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Journal of Clinical Microbiology, February 2000, p. 763-767, Vol. 38, No. 2
Department of Bacteriology and Immunology,
Haartman Institute and HD Laboratories, University and University
Central Hospital of Helsinki,1 and
Department of Obstetrics and Gynecology, Peijas Hospital,
Vantaa,2 Finland
Received 6 July 1999/Returned for modification 15 October
1999/Accepted 13 November 1999
Trichomonas vaginalis is a globally common sexually
transmitted human parasite. Many strains of T. vaginalis from around the world have been described to be
resistant to the current drug of choice, metronidazole. However, only a
few cases of metronidazole resistance have been reported from Europe.
The resistant strains cause prolonged infections which are difficult to
treat. T. vaginalis infection also increases the risk for
human immunodeficiency virus transmission. We present a practical
method for determining the resistance of T. vaginalis to 5-nitroimidazoles. The suggested method was
developed by determining the MICs and minimal lethal concentrations (MLCs) of metronidazole and ornidazole for
T. vaginalis under various aerobic and anaerobic
conditions. Using this assay we have found the first three
metronidazole-resistant strains from Finland, although the origin
of at least one of the strains seems to be Russia. Analysis of the
patient-derived and previously characterized isolates
showed that metronidazole-resistant strains were also resistant to
ornidazole, and MLCs for all strains tested correlated well with the
MICs. The suggested MICs of metronidazole for differentiation
of sensitive and resistant isolates are >75 µg/ml in an
aerobic 24-h assay and >15 µg/ml in an anaerobic 48-h assay.
Trichomonas vaginalis is
a flagellated protozoan and is the most common parasite that causes
sexually transmitted disease (24). The World Health
Organization has estimated that there are annually approximately 170 million infections worldwide (43). The main clinical
manifestations of T. vaginalis infections are vaginitis,
urethritis, and prostatitis. In addition, infection with trichomonads
can increase the risk of pelvic inflammatory disease and tubal
infertility (2). Since probably almost 50% of trichomonal
infections are asymptomatic (8), the infection can spread easily.
Infection with T. vaginalis may increase the risk of human
immunodeficiency virus (HIV) type 1 (HIV-1) transmission. In developing countries T. vaginalis is very common in the areas with the
highest prevalence of HIV-1 infections (15). Increased
shedding of HIV-1 in the semen in the presence of urethral infection
has been described (14). It has been postulated that the
increased amount of HIV-infected CD4+ lymphocytes in the
walls of the gynecological tract could facilitate congenital infections
with HIV-1 (20, 36).
The 5-nitroimidazoles, especially metronidazole, are the most
widely used antimicrobial agents for the treatment of
trichomoniasis. The mechanism of the protozooicidal effect of the
5-nitroimidazoles is thought to involve generation of nitro radicals,
which leads to subsequent DNA damage and cell death. Under normal
circumstances T. vaginalis cells use pyruvate-ferrodoxin
oxidoreductase (PFOR) and ferrodoxin-linked enzymes to oxidize acetate
from pyruvate via acetyl coenzyme A to gain ATP (6). When a
nitroimidazole is present, its nitro groups capture electrons from
ferrodoxin and nitro radicals are generated, leading to cell damage.
Since the introduction of 5-nitroimidazoles in the 1960s there have
been reports of at least 100 metronidazole-resistant strains of
T. vaginalis from the United States (5, 9, 12, 16, 21,
23, 29, 31, 32, 35). Only under 20 metronidazole-resistant strains have been described from Europe (3, 7, 12, 16, 19, 26, 40,
41). In addition, some preliminary reports have been published,
for example, from Russia (18) and Africa (13).
To overcome the clinical problems of metronidazole resistance, higher doses of metronidazole have usually been used to treat the
patients (11, 22). Also, despite the cross-resistance with
other 5-nitroimidazoles, tinidazole (10) and ornidazole (19) have been used to treat some patients infected with
metronidazole-resistant strains of T. vaginalis.
Furazolidone, a nitrofuran, has also shown trichomonicidal activity in
vitro (30). Paromomycin has been used as a topical treatment
for some patients with allergy to metronidazole or infections caused by
metronidazole-resistant strains of T. vaginalis (3,
31).
Resistance to nitroimidazoles has been studied by growing T. vaginalis strains in the presence of different drug concentrations under aerobic and anaerobic conditions in vitro. Resistance has been
suggested to be dependent on one or more of the following: a reduced
PFOR enzyme activity (19), an altered conformation of the
hydrogenosome (39), a ferrodoxin with an exceptional redox
potential (44), or a reduced amount of intracellular
ferrodoxin (27). In the resistant strains the intracellular
amounts of ferrodoxin are decreased by over 50% and the rate of
ferrodoxin gene transcription is reduced by as much as 40 to 65%
compared to those in sensitive isolates (33). Many of the
suggested mechanisms lead to fermentation of pyruvate in the cytosol
instead of the hydrogenosome, which means that the action of the
5-nitroimidazole drug is inhibited. The aerobic resistance to
nitroimidazoles is thought to be enhanced by free O2 in the
cytosol, as it is a potent electron acceptor from nitro radicals and
thus could inhibit the action of the drug (6). The suggested
mechanisms that lead to an excess of intracellular oxygen include
decreased amounts of oxidases and a decreased affinity of terminal
oxidases to oxygen (39).
In this report we suggest a practical in vitro method for determination
of the metronidazole susceptibility of T. vaginalis in
advanced clinical microbiology laboratories and report on three clinically metronidazole-resistant and in vitro metronidazole-resistant strains of T. vaginalis from Finland. The susceptibility to
metronidazole was tested under various oxygen concentrations. The
susceptibilities of the characterized strains of T. vaginalis to metronidazole and ornidazole were compared to those
of a set of patient-derived strains.
Reagents.
Metronidazole and ornidazole were purchased from
Sigma Chemical Co. (St. Louis, Mo.) and were dissolved in 0.15 M
phosphate buffer (pH 6.4) for the susceptibility assays just before
use. Dimethyl sulfoxide (DMSO) was purchased from Merck & Co.
(Darmstadt, Germany).
T. vaginalis strains and cultivation.
T.
vaginalis strains were cultured in 7-ml Wassermann glass tubes
containing 5 ml of Trypticase-yeast extract-maltose (TYM) medium
(4) complemented with 10% heat-inactivated horse serum and
a combination of 100 IU of streptomycin (Sigma) per ml and penicillin
(Orion Diagnostica, Espoo, Finland).
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Resistance of Trichomonas vaginalis to Metronidazole:
Report of the First Three Cases from Finland and Optimization of
In Vitro Susceptibility Testing under Various Oxygen
Concentrations
ABSTRACT
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
INTRODUCTION
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
MATERIALS AND METHODS
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
70°C) with DMSO by a
previously described method (42). For each assay new vials
were thawed. After thawing the strains were cultured for approximately
7 days to collect enough trophozoites. The possible presence of
bacteria or yeasts was examined by cultivating samples of all
T. vaginalis cultures in a thioglycolate medium (37°C
for 7 days) and on plates with blood or chocolate agar
(CO2 atmosphere) or fastidious anaerobic agar (anaerobic
atmosphere). Samples from thioglycolate medium-containing tubes with
any cloudy patches were cultivated on the plates. All cultivations were
performed by standard bacteriological methods.
Species identification by PCR. The species of all the strains was analyzed by PCR. In the PCR assay a highly conserved repeated DNA stretch specific for T. vaginalis was amplified with primers TVK3 and TVK4, which have been described elsewhere (17).
5-Nitroimidazole susceptibility assays. To examine the susceptibilities of the T. vaginalis strains to metronidazole and ornidazole under aerobic and anaerobic conditions, the trophozoites were cultured on 24-well tissue culture plates (Greiner, Gloucestershire, United Kingdom) in airtight jars with adjustable ventilators on the lid. Three plates with duplicate wells for each drug concentration were used in each suspectibility assay. All assays were run twice. Fresh TYM medium (200 µl) was mixed with 200 µl of prediluted 5-nitroimidazole (in 0.15 M phosphate buffer [pH 6.4]) in each well, and subsequently, 100 µl of medium containing live T. vaginalis trophozoites was added to each well. The final concentration of motile trophozoites was adjusted to approximately 105/ml in each well. The drug dilution buffer (phosphate buffer [pH 6.4]) was used as a positive control on each plate.
Anaerobic circumstances were created with the chemical oxygen consumption plate Anaerocult A (Merck & Co.) and were monitored with an anaerobic indicator (Oxoid, Hampshire, England). All incubations were performed at 37°C. The aerobic conditions were created by two different methods. The first assay used the same jars used for the anaerobic assay, but the ventilators were left open for access to room air. In the second assay the susceptibility of T. vaginalis to 5-nitroimidazoles was tested in the presence of different concentrations of oxygen in the culture atmosphere. The amounts of oxygen, nitrogen, and carbon dioxide were adjusted by using bottled gas (AGA Corp., Helsinki, Finland) and separate flow meters (Brooks Instrument B. V., Veeneendaal, The Netherlands). The purities of the gases used were 98, 99, and 97% for N2, O2, and CO2, respectively. The N2 and CO2 were free of O2. To prepare an anaerobic environment, 95% N2 and 5% CO2 were used. To prepare various aerobic environments, different amounts of O2 (0, 5, 10, 20, and 30%) were used to partially replace the N2. The gas mixture was allowed to flow through the inlet and outlet of the anaerobic jar for 30 min at a rate of 1,600 ml/h before the incubation and after the first check at 24 h. Anaerobic circumstances were monitored with an anaerobic indicator (Oxoid).Determination of MICs and MLCs. The viabilities of the trophozoites in the culture plate wells were assessed by examining visually the motilities of the cells with an inverted microscope at a ×400 magnification after 24 and 48 h of incubation. The MIC was the lowest concentration of the drug in the well in which no motile cells were detected. To check whether the evaluation of viability (MIC) reflected the effectiveness of the drug at actually killing the cells, the minimal lethal concentrations (MLCs) were also tested after cultivation of the trophozoites in the presence of different oxygen concentrations. The contents of each of the wells were inoculated into the bottoms of tubes containing 5 ml of fresh TYM medium, and the tubes were examined for the presence of motile T. vaginalis trophozoites after 5 and 10 days of cultivation.
Clinical data. The first (strain 1) and second (strain 2) clinically metronidazole-resistant isolates of T. vaginalis were obtained from female patients living in the Helsinki district in Finland. The third strain (strain 3) was from a female patient who is from the eastern part of Finland and whose husband had often visited Russia. All patients suffered from recurrent trichomonal infections and were treated with several courses (6, 3, and 10 courses for patients 1, 2, and 3, respectively) of metronidazole with a standard or an increased dose. All three patients were hospitalized and were treated with metronidazole intravenously (patient 1 with 1 g a day for 3 days, patient 2 with 500 mg four times a day for 7 days complemented with 100 g of metronidazole vaginally once a day for 10 days, and patient 3 with 750 mg three times a day for 5 days). After the treatment patients were symptomless for a follow-up period of 3 months, and the cultures of their samples were also negative for T. vaginalis.
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RESULTS |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Anaerobic MICs of metronidazole. The MICs of two 5-nitroimidazoles (metronidazole and ornidazole) for the different T. vaginalis strains were obtained under both aerobic and anaerobic conditions. The MICs of metronidazole were also determined under various oxygen concentrations. The MLCs were determined by cultivating the trophozoites in fresh nitroimidazole-free medium after incubation with metronidazole.
In the anaerobic assay the MICs of metronidazole were determined by cultivating the known resistant isolate (strain R), clinically resistant isolates (strains 1 to 3), the known sensitive isolate (strain S), and clinically sensitive isolates (strains 4 to 10) of T. vaginalis in the presence of different concentrations of metronidazole. Parasite motility was evaluated microscopically after 24 and 48 h. At the 24-h time point the MIC of metronidazole was 145 µg/ml for the known resistant strain (strain R), 23 µg/ml for clinically resistant strain 1, over 250 µg/ml for clinically resistant strains 2 and 3, 20 µg/ml for the known sensitive strain (strain S), and from 8.5 to 12 µg/ml for clinically sensitive strains 4 to 10. At the 48-h time point the MICs were 39 µg/ml (strain R), 16 µg/ml (strain 1), 24 µg/ml (strain 2), 36 µg/ml (strain 3), and from 1.0 to 9.8 µg/ml (strains 4 to 10) (Fig. 1A).
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Aerobic MICs. In the first aerobic assay the sensitivity of T. vaginalis to metronidazole was tested under ordinary room air conditions at 37°C. The MICs of metronidazole at the 24-h time point were 133 µg/ml for the known resistant strain (strain R), 77 µg/ml for clinically resistant strain 1, over 250 µg/ml for strains 2 and 3, 18 µg/ml for the known sensitive strain (strain S), and from 3.5 to 10 µg/ml for strains 4 to 10. After 48 h of cultivation the MICs were 8.4 µg/ml (strain R), 7.8 µg/ml (strain 1), 48 µg/ml (strain 2), 140 µg/ml (strain 3), 1.0 µg/ml (strain S), and from 1.0 to 2.0 µg/ml (strains 4 to 10) (Fig. 1B).
As the results of anaerobic and aerobic resistance for some strains, especially clinically resistant isolate 1, differed, a second aerobic sensitivity assay was performed to examine the effect of oxygen on drug tolerance. The T. vaginalis trophozoites were cultivated in the presence of different amounts of metronidazole under various concentrations of oxygen (0, 5, 10, 20, and 30%) in the atmosphere. It was found that the MIC of metronidazole for known resistant strain R was approximately 100 times higher than that for sensitive strain S when the amount of oxygen in the atmosphere exceeded 2% (Fig. 2). The corresponding MICs of metronidazole for clinically resistant strain 1 were approximately 20 times higher than those for sensitive strains 6 and 7.
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MICs of ornidazole. The MICs of ornidazole were determined for the known resistant strain (strain R), clinically resistant strain 1, the known sensitive strain (strain S), and clinically sensitive strains 4 to 7 in both the anaerobic and the aerobic assays. In the anaerobic assay the MICs of ornidazole after 24 h were 133 µg/ml for strain R, 37 µg/ml for strain 1, 2.0 µg/ml for strain S, and from 4.0 to 8.0 µg/ml for strains 4 to 7. After 48 h of cultivation the MICs of ornidazole were 8.4 µg/ml (strain R), 17 µg/ml (strain 1), 2.0 µg/ml (strain S), and from 4.0 to 8.0 µg/ml (strains 4 to 7) (Fig. 3A). In the aerobic assay the MICs were 200 µg/ml (strain R), 78 µg/ml (strain 1), 2.0 µg/ml (strain S), and from 2.0 to 4.0 µg/ml (strains 4 to 7) after 24 h of cultivation and 10 µg/ml (strain R), 18 µg/ml (strain 1), 1.0 µg/ml (strain S), and from 1.0 to 2.0 µg/ml (strains 4 to 7) after 48 h of cultivation (Fig. 3B).
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MLCs of metronidazole.
The MLCs were measured from the second
aerobic sensitivity assay. While the MIC was determined by microscopic
evaluation on the basis of cell motility at different drug
concentrations, the MLC was assayed to reveal the actual lethal
concentration on the basis of the growth after 5 and 10 days in fresh
medium after exposure to different concentrations of the drug. When no
oxygen was present the MLC for strains 1 and R was 6.0 µg/ml and the MLC for the clinically sensitive strains (strains S, 6, and 7) was 0.75 µg/ml (Table 1). The MLCs varied from 6 to 100% of the corresponding MICs. When the concentration of oxygen
was 
10% the sensitive strains died even in the absence of the drug.
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DISCUSSION |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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In the present study we have tested different in vitro conditions for determination of the 5-nitroimidazole resistance of T. vaginalis and suggest a relatively simple and easily interpretable method for laboratory testing of strains suspected of being metronidazole resistant. We describe the analysis of the first three metronidazole-resistant T. vaginalis strains, all of which were finally eradicated by intravenous metronidazole therapy.
Testing of drug susceptibility in vitro is necessary to ensure that the long-lasting T. vaginalis infection is really caused by a nonsensitive strain and that the patient is not experiencing a recurrent infection. We tested the susceptibilities of different resistant and sensitive strains of T. vaginalis under various conditions and at various time points. As a conclusion, we suggest that a combination of an aerobic 24-h cultivation and an anaerobic 48-h cultivation of patient-derived strains in the presence of different concentrations of metronidazole can be used to determine whether their susceptibilities to metronidazole are decreased. One of the patient-derived resistant strains (strain 1) described in this report was concluded to be a resistant isolate only from the aerobic assay. Anaerobic 24-h MICs were only slightly elevated for clinically resistant strain 1 and differed from those for the drug-susceptible control (strain S) only by 3 µg/ml.
Aerobic resistance has also been induced in vitro, and these strains were also drug sensitive under anaerobic conditions (38). Thus, both assays are needed in the laboratory analysis (5). A suitable anaerobic susceptibility testing protocol for diagnostics (InPouchTV test) is commercially available (1), but it should be complemented by an aerobic assay.
Interpretation of the MICs or MLCs for T. vaginalis has not been based on any widely accepted scheme. Some investigators have used a method in which the MIC is the lowest concentration of drug at which cell growth takes place and the MLC is the lowest concentration with motile cells. Both definitions are based on visual observation after a 48-h cultivation (23, 25, 28, 29, 38). In some studies the MLC is the original lowest drug concentration at which growth of the parasites in a drug-free medium no longer takes place (1, 12, 19). According to Narcici and Secor (30), the MIC of metronidazole was approximately fourfold higher than the concentration (MLC) that killed the isolates, but no data were presented. It seems that in the MIC assay the trophozoites had suffered irreversible damage but still retained motility. Narcici and Secor (30) used a 48-h cultivation for the determination of possible growth in drug-free medium. However, for some isolates it may take longer to recover from the effect of the drug because we found viable trophozoites after 5 days of cultivation. According to the present study the MIC for T. vaginalis is a suitable indicator of the actual MLC and can be used for diagnostic assessments.
Different threshold concentrations of the 5-nitroimidazole drugs for resistance have been proposed by many investigators. Müller et al. (28) have reported MLCs for 199 T. vaginalis strains and the treatment outcomes for the corresponding patients. According to their interpretation, the MLCs for a treatment-resistant strain were >100 µg/ml in an aerobic assay and >3.1 µg/ml in an anaerobic assay. They also found that treatment success overlapped between susceptible and resistant isolates. We found that following an aerobic 24-h cultivation and an anaerobic 48-h cultivation the MICs for clinically resistant isolates were >75 and >15 µg/ml, respectively. For clinically sensitive strains MICs were considerably lower in both assays (<19 and <10 µg/ml, respectively), and these values did not overlap with the values for the resistant strains. Many different methods are used in laboratories to test for drug susceptibility, and it is not possible to define accurate threshold values for resistant and sensitive strains. There is also uncertainty whether the MIC or MLC can be used as such to determine the suitable drug dosage for the patient (23, 34). We suggest that a patient-derived strain is judged to be resistant after comparing it to a known, highly resistant strain by an easily interpretable method.
In this study we found three patient samples with T. vaginalis strains that were clearly resistant to metronidazole in vitro. The finding correlated well with the clinical data for resistance to treatment. In earlier reports patients who carry resistant strains of T. vaginalis have usually been treated with longer courses of standard doses of metronidazole or with a considerably higher dosage (23). All patients described in this paper were initially treated with several courses of metronidazole per os. Finally, trichomonads were eradicated by using metronidazole intravenously. Some reports have suggested that other 5-nitroimidazoles, like tinidazole, ornidazole (19), or furazolidone (30), are curative for metronidazole-resistant isolates, and some reports have shown the opposite (7). However, oral metronidazole as a single dose of 1.5 g is still the drug of choice for the treatment of trichomoniasis (37), and the susceptibility assay is indicated only when the standard metronidazole dosage is repeatedly incapable of eradicating the infection from the patient and the partner(s). When the MIC for a patient-derived strain is high by a reliable assay, we suggest that the patient be treated with as high a dosage of the drug as possible to treat the infection and to prevent it from spreading.
The origins of our first two treatment-resistant T. vaginalis strains (strains 1 and 2) are not exactly known. The third strain (strain 3) came from a patient in the eastern part of Finland and is likely to have originated from a partner who had visited Russia several times. Tourism between Western Europe and Russia has increased a lot, and part of it is sex tourism in and out of Russia. No statistical data from Russia on how common T. vaginalis infections are and the current status of drug resistance in Russia are available. In Russia self-treatment with the usual doses of metronidazole is possible; thus, the time lag between a new diagnosis and effective treatment is increased. In Europe it is very important to start diagnosing possible resistance in vitro after, for example, 2 months of "recurrent" infections, to report the resistant strains, and to trace the sexual contacts, if possible. Recent epidemiological and in vitro evidence suggests that T. vaginalis infection may enhance the risk of HIV-1 transmission (36). If this connection is confirmed, T. vaginalis susceptibility testing becomes even more important in countries where infections are both frequent and inadequately controlled, for example, in Russia and tropical Africa. Patients infected with a resistant strain of T. vaginalis should be tested for HIV infection.
In summary, using metronidazole sensitivity testing under various oxygen concentrations, we found the first three metronidazole-resistant strains of T. vaginalis from Finland. It appears that the metronidazole resistance of T. vaginalis is an emerging threat in Europe. Thus, testing for metronidazole susceptibility in vitro and introduction of rapid and intense medication should be implemented more often. The in vitro diagnostic assays that we suggest can be relatively simply adopted for use in advanced clinical microbiology laboratories.
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ACKNOWLEDGMENTS |
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We thank all the involved hospitals for providing us with T. vaginalis strains and Suvi-Sirkku Kaukoranta-Tolvanen, Esa Korkeela, and Satu Suhonen for valuable clinical data on the patients.
This study was supported by a state subsidy to the Helsinki University Central Hospital.
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FOOTNOTES |
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* Corresponding author. Mailing address: Haartman Institute, P.O. Box 21, FIN-00029 University of Helsinki, Finland. Phone: 358-9-1912 6229. Fax: 358-9-1912 6382. E-mail: Taru.Meri{at}helsinki.fi.
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REFERENCES |
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Journal of Clinical Microbiology, February 2000, p. 763-767, Vol. 38, No. 2
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