Host range projection of SARS-CoV-2: South Asia perspective.

Rasel Ahmed1 Rajnee Hasan1 A M A M Zonaed Siddiki2 Md Shahidul Islam3,4
Affiliations 4 institutions
  1. Basic and Applied Research on Jute Project, Bangladesh Jute Research Institute, Dhaka, Bangladesh.
  2. Department of Pathology and Parasitology, Chittagong Veterinary and Animal Sciences University (CVASU), Khulshi, Chittagong, Bangladesh.
  3. Basic and Applied Research on Jute Project, Bangladesh Jute Research Institute, Dhaka, Bangladesh
  4. Bangladesh Jute Research Institute, Manik Mia Avenue, Dhaka 1207, Bangladesh. Electronic address: [email protected].

Abstract

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), the causing agent of Coronavirus Disease-2019 (COVID-19), is likely to be originated from bat and transmitted through intermediate hosts. However, the immediate source species of SARS-CoV-2 have not yet been confirmed. Here, we used diversity analysis of the angiotensin I converting enzyme 2 (ACE2) that serves as cellular receptor for SARS-CoV-2 and transmembrane protease serine 2 (TMPRSS2), which has been proved to be utilized by SARS-CoV-2 for spike protein priming. We also simulated the structure of receptor-binding domain of SARS-CoV-2 spike protein (SARS-CoV-2S RBD) with the ACE2s to investigate their binding affinity to determine the potential intermediate animal hosts that could spread the SARS-CoV-2 to humans in South Asia. We identified cow, buffalo, goat and sheep, which are predominant species in the household farming system in South Asia that can potentially be infected by SARS-CoV-2. All the bird species studied along with rat and mouse were considered less potential to interact with SARS-CoV-2. The interaction interfaces of SARS-CoV-2S RBD and ACE2 protein complex suggests pangolin as a potential intermediate host in SARS-CoV-2. Our results provide a valuable resource for the identification of potential hosts for SARS-CoV-2 in South Asia and henceforth reduce the opportunity for a future outbreak of COVID-19.

Supporting text Virus Host Location
ACE2 54 COVID-19 467 Host range 29 SARS-CoV-2 550 TMPRSS2 5 Angiotensin-Converting Enzyme 2 177 Animals 1948 Asia 13 COVID-19 425 Disease Vectors 12 Humans 1440 Phylogeny 805 SARS-CoV-2 453 Serine Endopeptidases 12 Species Specificity 84

Evidence records

1 total
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE4352
Key finding

SARS-CoV-2 uses ACE2 as its cellular receptor and TMPRSS2 for spike priming; structural simulations of the spike RBD–ACE2 interfaces were used to evaluate cross-species binding affinity.

Virus
Host
Location
Not specified
Supporting text

We used diversity analysis of the angiotensin I converting enzyme 2 (ACE2) that serves as cellular receptor for SARS-CoV-2 and transmembrane protease serine 2 (TMPRSS2), which has been proved to be utilized by SARS-CoV-2 for spike protein priming. We also simulated the structure of receptor-binding domain of SARS-CoV-2 spike protein (SARS-CoV-2S RBD) with the ACE2s to investigate their binding affinity.

Method
diversity analysis | structural simulation | receptor-binding domain modeling
Receptors
ACE2
Host factors
TMPRSS2