Department of Biological Sciences
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Item CHARACTERIZATION OF THE GUT MICROBIOME AND INFLAMMATORY MARKERS IN TREATMENT-NAIVE TRIPLE-NEGATIVE BREAST CANCER (TNBC) PATIENTS IN LAGOS, NIGERIA(Covenant University Ota, 2025-10) OGUNLEYE, Oluwanifemi Omodara; Covenant University DissertationTriple-negative breast cancer (TNBC) is an aggressive subtype lacking estrogen, progesterone, and HER2 receptors. Emerging studies suggest that gut microbial imbalance and chronic inflammation may contribute to breast cancer progression. This study investigated the gut microbiome profile and circulating inflammatory markers in treatment-naive TNBC patients compared with unknown subtypes and healthy controls to understand the microbiome–inflammation relationship in TNBC pathogenesis. Fecal DNA from TNBC, unknown subtype, and healthy control groups was extracted and analyzed using 16S rRNA sequencing through the Nephele QIIME2 pipeline. Alpha diversity was evaluated with the Shannon index, and group differences were tested using the Kruskal–Wallis and Mann–Whitney tests. Serum IL-6 and TNF-α levels were quantified using ELISA, and correlations were assessed using Pearson and Spearman analyses. Alpha diversity analysis revealed no statistically significant difference among groups (Kruskal–Wallis p = 0.298), though TNBC samples exhibited lower and more variable Shannon index values compared with controls. TNBC samples showed unstable high levels of Firmicutes, and Bacteriodota, and varying low levels of Proteobacteria and Actinobacteriota, indicating microbial imbalance. IL-6 and TNF-α levels did not differ significantly between TNBC and controls (p > 0.05), though TNBC patients displayed higher variability. A moderate positive correlation was found between IL-6 and TNF-α in TNBC (r = 0.5982), indicating co-regulated inflammatory activity. The PICRUSt functional prediction revealed altered microbial metabolic pathways in TNBC patients compared to controls, particularly a reduction in butyrate and propionate metabolism associated with short-chain fatty acid production. The findings suggest early gut dysbiosis and immune imbalance in TNBC despite the absence of significant statistical differences. Reduced microbial diversity, altered phylum-level composition, and cytokine co-regulation indicate biological perturbations in treatment-naive TNBC. These findings collectively support a potential link between microbial dysbiosis, altered short-chain fatty acid metabolism and elevated inflammatory activity in TNBC pathogenesis. It also highlights the need for larger, longitudinal studies to validate microbial and inflammatory biomarkers for early disease characterization.Item CHARACTERISATION OF THE GUT MICROBIOME AND FUNCTIONAL PROFILE IN ESTROGEN RECEPTOR-POSITIVE BREAST CANCER PATIENTS IN LAGOS, NIGERIA(Covenant University Ota, 2025-10) WILLIAMS, Moyosoreoluwa Mary; Covenant University DissertationEstrogen receptor-positive (ER+) breast cancer is the most prevalent molecular subtype globally, yet its association with gut microbial composition, functional potential and inflammatory drivers remains uncharacterised in sub-Saharan Africa. Employing the intersection of microbiology, oncology, and genomics, this study investigated the gut microbiome, predicted functional profiles, and systemic inflammatory markers in treatment-naïve ER+ breast cancer patients compared to healthy controls in Lagos, Nigeria. Faecal DNA samples from participants were extracted and analysed using 16S rRNA sequencing on the Illumina MiSeq platform using the QIIME2 pipeline. Microbial diversity was assessed through alpha (Shannon index) and beta diversity (NMDS, PCoA) metrics, and the group differences were tested using the Mann–Whitney test and Kruskal–Wallis, while PICRUSt2 predicted functional pathways with on focus on β-glucuronidase. Concurrently, systemic inflammation was evaluated through the quantification of Interleukin-6 (IL-6) and C-reactive protein (CRP) from blood serum. Analysis revealed no significant differences in alpha diversity between groups (p > 0.05). However, beta diversity demonstrated substantial compositional divergence (PERMANOVA R²=0.11, p=0.02), with cases showing an elevated Firmicutes/Bacteroidota ratio and depletion of Actinobacteriota, including Bifidobacterium and Collinsella. Functional prediction indicated heightened β-glucuronidase activity in ER+ cases, suggesting enhanced estrogen reactivation potential. Inflammatory markers displayed a complex profile, with significantly reduced IL-6 levels in patients despite stable CRP concentrations. These findings characterise distinct gut microbial dysbiosis and functional alterations in Nigerian ER+ breast cancer patients, revealing an estrobolome configuration potentially contributing to pathogenesis. The results underscore the necessity of population-specific microbiome studies and highlight potential biomarkers for early detection and targeted interventions in this understudied population.Item SINGLE NUCLEOTIDE POLYMORPHISMS OF Pfdhfr RESISTANCE GENE AMONG SYMPTOMATIC PATIENTS’ ISOLATES FROM SELECTED HOSPITALS IN IFO LGA, OGUN STATE(Covenant University Ota, 2025-10) SULE, Queen Elizabeth; Covenant University DissertationMalaria remains a primary universal health concern, particularly in endemic areas where drug resistance poses a serious threat to the effectiveness of key treatment and prevention strategies. Sulfadoxine-pyrimethamine (SP), commonly used for malaria prophylaxis, is increasingly compromised by resistance associated with mutations in the Plasmodium falciparum dihydrofolate reductase (Pfdhfr) gene. This study aimed to assess the prevalence of P. falciparum infection and identify the single-nucleotide polymorphisms (SNPs) in the Pfdhfr resistance gene among symptomatic patients in Ifo Local Government Area, Ogun State, Nigeria. Five hundred patients with severe P. falciparum infection were recruited, and demographic data were recorded. Blood samples were analysed for P. falciparum stages and parasitemia levels using microscopy. DNA was extracted from samples with high parasitemia and genotyped for Pfdhfr mutations using PCR, followed by visualisation on 1% agarose gel electrophoresis. Microscopy confirmed P. falciparum malaria in 300 patients (60%). A significantly higher prevalence (71.05%) was recorded in the 0–4 years’ age group, while males accounted for 64.31% of cases (p < 0.05). Parasitemia levels (greater than 200 parasites/100 μL) were more pronounced in males than in females, and were highest among individuals aged 0–4 years. Among the 10.67% Pfdhfr genotypes identified, males exhibited a higher frequency (6.0%) than females. The overall prevalence of pfdhfr SNPs in N51I, C59R, S108, and I64L was (96%), (96%), (100%), and (0%), respectively. tripple mutant halotype (N51I+ C59R+S108), prevance was 92%. Males have a higher mutation rate (60%) than females (40%). The overall prevalence of pfdhfr SNPs in N51I, C59R, S108, and I164L was (96%), (96%), (100%), and (0%), respectively. tripple mutant halotype (N51I+ C59R+S108), prevance was 92%. Males have a higher mutation rate (60%) than females (40%). Also, individuals aged 0-4 years (20%) and 15-20 years (20%) show higher SNPs than the other age groups. The study highlights a high prevalence of P. falciparum and emerging Pfdhfr resistance mutations, emphasising the need for continuous surveillance and targeted interventions in malaria-endemic regions, such as Ifo LGA, Nigeria.Item FUNGAL-MEDIATED VANILLIC ACID PRODUCTION THROUGH BIOCONVERSION OF GALLIC ACID OBTAINED FROM RICE BRAN(Covenant University Ota, 2025-08) OGUNBAJO, Oluwafemi Omolade; Covenant University DissertationGallic and vanillic acids are naturally occurring phenolic compounds widely used in the pharmaceutical, food, and cosmetic industries due to their antioxidant properties. Rice bran is a nutrient-rich agro-industrial by-product. However, there are challenges of improper disposal and underutilization as a substrate for the production of valuable bioactive compounds. This study investigated the fungal-mediated bioconversion of rice bran into gallic acid under solid-state fermentation (SSF) and its subsequent transformation into vanillic acid through submerged fermentation (SMF) using Aspergillus niger. It was inoculated into a fermentation medium containing pre-treated rice bran and mineral salts and incubated for 5 days at 30 °C. Fermentation was monitored for pH, temperature, UV-Vis absorbance (276nm), and titration. The produced gallic acid was characterized using HPLC, GC-MS, and FTIR. Thereafter, 1% Methanol was introduced into a mineral salt medium containing the produced gallic acid as the substrate, and inoculated 1ml of the inoculum and incubated at 30 °C for 5 days. This was monitored and characterized as in the gallic acid production. During fermentation, the temperature ranged 28-33 °C, pH decreased from 6.5 to 5.2, the absorbance rose from 0.205 to 0.681 nm, and titration increased from 0.016 to 0.075 mol (p<0.05). HPLC quantified 6552.2 mg/L total phenolics, with gallic acid at 2569.8 mg/L. FTIR revealed gallic acid functional groups such as O–H, C=O, and C=C, while GC-MS identified volatile compounds including O-toluic acid, 2(1H)-naphthalene derivatives, and 3H-Cyclodeca[b]furan-2-one. For the vanillic acid production, fermentation filtrate temperature stayed at 29-30 oC, with the pH increasing in acidity from 6.5 to 4.3 through the 5-day period. This corresponded with the results of the titration, showing 0.016 to 0.079 mol results.The GC-MS showed volatile organic compounds present in vanillic acid, including protocatechuic, catechol, and syringic acids. HPLC quantified a total of 15,31203 mg/L of vanillic acid. FTIR revealed vanillic acid functional groups such as OCH₃, OH, and C=O. The results of this study provides strategic insights for sustainable bioprocess approaches in support of SDGs 3 and 12.Item EXPRESSION PROFILES OF CYTOCHROME P450 GENES ASSOCIATED WITH PERMETHRIN RESISTANCE IN Anopheles gambiae s.l. IN ADO-ODO OTA, OGUN STATE(Covenant University Ota, 2025-10) AINA, Motunrayo Oluwabunmi; Covenant University DissertationMalaria remains a significant tropical public health threat, where resistance to insecticides constitutes a severe hindrance to the efficacy of its primary vector control methods. Routinely applied pyrethroid insecticides are increasingly facing resistance associated with the overexpression of cytochrome P450 genes in the Anopheles gambiae sensu lato, underscoring the urgent search into these associated genes. This study assessed the expression profile of cytochrome P450 genes associated with permethrin resistance in Anopheles gambiae sensu lato collected from three localities in Ado-Odo, Ota. Ethical approval was obtained from the Covenant Health Research Ethics Committee (CHREC). Based on the WHO standard, female adult An. gambiae larvae (n=300) were collected using the dipping method and reared into adults in the Insectary Laboratory. These laboratory-reared mosquitoes were phenotypically identified using microscopy and genotypically characterised using polymerase chain reaction (PCR) based on species-specific primers. Thereafter, a WHO susceptibility bioassay was conducted in vivo for mosquitocidal activity against these adult mosquitoes in four replicates at a 0.75% permethrin concentration each on day 3 post-adult emergence. The relative expression of the cytochrome P450 genes (CYP6M2 and CYP6P3) was carried out using the quantitative real-time PCR (qRT-PCR). Higher occurrence rate of An. gambiae sensu lato. was recorded in Nestle (80%)), Chelsea (78%)) compared Gasline (30%) localities of Ado-Odo. In vivo insecticide susceptibility testing revealed consistently low mortality rates across all the replicates, ranging from 20% to 32% indicating increased resistance to permethrin. Results of relative expression of cytochrome P450 genes showed higher fold changes in CYP6M2 ranging from 0.63 to 122.4 than in CYP6P3 0.63 to 34.39 across the tested mosquito replicates. Thus, this study has further emphasized the prevalence of An. gambiae sensu lato members in Ado-Odo, Ota. Additionally, the results of higher permethrin resistant and upregulation of CYP6M2 and CYP6P3 genes inform the imminent need for integrated resistance surveillance with newer vector management for improved malaria control.Item TARGET-SITE MUTATION GENOTYPING OF INSECTICIDE-RESISTANT FEMALE Anopheles MOSQUITOES IN OTA(Covenant University Ota, 2025-10) TAIWO, Damilare Isaiah; Covenant University DissertationMalaria control techniques in sub-Saharan Africa significantly depend on insecticide-based measures such as insecticide-treated nets (ITNs) and indoor residual spraying (IRS). However, the resistance emergence in Anopheles mosquitoes, driven by target-site mutations, undermines their effectiveness and threatens elimination efforts. Key resistance markers include knockdown resistance mutations (Kdr) in the voltage-gated sodium channel (VGSC) gene and the G119S mutation in the Ace-1 gene, both of which reduce insecticide efficacy. This study investigated the morphological and molecular composition of Anopheles populations, their insecticide resistance status, prevalence of Kdr and Ace-1 mutations, and assessed the genetic diversity, gene flow, and population structure across breeding sites in Ota, Ogun State, Nigeria. Using Coetzee’s key, a total of 478 adult female mosquitoes were obtained and morphologically identified, with molecular assays confirming a uniform species composition of Anopheles gambiae (390 bp) across all sites. Susceptibility assays revealed strong pyrethroid resistance, with permethrin mortality rates of 15–25%, far below the WHO threshold of 90%. However, bendiocarb produced 98–100% mortality, indicating high susceptibility. Genotypic analysis showed predominance of the Kdr-W (L1014F) allele, especially in Nestle and Iju, where homozygous resistant individuals were frequent. The Kdr-E (L1014S) allele was rare and largely confined to homozygous susceptible genotypes, suggesting it is not yet established. Deviations from the Hardy-Weinberg equilibrium were detected in Nestle populations, while sequence alignment confirmed L1014F mutations in Atan, Iju, and Chelsea. Population genetic analyses showed no strong subdivision (χ² = 0.7885, Fst = -1.3586, Gst = -0.0395, Kst = -0.13760), but high haplotype diversity (Hd = 0.94–1.00), moderate nucleotide diversity (π = 0.27–0.31), and substantial gene flow (Nm ≈ 8.24), supported by PCA and phylogenetic clustering. This study reveals widespread pyrethroid resistance but sustained carbamate susceptibility, providing the first genetic dataset from Ota to guide surveillance and resistance management strategies.Item ANALYSIS OF PHYTATE CONTENT VARIABILITY AND MOLECULAR CHARACTERISATION OF GENES IN COWPEA LANDRACES(Covenant University Ota, 2025-08) OMODIAGBE, David Eromosele; Covenant University DissertationPhytate is a naturally occurring phosphorus-storage compound in seeds, but it reduces the bioavailability of iron, zinc, and calcium in human diets. Cowpea (Vigna unguiculata (L.) Walp), an essential dietary protein source widely consumed in Nigeria, contains notable phytate levels, which may hinder micronutrient absorption with regular consumption. This study investigated phytate content in Nigerian cowpea accessions and explored candidate genes involved in its biosynthesis to guide future efforts for nutritional improvement. Thirty (30) cowpea landraces were obtained from the National Centre for Genetic Resources and Biotechnology (NACGRAB). Phytate concentration was quantified using acid digestion followed by filtration and titration. To explore the genetic basis of phytate accumulation, protein sequences of known phytate biosynthetic genes from Arabidopsis thaliana, Glycine max, and Phaseolus vulgaris were retrieved from Phytozome 14.0. These sequences were used for BLASTp searches to identify putative homologues in cowpea. Homologous cowpea sequences were aligned and subjected to phylogenetic analysis using the Neighbour-Joining method in MEGA v12.0.11 with 10,000 bootstrap replicates to assess evolutionary relationships. The results showed significant variation in phytate content, 3.96‒30.94mg/g (p < 0.001) across cowpea accessions. The cowpea sequences displayed strong homology to known phytate biosynthetic enzymes in seed, MIPS (Myo-inositol-3-phosphate synthase), ITPK (Inositol 1,3,4-triphosphate 5/6-kinase), IPK2 (Inositol 1,4,5-tris-phosphate kinase), MRP (Multidrug-resistance-associated protein ATP-binding cassette), IMP (Inositol monophosphate phosphatase), MIK (Myo-inositol kinase), and IPK1 (Inositol 1,3,4,5,6 pentakisphosphate 2-kinase), with low E-values and high identity percentages. Phylogenetic clustering of cowpea sequences alongside those from related legumes suggests potential functional conservation, although expression-level validation is necessary. Quantitative gene expression profiling to further clarify the roles of these genes in phytate biosynthesis and accumulation is needed. These identified genes could be prioritised for reverse genetics or transcriptomic studies, provided that tissue-specific expression and off-target impacts are carefully evaluatedItem EVALUATION OF EFFECTS OF Trichoderma asperellum STRAINS IN BIOCONTROL OF CHARCOAL-ROT CAUSING Macrophomina phaseolina (Tassi) Goidanich IN COWPEA(Covenant University Ota, 2025-09) OYESOLA, Olushola Luke; Covenant University ThesisMacrophomina phaseolina, a soil-borne fungal pathogen, is responsible for loss in cowpea at both seedling and adult stages. Synthetic fungicides, although proven effective in M. phaseolina control, lead to severe cowpea poisoning and pose significant health risks to humans and animals. Trichoderma are efficient bioagents for managing plant pathogens, representing a promising strategy for managing M. phaseolina. This study evaluated the antifungal efficacy of some Trichoderma asperellum strains against M. phaseolina. The Trichoderma isolates obtained from soil were macroscopically, microscopically and genotypically identified based on the Internal Transcribed Spacer genes. Bioactive compounds were isolated from selected Trichoderma species and evaluated using Gas Chromatography-Mass Spectrometry (GC-MS). The inhibitory potential of the suspensions of selected Trichoderma species against M. phaseolina was tested singly in vitro and in combination in vivo. The in vivo experiments were carried out in the screenhouse across pre-planting, post-germination and seed treatment for eighty days, and plant growth indicators such as plant height, stem girth and leaf number were assessed at ten-day intervals. Disease incidence and severity were also determined following standard methods. After the termination of the in vivo experiment, yield assessment was carried out to determine the cowpea pod number, pod weight, and seed number, as well as the fresh and dry weights of leaves, stems and roots. A histopathological assessment was carried out on the lower stems of the cowpea plants to determine the effect of M. phaseolina on the cowpea tissues. Phenotypic, microscopic and genotypic characterisation identified all the Trichoderma isolates as Trichoderma asperellum. Among the Trichoderma species isolated and tested, T. asperellum (Tric13), T. asperellum (Tric4) and T. asperellum (Tric12) exhibited significant inhibitory potential (p<0.05) against M. phaseolina in vitro, with inhibition values of 82.51%, 82.41%, and 81.95%, respectively. The production of volatile organic compounds varied among the Trichoderma species. Specifically, Tric13 yielded terpenoids, ketones, sesquiterpenes, cycloalkanes, and alcohols. In contrast, Tric4 produced fatty acids, aldehydes, alkanes, terpenoids, and aromatic and bicyclic compounds, while Tric12 generated carboxylic acids, terpenoids, phenolics, bicyclic and aromatic compounds. The in vivo results showed that Trt7 (plant height = 49.8000 cm; stem girth = 0.53625 cm; leaf number = 21.028), followed by Trt3 (plant height = 49.8250 cm; stem girth = 0.49986 cm; leaf number = 18.611), recorded higher cowpea biomass across the Trichoderma formulations than the negative control. Zero disease incidence was observed in Trt3 and Trt7 (0%) upon treatment with the Trichoderma formulations. Also, zero disease severity was noted in Trt3 and Trt7 (0%), compared to the negative controls, which displayed 100% incidence and severity. The cowpea yield assessment showed that the highest pod weight (11.3 g) and pod number (8) were recorded in Trt7 (pre-planting), and seed number (32) was recorded in Trt5 (seed treatment). The histopathological assessment of the cowpea showed the efficacy of the treatments in inhibiting the growth of M. phaseolina, minimising its tissue entry, and xylem vessel occlusion. This study established the efficacy of Trichoderma in M. phaseolina biomanagement and the synergistic potential of different Trichoderma asperellum strains in its biocontrol.Item MOLECULAR DOCKING, LIGAND QUALITY AND ANTIPLASMODIAL EVALUATION OF BENZAMIDE, COUMARIN AND BENZODIAZEPINE ANALOGS(Covenant University Ota, 2025-04) ADEBAYO GLORY PIPELOLUWA; Covenant University ThesisMalaria chemotherapy is an essential strategy for malaria elimination but resistance has challenged existing antimalarials, including frontline artemisinin combination therapy (ACT); hence, new antimalarial drugs must be discovered and developed. This study investigated the antiplasmodial efficacy and cytotoxicity through in vitro models while also testing the antiplasmodial efficacy, and the in vivo acute toxicity of benzamide, coumarin and benzodiazepine analogss. This study also evaluated the ligand quality of the molecules and their possible Plasmodium falciparum protein targets. Three molecules, 4- amino-N-hydroxybenzamide (AHB), ethyl 2-oxo-2H-chromene-3-carboxylate (ECC), and 2,2,4-trimethyl-2-3-dihyro-1H-benzo[b][1,4] diazepine (BDZ) were screened for their in vitro antiplasmodial activities tested against P. falciparum 3D7 standard strain using the SYBR Green Dye I measuring IC50 and their cytotoxicities against MCF-7 breast cancer cells using the [3(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] (MTT) assay. Their antiplasmodial efficacies were determined using Peter’s 4-day suppressive test against Plasmodium berghei in M. musculus while acute toxicities were investigated in the Mus musculus (mice). Ligand qualities were determined using ligand efficiency metrics, and molecular docking was conducted to determine the ligand interactions between ECC and the following enzymatic proteins, P. falciparum dihydroorotate dehydrogenase (PfDHOH) and P. falciparum purine nucleoside phosphorylase (PfPNP); and the molecular interaction between BDZ and PfDXR - Plasmodium falciparum 1-deoxy-D-xylulose-5-phosphate reductoisomerase, P. falciparum falcipain-2 and P. falciparum plasmepsin X (PfPMX). AHB showed no cytotoxicity against MCF-7 at (CC50) = 277.7 μM, while ECC showed inhibition with CC50= 3.930 μM, and BDZ showed no cytotoxicity CC50= 7373 μM. The in vitro antiplasmodial activity showed potency at (AHB)IC50 = 0.0020 ± 0.008 μM, (ECC) IC50= 0.0010 ± 0.002 μM, (BDZ) IC50= 0.0036 ± 0.003 μM respectively. BDZ showed the highest selectivity index at > 200,000, suggesting that it exhibited the best safety/efficacy among the three compounds. AHB displayed LD50 = >5000 mg/kg while ECC and BDZ displayed LD50 = 3162.28 mg/kg. Histopathological examinations showed non-toxicity by the three analogs on the liver and kidney of M. musculus. The percentage suppression of AHB (80.53 ± 3.26 %) at 400 mg/kg, was comparable to the standard chloroquine (81.71 ± 1.82 %) at 100 mg/kg where the mean survival time for both exceeded 30 days. ECC and BDZ showed excellent efficacies (70.98 ± 20.89 % and 83.66 ± 11.67 %) at 200 mg/kg, comparable to chloroquine 80.97 ± 5.82 %. The chemosuppression values for AHB and BDZ were significant at P value < 0.05. The ligand quality of ECC and BDZ displayed good Ligand Efficiency compared to chloroquine and artemisinin and higher enzyme affinities, and ligand efficiency dependent lipophilicity than the standard drugs. ECC and BDZ displayed good characteristics. The docking studies displayed strong hydrophobic interactions between ECC, PfDHODH, and PfPNP, suggesting good potency. BDZ’s binding with PfDXR, Pffalcipain-2, and PfPMX also displayed potency derived from hydrophobic and hydrogen interactions. Conclusively, this study showed AHB, ECC and BDZ were non-toxic to mammalian cells rodents’ liver and kidneys. These molecules exhibited good antiplasmodial inhibitory potential against both P. falciparum in vitro and P. berghei in vivo. ECC and BDZ displayed high ligand efficiency and strong molecular interactions with their protein targets. Therefore, all three analogs can be moved for further optimization in drug development.Item CHARACTERISATION OF PROSTATE TISSUE AND EXPRESSED PROSTATIC SECRETION IN PATIENTS WITH PROSTATE DISORDERS IN LAGOS NIGERIA(Covenant University Ota, 2025-01) SAMUEL ABOSEDE ESTHER; Covenant University OtaProstate cancer (PCa) is the second most prevalent cancer in men, particularly affecting those of Black African descent. Nigeria currently has the fourth highest risk for PCa mortality in the world. The microbiome of the prostate has emerged as a critical factor in understanding the aetiology and progression of prostate diseases, such as prostate cancer (PCa), benign prostatic hyperplasia (BPH), benign stromal hyperplasia (BSH) and prostatitis (PRO). This study was conducted to comparatively characterize the microbiome present in prostate tissue and expressed prostatic secretion (EPS) from patients diagnosed with PCa, BPH, BSH and PRO. A total of 30 study participants comprising of 15 prostate cancer, 10 benign prostatic hyperplasia, 2 benign stromal hyperplasia and 3 prostatitis subjects. Samples were collected from the urology clinic of Lagos State University Teaching Hospital Ikeja and analysed to identify and quantify bacterial species, assessing the diversity and composition of the microbial communities. Subjects without prostate (15) cancer were used as control subjects. By employing cultural and 16SrRNA sequencing techniques, uro-pathogens were isolated from the samples. The antibiotic susceptibility testing was carried out on these isolates. Prostate tissue and EPS samples from BPH patients demonstrated a higher prevalence of bacterial taxa, including Staphylococcus scuri, Bacillus mycoides, Staphylococcus aureus, Proteus vulgaris, Klebsiella pneumoniae, Pseudomonas aeruginosa, Streptococcus pyogene and Bacillus subtilis. Conversely, PCa patients exhibited an increased presence of pathogenic bacteria such as Escherichia coli Klebsiella oxytoca, Pseudomonas fluorescens, Citrobacter freudii, Pseudomonas putida, Staphylococcus condimentii, and Proteus mirabilis, which have been implicated in chronic inflammation and carcinogenesis. A high abundance of Lactobacillus vaginalis, Staphylococcus carnosus and Zymononas mobilis were observed in the prostate tissue. PCa-associated microbiome displayed reduced microbial diversity compared to other prostate disorders, suggesting a possible dysbiosis linked to cancer progression.