Detection of SARS-CoV-2 intra-host recombination during superinfection with Alpha and Epsilon variants in New York City
© 2022. The Author(s)..
Recombination is an evolutionary process by which many pathogens generate diversity and acquire novel functions. Although a common occurrence during coronavirus replication, detection of recombination is only feasible when genetically distinct viruses contemporaneously infect the same host. Here, we identify an instance of SARS-CoV-2 superinfection, whereby an individual was infected with two distinct viral variants: Alpha (B.1.1.7) and Epsilon (B.1.429). This superinfection was first noted when an Alpha genome sequence failed to exhibit the classic S gene target failure behavior used to track this variant. Full genome sequencing from four independent extracts reveals that Alpha variant alleles comprise around 75% of the genomes, whereas the Epsilon variant alleles comprise around 20% of the sample. Further investigation reveals the presence of numerous recombinant haplotypes spanning the genome, specifically in the spike, nucleocapsid, and ORF 8 coding regions. These findings support the potential for recombination to reshape SARS-CoV-2 genetic diversity.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2022 |
---|---|
Erschienen: |
2022 |
Enthalten in: |
Zur Gesamtaufnahme - volume:13 |
---|---|
Enthalten in: |
Nature communications - 13(2022), 1 vom: 25. Juni, Seite 3645 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Wertheim, Joel O [VerfasserIn] |
---|
Links: |
---|
Themen: |
Journal Article |
---|
Anmerkungen: |
Date Completed 28.06.2022 Date Revised 25.01.2023 published: Electronic Citation Status MEDLINE |
---|
doi: |
10.1038/s41467-022-31247-x |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM342736434 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM342736434 | ||
003 | DE-627 | ||
005 | 20231226014816.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2022 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1038/s41467-022-31247-x |2 doi | |
028 | 5 | 2 | |a pubmed24n1142.xml |
035 | |a (DE-627)NLM342736434 | ||
035 | |a (NLM)35752633 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Wertheim, Joel O |e verfasserin |4 aut | |
245 | 1 | 0 | |a Detection of SARS-CoV-2 intra-host recombination during superinfection with Alpha and Epsilon variants in New York City |
264 | 1 | |c 2022 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 28.06.2022 | ||
500 | |a Date Revised 25.01.2023 | ||
500 | |a published: Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2022. The Author(s). | ||
520 | |a Recombination is an evolutionary process by which many pathogens generate diversity and acquire novel functions. Although a common occurrence during coronavirus replication, detection of recombination is only feasible when genetically distinct viruses contemporaneously infect the same host. Here, we identify an instance of SARS-CoV-2 superinfection, whereby an individual was infected with two distinct viral variants: Alpha (B.1.1.7) and Epsilon (B.1.429). This superinfection was first noted when an Alpha genome sequence failed to exhibit the classic S gene target failure behavior used to track this variant. Full genome sequencing from four independent extracts reveals that Alpha variant alleles comprise around 75% of the genomes, whereas the Epsilon variant alleles comprise around 20% of the sample. Further investigation reveals the presence of numerous recombinant haplotypes spanning the genome, specifically in the spike, nucleocapsid, and ORF 8 coding regions. These findings support the potential for recombination to reshape SARS-CoV-2 genetic diversity | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Research Support, U.S. Gov't, P.H.S. | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 7 | |a Spike Glycoprotein, Coronavirus |2 NLM | |
650 | 7 | |a spike protein, SARS-CoV-2 |2 NLM | |
700 | 1 | |a Wang, Jade C |e verfasserin |4 aut | |
700 | 1 | |a Leelawong, Mindy |e verfasserin |4 aut | |
700 | 1 | |a Martin, Darren P |e verfasserin |4 aut | |
700 | 1 | |a Havens, Jennifer L |e verfasserin |4 aut | |
700 | 1 | |a Chowdhury, Moinuddin A |e verfasserin |4 aut | |
700 | 1 | |a Pekar, Jonathan E |e verfasserin |4 aut | |
700 | 1 | |a Amin, Helly |e verfasserin |4 aut | |
700 | 1 | |a Arroyo, Anthony |e verfasserin |4 aut | |
700 | 1 | |a Awandare, Gordon A |e verfasserin |4 aut | |
700 | 1 | |a Chow, Hoi Yan |e verfasserin |4 aut | |
700 | 1 | |a Gonzalez, Edimarlyn |e verfasserin |4 aut | |
700 | 1 | |a Luoma, Elizabeth |e verfasserin |4 aut | |
700 | 1 | |a Morang'a, Collins M |e verfasserin |4 aut | |
700 | 1 | |a Nekrutenko, Anton |e verfasserin |4 aut | |
700 | 1 | |a Shank, Stephen D |e verfasserin |4 aut | |
700 | 1 | |a Silver, Stefan |e verfasserin |4 aut | |
700 | 1 | |a Quashie, Peter K |e verfasserin |4 aut | |
700 | 1 | |a Rakeman, Jennifer L |e verfasserin |4 aut | |
700 | 1 | |a Ruiz, Victoria |e verfasserin |4 aut | |
700 | 1 | |a Torian, Lucia V |e verfasserin |4 aut | |
700 | 1 | |a Vasylyeva, Tetyana I |e verfasserin |4 aut | |
700 | 1 | |a Kosakovsky Pond, Sergei L |e verfasserin |4 aut | |
700 | 1 | |a Hughes, Scott |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Nature communications |d 2010 |g 13(2022), 1 vom: 25. Juni, Seite 3645 |w (DE-627)NLM199274525 |x 2041-1723 |7 nnns |
773 | 1 | 8 | |g volume:13 |g year:2022 |g number:1 |g day:25 |g month:06 |g pages:3645 |
856 | 4 | 0 | |u http://dx.doi.org/10.1038/s41467-022-31247-x |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 13 |j 2022 |e 1 |b 25 |c 06 |h 3645 |