Susceptibility to mice and potential evolutionary characteristics of porcine deltacoronavirus.

Honglei Zhang1,2 Qingwen Ding1 Jin Yuan1,2 Fangfang Han1 Zhanyong Wei1,2 Hui Hu1,2
Affiliations 2 institutions
  1. College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, Henan, China.
  2. Key Laboratory for Animal-derived Food Safety of Henan Province, Zhengzhou, Henan, China.

Abstract

Porcine deltacoronavirus (PDCoV) is a novel coronavirus that causes diarrhea in suckling piglets and has the potential for cross-species transmission, posing a threat to animal and human health. However, the susceptibility profile of different species of mice to PDCoV infection and its evolutionary characteristics are still unclear. In the current study, we found that BALB/c and Kunming mice are susceptible to PDCoV. Our results showed that there were obvious lesions in intestinal and lung tissues from the infected mice. PDCoV RNAs were detected in the lung, kidney, and intestinal tissues from the infected mice of both strains, and there existed wider tissue tropism in the PDCoV-infected BALB/c mice. The RNA and protein levels of aminopeptidase N from mice were relatively high in the kidney and intestinal tissues and obviously increased after PDCoV infection. The viral-specific IgG and neutralizing antibodies against PDCoV were detected in the serum of infected mice. An interesting finding was that two key amino acid mutations, D138H and Q641K, in the S protein were identified in the PDCoV-infected mice. The essential roles of these two mutations for PDCoV-adaptive evolution were confirmed by cryo-electron microscope structure model analysis. The evolutionary characteristics of PDCoV among Deltacoronaviruses (δ-CoVs) were further analyzed. δ-CoVs from multiple mammals are closely related based on the phylogenetic analysis. The codon usage analysis demonstrated that similar codon usage patterns were used by most of the mammalian δ-CoVs at the global codon, synonymous codon, and amino acid usage levels. These results may provide more insights into the evolution, host ranges, and cross-species potential of PDCoV.

Supporting text Virus Host Location
cross-species transmission 75 evolution 62 mammals 99 porcine deltacoronavirus (PDCoV) 5 susceptibility to mice 1 COVID-19 425 Swine Diseases 153 Amino Acids 14 Animals 1948 Antibodies, Neutralizing 80 CD13 Antigens 7 Deltacoronavirus 16 Humans 1440 Immunoglobulin G 24 Mammals 92 Mice 253 Phylogeny 805 RNA 9 Swine 258 Porcine coronavirus HKU15 7

Evidence records

3 total
Zoonotic Surveillance
1 records · 1 evidence types
Evidence type
1 records
OVE6214
Key finding

PDCoV RNA was detected in the lung, kidney, and intestinal tissues of infected BALB/c and Kunming mice, showing broad tissue tropism.

Virus
Host
Location
Not specified
Supporting text

PDCoV RNAs were detected in the lung, kidney, and intestinal tissues from the infected mice of both strains, and there existed wider tissue tropism in the PDCoV-infected BALB/c mice.

Method
RNA detection
Sample type
lung tissues | kidney tissues | intestinal tissues
Experimental Infection
1 records · 1 evidence types
Evidence type
1 records
OVE6213
Key finding

BALB/c and Kunming mice were experimentally shown to be susceptible to porcine deltacoronavirus infection.

Virus
Host
Location
Not specified
Supporting text

In the current study, we found that BALB/c and Kunming mice are susceptible to PDCoV.

Method
experimental infection | RT-PCR detection of viral RNA | histopathology | serological detection of viral-specific IgG and neutralizing antibodies
Sample type
lung tissues | kidney tissues | intestinal tissues
Experimental system
in vivo mouse infection model
Genomic Evolution
1 records · 1 evidence types
Evidence type
1 records