dc.description.abstract |
The marine environment is a source of biologically active metabolites with great potential
for the development of pharmaceuticals. Due to the rapidly increasing number of
pathogenic microbes and tumorous cells that possess resistance towards established
therapies causing a threat to public health, lead structures for the development of new
drugs are on high demand. This study aimed to isolate bacteria associated with marine
algae of the Kenyan coast, in an attempt to evaluate their antimicrobial and cytotoxic
activity and identify the compounds responsible for bioactivity. Bacterial endophytes and
epiphytes were isolated from 44 seaweed species of red, green and brown algal division,
collected at three sites (Mkomani, Mtwapa, and Kibuyuni) along the Kenya coast. The
obtained isolates were tested for their antimicrobial activity against eight human
pathogenic strains of Gram-positive bacteria (Staphylococcus aureus (ATCC 25922) and
Methicillin Resistant Staphylococcus aureus (MRSA), Gram-negative bacteria
(Escherichia coli (ATCC 25923) and Salmonella typhi), fungi (Candida albicans (ATCC
90028), Cryptococcus neoformans, Trichophyton metagrophyte and Microsporum
gypseum). Isolates that had a broad spectrum of inhibitory activity were further
investigated for anticancer activity against human larynx Hep-2 cells. The active isolates
were identified using the 16S ribosomal DNA gene sequence. Culture fermentation and
bioassay guided fractionation was carried out on the active isolates. The compounds
present in active factions were identified by GC-MS analysis. The study obtained 3493
bacterial isolates with bacterial epiphytes being the most abundant (54%) compared to
bacterial endophytes (46%). Initial antimicrobial screening results revealed that 695
isolates (20%) inhibited the growth of at least one test organism, while further screening
showed that 69 isolates (10%) had antimicrobial activity against three or more test
pathogens. The results also showed that there was significant difference (p=0.001) in the
mean susceptibility patterns of the Gram-negative and Gram-positive test strains, with
Gram-positive (16.64±9.81) being more susceptible compared to Gram negative
(12.37±6.94). The study showed there was a significant difference in the inhibitory
activities among the three sampling sites, suggesting that the geographical location
influences the production and bioactivity of secondary metabolites. A total of 33 isolates
(48%) showed cytotoxity against Hep-2 cell line. The Phylogenetic analysis of 16S
rDNA gene sequences showed they belong to the phyla Firmicutes (79%), Proteobacteria
(12%) and Actinobacteria (9%). The active marine bacteria were assigned to the genera
Bacillus, Geobacillus, Desulfovibrio, Massilia and Streptomyces. In addition, the
metabolites produced significant cytotoxic activity against the tumorous Hep-2 cells
compared to the normal cells (p<0.05). Cytotoxic profiles ranged from low IC50 value of
0.24mg/ml-1 to a high of 50.01 mg/ ml-1. Identification of the active metabolites showed
the presence of several compounds such as phenolics, fatty acids, alkaloids, esters,
indoles, alcohols, ketones, alkenes, alkanes, amines, nitriles, furan and azoles derivatives
in the bioactive metabolites. These diverse ranges of compounds are known to have
antimicrobial and cytotoxic activities. In conclusion, the study demonstrates that seaweed associated microbes produce antimicrobial and cytotoxic compounds, which represents a promising and potential resource of natural product drugs, possessing a broad-spectrum activity. |
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