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Article

Ethanolic Extracts of Datura innoxia Have Promising Acaricidal Activity against Rhipicephalus microplus as It Blocks the Glutathione S-Transferase Activity of the Target Tick

by
Saman Saman
1,†,
Chien-Chin Chen
2,3,4,†,
Nosheen Malak
1,
Afshan Khan
1,
Nasreen Nasreen
1,
Adil Khan
5,*,
Sadaf Niaz
1,
Gauhar Rehman
1,
Roger I. Rodriguez-Vivas
6 and
Raquel Cossío-Bayúgar
7
1
Department of Zoology, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan
2
Department of Biotechnology and Bioindustry Sciences, College of Bioscience and Biotechnology, National Cheng Kung University, Tainan 701, Taiwan
3
Department of Pathology, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi 600, Taiwan
4
Department of Cosmetic Science, Chia Nan University of Pharmacy and Science, Tainan 717, Taiwan
5
Department of Zoology, Bacha Khan University Charsadda, Charsadda 24631, Pakistan
6
Departamento de Salud Animal y Medicina Preventiva, Facultad de Medicina Veterinaria y Zootecnia, Universidad Autónoma de Yucatán, Merida 97000, Yucatán, Mexico
7
Departamento de Artropodología, Centro Nacional de Investigaciones Disciplinarias en Salud Animal e Inocuidad, Instituto Nacional de Investigaciones Forestales Agrícolas y Pecuarias (INIFAP), Boulevard Cuauhnahuac No. 8534, Jiutepec 62574, Morelos, Mexico
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Genes 2023, 14(1), 118; https://doi.org/10.3390/genes14010118
Submission received: 10 November 2022 / Revised: 14 December 2022 / Accepted: 27 December 2022 / Published: 31 December 2022
(This article belongs to the Section Epigenomics)
Browse Figures
Versions Notes

Abstract

:
Rhipicephalus microplus is a major bovine ectoparasite that negatively impacts the cattle industry. The acaricidal activity of Datura innoxia ethanolic plant extract against R. microplus, compared with trichlorfon, was examined using the adult immersion test (AIT), and larval packet test (LPT). In vitro acaricidal activity of the selected plant extract against R. microplus engorged females was evaluated at different concentrations (2.5, 5, 10, 20, and 40 mg/mL), and was the same for AIT and LPT. It was further supported by in silico molecular docking of D. innoxia’s 21 phytochemicals against the R. microplus Glutathione S-transferases (RmGST) protein’s three-dimensional (3D) structure predicted by the trRosetta server. The modeled 3D structure was then evaluated and confirmed with PROCHECK, ERRAT, and Verify3D online servers. To predict the binding mechanisms of these compounds, molecular docking was performed using Auto dock Vina software, and molecular dynamic (MD) simulations were used to investigate the protein atom’s dynamic motion. D. innoxia has a relatively higher inhibitory effect on oviposition (from 9.81% to 45.37%) and total larval mortality (42.33% at 24 h and 93.67% at 48 h) at 40 mg/mL. Moreover, the docking results showed that the chemicals norapoatropine and 7-Hydroxyhyoscyamine have strong interactions with active site residues of the target protein, with a docking score of −7.3 and −7.0 Kcal/mol, respectively. The current work also provided a computational basis for the inhibitors of Glutathione S-transferases that were studied in this research work, and this new knowledge should aid in creating new and effective acaricidal chemicals. Furthermore, this plant extract’s acaricide activity and its effect on oviposition and larval mortality were established in this work for the first time, indicating the possible use of this extract in the management of ticks.

Graphical Abstract

1. Introduction

Ticks negatively impact livestock because they are hematophagous ectoparasites [1]. Rhipicephalus microplus is one of the most extensively dispersed ticks in tropical and subtropical areas that is a concern for the livestock industry. The economic impact of this tick species on cattle production worldwide is estimated to be USD 30 billion annually [2,3]. Tick infestations can cause anemia, damage the hide, and spread diseases, including Anaplasma marginale, Babesia bovis, and Babesia bigemina [4].
Currently, various synthetic acaricides are used to control R. microplus. However, the continuous use of these acaricides has resulted in the selection of acaricide-resistant and multi-drug-resistant tick populations [5,6,7]. Plant extracts and oils may be a viable alternative to conventional pesticide approaches that have been overused and misused [8]. Plant extracts are associated with lower environmental and food contamination, result in slower development of arthropod resistance, and are of lower toxicity to animals and humans [9].
As a source of unrivaled chemo-diversity, medicinal plants’ pure chemicals and standardized extracts provide a bountiful supply of potential novel drugs. Modernization, standardization, quality control, and greater understanding of ethnomedicinal plant medicines’ active components and modes of action will affect their international acceptance. Steroids, alkaloids, terpenes, flavonoids, phenylpropanoids, amides, and lignans are among the plant metabolites that have drawn the most attention as potential bioactive compounds against ticks [10]. In addition, products from several angiosperm plant species have been used to control economically important tick species [11,12,13,14,15], including acaricide-resistant species such as organophosphate and pyrethroids-resistant R. microplus [16,17].
Datura innoxia Mill. (Solanaceae), commonly known as devil’s trumpet or thorn-apple, is a plant with ethnopharmacological significance and is native to China, Mexico, the United States, the Caribbean Islands, and Asia [18]. The plant holds a unique position in Ayurveda and has been used to treat various ailments, including rabies, leprosy, and other infectious diseases [19]; however, acute toxicity and delirium may occur if the extract is used without caution. In addition to atropine and other tropanes, D. innoxia contains scopolamine hyoscyamine and withanolides (lactones). When seed extracts from several Datura species were tested for their ability to neutralize the stable diphenylpicrylhydrazyl (DPPH) radical and scavenge free radicals, D. innoxia showed the highest antioxidant capability [20]. Recently, a novel dinoxin B and anolide isolated from methanol extracts of D. innoxia leaves displayed IC50 values in the micromolar range against multiple human cancer cell lines [21].
Multiple functions of the Glutathione S-transferases (GSTs; EC 2.5.1.18) tick enzyme include the degradation of toxic chemicals, the oxidative stress response, and the binding of intracellular ligands such as heme and porphyrin [22]. When consuming blood, parasites have developed several ways to minimize oxidative damage and control redox homeostasis; to avoid heme poisoning, ticks have highly active antioxidant systems in which antioxidant enzymes like Glutathione S-transferases (GST) play an essential role [22,23,24].
Redox balance mediated by GST also plays a significant role in the tick’s survival ability in the face of acaricides [25,26,27,28]. D. innoxia aerial component extracts may have anti-tick properties yet to be discovered. D. innoxia plant extract was used in this study to test its in vitro acaricidal efficacy on R. microplus larvae and engorged females. Further, in silico docking was used to investigate the molecular inhibition profiles of the more potent phytochemicals against R. microplus GST activity, all to limit tick acaricide resistance.

2. Materials and Methods

2.1. Preparation of Plant Extracts

Aerial plant leaves of D. innoxia were obtained from district Mardan of Khyber Pakhtunkhwa (KPK) province, Pakistan. The plant leaves were rinsed in running tap water to clean them from debris. The plant was then identified and deposited in the herbarium of the Department of Botany, Abdul Wali Khan University Mardan (AWKUM) for identification. The plant was verified and allotted an accession number Awkum. Bot. 223.9.7. The crude ethanolic extract of D. innoxia leaves was made by the maceration method according to the published procedure [29]. D. innoxia leaves were air dried for 2 weeks at room temperature (30 °C) and then pulverized into powder using a plant grinder (Panasonic Model MX-AC210, Osaka, Japan). D. innoxia leaf powder was weighed, and 50 g was added to 600 mL (1:12) of 96% ethanol and stored at room temperature (25 ± 3 °C). The solution was then agitated for 48 h in an orbital shaking incubator (Cole-Parmer Model EW-51700-14, Cole-Parmer, Vernon Hills, IL, USA) at 200 RPM. The extract was then concentrated for 24 h in a water bath (Model WTB15, Memmert GmbH and Co. KG, Schwabach, Germany) to obtain less than 10% of the original solution. The stock solution was refrigerated at −4 °C for further analysis. The stock solution was then diluted in distilled water to create different concentrations of 40, 20, 10, 5, and 2.5 mg/mL (w/v). Distilled water was used as a negative control, and trichlorfon as a positive control.

2.2. Collection of R. microplus Ticks

Totally engorged females of R. microplus from natural infestation were collected from the ground and cattle bodies kept on farms in and around the Mardan area. After collection, the ticks were cleaned using water to remove dirt and dried with absorbent paper. For oviposition, 200 ticks were transferred to Petri dishes (with holes in the lid allowing air to circulate) and incubated in laboratory conditions (28 ± 1 °C and 85 ± 5% relative humidity). The deposited eggs were transferred to fresh glass vials after complete egg laying and held for hatching under similar incubation circumstances for 20 days. The larval packet test (LPT) was performed on larvae aged 14 to 15 days. The remaining ticks, were used in the adult immersion test (AIT).

2.3. Adult Immersion Test (AIT)

The AIT was performed with minimal adjustments as described by [17]. Several concentrations of the extract were used, including 2.5, 5, 10, 20, and 40 mg/mL. A total of 75 (5 × 7 × 3 = 105) engorged adult ticks were used in this study. Three replicates were employed, each separately with five ticks at each concentration, keeping in mind that all the ticks in a replicate were collected from the same farm [30]. Engorged females in each replicate group were weighted. Adult female ticks were submerged in 1 mL of the extract concentrations for 5 min. The treated 5 ticks were then placed in a Petri dish with Whatman filter paper no. 1, and the dish was maintained in an incubator (Model BIBD-101, Toronto, ON, Canada), which was adjusted to 28 °C and 85 ± 5% RH. The weight of eggs laid in each replicate group was obtained. For surviving ticks, data on the influence of plant extracts on oviposition (egg-laying) inhibition was collected and analyzed as described by [31]. To determine the extract’s effectiveness against engorged females, the engorged female’s weight was measured, and the predicted mass of eggs produced by the female was then used to calculate the percent egg inhibition (inhibition of oviposition (% IO)) by using the following formula [32], with and without treatment:
%   IO = IE   control   group − IE   treated   group IE   control   group × 100
where the index of egg laying IE = mean weight of eggs laid ÷ mean weight of engorged females.

2.4. Larval Packet Test (LPT)

A bioassay was performed using 2.5, 5, 10, 20, and 40 mg/mL of ethanol extracts. A packet of 100 larvae were immersed in 200 μL of each extract concentration in 1.5 mL centrifuge tubes. Ten minutes after, the solution was pipetted out, and the entire tube was dried by absorbing the fluid with a filter paper strip. The tubes were then covered with cotton cloths and secured with rubber bands. Three replicates with each extract concentration were performed. The larval packets treated with LPT were put into the incubator at the same temperature and relative humidity described above. Larval mortality was determined by counting the number of live (only larvae that could walk were considered alive) and dead larvae (larvae without movement, ataxia, or movement only of appendages were considered dead) after 24 and 48 h.

2.5. Glutathione S-Transferases Protein Sequence of R. microplus

The protein sequence of glutathione S-transferases (RmGST) was obtained from the UniProt KB database, a publicly available library of protein sequences with comprehensive functional annotations. This particular protein’s accession number is E5L876.

2.6. Modeling the 3D Structure of RmGST

TrRosetta (“https://robetta.bakerlab.org/ (accessed on 1 August 2022)”), a protein prediction server based on continuous automated model assessment (CAMEO, “https://www.cameo3d.org/ (accessed on 1 August 2022)”), performed the 3D structure predictions (de novo or ab initio). TrRosetta predicts protein structure using a modeling technique based on deep machine learning [33].

2.7. Modeled Structure Validation

The verification of the stereochemical quality of the modeled structure of the query protein was made using the PROCHECK (“https://www.ebi.ac.uk/thornton-srv/software/PROCHECK (accessed on 5 August 2022)”), Verify3D (“http://servicesn.mbi.ucla.edu/Verify3D/ (accessed on 5 August 2022)”), and ERRAT (“https://servicesn.mbi.ucla.edu/ERRAT/ (accessed on 5 August 2022)”) servers.

2.8. Determining Binding Sites

To assess the potential binding sites of the selected proteins, the Computed Atlas of Surface Topology of Proteins (CASTp) was employed [34]. PyMOL (PyMOL Molecular Graphics System, Version 1.5.0.4, Schrödinger, LLC, New York, NY, USA) and Chimera 1.16 were used to visualize the predicted sites. The predicted binding sites with constrained areas and volumes, where no ligands could fit, were ignored [35].

2.9. Ligands, Protein Preparation for Molecular Docking

A PubChem database (“https://pubchem.ncbi.nlm.nih.gov/ (accessed on 8 August 2022)”) search was undertaken to identify compounds from D. innoxia; 21 compounds were found and selected. ChemDraw 16.0 was used to create and analyze the 2D structures (.mol) of all 21 compounds. Chem3D 16.0 transforms all of the chemicals into 3D designs (.pdb). All rotatable bonds in ligands were made flexible, and Gasteiger atomic partial charges were assigned using the AutoDockTools program [36]. In preparation for receptor docking using the AutoDockTools program, all water molecules were removed, the co-crystallized ligand was removed, Gasteiger atomic partial charges were assigned, and all receptors and ligands were converted to the PDBQT format. The grid box was constructed using 56, 56, and 40 grid points in the x, y, and z axes, respectively, with a grid point spacing of 0.347 Å. The coordinates of the main grid box are 33.494, 21.231, and −12.276. Nine alternative conformations were created for each ligand and ranked based on their binding energies using AutoDockVina scoring functions (https://vina.scripps.edu (accessed on 8 August 2022)). The Discovery studio visualizer (version 19.1.0.18287 BIOVIA, San Diego, CA, USA) was used for the post-docking experiments. The Discovery studio visualizer selected the conformations with the lowest (most advantageous) free binding energy to examine the interactions between the target receptor and ligands.

2.10. Statistical Analysis

All statistical analyses were made using R Statistical software (version 4.1.3) [37] and RStudio software (version 2022.12.0+353) [38]. One-way ANOVA followed by post hoc Tukey’s honesty significance difference (HSD) test was performed using the “agricolae” package to find the significant difference between larval mortalities at 24 and 48 h time intervals and % IO for different concentrations [39]. The lethal concentrations causing 50% and 90% mortalities (LC50 and LC90) (24 and 48 h) [40] and lethal time causing 50% mortality (LT50) for the ethanolic extract were calculated using probit analysis [41] by applying the R “ecotox” package [42], where the heterogeneity significance (p-value) was kept at 0.05, and the fiduciary confidence limit was set at 95%. All results were visually presented by the “ggplot2” package [43].

3. Results

3.1. Adult Immersion Test (AIT)

Table 1 displays the percentages observed for the in vitro effectiveness of D. innoxia ethanolic extract against R. microplus. According to Table 1 and Figure 1A,E, the % IO increased as extract concentration increased (from 9.86% IO at 2.5 mg/m to 45.37% IO at 40 mg/mL) at 48 h. Overall, with higher concentrations (≥5 mg/mL) and a longer treatment time (48 h), the plant extract could significantly increase larval mortality and have the potential to hamper the egg-laying activity of R. microplus.

3.2. Larval Packet Test (LPT)

D. innoxia plant extract showed significant larvicidal activity, with more than 50% larval mortality at all concentrations except 2.5 mg/mL after 48 h, comparable to the mortality induced by the positive control, trichlorfon. The LC50 value of the extract at 48 h of treatment is 4.06 (3.53–4.58) mg/mL, and its corresponding LC90 is 26.63 (22.56–32.56) mg/mL (Table 2), Figure 1C, whereas its LT50 value is 25.94 (24.53–27.26) h and its LT90 values are 43.47 (40.57–47.46) h at 40 mg/mL concentration (Table 3 and Figure 1D). The significant difference between different concentrations for mortality at 24 h and 48 h and % IO at 48 h treatment by post hoc Tukey’s HSD test is shown in Figure 1F.

3.3. Analysis of Protein Models and Validation

The amino acid sequence of the target protein, Glutathione S-transferases (RmGST) UniProt identifier E5L876, comprising 223 amino acid residues, was used to predict a full-length model structure using the trRosetta server template-free modeling (de novo or ab initio) technique (Figure 2A). This server has available five model structures. The models from trRosetta appear superior due to their domain area architecture. The predicted 3D structures were validated and quality-evaluated to produce suitable protein structures. The correctness of the models is determined by the Ramachandran plots produced by ERRAT, Verify3D, and PROCHECK.
The validation scores of model 1 from trRosetta are the preferred model among the RmGST protein structures. ERRAT generated the model’s quality factor of 95.814% (Figure 2B). Two lines were put on the error axis to represent the degree of certainty with which the regions that exceeded the error value may be rejected. It is presented as a percentage of the protein for which the estimated error value is less than the rejection level of 95%. Structures generating quality factors of 95% and higher are considered high resolution. The average quality factor for lower resolution (2.5–3.0 Å) is roughly 91%. By comparing highly enhanced predicted structures to statistical analysis, ERRAT provided the value of the error function and revealed confidence limits. As a result, 95.814% of the total value is considered significant and accurate.
The PROCHECK service evaluated the stereochemical quality of protein structures on a residue-by-residue basis and overall structural geometry. Ramachandran plots revealed the U and W distributions of non-glycine and non-proline residues and the distribution of residues (Figure 2D). To distinguish between favorable and unfavorable regions, the phi and psi angles were plotted against each other. These perspectives were used to assess the quality of different regions. PROCHECK results revealed that 93.9% of amino acid residues were in preferred areas, 5.6% were in allowed regions, 0.0% were in the generous region, and 0.5% were in prohibited areas (Figure 2D). The Verify-3D application confirmed the model’s stereochemical quality [44]. Residues with a score function more significant than 0.2 are regarded as acceptable. Furthermore, 85.2% of the residues received a score greater than 0.2. The results verify the high quality of the projected model [45], as shown in Figure 2C.

3.4. Active Site Prediction

CASTp was utilized to identify potential binding sites within the RmGST protein structure (Figure 3). Ligand binding sites on proteins tend to include the most prominent pockets or cavities [45,46,47]. Hence, pockets with relatively low areas and volumes, where no ligand could fit, were not examined [48,49]. The target protein’s active site consisted of the amino acids ARG18, LEU21, ALA22, ASP25, ALA26, LYS27, VAL28, ASP30, HIS193, ALA196, TYR197, SER200, and LYS202.

3.5. Docking Studies

After validating the RmGST three-dimensional (3D) structural model and defining the target pocket, the parameters for the docking analysis were determined using AutoDockVina software (version 4.2.6). The docking stage was used to find the ligands having the best interactions with protein residues. AutoDockVina was used for docking the selected chemicals and ranking complexes based on their greatest binding affinities. ChemDraw created and reduced the 2D structures of the 21 specified chemicals. The complex was chosen for its high binding affinity and examined for interactions between RmGST residues.
D. innoxia’s phytochemicals revealed a higher docking score at the active sites of the RmGST protein structure in molecular docking studies. All of the compounds demonstrated binding affinity within the co-crystallized ligand binding sites. The compound Norapoatropine shows the highest binding affinity of −7.3 Kcal/mol, producing one hydrogen bond connection with Ala196 and one residual hydrophobic interaction with Arg18, Ala22, Val28, Tyr197, and Lys202. Similarly, the compound 7-Hydroxyhyoscyamine also showed the maximum binding affinity of −7.0 Kcal/mol and showed persistent hydrophobic interactions with the amino acids Arg18, Ala22, Asp25, Val28, Asp30, Tyr197, and Lys202. In silico docking studies demonstrated that Norapoatropine and 7-Hydroxyhyoscyamine had high docked scores (−7.3 and −7.0 Kcal/mol, respectively), indicating that these compounds may be potent inhibitors of R. microplus RmGST protein (Figure 4).

3.6. Molecular Dynamics Simulation

The iMODS server was used to perform normal mode analysis (NMA) on proteins to investigate their stability. The complex’s deformability is determined by the individual deformation of each residue, which is represented by hinges in the chain (Figure 5B). The calculated eigenvalue, which indicates the complex’s motion stiffness, was 2.2614 × 10−4 (Figure 5D). An inverse connection was discovered between the eigenvalue and the variance of each normal mode (Figure 5C). The NMA-derived B-factor scores were comparable to the RMS (Figure 5A). The covariance matrix depicted the coupling between pairs of residues, with various pairings exhibiting correlated, anti-correlated, or uncorrelated movements, denoted by red, blue, and white, respectively (Figure 5E). Finally, an elastic network model (Figure 5F) was built, and it displayed the pairings of atoms linked by springs based on the degree of stiffness between them, with stiffer strings appearing as darker gray.

4. Discussion

Plants have an essential role in traditional medicine, and they contain several compounds that may be able to interfere with the metabolic processes and life cycle of ticks [50]. Rosado-Aguilar et al. evaluated the possible use of plant extracts to manage arthropods of veterinary importance; a few plants were found to be promising against ticks [51]. The acaricidal activity of the D. innoxia plant extract was discovered in this study, and this finding can contribute to the development of plant-based acaricides for tick management.
The in vitro components of this study show that the D. innoxia extract exhibits acaricidal properties directed at two phases of R. microplus development: larvae and adult females with higher concentrations (≥5 mg/mL) and a longer treatment time (48 h). These findings are consistent with previous research. A 95% ethanol extract from D. stramonium leaves generated 20% mortality against R. microplus within 72 h of treatment in an adult immersion bioassay [52]. Additionally, in vitro investigations revealed that the 95% methanol extract of D. stramonium suppressed R. microplus oviposition by 77% [30]. Leaf and seed extracts of D. stramonium produced 98% and 25% mortalities of spider mites (Tetranychus urticae Koche) after 24 h, respectively, where the death rate of T. urticae females rose when the concentration of leaf extract was increased from 2416 to 7250 ppm, but there was no change when the amount of seed extract of the same concentration was increased [53]. In this study, D. innoxia extracts killed the R. microplus larvae (73.67–93.67% at 10–40 mg/mL), and the concentration 40 mg/mL was similar to the positive control group (p < 0.0). D. innoxia extracts showed a strong effect, producing the inhibition of oviposition of engorged females (IO 15.73–45.37% at 5–40 mg/mL) compared with the negative control (IO 0.20%).
Computer modeling approaches are widely used in drug design. Computer-aided drug design is a common term for this approach, whereas “structure-based drug design” refers to drug development based on the 3D structure of the biomolecular target. This kind of drug design relies on an increasing number of computational programs developed to improve the affinity and stability of these protein-based therapeutics [54,55,56]. To predict the binding mechanisms of these drug-like compounds, 21 chosen compounds from the D. innoxia plant were docked to the target protein R. microplus Glutathione S-transferases using AutoDock Vina software. The findings revealed that the chemicals norapoatropine and 7-hydroxyhyoscyamine had significant interactions with active site residues of the target protein RmGST, making them a suitable RmGST inhibitor and comparable to reference ligands. Norapoatropine, with a docking score of −7.3 Kcal/mol among the 21 different docking compounds, was determined to be the most effective of the investigated compounds, followed by 7-Hydroxyhyoscyamine with a docking score of −7.0 Kcal/mol. Both of these compounds have good inhibitory activity and their docking score is in the region of certain standard ligands, such as Trichlorofon (−4.1 Kcal/mol). Furthermore, both these ligands exhibited good interaction with R. microplus RmGST protein. The most potent ligand, norapoatropine, formed one hydrogen interactions with a bond length of 1.461 Å with the Ala 196 active amino acid residue and hydrophobic (Pi-alkyl) interaction with Arg 18, Ala 22, Val 28, and Lys 201, and one Pi-Pi T shaped interaction with Tyr 127 amino acid residue. 7-Hydroxyhyoscyamine also demonstrated a higher binding affinity with residual amino acids compared with Trichlorofon, which formed three-carbon–hydrogen bond Arg 18, Ala 22, and Tyr 127 and three-Pi–cation bond with Asp 25, Asp 30 and Lys 202, and one Pi-alkyl bond Val 28 amino acid residue. The results of in silico docking showed that the compounds norapoatropine and 7-Hydroxyhyoscyamine had the highest docked scores (−7.3 and −7.0 Kcal/mol, respectively), compared to other compounds, and similar residual interactions to those of Trichlorofon within the binding pocket, indicating that these compounds are promising anti-tick agents against R. microplus. In summation, the current work establishes a computational basis for RmGST inhibitors. Future studies should focus more closely on the therapeutic efficacy of these chemicals, their method of action on ticks, and their proteins, thereby enabling the development of new tick control resources.

5. Conclusions

This study proved that plant extract from D. innoxia has in vitro acaricidal action against larvae and engorged females of R. microplus. Our results will help verify the conditions that stimulate acaricidal activity. In addition, the examined extracts may be helpful in the creation of a long-term strategy for tick management in the livestock industry due to their acaricidal characteristics. The in vitro bioassays and in silico methodologies explored in this study provide an opportunity to evaluate acaricidal effects by merging different disciplines. This study opens the opportunity for tick management in the cattle industry. Additional research must be done to assess their impact on the adult tick stage and acaricidal activity in vivo.

Author Contributions

Conceptualization, S.S. and N.N.; methodology, S.S. and N.M.; software, N.M. and A.K.; validation, N.N., S.S., C.-C.C. and G.R.; formal analysis, A.K. (Afshan Khan), N.M. and A.K. (Adil Khan); investigation, R.C.-B.; resources, S.N.; data curation, R.I.R.-V. and C.-C.C.; writing—original draft preparation, A.K. (Adil Khan), S.S. and C.-C.C.; writing—review and editing, N.M. and C.-C.C.; visualization, N.N.; supervision, N.N., C.-C.C. and S.N.; project administration, A.K. (Adil Khan); funding acquisition, S.N. and C.-C.C. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by HEC NRPU, grant number 14905 and “The APC was funded by R.C.”.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

All authors acknowledge the support of Higher Education Commission of Pakistan for their financial support for this research via project number 16905 NRPU.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Patoliya, P.; Raval, K.; Upadhyaya, V.; Dewry, R.K.; Maiti, S.; Mondal, G.; Mohanty, T.K.; Bhakat, M. Tick infestation and its herbal treatment approach in India: A review. Pharma Innov. J. 2022, SP-11, 1323–1339. [Google Scholar]
  2. Estrada-Peña, A.; García, Z.; Sánchez, H.F. The Distribution and Ecological Preferences of Boophilus microplus (Acari: Ixodidae) in Mexico. Exp. Appl. Acarol. 2006, 38, 307–316. [Google Scholar] [CrossRef]
  3. Grisi, L.; Leite, R.C.; Martins, J.R.; Barros, A.T.; Andreotti, R.; Cançado, P.H.; León, A.A.; Pereira, J.B.; Villela, H.S. Reassessment of the potential economic impact of cattle parasites in Brazil. Rev. Bras. Parasitol. Vet. 2014, 23, 150–156. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Miraballes, C.; Riet-Correa, F. A review of the history of research and control of Rhipicephalus (Boophilus) microplus, babesiosis and anaplasmosis in Uruguay. Exp. Appl. Acarol. 2018, 75, 383–398. [Google Scholar] [CrossRef] [PubMed]
  5. Abbas, R.Z.; Zaman, M.A.; Colwell, D.D.; Gilleard, J.; Iqbal, Z. Acaricide resistance in cattle ticks and approaches to its management: The state of play. Vet. Parasitol. 2014, 203, 6–20. [Google Scholar] [CrossRef]
  6. Luns, D.A.R.; Martins, R.; Pombal, S.; Rodilla, J.M.L.; Githaka, N.W.; Vaz, I.d.S.; Logullo, C. Effect of essential oils against acaricide-susceptible and acaricide-resistant Rhipicephalus ticks. Exp. Appl. Acarol. 2021, 83, 597–608. [Google Scholar] [CrossRef]
  7. Alota, S.L.; Edquiban, T.R.J.; Galay, R.L.; Bernardo, J.M.G.; Sandalo, K.A.C.; Divina, B.P.; Tanaka, T. Determination of resistance status to amitraz in the cattle tick Rhipicephalus (Boophilus) microplus from Luzon, Philippines, through bioassay and molecular analysis. Exp. Appl. Acarol. 2021, 83, 399–409. [Google Scholar] [CrossRef]
  8. De Souza Chagas, A.C.; de Sena Oliveira, M.C.; Giglioti, R.; Santana, R.C.M.; Bizzo, H.R.; Gama, P.E.; Chaves, F.C.M. Efficacy of 11 Brazilian essential oils on lethality of the cattle tick Rhipicephalus (Boophilus) microplus. Ticks Tick-Borne Dis. 2016, 7, 427–432. [Google Scholar] [CrossRef] [Green Version]
  9. Rosado-Aguilar, J.A.; Aguilar-Caballero, A.; Rodriguez-Vivas, R.I.; Borges-Argaez, R.; Garcia-Vazquez, Z.; Mendez-Gonzalez, M. Acaricidal activity of extracts from Petiveria alliacea (Phytolaccaceae) against the cattle tick, Rhipicephalus (Boophilus) microplus (Acari: Ixodidae). Vet. Parasitol. 2010, 168, 299–303. [Google Scholar] [CrossRef]
  10. Adenubi, O.T.; McGaw, L.J.; Eloff, J.N.; Naidoo, V. In vitro bioassays used in evaluating plant extracts for tick repellent and acaricidal properties: A critical review. Vet. Parasitol. 2018, 254, 160–171. [Google Scholar] [CrossRef]
  11. De Souza Chagas, A.C.; de Barros, L.D.; Cotinguiba, F.; Furlan, M.; Giglioti, R.; de Sena Oliveira, M.C.; Bizzo, H.R. In vitro efficacy of plant extracts and synthesized substances on Rhipicephalus (Boophilus) microplus (Acari: Ixodidae). Parasitol. Res. 2012, 110, 295–303. [Google Scholar] [CrossRef] [PubMed]
  12. Juliet, S.; Ravindran, R.; Ramankutty, S.A.; Gopalan, A.K.K.; Nair, S.N.; Kavillimakkil, A.K.; Bandyopadhyay, A.; Rawat, A.K.S.; Ghosh, S. Jatropha curcas (Linn) leaf extract–a possible alternative for population control of Rhipicephalus (Boophilus) annulatus. Asian Pac. J. Trop. Dis. 2012, 2, 225–229. [Google Scholar] [CrossRef]
  13. Kamaraj, C.; Rahuman, A.A.; Bagavan, A.; Elango, G.; Rajakumar, G.; Zahir, A.A.; Marimuthu, S.; Santhoshkumar, T.; Jayaseelan, C. Evaluation of medicinal plant extracts against blood-sucking parasites. Parasitol. Res. 2010, 106, 1403–1412. [Google Scholar] [CrossRef] [PubMed]
  14. Regnault-Roger, C.; Vincent, C.; Arnason, J.T. Essential oils in insect control: Low-risk products in a high-stakes world. Annu. Rev. Entomol. 2012, 57, 405–424. [Google Scholar] [CrossRef] [PubMed]
  15. Sunil, A.R.; Amithamol, K.K.; Juliet, S.; Nair, S.N.; Ajithkumar, K.G.; Soorya, V.C.; Divya, T.M.; Jyothymol, G.; Ghosh, S.; Ravindran, R. Acaricidal effect of Cassia fistula Linn. leaf ethanolic extract against Rhipicephlaus (Boophilus) annulatus. Trop. Biomed. 2013, 30, 231–237. [Google Scholar]
  16. Ghosh, S.; Sharma, A.K.; Kumar, S.; Tiwari, S.S.; Rastogi, S.; Srivastava, S.; Singh, M.; Kumar, R.; Paul, S.; Ray, D.D. In vitro and in vivo efficacy of Acorus calamus extract against Rhipicephalus (Boophilus) microplus. Parasitol. Res. 2011, 108, 361–370. [Google Scholar] [CrossRef]
  17. Ghosh, S.; Tiwari, S.S.; Srivastava, S.; Sharma, A.K.; Kumar, S.; Ray, D.D.; Rawat, A.K.S. Acaricidal properties of Ricinus communis leaf extracts against organophosphate and pyrethroids resistant Rhipicephalus (Boophilus) microplus. Vet. Parasitol. 2013, 192, 259–267. [Google Scholar] [CrossRef]
  18. Bagewadi, Z.K.; Muddapur, U.M.; Madiwal, S.S.; Mulla, S.I.; Khan, A. Biochemical and enzyme inhibitory attributes of methanolic leaf extract of Datura inoxia Mill. Environ. Sustain. 2019, 2, 75–87. [Google Scholar] [CrossRef]
  19. Neeraj, O.M.; Ayesha, K.; Balu, A.C. Rediscovering the medicinal properties of Datura sp.: A review. J. Med. Plants Res. 2013, 7, 2885–2897. [Google Scholar]
  20. Ramadan, M.F.; Zayed, R.; El-Shamy, H. Screening of bioactive lipids and radical scavenging potential of some solanaceae plants. Food Chem. 2007, 103, 885–890. [Google Scholar] [CrossRef]
  21. Vermillion, K.; Holguin, F.O.; Berhow, M.A.; Richins, R.D.; Redhouse, T.; O’Connell, M.A.; Posakony, J.; Mahajan, S.S.; Kelly, S.M.; Simon, J.A. Dinoxin b, a withanolide from Datura inoxia leaves with specific cytotoxic activities. J. Nat. Prod. 2011, 74, 267–271. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Guneidy, R.A.; Amer, M.A.; Hakim, A.E.E.; Abdel-Shafy, S.; Allam, S.A. Effect of polyphenols extracted from Punica granatum and Acacia saligna plants on glutathione S-transferase of the cattle tick Rhipicephalus (Boophilus) annulatus (Acari: Ixodidae). J. Parasit. Dis. 2021, 45, 524–538. [Google Scholar] [CrossRef] [PubMed]
  23. Sabadin, G.A.; Parizi, L.F.; Kiio, I.; Xavier, M.A.; da Silva Matos, R.; Camargo-Mathias, M.I.; Githaka, N.W.o.; Nene, V.; da Silva Vaz, I., Jr. Effect of recombinant glutathione S-transferase as vaccine antigen against Rhipicephalus appendiculatus and Rhipicephalus sanguineus infestation. Vaccine 2017, 35, 6649–6656. [Google Scholar] [CrossRef] [PubMed]
  24. Whiten, S.R.; Eggleston, H.; Adelman, Z.N. Ironing out the details: Exploring the role of iron and heme in blood-sucking arthropods. Front. Physiol. 2018, 8, 1134. [Google Scholar] [CrossRef] [Green Version]
  25. Balcı, N.; Türkan, F.; Şakiroğlu, H.; Aygün, A.; Şen, F. Purification and characterization of glutathione S-transferase from blueberry fruits (Vaccinium arctostaphylos L.) and investigated of some pesticide inhibition effects on enzyme activity. Heliyon 2019, 5, e01422. [Google Scholar] [CrossRef] [Green Version]
  26. Guneidy, R.A.; Shahein, Y.E.; Abouelella, A.M.K.; Zaki, E.R.; Hamed, R.R. Inhibition of the recombinant cattle tick Rhipicephalus (Boophilus) annulatus glutathione S-transferase. Ticks Tick-Borne Dis. 2014, 5, 528–536. [Google Scholar] [CrossRef]
  27. Hernandez, E.P.; Kusakisako, K.; Talactac, M.R.; Galay, R.L.; Hatta, T.; Matsuo, T.; Fujisaki, K.; Tsuji, N.; Tanaka, T. Characterization and expression analysis of a newly identified glutathione S-transferase of the hard tick Haemaphysalis longicornis during blood-feeding. Parasites Vectors 2018, 11, 1–16. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Sookrung, N.; Reamtong, O.; Poolphol, R.; Indrawattana, N.; Seesuay, W.; Saelim, N.; Tantilipikorn, P.; Bunnag, C.; Chaicumpa, W.; Tungtrongchitr, A. Glutathione S-transferase (GST) of American cockroach, Periplaneta americana: Classes, isoforms, and allergenicity. Sci. Rep. 2018, 8, 484. [Google Scholar] [CrossRef] [Green Version]
  29. Azwanida, N.N. A review on the extraction methods use in medicinal plants, principle, strength and limitation. Med. Aromat. Plants 2015, 4, 2167-0412. [Google Scholar]
  30. Shyma, K.P.; Gupta, J.P.; Ghosh, S.; Patel, K.K.; Singh, V. Acaricidal effect of herbal extracts against cattle tick Rhipicephalus (Boophilus) microplus using in vitro studies. Parasitol. Res. 2014, 113, 1919–1926. [Google Scholar] [CrossRef]
  31. Stendel, W. The relevance of different test methods for the evaluation of tick controlling substances. J. S Afr. Vet. Assoc. 1980, 51, 147–152. [Google Scholar] [PubMed]
  32. Sabatini, G.A.; Kemp, D.H.; Hughes, S.; Nari, A.; Hansen, J. Tests to determine LC50 and discriminating doses for macrocyclic lactones against the cattle tick, Boophilus microplus. Vet. Parasitol. 2001, 95, 53–62. [Google Scholar] [CrossRef] [PubMed]
  33. Yang, J.; Anishchenko, I.; Park, H.; Peng, Z.; Ovchinnikov, S.; Baker, D. Improved protein structure prediction using predicted interresidue orientations. Proc. Natl. Acad. Sci. USA 2020, 117, 1496–1503. [Google Scholar] [CrossRef] [PubMed]
  34. Tai, W.; He, L.; Zhang, X.; Pu, J.; Voronin, D.; Jiang, S.; Zhou, Y.; Du, L. Characterization of the receptor-binding domain (RBD) of 2019 novel coronavirus: Implication for development of RBD protein as a viral attachment inhibitor and vaccine. Cell. Mol. Immunol. 2020, 17, 613–620. [Google Scholar] [CrossRef]
  35. Agyapong, O.; Asiedu, S.O.; Kwofie, S.K.; Miller Iii, W.A.; Parry, C.S.; Sowah, R.A.; Wilson, M.D. Molecular modelling and de novo fragment-based design of potential inhibitors of beta-tubulin gene of Necator americanus from natural products. Inform. Med. Unlocked 2021, 26, 100734. [Google Scholar] [CrossRef]
  36. Morris, G.M.; Huey, R.; Lindstrom, W.; Sanner, M.F.; Belew, R.K. DS Goodsell i AJ Olson. J. Comput. Chem. 2009, 30, 2785–2791. [Google Scholar] [CrossRef] [Green Version]
  37. R Core Team. R: A Language and Environment for Statistical Computing, 4.1.3; R Foundation for Statistical Computing: Vienna, Austria, 2022. [Google Scholar]
  38. RStudio Team. RStudio: Integrated Development Environment for R; RStudio, PBC: Boston, MA, USA, 2022. [Google Scholar]
  39. De Mendiburu, F. Agricolae: Statistical procedures for agricultural research. R Package Version 2014, 1, 1–4. [Google Scholar]
  40. Shezryna, S.; Anisah, N.; Saleh, I.; Syamsa, R.A. Acaricidal activity of the essential oils from Citrus hystrix (Rutaceae) and Cymbopogon citratus (Poaceae) on the cattle tick Rhipicephalus (Boophilus) microplus larvae (Acari: Ixodidae). Trop. Biomed. 2020, 37, 433–442. [Google Scholar]
  41. Finney, D. Probit Analysis; Cambridge University Press: Cambridge, UK, 1971. [Google Scholar]
  42. Hlina, B.L.; Birceanu, O.; Robinson, C.S.; Dhiyebi, H.; Wilkie, M.P. The relationship between thermal physiology and lampricide sensitivity in larval sea lamprey (Petromyzon marinus). J. Great Lakes Res. 2021, 47, S272–S284. [Google Scholar] [CrossRef]
  43. Wickham, H. Data analysis. In Ggplot2; Springer: Cham, Switzerland, 2016; pp. 189–201. [Google Scholar]
  44. Eisenberg, D.; Lüthy, R.; Bowie, J.U. [20] VERIFY3D: Assessment of protein models with three-dimensional profiles. In Methods in Enzymology; Elsevier: Amsterdam, The Netherlands, 1997; Volume 277, pp. 396–404. [Google Scholar]
  45. Bowie, J.U.; Lüthy, R.; Eisenberg, D. A method to identify protein sequences that fold into a known three-dimensional structure. Science 1991, 253, 164–170. [Google Scholar] [CrossRef] [Green Version]
  46. Laskowski, R.A.; Luscombe, N.M.; Swindells, M.B.; Thornton, J.M. Protein clefts in molecular recognition and function. Protein Sci. A Publ. Protein Soc. 1996, 5, 2438. [Google Scholar]
  47. Liang, J.; Woodward, C.; Edelsbrunner, H. Anatomy of protein pockets and cavities: Measurement of binding site geometry and implications for ligand design. Protein Sci. 1998, 7, 1884–1897. [Google Scholar] [CrossRef] [Green Version]
  48. Broni, E.; Kwofie, S.K.; Asiedu, S.O.; Miller Iii, W.A.; Wilson, M.D. A molecular modeling approach to identify potential antileishmanial compounds against the cell division cycle (Cdc)-2-related kinase 12 (crk12) receptor of leishmania donovani. Biomolecules 2021, 11, 458. [Google Scholar] [CrossRef] [PubMed]
  49. Kwofie, S.K.; Broni, E.; Yunus, F.U.; Nsoh, J.; Adoboe, D.; Miller Iii, W.A.; Wilson, M.D. Molecular Docking Simulation Studies Identifies Potential Natural Product Derived-Antiwolbachial Compounds as Filaricides against Onchocerciasis. Biomedicines 2021, 9, 1682. [Google Scholar] [CrossRef]
  50. Ghosh, S.; Tiwari, S.S.; Kumar, B.; Srivastava, S.; Sharma, A.K.; Kumar, S.; Bandyopadhyay, A.; Julliet, S.; Kumar, R.; Rawat, A.K.S. Identification of potential plant extracts for anti-tick activity against acaricide resistant cattle ticks, Rhipicephalus (Boophilus) microplus (Acari: Ixodidae). Exp. Appl. Acarol. 2015, 66, 159–171. [Google Scholar] [CrossRef]
  51. Rosado-Aguilar, J.A.; Arjona-Cambranes, K.; Torres-Acosta, J.F.J.; Rodríguez-Vivas, R.I.; Bolio-González, M.E.; Ortega-Pacheco, A.; Alzina-López, A.; Gutiérrez-Ruiz, E.J.; Gutiérrez-Blanco, E.; Aguilar-Caballero, A.J. Plant products and secondary metabolites with acaricide activity against ticks. Vet. Parasitol. 2017, 238, 66–76. [Google Scholar] [CrossRef] [PubMed]
  52. Ghosh, S.; Tiwari, S.S.; Srivastava, S.; kumar, S.; Sharma, A.K.; Nagar, G.; Kumar, K.G.A.; Kumar, R.; Rawat, A.K.S. In vitro acaricidal properties of Semecarpus anacardium fruit and Datura stramonium leaf extracts against acaricide susceptible (IVRI-I line) and resistant (IVRI-V line) Rhipicephalus (Boophilus) microplus. Res. Vet. Sci. 2015, 101, 69–74. [Google Scholar] [CrossRef]
  53. Kumral, N.A.; Çobanoğlu, S.; Yalcin, C. Acaricidal, repellent and oviposition deterrent activities of Datura stramonium L. against adult Tetranychus urticae (Koch). J. Pest Sci. 2010, 83, 173–180. [Google Scholar] [CrossRef]
  54. Singla, R.K. In silico drug design & medicinal chemistry. Curr. Top. Med. Chem. 2015, 15, 971. [Google Scholar] [PubMed]
  55. Wang, C.; Xu, P.; Zhang, L.; Huang, J.; Zhu, K.; Luo, C. Current strategies and applications for precision drug design. Front. Pharmacol. 2018, 9, 787. [Google Scholar] [CrossRef]
  56. Zheng, M.; Zhao, J.; Cui, C.; Fu, Z.; Li, X.; Liu, X.; Ding, X.; Tan, X.; Li, F.; Luo, X. Computational chemical biology and drug design: Facilitating protein structure, function, and modulation studies. Med. Res. Rev. 2018, 38, 914–950. [Google Scholar] [CrossRef] [PubMed]
Genes 14 00118 g001 550
Figure 1. (A) Response curve graph for the inhibition of oviposition (% IO in AIT) at 48 h; (B) concentration–mortality curve for larval mortality at 24 and 48 h in LPT; (C,D) represent log-transformed LC50, LC90, LT50, and LT90 with error bars showing the corresponding log-transformed lower and upper confidence limits values of the LC and LT in LPT; (E,F) represent one-way ANOVA with post hoc Tukey HSD test for % IO and larval mortality, for AIT and LPT, respectively.
Figure 1. (A) Response curve graph for the inhibition of oviposition (% IO in AIT) at 48 h; (B) concentration–mortality curve for larval mortality at 24 and 48 h in LPT; (C,D) represent log-transformed LC50, LC90, LT50, and LT90 with error bars showing the corresponding log-transformed lower and upper confidence limits values of the LC and LT in LPT; (E,F) represent one-way ANOVA with post hoc Tukey HSD test for % IO and larval mortality, for AIT and LPT, respectively.
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Genes 14 00118 g002 550
Figure 2. (A) Rhipicephalus microplus glutathione S-transferases (RmGST) three-dimensional (3D) structure predicted by the trRosetta server; (B–D) ERRAT, Z-scores, and Ramachandran map, respectively, validate the protein structure and amino acid position of RmGST. The Ramachandran plot of RmGST indicates the percentage of residues in favored regions (red) and allowed regions (yellow) where the bars in the ERRAT plot represents the error value (white: error < 95%, yellow: error < 99%, and red: error > 99%).
Figure 2. (A) Rhipicephalus microplus glutathione S-transferases (RmGST) three-dimensional (3D) structure predicted by the trRosetta server; (B–D) ERRAT, Z-scores, and Ramachandran map, respectively, validate the protein structure and amino acid position of RmGST. The Ramachandran plot of RmGST indicates the percentage of residues in favored regions (red) and allowed regions (yellow) where the bars in the ERRAT plot represents the error value (white: error < 95%, yellow: error < 99%, and red: error > 99%).
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Figure 3. Determination of RmGST active sites using the CASTp server.
Figure 3. Determination of RmGST active sites using the CASTp server.
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Figure 4. (A,B) Docking of norapoatropine with binding sites of RmGST’s 3D complex structure and (C) their 2D interaction. (D,E) Docking of 7-hydroxyhyoscyamine with binding sites of RmGST’s 3D complex structure and (F) their 2D interaction.
Figure 4. (A,B) Docking of norapoatropine with binding sites of RmGST’s 3D complex structure and (C) their 2D interaction. (D,E) Docking of 7-hydroxyhyoscyamine with binding sites of RmGST’s 3D complex structure and (F) their 2D interaction.
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Figure 5. Result outputs of the normal mode analysis (NMA) through the iMODs server. (A) factor; (B) deformation plot; (C) variance plot; (D) eigenvalue; (E) covariance matrix plot; (F) elastic network model.
Figure 5. Result outputs of the normal mode analysis (NMA) through the iMODs server. (A) factor; (B) deformation plot; (C) variance plot; (D) eigenvalue; (E) covariance matrix plot; (F) elastic network model.
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Table
Table 1. Mean % larval mortality and inhibition of oviposition at different concentrations of D. innoxia plant extract against R. microplus in vitro in LPT and AIT, respectively.
Table 1. Mean % larval mortality and inhibition of oviposition at different concentrations of D. innoxia plant extract against R. microplus in vitro in LPT and AIT, respectively.
ExtractConcentration (mg/mL)% Mean ± Standard Deviation
% Larval Mortality% Inhibition of Oviposition (IO)
24 h48 h
D. innoxia4042.33 ± 2.08 b93.67 ± 1.53 a45.37 ± 2.60 b
2036.67 ± 2.08 bc86.33 ± 6.66 ab32.85 ± 1.63 c
1032.67 ± 3.06 c73.67 ± 5.13 b20.68 ± 2.80 d
525.33 ± 2.52 d55.67 ± 8.02 c15.73 ± 5.98 de
2.515.00 ± 1.00 e36.67 ± 1.53 d9.86 ± 4.01 ef
Control GroupTrichlorfon58.00 ± 3.00 a97.67 ± 2.52 a83.74 ± 5.02 a
Distilled water0 f1.00 ± 1.00 e0.20 ± 1.46 f
Means not sharing any letters in the same column were significantly different by Tukey’s HSD test at a 5% significance level (p < 0.05).
Table
Table 2. Medium lethal concentration causing 50% and 90% mortalities (LC50 and LC90 values) of D. innoxia plant leaf extract against R. microplus in vitro.
Table 2. Medium lethal concentration causing 50% and 90% mortalities (LC50 and LC90 values) of D. innoxia plant leaf extract against R. microplus in vitro.
Time (h)LC50 (mg/mL)95% Confidence LimitsLC90 (mg/mL)95% Confidence LimitsSlope ± S.E.Intercept ± S.E.Chi-Square (χ2)p-Value
LCLUCLLCLUCL
2466.4443.79127.556310.721754.2452,277.920.64 ± 0.08−1.18 ± 0.096.480.93
484.0603.5304.58626.63222.56432.561.56 ± 0.09−0.95 ± 0.0916.510.22
LCL: low confident limit, UCL: upper confident limit, S.E.: standard error.
Table
Table 3. Lethal time causing 50% and 90% mortalities (LT50 and LT90 values) at varying concentrations for D. innoxia against R. microplus in vitro.
Table 3. Lethal time causing 50% and 90% mortalities (LT50 and LT90 values) at varying concentrations for D. innoxia against R. microplus in vitro.
Concentration (mg/mL)LT50 (h)95% Confidence LimitsLT90 (h)95% Confidence LimitsSlope ± S. EIntercept ± SEChi-Square (χ2)p-Value
LCLUCLLCLUCL
2.567.3956.2193.62241.63150.14608.632.31 ± 0.38−4.22 ± 0.590.350.98
542.4638.6747.99127.7596.59203.912.67 ± 0.35−4.36 ± 0.555.880.21
1031.9929.7834.2572.717363.1289.093.59 ± 0.35−5.41 ± 0.553.560.47
2028.2826.6229.8852.5148.1758.764.77 ± 0.38−6.92 ± 0.587.880.09
4025.9424.5327.2643.4740.5747.465.71 ± 0.47−8.08 ± 0.651.140.89
LCL: low confident limit, UCL: upper confident limit, S.E.: standard error.
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Saman, S.; Chen, C.-C.; Malak, N.; Khan, A.; Nasreen, N.; Khan, A.; Niaz, S.; Rehman, G.; Rodriguez-Vivas, R.I.; Cossío-Bayúgar, R. Ethanolic Extracts of Datura innoxia Have Promising Acaricidal Activity against Rhipicephalus microplus as It Blocks the Glutathione S-Transferase Activity of the Target Tick. Genes 2023, 14, 118. https://doi.org/10.3390/genes14010118

AMA Style

Saman S, Chen C-C, Malak N, Khan A, Nasreen N, Khan A, Niaz S, Rehman G, Rodriguez-Vivas RI, Cossío-Bayúgar R. Ethanolic Extracts of Datura innoxia Have Promising Acaricidal Activity against Rhipicephalus microplus as It Blocks the Glutathione S-Transferase Activity of the Target Tick. Genes. 2023; 14(1):118. https://doi.org/10.3390/genes14010118

Chicago/Turabian Style

Saman, Saman, Chien-Chin Chen, Nosheen Malak, Afshan Khan, Nasreen Nasreen, Adil Khan, Sadaf Niaz, Gauhar Rehman, Roger I. Rodriguez-Vivas, and Raquel Cossío-Bayúgar. 2023. "Ethanolic Extracts of Datura innoxia Have Promising Acaricidal Activity against Rhipicephalus microplus as It Blocks the Glutathione S-Transferase Activity of the Target Tick" Genes 14, no. 1: 118. https://doi.org/10.3390/genes14010118

APA Style

Saman, S., Chen, C.-C., Malak, N., Khan, A., Nasreen, N., Khan, A., Niaz, S., Rehman, G., Rodriguez-Vivas, R. I., & Cossío-Bayúgar, R. (2023). Ethanolic Extracts of Datura innoxia Have Promising Acaricidal Activity against Rhipicephalus microplus as It Blocks the Glutathione S-Transferase Activity of the Target Tick. Genes, 14(1), 118. https://doi.org/10.3390/genes14010118

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