Kennedy D. Mwambete has completed his PhD at the age of 35 years from Universidad Complutense de Madrid, Spain majoring in Molecular Biology. Currently, he works for Muhimbili University of Health and Allied Sciences in Dar es Salaam, Tanzania as an Associate Professor of Pharmaceutical Microbiology. He is also the Associated Dean of School of Pharmacy since 2007 and the school curriculum chairperson since 2009. He has published more than 35 papers in reputed journals and serving as potential reviewer of several reputable journals. Kennedy D. Mwambete, BPharm, PhD, is an Associate Professor of pharmaceutical microbiology and the Associate Dean of the MUHAS School of Pharmacy. He is Curriculum Committee Chair for the school of pharmacy and led the school's curriculum revision process.


Trimethoprim-sulfamethoxazole [co-trimoxazole (CXT)] has been recommended by WHO as prophylactic drug for HIV/AIDS-patients against opportunistic infections. However, daily administration of CXT may reduce its efficacy to commensal intestinal Escherichia coli, thus increasing burden of CXT-resistant pathogens. CXT-resistance among enteric pathogens may impede empiric treatment strategies and worsen HIV/AIDS-patients conditions. We investigated incidences of fecalE. coli resistanceto CXTin 188 HIV/AIDS-patients over 18 years old, and determined changes in susceptibility of the bacteria to the drug. It was a prospective study conducted in Dar es Salaam, Tanzaniainvolving collection of stool specimens prior to initiating CXT prophylaxis and after.Specimens were collected from patients on the 1st, 4th, and 24th weeks upon commencing CXT prophylaxis. Susceptibility profiling of E. coli and other enteric bacteria to CXT and other widely used antibiotics were done using Kirby-Bauer disk diffusion method. On first visit, 143 (76.1%) enteric bacteria were isolates from 188 HIV/AIDS-patients. Of those, 123 (86%) were E. coli. About 98.6% (n= 141) were resistant to CXT. On second visit, 76 (74.5%) E. coli isolate and 10 (9.8%) mixture of E. coli and other microbes and were isolated from 102 (54.2%) patients. Of those, 100 (98.4%) isolates exhibited resistance to CXT. On third visit, only 64 (34%) of 188 HIV/AIDS-patients had significant enteric bacteria, and of those 63 (98.4%) were resistant to CXT: 39(62.6%) E. coli, 13(15.9%) S. aureusand 10(16%) E. coli plus others. About 53.2% (n=100) bacterial isolates were resistant to ciprofloxacin and ampicillin.Continuing use of CXT prophylaxis in HIV/AIDS-patients in Tanzania should be re-examined because of high antibacterial resistance revealed in our study.

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