AnimalNet Dec. 1/03 -- II
African
biosciences facility

Back at the
ranch, a horror story

Factors
influencing fluoroquinolone resistance

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African
biosciences facility
December 1, 2003
FAO BiotechNews
http://www.fao.org/biotech/index.asp
A Biosciences Facility for Eastern and Central Africa is being established as
part of NEPAD's (New Partnership for Africa's Development) continent-wide
network of centres of excellence. Establishment of the new Facility has been
made possible by an initial investment of more than Canadian $30 million by the
Canada Fund for Africa through the Canadian International Development Agency.
The facilities will be hosted by the International Livestock Research Institute,
in Nairobi, Kenya. Biosciences embrace a wide range of biological
specialisations related to all living organisms, including animals, microbes,
plants and trees. See http://www.doylefoundation.org/BiosciencesBrochure.pdf
(1.68 MB) or contact ILRI-Kenya@cgiar.org for more information.
Back
at the ranch, a horror story
December 1, 2003
LA Times
Peter Singer and Karen Dawn write in this op-ed that a ranch owner in San Diego
County disposes of 30,000 nonproductive egg-laying hens by feeding them into a
wood chipper.
The authors say that such "spent hens" are often packed into
containers and bulldozed into the ground buried alive. Or they are often
gassed using carbon dioxide distributed unevenly among tens of thousands of
birds; it's common for them to die slow, painful deaths.
California's anti-cruelty statutes, which are separate from the humane slaughter
laws, supposedly cover these animals, but it can be difficult to prosecute what
is called "standard industry practice." And district attorneys don't
like to bring cases they don't think they will win.
When a horrified neighbor saw ranchers cramming live chickens into a chipper,
animal advocates thought they had a winning case. Karen Davis of United Poultry
Concerns led the push for prosecution.
Unfortunately, the authors say, a San Diego deputy district attorney found no
criminal intent on the part of the owners, concluding that they "were just
following professional advice" from two veterinarians. The ranchers named
Dr. Gregg Cutler as one. Cutler denies directly authorizing the use of a chipper
in the case but says he has no problem with the procedure. He is on the animal
welfare committee of the American Veterinarian Medical Assn.
In order to dispel notions that the association had condoned the act, the
organization's Web site displays the following quote from Executive Vice
President Dr. Bruce W. Little: "It is absolutely absurd and ludicrous to
believe that any veterinary medical association, especially an association that
has for more than 150 years been the leading voice for humane and proper care of
animals, could or would advocate throwing live chickens into a wood chipper as
an appropriate method of euthanasia." Yet the man who reportedly condoned
such "ludicrous" action remains on the organization's animal welfare
committee.
Further, the AVMA has let farmed animals down in other areas. The majority of
laying hens in the United States are forced to go into an unnatural molt by the
sudden withdrawal of food for up to 14 days. This process shocks them into
another round of laying. Even though this violates California's anti-cruelty
statute, which states that a person who causes an animal to be "deprived of
necessary sustenance" is guilty of a crime, but cases are not prosecuted.
Forced molting is outlawed in Europe. Even McDonald's does not permit its
suppliers to starve hens. Yet the AVMA has refused to take a clear stance
against forced molting. And those with the power to prosecute people who starve
animals look to that organization for expert advice.
The story adds that Assemblywoman Loni Hancock (D-Berkeley) introduced a bill
this year that would ban the housing of pregnant sows and veal calves in crates
so small that the animals are unable to turn around or lie down with limbs
outstretched. She was forced to defer her bill for lack of committee votes. The
California Veterinary Medical Assn., which led the opposition, based its stance
on the national group's policies. Florida residents, in a referendum, passed a
ban on sow gestation crates last year despite AVMA opposition.
A Gallup survey in May found that 62% of Americans supported strict laws
concerning the treatment of farmed animals. Yet AVMA policy on farmed animal
welfare interferes with the enforcement of existing law and too often blocks
legislation that would protect animals. And a veterinarian who apparently
condones putting live hens into chippers remains on the organization's welfare
committee. If the AVMA hopes to continue to be seen as "the leading voice
for humane and proper care of animals," it is time for change.
Factors
influencing fluoroquinolone resistance
December 2003
CDC Emerging Infectious Diseases Vol 9, No 12
Daniel F. Sahm,* Clyde Thornsberry,* Mark E. Jones,* and James A. Karlowsky*
*Focus Technologies, Herndon, Virginia, USA
Suggested citation for this article: Sahm DF, Thornsberry C, Jones ME, Karlowsky
JA. Factors influencing fluoroquinolone resistance. Emerg Infect Dis [serial
online]. 2003 Dec. [date cited]. Available from: URL: http://www.cdc.gov/ncidod/EID/vol9no12/03-0168.htm
To the Editor: Recently, Scheld summarized factors that he considered to have an
influence on the efficacy of fluoroquinolones (1). In the review, ciprofloxacin
was presented as the most active fluoroquinolone against Pseudomonas aeruginosa
with MICs typically two- to eightfold lower than those for levofloxacin,
moxifloxacin, or gatifloxacin. However, because the National Committee for
Clinical Laboratory Standards (NCCLS) MIC interpretative breakpoints are
fluoroquinolone-specific, percent susceptibility is considered to be a better
measure by which to compare fluoroquinolone activities. Our company has
conducted annual investigations called TRUST (Tracking Resistance in the United
States Today) since 1996. These surveillance studies have consistently shown
similar susceptibility rates for levofloxacin (67.7% in 2002) and ciprofloxacin
(67.4% in 2002) against P. aeruginosa (2,3). Both agents show higher in vitro
activity against P. aeruginosa than gatifloxacin and moxifloxacin (24). A
critique of antipseudomonal fluoroquinolone activity should also consider peak
achievable fluoroquinolone levels at a site of infection, the area under the
serum concentration curve in 24 hours (AUC24h), and the AUC24h/MIC ratio (5). At
equivalent dosages for nosocomial pneumonia, levofloxacin (750 mg intravenously,
once daily) has a threefold higher peak serum level (Cmax) and threefold higher
AUC24h than ciprofloxacin (400 mg intravenously, every 8 hours) (package inserts
for Levaquin and Cipro). While certain P. aeruginosa isolates have lower
ciprofloxacin than levofloxacin MICs, the two fluoroquinolones have equivalent
activity against P. aeruginosa because of their equivalent AUC24h /MIC ratios
(6). We agree strongly with Schelds suggestion that the fluoroquinolone used
clinically should be the fluoroquinolone tested by the laboratory and reported;
surrogate testing of fluoroquinolones may lead to major errors in reporting,
particularly for Enterobacteriaceae (2,3,7).
The review also stated that levofloxacin-resistant strains of P. aeruginosa
emerge at a significantly higher rate than with ciprofloxacin. However, a recent
study of P. aeruginosa isolated from cystic fibrosis patients reported that
fewer resistant mutants were isolated after exposure to levofloxacin (11
mutants) than to ciprofloxacin (28 mutants) (8).
With regards to S. pneumoniae, the review stated that in vitro studies have
demonstrated that ciprofloxacin (14 mg/L) and levofloxacin (12 mg/L) are
not as active as moxifloxacin (0.060.25 mg/L) and gatifloxacin (0.51 mg/L)
against pneumococci. As with P. aeruginosa, fluoroquinolone comparisons against
S. pneumoniae should not be limited to MICs alone because pharmacokinetic and
pharmacodynamic characteristics differ for each fluoroquinolone. Pneumococcal
time-kill studies with levofloxacin, gatifloxacin, and moxifloxacin in a
pharmacodynamic model have demonstrated that these three agents possess equal
bactericidal activity and are equally effective in preventing resistance
development because the lower in vitro MICs for gatifloxacin and moxifloxacin
were offset by the higher serum and tissue levels of levofloxacin (9). In the
same study, ciprofloxacin did not exhibit rapid killing and selected for
resistance faster than the other three agents (9). TRUST and other U.S.
surveillance studies, using the NCCLS-recommended broth-dilution method, have
shown that S. pneumoniae remain highly susceptible to levofloxacin with
resistance rates in the United States of <1%; the MIC90 for levofloxacin in
these studies has remained at 1 mg/L from 1997 through 2002 (1015). Further,
levofloxacin, gatifloxacin, and moxifloxacin are equally effective in rates of
clinical cure and microbiologic eradication of pneumococcal respiratory
infections (16, and FDA website; available from: URL: http://www.fda.gov/cder/foi/nda/99/21061_Tequin.htm
and http://www.fda.gov/cder/foi/nda/2001/21277_Avelox.htm)
The review implied that, in general, higher AUC24h/MIC ratios were associated
with better patient outcomes. For S. pneumoniae, several pharmacodynamic studies
have demonstrated that a target AUC24h/MIC ratio of 30 to 35 for
fluoroquinolones is the best correlate for successful bacteriologic eradication,
clinical cure, and prevention of emergence of resistance during therapy
(5,9,1719). Levofloxacin, gatifloxacin, and moxifloxacin all achieve this
AUC24h/MIC ratio (9). Zhanel et al. demonstrated that AUC24h/MIC ratios above
the target value of 30 to 35 did not improve bacteriologic eradication or reduce
the emergence of resistance (9). Moreover, no clinical data support the claim
that higher AUC24h/MIC ratios correlate with better patient outcomes.
The review discusses the question of whether C-8-methoxyquinolones (moxifloxacin
and gatifloxacin) have a lower propensity to select resistant mutants of S.
pneumoniae compared with levofloxacin. Mutation prevention concentration is a
theoretical laboratory concept based on agar dilution methodology, and no
published data have shown any clinical correlation between this theory and
clinical outcomes. NCCLS does not recommend agar dilution for susceptibility
analysis of S. pneumoniae. Moreover, the extremely low levels of resistance in
S. pneumoniae (<1%) after many years of fluoroquinolone use do not support
the theory of mutation prevention concentration. The review did not reference an
analysis of 16 penicillin-resistant S. pneumoniae strains by Kolhepp et al.
(20). In that broth-dilution study, in vitro resistance developed in a greater
proportion of strains exposed to gatifloxacin (11/16) and moxifloxacin (8/16)
than to levofloxacin (2/16). Similarly, in a study by Klepser et al. that used
an in vitro pharmacodynamic model, levofloxacin was less likely than
moxifloxacin to select for resistant isolates of S. pneumoniae; moreover, after
24 hours of exposure, levofloxacin MICs remained unchanged while moxifloxacin
MICs increased two- to eightfold (21).
Levofloxacin, gatifloxacin, and moxifloxacin all have susceptibility rates
>99% for S. pneumoniae (22,23). Although resistance is rare, considerable
cross-resistance among fluoroquinolones is observed once two or more key
mutations (e.g., Ser79 in ParC, Ser81 in GyrA) are detected (24,25). Using
topoisomerase IV-selecting fluoroquinolones (ciprofloxacin and levofloxacin) in
the same patient population as DNA gyrase-selecting fluoroquinolones (gatifloxacin
and moxifloxacin) could potentially accelerate the development of double mutants
(ParC and GyrA) and clinically important class resistance because selective
pressure would be applied to both enzyme targets (26).
The review stated that, since 1999, at least 20 case reports of pulmonary
infection that did not respond to levofloxacin therapy have been published. This
number is remarkably small considering that >250 million patients have been
treated with levofloxacin worldwide. A number of the treatment failures cited
had documentation of prior ciprofloxacin use and ciprofloxacin failure, and many
isolates were not tested for levofloxacin susceptibility before treatment (27).
We agree with the recommendation in the cited Davidson et al. reference: a
patients failure to respond to one fluoroquinolone is sufficient reason not
to use other fluoroquinolones (27). Isolated clinical failures will occur with
the use of any antimicrobial agent when treating pneumococcal pneumonia.
The notion that fluoroquinolone therapy can be targeted for an indication
requires challenge as fluoroquinolone therapy will always result in systemic
drug levels. Evidence does not indicate that the use of two fluoroquinolones,
such as ciprofloxacin and moxifloxacin, minimizes fluoroquinolone resistance.
Targeted fluoroquinolone therapy may in fact have adverse implications for the
patient and for overall institutional resistance patterns. For example, the use
of ciprofloxacin for urinary tract infections exposes resident streptococci in
the respiratory tract to an agent that has demonstrated weaker activity against
pneumococci, thus potentially selecting for pneumococcal resistance (9).
Moreover, 20%-35% of ciprofloxacin is excreted through the intestinal tract (Cipro
package insert), compared to 4% of levofloxacin (Levaquin package insert).
Studies have shown that ciprofloxacin displays weaker in vitro activity (lower
percentage of isolates susceptible) than levofloxacin for several gram-negative
enteric bacteria (2,3). Stepwise adaptive changes towards fluoroquinolone
resistance in enteric bacteria may be selected by fluoroquinolones with weaker
in vitro activity and higher levels of exposure in the intestinal tract.
Therefore, ciprofloxacin would have a greater potential than levofloxacin for
the selection of resistant strains of intestinal gram-negative pathogens. A
recent report stated that ciprofloxacin-resistant Escherichia coli were isolated
from the feces of 48% of patients treated with ciprofloxacin for prostatitis;
before ciprofloxacin therapy, only ciprofloxacin-susceptible E. coli were
isolated from the feces of these patients (28). Further, given that 25% of
moxifloxacin is excreted through the intestinal tract (Avelox package insert),
the use of moxifloxacin for respiratory infections exposes bacteria in the
intestinal tract to a fluoroquinolone with greater activity against Bacteroides
fragilis and other intestinal anaerobes than levofloxacin (29,30). Moxifloxacin
has a greater potential than other fluoroquinolones to alter the normal
intestinal flora and select for vancomycin-resistant enterococci (31) and
intestinal gram-negative strains with increased fluoroquinolone resistance.
In conclusion, we believe that the data we have briefly presented here
supplements the previous discussion by Scheld (1) and will help facilitate an
improved understanding of the factors influencing the maintenance of
fluoroquinolone efficacy.
Focus Technologies is the central testing laboratory for the TRUST antimicrobial
susceptibility testing surveillance program, sponsored by Ortho-McNeil
Pharmaceutical.
References
1. Scheld WM. Maintaining fluoroquinolone class efficacy: review of influencing
factors. Emerg Infect Dis 2003;9:19.
2. Karlowsky JA, Kelly LJ, Thornsberry C, Jones ME, Evangelista AT, Critchley
IA, et al. Susceptibility to fluoroquinolones among commonly isolated
Gram-negative bacilli in 2000: TRUST and TSN data for the United States. Int J
Antimicrob Agents 2002;19:2131.
3. Blosser-Middleton RS, Sahm D, Evangelista AT, Thornsberry C, Jones ME,
Critchley IA, Karlowsky JA. Antimicrobial susceptibilities of common pathogens
causing nosocomial pneumonia: 20012002 TRUST surveillance. Annual Meeting
Infectious Disease Society of America, 2002, abstract 71.
4. Milatovic D, Schmitz F-J, Brisse S, Verhoef, Fluit AC. In vitro activities of
sitafloxacin (DU-6859a) and six other fluoroquinolones against 8,796 clinical
bacterial isolates. Antimicrob Agents Chemother 2000;44:11027.
5. Craig WA. Does dose matter? Clin Infect Dis 2001;33(Suppl 3):S2337.
6. MacGowan AP, Wootton M, Holt HA. The antibacterial efficacy of levofloxacin
and ciprofloxacin against Pseudomonas aeruginosa assessed by combining
antibiotic exposure and bacterial susceptibility. J Antimicrob Chemother
1999;43:3459.
7. Sahm DF, Thornsberry C, Jones ME, Blosser R, Critchley IA, Evangelista AT,
Karlowsky JA. Antimicrobial susceptibility of Enterobacteriaceae and Pseudomonas
aeruginosa from inpatient infections in the U.S.: 19992002 TRUST
surveillance. Critical Care Congress, 2003, Abstract 22015.
8. Gillespie T, Masterton RG. Investigation into the selection frequency of
resistant mutants and the bacterial kill rate by levofloxacin and ciprofloxacin
in non-mucoid Pseudomonas aeruginosa isolates from cystic fibrosis patients. Int
J Antimicrob Agents 2002;19:37782.
9. Zhanel GG, Walters M, Laing N, Hoban DJ. In vitro pharmacodynamic modeling
simulating free serum concentrations of fluoroquinolones against multidrug-resistant
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10. Thornsberry C, Ogilvie PT, Holley HP Jr, Sahm DF. Survey of susceptibilities
of Streptococcus pneumoniae, Haemophilus influenzae, and Moraxella catarrhalis
isolates to 26 antimicrobial agents: a prospective U.S. study. Antimicrob Agents
Chemother 1999;43:261223.
11. Biedenbach DJ, Barrett MS, Croco MA, Jones RN. Bay 12-8039, a novel
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12. Jones RN, Pfaller MA. In vitro activity of newer fluoroquinolones for
respiratory tract infections and emerging patterns of antimicrobial resistance
data from the Sentry antimicrobial surveillance program. Clin Infect Dis
2000;31(Suppl 2):S1623.
13. Doern GV, Heilmann KP, Huynh HK, Rhomberg PR, Coffman SL, Brueggemann AB.
Antimicrobial resistance among clinical isolates of Streptococcus pneumoniae in
the United States during 1999-2000, including a comparison of resistance rates
since 19941995. Antimicrob Agents Chemother 2001;45:17219.
14. Thornsberry C, Sahm DF, Kelly LJ, Critchley IA, Jones ME, Evangelista AT, et
al. Regional trends in antimicrobial resistance among clinical isolates of
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the United States: results from the TRUST surveillance program, 1999-2000. Clin
Infect Dis 2002;34(Suppl 1):S416.
15. Sahm DF, Thornsberry C, Jones ME, Blosser RS, Critchley IA, Evangelista AT,
et al. Correlation of antimicrobial resistance among Streptococcus pneumoniae in
the U.S.: 20012002 TRUST surveillance. Interscience Conference on
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16. Zhanel GG, Ennis K, Vercaigne L, Walkty A, Gin AS, Embil J, et al. A
critical review of the fluoroquinolones: focus on respiratory infections. Drugs
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17. Lacey MK, Lu W, Xu X, Tessier PR, Nicolau DP, Quintiliani R, Nightingale CH.
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against Streptococcus pneumoniae in an in vitro model of infection. Antimicrob
Agents Chemother 1999;43:6727.
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pharmacokinetics of levofloxacin. Chemotherapy 2000;46(Suppl 1):614.
19. Ambrose PG, Grasela DM, Grasela TH, Passarell J, Mayer HB, Pierce PF.
Pharmacodynamics of fluoroquinolones against Streptococcus pneumoniae in
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Chemother 2001;45:27937.
20. Kolhepp SJ, Grunkemeier G, Leggett JE, Dworkin RJ, Slaughter SE, Gilbert DN.
Phenotypic resistance of penicillin-susceptible and penicillin-resistant
Streptococcus pneumoniae after single and multiple in vitro exposures to
ciprofloxacin, gatifloxacin, levofloxacin, moxifloxacin, and trovofloxacin.
Annual Meeting Infectious Diseases Society of America, 2000, Abstract 97.
21. Klepser M, Ernst E, Petzold CR, Rhomberg P, Doern GV. Comparative
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in a dynamic in vitro model. Antimicrob Agents Chemother 2001;45:6738.
22. Low D, de Azavedo J, Weiss K, Mazzulli T, Kuhn M, Church D, et al.
Antimicrobial resistance among clinical isolates of Streptococcus pneumoniae in
Canada during 2000. Antimicrob Agents Chemother 2002;46:1295301.
23. Brueggemann AB, Coffman SL, Rhomberg P, Huynh H, Almer L, Nilius A, et al.
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19941995. Antimicrob Agents Chemother 2002;46:6808.
24. Evangelista AT, Loeloff M, Pfelger S, Davies T, Bush K, Mauriz Y, et al.
Cross-resistance among fluoroquinolone-resistant clinical isolates of
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P50.
25. Davies TA, Pfleger S, Goldschmidt R, Bush K, Sahm DF, Evangelista AT.
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20002001 that are cross-resistant to ciprofloxacin, gatifloxacin,
levofloxacin, and moxifloxacin. Annual Meeting Infectious Disease Society of
America 2002, Abstract 78.
26. Davies TA, Evangelista A, Pfleger S, Bush K, Sahm DF, Goldschmidt R.
Prevalence of single mutations in topoisomerase type II genes among levofloxacin-susceptible
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19921996 and 19992000. Antimicrob Agents Chemother 2002;46:11924.
27. Davidson R, Covalcanti R, Brunton JL, Bast DI, de Azavedo JC, Kibsey P, et
al. Resistance to levofloxacin and failure of treatment of pneumococcal
pneumonia. N Engl J Med 2002;346:74750.
28. Horcajada JP, Vila J, Moreno-Martํnez A, Ruiz J, Martํnez J, Sแnchez M,
Soriano E, et al. Molecular epidemiology and evolution of resistance to
quinolones in Escherichia coli after prolonged administration of ciprofloxacin
in patients with prostatitis. J Antimicrob Chemother 2002;49:559.
29. Hoellman DB, Kelly LM, Jacobs MR, Appelbaum PC. Comparative antianaerobic
activity of BMS 284756. Antimicrob Agents Chemother 2001;45:58992.
30. Ednie LM, Jacobs, Appelbaum PC. Activities of gatifloxacin compared to those
of seven other agents against anaerobic organisms. Antimicrob Agents Chemother
1998;42:245962.
31. Zhanel GG, Laing NM, DeCorby M, Nichol KA, Hoban DJ. Pharmacodynamic
activity of fluoroquinolones in a mixed infection simulationg an artificial
bowel: effect of eradicating Bacteroides fragilis. American Society for
Microbiology, 2002, Abstract A-145.
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