CD163 and pAPN double-knockout pigs are resistant to PRRSV and TGEV and exhibit decreased susceptibility to PDCoV while maintaining normal production performance

Author:

Xu Kui1ORCID,Zhou Yanrong2,Mu Yulian1,Liu Zhiguo1ORCID,Hou Shaohua1,Xiong Yujian2,Fang Liurong2,Ge Changli3,Wei Yinghui1,Zhang Xiuling1,Xu Changjiang1,Che Jingjing1,Fan Ziyao1,Xiang Guangming1,Guo Jiankang1,Shang Haitao4ORCID,Li Hua5,Xiao Shaobo2,Li Julang6,Li Kui1ORCID

Affiliation:

1. State Key Laboratory of Animal Nutrition and Key Laboratory of Animal Genetics, Breeding and Reproduction of Ministry of Agriculture and Rural Affairs of China, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing, China

2. State Key Laboratory of Agricultural Microbiology and Key Laboratory of Preventive Veterinary Medicine in Hubei Province, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China

3. Shandong Landsee Genetics Co., Ltd., Rizhao, China

4. Shenzhen Kingsino Technology Co., Ltd., Shenzhen, China

5. College of Life Science and Engineering, Foshan University, Foshan, China

6. Department of Animal BioSciences, University of Guelph, Ontario, Canada

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) and transmissible gastroenteritis virus (TGEV) are two highly infectious and lethal viruses causing major economic losses to pig production. Here, we report generation of double-gene-knockout (DKO) pigs harboring edited knockout alleles for known receptor proteins CD163 and pAPN and show that DKO pigs are completely resistant to genotype 2 PRRSV and TGEV. We found no differences in meat-production or reproductive-performance traits between wild-type and DKO pigs, but detected increased iron in DKO muscle. Additional infection challenge experiments showed that DKO pigs exhibited decreased susceptibility to porcine deltacoronavirus (PDCoV), thus offering unprecedented in vivo evidence of pAPN as one of PDCoV receptors. Beyond showing that multiple gene edits can be combined in a livestock animal to achieve simultaneous resistance to two major viruses, our study introduces a valuable model for investigating infection mechanisms of porcine pathogenic viruses that exploit pAPN or CD163 for entry.

Funder

National Transgenic Breeding Project

Chinese Academy of Agricultural Sciences

Shandong Landsee Genetics Co., Ltd.

National Natural Science Foundation of China

Shenzhen Key Technology Projects

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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