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Bacterial chromosome
circular
Eukaryotic chromosome
linear in nucleus
Eukaryotic Ribosomes
40S, 60S, 80S
Bacterial ribosomes
30S, 50S, 70S
Cell wall
bacteria have this, most human cells do not
Bacterial DNA modifying enzymes
gyrase, topoisomerase IV
Folic acid synthesis
done by bacteria, not by human cells
Plasmid
loop of DNA separate from the chromosome in bacteria that replicate separately and give the bacteria extra genes
Capsule
bacterial covering made of polysaccharides that prevents phagocytosis and aids in attachment; responsible for differences in serotypes
Bactericidal agents
kill bacteria
Bacteriostatic agents
Inhibit bacterial growth
DNA gyrase
enzyme that allows bacteria to unwind their DNA for replication, lethal to bacteria if inhibited
topoisomerase IV
cuts DNA to relieve twisting forces during unwinding and replication, lethal to bacteria if inhibited
folic acid
humans acquire this from diet, cofactor in DNA precursor synthesis of thymidine, bacteria synthesize it using enzymes using dihydropteroate, PABA, and glutamic acid, inhibition of this synthesis pathway is lethal to bacteria
folic acid synthesis enzymes
dihydropteroate synthase and dihydrofolate reductase
Aminoglycosides
water-soluble, bactericidal, bind to 30S subunit, cause misreading mRNA, forms aberrant proteins that kill the cell
Tetracyclines
bacteriostatic, protein synthesis inhibitor, binds to 30S ribosome, prevents incoming tRNA from binding to the A site
Macrolides
bacteriostatic, protein synthesis inhibitor, bind to 50S subunit in the P-site, inhibit peptide transfer, shortened peptides are formed
Sulfamethoxazole
inhibits dihydropteroate synthase
Trimethoprim
inhibits dihydrofolate reductase
Nonsterile sites
mouth, sputum, GI tract, skin, outer parts of the female reproductive tract
Sterile sites
internal organs, blood, CSF, urine, lungs, biliary tract, liver, kidneys, spleen, pancreas
Colonization
presence of microorganisms that are not causing disease
Infection
presence of microorganisms that are causing disease
Empiric therapy
broad-spectrum agents to treat suspected pathogens
Definitive therapy
treating known pathogens when sensitivity results are available
Nose
colonized by Staphylococcus aureus
Mouth
colonized by Viridans streptococci and anaerobes
Upper respiratory tract
colonized by Streptococci, viridans streptococci, S. pyogenes, S. pneumonia, Haemophilus influenza, and Moxarella catarrhalis
Lower respiratory tract
colonized by Streptococcus pneumonia, Haemophilus influenza, and atypicals such as mycoplasma pneumoniae, chlamydia pneumoniae, and legionella sp.
Skin
colonized by Staphylococcus epidermidis, Staphylococcus aureus, and Streptococci, especially S. pyogenes
GI tract
colonized by enteric Gram-negative rods such as E. coli and Klebsiella, anaerobes such as B. fragilis, Enterococci, and Streptococci
Urinary tract
colonized by E. coli, S. saprophyticus, and group B streptococci
Staphylococcus aureus
gram positive coccus in clusters, catalase positive, coagulase positive
MSSA
nafcillin, oxacillin, cefazolin
MRSA
vancomycin IV, daptomycin, linezolid
Staphylococcus epidermidis
gram positive coccus in clusters, catalase positive, coagulase negative
MSSE
nafcillin, oxacillin, cefazolin
MRSE
vancomycin, daptomycin, linezolid with or without rifampin
Staphylococcus saprophyticus
gram positive coccus in clusters, catalase positive, coagulase negative, treated with Bactrim or nitrofurantoin
Viridans streptococci
gram positive cocci in chains and pairs, alpha-hemolytic, treated with penicillin or amoxicillin
Streptococcus pneumoniae
gram positive coccus in pairs, alpha-hemolytic, treated with penicillin, azithromycin, ceftriaxone, respiratory fluoroquinolones, or vancomycin
Streptococcus pyogenes
group A, gram positive coccus in chains and pairs, beta-hemolytic, treated with penicillin and amoxicillin
Streptococcus agalactiae
group B, gram positive coccus in chains and pairs, beta-hemolytic, lives in GI and female reproductive tracts, treated with penicillin and amoxicillin
Enterococcus faecalis/faecium
group D, gram positive coccus in chains and pairs, gamma-hemolytic, treated with ampicillin or vancomycin with or without an aminoglycoside
Vancomycin resistant enterococcus
treated with daptomycin or linezolid
mecA gene
causes S. aureus to be resistant to methicillin
Biofilms
glycocalyx-producing strains of S. epidermidis make these, allowing them to live on and cause infectious through prosthetic valves and indwelling catheters, infections with these can be more challenging to treat
Alpha hemolytic
partial lysis of RBCs forming a green zone
Beta hemolytic
complete lysis of RBCs, forming a clear zone
Gamma hemolytic
no lysis of RBCs
Amoxicillin
Amoxil
Amoxil therapeutic class
beta lactam, amino-penicillin
Amoxicillin/clavulanate
Augmentin
Augmentin therapeutic class
beta lactam, amino-penicillin/PO beta-lactamase inhibitor
Ampicillin/sulbactam
Unasyn
Unasyn therapeutic class
beta-lactam, amino-penicillin/IV beta-lactamase inhibitor
Piperacillin/tazobactam
Zosyn
Zosyn therapeutic class
beta lactam, penicillin/beta-lactamase inhibitor
cefazolin
Ancef
Ancef therapeutic class
beta lactamase, 1st generation cephalosporin
cephalexin
Keflex
Keflex therapeutic class
beta lactam, 1st generation cephalosporin
Cefuroxime
Ceftin
Ceftin therapeutic class
beta lactam, 2nd generation cephalosporin
ceftriaxone
Rocephin
Rocephin therapeutic class
beta lactam, 3rd generation cephalosporin
cefepime
Maxipime
Maxipime therapeutic class
beta lactam, 4th generation cephalosporin
meropenem
Merrem
Merrem therapeutic class
carbapenem
imipenem
Primaxin
Primaxin therapeutic class
carbapenem
vancomycin
Vancocin
Vancocin therapeutic class
glycopeptide
daptomycin
Cubicin
Cubicin therapeutic class
lipopeptide
linezolid
Zyvox
Zyvox therapeutic class
lipoglycopeptide
azithromycin
Zithromax
Zithromax therapeutic class
macrolide
ciprofloxacin
Cipro
Cipro therapeutic class
fluoroquinolone
levofloxacin
Levaquin
Levaquin therapeutic class
fluoroquinolone
sulfamethoxazole/trimethoprim
Bactrim
Bactrim therapeutic class
sulfonamide
Beta-lactam mechanism of action
inhibits bacterial cell-wall synthesis by binding to penicillin-biding proteins, which stop peptoglycan synthesis
carbapenem mechanism of action
inhibits bacterial cell-wall synthesis by binding to penicillin-biding proteins, which stop peptoglycan synthesis
Glycopeptide mechanism of action
prevents glycopeptide polymerization by binding to D-alanyl-D-alanine part of the cell wall precursor, inhibiting bacterial cell wall synthesis
Lipoglycopeptide mechanism of action
binds to bacterial 23S rRNA from the 50S subunit, preventing the formation of a whole ribosome, bacteriostatic against enterococci and staphylococci and bactericidal against most streptococci
Lipopeptide mechanism of action
binds to cell membrane components, causes depolarization which inhibits the synthesis of DNA, RNA, and proteins, bactericidal
fluoroquinolone mechanism of action
inhibits DNA gyrase