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Efficacy of eleven antimicrobials against a gregarine parasite (Apicomplexa: Protozoa)
Annals of Clinical Microbiology and Antimicrobialsvolume 6, Article number: 15 (2007)
The Apicomplexa are a diverse group of obligate protozoan parasites infesting a wide range of invertebrate and vertebrate hosts including humans. These parasites are notoriously difficult to control and many species continue to evolve resistance to commercial antibiotics. In this study, we sought to find an effective chemotherapeutic treatment against arthropod gregarines (Apicomplexa), and to identify candidate compounds for testing against other groups of protozoan parasites.
We tested eleven commercial antibiotics against a gregarine parasite of Romalea microptera grasshoppers. Infected insects were fed daily, lettuce containing known amounts of specific antibiotics. On Days 15 or 20, we measured the number of gregarines remaining in the digestive tract of each grasshopper.
Treatment with metronidazole and griseofulvin in host insects significantly reduced gregarine counts, whereas, gregarine counts of insects fed, albendazole, ampicillin, chloramphenicol, fumagillin, quinine, streptomycin, sulfadimethoxine, thiabendazole or tetracycline, were not significantly different from the controls. However, albendazole produced a strong, but non-significant reduction in gregarine count, and streptomycin exhibited a non-significant antagonistic trend.
Our results confirm that gregarine infections are difficult to control and suggest the possibility that streptomycin might aggravate gregarine infection. In addition, the insect system described here, provides a simple, inexpensive, and effective method for screening antibiotics.
The phylum Apicomplexa consists of unicellular protozoan parasites, infesting a wide range of Metazoa [1, 2]. Included are numerous genera that attack humans or domesticated animals (e.g., Plasmodium, Toxoplasma, Cryptosporidium, Neospora, Theileria, Babesia, and Eimeria) [3, 4]. In aggregate, these parasites cause great suffering and economic damage, and contribute to millions of human deaths each year . Chemotherapeutic control ranges from non-existent to fairly effective; however, many species of Apicomplexa continue to evolve resistance to commercial antibiotics. For example, although most Plasmodium infections can still be cured by appropriate antimalarial drugs if treatment is administered early enough, resistance is increasing rapidly to essentially all compounds in use . Clearly there is an urgent need to develop novel chemotherapeutic approaches against these diseases.
Gregarines (Apicomplexa of the subclass Gregarinia Dufour, 1828) are perhaps the most ubiquitous and taxonomically diverse of all parasites, infecting a wide range of invertebrate hosts, including arthropod vectors of vertebrate diseases [1, 6–11]. Gregarines are considered to represent an early diverging apicomplexan lineage, thus making them a key group for questions regarding apicomplexan evolution . Phylogenetic analysis of the small subunit (SSU) ribosomal RNA (rRNA) gene suggest that the gregarines are a sister group to the Cryptosporidium, a group parasitic on vertebrates [13–15]. Moreover, gregarines and Cryptosporidium share many life cycle features [16, 17], and both groups lack a plastid genome, which is present in other apicomplexans [12, 18]. Gregarines do not appear to directly impact human health. However, one gregarine species influences a human disease; the gregarine parasite Ascogregarina culicis apparently helps to maintain Chikungunya virus in vector mosquitoes , thereby fostering febrile epidemics in Southeast Asia and Africa [20–22], and recently spreading over Europe [23–25].
Although gregarines do not attack vertebrates, they have harmed, and continue to harm, scientific research, including research on arthropod vectors of human and animal diseases. This is because gregarines are extremely common in both field and laboratory arthropods [11, 26, 27] yet few researchers are aware of their presence or how these parasites may influence their experiments [10, 28–30]. Gregarines are often considered to be sub-lethal or even harmless to their hosts, but in fact, they divert host nutrients to their own use, occupy space, alter host immune systems, and damage host cell walls when emerging, and thus foster microbial attack. As such, they can reduce longevity, vitality, or fecundity, or cause rapid mortality [27, 31–38]. The effects of gregarines are seldom examined by researchers who study arthropod vectors of vertebrate diseases. Yet recent studies demonstrate that gregarine infection significantly increases the effectiveness of both chemical and microbial control measures against insect pest . Hence, controlling an arthropod vector may hinge on the presence of gregarines.
Knowing the effects of gregarine parasites on their hosts requires a comparison of gregarine-infested and gregarine-free hosts. However, there are few effective antibiotic treatments to eliminate gregarines; typically, parasite numbers can be reduced, but seldom completely eliminated [39–41]. Sanitation and sterilization are commonly employed to combat gregarines, but these methods are sometimes laborious and ineffective [24, 29]. The main problem with sterilization of host eggs and subsequent rearing is that it takes too long, especially for hosts that undergo only a single generation per year. Hence, there is a need to rapidly eliminate gregarines from hosts. Controlling other Apicomplexa is important as well. We are seeing increased levels of Apicomplexa infection in immune-repressed, HIV-infected patients, in part because of the evolution of drug resistance . Numerous other human apicomplexan diseases like cryptosporidiosis are likewise difficult to treat [5, 42]. Thus, there is a need to identify new antimicrobials for use against this group.
In this paper, we test 11 different commercial antibiotics for control of a gregarine (Gregarina sp.) in an insect, the Eastern Lubber Grasshopper, Romalea microptera (Beauvois). Our primary goal is to find an effective chemotherapeutic treatment against arthropod gregarines, and identify candidate compounds for testing against other related groups of apicomplexan parasites. Our secondary goal is to develop an inexpensive and effective insect-based system for rapidly testing large numbers of antibiotics in vivo.
All experiments were conducted on Eastern Lubber grasshoppers, Romalea microptera obtained from stock colonies at Illinois State University . The colony was established in 1997 from wild animals collected from Copeland, Florida, USA. A survey of the colony in 2003 indicated ~96% prevalence of gregarine infection. The origin of this infection is unknown.
We used an unknown species of Gregarina. Placement into this genus was based on trophozoite with papillae shaped epimerite, early association, and gametocysts dehiscing through multiple sporoduct (Fig. 1A-D) [1, 11] (Johny and Whitman, unpubl.). The natural occurrence and host range of this specific parasite is unknown. Indeed, probably more than 95% of the world's gregarine fauna awaits identification . Gregarine gametocysts were collected from the faeces of captive male and female grasshoppers, washed with sterile distilled water 3–5 times, and incubated in air at 30°C under 90% RH , until dehiscence occurred. The resulting oocyst coils were disrupted by centrifugation in sterile distilled water at 1000 rpm for 5 minutes, resuspended, and then fed to grasshoppers. The oocyst concentration was determined using a haemocytometer, as per Undeen and Vavra .
We tested the following 11 commercially available products: albendazole, powder, 100% methyl 5-(propylthio)-2-benzimidazole carbonate (Sigma-Aldrich Inc., St. Louis); ampicillin, sodium salt, 100% monosodium D-(-)-6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0]heptane-2-carboxylate (Research Products International, Mt. Prospect, IL); chloramphenicol, powder, 100% 2,2-dichloro-N-(2-hydroxy-1-[hydroxymethyl]-2-[4-nitrophenyl]ethyl)-, (R-[R*,R*]) (Research Products International); fumagilin-B (fumagillin), powder, 2.1% bicyclohexylammonium fumagillin (Medivet Pharmaceuticals Ltd., High River, Alberta, Canada); griseofulvin, powder, 95% (2S,6'R)-7-chloro-2',4,6-trimethoxy-6'-methyl-3H,4'H-spiro [1 benzofuran-2,1'-cyclohexene]-3,4'-dione (Sigma-Aldrich); metronidazole, powder, 100% (1-(beta-hydroxyethyl)-2-methyl-5-nitroimidazole (Sigma-Aldrich); quinine hemisulfate, salt, 94% (9R)-6'-methoxycinchonan-9-ol (Sigma-Aldrich); streptomycin sulfate, powder, 100% O-2-deoxy-2-(methylamino)-alpha-L-glucopyranosyl-(1-2)-O-5-deoxy-3-C-formyl-alpha-L-lyxofuranosyl-(1–4)-N,N'-bis-(aminoiminomethyl)-D-streptamine (Research Products International); sulfadimethoxine, powder, 100% 4-amino-N-[2,6-dimethoxy-4-pyrimidinyl]-benzenesulfonamide, (sodium salt) (Sigma-Aldrich); tetracycline HCl, powder, 100% 2-naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, (4S-[4alpha,4aalpha,5aalpha,6beta,12aalpha]) (Research Products International); and thiabendazole, powder, 99% 2-(4'-thiazolyl) benzimidazole (Sigma-Aldrich).
Preparation of test compounds
We prepared oral doses of the various antibiotics by mixing them with juice from fresh carrot (Daucus carota) leaves. Carrot leaf juice is a strong phagostimulant for R. microptera. Juice was prepared without adding water, using a commercial juicer, and then filtered through cheesecloth. The water-soluble drugs were directly mixed with the filtrate. The hydrophobic drugs (albendazole, griseofulvin, metronidazole, and quinine) were first mixed with dry powdered sucrose, then blended into the pure juice, to produce suspensions. We then applied 20 μl of juice, containing a known concentration of drug onto 2 cm2 pieces of fresh Romaine lettuce leaves, spreading the juice evenly over the surface. We allowed the juice to dry at air temperature (~10 min) and then fed one leaf to each grasshopper. All test compound mixtures were prepared immediately prior to feeding.
Determination of proper doses for antibiotics
We prepared a wide range of concentrations of each antibiotic in carrot juice, as above, and then determined the maximum concentrations acceptable to adult male grasshoppers (the highest dose that 90% of hungry grasshoppers would consume). Once the maximum accepted dose was determined, we then selected our test doses as 50% of the maximum accepted dose (Table 1). Note that our purpose was not to compare identical doses of different antibiotics, but to identify a specific oral dose of antibiotic that was both palatable to grasshoppers and effective in eliminating gregarine infection in our test animal.
Ten male Romalea microptera (5- to 40-day-old adults) were tested with each drug. Grasshoppers were numbered individually with permanent markers and placed into individual, ventilated, 500-ml transparent plastic containers. Each day, for the next 19 days, each grasshopper was starved for12 hr, then fed a 2 cm2 piece of Romaine lettuce smeared with 20 μl of juice + antibiotic. Insects were allowed to feed on the treated lettuce for 4 hr, and the amount of chemical ingested was calculated based on the amount of lettuce eaten by the insect. Note that not all insects consumed a full dose of antibiotic each day; hence, the dose consumed differs from the dose offered (Table 1). A control group of 40 insects received lettuce with pure carrot juice. After each day's antibiotic feeding, grasshoppers were fed ad lib Romaine lettuce and oatmeal for 8 hr, followed by the next 12 hr starvation period. Insects were maintained at 26 ± 2°C; 60–85% RH, and 14:10 (L:D) photoperiod. On Day 10, the control and treatment groups were inoculated with ~3000 gregarine oocysts/grasshopper by feeding each 1 cm2 of Romaine lettuce contaminated with oocysts (collected as previously described). On Days 5 and 10, one or two grasshoppers from each treatment group and five from the control were dissected and examined for gregarines. These examinations looked for early and profound control; however, no dramatic effects were found in these early inspections, and therefore, these low-n results are not reported here. On Day 15, we dissected one or two grasshoppers from each treatment group, and on Day 20, all survivors were dissected and examined for gregarines.
Evaluation of drug effect
To quantify the gregarines in individual insects, we removed and opened the host's digestive tract, under Yeager's physiological saline . We examined the gut contents under a dissecting microscope, and counted the number of trophozoites, gamonts, and gametocysts. In this species, gamonts were always associated (conjugation), and such associated gamonts and gametocyst were counted as two individuals. Thus the total number of gregarines per grasshopper = # trophozoites + 2 × (# associated gamonts + # gametocysts). Our gregarine parasite requires more than 20 days to complete its life cycle at 26 ± 2°C. Hence, in our experiment, when we found individuals to be gregarine-free on days 15 or 20, we assumed that this had resulted from antibiotic treatment. We analyzed the combined data for Days 15 and 20 by one way ANOVA weighted for unequal variances, and the difference among treatment groups were identified using Tukey's honesty significant difference test. The data were normalized by log transformation before carrying out the ANOVA. All analysis were completed using Statistica 5.5 (StatSoft, Inc. Tulsa, OK, U.S.A) with α = 0.05.
The mean densities of gregarines (pooled data for Days 15 and 20) for the different treatment groups are presented in Figure 2. Grasshoppers treated with metronidazole (ANOVA followed by Tukey HSD test, P < 0.01) and griseofulvin (ANOVA followed by Tukey HSD test, P < 0.05) exhibited significantly lower gregarine counts than control insects (Fig. 2). No other treatments were significantly different from the control; however, albendazole treatment exhibited a strong, but non-significant trend for reduced gregarine count (P > 0.05; Fig. 2). In contrast, a non-significant antagonistic trend was observed in the streptomycin treatment, which showed higher gregarine counts in comparison to the control (P > 0.05) (Fig. 2). Of the 98 animals dissected in Fig. 2, 1 control, 1 fumagillin-, 2 griseofulvin- and 4 metronidazole-treated animals lacked gregarines in their guts.
Of the 11 antimicrobials tested in this experiment, griseofulvin was the most effective in reducing gregarine parasites in the gut lumina of grasshoppers, followed by metronidazole. Griseofulvin, a chlorine-containing metabolite of the fungus Penicillium griseofulvum Direck , has been successfully used against onychomycosis (fungus), and used for more than three decades to treat dermatomycoses in humans and animals. It inhibits nucleic acid synthesis and its main effect on mitosis is due to disorganization of spindle microtubules in the M phase [48, 49]. To our knowledge, griseofulvin has never been used to treat any apicomplexan parasite groups. Hence the potential use of griseofulvin against gregarines and related apicomplexan groups should be explored.
Metronidazole is a benzimidazole, known for its strong antiprotozoan activity, first used to treat Trichomonas vaginalis (Phylum: Zoomastigina) and later Entamoeba histolytica (Phylum: Sarcomastigophora), Giardia lamblia (Sarcomastigophora) and Cryptosporidium sp. (Phylum: Apicomplexa) [50–53]. It is administered in an inactive form and enters cells by passive diffusion . The drug is then activated in cells via electron transfer from ferredoxin to its nitro group, resulting in the therapeutically active intermediate . In the present study, metronidazole reduced gregarine mean intensities by 90% over controls, an effect comparable with the 71% reduction reported by Smith and Clopton  for treatment with metronidazole in their gregarine-cockroach model system. The dosage used in the present study (20 mg/kg body weight/day) is 50-fold higher than the dosage (0.4 mg/kg body weight/day) used by Smith and Clopton . Moreover, their treatment regime was only for 5 days, whereas we administered metronidazole up to 19 days. However, on Day 10, we introduced a large dose of gregarine oocysts (~3000) into our test animals. Overall, our study reaffirms that metronidazole is a strong gregarinostat.
Albendazole, another benzimidazole with broad-spectrum antihelminthic and antifungal activity, is also effective against various protozoa . It binds to tubulin and affects cytoskeletal microtubules; this property makes it potentially useful in the treatment of some protozoan infections in addition to its more established roles in therapy for helminthic infections. Albendazole is also strongly active against Plasmodium berghei and P. falciparum [57–59]. In our experiments, treatment with albendazole resulted in a strong, but non-significant decrease in the gregarine count. The lack of significance may be due to the poor absorption rate of albendazole across the gut. However, albendazole absorption is enhanced in mammals by taking it with fatty meals .
Earlier reports suggested that sulfadimethoxine displays some apicomplexan toxicity and this, and related compounds, are commonly used for prophylactic control of coccidians in livestock and poultry [1, 61, 62]. Recently Clopton and Smith  evaluated the activity of sulfadimethoxine against Gregarina cubensis and Protomagalhaensia granulosae (Apicomplexa: Eugregarinida), infecting the Death's Head cockroach, Blaberus discoidalis, and found that sulfadimethoxine significantly reduced the mean gregarine intensities, but did not eliminate the gregarine infection completely. In our test, sulfadimethoxine did not significantly reduce the gregarine numbers even after 19 days of treatment. One possible reason might be due to the dosage: the 30 mg/kg body weight used in our experiment is 5–6 times lower than the dosage (170 mg/kg body weight) used by Clopton and Smith  in their cockroach-gregarine model. Mourya et al.  assessed the efficacy of sulfadimethoxine against Ascogregarina culicis (Eugregarinida: Lecudinidae) infecting larval Aedes aegypti mosquitoes. Though high concentration of sulfadimethoxine (0.5 mg/ml culture water) reduced the mean gregarine intensity, it also resulted in host mortality of upto 52%.
In our study, streptomycin-treated animals had, on average, double the gregarine load of control animals. Although the difference was not significant, it suggests the possibility that streptomycin aggravated gregarine infection. In humans, gut microbiota effectively limit the capacity of invading micro-organisms, including pathogens, to colonize the gut, giving rise to what has been termed 'colonisation resistance' . Streptomycin is a strong bacterial antibiotic which inhibits protein synthesis by binding to the 30S ribosomal subunit . In the present study, streptomycin may have reduced midgut bacteria in grasshoppers, thereby increasing the survival of gregarines. Toure et al.  reported that combination antibiotics such as gentamicin, penicillin, and streptomycin reduced the bacterial flora in the mosquito midgut, which in turn increased the infectivity of Plasmodium falciparum in Anopheles mosquitoes. Likewise, Culex bitaeniorhynchus mosquitoes treated with tetracycline showed an increased susceptibility to the Japanese encephalitis (JE) virus .
The gregarines (Apicomplexa) appear to be highly resistant to chemotherapy, although our results suggest that metronidazole and griseofulvin have moderate antibiotic effects. Streptomycin might aggravate gregarine infections. Apicomplexa parasites have a global impact on economic development and on the health and survival of millions of people and domesticated animals worldwide. New therapies for the diseases they cause are urgently required, but many drugs have proven ineffective  or are becoming increasingly ineffective because of increased antibiotic resistance in pathogens . The insect system described here is a simple method for evaluation of drugs against gregarines. It can also serve as a model system to identify compounds with a potential broad activity against other Apicomplexa. Insects can be cheaply mass-reared, require less laboratory space and support facilities, do not suffer from the ethical problems of using mammals as experimental hosts, and share some common immune-response features with vertebrates . Insects can be infected by virtually all pathogen and parasite taxa, including viruses, rickettsiae, bacteria, fungi, protozoa, and nematodes, etc. Therefore, insects can be exploited, not only to examine pathogens of arthropods, but also to screen new drugs for potential use against a wide range of pathogens and parasites of vertebrates [40, 41, 68]. Finally, the effects of gregarines on arthropod vectors of vertebrate diseases have been largely ignored. Understanding such effects will require the ability to culture gregarine-free hosts. This research contributes to that goal.
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We thank Carrie Booth for laboratory assistance. This study was supported by the Undergraduate Research Training Program/CRUI at Illinois State University, and by NSF grants BIR 9510979A000 and DBI-0442412.
SJ and AM performed experimental work. DWW and SJ designed the study, collected and analyzed the data and drafted the manuscript. All authors read and approved the final manuscript.