Fractionation Coupled to Molecular Networking: Towards Identification of Anthelmintic Molecules in Terminalia leiocarpa (DC.) Baill

Terminalia leiocarpa is a medicinal plant widely used in ethnoveterinary medicine to treat digestive parasitosis whose extracts were shown to be active against gastrointestinal nematodes of domestic ruminants. The objective of our study was to identify compounds responsible for this activity. Column fractionation was performed, and the activity of the fractions was assessed in vitro on Haemonchus contortus and Caenorhabditis elegans as well as their cytotoxicity on WI38 fibroblasts. Two fractions were the most active on both nematode models and less cytotoxic. LC-MS/MS analysis and manual dereplication coupled to molecular networking allowed identification of the main compounds: ellagic acid and derivatives, gallic acid, astragalin, rutin, quinic acid, and fructose. Other potentially identified compounds such as shikimic acid, 2,3-(S)-hexahydroxydiphenoyl-D-glucose or an isomer, quercetin-3-O-(6-O-galloyl)-β-D-galactopyranoside or an isomer, and a trihydroxylated triterpenoid bearing a sugar as rosamultin are reported in this plant for the first time. Evaluation of the anthelmintic activity of the available major compounds showed that ellagic and gallic acids were the most effective in inhibiting the viability of C. elegans. Their quantification in fractions 8 and 9 indicated the presence of about 8.6 and 7.1 µg/mg ellagic acid and about 9.6 and 2.0 µg/mg gallic acid respectively. These concentrations are not sufficient to justify the activity observed. Ellagic acid derivatives and other compounds that were found to be positively correlated with the anthelmintic activity of the fractions may have additive or synergistic effects when combined, but other unidentified compounds could also be implicated in the observed activity.

[1]  J. Quetin-Leclercq,et al.  Anthelmintic Activity, Cytotoxicity, and Phytochemical Screening of Plants Used to Treat Digestive Parasitosis of Small Ruminants in Benin (West Africa) , 2022, Animals : an open access journal from MDPI.

[2]  O. Anjos,et al.  Identification of gallotannins and ellagitannins in aged wine spirits: A new perspective using alternative ageing technology and high-resolution mass spectrometry. , 2022, Food chemistry.

[3]  J. Quetin-Leclercq,et al.  Dereplication and Quantification of Major Compounds of Convolvulus arvensis L. Extracts and Assessment of Their Effect on LPS-Activated J774 Macrophages , 2022, Molecules.

[4]  E. Filaire,et al.  Feature-Based Molecular Networks Identification of Bioactive Metabolites from Three Plants of the Polynesian Cosmetopoeia Targeting the Dermal Papilla Cells of the Hair Cycle , 2021, Molecules.

[5]  Xunhong Liu,et al.  Quality Evaluation of Taxilli Herba from Different Hosts Based on Simultaneous Determination of Multiple Bioactive Constituents Combined with Multivariate Statistical Analysis , 2021, Molecules.

[6]  J. Quetin-Leclercq,et al.  Ethnoveterinary knowledge of sheep and goat farmers in Benin (West Africa): effect of socioeconomic and environmental factors , 2021, Heliyon.

[7]  S. Ercişli,et al.  LC-MS/MS Screening of Phenolic Compounds in Wild and Cultivated Grapes Vitis amurensis Rupr. , 2021, Molecules.

[8]  E. Abdel-Sattar,et al.  Unravelling the anthelmintic bioactives from Jasminum grandiflorum L. subsp. Floribundum adopting in vitro biological assessment. , 2021, Journal of ethnopharmacology.

[9]  S. Ignatova,et al.  Laguncularia racemosa Phenolics Profiling by Three-Phase Solvent System Step-Gradient Using High-Performance Countercurrent Chromatography with Off-Line Electrospray Mass-Spectrometry Detection , 2021, Molecules.

[10]  E. Andersen,et al.  Caenorhabditis elegans in anthelmintic research – Old model, new perspectives , 2020, International journal for parasitology. Drugs and drug resistance.

[11]  R. Julkunen‐Tiitto,et al.  Potential Anti-Tuberculosis Activity of the Extracts and Their Active Components of Anogeissus leiocarpa (DC.) Guill. and Perr. with Special Emphasis on Polyphenols , 2020, Antibiotics.

[12]  Samantha M. Martins,et al.  Isolation and characterization of flavonoids from Tapirira guianensis leaves with vasodilatory and myeloperoxidase-inhibitory activities , 2020, Natural product research.

[13]  Christine M. Aceves,et al.  Reproducible molecular networking of untargeted mass spectrometry data using GNPS , 2019, Nature Protocols.

[14]  Mingxun Wang,et al.  Bioactivity-Based Molecular Networking for the Discovery of Drug Leads in Natural Product Bioassay-Guided Fractionation. , 2018, Journal of natural products.

[15]  Bill C. H. Chang,et al.  Screening of a small, well-curated natural product-based library identifies two rotenoids with potent nematocidal activity against Haemonchus contortus. , 2017, Veterinary parasitology.

[16]  R. Martin,et al.  A brief review on the mode of action of antinematodal drugs , 2017, Acta veterinaria.

[17]  Pieter C Dorrestein,et al.  Molecular Networking As a Drug Discovery, Drug Metabolism, and Precision Medicine Strategy. , 2017, Trends in pharmacological sciences.

[18]  M. Kanninen,et al.  Tannins, flavonoids and stilbenes in extracts of African savanna woodland trees Terminalia brownii, Terminalia laxiflora and Anogeissus leiocarpus showing promising antibacterial potential , 2017 .

[19]  D. Yadav,et al.  The genus Anogeissus: A review on ethnopharmacology, phytochemistry and pharmacology. , 2016, Journal of ethnopharmacology.

[20]  F. Bucar,et al.  LC-PDA-ESI-MSn analysis of phenolic and iridoid compounds from Globularia spp. , 2016, Journal of mass spectrometry : JMS.

[21]  Jonathan Bisson,et al.  Integration of Molecular Networking and In-Silico MS/MS Fragmentation for Natural Products Dereplication. , 2016, Analytical chemistry.

[22]  B. Roy,et al.  IN VITRO ANTHELMINTIC EFFICACY OF ALPINIA NIGRA AND ITS BIOACTIVE COMPOUND, ASTRAGALIN AGAINST FASCIOLOPSIS BUSKI , 2015 .

[23]  E. Williamson,et al.  Synergistic inhibition of Haemonchus contortus exsheathment by flavonoid monomers and condensed tannins , 2015, International journal for parasitology. Drugs and drug resistance.

[24]  E. Llorent-Martínez,et al.  HPLC-ESI-MSn characterization of phenolic compounds, terpenoid saponins, and other minor compounds in Bituminaria bituminosa , 2015 .

[25]  Md. Saidur Rahman,et al.  Anthelmintic activity of ellagic acid, a major constituent of Alternanthera sessilis against Haemonchus contortus. , 2015 .

[26]  I. Cock,et al.  GC-MS and LC-MS analysis of Kakadu plum fruit extracts displaying inhibitory activity against microbial triggers of multiple sclerosis , 2015 .

[27]  M. Grace,et al.  Anthelmintic Activity of Punicalagin from nogeissus Leiocarpus , 2015 .

[28]  M. Lafosse,et al.  Isolation by pressurised fluid extraction (PFE) and identification using CPC and HPLC/ESI/MS of phenolic compounds from Brazilian cherry seeds (Eugenia uniflora L.). , 2014, Food chemistry.

[29]  E. Liebau,et al.  Anthelmintic activity of phenolic acids from the axlewood tree Anogeissus leiocarpus on the filarial nematode Onchocerca ochengi and drug-resistant strains of the free-living nematode Caenorhabditis elegans , 2013, Journal of Helminthology.

[30]  B. Bonfoh,et al.  In vivo anthelmintic activity of Anogeissus leiocarpus Guill & Perr (Combretaceae) against nematodes in naturally infected sheep , 2013, Parasitology Research.

[31]  E. Liebau,et al.  Anogeissus leiocarpus extract on the parasite nematode Onchocerca ochengi and on drug resistant mutant strains of the free-living nematode Caenorhabditis elegans. , 2012, Veterinary parasitology.

[32]  E. Papadopoulos,et al.  Anthelmintic resistance in parasites of small ruminants: sheep versus goats , 2011, Helminthologia.

[33]  L. Lagnika,et al.  In vitro antiplasmodial and antileishmanial activities of flavonoids form Anogeissus leiocarpus (Combretaceae) , 2011 .

[34]  J. Eloff,et al.  In vitro anthelmintic effect of Anogeissus leiocarpus (DC.) Guill. & Perr. leaf extracts and fractions on developmental stages of Haemonchus contortus. , 2011, African journal of traditional, complementary, and alternative medicines : AJTCAM.

[35]  K. Adama,et al.  In vitro anthelmintic effect of two medicinal plants (Anogeissus leiocarpus and Daniellia oliveri ) on Haemonchus contortus , an abosomal nematode of sheep in Burkina Faso , 2009 .

[36]  V. Cardile,et al.  Antiproliferative activity of Pteleopsis suberosa leaf extract and its flavonoid components in human prostate carcinoma cells. , 2006, Planta medica.

[37]  G. von Samson-Himmelstjerna,et al.  The detection of anthelmintic resistance in nematodes of veterinary importance. , 2006, Veterinary parasitology.

[38]  F. Moharram,et al.  Pharmacologically active ellagitannins from Terminalia myriocarpa. , 2002, Planta medica.

[39]  J. Quetin-Leclercq,et al.  Cytotoxic aporphine alkaloids from Cassytha filiformis. , 2002, Planta medica.

[40]  S. Srivastava,et al.  Triterpenoid glycoside from the roots of Terminalia alata. , 2001, Fitoterapia.

[41]  P. Douch,et al.  Improved bioassay for estimation of inhibitory effects of ovine gastrointestinal mucus and anthelmintics on nematode larval migration. , 1994, International journal for parasitology.

[42]  Takashi Tanaka,et al.  Tannins and Related Compounds. CIII. Isolation and Characterizatino of New Monomeric, Dimeric and Trimeric Ellagitannins, Calamansanin and Calamanins A, B and C, from Terminalia calamansanai (BLANCO) ROLFE , 1991 .

[43]  D. Waldi Spray Reagents for Thin-Layer Chromatography , 1965 .