Apinda Nisachon, Muenthaisong Anucha, Chomjit Paweena, Sangkakam Kanokwan, Nambooppha Boondarika, Rittipornlertrak Amarin, Koonyosying Pongpisid, Yao Yongxiu, Nair Venugopal, Sthitmatee Nattawooti
Department of Veterinary Biosciences and Veterinary Public Health, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand.
Department of Food Animal Clinic, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai 50100, Thailand.
Vaccines (Basel). 2022 Aug 19;10(8):1358. doi: 10.3390/vaccines10081358.
Duck enteritis virus and are major duck pathogens that induce duck plague and fowl cholera, respectively, in ducks and other waterfowl populations, leading to high levels of morbidity and mortality. Immunization with live attenuated DEV vaccine containing outer membrane protein H (OmpH) can provide the most effective protection against these two infectious diseases in ducks. We have recently reported the construction of recombinant DEV expressing ompH gene using the CRISPR/Cas9 gene editing strategy with the goal of using it as a bivalent vaccine that can simultaneously protect against both infections. Here we describe the findings of our investigation into the systemic immune responses, potency and clinical protection induced by the two recombinant DEV-ompH vaccine constructs, where one copy each of the ompH gene was inserted into the DEV genome at the UL55-LORF11 and UL44-44.5 intergenic regions, respectively. Our study demonstrated that the insertion of the ompH gene exerted no adverse effect on the DEV parental virus. Moreover, ducklings immunized with the rDEV-ompH-UL55 and rDEV-ompH-UL44 vaccines induced promising levels of OmpH-specific as well as DEV-specific antibodies and were completely protected from both diseases. Analysis of the humoral and cellular immunity confirmed the immunogenicity of both recombinant vaccines, which provided strong immune responses against DEV and . This study not only provides insights into understanding the immune responses of ducks to recombinant DEV-ompH vaccines but also demonstrates the potential for simultaneous prevention of viral and bacterial infections using viral vectors expressing bacterial immunogens.
鸭肠炎病毒和禽霍乱杆菌分别是导致鸭瘟和禽霍乱的主要鸭病原体,可在鸭和其他水禽种群中引发高发病率和死亡率。用含有外膜蛋白H(OmpH)的鸭肠炎病毒减毒活疫苗进行免疫接种,可为鸭提供针对这两种传染病的最有效保护。我们最近报道了使用CRISPR/Cas9基因编辑策略构建表达ompH基因的重组鸭肠炎病毒,目的是将其用作一种能同时预防两种感染的双价疫苗。在此,我们描述了对两种重组鸭肠炎病毒-ompH疫苗构建体诱导的全身免疫反应、效力和临床保护作用的研究结果,其中ompH基因的一个拷贝分别插入到鸭肠炎病毒基因组的UL55-LORF11和UL44-44.5基因间隔区。我们的研究表明,ompH基因的插入对鸭肠炎病毒亲本病毒没有不利影响。此外,用rDEV-ompH-UL55和rDEV-ompH-UL44疫苗免疫的雏鸭诱导产生了可观水平的OmpH特异性抗体以及鸭肠炎病毒特异性抗体,并对这两种疾病都具有完全的保护作用。对体液免疫和细胞免疫的分析证实了两种重组疫苗的免疫原性,它们对鸭肠炎病毒和禽霍乱杆菌都产生了强烈的免疫反应。这项研究不仅为理解鸭对重组鸭肠炎病毒-ompH疫苗的免疫反应提供了见解,还证明了使用表达细菌免疫原的病毒载体同时预防病毒和细菌感染的潜力。