Complete Genome Sequencing, Annotation, and Mutational Profiling of the Novel Clade I Human Mpox Virus, Kamituga Strain

• Published in: Journal of infection in developing countries Vol. 18; no. 4; pp. 600 - 608
• Main Authors: Masirika, Leandre Murhula, Kumar, Anuj, Dutt, Mansi, Ostadgavahi, Ali Toloue, Hewins, Benjamin, Nadine, Maliyamungu Bubala, Steeven, Bilembo Kitwanda, Mweshi, Franklin Kumbana, Mambo, Léandre Mutimbwa, Mbiribindi, Justin Bengehya, Siangoli, Freddy Belesi, Kelvin, Alyson A, Udahemuka, Jean Claude, Kelvin, Patricia, Flores, Luis, Kelvin, David J, Sganzerla Martinez, Gustavo
• Format: Journal Article
• Language: English
• Published: Italy Journal of Infection in Developing Countries 01.04.2024; The Journal of Infection in Developing Countries
• Subjects: Adolescent; Adult; Annotations; Child; Child, Preschool; Clade I; Cohort Studies; Cross-Sectional Studies; Democratic Republic of the Congo - epidemiology; Disease Outbreaks; DRC; Epidemics; Female; Genome, Viral; Genomes; hMPXV; Humans; Kamituga outbreak; Male; Middle Aged; Monkeypox virus - classification; Monkeypox virus - genetics; Mpox; Mpox (monkeypox) - epidemiology; Mpox (monkeypox) - virology; Mutation; Phylogenetics; Phylogeny; Sequencing; Whole Genome Sequencing; Young Adult; Democratic Republic of the Congo; Congo-Democratic Republic of Congo; Clade I; DRC; hMPXV; South Kivu; Mpox; Sequencing; Kamituga outbreak
• ISSN: 1972-2680; 2036-6590; 1972-2680
• DOI: 10.3855/jidc.20136

Introduction: Human Mpox (formerly monkeypox) infection is an emerging zoonotic disease caused by the Mpox virus (MPXV). We describe the complete genome annotation, phylogeny, and mutational profile of a novel, sustained Clade I Mpox outbreak in the city of Kamituga in Eastern Democratic Republic of the Congo (DRC). Methodology: A cross-sectional, observational, cohort study was performed among patients of all ages admitted to the Kamituga Hospital with Mpox infection symptoms between late September 2023 and late January 2024. DNA was isolated from Mpox swabbed lesions and sequenced followed by phylogenetic analysis, genome annotation, and mutational profiling. Results: We describe an ongoing Clade I Mpox outbreak in the city of Kamituga, South Kivu Province, Democratic Republic of Congo. Whole-genome sequencing of the viral RNA samples revealed, on average, 201.5 snps, 28 insertions, 81 deletions, 2 indels, 312.5 total variants, 158.3 amino acid changes, 81.66 intergenic variants, 72.16 synonymous mutations, 106 missense variants, 41.16 frameshift variants, and 3.33 inframe deletions across six samples. By assigning mutations at the proteome level for Kamituga MPXV sequences, we observed that seven proteins, namely, C9L (OPG047), I4L (OPG080), L6R (OPG105), A17L (OPG143), A25R (OPG151), A28L (OPG153), and B21R (OPG210) have emerged as hot spot mutations based on the consensuses inframe deletions, frameshift variants, synonymous variants, and amino acids substitutions. Based on the outcome of the annotation, we found a deletion of the D14L (OPG032) gene in all six samples. Following phylogenetic analysis and whole genome assembly, we determined that this cluster of Mpox infections is genetically distinct from previously reported Clade I outbreaks, and thus propose that the Kamituga Mpox outbreak represents a novel subgroup (subgroup VI) of Clade I MPXV. Conclusions: Here we report the complete viral genome for the ongoing Clade I Mpox Kamituga outbreak for the first time. This outbreak presents a distinct mutational profile from previously sequenced Clade I MPXV oubtreaks, suggesting that this cluster of infections is a novel subgroup (we term this subgroup VI). These findings underscore the need for ongoing vigilance and continued sequencing of novel Mpox threats in endemic regions.