Mutations in Coding and Non-Coding Regions in Varicella-Zoster Virus Causing Fatal Hemorrhagic Fever Without Rash in an Immunocompetent Patient: Case Report

• Published in: Infectious diseases and therapy 2023-11, Vol.12 (11), p.2621-2630
• Main Authors: Camacho, Juan, Negredo, Anabel, Carrilero, Bartolomé, Segovia, Manuel, Moreno, Antonio, Pozo, Francisco, Echevarría, Juan-Emilio, Echevarría, José-Manuel, Sánchez-Seco, M. Paz, Tarragó, David
• Format: Article
• Language: English
• Subjects: Analysis; Case Report; Case reports; Chicken pox; Chickenpox; Developing countries; Development and progression; DNA sequencing; Ebola virus; Epidemiology; Genes; Genetic aspects; Genomes; Genomics; Health aspects; Hemorrhagic fever; Immigration policy; Immunization; Immunocompetence; Infection; Infectious Diseases; Internal Medicine; Laboratory tests; LDCs; Liver; Medicine; Medicine & Public Health; Metagenomic whole genome sequencing (mWGS); Mutation; Nucleotide sequencing; Patients; Rash (Dermatology); Shingles (Disease); Skin; Vaccines; Varicella-zoster virus; Varicella-zoster virus clades; Varicella-zoster virus mutations; Varicella-zoster virus virulence; Virulence
• ISSN: 2193-8229; 2193-6382
• DOI: 10.1007/s40121-023-00884-0

Introduction We report the case of a fatal hemorrhagic varicella primary infection in an immunocompetent man and whole-genome characterization of the virus for the investigation of biomarkers of virulence. Case A 38-year-old patient born in Nigeria presented to the emergency department with abdominal pain and subsequently developed fatal hemorrhagic disease without skin rash. Extensive laboratory tests including serology and PCR for arenaviruses, bunyaviruses and ebolaviruses were negative. Varicella-zoster virus (VZV) PCR of sera, liver and spleen tissue samples from autopsy revealed the presence of VZV DNA. Primary infection by varicella-zoster virus with hemorrhagic manifestations was diagnosed after virological testing. The VZV genome was sequenced using a mWGS approach. Bioinformatic analysis showed 53 mutations across the genome, 33 of them producing non-synonymous variants affecting up to 14 genes. Some of them, such as ORF11 and ORF 62, encoded for essential functions related to skin or neurotropism. To our knowledge, the mutations reported here have never been described in a VZV causing such a devastating outcome. Discussion In immunocompetent patients, viral factors should be considered in patients with uncommon symptoms or severe diseases. Some relevant mutations revealed by using whole genome sequencing (WGS) directly from clinical samples may be involved in this case and deserves further investigation. Conclusion Differential diagnosis of varicella-zoster virus in immunocompetent adults should be considered among patients with suspected VHF, even if the expected vesicular rash is not present at admission and does not arise thereafter. Whole genome sequencing of strains causing uncommon symptoms and/or mortality is needed for epidemiological surveillance and further characterization of putative markers of virulence. Additionally, this report highlights the recommendation for a VZV vaccination policy in non-immunized migrants from developing countries.