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Antimicrobial Agents and Chemotherapy, May 1999, p. 1291-1293, Vol. 43, No. 5
Departments of Pharmacy
Practice1 and Internal
Medicine,2 University of Nebraska Medical
Center, Omaha, Nebraska 68198
Received 4 May 1998/Returned for modification 27 October
1998/Accepted 19 February 1999
The antimicrobial activity of concentrations of selected macrolides
found in epithelial cell lining fluid was investigated. Clarithromycin demonstrated greater potency and a significantly longer
postantibiotic effect (PAE) than azithromycin against
Streptococcus pneumoniae. Azithromycin displayed greater
potency, faster killing, and a longer PAE than clarithromycin against
Haemophilus influenzae. Drug concentrations in epithelial
cell lining fluid similar to those found in tissue did not improve the
synergistic potential of 14-hydroxy-clarithromycin and indicate that a
maximal PAE may exist despite increasing concentrations of drug.
The bacterial pathogens most
commonly responsible for community-acquired pneumonia (CAP)
infections include Streptococcus pneumoniae and
Haemophilus influenzae (2, 10). Institution of
appropriate empiric antimicrobial therapy is the cornerstone of
treatment for CAP (1). Newer macrolides, specifically
clarithromycin and azithromycin, are used in the treatment of CAP
based on enhanced antibacterial spectra and unique
pharmacokinetic properties in comparison to those of
erythromycin. Clarithromycin possesses increased activity against
H. influenzae and most streptococcal species
(11, 17), and its active metabolite,
14-hydroxy-clarithromycin, has demonstrated greater activity
against H. influenzae and additive or synergistic
properties when combined with clarithromycin (9, 16, 18).
The azalide antibiotic azithromycin exhibits two to four times
the bactericidal potency of erythromycin against H. influenzae (5, 17, 21, 26).
In addition to enhanced spectra, clarithromycin and azithromycin
display unique pulmonary tissue pharmacokinetics. Clarithromycin concentrations in lung epithelial cell lining fluid (ELF), a proposed site of infection in CAP (4), have ranged from 10 to
30 times higher than those in serum (12, 25, 27).
14-Hydroxy-clarithromycin also achieves concentrations in ELF
that are superior to those in serum (6, 12, 27).
Azithromycin consistently demonstrates high and sustained
concentrations in lung ELF and alveolar macrophages (13, 24,
27). Data illustrating the effect of these antibiotic concentrations at the site of infection on bacterial growth is limited.
Our purpose was to define the antimicrobial effects of concentrations of clarithromycin, 14-hydroxy-clarithromycin,
and azithromycin in ELF on in vitro growth characteristics of
H. influenzae and S. pneumoniae, as
evidenced by MICs and MBCs, time-kill curves, and postantibiotic
effects (PAEs).
One reference strain and four clinical strains each of
S. pneumoniae and H. influenzae
were studied. Antimicrobial agents were obtained from their
respective manufacturers. S. pneumoniae was
grown in cation-adjusted Mueller-Hinton broth (Difco, Detroit, Mich.) supplemented with 2% lysed horse blood (Colorado Serum Co., Denver), and viability counts were performed with 5% sheep blood agar plates (Remel, Lenexa, Kans.). H. influenzae was grown in Haemophilus test medium
(Remel), and viability counts were performed with chocolate agar plates (Remel).
The MICs and MBCs of clarithromycin and azithromycin were determined by
the standard broth microdilution method (20, 22). Viability
counts were determined from plates yielding 30 to 300 colonies.
Time-kill experiments were performed with clarithromycin, azithromycin,
14-hydroxy-clarithromycin, and a combination of clarithromycin and
14-hydroxy-clarithromycin at the following concentrations found in lung
ELF: clarithromycin, 30 µg/ml; azithromycin, 3 µg/ml; and
14-hydroxy-clarithromycin, 2 µg/ml (3, 7, 19, 24,
27). An initial log-phase inoculum of 6 × 105 CFU/ml was added, and the suspensions were incubated
aerobically at 37°C with shaking at 100 rpm. Viable-cell counts were
performed at 0, 1, 3, 6, and 24 h with plates incubated in 5%
CO2.
In vitro determination of PAE at the aforementioned concentrations in
lung ELF was performed by the broth technique (8). A final
log-phase inoculum of 106 to 107 CFU/ml was
used. Organisms were exposed to drugs for 1 h while incubating at
37°C with shaking at 100 rpm, followed by a 10 Broth microdilution MICs and MBCs for clarithromycin and azithromycin
are presented in Table 1. Mean MICs of
clarithromycin and azithromycin for H. influenzae were
3.6 and 0.7 µg/ml, respectively; those for S. pneumoniae were 0.03 and 0.09 µg/ml, respectively.
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Antimicrobial Activities and Postantibiotic Effects of
Clarithromycin, 14-Hydroxy-Clarithromycin, and Azithromycin in
Epithelial Cell Lining Fluid against Clinical Isolates of
Haemophilus influenzae and Streptococcus
pneumoniae
ABSTRACT
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dilution in prewarmed media. One residual antibiotic control containing
drugs at 104 dilutions of the ELF test concentrations for
each of the tested agents was also included in each
experiment. Viability counts were performed at the time of drug
removal (T0) and at 1-h intervals until cultures
reached marked turbidity. PAEs were quantified as previously described
(8).
TABLE 1.
Broth microdilution MICs and MBCs for clarithromycin and
azithromycin against H. influenzae and
S. pneumoniae
Azithromycin at the concentrations found in ELF displayed the most
rapid killing effect on all strains of H. influenzae,
with 
99.9% killed within 6 h for four of five strains.
14-Hydroxy-clarithromycin alone showed the poorest activity against
H. influenzae. All agents tested demonstrated
statistically similar killing kinetics against S. pneumoniae at the concentrations found in ELF.
Mean PAEs of drugs at the concentrations found in ELF for H. influenzae and S. pneumoniae are presented in Figure 1. Although the PAE of azithromycin against H. influenzae was 83.3% longer than that of clarithromycin, this difference was not statistically significant. Clarithromycin produced a significantly longer PAE against S. pneumoniae than azithromycin (P < 0.05), as did the clarithromycin-14-hydroxy-clarithromycin combination (P < 0.001). Although the addition of 14-hydroxy-clarithromycin to its parent compound prolonged the PAEs of clarithromycin against H. influenzae and S. pneumoniae by 29.2 and 22.7%, respectively, these changes were not statistically significant. Clarithromycin, 14-hydroxy-clarithromycin, and the combination of the two produced significantly longer PAEs against S. pneumoniae than against H. influenzae (P < 0.01, P < 0.01, and P < 0.001, respectively). The PAEs of azithromycin against H. influenzae and S. pneumoniae did not differ significantly.
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Lung ELF provides a quantifiable site for study of antibiotic tissue concentration effects on lung infection. Clarithromycin and azithromycin concentrations in ELF employed in this experiment exceeded the MICs for the H. influenzae and S. pneumoniae strains studied, clarithromycin concentrations being >8 times and 1,000 times the mean MICs and azithromycin concentrations being >4 times and >33 times mean MICs for H. influenzae and S. pneumoniae, respectively. The significance of these concentrations is substantiated by efficacy and favorable outcomes of azithromycin therapy while concentrations in serum remain below MICs.
Our findings support previous data (28) indicating that the synergistic relationship between clarithromycin and its major metabolite is not improved by high concentrations in pulmonary tissue. Although addition of 14-hydroxy-clarithromycin to clarithromycin resulted in prolongation of the PAE against H. influenzae and S. pneumoniae, it is not clear whether this relatively small increase would result in a clinically significant effect.
Increasing the concentration above the MIC has produced increased durations of PAEs, at times reaching a maximum effect (8). PAEs observed in the present study are comparable to the PAEs of clarithromycin and azithromycin, at concentrations equal to 10 times the MIC, previously reported in the literature (14, 23). These findings suggest that comparable PAEs for clarithromycin and azithromycin exist once a maximum effect is achieved.
In vitro simulation of fluctuating drug concentrations in the in vivo environment continues to be a limitation of studies examining antibiotic activity, such as in vitro PAE determination. Concentrations in ELF exceeded the MICs for both organisms tested; thus, the clinical significance of the PAEs obtained in vitro is questioned. The accuracy of measurements of concentrations in ELF and the role of active metabolites in infection have also been challenged.
Our results have shown that clarithromycin exhibited greater potency and a significantly longer PAE than azithromycin against S. pneumoniae at concentrations found in ELF. Azithromycin demonstrated greater potency, killing, and PAE than clarithromycin against H. influenzae at concentrations found in ELF. The data presented question the clinical significance of 14-hydroxy-clarithromycin killing, PAE, and synergistic potential with H. influenzae at concentrations found in ELF. This study also indicates that a maximal PAE may exist despite increasing concentrations of drug.
Overall, the activity of clarithromycin and azithromycin at physiological levels against H. influenzae and S. pneumoniae is an important consideration in the design of tissue-directed antimicrobial therapy. Models of localized infection indicate a correlation between adequate concentrations of appropriate antimicrobials in tissue and decreased morbidity and mortality from infection (15). Additional efforts in examining the importance of antimicrobial activity at concentrations found at the site of infection are required for optimum tissue-directed therapeutic decisions and determination of clinical relevance.
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ACKNOWLEDGMENTS |
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This study was supported in part through a grant from Abbott Pharmaceuticals, Abbott Park, North Chicago, Ill.
We thank Amy Arnold for her laboratory assistance.
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FOOTNOTES |
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* Corresponding author. Mailing address: 984031 Nebraska Medical Center, Omaha, NE 68198-4031. Phone: (402) 559-8650. Fax: (402) 559-8300. E-mail: merupp{at}.unmc.edu.
Present address: Department of Pharmacy Practice, Kansas University
Medical Center, Kansas City, KS 66160-7231.
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Antimicrobial Agents and Chemotherapy, May 1999, p. 1291-1293, Vol. 43, No. 5
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