Festus Chukwuemeka Onwuliri
Federal University Lafi a, Nigeria
Professor Festus Chukwuemeka Onwuliri got his Ph.D at the age of 35years from University of Jos. He has previously had his B.Sc., M.Sc and AIML from the University of Nigeria Nsukka, University of Jos and Medical Laboratory College Vom, Nigeria respectively. He has acquired a wide range of administrative experience. He was the Head of Department of Plant Science and Technology, University of Jos and is the Director of Victory medical laboratory service, Jos Nigeria. Professor F. C. Onwuliri has published about 65 papers in both national and international Journals. He has supervised 54 Post Graduate students both at Ph.D and M.Sc levels in the area of Microbiology and Biotechnology. He has also supervised over 150 undergraduate students. He has held several other positions and served in several committees, both ad-hoc and statutory, within the University of Jos and other Universities in Nigeria. He has several memberships including memberships Association of Medical Laboratory Scientists of Nigeria, Nigerian Society for Microbiology, Nigerian Mycological Society, Botanical Society of Nigeria, Nigerian Society for Parasitology, Biotechnology Society of Nigeria, International Biotechnology. Professor Onwuliri participated in the 4th world congress on Biotechnology in North Carolina, USA and the 5th world congress on Biotechnology in Valencia, Spain. He has many Scholastic Honours and Awards.
Faco’s medium is a novel, differential culture medium obtained from the mixture of extracts of Acha (Digitaria exilis and Digitaria iburua) and pooled human urine that is claimed to facilitate the isolation and presumptive identification of some clinical important bacterial isolates from clinical samples. The microbiological performance and efficacy of Faco’s medium was compared to that of blood and MacConkey agar for the isolation and presumptive identification of bacteria responsible for urinary tract infections. This study included consecutively collected midstream and/or catheter-catch urine samples obtained from patients. All urine samples were inoculated on Blood agar, MacConkey agar, and Faco’s medium medium and incubated overnight aerobically at 370 C and examined. Of the 2700 urine samples tested, 71.3% produced significant growth on the test media and about 14 potentially significant organisms were recovered on at least one of the three media. 743(95.8%) were uni-microbial, 32(4.12%) were poly microbial. Faco’s medium medium succeeded in detecting all the urine pathogens that were detected by the reference media, including Gram-negative bacilli, Staphylococci, Streptococci, and Yeasts. Colony colour and morphology on Faco’s medium agar accurately differentiated Escherichia coli, Proteus species, Klebsiella, Pseudomonas and Acinetobacter spp. The result suggests that Faco’s medium agar media can be used as a single medium for the isolation of uropathogens. Presumptive identification of isolates is time consuming and requires a great deal of experience when using traditional media. On Faco’s medium it is easier and will improve the quality of urine culture by contributing to a more uniform interpretation of Uropathogens on culture media. The performance of Faco’s medium was also determined using bacterial growth curve and the result obtained showed that there was significant increase in the performance of Faco’s media compared to that of Nutrient Broth. The result obtained also showed that there was significant difference (P˂0.05) between the growth of E. coli when grown in Faco’s media containing two different substrates. Growth in medium containing Nitrophenyl-B-D-galactoside was better than the growth of E. coli in the medium containing glucose. The activity of the enzyme B-galactosidase induced was then determined. The implications of the results are discussed.