Micro chapter 12
Cell wall inhibitors
Block synthesis and repair (ex: PCNS and vancomycin)
Nucleic Acids (DNA/RNA) synthesis can be blocked at any step in it's pathway
Block synthesis of nucleotides (building blocks of DNA, RNA) Inhibit replication of DNA, RNA Stop transcription: DNA-->RNA Example: Cipro, AZT
Antibacterial Drugs Targeting DNA or RNA
Fluoroquinolones - Norfloxacin, Ciprofoxacin
Selective Toxicity
Goal of antimicrobial chemotherapy: administer a drug to an infected person, which destroys the infective agent without harming the host's cells (rather hard to achieve this goal)
Considerations in Selecting an Antimicrobial Drug: Three factors must be known
- The nature of the microorganism causing the infection - The degree of the microorganism's susceptibility to various drugs - The overall medical condition of the patient
Interferon (IFN): An Alternative to Artificial Drugs
Antiviral compound produced by cells of the body Often results in serious side effects - flu-like symptoms, depression, fatigue, diarrhea, nausea
Mechanisms of Drug Action
Inhibition of cell wall synthesis- selective Inhibition of nucleic acid structure and function Inhibition of protein synthesis- selective Interference with cell membrane structure or function Inhibition of folic acid synthesis- selective
Antimicrobial Drugs that Block Protein Synthesis
Inhibits protein synthesis by blocking any of the steps in translation: RNA -->protein
Superinfection: cephalosporin
Using a broad-spectrum cephalosporin for a urinary tract infection; destroys lactobacilli in the vagina; without the lactobacilli, Candida albicans can proliferate and cause a yeast infection
Therapeutic Index
What is the best drug to use? Lowest risk of side effects versus Highest probability of killing the pathogen Higher T.I. are better
superinfection
When beneficial species are destroyed, microbes that were once kept in small numbers can begin to overgrow and cause disease
Antibacterial Drugs Targeting Cell Membranes
Polymyxins, Daptomycin
Semisynthetic drugs
drugs that are chemically modified in the laboratory after being isolated from natural sources
Quinine
extracted from the bark of the cinchona tree
Biota
normal colonists or residents of healthy body surfaces - Usually harmless or beneficial bacteria - Small number can be pathogens
Antimicrobial Drugs that Affect the Bacterial Cell Wall
- Active cells must constantly synthesize new peptidoglycan and transport it to the proper place in the cell envelope - Penicillins and cephalosporins react with one or more of the enzymes required to complete this process - Known as Bactericidal antibiotics
Antiviral drugs: 3 modes of action
- Barring penetration of the virus into the host cell (Tamiflu) - Blocking the transcription (blocks DNA synthesis) and translation of viral molecules (Acyclovir, AZT) - Preventing the maturation of viral particles/release - Protease inhibitors
Interactions Between Microbes and Drugs: The Acquisition of Drug Resistance
- Can be intrinsic (will be resistant to any antimicrobial it produces) or acquired - Microbes become newly resistant to a drug after: Spontaneous mutations in critical chromosomal genes Acquisition of entire new genes or sets of genes via transfer from another species (plasmids called resistance (R) factors) - Specific Mechanisms of Drug Resistance
The Origins of Antimicrobial Drugs
- Chemists have created new drugs by altering the structure of naturally occurring antibiotics - Also Searching for metabolic compounds with antimicrobial effects in species other than bacteria and fungi (plants and animals)
Antimicrobial Drugs that Disrupt Cell Membrane Function
- Damaged membrane invariably results in death from disruption in metabolism or lysis - Specificity for particular microbial groups based on differences in the types of lipids in their cell membranes - Toxic to humans due to similarities in membrane structure - Polymyxins, Nystatin
Considerations in Selecting an Antimicrobial Drug: Identifying the Agent
- Direct examination of body fluids, sputum, or stool is a rapid initial method - The choice of drug will be based on experience with drugs that are known to be effective against the microbe: the "informed best guess"
Goal of antimicrobial drugs
- Disrupt the cell processes or structures of bacteria, fungi, and protozoa - Or inhibit virus replication
Antihelminthic Drug Therapy
- Flukes, tapeworms, and roundworms have greater similarities to human physiology - Using drugs to block their reproduction is usually not successful in eradicating adult worms - Most effective drugs immobilize, disintegrate, or inhibit the metabolism of all stages of the life cycle ex mebendazole, thiabendazole
Fluoroquinolones - Norfloxacin, Ciprofoxacin
- High potency, easily absorbed - Broad spectrum - Inhibit a wide variety of gram-positive and gram-negative bacterial species even in minimal concentrations
Fungal cells are eukaryotic, so present special problems
- Majority of chemotherapeutic drugs are designed to act on bacteria and are ineffective for fungal infections - Similarities between fungal and human cells- toxicity to humans - Lengthy duration of treatment - Nystatin, amphotericin B, Griseofulvin, miconazole
The Cephalosporin Group of Drugs
- Newer group - similar to penicillin - Currently account for a majority of all antibiotics administered - Broad spectrum - Most resistant to penicillinase - Fewer allergic reactions Other drugs targeting cell wall: bacitracin, vancomycin
Aminoglycoside Drugs
- Products of various species of soil actinomycetes in the genera Streptomyces and Micromonospora - Relatively broad spectrum because they inhibit protein synthesis - Streptomycin, Gentamicin, Tetracyclines, Erythromycin, Chloramphenicol, Clindamycin
Polymyxins, Daptomycin
- used in limited circumstances for infections not responsive to other drugs - toxic to kidneys
Interferon (IFN): An Alternative to Artificial Drugs: Known therapeutic benefits
-- Reducing the time of healing and some of the complications in certain infections - Preventing or reducing some symptoms of cold and papillomaviruses (HPV) - Slowing the progress of certain cancers
Penicillin
1St antibiotic - discovered by Fleming
Survey of Major Antimicrobial Drug Groups
About 260 different antimicrobial drugs Classified in 20 drug families Largest number of antimicrobial drugs are for bacterial infections
Antibacterial Drugs Targeting Protein Synthesis
Aminoglycoside Drugs
Metronidazole (Flagyl)
Amoebicide can also apply to infections by Giardia lamblia and Trichomonas vaginalis
Testing for the Drug Susceptibility of Microorganisms
Kirby Bauer Disc Diffusion Test
Disk Diffusion Assays
Kirby-Bauer Standardized conditions Zones of inhibition Larger zone indicates more susceptible Smaller zone indicates more resistant
Chemotherapy for Other Protozoan Infections
Metronidazole (Flagyl)
Penicillin group
Most end in the suffix -cillin All consist of three parts: a thiazolidine ring, a beta-lactam ring, and a variable side chain
Interactions Between Drug and Microbe
Most interfere with the function of enzymes required to synthesize or assemble macromolecules or destroy structures already formed in the cell
New Approaches to Antimicrobial Therapy
Often researchers try to find new targets in the bacterial cell and custom-design drugs that aim for them Targeting iron-scavenging capabilities of bacteria
Superinfection: Oral therapy
Oral therapy with tetracyclines, clindamycin, and broad-spectrum penicillins and cephalosporins is associated with antibiotic-associated colitis
Antimalarial Drugs
Quinine and Its Relatives
Antiviral Chemotherapeutic Agents: Selective toxicity
almost impossible to achieve because a single metabolic system is responsible for the well-being of both virus and host
narrow spectrum (limited spectrum)
antimicrobials effective against a limited array of microbial types
broad spectrum (extended spectrum)
antimicrobials effective against a wide array of microbial types
chemotherapeutic drug
any chemical used in the treatment, relief, or prophylaxis of disease
Antiviral Chemotherapeutic Agents: Several antiviral drugs
been developed that target specific points in the infectious cycle of viruses
Folic acid synthesis
block pathways and inhibit metabolism (ex: sulfa drugs)
Sulfa drugs
block the enzyme need for folic acid synthesis, thus DNA cannot be synthesized.
Sulfonamides (Sulfa - 1st antimicrobial)
blocks DNA synthesis by competitive inhibition
Cell membrane
cause loss of selective permeability (ex: polymyxins and daptomycin)
The Origins of Antimicrobial Drugs: Antibiotics
common metabolic products of aerobic bacteria and fungi - more than ½ of antibiotics come from: Bacteria: Streptomyces and Bacillus Molds: Penicillium and Cephalosporium
Chemotherapeutic agents
described with regard to their origin, range of effectiveness, and whether they are naturally produced or chemically synthesized
broad-spectrum antimicrobial
destroys both infectious agents but also some beneficial species
Probiotics
ingesting live microorganisms
Prebiotics
ingesting nutrients that encourage the growth of beneficial microbes soybean, onion, chicory root, asparagus etc
Protein synthesis
inhibitors acting on ribosomes
DNA/RNA
inhibits replication and transcription
Disadvantage: Penicillin
some are destroyed by bacteria that produce penicillinase (cleaves beta-lactam ring). Another disadvantage: allergies
Antibiotics
substance produced by the natural metabolic processes of some microorganisms that can inhibit or destroy other microorganisms
Folic acid
synthesized by the bacterial cell and necessary for DNA synthesis. In eukaryotes folic acid is supplied in the diet
Synthetic drugs
the use of chemical reactions to synthesize antimicrobial compounds in the laboratory
Antimicrobial chemotherapy
the use of chemotherapeutic drugs to control infection
Drugs should be selectively toxic
they kill or inhibit microbial cells without damaging host tissues
Prokaryotic ribosomes are different from eukaryotic ribosomes
thus a drug affecting a bacterial cell will not affect a eukaryotic cell (you) - Good example of Selective Toxicity
Prophylaxis
use of drug to prevent imminent infection of a person at risk