes cerebellar problems (ataxia, dizziness, slurred speech) |
|
what 2 drugs inhibit influenza neuraminidase?
|
Zanamivir, oseltamivir
|
|
Acyclovir
clinical use? MOA? Requirement? |
for HSV, VZV, EBV
monophosphorylated by HSV/VZV thymidine kinase. Guanosine analog --> inhibit viral DNA polymerase |
|
Ganciclovir
clinical use? MOA? Requirement? |
for CMV, esp. immunocompromised pts
Guianosine analog --> inhibit viral DNA polymerase activated by CMV kinase or HSV/VZV thymidine kinase |
|
Which one is more toxic: Acyclovir or Ganciclovir?
|
Ganciclovir
can cause leukopenia, neutropenia, throbocytopenia, renal toxicity. |
|
Foscarnet
MOA? Clinical use? |
viral DNA polymerase inhibitor; does not require activation by viral kinase
CMV retinitis in immunocompromised pts when ganciclovir fails in acyclovir-resistant HSV |
|
Protease inhibitor
common postfix? toxicity? |
all end in -navir; e.g. Squinavir, indinavir
hyperglycemia, lipodystrophy (sunken cheeks and buffalo humps) thrombocytopenia (indinavir) |
|
Enfuvirtide
MOA? |
fusion inhibitor by binding to viral gp41 subunit
|
|
Zidovudine
MOA? toxicity? |
nucleosides reverse transcriptase inhibitors
lactic acidosis megalobalstic anemia |
|
HAART
indication? |
highly active antiretroviral therapy
initiated when pts have low CD4 counts (< 500) or high viral load. also used as prophylactic tx in general population and during pregnancy |
|
Nevirapine, Efavirenz, Delavirdine
class? |
non-nucleoside reverse transcriptase inhibitor used in HIV therapy
|
|
List antibiotics to avoid in pregnancy (9).
|
SAFE Moms Take Really Good Care
Sulfonamides: kernicterus Aminoglycosides: ototoxicity Fluoroquinolone: cartilage damage Erythromycin: acute cholestatic hepatitis in mom (and clarithromycin is embryotoxic) Metronidazole: mutagenesis Tetracycline: discolored teeth, inhibition of bone growth Ribavirin: teratogenic Griseofulvin: teratogenic Chloramphenicol: gray baby syndrome |
|
Rifampin
clinical use? |
1. Mtb (must use with other agents such as INH, Prayzinamide Ethambutol)
2. delays resistance to dapsone when used for leprosy 3. prophylaxis for meningococcal infection 4. chemoprophylaxis for contacts with children with Haemophilus influenzae type B |