Association of genotype III of dengue virus serotype 3 with disease outbreak in Eastern Sudan, 2019

• Published in: Virology journal Vol. 17; no. 1; pp. 1 - 118
• Main Authors: Eldigail, Mawahib H, Abubaker, Hazem A, Khalid, Fatima A, Abdallah, Tajeldin M, Musa, Hassan H, Ahmed, Mohamed E, Adam, Gamal K, Elbashir, Mustafa I, Aradaib, Imadeldin E
• Format: Journal Article
• Language: English
• Published: London BioMed Central Ltd 30.07.2020; BioMed Central; BMC
• Subjects: Analysis; Antibodies; Dengue fever; Dengue virus; ELISA; Enzyme-linked immunosorbent assay; Enzymes; Epidemics; Fever; Genetic aspects; Genomes; Genotypes; Headaches; Health aspects; Identification; Immunoglobulins; Infections; Mosquitoes; Outbreaks; Pain; Phylogenetics; Phylogeny; Polymerase chain reaction; Public health; Ribonucleic acid; RNA; RT-PCR; sequence analysis; Sudan; Thermal cycling; Red Sea; United States > US; Darfur Sudan; Germany; Sudan
• ISSN: 1743-422X; 1743-422X
• DOI: 10.1186/s12985-020-01389-9

Dengue fever (DF) is an arthropod-borne disease caused by dengue virus (DENV). DENV is a member of the genus Flavivirus in the family Flaviviridae. Recently, DENV has been reported as an important emerging infectious viral pathogen in Sudan. Multiple outbreaks and sporadic cases of DF have been frequently reported in the eastern region of Sudan. The present study was conducted to confirm DENV outbreak in Kassala State, eastern Sudan, 2019, and to provide some information on the molecular characterization of the DENV isolate associated with the disease outbreak. A hundred serum samples were collected during the outbreak from residents of Kassala State, Sudan, 2019. ELISA was used to detect DENV non structural protein NS1 (DENV-NS1) in acute phase sera sampled during the disease outbreak. RT-PCR assays were used to amplify a fragment of the capsid/pre-membrane region (CprM) of the viral polyprotein gene. The PCR products of the amplified CprM region of the viral polyprotein gene were purified and partial sequences were generated and used to confirm the specificity of DENV sequences and to identify the virus serotype. Phylogenetic tree was constructed to determine the genotype of DENV associated with the outbreak. Using DENV-NS1 ELISA assay, DENV infection was confirmed in 23% sampled sera. The detection of DENV RNA was made possible using group-specific RT-PCR assay. The virus was serotyped as DENV serotype 3 (DENV-3) using DENV serotype-specific RT-PCR assay. Phylogenetic analysis of the partial CprM sequences of the viral polyprotein gene indicates that the virus belonged to genotype III of DENV-3. The scientific data presented in this investigation confirmed that genotype III of DENV-3 was associated with the disease outbreak in eastern Sudan, 2019. The study represents the first report on molecular characterization of DENV-3 in Sudan.