MOLECULAR DETECTION OF THE PLASMODIUM FALCIPARUM OBTAINED FROM OUT-PATIENTS FROM SELECTED HOSPITALS IN KADUNA STATE
Abstract
Molecular detection of Plasmodium falciparum based on PCR amplification is generally very specific and sensitive test for determining the species of Plasmodium present in the blood of an individual than the microscopy-based diagnosis from blood smears. Thirty-two (32) microscopic malaria positive blood samples were collected from some patients between November 2013 to March 2014 from three major hospitals.Plasmodium DNA was extracted from the 32 blood samples collected from the malaria-positive patients confirmed by microscopy and the DNA amplification was done by using Polymerase Chain Reaction (PCR). The amplified COX3 gene of each malaria isolates were further characterized using Agarose gel electrophoresis while sequence identification was performed by using GenBank’s BLAST algorithm. After the completion of the agarose gel electrophoresis the bands indicating amplified Cox3 gene by PCR was observed in four (4) plasmodium positive blood samples out of the 32 samples analyzed. Amplified band for COX3 gene was located at 300bp position on the DNA ladder on the agarose gel plate for sample 1, 9 and 24 all from Kagarko general hospital while sample 28 was from GwannaAwan general hospital. The BLAST results showed that the P. falciparum DNA sequences aligned at 98-99% similarity with those deposited in the GenBank confirming the parasite isolated from the patients were P. falciparum. The use of PCR diagnosis to compliment microscopy examination of stained blood smears in our medical centres is strongly recommended so that an accurate detection of malaria parasites in blood will help to institute proper drug therapy
References
Abubakar, U. B, Bala, S. H, Abayomi, A. O, Mahmood, M. D, Ibrahim, B. S, Muhammed S. I, Ayo S. A, Babatunde O. A, Mohammed Y, Ike O.O. A, Patrick M. N, and Olufemi O. A (2019). Trend of Malaria Cases in Kaduna State Using Routine Surveillance Data, 2011-2015. Pan African Medical Journal.32(1):8.Retrieved August 2021[doi:10.11604/pamj.supp.2019.32.1.13735]https://www.panafrican-med journal.com/content/series/32/1/8/full
Alaeddini, R. (2012). Forensic Implications of PCR Inhibition—A review. Forensic Science International: Genetics, 6 (3): 297–305. doi: 10.1016/j.fsigen.2011.08.006.
Bello B, and Ishaleku D (2018). Prevalence of Malaria Infection Among People Living with HIV/AIDS at Federal Medical Center Keffi Nasarawa State, Nigeria. Journal of Advances in Microbiology 11: 1-6.
Buppan P., Putaporntip C., and Jongwutiwes S. (2011). Improved Performance With Saliva and Urine As Alternative DNA Sources For Malaria Diagnosis By Mitochondrial DNA-based PCR assays. Clinical Microbiology Infectious, 17:1484-91.
Caraballo, H. (2014). “Emergency Department Management of Mosquito-borne Illness: Malaria, Dengue and West Nile Virusâ€. Emergency Medicine Practice, 16(5): 1-23.
Eke S.S, Omalu I.C.J, Olayemi I.K, Egwim E.C, and Hassan S.C,(2018). Malaria Parasitaemia Among Patients Attending General Hospital Minna, North Central Nigeria. Journal of Bioscience and Biotechnology Discovery 3: 78-82.
FMOH, (2008). National Malaria Control Programme, Abuja, Nigeria. Strategic, Plan 2009–2013. A Road Map for Malaria Control in Nigeria. http://www.nationalplanningcycles.org/sites/default/files/country/nigeria_.pdf.
Ikpa, T.F., Auta, K. I. and Ikpa, G. I. (2017). Evidence of Inconsistency Among Laboratory Technicians Collecting Dry Blood Spots for Molecular Analysis of
Plasmodium falciparum dhfr gene. Nigeria. Nigerian Journal of Parasitology 38 (1) 7 - 13.
Jyothi K., Surendra K.B., Nancy C.K. and Kashyap A. (2012). Identification and Isolation of Hydrocarbon Degrading Bacteria by Molecular Characterization. Helix, 2: 105-111.
Kalu K.M, Obasi N.A, Nduka F.O, and Oko M.O (2012). Prevalence of malaria parasitaemia in Umuchieze and Uturu Communities of Abia State, Nigeria. Asian Journal of Epidemiology 5: 95-102.
Kloos H., Seils J., Abranches J., Burne R.A., Bowen W.H., and Quivey R.G.(2006). Influence of Apigenin on gtf gene expression in Streptococcus mutants UA159. Antimicrobial Agents Chemotherapy, 50:542–546.
Maina A. T., Auta K. I. and Nock I. H. (2017): Prevalence of Plasmodium falciparium in participants at selected hospitals, Kaduna Metropolis. Nigerian Journal Parasitology 3:82) page 210 – 214.
Martinez-Perez G, Lansana D.P, Omeonga S, Gupta H, and Breeze-Barry B,(2018). Prevalence of Plasmodium falciparum infection among pregnant women at first antenatal visit in post-Ebola Monrovia, Liberia. Malaria Journal 17: 357-370
Max Lock, (2003): Executive Summary of Kaduna Master Plan Revision. Max Lock Consultancy Nigeria Limited, Kaduna.
National Malaria Control Programme (2014). Federal Ministry of Health – National guidance and strategies for malaria prevention and control during pregnancy. Retrieved June 2016 http://www.ihi.eprints.org.malaria.Strategic_Plan_Full_Version_02_27_14.pdf
National Population Commission (NPC) (2006). Nigeria National Demographic Survey, http://population.gov.ng/core-activities/surveys/dataset/2006-phc-priority-tables/ Retrieved 24th May, 2018.
Nwuba, R. I., Sodeinde, O. and Anumudu, C. (2002).The Human Immune Response to Plasmodium falciparum Antibodies that Inhibit Merozoite Surface Protein-1 Processing and Blocking Antibodies. Infectious Immunology. 70:5328-5331.
Obafemi B. J and Gidado S.(2014). Evaluation of Malaria Control Strategies Implementation in Kaduna State, Nigeria January 2011-June 2014. In: Afenet Conference. 2016.
Oladele O.V, Onuoha S.C, Hamafyelto H.S, Onisope O, Abayomi F,(2018). Prevalence of Malaria Infection among Patients Attending Murtala Mohammed Specialist Hospital Kano, Nigeria. African Journal of Clinical and Experimental Microbiology 19: 214-220.
Okokon I.I, Ubong A.U, Kenneth O.I and Anthony A.I (2017). Climate and Plasmodium falciparum infection on the Jos Plateau, Nigeria. International Journal of Microbiology and Biotechnology 2: 161-165.
Purfield A, Nelson A, Laoboonchai A, Congpuong K, McDaniel P, Miller R.S, Welch K, Wongsrichanalai C and Meshnick S.R (2004). A New Method for Detection of Pfmdr1 Mutations in Plasmodium falciparum DNA using Real-time PCR. Malaria Journal, 3:9.
Ricke, C. H., Stealsoe, T., Koram, K., Akanmori, B.D., Riley, E.M.,Theauder, T.G. and Hviid, L. (2000). Plasma Antibodies From Malaria Exposed Pregnant Women Recognize Variant Surface Antigen on Plasmodium Falciparum Infected Erythrocytes In A Parity Dependent Manner and Blood Parasite Adhesion to Chondroitin Sulfate. American Journal of Immunology 165:3309-3316.
Somvanshi V., Sloup R., Crawford J., Martin A., Heidt A., Kim K., (2012). A Single Promoter Inversion Switches Photorhabdus between Pathogenic and Mutualistic States. Science, 337:88-93.
Snounou, G., Viriyakosol, S.S, Zhu, X.P, Jarra, W, Pinheiro, L.V, De Rosario, E., Thaithong, S and Brown, K.N (1993). High Sensitivity of Detection of Human Malaria Parasites by the Use of Nested Polymerase Chain Reaction. Molecular Biochemistry Parasitology, 61:315-320.
World Health Organization (2014). World malaria report .WHO, Geneva, Switzerland. Retrieved March 2016, Available at http://www.who.int/malaria/publications/world_malaria_report_/2014.
WHO (2015). World Malaria Report. Retrieved October 2018. Available from http://www.who.int/malaria/publications/world-malaria-report-2015/en/
WHO (2016). World Malaria Report: Geneva. Retrieved October 2018;https://www.who.reliefweb.int/report/world/world-malaria-report-2016/en/
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