1 Recurrence of pandemics/epidemics is a common occurrence! Just think of; Bird fu (H5N1) 1996/7 Swine flu (H1N1) 2009/10 Zika virus epidemic 2015 SARS covid-19 2019 SCIENCE is expected to deliver the much needed interventions! These include; rapid and efficient diagnostic tools to inform intervention measures new and effective vaccines efficient drug/vaccine delivery methods novel therapeutic approaches 2 Can Biotechnology deliver to these demands? Yes it can! And, it has tremendous potential because of the Genomics revolution currently taking place Biotechnology can deliver through; Molecular diagnostic technologies a) PCR and related materials uses very small (ml) volumes, has low detection limit, yet fast and accurate exploits pathogen-specific DNA sequence in very small volume of body fluid to accurately detect infection in an individual this technique produces results in hours (commonly ≤ 4 hrs) NB: Suitable and reliable reagents are necessary for 3 delivering reliable PCR assays! Through multiplex PCR, more than one infection or disease can be detected in the same small body fluid of an individual Through the PCR technique, we are now better enabled to accurately diagnose HIV, malaria, cancer, TB indeed many other diseases b) Antibody-coated dipsticks A very sensitive molecular diagnostic approach that is very suitable to many developing country situations Why developing country situations? these devices are used anywhere without need for lab space, running water or electricity HIV Determine test kit 4 OptiMal for malaria detection c) Vaccines have enabled modern medicine to provide better quality of life hence, smallpox has been eradicated eradication of polio is imminent! other infectious disease incidents have also been significantly reduced The momentum is expected to spread to non-communicable diseases like cancer! Applications of Recombinant DNA technology is an integral part of the vaccine pursuit
Recombinant DNA technology
makes it possible to produce a single protein or DNA strand outside the pathogen and then use the produced 5 protein/DNA strand to challenge the human host this avoids contact with the pathogen as would be the case with attenuated vaccines this may be rendered cheap by using “cheap-to-grow” producer organism(s) DNA vaccines are thermostable and may be cheaper to make But, thermostability can be improved for either DNA or protein vaccines! Some challenges need to be overcome for ex situ synthesised / ‘engineered’ vaccines correct presentation of recombinant antigens to the immune system lengthening the lifespan of the ‘engineered’ vaccine in the body 6 in-built resistance to breakdown RTS,S/ASO2 a malaria vaccine based on the circumsporozoite protein of P. falciparum is synthesised in mice and excreted in milk After ‘Dolly the sheep’, transgenic goats for production of this vaccine are possible! Please read: Aide et al 2010: doi: 10.1371/journal.pone.0013838 Mtb8.4 peptide-linked surface antigen for vaccination against TB AND, Please also read: Gong et al (2021) Frontiers in Immunology https://doi.org/10.3389/fimmu.2021.666290 7 Day et al (2003) J. Immunol. 170: 1498-
Prediction of Conserved Epitopes of Hemagglutinin Neuraminidase From New Castle Disease Virus Isolated in Madagascar Between 1992 and 2011 An in Silico Study
International Journal of Innovative Science and Research Technology