Susceptibility of Cell Lines from Different Species to Porcine Deltacoronavirus.

Hui Jiang1 Baoguo Lu2,3 Yimin Chu2,3 Mingyue Ma2,3 Nannan Zhang2,3 Yanyan Xu2,3 Yanying Chen2,3 Qingyang Xiao4 Ting Wang2,3 Qi Peng2,3
Affiliations 4 institutions
  1. College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang 330045, China.
  2. Institute of Pathogenic Microorganism, Jiangxi Agricultural University, Nanchang 330045, China.
  3. College of Bioscience and Engineering, Jiangxi Agricultural University, Nanchang 330045, China.
  4. School of Medical and Information Engineering, Gannan Medical University, Ganzhou 341000, China.

Abstract

Porcine deltacoronavirus (PDCoV) is an emerging swine enteric coronavirus that causes severe diarrhea in piglets, leading to extensive economic losses in the global swine industry. Previous studies have reported that PDCoV can experimentally infect multiple animal species. However, the replication capability of PDCoV in non-natural host cell lines remains largely unknown. Herein, we investigated the effects of exogenous trypsin on PDCoV replication and systematically evaluated the susceptibility of various cell lines derived from human, murine, and feline to PDCoV. The results showed that highly permissive cell lines (H1299, Caco-2, MC-38) supported efficient viral replication without the requirement for exogenous trypsin, and high concentrations of trypsin induced prominent syncytia formation in infected H1299, U251, and Neuro-2a cells. Furthermore, this study also found that trypsin can enhance PDCoV replication in a concentration-dependent manner in semi-permissive cell lines. PDCoV can replicate in multiple cell lines of human, murine, and feline origin. Human cells (H1299, Caco-2) and murine MC-38 are highly susceptible to PDCoV infection, whereas MCF-7, TE-10, and KYSE-410 cells were completely non-permissive. The results also revealed a potential correlation between basal APN expression and cellular susceptibility to PDCoV. Collectively, this study provides a basis for assessing the interspecies transmission and zoonotic risk of PDCoV.

Supporting text Virus Host Location
aminopeptidase N 3 cell line susceptibility 1 porcine deltacoronavirus 8 trypsin 6

Evidence records

5 total
Experimental Infection
4 records · 2 evidence types
Evidence type
1 records
OVE11857
Key finding

High concentrations of trypsin triggered prominent syncytia formation in PDCoV-infected H1299, U251, and Neuro-2a cells.

Virus
Host
Experimental system Experimental system Experimental system
Location
Not specified
Supporting text

high concentrations of trypsin induced prominent syncytia formation in infected H1299, U251, and Neuro-2a cells.

Method
trypsin treatment during infection | cytopathic effect observation (syncytia formation)
Experimental system
in vitro infected cell line model
Evidence type
3 records
OVE11854
Key finding

PDCoV replicated efficiently without exogenous trypsin in human H1299 and Caco-2 cells and murine MC-38 cells, indicating high permissiveness.

Virus
Host
Experimental system Experimental system Experimental system
Location
Not specified
Supporting text

The results showed that highly permissive cell lines (H1299, Caco-2, MC-38) supported efficient viral replication without the requirement for exogenous trypsin

Method
virus infection of cell lines | replication assay/virus growth assessment | trypsin supplementation testing
Experimental system
cell-culture system (human and murine cell lines)
OVE11855
Key finding

Human H1299 and Caco-2 and murine MC-38 cells were highly susceptible to PDCoV, whereas MCF-7, TE-10, and KYSE-410 were non-permissive.

Virus
Host
Experimental system Experimental system Experimental system Experimental system Experimental system Experimental system
Location
Not specified
Supporting text

Human cells (H1299, Caco-2) and murine MC-38 are highly susceptible to PDCoV infection, whereas MCF-7, TE-10, and KYSE-410 cells were completely non-permissive.

Method
virus infection of cell lines | susceptibility/permissiveness assessment | replication/cytopathic effect evaluation
Experimental system
cell-culture system (human and murine cell lines)
OVE11856
Key finding

Exogenous trypsin enhanced PDCoV replication in semi-permissive cell lines in a concentration-dependent manner.

Virus
Host
Experimental system
Location
Not specified
Supporting text

this study also found that trypsin can enhance PDCoV replication in a concentration-dependent manner in semi-permissive cell lines.

Method
virus infection of cell lines | trypsin supplementation testing | dose–response replication assessment
Experimental system
cell-culture system with exogenous trypsin modulation
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE11858
Key finding

Basal APN expression correlates with cellular susceptibility to PDCoV across tested cell lines.

Virus
Host
Not specified
Location
Not specified
Supporting text

The results also revealed a potential correlation between basal APN expression and cellular susceptibility to PDCoV.

Genes or proteins
APN
Receptors
APN
Host factors
APN
Mechanism types
receptor usage | host-range expansion | tissue tropism