Molecular surveillance of arboviruses in Nigeria

• Published in: BMC infectious diseases Vol. 23; no. 1; pp. 1 - 538
• Main Authors: Shaibu, Joseph Ojonugwa, Akinyemi, Kabiru Olusegun, Uzor, Oshilonyah Henry, Audu, Rosemary Ajuma, Bola Oriowo Oyefolu, Akeeb
• Format: Journal Article
• Language: English
• Published: London BioMed Central Ltd 18-08-2023; BioMed Central; BMC
• Subjects: Analysis; Arboviruses; Care and treatment; Chikungunya virus; Clustering; Coccidioidomycosis; Complications and side effects; Control; Dengue fever; Dengue viruses; Disease transmission; DNA probes; Ethics; Ethylenediaminetetraacetic acid; Genomes; Genomics; Genotypes; Guillain-Barre syndrome; Health aspects; Identification and classification; Infection; Infections; Medical research; Molecular; Nervous system diseases; Outbreaks; Pandemics; Pathogens; Phylogenetics; Phylogeny; Polymerase chain reaction; Prevention; Public health; Ribonucleic acid; Rift Valley fever; Risk factors; RNA; Sequencing; Serology; Surveillance; Tropical diseases; Vector-borne diseases; Viral diseases; Viral infections; Virus diseases; Viruses; West Nile fever; West Nile virus; Yellow fever; Yellow fever, Virus, Arbovirus; Zika virus; Nigeria; Kenya; Germany
• ISSN: 1471-2334; 1471-2334
• DOI: 10.1186/s12879-023-08526-z

Arboviral infections are fast becoming a global public health concern as a result of its high fatality rate and sporadic spread. From the outbreak of Zika virus in the Americas, the endemicity of Yellow fever in West Africa and South America, outbreaks of West Nile virus in South Africa to the year-round and national risk of Dengue fever in Mainland China and India. The war against emerging and re-emerging viral infection could probably lead to the next pandemic. To be above the pending possible arboviral pandemic, consistent surveillance of these pathogens is necessary in every society. This study was aimed at conducting a surveillance for Yellow fever virus, Zika virus, Chikungunya virus, Dengue virus and Rift Valley fever virus in four states in Nigeria using molecular techniques. A cross-sectional study involving 1600 blood samples collected from febrile patients in Lagos, Kwara, Ondo and Delta States between 2018 and 2021 was conducted using Real time polymerase chain reaction for detection of the pathogens. Extraction and purification of viral RNA were done using Qiagen Viral RNA Mini Kit. Samples were analyzed using One Step PrimeScript III RT-PCR mix (Takara Bio) alongside optimized primers and probes designed in-house. Positive samples were sequenced on MinION platform (Nanopore technologies). Bioinformatic and phylogenetic analysis were performed with DNASTAR Lasergene 17.3. All the RNA extracted from samples collected from the four states were negative for ZIKV RNA, RVFV RNA, CHIKV RNA and DENV RNA. However, twelve of the samples (2%) tested positive for YFV RNA. Three full genomes of sizes 10,751 bp, 10,500 bp and 10,715 bp were generated and deposited in GenBank with accession numbers: ON323052, ON323053 and ON323054 respectively. Phylogenetic analysis shows clustering within lineage 3 of West African genotype. This result shows an active spread of Yellow fever in Delta State, Nigeria. However, there is no emergence of a new genotype There is a need for an intense surveillance of Yellow fever virus in Nigeria to avert a major outbreak.