Emerging Mechanisms of Fluoroquinolone Resistance: Special Issue
Emerging Mechanisms of Fluoroquinolone Resistance: Special Issue
Emerging Mechanisms of
Fluoroquinolone Resistance
David C. Hooper
Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA
Broad use of fluoroquinolones has been followed by emergence of resistance, which has been due
mainly to chromosomal mutations in genes encoding the subunits of the drugs’ target enzymes, DNA gyrase
and topoisomerase IV, and in genes that affect the expression of diffusion channels in the outer membrane
and multidrug-resistance efflux systems. Resistance emerged first in species in which single mutations were
sufficient to cause clinically important levels of resistance (e.g., Staphylococcus aureus and Pseudomonas
aeruginosa). Subsequently, however, resistance has emerged in bacteria such as Campylobacter jejuni,
Escherichia coli, and Neisseria gonorrhoeae, in which multiple mutations are required to generate clinically
important resistance. In these circumstances, the additional epidemiologic factors of drug use in animals
and human-to-human spread appear to have contributed. Resistance in Streptococcus pneumoniae, which
is currently low, will require close monitoring as fluoroquinolones are used more extensively for treating
respiratory tract infections.
The fluoroquinolone class of antimicrobial agents has reaction results in introduction (or removal) of DNA
had broad acceptance in hospitalized and community supercoils, thus affecting the negative supercoiling of DNA
patients, and usage appears to be increasing (1,2). Although necessary to initiate DNA replication and remove positive
some members of the class (temafloxacin, grepafloxacin, and supercoils that accumulate before an advancing replication
trovafloxacin) have been withdrawn or restricted because of fork. For topoisomerase IV, the topoisomerization reaction
adverse events, new members continue to be developed and results in separation of the interlocking of daughter DNA
approved (gatifloxacin and moxifloxacin). The last six strands that develop during replication; this facilitates the
released fluoroquinolones are for treating patients with segregation of daughter DNA molecules into daughter cells.
respiratory tract infections, the single most common group of In both cases, fluoroquinolones appear to trap the enzyme on
infections (3). This fact, plus the convenience of DNA during the topoisomerization reaction, forming a
fluoroquinolones (once or twice a day oral dosing), suggests physical barrier to the movement of the replication fork (4),
that use will increase (1). RNA polymerase (5), and DNA helicase (6). The collision of
As we approach the halfway point of the second decade of the replication fork with these trapped complexes triggers
fluoroquinolone use, resistance has already emerged in some other poorly defined events within the cell that ultimately
species of bacteria and some clinical settings. We examine the result in cell death.
mechanisms of fluoroquinolone resistance and discuss
epidemiologic factors that may have contributed to the Mechanisms of Fluoroquinolone Resistance
prevalence of antibiotic resistance in clinical settings. In all species studied, mechanisms of fluoroquinolone
resistance include one or two of the three main mechanistic
Mechanism of Fluoroquinolone Action categories, alterations in the drug target, and alterations in
Fluoroquinolones (and earlier quinolones) are novel the permeation of the drug to reach its target. No specific
among antimicrobial agents in clinical use because they quinolone-modifying or -degrading enzymes have been found
directly inhibit DNA synthesis. Inhibition appears to occur as a mechanism of bacterial resistance to fluoroquinolones,
by interaction of the drug with complexes composed of DNA although some fungi can degrade quinolones by metabolic
and either of the two target enzymes, DNA gyrase and pathways (7).
topoisomerase IV. These enzymes are structurally related to
each other, both being tetrameric with pairs of two different Alterations in Target Enzymes
subunits. The GyrA and GyrB subunits of DNA gyrase are Most extensively studied have been alterations in target
respectively homologous with the ParC and ParE subunits of enzymes, which are generally localized to specific domains of
topoisomerase IV. Both enzymes are type 2 topoisomerases, each subunit type. These alterations arise from spontaneous
which act by breaking both strands of a segment of DNA, mutations in the genes encoding the enzyme subunits and
passing another segment through the break, and then thus can exist in small numbers (1 in 106 to 1 in 109 cells) in
resealing the break. For DNA gyrase, this topoisomerization large bacterial populations. With GyrA and ParC subunits of
resistant bacteria, amino acid changes are generally localized
to a region of the enzyme in the amino terminus that contains
Address for correspondence: David C. Hooper, Division of Infectious the active site, a tyrosine that is covalently linked to the
Diseases, Massachusetts General Hospital, 55 Fruit Street, Boston, broken DNA strand during enzyme action. Resistance-
MA 02114-2696, USA; fax: 617-726-7416; e-mail: [email protected] causing amino acid changes are also clustered in three
dimensions, based on the structure of a fragment of GyrA that or killed by these concentrations. Furthermore, the greater
has been solved by x-ray crystallography, suggesting that this the extent to which a fluoroquinolone has similar (and
region constitutes part of a quinolone-binding site on the ultimately equal) potency against both enzyme targets, the
enzyme (8). One of the common resistance mutations in GyrA, lower the MIC increment for a first-step drug target mutant.
which causes a change from serine at position 83 to Thus, for drugs with low increments in resistance for first-
tryptophan, causes reduced binding of norfloxacin to the step mutants because of similar activities against both target
gyrase-DNA complex (9). enzymes, the extent to which drug concentrations can exceed
For the GyrB and ParE subunits of resistant bacteria, the MIC of first-step mutants may be enhanced. These
amino acid changes, when present (mutations in these principles would predict that selection of fluoroquinolone
subunits are much less common than those in GyrA or ParC), resistance could occur readily with ciprofloxacin against
are usually localized to the mid-portion of the subunit in a species such as Staphylococcus aureus and Pseudomonas
domain involved in interactions with their complementary aeruginosa, organisms in which single mutations cause MICs
subunits (GyrA and ParC, respectively). The original crystal of ciprofloxacin that approach or exceed achievable serum
structure of yeast topoisomerase II, which is related to DNA concentrations. This prediction has been borne out by
gyrase and topoisomerase IV, had suggested that this surveillance data (16).
resistance-determining domain was not in proximity to the
resistance-determining domains of GyrA and ParC (10); Alterations in Drug Permeation
however, structures of other enzyme conformations suggested To reach their targets in the cell cytoplasm,
that the resistance-determining regions of both types of fluoroquinolones must cross the cytoplasmic membrane and,
subunits might be in proximity during certain parts of the in gram-negative bacteria, the outer membrane as well.
enzyme catalytic cycle, perhaps defining an enzyme Fluoroquinolones are sufficiently small and have charge
conformation to which quinolones bind (11). No crystal characteristics that allow them to cross the outer membrane
structures in which a quinolone is bound to the enzyme-DNA through porin proteins, which form general diffusion
complex have been solved; thus, contact points between drug, channels; they also appear to cross the cytoplasmic
enzyme, and DNA have not been directly determined. Also membrane by diffusion (17). Resistance to fluoroquinolones in
unknown is how different amino acid changes effect gram-negative bacteria is associated with reductions in
resistance. porins and reduced bacterial accumulation of drug, but
measurements of diffusion rates suggest that porin
Differences in Fluoroquinolone Targets and Resistance reductions alone are generally not sufficient to account for
The interaction of a fluoroquinolone with the complexes resistance (18).
of either DNA gyrase or topoisomerase IV with DNA may More recently, resistance caused by reduced accumula-
block DNA synthesis and result in cell death (12). The tion has been shown to require the presence and enhanced
antibacterial potency of a quinolone is defined in part by its expression of endogenous efflux systems that actively pump
potency against the two enzyme targets; the more sensitive of drug from the cytoplasm. In gram-negative bacteria, these
the two enzymes within a cell is the primary target. Many systems typically have three components: the efflux pump
fluoroquinolones have differing potencies against DNA located in the cytoplasmic membrane, an outer membrane
gyrase and topoisomerase IV. A general pattern for most protein, and a membrane fusion protein thought to link the
quinolones has emerged: DNA gyrase is the primary drug two. Drug is actively extruded from the cytoplasm or
target in gram-negative bacteria, and topoisomerase IV is the cytoplasmic membrane across the periplasm and outer
primary target in gram-positive bacteria. These differences membrane to the cell exterior; the energy for this process is
correlate with relative drug sensitivities in several cases, the derived from the proton gradient across the membranes.
more sensitive of the two enzymes being the primary target Pumps of this type also exist in gram-positive bacteria, and
defined by genetic tests (13-15). The first step in mutational increased amounts of these pumps have been associated with
resistance in the drug target usually occurs by an amino acid low levels of fluoroquinolone resistance. These efflux systems
change in the primary enzyme target, with a rise in MIC of the are typically capable of causing resistance to compounds of
cell predicted to be determined by the effect of the mutation diverse structural types and thus are referred to as multidrug
itself or by the level of intrinsic sensitivity of the secondary resistance (MDR) pumps. They appear to be present in many
drug target (whichever is lower). Higher levels of resistance if not all bacteria. The natural substrates for these systems
may then occur by second mutational steps, in which amino are generally unknown, but current models envision a general
acid changes are selected in the secondary target enzyme. role in removing toxic compounds from the cytoplasm or
Further mutations result in additional amino acid changes in cytoplasmic membrane (19). Although fluoroquinolones are
either enzyme, depending on which was least resistant in the synthetic antimicrobial agents, a number of them are
cell under selection. On mechanistic grounds, this pattern of substrates for a range of efflux systems. Among pathogenic
stepwise mutations in alternating target enzymes implies bacteria, Escherichia coli, P. aeruginosa, S. aureus, and
that both high intrinsic potency against the primary target Streptococcus pneumoniae have been most extensively
and the similarity of potency against both targets will affect studied for efflux systems causing fluoroquinolone resistance
the likelihood of selection of first-step resistant mutants. (Table). In most cases, expression of the components of the
Thus, fluoroquinolones with a high therapeutic index (defined efflux system is regulated, and resistance occurs by
as the concentration of drug at the site of infection divided by chromosomal mutation that causes coordinated increased
the MIC of the drug for the target bacterium), in which drug expression of pump components. The conditions under which
concentration exceeds the MIC of a first-step mutant, are there is physiologically increased expression of these systems
unlikely to select spontaneous first-step mutants present in are largely unknown. In P. aeruginosa, four such efflux
the infecting bacterial population; such mutants are inhibited systems have been identified, each differing by which
Table. Components of multidrug transport systems in selected bacterial fluoroquinolones. In the case of S. aureus and coagulase-
pathogens negative staphylococci, methicillin-resistant strains devel-
Efflux components oped fluoroquinolone resistance more rapidly than methicil-
Mem- Outer lin-susceptible strains (1,24). This difference is in part
brane mem- Regulatory explained by nosocomial transmission in some settings and by
fusion brane gene or the potential for coselection with several antimicrobial agents
Species Pump protein protein mutation (because of the common multidrug resistance phenotype of
Gram-negative bacteria methicillin-resistant strains [25]). Case-control studies have
Pseudomonas aeruginosa MexB MexA OprM mexR identified fluoroquinolone use as a risk factor for resistance.
MexD MexC OprJ nfxB Fluoroquinolone resistance has also increased substan-
MexF MexE OprN mexT tially in some settings in species in which multiple
MexY MexX OprM mexZ mutational events are required for resistance to occur (e.g.,
Escherichia coli AcrB AcrA TolC acrR, Campylobacter jejuni [26], E. coli [27], and Neisseria
marA, gonorrhoeae [28]). Emergence in these species would not have
robA, been predicted on molecular grounds, suggesting that other
soxS epidemiologic factors may have come into play. For C. jejuni,
Gram-positive bacteria resistance emerged in parallel in animal and human
Staphylococcus aureus NorA -- -- flqB populations (29) shortly after fluoroquinolones were
promoter introduced for use in humans and other quinolones were
mutation, introduced in food animal production, particularly poultry, in
arlRS parts of Europe. In the United States, where use of quinolones
Streptococcus pneumoniae PmrA -- -- ? in food animals was introduced later, demonstrating a link
between resistant C. jejuni strains from poultry and food
fluoroquinolones are preferred substrates (20). It appears products and those causing human disease was possible (26).
Thus, for a known zoonotic pathogen such as C. jejuni,
likely that most bacteria will have multiple MDR efflux
systems. resistance was augmented by selection pressures in an
The structural features of a fluoroquinolone that animal reservoir of campylobacters.
Fluoroquinolone resistance in E. coli has emerged in
determine whether it is affected by an efflux system are not
fully defined but correlate with hydrophilicity in the NorA Europe, particularly in patients with urinary tract infections
pump of S. aureus (21). The risk for acquisition of resistance (30) and neutropenic cancer patients with bacteremia that
developed during fluoroquinolone prophylaxis (31). Fecal
may be reduced for quinolones that are poor substrates for
efflux pumps, since overexpression of such pumps would be carriage of resistant E. coli, however, appears to be common in
unlikely to be effective as a resistance mechanism. Inhibition both healthy adults and children in Spain (27). Carriage of
resistant strains by children, a group in which fluoroquinolones
of pump function by other compounds is also under
are rarely used, and by adults without prior quinolone
investigation as a means of reducing the frequency of
resistance selections (22) and enhancing intrinsic activity of exposures (30) suggests acquisition of resistant strains by the
population at large. This occurrence (in the context of
fluoroquinolones and other drugs that are also pump
documented high rates of fluoroquinolone resistance in E. coli
substrates.
isolated from poultry in Spain [32] and, by analogy, to what
has been documented with campylobacters) suggests that
Other Mechanisms of Resistance
acquisition of resistant strains from food sources may have
The dominant mechanisms of fluoroquinolone resistance
identified are 1) chromosomal mutations causing reduced resulted in substantial colonization of the human population
with resistant E. coli, creating a reservoir of resistant
affinity of DNA gyrase and topoisomerase IV for
organisms. Fluoroquinolone use in humans, which has also
fluoroquinolones and 2) overexpression of endogenous MDR
pumps. One report, however, has documented plasmid- been shown to be a risk factor for having a resistant strain,
may operate in this context to select either already fully
mediated fluoroquinolone resistance in clinical isolates of
resistant or intermediately resistant strains, accounting for
Klebsiella pneumoniae, transferable to E. coli in the
laboratory (23). Neither the mechanism of this transferable the high levels of resistance and multiple mutations reported
in resistant strains causing infections in humans. Whether
resistance nor the prevalence of fluoroquinolone-resistance
similar problems with fluoroquinolone-resistant E. coli will
plasmids in clinical settings is known.
emerge in the United States is not known, but the situation is
being monitored.
Clinical Occurrence of Fluoroquinolone Resistance Humans are the sole reservoir for infections with
Fluoroquinolone resistance emerged shortly after these
N. gonorrhoeae. In the United States, fluoroquinolone
drugs were introduced; two species were particularly affected, resistance in this organism has resulted largely from clonal
S. aureus and P. aeruginosa. Ciprofloxacin and ofloxacin were outbreaks caused by human-to-human spread (33). Thus, for
the most extensively used fluoroquinolones during this early
all three organisms in which fluoroquinolone resistance has
period. The emergence of resistance was predicted on become problematic despite a requirement for multiple
molecular grounds because, in these species, single mutations, other epidemiologic factors (of transmission and
mutations, which raise the MIC of ciprofloxacin of these
ongoing selection in reservoir populations of organisms)
organisms 4- to 16-fold, produce a level of resistance at or appear to be at work.
above peak drug concentrations achievable in serum, Newer fluoroquinolones are now incorporated into
providing an opportunity for spontaneous first-step mutants
guidelines for treatment of patients with lower respiratory
to survive and emerge when a patient is exposed to
tract infections because of rising resistance to beta-lactams 13. Blanche F, Cameron B, Bernard FX, Maton L, Manse B, Ferrero L,
and other agents in S. pneumoniae, the most commonly et al. Differential behaviors of Staphylococcus aureus and
identified bacterial pathogen in patients with community- Escherichia coli type II DNA topoisomerases. Antimicrob Agents
acquired pneumonia (34). Only recently has fluoroquinolone Chemother 1996;40:2714-20.
resistance begun to emerge in this organism, albeit at low 14. Pan XS, Fisher LM. Streptococcus pneumoniae DNA gyrase and
levels (2). In some cases, fluoroquinolone-resistant strains, topoisomerase IV: overexpression, purification, and differential
like those resistant to beta-lactams, have emerged because of inhibition by fluoroquinolones. Antimicrob Agents Chemother
clonal spread (35). Because the newest fluoroquinolones are 1999;43:1129-36.
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increasing selection pressure for resistance is possible. This the specificity of antibacterial fluoroquinolones: benzenesulfonamide
concern is especially great for drugs developed for use in modifications at C-7 of ciprofloxacin change its primary target in
children, who are a major reservoir of S. pneumoniae (36). Streptococcus pneumoniae from topoisomerase IV to gyrase.
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Monitoring will be necessary, as will studies to indicate
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Dr. Hooper is chief of the Infection Control Unit of Massachusetts Updates 1999;2:38-55.
General Hospital and program director for the Massachusetts General 18. Nikaido H, Thanassi DG. Penetration of lipophilic agents with
Hospital/Brigham and Women’s Hospital Joint Fellowship in Infectious multiple protonation sites into bacterial cells: tetracyclines and
Diseases at Harvard Medical School. He is an associate professor of fluoroquinolones as examples. Antimicrob Agents Chemother
medicine at Harvard Medical School. His research interests include the 1993;37:1393-9.
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