Susceptibility of Toxoplasma gondii to Ethanolic Extract of Tinospora crispa in Vero Cells

Author:

Sharif Alhassan Abdullahi12ORCID,Unyah Ngah Zasmy1,Nordin Norshariza1ORCID,Basir Rusliza1,Wana Mohammed Nasiru13,Alapid Ahmad Ashraf14,Mustapha Tijjani15,Majid Roslaini Abd.1ORCID

Affiliation:

1. Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia

2. Faculty of Clinical Sciences, College of Health Sciences, Bayero University Kano, PMB 3011, Kano, Nigeria

3. Department of Biological Sciences, Faculty of Sciences, Abubakar Tafawa Balewa University, Bauchi, Nigeria

4. Department of Zoology, Faculty of Science-Alassaba, University of Gharyan, Garyan, Libya

5. Department of Biological Sciences, Faculty of Science, Yobe State University, PMB 1104, Damaturu, Nigeria

Abstract

Background. Toxoplasmosis remains widely distributed globally and is one of the major neglected parasitic zoonotic infections. The infection is still endemic in most parts of the world due to poor control as well as challenges of the currently used medications which can be overcome by using natural products. This study evaluated the effect of ethanolic extract from the stem of Tinospora crispa (EETC) on host cell invasion and intracellular replication of Toxoplasma gondii. Method. The stem powder of T. crispa was soaked in absolute ethanol for 72 hours. The resulting ethanolic extract was screened for the presence of phytochemicals. Vero cells monolayer in 96-well plate was infected with RH strain of T. gondii and treated with concentrations of the EETC, Veratrine alkaloid, and clindamycin ranging from 1.56 to 200 μg/mL. MTT assay was conducted after 24 hours to evaluate the cytotoxicity and antiparasitic activities of the EETC. Four and 24 hours treatment models were adapted to assess the infection index and intracellular proliferation of T. gondii in vitro. Microscopic analysis was conducted after 24 and 48 hours exposure to EETC in both treatment models. Results. The study revealed that the EETC had no cytotoxic effects on Vero cells with IC50 = 179 μg/mL, as compared to clindamycin (IC50 = 116.5 μg/mL) and Veratrine alkaloid (IC50 = 60.4 μg/mL). The EETC had good anti-toxoplasma activities with IC50 = 6.31 μg/mL in comparison with clindamycin (IC50 = 8.33 μg/mL) and Veratrine alkaloid (IC50 = 14.25 μg/mL). The EETC caused more than 70% and 80% reduction in infection index and intracellular proliferation in both treatment models, respectively. Conclusion. This in vitro study showed that the EETC contains promising phytochemicals effective against T. gondii and safe to the host cells.

Funder

Ministry of Higher Education, Malaysia

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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