The Scientific World Journal
Volume 2014 (2014), Article ID 936560, 9 pages
http://dx.doi.org/10.1155/2014/936560

Research Article

The In Vitro Effect of Ivermectin on the Activity of Trehalose Synthesis Pathway Enzymes and Their mRNA Expression in the Muscle of Adult Female Ascaris suum (Nematoda)

Małgorzata Dmitryjuk, Elżbieta Łopieńska-Biernat, and Ewa Anna Zaobidna

Biochemistry Department, Faculty of Biology and Biotechnology, University of Warmia and Mazury, Oczapowski 1A Street, 10-719 Olsztyn, Poland

Received 10 July 2014; Accepted 21 August 2014; Published 27 October 2014

Academic Editor: Mehmet Yakup Arica

Copyright © 2014 Małgorzata Dmitryjuk et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

The in vitro effect of ivermectin lethal dose on the activity of trehalose-6-phosphate synthase (TPS) and phosphatase (TPP) and the expression of their mRNA (tps1, tps2, and tpp genes) in the muscle of adult female Ascaris suum was investigated. The presence of ivermectin in the medium caused a decrease in TPS and TPP activities during the experiment compared with the start and control groups. The exception was the group of worms grown for 8 hours in a IVM solution, in which there was a little higher TPS activity than in the control. Real-time qPCR analysis showed reduced expression of tps1 and tps2, and unchanged tpp expression after 20 hours of incubation relative to the expression at time zero. Relative to the appropriate control groups, the expression of tps2 gene was slight increased but the other two genes were reduced after 8-hours of IVM-treatment. Then the expression of all three genes was lower at the end of cultivation. The level of gene expression was positively correlated with the activity of specific enzymes. In the case of tpp gene there was only a weak correlation. Prolonged exposure to ivermectin was effective in lowering TPS and TPP activity and their mRNA expression. However, the drug did not block the pathway.

1. Introduction

Ivermectin (IVM) is the 22,23-dihydroderivative of avermectin B1, a strong macrocyclic lactone produced by an actinomycete, Streptomyces avermitilis [1]. The action of this drug appears to depend on its effect on nerve impulse conduction [2]. Although previously it was thought that IVM acts via γ-aminobutyric acidergic (GABAergic) regulation [1], it has been shown that IVM induces an influx of chloride ions through channels that are not regulated by the neurotransmitter GABA. There is ample evidence that GABA plays a little part in the antiparasitic action of IVM; for example, GABA-linked Cl⁻ channels in cell membranes of Ascaris suum are less sensitive to IVM than are other types of channel [3]; specific IVM-binding proteins in cell membranes of Caenorhabditis elegans and Drosophila melanogaster have been identified [4]; and also IVM is insensitive to GABA but sensitive to the neurotransmitter L-glutamate in specially prepared oocytes of the frog Xenopus laevis after C. elegans mRNA injection [5, 6]. It may be possible that IVM acts on a novel type of ion channel [2].

Although the mechanism of IVM binding is unclear, it is known that it is collected in the outer monolayer of the muscle membrane and following an irreversible change in membrane potential the muscles of parasites are paralysed [7]. IVM is absorbed into the blood of the host after oral administration and is almost completely excreted in the faeces. Maximum plasma concentrations are reached approximately 4 hours after oral administration. The half-life of IVM is about 12 hours, but trace amounts of the drug are present in the blood of the host up to 3 days after administration [2]. Due to the broad spectrum of activity and large safety margin, IVM has become a medicine used for the control of nematodes and arthropod parasites in cattle, horses, sheep, goats, dogs, pigs, and humans [1, 2, 8].

The effect of IVM and other nonbenzimidazole compounds on embryonation and infectivity of A. suum eggs has been studied. These studies have shown that the anthelmintic treatment of pigs with IVM has only a limited effect on both embryonation and infectivity of A. suum eggs isolated from expelled worms [9]. On the other hand, the efficacy of the drug in inactivation of larval and adult form of A. suum is high, nearing 100% [10, 11].

In the present study we decided to investigate the in vitro influence of IVM on trehalose synthesis in muscles of adult female A. suum. Trehalose (-D-glucopyranosyl-(1,1)--D-glucopyranoside) in nematodes is usually present at a higher concentration than the free glucose [12, 13] and has a number of important functions: it protects cellular structures during periods of stress such as high osmotic pressure, drying, and freezing; it provides energy and is the major circulating sugar; it is also important in the process of egg hatching [14–16]. In most eukaryotes, including nematodes, trehalose synthesis is catalysed by the action of two enzymes: trehalose-6-phosphate (T6P) synthase (TPS; EC 2.4.1.15), which catalyses the transfer of glucose from uridine diphosphate glucose (UDPG) to glucose-6-phosphate (G6P) to produce T6P, and T6P phosphatase (TPP; EC 3.1.3.12), which converts T6P to free trehalose and inorganic phosphate [15]. The activity of both enzymes participating in trehalose synthesis has been confirmed in the muscles, haemolymph, and reproductive system of A. suum [13]. TPS was isolated from muscles of A. suum and its properties have been detected. Also two genes encoding TPS, tps1 (JF412033.2) and tps2 (JF412034.2), were isolated and sequenced from muscles of the parasite [17]. The activity and preliminary properties of TPP (optimum of pH and temperature, thermostability, activators, and inhibitors) were detected in muscles of A. suum [18]. In the nematodes, TPP was first identified in C. elegans in a forward genetic screen for intestinal defects where the loss of tpp (gob-1) function resulted in early larval lethality due to a blocked intestinal lumen and consequent starvation [19]. Kushwaha et al. [20] reported on the cloning, expression, and purification of Brugia malayi TPP that was found to be an unusual phosphatase. These researchers have shown that tpp gene silencing was lethal for stage 3 (L₃) larvae of B. malayi and that those defined lethal effects resulted in impaired in vivo development [21]. The World Health Organization has included the B. malayi TPP enzyme in the priority list of prospective antifilarial drug targets for lymphatic filariasis [22]. Therefore, the trehalose synthesis pathway in A. suum may play an important role in therapeutic aims and this pathway can be a target for antiascariasis drugs, especially since the pathway does not occur in mammalian hosts of Ascaris sp. In the current study, we evaluated whether IVM, a well-known antiparasitic drug, affected the activity of trehalose synthesis enzymes and expression of their mRNA. We try to find answers to the following questions: is roundworms trehalose metabolism activated to protect against lethal effects of the drug? At what level is this done? Is there a positive correlation between the activity of the trehalose synthesis pathway enzymes and their mRNA expression?

2. Materials and Methods

2.1. Chemicals

Purified bovine serum albumin (BSA), T6P dipotassium salt, uridine 5′-diphosphoglucose disodium salt from Saccharomyces cerevisiae (UDPG), D-glucose-6-phosphate disodium salt hydrate (G6P), and alkaline phosphatase from bovine intestinal mucosa (lyophilized powder, 10–30 defined enzyme activity (DEA) units/mL solid), penicillin G sodium salt, nystatin, IVM, 4-(2-hydroxyethyl)-piperazine-1-ethanesulfonic acid (HEPES), agarose, and ethidium bromide were purchased from Sigma-Aldrich (Germany and USA). Total RNA Kit, TranScriba Kit, and SYBR Green B PCR-MIX Taq were obtained from A&A Biotechnology (Poland). The components of 0.1 M acetic acid-ammonia buffer and 0.1 M phosphoric buffer (resp., pH 4.2 and pH 7.0) (acetic acid, ammonia, NaH₂PO₄, and Na₂HPO₄  × 7H₂O₂) and of Ascaris Ringer’s Solution (ARS) medium (KCl, CaCl₂  × 2H₂O, MgCl₂  × 6H₂O, NaCl, and sodium acetate) were of high purity grade and were purchased from Chempur (Poland) and P.P.H. Stanlab (Poland).

The water used for the analysis was deionized with the use of a Direct-Q Ultrapure UV3 Water System (EMD Millipore, USA). The water, media, sodium saline, and surgical instruments were sterilized using a Classic Standard Prestige Medical autoclave (Ma-Je-R, Poland).

2.2. Acquisition of Material and In Vitro Cultures

Living mature female roundworms (Ascaris suum Goeze, 1782) were isolated from the intestines of pigs in a nearby slaughterhouse and transported in ARS medium [22] within 1 hour of collection. ARS medium was formulated from 25 mM potassium chloride, 15 mM calcium chloride, 10 mM magnesium chloride, 4 mM sodium chloride, and 125 mM sodium acetate and next buffered to pH 7.4 using 5 mM HEPES. In the laboratory, pig roundworms were washed in sterile saline and next in ARS medium containing antibiotics (1.2 million units of penicillin and 1 g of nystatin per litre) for 4 hours. This was followed by two equal in vitro cultures. The first culture was grown in ARS medium supplemented with antibiotics at the above concentrations (control group). The second was grown in a saturated solution of unlabelled IVM (11.44 μM) in ARS supplemented with antibiotics (study group, IVM). The start group (S) consisted of washed living worms before the foundation of the cultures. Single individuals were cultured in sterile 50 mL culture flasks at 37°C under 5% CO₂ in air. During the culturing the motility of the parasites was observed. After 4, 8, and 20 hours samples of muscle from 5 worms were taken equally from both cultures under sterile conditions. Then, samples for enzyme assays and molecular analysis were frozen in liquid nitrogen and stored at −70°C.

2.3. Enzyme Assays

Samples of prepared muscle tissue were homogenized in an Omni TH-02 (5,000–35,000 revolutions per min; Omni International, USA) homogenizer in a 1 : 4  (w/v) ratio in 0.9% NaCl. The homogenates were centrifuged at 1500 g for 15 min at 4°C using an Eppendorf Centrifuge 5804 R (USA). The supernatant fraction was a crude extract used for enzyme assays. The activity of TPS and TPP was determined using modified methods described by Giaever et al. [23] and Kaasen et al. [24], respectively. The reaction mixture for TPS activity contained 0.2 mL of 0.1 M acid-ammonia buffer (pH 4.2), 0.1 mL of 10 mM MgCl₂, 50 μL of 2 mM UDPG, 50 μL of 2 mM G6P, and 0.1 mL of the crude extract of enzyme. After mixing, appropriate control samples were incubated at 100°C for 5 min; tested samples were incubated at 37°C for 30 min and after that at 100°C for 5 min to complete the reaction. In a second step, the resulting T6P was decomposed by the addition of 0.1 mL of the alkaline phosphatase solution (1 U) in 0.1 M phosphoric buffer (pH 8.0) at 37°C for 30 min. The reaction mixture for TPP activity contained 0.2 mL of 0.1 M phosphoric buffer (pH 7.0), 0.1 mL of 10 mM MgCl₂, 0.1 mL of 2 mM T6P, and 0.1 mL of the crude extract of enzyme. After mixing, appropriate control samples were incubated at 100°C for 5 min; tested samples were incubated at 37°C for 60 min and after that at 100°C for 5 min to complete the reaction. The end product of the activities of both the enzymes, trehalose, was assayed by high-performance liquid chromatography (HPLC) using a method described by Dmitryjuk et al. [13]. The activities of TPS and TPP were expressed in units (U) per mg protein measured using the Bradford [25] method with BSA as a standard. One unit defines the quantity of trehalose (nmol) formed during 1 min at 37°C.

2.4. Real-Time Quantitative Polymerase Chain Reaction

Total RNA extraction was performed using a Total RNA Kit according to the manufacturer’s protocol (A&A Biotechnology). The RNA was spectrophotometrically quantified (A260 nm), and its quality was determined by gel electrophoresis on 1% agarose containing 0.01% ethidium bromide. A TranScriba Kit was used for first-strand cDNA synthesis. First, 1 μg of total RNA was preincubated with 1 μL of 10 mM appropriate reverse primer (Table 1) in a total volume of 10 μL (in the nuclease-free water) in an Applied Biosystems Veriti 96-well Thermal Cycler (Life Technologies, USA) at 65°C for 5 min to denature the RNA template secondary structures and then cooled on ice for 5 min. After that, 4 μL of 5x reaction buffer, 2 μL of 10 mM mix of triphosphate deoxyribonucleotides (dNTPs), and 4 μL of TranScriba reverse transcriptase (20 U/μL) were added to the mixture and incubated at 41°C for 60 min and for the next 5 min at 70°C. Real-time reverse transcriptase qPCR (qRT-PCR) was performed using SYBR Green B PCR-MIX Taq. The reaction mixture consisted of 2 μL cDNA, 5 μL SYBR Green PCR-MIX, 1 μL 10 mM of both appropriate forward and reverse primers (Table 1), and 0.15 μL ROX (5-carboxy-X-rhodamine) reference dye, and the volume was raised to 10 μL with nuclease-free water. Mean values and standard deviations were used for the analysis of relative transcript levels for each time point using the method [26]. The data were presented as the fold change in gene expression normalized to an endogenous reference gene gapdh (glyceraldehyde-3-phosphate dehydrogenase; housekeeping gene; Table 1) and relative to the untreated control (relative quantification (RQ) = 1; start group or control group). Transcript levels were shown by AB analysis software (7500 v2.0). All samples were tested in triplicate on Applied Biosystems 7500 Fast Real-Time PCR Systems (Life Technologies, USA). Melting curves were constructed after amplification.

Table 1: Primer sequences.

Enzyme
Gene
Primer name
Sequence ()
GenBank accession number
of target sequence

Trehalose-6-phosphate synthase (TPS)
tps1
Forward
CTCGTCGTTGTGCACAGTTT
JF412033.2

Reverse
GCTGTTCCAGCAGTTCTTCC

tps2
Forward
CCACATGCGGGTCTTATTCT
JF412034.2

Reverse
ACTCTCGGTGGCTGCACTAT

Trehalose-6-phosphate phosphatase (TPP)
tpp
Forward
CATGGCACTCTTTGTTGGTG
JI169681.1

Reverse
AGCGTTATTCAGTGCCTCGT

Glyceraldehyde-3-phosphate dehydrogenase (GAPDH)
gapdh
Forward
CGGTTGTATCGACGGACTTT
AB058666.1

Reverse
TGAGGCTTTGACGTTCAGTG

2.5. Statistical Analysis

Data were expressed as means ± standard deviation by one-way ANOVA using Statistica 10 (StatSoft Inc., Tulsa, Oklahoma, USA). Tukey’s honestly significant different (HSD) test was used to assess differences between means. Pearson’s correlation test was used for determination of correlation between TPS or TPP relative activity and their mRNA expression over time. The value less than 0.05 () was considered statistically significant. All the experiments were performed in triplicate.

3. Results

3.1. Observation of the Mobility of Worms during In Vitro Cultivation

Worms in the control group were highly mobile to the end of the in vitro cultivation. However, A. suum in the IVM medium displayed a gradual decrease in motility. After 4 hours IVM roundworms showed negligible mobility. Paralysis of the worms increased further after 8 hours of the culture. The in vitro culture was terminated after 20 hours, when the roundworms from the IVM-group did not show any movement.

3.2. Activity of Enzymes in the Trehalose Synthesis Pathway

TPS and TPP activities were observed during 20 hours of in vitro cultivation of adult female A. suum (Table 2). In the case of TPS, a gradual decrease in the activity was observed in the control group. Differences between means were statistically significant here. After 20 hours of incubation, the enzyme showed activity equal to of the starting (Table 2; Figure 1(a)). In the group supplemented with IVM a significant decrease in the activity of TPS was initially observed (after 4 hours to ). After 8 hours of incubation in IVM-group was observed a slight increase of TPS activity relative to 4-hours culture (up to ) in contrast to the control group where a further decrease in enzyme activity was noted. After 20 hours of culture, again there was a greater decrease to a value slightly lower than that of the control group (). Also, there were statistically significant differences compared with the means of the start (S) group in all groups (Figure 1(b)). TPP activity in the IVM-group was lower than that in the control group, after 4, 8, and 20 hours of incubation of the worms. In addition, the activity of TPP decreased during incubation in the control group and these changes were statistically significant (Figure 2(a)) but slightly increased in the IVM-group after 8 and 20 hours (Table 2; Figure 2(b)).

Table 2: Activity of trehalose-6-phosphate synthase (TPS) and phosphatase (TPP) and their mRNA expression (tps1, tps2, and tpp genes) during in vitro cultivation of adult female Ascaris suum in control (C-group) and ivermectin-supplemented medium (IVM-group).

Group of worms
Activity of TPS   [nM/mg]
Activity of  TPS relative to the start [%]
tps1 RQ to  the start
tps2 RQ to  the start
Activity of TPS relative to the control  [%]
tps1 RQ to  the control
tps2 RQ to  the control

S-group

100
1
1
—
—
—

4 h C-group

67.13 ± 2.56

100
1
1

8 h C-group

53.85 ± 2.03

100
1
1

20 h C-group

33.64 ± 3.07

100
1
1

Correlation coefficient

4 h IVM-group

54.12 ± 1.74

8 h IVM-group

64.64 ± 4.4

20 h IVM-group

31.13 ± 1.85

Correlation coefficient

Group of worms
Activity of TPP  [nM/mg]
Activity of TPP relative to the start [%]
tpp RQ to  the start
Activity of TPP relative to the control [%]
tpp RQ to the  control

S-group

100
1
—
—

4 h C-group

63.48 ± 0.84

100
1

8 h C-group

45.97 ± 1.33

100
1

20 h C-group

41.13 ± 1.15

100
1

Correlation coefficient

4 h IVM-group

26.35 ± 0.74

8 h IVM-group

30.88 ± 1.85

20 h IVM-group

32.26 ± 2.18

Correlation coefficient

Pearson’s correlation coefficient between gene expression and appropriate enzyme activity changes over time with respect to the start group (S); **Pearson’s correlation coefficient between gene expression and appropriate enzyme activity changes over time with respect to the C-group.

(a)

(b)

Figure 1: Relative activity of trehalose-6-phosphate synthase (TPS) and its mRNA (tps1, tps2 genes) expression normalized to the endogenous reference gapdh (glyceraldehyde-3-phosphate dehydrogenase) gene and relative to the expression at time zero (start group). IVM: ivermectin; RQ: relative quantification; (a) control group; (b) IVM-group; change at and change at with respect to the start group.

(a)

(b)

Figure 2: Relative activity of trehalose-6-phosphate phosphatase (TPP) and its mRNA (tpp gene) expression normalized to the endogenous reference gapdh (glyceraldehyde-3-phosphate dehydrogenase) gene and relative to the expression at time zero (start group). IVM: ivermectin; RQ: relative quantification; (a) control group; (b) IVM-group; change at with respect to the start group.

3.3. Real-Time Quantitative Polymerase Chain Reaction

3.3.1. Expression of Trehalose-6-phosphate Synthase and Phosphatase mRNA Relative to Expression at Time Zero (Start Group)

TPS mRNA was expressed in all groups. However, differences in the expression of tps1 and tps2 genes were noted during the in vitro culturing of A. suum (Figures 1(a) and 1(b)). Initially, tps1 expression in both groups increased several times relative to the expression at time zero and this was a statistically significant increase. After 8 hours, expression of the gene slightly increased and then decreased again after 20 hours in IVM-group relative to the control group (Figures 1(a) and 1(b)). Between tps1 gene expression and TPS activity was observed a fairly strong correlation in the control group () and a moderate correlation () in the case of IVM-group with respect to the start (Table 2).

Expression of the tps2 gene increased in both groups, but the increase of this gene expression was about half lower in the group cultured in medium supplemented with IVM than in the control group. In both cases statistically significant differences were noted. After 8 hours of incubation in the IVM medium, tps2 expression level was higher than at the start and control (RQ = ; Figures 1(a) and 1(b)). Between tps2 gene expression and TPS activity was observed a weak correlation in the control group () and a very strong correlation () in the case of IVM-group (Table 2).

The expression level of the gene encoding TPP also fluctuated during worm cultivation (Figures 2(a) and 2(b)). After 4, 8, and 20 hours of incubation, tpp expression level was a little higher relative to the start. The highest level of gene expression was achieved after eight-hour incubation in IVM-group (RQ = ). At the end of the culture, this gene expression increased in the control group; however, in the group treated with IVM tpp expression dropped to the level of start expression (RQ = ; Figures 2(a) and 2(b)). A fairly strong correlation () in the control group and a weak correlation () in the case of IVM-group between tpp gene expression and TPP activity were observed (Table 2).

3.3.2. Expression of Trehalose-6-phosphate Synthase and Phosphatase mRNA Relative to the Control Groups

A subsequent real-time quantitative PCR analysis tested the expression of trehalose synthesis genes relative to the control groups. The tps1 expression was always at a lower level relative to the control group. Initially, tps1 gene expression was the lowest among the tested genes (RQ = ). After 8 hours expression increased to RQ = 0., but after 20 hours it decreased to RQ = (Table 2). Differences between means for the IVM-group after 4 and 20 hours of culture were statistically significant with respect to the control (Figure 3(a)). Between tps1 gene expression and TPS activity was observed a fairly strong correlation (; Table 2).

(a)

(b)

Figure 3: Relative activity of trehalose-6-phosphate synthase (TPS) and phosphatase (TPP) and their mRNA expression (tps1, tps2, and tpp genes) normalized to the endogenous reference gapdh (glyceraldehyde-3-phosphate dehydrogenase) gene and relative to the control groups. IVM: ivermectin; RQ: relative quantification; (a) relative activity of TPS and tps1, tps2 expression; (b) relative activity of TPP and tpp expression; change at and change at with respect to the control group.

Expression of the tps2 gene after 4 and 20 hours was lower than that of the control group (RQ = and RQ = , resp.). After 8-hour incubation expression of this gene was a little higher than in the control but it was not a statistically significant change relative to the control (RQ = ; Table 2; Figure 3(a)). As with tps1, between tps2 gene expression and TPS activity was observed a fairly strong correlation (; Table 2).

The level of TPP mRNA expression was lower relative to the control group during the cultivation. The highest expression of tpp was also observed after 8 hours of the culture (RQ = ; Table 2; Figure 3(b)). The weak Pearson’s correlation was here between tpp gene expression and TPP activity (; Table 2).

4. Discussion

Trehalose metabolism may provide a new target for combating parasitic nematodes in mammals [27, 28]. This is particularly true for the destruction of the T6P pathway, which is likely to be toxic for nematodes. As mentioned in the Introduction, Kormish and McGhee [19] discovered gob-1 lethality in C. elegans, which is not due to low trehalose levels but rather to the buildup of the intermediate T6P. In addition, mutations in tps1 and tps2 almost completely suppress the gob-1 loss-of-function phenotype. The results of these studies suggest that TPP could be a good target for new anthelmintic drugs. Promising results were obtained by Kushwaha et al. [21], who investigated the silencing of B. malayi TPP in vitro. Silencing of the tpp gene had the effect of reducing fertility in B. malayi males and females, resulted in violations of embryogenesis in the interior of females, was lethal to L₃ larvae, and led to fatal effects during the development of the parasite in the host. In the present research, we decided to investigate if there would be a similar effect to the above on the trehalose synthesis pathway with the use of the antiparasitic drug IVM in in vitro cultures of mature female A. suum.

IVM is a widely used antiparasitic agent. It was used in in vitro cultures of adult male cattle parasite Onchocerca ochengi [29]. Previous research has used, like us, a saturated solution of unlabelled IVM (11.44 μM) for the cultivation of adult parasites. Although it was not a lethal dose for O. ochengi, it is the drug concentration administrated to pigs in feed and is sufficient to kill nonfilarial nematodes. In O. ochengi uptake of IVM was high by 3 hours of exposure, and uptake continued for up to 12 hours. This process occurred predominantly by the transcuticular route. In our study, after only 4 hours of IVM exposure, we noticed a significant paralysis and loss of mobility in the adult female A. suum. In the subsequent hours of incubation, worm shock deepened. After 20 hours, the roundworms were straight and showed no movement, while in the control worms we observed complete motility.

In the available literature there are several reports regarding IVM efficacy against larval and adult A. suum and A. lumbricoides in vivo [10, 11, 30, 31]. It is likely that IVM does not penetrate the shell of parasite eggs, because the larvae that develop in the eggs from IVM-treated groups appear fully infective for mice [9]. The impact of IVM on the trehalose metabolism of parasitic organisms seems particularly interesting, because this disaccharide acts as a key survival strategy of nematodes during exposure to various environmental stressors [15]. In addition, these studies are part of the current trend of the antiparasitic drugs research, which mostly revolve around pathways of trehalose synthesis. For example, Farelli et al. [32] recent results showed that structure of the trehalose-6-phosphate phosphatase from B. malayi reveals key design principles for anthelmintic drugs.

It is known that the ivermectin was located in the outer monolayer of the A. suum muscle membrane and nerve cord [7]. In our studies, we showed that IVM affects the profile of enzyme activity of the trehalose synthesis pathway and the expression of the mRNA of these enzymes in the muscle of A. suum. However, it is worth noting that the drug does not block the metabolic pathway. In the control groups, we observed a gradual decrease in the activity of both TPS and TPP in the muscle of the parasites. This may be because the culture medium does not contain nutritional components. TPS activity increased after 8 hours of incubation in the IVM-group in relation to the 4-hour cultures of IVM-group and control. It is possible that stress induced by the administration of IVM was stronger than starvation and affects T6P synthesis from accumulated reserve components such as glycogen. It is also clear that an efficient excretory system would detoxify the parasite and make it less susceptible to the therapeutic action of drugs [7]. The fact that tps2 expression was two times higher relative to the start and slightly rose relative to the control, at relatively lower expression of the tps1 gene, leads to the conclusion that the tps2 gene here is responsible for the increased activity of TPS in worms being IVM-treated here at this time.

In both groups there was a positive correlation between gene expression and the specific enzymes activity relative to the start. The highest level of correlation between the activity of a specific enzyme and the gene expression was observed for the tps2 gene at IVM-group, while, in the control group, this correlation was weak. It was observed a high correlation of the tps1 gene expression with the TPS activity in the control group and moderate in IVM-group with respect to the start. In the case of tpp, the correlation between gene expression and the TPP activity was strong in the control group and weak in the IVM-group.

Relative to the appropriate control groups we noted the highest correlation coefficient between the activity of a specific enzyme with tps2 gene expression. Also in the case of tps1 there was fairly strong correlation. Between the activity of TPP and the tpp expression relative to control was observed a weak correlation, as in the case of analysis with respect to the starting. To summarize, we can say that T6P synthase activity in the IVM-group is positively correlated mainly with the tps2 gene expression. In the case of T6P phosphatase the same relationship was not observed.

Expression profiles of mRNA were different for each of the three examined genes. There was a decrease in tps1 and tps2 gene expression after 20 hours in the IVM medium, relative to the expression at time zero. However, the level of tpp expression at this time was very similar to the start. Relative to the control, the expression level was lower for all three genes at the end of the culture; however, expression of tps2 was a little higher after 8 hours in the IVM-group. Results of this study could suggest that this concentration of IVM acts mainly by lowering the expression of the tps1 and tpp genes. It is worth noting that in the 8-hour incubation in IVM medium an increase in expression of all three genes in relation to measurements occurred at 4 hours of incubation. In the case of tpp gene it was an increase above the control value. In addition, it is positively correlated with increased activity of trehalose synthesis enzymes. The 8-hour incubation seems to be a key moment of the impact of IVM to stimulate the metabolism of trehalose in adult worms. Further culturing worms in the drug solution caused a rapid decreasing of studied parameters. Given that the decrease in activity of a satisfactory effect of the enzymes and their mRNA expression was obtained after 20 h of incubation, when the worms were completely nonmotile, the effect of the drug on the trehalose metabolism of adult worms present in the intestine of the host in vivo appears to be negligible, because IVM enters the blood as early as 4 hours after oral administration [2]. It seems that IVM may more negatively affect the trehalose synthesis of A. suum larvae in host body.

5. Conclusions

Based on the results of our research it can be concluded that the search for new drugs that block the trehalose synthesis path in A. suum is justified to enhance the action of ivermectin and maybe another drugs. Addition of trehalose synthesis pathway inhibitors can contribute to more effective control of the parasites in the future. The study also confirms that trehalose metabolism is activated to protect against lethal effects of the drug in the 8 hours of cultivating and this process is regulated at the molecular level. In addition, it correlates positively with the activity of specific enzymes. We can also say that trehalose synthesis pathway is activated in stress conditions, more during treatment with the use of antiparasitic drug than starvation.

Although the lethal dose of IVM reduces mRNA expression of trehalose synthesis enzymes by roundworms cultivated in vitro, it does not block the path completely and the time necessary to obtain a satisfactory result is too long. Because of this and the progressive drug resistance of parasites, it seems reasonable to study trehalose synthesis pathway gene silencing in the future.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

W. C. Campbell, M. H. Fisher, E. O. Stapley, G. Albers-Schönberg, and T. A. Jacob, “Ivermectin: a potent new antiparasitic agent,” Science, vol. 221, no. 4613, pp. 823–828, 1983.

A. Ottesen and W. C. Campbell, “Ivermectin in human medicine,” Journal of Antimicrobial Chemotherapy, vol. 34, no. 2, pp. 195–203, 1994.

R. J. Martin and A. J. Pennington, “A patch-clamp study of effects of dihydroavermectin on Ascaris muscle,” British Journal of Pharmacology, vol. 98, no. 3, pp. 747–756, 1989.

S. P. Rohrer, P. T. Meinke, E. C. Hayes, H. Mrozik, and J. M. Schaeffer, “Photoaffinity labeling of avermectin binding sites from Caenorhabditis elegans and Drosophila melanogaster,” Proceedings of the National Academy of Sciences of the United States of America, vol. 89, no. 9, pp. 4168–4172, 1992.

J. P. Arena, K. K. Liu, P. S. Paress, and D. F. Cully, “Avermectin-sensitive chloride currents induced by Caenorhabditis elegans RNA in Xenopus oocytes,” Molecular Pharmacology, vol. 40, no. 3, pp. 368–374, 1991.

J. P. Arena, K. K. Liu, P. S. Paress, J. M. Schaeffer, and D. F. Cully, “Expression of a glutamate-activated chloride current in Xenopus oocytes injected with Caenorhabditis elegans RNA: evidence for modulation by avermectin,” Molecular Brain Research, vol. 15, no. 3-4, pp. 339–348, 1992.

R. J. Martin, J. R. Kusel, S. J. Robertson, A. Minta, and R. P. Haugland, “Distribution of a fluorescent ivermectin probe, bodipy ivermectin, in tissues of the nematode parasite Ascaris suum,” Parasitology Research, vol. 78, no. 4, pp. 341–348, 1992.

I. O. Ademola, B. O. Fagbemi, and O. S. Idowu, “Comparative in-vitro studies on the efficacy of ivermectin against gastrointestinal sheep nematode,” Tropical Journal of Pharmaceutical Research, vol. 2, no. 2, pp. 235–238, 2003.

J. Boes, L. Eriksen, and P. Nansen, “Embryonation and infectivity of Ascaris suum eggs isolated from worms expelled by pigs treated with albendazole, pyrantel pamoate, ivermectin or piperazine dihydrochloride,” Veterinary Parasitology, vol. 75, no. 2-3, pp. 181–190, 1998.

C. A. Lichtensteiger, J. A. Dipietro, A. J. Paul, E. J. Neumann, and L. Thompson, “Persistent activity of doramectin and ivermectin against Ascaris suum in experimentally infected pigs,” Veterinary Parasitology, vol. 82, no. 3, pp. 235–241, 1999.

F. H. M. Borgsteede, C. P. H. Gaasenbeek, S. Nicoll, R. J. Domangue, and E. M. Abbott, “A comparison of the efficacy of two ivermectin formulations against larval and adult Ascaris suum and Oesophagostomum dentatum in experimentally infected pigs,” Veterinary Parasitology, vol. 146, no. 3-4, pp. 288–293, 2007.

D. Fairbairn, “Trehalose and glucose in helminths and other invertebrates,” Canadian Journal of Zoology, vol. 36, no. 5, pp. 787–795, 1958.

M. Dmitryjuk, E. Łopieńska-Biernat, and M. Farjan, “The level of sugars and synthesis of trehalose in Ascaris suum tissues,” Journal of Helminthology, vol. 83, no. 3, pp. 237–243, 2009.

R. N. Perry, “Dormancy and hatching of nematode eggs,” Parasitology Today, vol. 5, no. 12, pp. 377–383, 1989.

C. A. Behm, “The role of trehalose in the physiology of nematodes,” International Journal for Parasitology, vol. 27, no. 2, pp. 215–229, 1997.

A. D. Elbein, Y. T. Pan, I. Pastuszak, and D. Carroll, “New insights on trehalose: a multifunctional molecule,” Glycobiology, vol. 13, no. 4, pp. 17–27, 2003.

M. Dmitryjuk, M. Dopieralska, E. Łopieńska-Biernat, and R. J. Fraȩczek, “Purification and partial biochemical-genetic characterization of trehalose 6-phosphate synthase from muscles of adult female Ascaris suum,” Journal of Helminthology, vol. 87, no. 2, pp. 212–221, 2013.

M. Dmitryjuk, E. Łopieńska-Biernat, and B. Sawczuk, “Properties of trehalose-6-phosphate phosphatase from Ascaris suum muscles—preliminary studies,” Russian Journal of Nematology, vol. 20, no. 1, pp. 9–14, 2012.

J. D. Kormish and J. D. McGhee, “The C. elegans lethal gut-obstructed gob-1 gene is trehalose-6-phosphate phosphatase,” Developmental Biology, vol. 287, no. 1, pp. 35–47, 2005.

S. Kushwaha, P. K. Singh, A. K. Rana, and S. Misra-Bhattacharya, “Cloning, expression, purification and kinetics of trehalose-6-phosphate phosphatase of filarial parasite Brugia malayi,” Acta Tropica, vol. 119, no. 2-3, pp. 151–159, 2011.

S. Kushwaha, P. K. Singh, M. Shahab, M. Pathak, and S. M. Bhattacharya, “In vitro silencing of Brugia malayi trehalose-6-phosphate phosphatase impairs embryogenesis and in vivo development of infective larvae in jirds,” PLoS Neglected Tropical Diseases, vol. 6, no. 8, Article ID e1770, 2012.

N. F. H. Ho, T. G. Geary, C. L. Barsuhn, S. M. Sims, and D. P. Thompson, “Mechanistic studies in the transcuticular delivery of antiparasitic drugs II: ex vivo/in vitro correlation of solute transport by Ascaris suum,” Molecular and Biochemical Parasitology, vol. 52, no. 1, pp. 1–14, 1992.

H. M. Giaever, O. B. Styrvold, I. Kaasen, and A. R. Strøm, “Biochemical and genetic characterization of osmoregulatory trehalose synthesis in Escherichia coli,” Journal of Bacteriology, vol. 170, no. 6, pp. 2841–2849, 1988.

I. Kaasen, P. Falkenberg, O. B. Styrvold, and A. R. Strom, “Molecular cloning and physical mapping of the otsBA genes, which encode the osmoregulatory trehalose pathway of Escherichia coli: evidence that transcription is activated by KatF (AppR),” Journal of Bacteriology, vol. 174, no. 3, pp. 889–898, 1992.

M. M. Bradford, “A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding,” Analytical Biochemistry, vol. 72, no. 1-2, pp. 248–254, 1976.

K. J. Livak and T. D. Schmittgen, “Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method,” Methods, vol. 25, no. 4, pp. 402–408, 2001.

F. I. Pellerone, S. K. Archer, C. A. Behm, W. N. Grant, M. J. Lacey, and A. C. Somerville, “Trehalose metabolism genes in Caenorhabditis elegans and filarial nematodes,” International Journal for Parasitology, vol. 33, no. 11, pp. 1195–1206, 2003.

S. Gupta and A. K. Srivastava, “Biochemical targets in filarial worms for selective antifilarial drug design,” Acta Parasitologica, vol. 50, no. 1, pp. 1–18, 2005.

H. F. Cross, A. Renz, and A. J. Trees, “In-vitro uptake of ivermectin by adult male Onchocerca ochengi,” Annals of Tropical Medicine and Parasitology, vol. 92, no. 6, pp. 711–720, 1998.

D. O. Freedman, W. S. Zierdt, A. Lujan, and T. B. Nutman, “The efficacy of ivermectin in the chemotherapy of gastrointestinal helminthiasis in humans,” The Journal of Infectious Diseases, vol. 159, no. 6, pp. 1151–1153, 1989.

C. Naquira, G. Jimenez, J. G. Guerra et al., “Ivermectin for human strongyloidiasis and other intestinal helminths,” The American Journal of Tropical Medicine and Hygiene, vol. 40, no. 3, pp. 304–309, 1989.

J. D. Farelli, B. D. Galvin, Z. Li et al., “Structure of the trehalose-6-phosphate phosphatase from Brugia malayi reveals key design principles for anthelmintic drugs,” PLoS Pathogens, vol. 10, no. 7, Article ID e1004245, 2014.