MYADM binds human parechovirus 1 and is essential for viral entry

• Published in: Nature communications 2024-04, Vol.15 (1), p.3469-3469, Article 3469
• Main Authors: Qiao, Wenjie, Richards, Christopher M., Kim, Youlim, Zengel, James R., Ding, Siyuan, Greenberg, Harry B., Carette, Jan E.
• Format: Article
• Language: English
• Subjects: 13; 13/106; 14; 14/19; 45; 45/70; 49; 49/47; 631/1647/2163; 631/326/596/2555; 631/326/596/2557; Amino acids; Cell Line; Cell lines; CRISPR; CRISPR-Cas Systems; Genomes; Genotypes; HEK293 Cells; Humanities and Social Sciences; Humans; Immunoprecipitation; Infections; Meningitis; multidisciplinary; Neonates; Organoids; Organoids - metabolism; Organoids - virology; Parechovirus - genetics; Parechovirus - metabolism; Picornaviridae Infections - metabolism; Picornaviridae Infections - virology; Protein Binding; Receptors; Receptors, Virus - genetics; Receptors, Virus - metabolism; Respiratory diseases; Science; Science (multidisciplinary); Sepsis; Virus Internalization
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-024-47825-0

Human parechoviruses (PeV-A) are increasingly being recognized as a cause of infection in neonates and young infants, leading to a spectrum of clinical manifestations ranging from mild gastrointestinal and respiratory illnesses to severe sepsis and meningitis. However, the host factors required for parechovirus entry and infection remain poorly characterized. Here, using genome-wide CRISPR/Cas9 loss-of-function screens, we identify myeloid-associated differentiation marker (MYADM) as a host factor essential for the entry of several human parechovirus genotypes including PeV-A1, PeV-A2 and PeV-A3. Genetic knockout of MYADM confers resistance to PeV-A infection in cell lines and in human gastrointestinal epithelial organoids. Using immunoprecipitation, we show that MYADM binds to PeV-A1 particles via its fourth extracellular loop, and we identify critical amino acid residues within the loop that mediate binding and infection. The demonstrated interaction between MYADM and PeV-A1, and its importance specifically for viral entry, suggest that MYADM is a virus receptor. Knockout of MYADM does not reduce PeV-A1 attachment to cells pointing to a role at the post-attachment stage. Our study suggests that MYADM is a multi-genotype receptor for human parechoviruses with potential as an antiviral target to combat disease associated with emerging parechoviruses. Host factors required for parechovirus entry are not well understood. Here, the authors identify MYADM as an essential host entry factor that directly binds human parechovirus 1 and that is required for PeV-A infection in cell lines and human gastrointestinal epithelial organoids.