Temporal intra‐host variability of mpox virus genomes in multiple body tissues

Author:

Rueca Martina1,Tucci Fabio Giovanni1,Mazzotta Valentina2ORCID,Gramigna Giulia1,Gruber Cesare Ernesto Maria1ORCID,Fabeni Lavinia1,Giombini Emanuela1,Matusali Giulia1,Pinnetti Carmela2,Mariano Andrea2,Butera Ornella3,Specchiarello Eliana1,Mondi Annalisa2ORCID,Lanini Simone2,Carletti Fabrizio1,Girardi Enrico4,Vaia Francesco5,Nicastri Emanuele2,Antinori Andrea2,Maggi Fabrizio1

Affiliation:

1. Laboratory of Virology National Institute for Infectious Diseases “L. Spallanzani”—IRCCS Rome Italy

2. Department of Clinical and Research Infectious Diseases National Institute for Infectious Diseases “L. Spallanzani”—IRCCS Rome Italy

3. Laboratory of Microbiology National Institute for Infectious Diseases “L. Spallanzani”—IRCCS Rome Italy

4. Scientific Direction National Institute for Infectious Diseases “L. Spallanzani”—IRCCS Rome Italy

5. General Direction National Institute for Infectious Diseases “L. Spallanzani”—IRCCS Rome Italy

Abstract

AbstractWhole‐genome sequencing (WGS) has been widely used for the genomic characterization and the phylogenesis of mpox virus (MPXV) 2022 multi‐country outbreak. To date, no evidence has been reported on intra‐host evolution within samples collected over time from a single patient with long‐term infection. Fifty‐one samples were collected from five patients at different time points post‐symptom onset. All samples were confirmed as MPXV DNA positive, amplified by a multiplexed PCR amplicon, and sequenced by WGS. Complete MPXV genomes were assembled by reference mapping and then aligned to perform phylogenetic and hierarchical clustering analysis. Large intra‐host variability was observed among the MPXV genomes sequenced from samples of two immunocompromised with advanced HIV‐1 infection patients with prolonged MPXV shedding. Overall, 20 nucleotide mutations were identified in the 32 genomes from HIV patients, differently distributed in samples collected from different tissues and at different time points. No sequence compartmentalization nor variation was observed in the three patients with rapid viral clearance. MPXV exhibits adaptation to changing environments within the infected host and consequently demonstrates tissue compartmentalization. Further studies are needed to elucidate the role of this adaptation in forming a pool of genetic variability and contributing to viral persistence and its clinical implications.

Publisher

Wiley

Subject

Infectious Diseases,Virology

Reference31 articles.

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5. CDC. Mpox Cases by Age and Gender and Race/Ethnicity. 2023.https://www.cdc.gov/poxvirus/monkeypox/response/2022/demographics.html

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