Anthelmintic effect of Indigofera tinctoria L on Haemonchus contortus obtained from sheep in Indonesia.

BACKGROUND AND AIM: Hemonchosis has resulted in huge economic losses for sheep farmers worldwide. Secondary metabolite compounds from Indigofera tinctoria L. can be used as anthelmintics. This study aimed to evaluate the in vitro and in vivo effects of I. tinctoria L. aqueous extract (IAE) as an anthelmintic against adult Haemonchus contortus isolated from sheep.
MATERIALS AND METHODS: Ten active adult worms were placed in each Petri dish containing 25 mL of IAE, each having a different concentration of IAE (at concentrations 100, 120, 140, 160, 180, 200, and 220 mg/mL). Each experiment was repeated. The positive control used 1% albendazole, and the negative control used 0.62% saline water. The number of immobile worms and the time of mortality were recorded after 2, 4, 6, and 8 h. The dead worms were subsequently tested using scanning electron microscopy (SEM) and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. In the in vivo study, 15 sheep with an average fecal egg count (FEC) of 1000 eggs per gram were treated with IAE for 9 days: Group A (negative control, saline water 0.62%), Group B (21 mg/mL), Group C (41 mg/mL), Group D (62 mg/mL), and Group E (positive control, albendazole 100 mg/mL). Measurements of the body weight, FEC reduction test, and hematology testing were performed on days 0, 7, and 14. SEM was performed using worms found from the abomasum of slaughtered sheep.
RESULTS: The leaves of I. tinctoria L. contained a number of secondary metabolites, including total tannins, saponins, flavonoids, and alkaloids. The most effective concentration that killed the adult H. contortus worms was 220 mg/mL (93.33% mortality) after 8 h of treatment. The electrophoresis results showed that the protein band at a dose of 22% was less than that of the control. The highest FECR value of the treatment group on the 14th day after treatment was at a dose of 62 mg/mL. The highest weight gain as well as the highest increased hemoglobin (Hb), packed cell volume (PCV), and total erythrocyte count (TEC) values on the 14th day after treatment were at a dose of 41 mg/mL. The SEM results showed that IAE treatment caused the worms' anterior parts to become wrinkled with thick creases and cuticle abrasion (in vitro) and the anterior part to shrink along with the presence of aggregates in the worm cuticle (in vivo).
CONCLUSION: The aqueous extract of I. tinctoria contains tannins, saponins, flavonoids, and alkaloids and has an anthelmintic effect with decreased FEC, increased weight gain, Hb, PCV, and TEC, causing damage to the worms' body and reducing the protein profile of adult H. contortus worms. Copyright: © Muda, et al.

Introduction

Haemonchus contortus is a blood-sucking gastrointestinal worm from the nematode class (Familia: Trichostrongylidae). In the sheep husbandry business, hemonchosis has caused huge economic losses. H. contortus infestation disrupts the health of farmed sheep in Indonesia. In sheep, hemonchosis can cause mortality, decreased production, stunted growth, and low body weight [1].

The prevalence of hemonchosis in sheep is still quite high. Baihaqi et al. [2] stated that the prevalence of Haemonchus sp. in thin-tailed sheep in Wonosobo, Indonesia, was 55.41%. Abdo et al. [3] stated that the hemonchosis infection rate in sheep slaughtered at a slaughterhouse in Bishoftu, Ethiopia was 69.6%, with a prevalence in young and adult cattle of 66.9% and 59%, respectively. Bibi et al. [4] reported that the prevalence of hemonchosis in sheep in Pakistan was 55%. Secondary metabolite compounds from plant extracts can be used as anthelmintics. Indigofera tinctoria L. is very commonly grown and can be easily found in Indonesia. Kusumawati et al. [5] stated that I. tinctoria contains tannins. Renukadevi and Sultana [6] added that the leaf extract of I. tinctoria contains flavonoids, saponins, sterols, terpenoids, phenolic acids, quinones, and tannins. Some plants that are the sources of tannins have an anthelmintic effect on nematodes [7]. Maestrini et al. [8] added that saponins also have an anthelmintic effect. Tannin and flavonoids have effective anthelmintic effects against worm eggs and larvae [9].

This study aimed to evaluate the in vitro and in vivo effects of I. tinctoria L. aqueous extract as an anthelmintic against adult H. contortus isolated from sheep.

Materials and Methods

Ethical approval

This study was approved by the Institutional Ethical Committee, Faculty of Veterinary Medicine, Universitas Gadjah Mada, Yogyakarta, Indonesia (No. 0016/EC-FKH/Int/2019).

Study period and location

The study was conducted from April 2019 to October 2020. All samples were processed in the Parasitology Laboratory of Veterinary Faculty of Gadjah Mada University, except for scanning electron microscopy (SEM) samples that were processed in the Laboratory of Indonesian Institute of Sciences.

Plant collection and extraction

The leaves of I. tinctoria L. were obtained from Maguwoharjo Village, Depok District, Sleman Regency, Yogyakarta (7.46’43″ “S, 110.23’21”″ E, and 140 MASL). The plant specimens were identified at the Plant Taxonomy Laboratory of the Biology Faculty, Universitas Gadjah Mada, Yogyakarta, Indonesia. A number of I. tinctoria L. leaves were cleaned, dried in a drying room, and stored until they were used for the extraction process. Each of the dry I. tinctoria leaves (10, 12, 14, 16, 18, 20, and 22 g) was placed in 100 mL of distilled water and then incubated at 90°C for 15 min. The solution was filtered using filter paper, and the filtrate (100, 120, 140, 160, 180, 200, and 220 mg/mL) was stored in the refrigerator until SEM and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) were conducted [10].

Determinination of qualitative plant phytochemical

The content of secondary metabolites in I. tinctoria leaves was determined using the spectrophotometric method. The total equivalent tannic acid was determined as described previously [11,12]. Total flavonoids were determined using the spectrophotometric method [13]. The results of the total equivalent tannic acid, saponins, flavonoids, and alkaloid equivalent quinine were expressed as %w/w (weight of tannins or flavonoids or saponin or alkaloid per weight of sample × 100).

In vitro study

The H. contortus worms were obtained directly from the abomasum of naturally infected sheep slaughtered at a slaughterhouse in Sleman, Yogyakarta, Indonesia. This abomasum was taken to the Parasitology Laboratory of the Faculty of Veterinary Medicine, Universitas Gadjah Mada, Yogyakarta. The worm collection was done by opening the abomasum and cutting the curvature. Subsequently, the abomasum contents were poured out carefully, and the visible worms were collected and put into a container containing 0.62% physiological NaCl solution [10].

The I. tinctoria L. aqueous extract (IAE) was prepared 1 day before the worm mortality test according to the treatment dose. Ten active adult worms were placed in a Petri dish containing 25 mL of IAE. This experiment with each treatment group (negative control, 100, 120, 140, 160, 180, 200, and 220 mg/mL IAE, and positive control) was repeated. The positive control was administered albendazole 1%, and the negative control was administered 0.62% physiological NaCl. Observations were made after 2, 4, 6, and 8 h. The time of mortality and the number of immobile worms were recorded. Worm mortality was characterized by worms that did not move when the Petri dish was shaken or touched with a needle. The dead worms were put in an absolute ethanol solution and stored at 4°C until they were used for SEM and SDS-PAGE [10].

In vivo study

Fifteen sheep with an average fecal egg count (FEC) of 1000 egg per gram (EPG) that was infected with L3 H. contortus were treated with IAE for 9 days: Negative control (saline water 0.62%), Group B (21 mg/mL), Group C (41 mg/mL), Group D (62 mg/mL), and positive control (albendazole 100 mg/mL). The variables analyzed included body weight, EPG, hematology results, and SEM. Observations, data collection, and testing were carried out on days 0, 7, and 14 [14]. SEM was performed using worms found in the abomasum of slaughtered sheep.

SEM

Adult worms that had died from the anthelmintic test (in vitro) and adult worms found in the abomasum (in vivo) were used in this test. The worm samples were fixed in absolute ethanol. Subsequently, the following were carried out: Solid specimen preparation by cleaning in a cacodylate buffer for 2 h, prefixation in 2.5% glutaraldehyde for 48 h, fixation in 2% tannic acid with four washes in cacodylate buffer and distilled water, dehydrated in graded alcohol, and dried in tertiary butanol. Dry samples were coated with copper for 15 min and observed with SEM (JEOL JSM-5319LV, JEOL USA, Inc.) [15].

SDS-PAGE

This test used adult worms that died from the anthelmintic test. The specimens were washed several times using phosphate-buffered saline (PBS) to remove debris and host-derived materials. The specimens were crushed in 100 uL of PBS. The dissolved protein was isolated through 1200× centrifugation for 5 min and used for electrophoresis. Electrophoresis was carried out based on the method used by Sambodo et al. [10]. Dissolved protein samples and markers (Thermo Scientific, Lithuania) were boiled for 2 min in a sample buffer with a volume ratio of 4:1 containing 50% glycerol, 10% SDS, 2.5% DTT, and 0.05% (w/v) bromophenol blue liquid as a marker dye. Electrophoresis was carried out at 100 V in a vertical slab gel system. After electrophoresis, the gel was stained with 0.2% (w/v) Coomassie blue.

Fecal egg-count reduction test (FECRT)

Fecal sample collection was performed directly from the rectum. The EPG calculation was carried out using the McMaster egg counting technique (flotation procedures). The percentage decrease in the number of worm EPG of feces or FECR was calculated according to the following:

Hematology

Blood was collected from all sheep through the jugular vein (2 mL/sheep). The parameters analyzed included hemoglobin (Hb), packed cell volume (PCV), and total erythrocyte count (TEC) [14].

Statistical analysis

Adult worm mortality, body weight, EPG, and hematology data were analyzed using a one-way analysis of variance (ANOVA). The SEM and SDS-PAGE results were analyzed descriptively.

Results

Determining qualitative plant phytochemical

The quantitative phytochemical analysis showed that the leaves of I. tinctoria L. contained a number of secondary metabolites such as total tannins, saponins, flavonoids, and alkaloids (Table-1). The largest secondary metabolite compound was total tannins (5.43% w/w) and flavonoids (3.45% w/w).

Table-1

Quantitative phytochemical analysis.

Secondary metabolite compounds	%w/w
Total Tannins	5.43
Total Saponins	1.22
Total Flavonoids	3.45
Total Alkaloids	0.11

Table-2 shows that IAE had a statistically significant effect on the mortality rate of H. contortus after 8 h of treatment (p<0.05). H. contortus deaths occurred after 8 h of immersion at a dose of 120 mg/mL and after 6 h at a dose of 160 mg/mL. In the negative control group, there was no worm mortality within 8 h of immersion. The most effective concentration that terminated adult H. contortus worms was obtained at a 220 mg/mL concentration, which resulted in 93.33% mortality (Table-2).

Table-2

Effect of IAE concentrations on the mortality rate of Haemonchus contortus after 8 h of immersion.

Treatment	Time of death (h)
	2	4	6	8
NaCl 0.62%	0.00+0.00	0.00+0.00	0.00+0.00a	0.00+0.00a
IAE 100 mg/mL	0.00+0.00	0.00+0.00	0.00+0.00a	0.00+0.00a
IAE 120 mg/mL	0.00+0.00	0.00+0.00	0.00+0.00a	13.33+11.54b
IAE 140 mg/mL	0.00+0.00	0.00+0.00	0.00+0.00a	16.67+5.77b
IAE 160 mg/mL	0.00+0.00	0.00+0.00	10.00+17.32b	36.66+5.77c
IAE 180 mg/mL	0.00+0.00	0.00+0.00	16.66+20.81b	56.66+15.27d
IAE 200 mg/mL	0.00+0.00	0.00+0.00	33.33+28.8c	76.66+5.77e
IAE 220 mg/mL	0.00+0.00	0.00+0.00	56.66+15.27c	93.33+11.54f
Albendazole 1 mg/mL	3.33+5.77	96.66+5.77	100.00+0.00d	100.00+0.00f

a,b,c,d,e,fDifferent superscripts within the same column indicates significant differences (p<0.05). IAE=Indigofera tinctoria crude aqueous extract

Figures-1 and 2 show the significant ultrastructural changes in adult H. contortus worms after in vitro immersion in IAE. In the control worms, their anterior part did not shrink, their cuticle had no aggregate, and there was no damage to the cuticle surface. However, damage occurred in the treatment worms (Figures-1, 2b, and 1, 2c). Their anterior end was wrinkled with thick folds, and their cuticles were abraded.

Figure-1

Ultrastructure of the anterior part of the worm: (a) Negative control. (b) A dose of 100 mg/mL: Anterior end was constricted. (c) A dose 220 mg/mL: Anterior end was constricted with thick folds.

Figure-2

Ultrastructure of the midsection cuticle of the worm’s body: (a) Negative control. (b) A dose of 100 mg mL: Cuticle surface abraded. (c) A dose 220 mg/mL: The cuticle surface was wavy and abraded.

Figure-3 shows that the electrophoresis of the soluble protein of H. contortus after treatment produced five protein bands with molecular weights of 10.8, 15.8, 35.4, and 51.7 kDa in 22% IAE. Conversely, at a dose of 10%, there were six protein bands. There were eight protein bands with molecular weights of 10.8, 15.8, 35.4, 40.8, 47.0, 51.7, 56.9, and 72.1 kDa in the control group.

Figure-3

Sodium dodecyl sulfate-polyacrylamide gel electrophoresis electropherogram of Haemonchus contortus. Line 1 protein marker (Mr), line 2 worm protein of negative control (C), line 3, and 4 worm protein after immersion in 10% and 22% Indigofera tinctoria L. aqueous extract.

Table-3 shows the highest FECRT value in the treatment group on the 14th day after treatment at a dose of 62 mg/mL. The results of the ANOVA showed significant differences (p<0.05). Table-4 shows that the highest weight gain on the 14th day after treatment at a dose of 41 mg/mL, which is 0.57 kg or 2.55%, and in the negative control, a weight loss of 0.40 kg or 2.08%. The highest increased Hb, PCV, and TEC values at day 14 were at a dose of 41 mg/mL, although the ANOVA did not show a significant difference (p<0.05; Table-5). The SEM results showed that IAE in vivo treatment caused the anterior part to shrink and aggregate to appear in the worm cuticle (Figure-4).

Table-3

The effect of IAE on fecal egg counts.

Dose of IAE (mg/mL)	Eggs per gram			Fecal egg-count reduction test (%)
	Pre-treatment	Post-treatment day 7	Post-treatment day 14
Saline water 0.62%	1250.00±317.54a	666.67±44.10a	383.33±83.33a	69.36
21	800.00±200.00a	416.67±116.67a	50.00±50.00b	93.75
41	850.00±202.07a	583.33±216.67a	50.00±28.87a	94.12
62	750.00±325.32a	350.00±76.38a	16.67±16.67c	97.87
Albendazole	1383.33±231.54a	0.00±0.00b	0.00±0.00d	100

a,b,c,dDifferent superscripts indicate significant differences (p<0.05). IAE=Indigofera tinctoria crude aqueous extract

Table-4

The effect of IAE on sheep body weight (kg).

Dose of IAE (mg/mL)	Pre-treatment	Post-treatment day 79	Post-treatment day 14
Saline water 0.62%	19.25±0.70a	20.10±0.89a	18.85±0.60a
21	22.10±0.40a	22.42±0.52a	21.88±0.06b
41	22.33±0.68a	23.20±0.73a	22.90±0.89b
62	20.43±0.96a	20.80±1.00a	20.67±0.71b
Albendazole	21.55±1.68a	22.08±1.86a	22.08±1.52b

a,bDifferent superscripts indicate significant differences (p<0.05). IAE=Indigofera tinctoria crude aqueous extract

Table-5

The effect of IAE on sheep hematology.

Blood parameters	Dose of IAE (mg/mL)	Pre-treatment	Post-treatment day 7	Post-treatment day 14
Hb (g/dl)	Saline water 0.62%	12.56±0.73	12.40±0.30	12.47±0.64
	21	11.23±0.98	10.73±0.54	11.33±0.95
	41	9.83±0.82	11.23±0.39	12.43±0.34
	62	10.70±0.69	10.73±0.70	11.13±0.75
	Albendazole	10.30±0.35	9.90±0.0.11	11.00±0.30
PCV (%)	Saline water 0.62%	35.10±1.95	36.50±1.31	35.47±1.74
	21	32.63±3.28	31.20±1.70	33.00±2.56
	41	29.67±1.51	33.57±0.99	35.97±1.81
	62	32.73±2.44	32.50±2.51	32.23±1.98
	Albendazole	31.57±1.14	29.93±1.23	32.47±1.46
TEC (million/UI)	Saline water 0.62%	12.92±0.84	13.45±0.50	13.24±0.88
	21	12.12±0.67	11.83±0.63	12.32±0.59
	41	10.04±1.97	11.34±1.41	12.15±0.89
	62	10.99±0.15	10.88±0.64	11.00±0.92
	Albendazole	10.55±1.15	10.12±0.69	11.04±0.73

Overall values do not differ significantly (p<0.05); Hb=Hemoglobin, PCV=Packed cell volume, TEC=Total erythrocyte count, SE=Standard error

Figure-4

Ultrastructure of the anterior and the midsection part of the worm: (a) Negative control. (b) a dose 21 mg/mL.

Discussion

The quantitative phytochemical analysis showed that I. tinctoria L. contained secondary metabolites with the highest amount of total tannins and flavonoids. The previous studies conducted by Rahman et al. [16] and Verma and Suresh [17] found that I. tinctoria leaves contain flavonoids and alkaloids. Mishra et al. [18] also found that tannins and saponins are present in I. tinctoria. Tannins, saponins, flavonoids, and alkaloids in the extract of P. falcaria have previously been shown to have an anthelmintic effect against H. contortus [19]. Klongsiriwet et al. [20] added that the combination of flavonoids and tannins had a synergistic anthelmintic effect against H. contortus. Joshua et al. [11] stated that the medicinal potential of plant leaf extracts could be identified from their phytochemical components.

In the current study, the highest mortality in H. contortus occurred after 8 h of immersion, which was believed to be caused by the reaction of the collective presence of bioactive compounds in the plant extracts. This study’s findings are similar to those of Ferreira et al. [21], who reported that the leaf extract of Annona muricata L. could completely inhibit the motility of adult H. contortus worms in the first 6-8 h. Ahmed et al. [22] stated that Artemisia herba-alba and Punica granatum had a significant effect on the mortality rate of adult H. contortus after 7 h of exposure. Zaman et al. [23] reported that herbal complex extracts could cause 100% death in adult H. contortus worms 8 h post-exposure. Widiarso et al. [24] stated that the infusion of Gigantochloa apus could cause 100% mortality against H. contortus after 4 h of immersion. H. contortus adult worms’ mortality is an effect of the tannins in the plant extract. Tannins can directly affect adult H. contortus worms by impairing the protective function and absorption of H. contortus [25]. Maestrini et al. [8] added that saponins could cause death by increasing the cell membrane permeability. Alkaloids work by affecting the activity of the worm muscles [26].

The damage to the anterior end and cuticle that experienced abrasion proved that IAE interacted with the nematode cuticle. Baihaqi et al. [19] stated that an in vitro extract of P. falcataria’s bark waste caused damage to the buccal area, and aggregate built up in the cuticle annular. Acevado-Ramírez et al. [27] stated that Castanea sativa caused damage around the mouth, anus, vulva, copular bursa, and cuticle of worms. Martínez-ortíz-de-montellano et al. [28] added that the leaf extracts of Onobrychis viciifolia and Lysiloma latisiliquum caused changes in the transferal fold and thickening of the cuticle of adult H. contortus worms. Yoshihara et al. [29] added that Acacia mearnsii extract caused ruptures of the cuticle and transverse wrinkles on the body surface of adult H. contortus. Barone et al. [30] added that Cranberry vine extract caused aggregate accumulation in the cuticle and buccal areas of H. contortus. The peeling and wrinkling of adult H. contortus cuticle after soaking with Biophytum petersianum were reported by Sambodo et al. [10]. Tresia et al. [31] stated that cuticle damage and changes in the permeability of the worm cuticle were related to the active ingredients found in plants. Damage to the cuticle disrupts the protective function and absorption of nutrients, resulting in malnutrition and impaired motility, which causes the worms to die. The mechanism of cuticle damage occurs through the insertion of tannins into the lipid layer in the cuticle (glycosylation) and interaction with the proline and hydroxyproline collagen layers in the cuticle, resulting in changes in the cells [32].

Soaking H. contortus in I. tinctoria extract showed a decrease in the number of protein bands. Several studies have shown different numbers of protein bands. Sambodo et al. [10] stated that H. contortus soaked in a 10% dose of B. petersianum showed five protein bands with sizes of 9.3, 17.1, 50, 63.2, and 72.7 kDa. Mubarokah et al. [15] stated that A. catechu extract decreased the number of protein bands. Jaiswal et al. [33] added that in H. contortus females, there were 35 protein bands. In this study, the decrease in the number of protein bands was caused by secondary metabolites that disrupted the protein binding in the worms. Hoste et al. [34] stated that tannins could bind proline and hydroxyproline, while worm bodies are known to contain lots of proline and hydroxyproline. Zong et al. [25] added that tannins binding to proteins affected the physiological processes of worms and/or modified the host immune response in eliminating adult worms.

The decreased EPG value after treatment was the same as the results of research conducted by Simon et al. [35], who stated that Combretum molle extract decreased the FEC in sheep infected with H. contortus. González-Cortazar et al. [36] stated that the aqueous extract of L. acapulcensis leaves reduced the EPG value of gastrointestinal nematodes in sheep. Sambodo et al. [14] also stated that the aqueous extract of Biophytum petersianum decreased the EPG value of H. contortus in goats. The decrease in the EPG value is believed to be caused by secondary compounds in I. tinctoria. The presence of flavonoids, tannins, saponins, and alkaloids in C. molle may be responsible for the anthelmintic effect of these plants [35]. González-Cortazar et al. [36] added that myricitrin (a flavonoid) is the main component for reducing the EPG value.

The treatment group’s increased body weight is believed to be due to the loss of most of the worms in the abomasum of the treated animals so that the absorption of nutrients from the feed was improved. These results are consistent with those of Sambodo et al. [14], who stated that B. petersianum extract increased the body weight of goats infected with H. contortus. Eguale et al. [37] stated that this could occur in livestock due to reduced blood plasma and protein associated with the presence of parasites.

The blood test results in this study were similar to those of Meenakshisundaram et al. [38], who stated that the ethanol extract treatment of I. tinctoria increased the Hb, PCV, and TEC values in sheep infected with gastrointestinal parasites. Eguale et al. [37] stated that Coriandrum sativum extract increased the PCV value 7 days after treatment. The increased hematological values are believed to be due to the loss of worm parasites in the abomasum so that the blood components can be better absorbed by the body. The increased Hb is probably due to increased iron absorption [38].

The SEM results at an in vivo stage are consistent with the SEM results at the in vitro stage. Changes in the ultrastructure of helminth parasites prove a strong interaction with IAE. This study’s results are similar to those of Martínez-ortíz-de-montellano et al. [28], which found that Tzalam leaf extract causes aggregates in the anterior end of H. contortus.

Conclusion

IAE contains tannins, saponins, flavonoids, and alkaloids. Aqueous extract of I. tinctoria L. has an anthelmintic effect, resulting in decreased FEC, increased weight gain, Hb, PCV, and TEC, causing damage to the worms’ body and reducing the protein profile of adult H. contortus worms.

Authors’ Contributions

JP and IM: Designed and managed the study. IM: Collected and analyzed the samples. IM and SS: Wrote the manuscript. JK and WN: Reviewed the manuscript. All authors have read and approved the final manuscript.