Abstract:
Epidemics of infection due to drug resistance and unknown microbial
organisms remain the public health concern. Consequently, there is the strong need for
renewed strategies on treatment and prevention in which fungi because of its great
biodiversity cannot be overlooked. Investigations were conducted to assay the
antimicrobial and therapeutic potentials of selected endophytic fungi as well as edible
and poisonous mushrooms. Employing molecular techniques, eighteen (18) fungal
species were identified. Methanol and hot water extracts of five mushrooms and three
endophytic fungi species were investigated for their antimicrobial activity using agar
well diffusion and disc diffusion methods against six clinical bacterial and two fungal
pathogens. The sensitivity patterns of typed cultures to the fungal extracts were also
evaluated. Standard antibiotics (0.5 μg Ciprofloxacin) used against the bacteria showed
the highest inhibitory activity (27 mm) against Pseudomonas aerugenosa and the least
(13 mm) against Staphylococcus aureus. The standard antifungal agent (10 mg/ml
Fluconazole) showed highest inhibition (15 mm) against Aspergilus flavus and least (9
mm) against Candida albicans. Mushroom extracts showed antibacterial activity
ranging from 6 to 18 mm and antifungal activity of 3 to 12 mm. Endophytic fungal
extracts induced broad spectrum antimicrobial activity with zones of inhibition ranging
from 7 to 12 mm. At 200 μg/ml concentration the bioactive fractions obtained from
methanol extract of Pleurotus ostreatus and Trametes versicolor produced appreciable
broad spectrum antimicrobial activity. The mushroom extracts showed Minimum
Inhibitory Concentration (MIC) ranging from 6.25 to 100 mg/ml and Minimum
Bactericidal Concentration (MBC) ranging from 50 to 100 mg/ml. The phytochemical
constiuents such as terpenoids, cardiac glycosides and steroids were significantly
higher (P < 0.05) in hot water extract when compared with methanol extract. Total
viii
Phenolic constituents, antioxidants and scavenging capacity against free radicals were
in appreciable amount in all the fungal species. Phomopsis liquidambaris hosted in the
leaf and petiole of Bryophyllum pinnatum had the best scavenging capacity and the
Inhibitory Concentration (IC50) against Diphenyl Picry Hydrazyl was 0.04±0.01. Total
phenol and free radical scavenging potency was higher in P. ostreatus as compared
with T. versicolor. The Fourier Transform-Infrared (FT-IR) Spectra and Gas
Chromatography Mass Spectra (GC-MS) revealed the bioactive compounds inherent in
the mushroom species. The in vivo study of P. ostreatus was conducted on
Staphylococcus aureus infected Wistar albino rats of weight range 63 g - 114 g. P.
ostreatus methanol extract Lethal dose for 50 % of the animals which was greater than
5000 mg/kg (LD 50 > 5000 mg/kg) was used to determine the graded doses for
therapeutic study. Infected untreated and treated rats with 625 mg/kg body weight
extract (low dose) had skin ulceration while moderate to high dose treatment produced
apparently healthy skin. Bacterial count in blood culture after 7 days post treatment was
significantly high in the untreated and low dose (32.00 x 104 ± 6.10b; 43.40 x 104 ±
6.20b Cfu/ml) P < 0.05. Haematological and serum biochemical values were not
significantly P < 0.05 affected. Chronic administration of P. ostreatus had no ill effect
on any of the vital organs including the heart, kidney, liver, lungs and spleen. This
could form a basis for the production of a novel antimicrobial of commercial value.