micro 260 antimicrobial agents

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  • 8/10/2019 Micro 260 Antimicrobial Agents

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    Chapter 12 Drugs, Microbes, Hos.~

    The Elements of Chemotherapy

    Building Your Knoledge,

    1) In 1900, what percentage of all children in the United States died of infectious disease beforeage 51 . .

    ) !"plain the concept of selecti#e to"icit$ .

    %

    &) 'esign the perfect antibiotic. (lease consider ease of adinistration, target icrobe, distribution

    throughout the bod$ *if necessar$ for the targeted icrobe) length of acti#it$, host to"icit$ and

    potential for the de#elopent of antibiotic resistance to the drug .

    . .

    'oes the perfect antibiotic actuall$ e"ist+ h$ or wh$ not+

    -) opare and contrast narrow and broad spectru antibiotics .

    If $ou /now what the causati#e agent of a disease is, which would $ou want to use+

    If a patient is septic *seriousl$ ill) with an un/nown organis, which would $ou recoend+

    5) here do ost antibiotics originate, in the lab or fro nature+

    h$ is this the case+

    ..

    ) hich drugs are ost selecti#el$ to"ic to bacterial cells *in general)+

    hich are the least selecti#el$ to"ic+

    h$+

    ~9%

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    ) 2re drugs that target the cell wall 3ore or less selecti#el$ to"ic than those that target the plasa

    ebrane+ h$+

    4) 2re ost penicillin and penicillin%li/e antibiotics ore effecti#e against acti#el$ growing cells, or

    old, dorant cells+ h$+

    2re the$ ore effecti#e against ra%positi#e or ra%negati#e cells+ h$+

    %.

    9) hat is copetiti#e inhibition and what does it ha#e to do with sulfonaide acti#it$ against

    bacterial cells+

    I6).h$ don3t sulfonaides daage host cells as uch as the$ do bacterial cells+

    11) 2re the ebrane%disrupting drugs generall$ used topicall$ *on bod$ surfaces) or adinisteredinternall$+ t ) ,

    1) 7ill in the diagra with se#eral e"aple antibiotics that target each of the following structures or

    processes in a bacterial cell.

    Block synthesis and repair

    >.

    Inhibit replication and transcription

    Inhibit gyrase (unwinding enzyes)

    Inhibit !"# polyerase

    ..

    Inhlbit $olic acid etabolis

    % 9& %I

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    1&) How is ost penicillin produced+,

    ,

    1-) ist & ebers of the penicillin fail$.

    a.

    b.

    ...

    c.,

    15) hat is the ad#antage of using sei%s$nthetic penicillins, li/e apicillin or nafcillin+

    1) h$ add cla#ulanic acid to penicillins *e.g., 2ugentin)+%,

    1) hat are the two a:or3probles that liit the usefulness of the penicillin antiicrobials+

    ,

    14) hat are cephalosporins+~, ;

    & .'

    How arethe$ generall$ adinistered+ h$+

    hat are the

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    &) hat are the bacillus antibiotics+

    hat is their echanis of action+

    h$ are the$ generall$ not gi#en s$steicall$+

    .

    -) 'escribe the new classes of antibiotics recentl$ disco#ered and appro#ed b$. the 7'2+

    &

    5) here do sulfaides coe fro+,

    How does this origin differ fro that of penicillins and cephalosporins+

    ) hat are fosof$cin and s$nercid+. t( ),

    h$ are the$ not widel$ used+r

    ,

    ) h$ are scientists hopeful that resistance to the@o"a=olidinones will be slow to de#elop+

    4) h$ did the ' change the recoendation fro ciproflo"acin to do"$c$cline for the treatent

    of anthra" in 001 +

    9) h$ are anti%fungals generall$ ore to"ic to huan tissues than antibacterial agents+

    &0) ist - separate antifungals and the conditions the$ treat.I

    !ntifun gal a gent Condition"s# treated,

    .

    &

    . .

    .

    .

    % 95 %8

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    &1) h$ are pol$enes effecti#e against fungal cells, but not bacterial cells+%,

    &) h$ are there few effecti#e anti%parasite drugs+

    hat drugs are used to treat alaria+

    hat drugs are used to treat roundwor+

    .

    &&) h$ is selecti#e to"icit$ so difficult to achie#e in anti%#iral therapies+

    ,

    &-) h$ are. #iral diseases li/e easles and ups fairl$ rare in the U.S.+

    &5) hat are & basic echaniss of action of anti%#iral agents+,

    a.

    b.

    c.

    &) h$ is the fact HIA is a retro#irus significant when designing anti%#iral therapies+

    &) How does chroosoal drug resistance originate+ 'oes this t$peof resistance spread in apopulation+

    .

    &4) hat 3is the difference between intrinsic and e"trinsic drug resistance+ hich is of ore concern+

    &9) hat are B factors+ 'o these spread through a bacterial population+

    ,

    ,

    % *+%

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    -0) 'escribe - distinct wa$s bacteria .a$becoe resistant to antibiotics the$ were once sensiti#e to .

    a .

    b.f

    c.

    d.

    -1) hat are beta%lactaases and what antiicrobial drugs do the$ confer resistance to+?

    -) 'o pups generall$ confer resistance to 1 t$pe of antiicrobial or an$+ h$+

    How do bacteria becoe resistant to rifapin or strepto$cin+

    -&) How do bacteria becoe resistant to sulfonaide+

    --) 'oes e"posure to an antibiotic increase or decrease the percentage of resistant cells in a

    population+ !"plain .

    -5) h$ does cobining drug therapies liit the spread of drug resistance+

    -) hat are prebiotics, probiotics and lantibiotics+

    ,

    ,

    &

    How does each pre#ent disease+

    % 9 % %

    ,

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    -) Chere are & a:or categories of antibiotic side%effects. Dae the .

    a.

    b.

    c.

    -4) h$ are the li#er and /idne$s often daaged b$ antibiotics+

    .

    -9) h$ are tetrac$clines not gi#en to pregnant woen or $oung children+

    50) How a$ antibiotics cause diarrhea+ *list wa$s)

    51) If a person ta/es penicillin once and does not ha#e an allergic reaction to it, does that ean the$

    are not allergic+3 !"plain, .

    ,

    5) hat & factors do doctors generall$ consider when choosing antiicrobial therapies+.

    a.

    b.

    c.

    5&) If the causati#e agent of a disease is un/nown, do doctors generall$ gi#e narrow%spectru or

    broad%spectru antibiotics+ h$+

    5-) hat ethods are coonl$ used to tell which antibiotics are ost and least effecti#e against a

    gi#en pathogen+ .,

    a.

    b.

    % 94%

    ,

    . ,

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    $rgani%ing Your Knoledge

    !ntimicrobial !gent

    penicillin

    sulfonaide

    chloroEuine

    gentaicin

    pol$$"ins .

    n$statin

    rifapicin

    ebenda=ole

    Mechanism of !ction oonl$ &sed to Treat

    etronida=ole

    riba#irin ,

    #-&

    aphotericin F

    chloraphenicol,

    tetrac$cline

    #anco$ci

    n

    .,

    ,

    %, '

    ,

    % 100%,

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    ,

    2ntiicrobial 'rug roup %

    , ,

    Gechanis of 2ction .Gechanis of ,.

    Besistance

    #anco$ci

    n .

    ,tetrac$cline ,

    .

    sulfonaide%

    ..

    rifapicin ,

    riba#irin. .

    pol$$"ins . . .

    ,

    ,

    penicillin .

    ,

    n$statin ,

    etroriida=ole &

    &

    ebenda=ole

    . gentaicinI

    I , ., i

    ,

    &

    chloroEuine

    .

    chloraphenicol ,

    2C &

    aphotericin F .

    (racticing .our Jnowledge

    1. hich of the following is D6C a coon

    target for antibacterial drugs+

    a. cell wall s$nthesis

    b. nucleic acid structure

    c. protein s$nthesis

    d. bacterial cell nucleus

    . 2ll of the following antibiotics target

    procar$otic ribosoes !K!(C .

    a. strepto$cin.

    b. cephale"iii