TY - JOUR
T1 - SARS-CoV-2 Omicron BA.1 Variant Infection of Human Colon Epithelial Cells
AU - Antia, Avan
AU - Alvarado, David M.
AU - Zeng, Qiru
AU - Casorla-Perez, Luis A.
AU - Davis, Deanna L.
AU - Sonnek, Naomi M.
AU - Ciorba, Matthew A.
AU - Ding, Siyuan
N1 - Publisher Copyright:
© 2024 by the authors.
PY - 2024/4
Y1 - 2024/4
N2 - The Omicron variant of SARS-CoV-2, characterized by multiple subvariants including BA.1, XBB.1.5, EG.5, and JN.1, became the predominant strain in early 2022. Studies indicate that Omicron replicates less efficiently in lung tissue compared to the ancestral strain. However, the infectivity of Omicron in the gastrointestinal tract is not fully defined, despite the fact that 70% of COVID-19 patients experience digestive disease symptoms. Here, using primary human colonoids, we found that, regardless of individual variability, Omicron infects colon cells similarly or less effectively than the ancestral strain or the Delta variant. The variant induced limited type III interferon expression and showed no significant impact on epithelial integrity. Further experiments revealed inefficient cell-to-cell spread and spike protein cleavage in the Omicron spike protein, possibly contributing to its lower infectious particle levels. The findings highlight the variant-specific replication differences in human colonoids, providing insights into the enteric tropism of Omicron and its relevance to long COVID symptoms.
AB - The Omicron variant of SARS-CoV-2, characterized by multiple subvariants including BA.1, XBB.1.5, EG.5, and JN.1, became the predominant strain in early 2022. Studies indicate that Omicron replicates less efficiently in lung tissue compared to the ancestral strain. However, the infectivity of Omicron in the gastrointestinal tract is not fully defined, despite the fact that 70% of COVID-19 patients experience digestive disease symptoms. Here, using primary human colonoids, we found that, regardless of individual variability, Omicron infects colon cells similarly or less effectively than the ancestral strain or the Delta variant. The variant induced limited type III interferon expression and showed no significant impact on epithelial integrity. Further experiments revealed inefficient cell-to-cell spread and spike protein cleavage in the Omicron spike protein, possibly contributing to its lower infectious particle levels. The findings highlight the variant-specific replication differences in human colonoids, providing insights into the enteric tropism of Omicron and its relevance to long COVID symptoms.
KW - SARS-CoV-2 Delta
KW - SARS-CoV-2 Omicron BA.1
KW - SARS-CoV-2 WA1
KW - human primary colonoids
KW - interferon responses
KW - intestinal infection
KW - intestinal permeability
KW - spike processing
UR - http://www.scopus.com/inward/record.url?scp=85191593126&partnerID=8YFLogxK
U2 - 10.3390/v16040634
DO - 10.3390/v16040634
M3 - Article
C2 - 38675974
AN - SCOPUS:85191593126
SN - 1999-4915
VL - 16
JO - Viruses
JF - Viruses
IS - 4
M1 - 634
ER -