Okalang Uthman, Nanteza Ann, Matovu Enock, Lubega George W
Department of Biology, Faculty of Science and Education, Busitema University Tororo, Uganda.
Int J Biochem Mol Biol. 2013 Jul 29;4(2):73-82. Print 2013.
Animal African trypanosomiasis (AAT) also known as Nagana is a devastating disease among domestic animals in large parts of Sub-Saharan Africa causing loses in milk and meat production as well as traction power. However, there is currently no commercial vaccine against AAT. The parasites have also developed resistance to some of the drugs in use. Moreover, the use of affordable computer-aided wet bench methods in the search for vaccine and/or new drug targets against this disease have not yet been fully explored in developing countries. This study, therefore, explored the use of PCR to screen a freshly prepared bloodstream form Trypanosoma brucei brucei (T. b. brucei) expression library for coding sequences followed by bioinformatics analyses specifying the functions and importance of these proteins to parasite survival. Eleven protein coding sequences were identified from twenty nine purified clones. The putative retro transposon hot spot protein 4 (RHSP 4) was the only protein with a fully annotated DNA sequence. All the others were hypothetical or had partial or unqualified annotations. RHSP 4 and pyruvate dehydrogenase E1 component, alpha sub-unit (PDE1α) are involved in aerobic respiration whereas succinyl-Co A-3-ketoacid-coenzyme A transferase mitochondrial precursor (SKTMP) is predicted to be involved in ketone body catabolism. Cystathionine beta-synthase (CBS) and alpha-1,3-mannosyltransferase (αMT) have been predicted in cysteine biosynthesis and vesicular transport respectively. The functions of the hypothetical proteins encountered have neither been experimentally determined nor predicted. We hypothesize that both CBS and PDE1α are good drug targets. Overall, about 300 plates are required to PCR screen the entire Trypanosoma brucei genome in approximately eight months. This method is therefore, applicable and affordable in the search for new drug targets under conditions of limited resources among developing countries.
动物非洲锥虫病(AAT),也称为那加那病,是撒哈拉以南非洲大部分地区家畜中的一种毁灭性疾病,会导致牛奶、肉类产量以及牵引力下降。然而,目前尚无针对AAT的商业疫苗。这些寄生虫也对一些正在使用的药物产生了耐药性。此外,在发展中国家,尚未充分探索使用经济实惠的计算机辅助湿实验室方法来寻找针对这种疾病的疫苗和/或新药物靶点。因此,本研究探索了使用聚合酶链反应(PCR)筛选新制备的布氏布氏锥虫(T. b. brucei)血流形式表达文库中的编码序列,随后进行生物信息学分析,以确定这些蛋白质对寄生虫生存的功能和重要性。从29个纯化克隆中鉴定出11个蛋白质编码序列。推定的逆转录转座子热点蛋白4(RHSP 4)是唯一具有完全注释DNA序列的蛋白质。其他所有蛋白质都是假设性的,或者具有部分或不合格的注释。RHSP 4和丙酮酸脱氢酶E1组分α亚基(PDE1α)参与有氧呼吸,而琥珀酰辅酶A - 3 - 酮酸辅酶A转移酶线粒体前体(SKTMP)预计参与酮体分解代谢。胱硫醚β合酶(CBS)和α - 1,3 - 甘露糖基转移酶(αMT)分别被预测参与半胱氨酸生物合成和囊泡运输。所遇到的假设性蛋白质的功能既未通过实验确定,也未被预测。我们假设CBS和PDE1α都是良好的药物靶点。总体而言,在大约八个月内,需要约300个平板来对整个布氏锥虫基因组进行PCR筛选。因此,这种方法在发展中国家资源有限的条件下,适用于寻找新的药物靶点且成本低廉。