Literature detail

Molecular Basis of Binding between Middle East Respiratory Syndrome Coronavirus and CD26 from Seven Bat Species.

Yuan Yuan1 Jianxun Qi1 Ruchao Peng1 Chunrui Li1 Guangwen Lu2 Jinghua Yan1,3,4 Qihui Wang5,4 George Fu Gao6,4,7,8
Affiliations 8 institutions
  1. CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
  2. West China Hospital Emergency Department, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center of Biotherapy, Chengdu, Sichuan, China.
  3. CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China.
  4. Shenzhen Key Laboratory of Pathogen and Immunity, Shenzhen Third People's Hospital, Shenzhen, China.
  5. CAS Key Laboratory of Microbial Physiological and Metabolic Engineering, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China [email protected] [email protected].
  6. CAS Key Laboratory of Pathogenic Microbiology and Immunology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, China [email protected] [email protected].
  7. Savaid Medical School, University of Chinese Academy of Sciences, Beijing, China.
  8. National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
PMID 31776269 2020 J Virol eng epublish
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Article

Publication summary

Continued reports of Middle East respiratory syndrome coronavirus (MERS-CoV) infecting humans have occurred since the identification of this virus in 2012. MERS-CoV is prone to cause endemic disease in the Middle East, with several dozen spillover infections to other continents. It is hypothesized that MERS-CoV originated from bat coronaviruses and that dromedary camels are its natural reservoir. Although gene segments identical to MERS-CoV were sequenced from certain species of bats and one species experimentally shed the virus, it is still unknown whether other bats can transmit the virus. Here, at the molecular level, we found that all purified bat CD26s (bCD26s) from a diverse range of species interact with the receptor binding domain (RBD) of MERS-CoV, with equilibrium dissociation constant values ranging from several to hundreds at the micromolar level. Moreover, all bCD26s expressed in this study mediated the entry of pseudotyped MERS-CoV to receptor-expressing cells, indicating the broad potential engagement of bCD26s as MERS-CoV receptors. Further structural analysis indicated that in the bat receptor, compared to the human receptor, substitutions of key residues and their adjacent amino acids leads to decreased binding affinity to the MERS-RBD. These results add more evidence to the existing belief that bats are the original source of MERS-CoV and suggest that bCD26s in many species can mediate the entry of the virus, which has significant implications for the surveillance and control of MERS-CoV infection.<b>IMPORTANCE</b> In this study, we found that bat CD26s (bCD26s) from different species exhibit large diversities, especially in the region responsible for binding to the receptor binding domain (RBD) of Middle East respiratory syndrome coronavirus (MERS-CoV). However, they maintain the interaction with MERS-RBD at varied affinities and support the entry of pseudotyped MERS-CoV. These bat receptors polymorphisms seem to confer evolutionary pressure for the adaptation of CD26-binding virus, such as the ancestor of MERS-CoV, and led to the generation of diversified CD26-engaging CoV strains. Thus, our data add more evidence to support that bats are the reservoir of MERS-CoV and similar viruses, as well as further emphasize the necessity to survey MERS-CoV and other CoVs among bats.

bat CD26 evolution interspecies transmission MERS-CoV MERS-RBD receptor Dipeptidyl Peptidase 4 Middle East Respiratory Syndrome Coronavirus Virus Attachment Animals Cell Line Chiroptera Humans Protein Domains Species Specificity

Structured evidence records

Evidence records

3 total
1 records
Extraction confidence 0.70
Key finding

Comparative sequence and structural analysis showed that amino acid differences in bat CD26 reduce MERS-CoV RBD binding affinity, indicating evolutionary adaptations influencing host range and supporting a bat origin of MERS-CoV.

Virus
Host
Location
Not specified
Supporting text

Bat CD26s from seven species exhibited large sequence diversity, particularly in the receptor binding site, where substitutions of key residues compared to human CD26 led to decreased binding affinity to the MERS-RBD.

Genes or proteins
CD26; RBD
Analysis methods
comparative sequence analysis; structural analysis
1 records
Extraction confidence 0.95
Key finding

Bat CD26 receptors with specific amino acid substitutions show reduced binding affinity to the MERS-CoV receptor-binding domain, indicating molecular determinants of host-specific viral adaptation.

Virus
Host
Not specified
Location
Not specified
Supporting text

All purified bat CD26s from a diverse range of species interact with the receptor binding domain (RBD) of MERS-CoV, and structural analysis indicated that substitutions of key residues in bat CD26 compared to the human receptor lead to decreased binding affinity to the MERS-RBD.

Genes or proteins
receptor binding domain (RBD); CD26
Receptors
CD26
Mechanism types
receptor_binding; cell_entry; host_factor_interaction
1 records
Extraction confidence 1.00
Key finding

Bat CD26 proteins from multiple bat species bind to the MERS-CoV receptor binding domain and can mediate pseudotyped virus entry, confirming CD26 as the receptor for MERS-CoV across bat species with varied affinities.

Virus
Host
Location
Not specified
Supporting text

All purified bat CD26s (bCD26s) from a diverse range of species interact with the receptor binding domain (RBD) of MERS-CoV and mediated the entry of pseudotyped MERS-CoV to receptor-expressing cells.

Method
binding assay; pseudovirus assay; structural analysis
Receptors
CD26