2022
DOI: 10.1101/2022.08.09.22278589
|View full text |Cite
Preprint
|
Sign up to set email alerts
|

Recombination shapes 2022 monkeypox outbreak

Abstract: Here we report the first evidence of recombination of monkeypox genome in natural transmission by analyzing six tandem repeats (TRs) among 415 sequences collected between January to July 2022. The 2022 monkeypox viral population has diverged into 11 subgroups based on various TRs and their copy numbers. Here we identify 8 new recombinants (six from Slovenia, one from Australia, one from Italy). Our results indicate that the monkeypox genome is evolving and expanding quickly during the 2022 pandemic (Zeng E = -… Show more

Help me understand this report
View published versions

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
6
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
2
2

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(7 citation statements)
references
References 50 publications
0
6
0
Order By: Relevance
“…However, MPXV can inhibit host immune responses, although a recombinant VACV expressing the MPXV F3L gene did not inhibit host PKR activation ( Arndt et al., 2015 ), suggesting that MPXV has evolved to encode for yet undiscovered proteins that compensate for the missing N-terminal amino acids of F3 in limiting host antiviral activities. As previously mentioned, MPXV CCP ( D14L gene) is completely absent in Clade II isolates, whereas the Clade I strains are predicted to express CCP, albeit with a truncated fourth short consensus repeat ( Yeh and Contreras, 2022 ). Loss of expression of CCP/MOPICE limited the adaptive immune response against MPXV infection in rhesus macaques ( Estep et al., 2011 ).…”
Section: Infection Biology and Pathophysiologymentioning
confidence: 92%
See 2 more Smart Citations
“…However, MPXV can inhibit host immune responses, although a recombinant VACV expressing the MPXV F3L gene did not inhibit host PKR activation ( Arndt et al., 2015 ), suggesting that MPXV has evolved to encode for yet undiscovered proteins that compensate for the missing N-terminal amino acids of F3 in limiting host antiviral activities. As previously mentioned, MPXV CCP ( D14L gene) is completely absent in Clade II isolates, whereas the Clade I strains are predicted to express CCP, albeit with a truncated fourth short consensus repeat ( Yeh and Contreras, 2022 ). Loss of expression of CCP/MOPICE limited the adaptive immune response against MPXV infection in rhesus macaques ( Estep et al., 2011 ).…”
Section: Infection Biology and Pathophysiologymentioning
confidence: 92%
“…The low clade supports are probably due to very low genetic variability among isolates (Scarpa et al, 2022). Polytomy within lineage B.1 could be an indication of uncertainty in the relatedness of isolates or the belief that those isolates evolved independently from a single origin (Slowinski, 2001;Phylogenetic pitchforks -Understanding Evolution, 2023), although recombination cannot be excluded (Yeh et al, 2022).…”
Section: Phylogenomics and Phylodynamicsmentioning
confidence: 99%
See 1 more Smart Citation
“…This is an important distinction because we are still unsure about the precise transmission mechanisms, that is to say whether contagion is occurring through body fluids exchanged during sexual intercourse, or via contact with mucosal surfaces, scarification, or even respiratory exposures via droplets. 13 On the other hand, this new epidemiological trend seems to suggest that the monkeypox virus may have mutated, 14 adapted, and found a niche in high income countries among subjects with patterns of high frequencies of close, physical contact, like the MSM community. 15 Canada has become one of the most affected countries in the WHO Region of the Americas, reporting 1400 monkeypox cases (2.1% of all the cases worldwide), across 9 provinces or territories, 38 of which requiring hospitalization.…”
Section: Introductionmentioning
confidence: 99%
“…Like all orthopoxviruses, its genome comprises two terminal ends, called Telomeres. These contain identical but oppositely oriented adjacent repetitive nucleotide sequences, called Inverted Terminal Repeats (ITRs); they make up about 3% of monkeypox viral genome and are responsible for genetic variation and mutations (35). The monkeypox genome encodes several essential viral proteins that are categorized into three groups: i) Viral proteins that assist the virus to invade host cells by attaching to their glycoprotein receptors and enter via macropinocytosis; ii) viral proteins that liberate intracellularly proliferated viral replicas into the extracellular environment; iii) proteins that serve as immune modulators to host cell defenses.…”
mentioning
confidence: 99%