{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,20]],"date-time":"2026-03-20T05:04:12Z","timestamp":1773983052629,"version":"3.50.1"},"reference-count":1,"publisher":"Polish Academy of Sciences Chancellery","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:p>An animal body\u2019s immune response to viruses might vary depending on various factors. The relationship between 2\u2019-5\u2019-oligoadenylate synthetase like (OASL), interferon alpha (IFN-\u03b1), and duck hepatitis A virus type 3 (DHAV-3) virus genome copy number in duck embryo tissues was studied to investigate duck\u2019s natural antiviral immunity mechanism. 15-day-old SPF duck embryos were infected with DHAV-3 and their organs and tissues were collected at various times after inoculation. RT real-time PCR was used to determine OASL and IFNA mRNA expression levels and the DHAV-3 copy number. Compared with that at 0 hours, liver OASL transcription increased significantly at 24 hours, and extremely significantly in the liver, heart, gizzard, small intestine, and muscle at 48 hours. The heart had the highest expression level, followed by the liver, with lower expression in the other tissues. There was no significant difference in IFNA expression between the heart and liver at 12 hours, but it started to rise at 24 hours, reaching its maximum at 48 hours. Although IFNA expression increased in the gizzards, small intestines, and muscles, its relative expression levels were lower than those in the heart and liver. In the tissues, the virus genome copy number peaked at 24 hours, and then decreased. The liver had the highest virus genome copy number, followed by the heart. The results implied that the differences in OASL transcription in the tested tissues were similar to those of IFNA. Thus, the immune response (OASL and IFN-\u03b1 levels) of duck embryos to DHAV-3 shows tissue differences, especially in the liver and heart.<\/jats:p>","DOI":"10.24425\/pjvs.2025.154010","type":"journal-article","created":{"date-parts":[[2025,3,20]],"date-time":"2025-03-20T10:06:10Z","timestamp":1742465170000},"page":"25-33","source":"Crossref","is-referenced-by-count":1,"title":["Research on expression patterns of endogenous OASL and IFN-\u03b1 in duck embryos infected with DHAV-3"],"prefix":"10.24425","author":[{"ORCID":"https:\/\/orcid.org\/0009-0008-7751-7741","authenticated-orcid":false,"given":"H.","family":"Zhang","sequence":"first","affiliation":[{"name":"Independent researcher, New York, NY 11355, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Y.","family":"Tang","sequence":"additional","affiliation":[{"name":"Institute of Comparative Medicine, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu 225009, China"},{"name":"Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu 225009, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"X.","family":"Hong","sequence":"additional","affiliation":[{"name":"Institute of Comparative Medicine, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu 225009, China"},{"name":"Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu 225009, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"S.","family":"Zhou","sequence":"additional","affiliation":[{"name":"Institute of Comparative Medicine, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu 225009, China"},{"name":"Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu 225009, China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"T.","family":"Zhang","sequence":"additional","affiliation":[{"name":"Institute of Comparative Medicine, College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu 225009, China"},{"name":"Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu 225009, China"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"37468","published-online":{"date-parts":[[2025,3,20]]},"reference":[{"key":"ref0","unstructured":"Bi K, Han K, Liu Q, Zhao D, Huang X, Liu Y, Yang J, Li Y (2017) Molecular cloning, characterization, and expression of duck 2\u2019-5\u2019-oligoadenylate synthetase-like gene. Gene 629: 43-51. Cao J, Zhang Y, Chen Y, Liang S, Liu D, Fan W, Xu Y, Liu H, Zhou Z, Liu X, Hou S (2020) Dynamic Transcriptome Reveals the Mechanism of Liver Injury Caused by DHAV-3 Infection in Pekin Duck. Front Immunol 11: 568565. Chen, Y, Hu, S, Lin, X, Tian, J, Lv, J, Wang, M, Luo, X, Pei, Y, Hu, R, Song, Z, Holmes, E, Zhang, Y (2023). Host traits shape virome composition and virus transmission in wild small mammals. Cell 186: 4662-4675.e4612. Cheng G, Hu X, Zhou S, Xiong D(1996) Determining the Location of Duck Hepatitis Virus in Inoculated Ducklings by Monoclonal Antibody-pap Technique. J Huazhong Agric Univ. 15: 568-572. Feh\u00e9r E, Jakab S, Bali K, Kaszab E, Nagy B, Ih\u00e1sz K, B\u00e1lint \u00c1, Palya V, B\u00e1nyai K(2021) Genomic Epidemiology and Evolution of Duck Hepatitis A Virus.&nbsp;Viruses 13: 1352. Fu Y,&nbsp;Chen Z,&nbsp;Li C,&nbsp;Liu G (2012) Establishment of a duck cell line susceptible to duck hepatitis virus type 1. J Virol Methods 184: 41-45. Ishibashi M, Wakita T, Esumi M(2010) 2\u2019,5\u2019-Oligoadenylate synthetase-like gene highly induced by hepatitis C virus infection in human liver is inhibitory to viral replication in vitro. Biochem Biophys Res Commun. 392: 397-402. Jones LL, Vignali DAA (2011) Molecular interactions within the IL-6\/IL-12 cytokine\/receptor superfamily. Immunol Res 51: 5-14. Kim MC, Kim MJ. Kwon Y K, Lindberg A M, Joh S K, Kwon H M, Lee Y J, Kwon J H (2009) Development of duck hepatitis A virus type 3 vaccine and its use to protect ducklings against infections. Vaccine 27: 6688-6694 Kutlu B, Cardozo AK, Darville MI, Kruh\u00f8ffer M, Magnusson N, \u00d8rntoft T, Eizirik DL (2003) Discovery of gene networks regulating cytokine-induced dysfunction and apoptosis in insulin-producing INS-1 cells. Diabetes 52: 2701-2719. Levine P, Fabricant J (1950) A hitherto-undescribed virus disease of ducks in North America.&nbsp;Cornell Vet 40: 71-86. Luo HL, Fan WM, Zhang JY, Liu JP (1996) Research of cell culture technique of duck Hepatitis virus. Jiangsu Agric Sci 06: 53-54. Ou XM (2021) The attenuation of DHAV vaccine and its immune responses in breeding ducks. Master\u2019s Thesis. Sichuan Agric Univ. Chengdu, China Ou X, Mao S, Cao J, Ma Y, Ma G, Cheng A, Wang M, Zhu D, Chen S, Jia R, Liu M, Sun K, Yang Q, Wu Y, Chen X (2017) The neglected avian hepatotropic virus induces acute and chronic hepatitis in ducks: an alternative model for hepatology.&nbsp;Oncotarget&nbsp;8: 81838-81851. Peinnequin A, Mouret C, Birot O, Alonso A, Mathieu J, Claren\u00e7on D, Agay D, Chancerelle Y, Multon E (2003) Rat pro-inflammatory cytokine and cytokine related mRNA quantification by real-time polymerase chain reaction using SYBR green. BMC Immunol. 5: 3. Perelygin AA, Zharkikh AA, Scherbik SV, Brinton MA (2006) The mammalian 2\u2019-5\u2019 oligoadenylate synthetase gene family: evidence for concerted evolution of paralogous Oas1 genes in Rodentia and Artiodactyla. J Mol Evol 63: 562-576. Reed LJ, Muench H (1938) A simple method of estimating fifty percent endpoints. Am J Epidemiol 27: 493-497. Schneider WM, Chevillotte MD, Rice CM (2014) Interferon-stimulated genes: a complex web of host defenses. Annu Rev Immunol 32: 513-545. Song C, Yu S, Duan Y, Hu Y, Qiu X, Tan L, Sun Y, Wang M, Cheng A, Ding C (2014) Effect of age on the pathogenesis of DHV-1 in Pekin ducks and on the innate immune responses of ducks to infection. Arch Virol 159: 905-914. Su J, Huang Y, He R, Zhao J, Gu Y (2002) Screening and primary identification of new type duck hepatitis virus. Chin J Vet Sci Technol 32: 15-16. Tjiong MY, van der Vange N, ten Kate FJ, Tjong-A-Hung SP, ter Schegget J, Burger MP, Out TA (1999) Increased IL-6 and IL-8 levels in cervicovaginal secretions of patients with cervical cancer. Gynecol Oncol 73: 285-291. Tseng CH, Tsai HJ (2007) Molecular characterization of a new serotype of duck hepatitis virus. Virus Res 126: 19-31. Wang L, Pan M, Fu Y, Zhang D(2008) Classification of duck hepatitis virus into three genotypes based on molecular evolutionary analysis.&nbsp;Virus Genes 37: 52-59. Wang MS, An AC, Chen XY(1997) Study on duck viral hepatitis distribution and excretion of virulent duck hepatitis virus in duckling and adult duck Chin J Vet Sci 17: 254-257. Wei R (2020) Cloning and polymorphism analysis of OASL gene in Gaoyou duck and study on the effect of DHAV-3 on OASL expression. Master\u2019s Thesis. Yangzhou Univ. Yangzhou, China Wen X,&nbsp;Zhu D,&nbsp;Cheng A, Wang M,&nbsp;Chen S, Jia R, Liu M, Sun K,&nbsp;Zhao X,&nbsp;Yang Q,&nbsp;Wu Y,&nbsp;Chen X (2018) Molecular epidemiology of duck hepatitis a virus types 1 and 3 in China, 2010\u20132015.&nbsp;Transbound Emerg Dis&nbsp;65: 10-15. Woolcock PR, Chalmers WS, Davis D (1982) A plaque assay for duck hepatitis virus. Avian Pathol 11: 607-610. Xie J,&nbsp;Wang M,&nbsp;Cheng A,&nbsp;Zhao X, Liu M,&nbsp;Zhu D,&nbsp;Chen S, Jia R,&nbsp;Yang Q,&nbsp;Wu Y,&nbsp;Zhang S, Liu Y,&nbsp;Yu Y,&nbsp;Zhang L, Sun K, Chen X (2018) Cytokine storms are primarily responsible for the rapid death of ducklings infected with duck hepatitis A virus type 1. Sci Rep 8: 6596. Yang C, Chen S, Wang MS, Cheng AC (2017) Research progress of the association between the 2\u2019, 5\u2019-oligoadenylate synthetase and antiviral mechanism. Chin J Prev Vet Med 39: 682-685. Ye L, Zhou S, Zhang H, Zhang T, Yang D, Hong X (2023) A meta-analysis for vaccine protection rate of duck hepatitis a virus in mainland China in 2009-2021. BMC Vet Res 19: 179. Yugo DM, Hauck R, Shivaprasad HL, Meng XJ (2016) Hepatitis virus infections in poultry. Avian Dis 60: 576- 588. Zhang H, Pi J, Tang C, Yue H, Yang F(2012)&nbsp;An experimental study of the pathogenicity of a duck hepatitis A virus genotype C isolate in specific pathogen free ducklings. Avian Pathol&nbsp;41: 613\u2013620. Zhang Y, Wu S, Liu W, Hu Z(2023) Current status and future direction of duck hepatitis A virus vaccines. Avian Pathol 52: 89-99. Zhu F, Gu C, Cheng G, Su J, She R, Hu X(2007) Dynamic distribution of new type duck hepatitis virus in experimental infectious duckling. Huazhong Agric Univ 26: 511-513. Zhu J,&nbsp;Zhang Y,&nbsp;Ghosh A,&nbsp;Cuevas RA,&nbsp;Forero A,&nbsp;Dhar J, Ibsen MS,&nbsp;Schmid-Burgk JL,&nbsp;Schmidt T, Ganapathiraju MK,&nbsp;Fujita T,&nbsp;R. Hartmann R,&nbsp;Barik S, Hornung V,&nbsp;Coyne CB,&nbsp;Sarkar SN(2014) Antiviral activity of human OASL protein is mediated by enhancing signaling of the RIG-I RNA sensor. Immunity 40: 936-948. Zhu Y, Wang M, Cheng A, Zhu D, Jia R, Liu M, Chen S, Zhao X, Yang Q, Wu Y, Chen X (2018) Distribution of duck hepatitis A virus type 3 in artificial infected ducklings and analysis of the relationship between histopathological changes and expression of cytokines in the livers. Acta Vet Zootech Sin 49: 164-172.&nbsp;"}],"container-title":["Polish Journal of Veterinary Sciences"],"original-title":[],"language":"pl","link":[{"URL":"https:\/\/journals.pan.pl\/Content\/134447\/PDF\/3%20_%20Zhang.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,3,20]],"date-time":"2025-03-20T14:03:01Z","timestamp":1742479381000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.pan.pl\/dlibra\/publication\/154010\/edition\/134447\/content"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2025,3,20]]},"references-count":1,"URL":"https:\/\/doi.org\/10.24425\/pjvs.2025.154010","relation":{},"ISSN":["1505-1773"],"issn-type":[{"value":"1505-1773","type":"print"}],"subject":[],"published":{"date-parts":[[2025,3,20]]}}}