Reverse Genetic Assessment of the Roles Played by the Spike Protein and ORF3 in Porcine Epidemic Diarrhea Virus Pathogenicity

被引:10
|
作者
Kristen-Burmann, Claudia [1 ,8 ]
Rogger, Peter [2 ,3 ,4 ,9 ]
Veiga, Ines Berenguer [2 ,3 ,5 ]
Riebesehl, Stefanie [1 ,10 ]
Rappe, Julie [2 ,3 ,4 ,11 ]
Ebert, Nadine [2 ,3 ,4 ]
Sautter, Carmen A. A. [2 ,3 ,4 ,12 ]
Kelly, Jenna N. N. [3 ]
Stalder, Hanspeter [2 ,3 ,4 ]
Ehmann, Rosina [1 ,13 ]
Huber, Michael [6 ]
Posthaus, Horst [5 ,7 ]
Ruggli, Nicolas [2 ,3 ,4 ]
Thiel, Volker [2 ,3 ,4 ]
Tekes, Gergely [1 ,14 ]
机构
[1] Justus Liebig Univ Giessen, Inst Virol, Giessen, Germany
[2] Inst Virol & Immunol IVI, Bern, Switzerland
[3] Inst Virol & Immunol IVI, Mittelhausern, Switzerland
[4] Univ Bern, Vetsuisse Fac, Dept Infect Dis & Pathobiol, Bern, Switzerland
[5] Univ Bern, Inst Anim Pathol, Vetsuisse Fac, Bern, Switzerland
[6] Univ Zurich, Inst Med Virol, Zurich, Switzerland
[7] Univ Bern, COMPATH, Bern, Switzerland
[8] Dept Vet Med, Hessian State Lab, Giessen, Germany
[9] Vet Cantonal Off, Zurich, Switzerland
[10] Vet Practice Sandra Meyer, Bad Homburg, Germany
[11] Sci Div Vetoquinol, Lure, France
[12] Drs Paul & Ursula Trachsel, Livestock Anim Practice, St Antoni, Switzerland
[13] Bundeswehr Inst Microbiol, Munich, Germany
[14] Elanco Anim Hlth, Bad Homburg, Germany
关键词
porcine epidemic diarrhea virus; synthesized DNA; vaccinia virus reverse genetics; spike gene; ORF3; LENGTH INFECTIOUS CDNA; SEQUENCE-ANALYSIS; UNITED-STATES; IN-VITRO; FELINE CORONAVIRUS; GENOME; STRAIN; SWINE; RECOMBINATION; OUTBREAK;
D O I
10.1128/jvi.01964-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Porcine epidemic diarrhea virus is a swine pathogen that has been responsible for significant animal and economic losses worldwide in recent years. In this manuscript, we report the generation of a reverse genetics system C(RGS) for the highly virulent US PEDV strain Minnesota (PEDV-MN; GenBank accession number ), which was based on the assembly and cloning of synthetic DNA, using vaccinia virus as a cloning vector. Viral rescue was only possible following the substitution of 2 nucleotides within the 5 & PRIME;UTR and 2 additional nucleotides within the spike gene, based on the sequence of the cell culture-adapted strains. Besides displaying a highly pathogenic phenotype in newborn piglets, in comparison with the parental virus, the rescued recombinant PEDV-MN was used to confirm that the PEDV spike gene has an important role in PEDV virulence and that the impact of an intact PEDV ORF3 on viral pathogenicity is modest. Moreover, a chimeric virus with a TGEV spike gene in the PEDV backbone generated with RGS was able to replicate efficiently in vivo and could be readily transmitted between piglets. Although this chimeric virus did not cause severe disease upon the initial infection of piglets, there was evidence of increasing pathogenicity upon transmission to contact piglets. The RGS described in this study constitutes a powerful tool with which to study PEDV pathogenesis and can be used to generate vaccines against porcine enteric coronaviruses.IMPORTANCE PEDV is a swine pathogen that is responsible for significant animal and economic losses worldwide. Highly pathogenic variants can lead to a mortality rate of up to 100% in newborn piglets. The generation of a reverse genetics system for a highly virulent PEDV strain originating from the United States is an important step in phenotypically characterizing PEDV. The synthetic PEDV mirrored the authentic isolate and displayed a highly pathogenic phenotype in newborn piglets. With this system, it was possible to characterize potential viral virulence factors. Our data revealed that an accessory gene (ORF3) has a limited impact on pathogenicity. However, as it is also now known for many coronaviruses, the PEDV spike gene is one of the main determinants of pathogenicity. Finally, we show that the spike gene of another porcine coronavirus, namely, TGEV, can be accommodated in the PEDV genome background, suggesting that similar viruses can emerge in the field via recombination.
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页数:24
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