In common usage, an antibiotic (from the Ancient Greek: ἀντί – anti, "against", and βίος – bios, "life") is a substance or compound that kills or inhibits the growth of bacteria. Antibiotics belong to the broader group of antimicrobial compounds, used to treat infections caused by microorganisms, including fungi and protozoa.
The term "antibiotic" was coined by Selman Waksman in 1942 to describe any substance produced by a microorganism that is antagonistic to the growth of other microorganisms in high dilution. This original definition excluded naturally occurring substances that kill bacteria but are not produced by microorganisms (such as gastric juice and hydrogen peroxide) and also excluded synthetic antibacterial compounds such as the sulfonamides. Many antibiotics are relatively small molecules with a molecular weight less than 2000 Da.
With advances in medicinal chemistry, most antibiotics are now semisynthetic — modified chemically from original compounds found in nature, as is the case with beta-lactams (which include the penicillins, produced by fungi in the genus Penicillium, the cephalosporins, and the carbapenems). Some antibiotics are still produced and isolated from living organisms, such as the aminoglycosides, and others have been created through purely synthetic means: the sulfonamides, the quinolones, and the oxazolidinones. In addition to this origin-based classification into natural, semisynthetic, and synthetic, antibiotics may be divided into two broad groups according to their effect on microorganisms: those that kill bacteria are bactericidal agents, while those that only impair bacterial growth are known as bacteriostatic agents.
Antibiotic resistance
The emergence of antibiotic resistance is an evolutionary process that is based on selection for organisms that have enhanced ability to survive doses of antibiotics that would have previously been lethal. Antibiotics like Penicillin and Erythromycin which used to be one-time miracle cures are now less effective because bacteria have become more resistant. Antibiotics themselves act as a selective pressure which allows the growth of resistant bacteria within a population and inhibits susceptible bacteria. Antibiotic selection of pre-existing antibiotic resistant mutants within bacterial populations was demonstrated in 1943 by the Luria-Delbrück experiment. Survival of bacteria often results from an inheritable resistance. Any antibiotic resistance may impose a biological cost and the spread of antibiotic resistant bacteria may be hampered by the reduced fitness associated with the resistance which proves disadvantageous for survival of the bacteria when antibiotic is not present. Additional mutations, however, may compensate for this fitness cost and aids the survival of these bacteria.
The underlying molecular mechanisms leading to antibiotic resistance can vary. Intrinsic resistance may naturally occur as a result of the bacteria's genetic makeup. The bacterial chromosome may fail to encode a protein which the antibiotic targets. Acquired resistance results from a mutation in the bacterial chromosome or the acquisition of extra-chromosomal DNA. Antibiotic-producing bacteria have evolved resistance mechanisms which have been shown to be similar to and may have been transferred to antibiotic resistant strains. The spread of antibiotic resistance mechanisms occurs through vertical transmission of inherited mutations from previous generations and genetic recombination of DNA by horizontal genetic exchange. Antibiotic resistance exchanged between different bacteria by plasmids that carry genes which encode antibiotic resistance which may result in co-resistance to multiple antibiotics. These plasmids can carry different genes with diverse resistance mechanisms to unrelated antibiotics but because they are located on the same plasmid multiple antibiotic resistance to more than one antibiotic is transferred. Alternatively, cross-resistance to other antibiotics within the bacteria results when the same resistance mechanism is responsible for resistance to more than one antibiotic is selected for.
Antibiotics by class
Generic name
Brand names
Common uses
Possible side effects
Mechanism of action
Aminoglycosides
Amikacin
Amikin
Infections caused by Gram-negative bacteria, such as Escherichia coli and Klebsiella particularly Pseudomonas aeruginosa. Effective against Aerobic bacteria (not obligate/facultative anaerobes) and tularemia.
Hearing loss
Vertigo
Kidney damage
Binding to the bacterial ribosomal subunit (some work by binding to the 50S subunit), inhibiting the translocation of the peptidyl-tRNA from the A-site to the P-site and also causing misreading of mRNA, leaving the bacterium unable to synthesize proteins vital to its growth.
Gentamicin
Garamycin
Kanamycin
Kantrex
Neomycin
Mycifradin
Netilmicin
Netromycin
Streptomycin
Tobramycin
Nebcin
Paromomycin
Humatin
Ansamycins
Geldanamycin
Experimental, as antitumor antibiotics
Herbimycin
Carbacephem
Loracarbef
Lorabid
prevents bacterial cell division by inhibiting cell wall synthesis.
Carbapenems
Ertapenem
Invanz
Bactericidal for both Gram-positive and Gram-negative organisms and therefore useful for empiric broad-spectrum antibacterial coverage. (Note MRSA resistance to this class.)
Gastrointestinal upset and diarrhea
Nausea
Seizures
Headache
Rash and allergic reactions
Inhibition of cell wall synthesis
Doripenem
Finibax
Imipenem/Cilastatin
Primaxin
Meropenem
Merrem
Cephalosporins (First generation)
Cefadroxil
Duricef
Gastrointestinal upset and diarrhea
Nausea (if alcohol taken concurrently)
Allergic reactions
Same mode of action as other beta-lactam antibiotics: disrupt the synthesis of the peptidoglycan layer of bacterial cell walls.
Cefazolin
Ancef
Cefalotin or Cefalothin
Keflin
Cefalexin
Keflex
Cephalosporins (Second generation)
Cefaclor
Ceclor
Gastrointestinal upset and diarrhea
Nausea (if alcohol taken concurrently)
Allergic reactions
Same mode of action as other beta-lactam antibiotics: disrupt the synthesis of the peptidoglycan layer of bacterial cell walls.
Cefamandole
Mandole
Cefoxitin
Mefoxin
Cefprozil
Cefzil
Cefuroxime
Ceftin, Zinnat
Cephalosporins (Third generation)
Cefixime
Suprax
Gastrointestinal upset and diarrhea
Nausea (if alcohol taken concurrently)
Allergic reactions
Same mode of action as other beta-lactam antibiotics: disrupt the synthesis of the peptidoglycan layer of bacterial cell walls.
Cefdinir
Omnicef, Cefdiel
Cefditoren
Spectracef
Cefoperazone
Cefobid
Cefotaxime
Claforan
Cefpodoxime
Vantin
Ceftazidime
Fortaz
Ceftibuten
Cedax
Ceftizoxime
Ceftriaxone
Rocephin
Cephalosporins (Fourth generation)
Cefepime
Maxipime
Gastrointestinal upset and diarrhea
Nausea (if alcohol taken concurrently)
Allergic reactions
Same mode of action as other beta-lactam antibiotics: disrupt the synthesis of the peptidoglycan layer of bacterial cell walls.
Cephalosporins (Fifth generation)
Ceftobiprole
Used to treat MRSA
Gastrointestinal upset and diarrhea
Nausea (if alcohol taken concurrently)
Allergic reactions
Same mode of action as other beta-lactam antibiotics: disrupt the synthesis of the peptidoglycan layer of bacterial cell walls.
Nausea, vomiting, and diarrhea (especially at higher doses)
Jaundice
inhibition of bacterial protein biosynthesis by binding irreversibly to the subunit 50S of the bacterial ribosome, thereby inhibiting translocation of peptidyl tRNA.
Clarithromycin
Biaxin
Dirithromycin
Dynabac
Erythromycin
Erythocin, Erythroped
Roxithromycin
Troleandomycin
TAO
Telithromycin
Ketek
Pneumonia
Visual Disturbance, Liver Toxicity.
Spectinomycin
Antimetabolite, Anticancer
Monobactams
Aztreonam
Azactam
Same mode of action as other beta-lactam antibiotics: disrupt the synthesis of the peptidoglycan layer of bacterial cell walls.
Penicillins
Amoxicillin
Novamox, Amoxil
Wide range of infections; penicillin used for streptococcal infections, syphilis, and Lyme disease
Gastrointestinal upset and diarrhea
Allergy with serious anaphylactic reactions
Brain and kidney damage (rare)
Same mode of action as other beta-lactam antibiotics: disrupt the synthesis of the peptidoglycan layer of bacterial cell walls.
Ampicillin
Principen
Azlocillin
Carbenicillin
Cloxacillin
Tegopen
Dicloxacillin
Dynapen
Flucloxacillin
Floxapen
Mezlocillin
Meticillin
Nafcillin
Oxacillin
Penicillin
Piperacillin
Ticarcillin
Polypeptides
Bacitracin
Eye, ear or bladder infections; usually applied directly to the eye or inhaled into the lungs; rarely given by injection
Kidney and nerve damage (when given by injection)
Inhibits isoprenyl pyrophosphate, a molecule which carries the building blocks of the peptidoglycan bacterial cell wall outside of the inner membrane
Colistin
Interact with the bacterial cytoplasmic membrane, changing its permeability.
Nausea (rare), irreversible damage to central nervous system (uncommon), tendinosis (rare)
inhibit the bacterial DNA gyrase or the topoisomerase IV enzyme, thereby inhibiting DNA replication and transcription.
Enoxacin
Penetrex
Gatifloxacin
Tequin
Levofloxacin
Levaquin
Lomefloxacin
Maxaquin
Moxifloxacin
Avelox
Norfloxacin
Noroxin
Ofloxacin
Floxin, Ocuflox
Trovafloxacin
Trovan
Withdrawn
Grepafloxacin
Raxar
Withdrawn
Sparfloxacin
Zagam
Withdrawn
Temafloxacin
Omniflox
Withdrawn
Sulfonamides
Mafenide
Urinary tract infections (except sulfacetamide and mafenide); mafenide is used topically for burns
Nausea, vomiting, and diarrhea
Allergy (including skin rashes)
Crystals in urine
Kidney failure
Decrease in white blood cell count
Sensitivity to sunlight
Folate synthesis inhibition. They are competitive inhibitors of the enzyme dihydropteroate synthetase, DHPS. DHPS catalyses the conversion of PABA (para-aminobenzoate) to dihydropteroate, a key step in folate synthesis. Folate is necessary for the cell to synthesize nucleic acids (nucleic acids are essential building blocks of DNA and RNA), and in its absence cells will be unable to divide.
Syphilis, chlamydial infections, Lyme disease, mycoplasmal infections, acne rickettsial infections, malaria. Note: Malaria is caused by a protist and not a bacterium.
Potentially Permanent
Gastrointestinal upset
Sensitivity to sunlight
Potential toxicity to mother and fetus during pregnancy
Enamel hypoplasia (staining of teeth)
transient depression of bone growth
inhibiting the binding of aminoacyl-tRNA to the mRNA-ribosome complex. They do so mainly by binding to the 30S ribosomal subunit in the mRNA translation complex.
Doxycycline
Vibramycin
Minocycline
Minocin
Oxytetracycline
Terramycin
Tetracycline
Sumycin, Achromycin V, Steclin
Others
Arsphenamine
Salvarsan
Spirochaetal infections (obsolete)
Chloramphenicol
Chloromycetin
meningitis,
Rarely: aplastic anemia.
Inhibits bacterial protein synthesis by binding to the 50S subunit of the ribosome
Clindamycin
Cleocin
acne infections, prophylaxis before surgery
Lincomycin
Lincocin
acne infections, prophylaxis before surgery
Ethambutol
Myambutol
Antituberculosis
Fosfomycin
Monurol
Fusidic acid
Fucidin
Furazolidone
Isoniazid
I.N.H.
Antituberculosis
Linezolid
Zyvox
VRSA
Metronidazole
Flagyl
Giardia
Mupirocin
Bactroban
Nitrofurantoin
Macrodantin, Macrobid
Platensimycin
Pyrazinamide
Antituberculosis
Quinupristin/Dalfopristin
Syncercid
Rifampicin (Rifampin in US)
mostly Gram-positive and mycobacteria
Reddish-orange sweat, tears, and urine
Binds to the β subunit of RNA polymerase to inhibit transcription
Thiamphenicol
Gram-negative, Gram-positive, anaerobes. Widely used in veterinary medicine.
Lacks known anemic side-effects.
A chloramphenicol analog. May inhibit bacterial protein synthesis by binding to the 50S subunit of the ribosome
Regarding the effect: I do notice an increase in bloodflow and a better
stamina using the pills (I use 50mg). A side-effect I have noticed is that
my nose clogs up so I seem like I have a cold for an hour or so after taking
one pill. No other side-effects than that.