Quinolones and the Clinical Laboratory
- What are quinolones?
- How many fluoroquinolones are approved for human use?
- Why are there so many fluoroquinolones on the market?
- Why is resistance to quinolones important?
- How does resistance to quinolones develop?
- What causes different levels of fluoroquinolone resistance?
- Can an isolate be resistant to one quinolone and susceptible to another?
- What organisms can be resistant to quinolones?
What are quinolones?
Quinolones are antimicrobial agents effective in the treatment of selected community-acquired and nosocomial infections. They are usually administered orally, but some can be given intravenously for treatment of serious infections.
Quinolones are bactericidal and exhibit concentration-dependent killing. The targets of quinolone activity are the bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication and transcription.
Quinolone activity: Early quinolones, such as nalidixic acid, had poor systemic distribution and limited activity and were used primarily for Gram-negative urinary tract infections. The next generation of quinolone agents, the fluoroquinolones (i.e., ciprofloxacin, ofloxacin, norfloxacin, lomefloxacin, and enoxacin), were more readily absorbed and displayed increased activity against Gram-negative bacteria. Newer fluoroquinolones (i.e., levofloxacin, sparfloxacin, trovafloxacin, and grepafloxacin) are broad-spectrum agents with enhanced activity against many Gram-negative and gram-positive organisms.
How many fluoroquinolones are approved for human use?
In the United States, nine fluoroquinolones are currently approved for human use. Norfloxacin was the first fluoroquinolone approved for human use (1986), followed by ciprofloxacin (1987), ofloxacin (1990), enoxacin (1991), lomefloxacin (1992), levofloxacin (1996), trovafloxacin (1997), gatifloxacin (1999), and moxifloxacin (1999). Gemifloxacin is currently undergoing clinical investigation in the United States.
Why are there so many fluoroquinolones on the market?
As a class, the newer fluoroquinolones possess many characteristics that make them useful antimicrobial agents, including a broad spectrum of activity against Gram-negative and gram-positive organisms, good oral absorption and tissue penetration, relatively long serum elimination half-lives that allow once or twice daily dosing, predictable drug-drug interactions, and a relatively low incidence of serious side effects. However, not all fluoroquinolones show all of these characteristics. In addition, several of the fluoroquinolones continue to be expensive alternatives to other regimens.
Why is resistance to quinolones important?
- Resistance to quinolones limits drug selection for treatment of many infections.
- Organisms resistant to quinolones often are resistant to other classes of antimicrobials.
- Quinolones are frequently prescribed before culture results are known. Prompt reporting of resistance reduces the risk of complications of illnesses caused by inadvertent treatment of resistant organisms.
- Reporting susceptibilities to various quinolones provides the information necessary to choose an appropriate therapy that will minimize the selection of mutations leading to resistance.
How does resistance to quinolones develop?
Quinolones inhibit two enzymes that are required for bacterial DNA synthesis, i.e., DNA gyrase and topoisomerase IV. Resistance to quinolones occurs through chromosomal mutations in the genes encoding these enzymes and by porin and efflux mutations. The enzyme mutations result in an alteration of the target region where the drug binds to the enzyme; the drug exhibits reduced affinity for the target site and becomes ineffective. Mutations that result in alterations of the outer membrane porin proteins of Gram-negative organisms lead to decreased permeability of the drug through the outer membrane so less drug reaches the target enzyme. Mutations that enhance the organism's efflux capability increase the amount of drug pumped out of the cell. The enzyme target site, porin, and efflux mutations may result from the selective pressure of exposure of the organism to antimicrobial agents during therapy and may cause treatment failure.
What causes different levels of fluoroquinolone resistance?
The number and location of mutations affecting critical sites determine the level of resistance. Organisms may have alterations in more than one enzyme target site and, in Gram-negative organisms, may contain more than one porin change. Many resistant organisms have multiple enzyme target site, porin, and efflux mutations, producing high-level resistance to quinolones. In contrast, organisms with decreased susceptibility produced only by porin changes usually have lower minimum inhibitory concentrations (MICs).
Can an isolate be resistant to one quinolone and susceptible to another?
Yes. The fluoroquinolone susceptibility profile for each clinical isolate is determined by the number and location of mutational changes in specific enzyme target sites, porin proteins, and efflux mechanisms. The effect of each mutation in an isolate is not equivalent for all fluoroquinolones, due to variations of the chemical structures among this class of agents. Therefore, an organism with one or more mutations may have resistant MICs/zone sizes to one quinolone but have intermediate or susceptible MICs/zone sizes to another quinolone.
During therapy, the potential exists for an organism with a single mutation to acquire a second mutation, leading to high-level resistance. After multiple mutations occur, an organism is generally highly resistant to all quinolones.
What organisms can be resistant to quinolones?
Resistance to quinolones has been reported in a variety of important bacterial pathogens, including Escherichia coli, Klebsiella pneumoniae, and other enteric organisms; Pseudomonas aeruginosa; Chlamydia trachomatis and Mycoplasma pneumoniae; Campylobacter jejuni; Burkholderia cepacia; Stenotrophomonas maltophilia; Neisseria gonorrhoeae; Staphylococcus aureus (especially oxacillin-resistant strains); Enterococcus faecium; and Streptococcus pneumoniae.