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

Authors

  • Leandre Murhula Masirika Centre de Recherche en Sciences Naturelles de Lwiro, South Kivu, DS Bukavu, Democratic Republic of the Congo
  • Anuj Kumar Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada
  • Mansi Dutt Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada
  • Ali Toloue Ostadgavahi Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada
  • Benjamin Hewins Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada
  • Maliyamungu Bubala Nadine Hospital General de Reference de Kamituga, South Kivu, Democratic Republic of the Congo
  • Bilembo Kitwanda Steeven Hospital General de Reference de Kamituga, South Kivu, Democratic Republic of the Congo
  • Franklin Kumbana Mweshi Hospital General de Reference de Kamituga, South Kivu, Democratic Republic of the Congo
  • Léandre Mutimbwa Mambo Zone de Santé de Kamituga, South Kivu, Democratic Republic of the Congo
  • Justin Bengehya Mbiribindi Division Provinciale de la Santé, South Kivu, Democratic Republic of the Congo
  • Freddy Belesi Siangoli Division Provinciale de la Santé, South Kivu, Democratic Republic of the Congo
  • Alyson A Kelvin Vaccine and Infectious Disease Organization (VIDO), University of Saskatchewan, Saskatoon, Canada
  • Jean Claude Udahemuka Department of Veterinary Medicine, University of Rwanda, Nyagatare, Rwanda
  • Patricia Kelvin Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada
  • Luis Flores Centre de Recherche en Sciences Naturelles de Lwiro, South Kivu, DS Bukavu, Democratic Republic of the Congo
  • David J Kelvin Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada
  • Gustavo Sganzerla Martinez Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada

DOI:

https://doi.org/10.3855/jidc.20136

Keywords:

DRC, Mpox, Kamituga outbreak, hMPXV, Clade I, Sequencing, South Kivu

Abstract

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.

Author Biographies

Anuj Kumar, Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada

1Department of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, Canada

 

2Laboratory of Immunity, Shantou University Medical College, Jinping, Shantou, Guangdong, China

Mansi Dutt, Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada

1Department of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, Canada

2Laboratory of Immunity, Shantou University Medical College, Jinping, Shantou, Guangdong, China

Ali Toloue Ostadgavahi, Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada

1Department of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, Canada

2Laboratory of Immunity, Shantou University Medical College, Jinping, Shantou, Guangdong, China

Benjamin Hewins, Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada

1Department of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, Canada

2Laboratory of Immunity, Shantou University Medical College, Jinping, Shantou, Guangdong, China

David J Kelvin, Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada

1Department of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, Canada

2Laboratory of Immunity, Shantou University Medical College, Jinping, Shantou, Guangdong, China

Gustavo Sganzerla Martinez, Department of Microbiology and Immunology, Canadian Center for Vaccinology (CCfV), Faculty of Medicine, Dalhousie University, Halifax, Canada

1Department of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, Canada

2Laboratory of Immunity, Shantou University Medical College, Jinping, Shantou, Guangdong, China

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Published

2024-04-30

How to Cite

1.
Masirika LM, Kumar A, Dutt M, Ostadgavahi AT, Hewins B, Nadine MB, Steeven BK, Mweshi FK, Mambo LM, Mbiribindi JB, Siangoli FB, Kelvin AA, Udahemuka JC, Kelvin P, Flores L, Kelvin DJ, Sganzerla Martinez G (2024) Complete Genome Sequencing, Annotation, and Mutational Profiling of the Novel Clade I Human Mpox Virus, Kamituga Strain. J Infect Dev Ctries 18:600–608. doi: 10.3855/jidc.20136

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Original Articles