In vitro antifungal activity of Embelia schimperi (Vatke) and Conyza floribunda

Paper Details

Research Paper 01/09/2018
Views (607)
current_issue_feature_image
publication_file

In vitro antifungal activity of Embelia schimperi (Vatke) and Conyza floribunda

Elibariki Eliangilisa Kowero, Cecilia Leweri, Musa Chacha
Int. J. Biosci. 13(3), 45-50, September 2018.
Copyright Statement: Copyright 2018; The Author(s).
License: CC BY-NC 4.0

Abstract

The study aimed to investigate antifungal activity of 2 medicinal plants namely Embelia schimperi and Conyza floribunda used in Tanzania to treat infectious diseases. Micro-dilution method was used to evaluate antifungal activity of plant extracts against Cryptococcus neuformans and Candida albicans. The study revealed that tested extracts have different levels of antifungal activity with minimum inhibition concentration (MIC) range of 0.78 mg/mL to >25 mg/mL. The Conyza floribunda root chloroform extract (CFRC) inhibited both C. albicans and C. neoformans at MIC value of 0.78 mg/mL. Conyza floribunda leaf ethyl acetate (CFLE) and Embelia schimperi stem methanolic extract (ESSM) exhibited antifungal activity at MIC value of 0.78 mg/mL against C. neoformans. The results obtained suggest that CFRC, CFLE and ESSM is a potential source of antifungal secondary metabolites.

Arot LOM, Williams LA. 1997. A flavonol glycoside from Embelia schimperi leaves. Phytochemistry 44(7), 1397-1398.

Brown GD, Denning DW, Gow NA, Levitz SM, Netea MG, White TC .2012. Hidden killers: human fungal infections. Science translational medicine, 4(165), 165rv13-165rv13. https://doi.org/10.1126/scitranslmed.3004404

Chepkwony KP, Ngari AG, Kipkemboi PK, Andrew AO, Kiprop A. 2011.Antimicrobial Activity of Emblem from Embelia shimperi and its Synthetic Derivatives. Journal of Agriculture, Pure and Aplied Science and Technology 7, 25-29.

Debebe Y, Tefera M, Mekonnen W, Abebe D, Woldekidan S, Abebe A, Belete Y, Menberu T, Belayneh B, Tesfaye B. 2015. Evaluation of anthelmintic potential of the Ethiopian medicinal plant Embelia schimperi Vatke in vivo and in vitro against some intestinal parasites. BMC complementary and alternative medicine 15(1), 187. https://doi.org/10.1186/s12906-015-0711-7

Eggimann P, Garbino J, Pittet D. 2003. Epidemiology of Candida species infections in critically ill non-immunosuppressed patients. The Lancet infectious diseases  3(11), 685-702. https://doi.org/10.1016/S1473-3099(03)00801-6

Eliopoulos GM, Perea S, Patterson TF. 2002. Antifungal resistance in pathogenic fungi. Clinical Infectious Diseases 35(9), 1073-1080. https://doi.org/10.1086/344058

Eloff J. 1998. A sensitive and quick microplate method to determine the minimal inhibitory concentration of plant extracts for bacteria. Planta medica  64(8), 711-713.

Jackson A, Hosseinipour MC. 2010. Management of cryptococcal meningitis in sub-Saharan Africa. Current HIV/AIDS Reports 7(3), 134-142.

Kiprono C, Midiwo J, Kipkemboi P, Ladogana S. 2004. Larvicidal benzoquinone from Embelia schimperi. Bulletin of the Chemical Society of Ethiopia 18(1).

Kokwaro J. 1993. Medicinal plants of East Africa, East Africa Literature Bureau, Kampala, Nairobi, and Dar-es-Salaam.

Machocho AK, Kiprono PC, Grinberg S, Bittner S. 2003. Pentacyclic triterpenoids from Embelia schimperi. Phytochemistry 62(4), 573-577. https://doi.org/10.1016/S0031-9422(02)00619-2

Manguro L, Ogur JA, Opiyo SA. 2010. Antimicrobial Constituents of Conyza Floribunda 1(9). https://doi.org/10.9754/journal.wmc.2010.00842

Martins N, Ferreira IC, Barros L, Silva S, Henriques M. 2014. Candidiasis: predisposing factors, prevention, diagnosis and alternative treatment. Mycopathologia 177 (5-6), 223-240. https://doi.org/10.1007/s11046-014-9749-1

WHO. 2014. Antimicrobial resistance: Global report on surveillance: World Health Organization.

Park BJ, Wannemuehler KA, Marston BJ, Govender N, Pappas PG, Chiller TM. 2009. Estimation of the current global burden of cryptococcal meningitis among persons living with HIV/AIDS. Aids 23(4), 525-530.

Perfect JR, Cox GM. 1999. Drug resistance in Cryptococcus neoformans. Drug resistance updates  2(4), 259-269. molecular mechanisms and clinical consequences. The Lancet infectious diseases 2(2), 73-85.

Sloan DJ, Parris V. 2014. Cryptococcal meningitis: epidemiology and therapeutic options. Clinical epidemiology  6, 169.

Stevens DA. 2002. Diagnosis of fungal infections: current status. Journal of Antimicrobial Chemotherapy 49( 1), 11-19.

Shah NZ, Muhammad N, Azeem S, Khan AZ, Samie M, Khan H. 2013. Antimicrobial and phytotoxic properties of Conyza bonariensis. Pharmacy and Pharmacology Research 1(1), 8-11.

Vázquez-González D, Perusquía-Ortiz AM, Hundeiker M, Bonifaz A. 2013. Opportunistic yeast infections: candidiasis, cryptococcosis, trichosporonosis and geotrichosis. JDDG: Journal der Deutschen Dermatologischen Gesellschaft 11(5), 381-394.

Walsh T, Groll A. 1999. Emerging fungal pathogens: evolving challenges to immunocompromised Patients for the twenty-first century. Transplant infectious disease 1(4), 247-261. https://doi.org/10.1034/j.1399-3062.1999.010404.x

Warnock D. 2004. Emerging fungal diseases. Paper presented at: 42nd Annual Meeting. Idsa.

Related Articles

The protective effect of black pepper (Piper nigrum) on liver enzymes in streptozotocin-induced diabetic rats

Amani A. R. Filimban, Khulud A. Wathi, Int. J. Biosci. 27(4), 140-149, October 2025.

Production of bioplastics (PHB) using waste paper as feed stock by Cupriavidus taiwanensis

Ajeena Davis, Jini Joseph, Int. J. Biosci. 27(4), 130-139, October 2025.

Gill ectoparasites of the mugilidae from the Ebrié lagoon, Abidjan (Côte d’Ivoire)

Eby Yoboué Gnamma Honorine Alla, Carel Wilfried Bermian Dibi-Ahui, Fidèle Kouassi Kouakou, Abouo Béatrice Adepo-Gourene, Int. J. Biosci. 27(4), 123-129, October 2025.

Impacts of diverse water management systems on growth and yield of two prominent boro rice cultivars in Bangladesh

Zahidul Islam, Md Ekhlasur Rahman, Md Khayrul Islam Bashar, Sharmin Sultana, Md Taharat Al Tauhid, Md Rabiul Islam, Md Shahed Hossain, Md Musa Mondal, Pradip Kumar Biswas, Int. J. Biosci. 27(4), 110-122, October 2025.

First record of Brachymeria excarinata Gahan, 1925 (Hymenoptera: Chalcididae) parasitizing Plutella xylostella (L.) (Lepidoptera: Plutellidae) in west Africa

Babacar Labou, Etienne Tendeng, El hadji Sérigne Sylla, Mamadou Diatte, Karamoko Diarra, Int. J. Biosci. 27(4), 104-109, October 2025.

Assessment of adsorption isotherms of three plantain flours (Musa paradisiaca L. var. Horn 1, FHIA 21 and PITA 3) and cassava flour (Manihot esculenta Crantz var. Bonoua 2)

Brou Koffi Siméon, Yue Bi Yao Clément, Kane Fako, Douali Gohi Bi Douali Jean-Sory, Tano Kablan, Int. J. Biosci. 27(4), 93-103, October 2025.

Exploring the antioxidant efficacy of boldine: A natural compound with broad-spectrum activity

Maharani Jaganathan, Kathiresan Suresh, Manickam John, Rajeswari Vasu, Theerthu Azhamuthu, Nihal Ahamed Abulkalam Asath, Ravichandran Pugazhendhi, Pratheeba Veerapandiyan, Int. J. Biosci. 27(4), 82-92, October 2025.

Assessment of genetic parameters and yield trait stability in sweet sorghum genotypes through AMMI and GGE biplot approaches

A. H. Inuwa, H. A. Ajeigbe, Y. Mustapha, B. S. Aliyu, I. I. Angarawai, Int. J. Biosci. 27(4), 69-81, October 2025.