Literature detail

Independent infections of porcine deltacoronavirus among Haitian children.

John A Lednicky1,2 Massimiliano S Tagliamonte1,3 Sarah K White1,2 Maha A Elbadry1,2 Md Mahbubul Alam1,2 Caroline J Stephenson1,2 Tania S Bonny1,2 Julia C Loeb1,2 Taina Telisma4 Sonese Chavannes4 David A Ostrov1,3 Carla Mavian1,3 Valery Madsen Beau De Rochars1,5 Marco Salemi6,7 J Glenn Morris8,9
Affiliations 9 institutions
  1. Emerging Pathogens Institute, University of Florida, Gainesville, FL, USA.
  2. Department of Environmental and Global Health, College of Public Health and Health Professions, University of Florida, Gainesville, FL, USA.
  3. Department of Pathology, Immunology and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, FL, USA.
  4. Christianville Foundation, Gressier, Haiti.
  5. Department of Health Services Research, Management and Policy, College of Public Health and Health Professions, University of Florida, Gainesville, FL, USA.
  6. Emerging Pathogens Institute, University of Florida, Gainesville, FL, USA. [email protected].
  7. Department of Pathology, Immunology and Laboratory Medicine, College of Medicine, University of Florida, Gainesville, FL, USA. [email protected].
  8. Emerging Pathogens Institute, University of Florida, Gainesville, FL, USA. [email protected].
  9. Department of Medicine, College of Medicine, University of Florida, Gainesville, FL, USA. [email protected].
PMID 34789872 2021 Nature eng ppublish
PubMed DOI Browse context

Article

Publication summary

Coronaviruses have caused three major epidemics since 2003, including the ongoing SARS-CoV-2 pandemic. In each case, the emergence of coronavirus in our species has been associated with zoonotic transmissions from animal reservoirs<sup>1,2</sup>, underscoring how prone such pathogens are to spill over and adapt to new species. Among the four recognized genera of the family Coronaviridae, human infections reported so far have been limited to alphacoronaviruses and betacoronaviruses<sup>3-5</sup>. Here we identify porcine deltacoronavirus strains in plasma samples of three Haitian children with acute undifferentiated febrile illness. Genomic and evolutionary analyses reveal that human infections were the result of at least two independent zoonoses of distinct viral lineages that acquired the same mutational signature in the genes encoding Nsp15 and the spike glycoprotein. In particular, structural analysis predicts that one of the changes in the spike S1 subunit, which contains the receptor-binding domain, may affect the flexibility of the protein and its binding to the host cell receptor. Our findings highlight the potential for evolutionary change and adaptation leading to human infections by coronaviruses outside of the previously recognized human-associated coronavirus groups, particularly in settings where there may be close human-animal contact.

Amino Acid Sequence Animals Bayes Theorem Child Chlorocebus aethiops Conserved Sequence Coronavirus Infections Deltacoronavirus Female Haiti Humans Male Models, Molecular Mutation Phylogeny Swine Vero Cells Viral Zoonoses

Structured evidence records

Evidence records

4 total
1 records
Extraction confidence 0.90
Key finding

Genomic and evolutionary analyses of porcine deltacoronavirus showed at least two distinct viral lineages infecting Haitian children, both independently acquiring identical mutations in Nsp15 and spike genes.

Virus
Location
Not specified
Supporting text

Genomic and evolutionary analyses reveal that human infections were the result of at least two independent zoonoses of distinct viral lineages that acquired the same mutational signature in the genes encoding Nsp15 and the spike glycoprotein.

Genes or proteins
Nsp15; spike glycoprotein
Analysis methods
genomic analysis; evolutionary analysis
1 records
Extraction confidence 0.93
Key finding

Distinct porcine deltacoronavirus lineages infecting humans independently evolved identical mutations in Nsp15 and the spike glycoprotein, with a spike S1 subunit change predicted to alter receptor binding and support adaptation to human hosts.

Virus
Host
Not specified
Location
Not specified
Supporting text

Genomic and evolutionary analyses reveal that human infections were the result of at least two independent zoonoses of distinct viral lineages that acquired the same mutational signature in the genes encoding Nsp15 and the spike glycoprotein. In particular, structural analysis predicts that one of the changes in the spike S1 subunit, which contains the receptor-binding domain, may affect the flexibility of the protein and its binding to the host cell receptor.

Genes or proteins
Nsp15; spike glycoprotein; spike S1 subunit
Receptors
host cell receptor
Mechanism types
receptor_binding; molecular_adaptation; host_range_expansion
1 records
Extraction confidence 0.78
Key finding

A mutation in the porcine deltacoronavirus spike S1 receptor-binding domain may alter receptor binding and mediate adaptation to human host cells.

Virus
Location
Not specified
Supporting text

Structural analysis predicts that one of the changes in the spike S1 subunit, which contains the receptor-binding domain, may affect the flexibility of the protein and its binding to the host cell receptor.

Method
structural analysis
Receptors
host cell receptor
1 records
Extraction confidence 0.98
Key finding

Porcine deltacoronavirus was transmitted independently from pigs to humans in Haiti, causing infection in children.

Virus
Location
Supporting text

Genomic and evolutionary analyses reveal that human infections were the result of at least two independent zoonoses of distinct viral lineages, identifying porcine deltacoronavirus strains in plasma samples of three Haitian children.

Method
genomic analysis; evolutionary analysis
Study design
genomic surveillance
Transmission direction
animal-to-human
Geographic raw
Haiti
Country inferred
Haiti