2022
DOI: 10.1128/spectrum.03157-22
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The Role of Histo-Blood Group Antigens and Microbiota in Human Norovirus Replication in Zebrafish Larvae

Abstract: Despite causing over 700 million infections yearly, many gaps remain in the knowledge of human norovirus (HuNoV) biology due to an historical lack of efficient cultivation systems. Fucose-containing carbohydrate structures, named histo-blood group antigens, are known to be important (co)receptors for viral entry in humans, while the natural gut microbiota is suggested to enhance viral replication.

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Cited by 5 publications
(3 citation statements)
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“…In addition, the zebrafish larvae model has been employed to investigate the role of HBGAs and the host microbiota during HuNoV infection. The findings showed that successful HuNoV infection in zebrafish larvae depends on the presence of terminal fucoses, an integral part of HBGAs [120]. This aligns with infections observed in humans and in other recently established in vitro HuNoV models, emphasizing the consistent requirement for fucose residues on intestinal cells and suggesting a shared entry mechanism for HuNoV infection in zebrafish.…”
Section: Zebrafish Model For Detecting Infectious Human Norovirussupporting
confidence: 83%
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“…In addition, the zebrafish larvae model has been employed to investigate the role of HBGAs and the host microbiota during HuNoV infection. The findings showed that successful HuNoV infection in zebrafish larvae depends on the presence of terminal fucoses, an integral part of HBGAs [120]. This aligns with infections observed in humans and in other recently established in vitro HuNoV models, emphasizing the consistent requirement for fucose residues on intestinal cells and suggesting a shared entry mechanism for HuNoV infection in zebrafish.…”
Section: Zebrafish Model For Detecting Infectious Human Norovirussupporting
confidence: 83%
“…This aligns with infections observed in humans and in other recently established in vitro HuNoV models, emphasizing the consistent requirement for fucose residues on intestinal cells and suggesting a shared entry mechanism for HuNoV infection in zebrafish. Additionally, this study also demonstrated that neither the zebrafish microbiota nor the presence of HBGA-expressing bacteria in the zebrafish intestine amplified HuNoV replication during the early larval stages of their development [120]. This differs from the results seen in B-cells, where the presence of HBGA-expressing enteric bacteria was required for HuNoV infection [108].…”
Section: Zebrafish Model For Detecting Infectious Human Noroviruscontrasting
confidence: 77%
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