Department of Parasitology, Medical College, Zhengzhou University, Zhengzhou, People's Repuplic of China.
PLoS Negl Trop Dis. 2022 Nov 29;16(11):e0010929. doi: 10.1371/journal.pntd.0010929. eCollection 2022 Nov.
Trichinella spiralis is a foodborne parasitic nematode which is a serious risk to meat safety. Development of anti-Trichinella vaccine is needed to control Trichinella infection in food animals. In this study, two novel T. spiralis genes (calreticulin and serine protease 1.1) in combination were used to construct oral DNA vaccines, and their induced protective immunity was evaluated in a murine model.
METHODOLOGY/PRINCIPAL FINDINGS: TsCRT+TsSP1.1, TsCRT and TsSP1.1 DNA were transformed into attenuated Salmonella typhimurium ΔcyaSL1344. Oral vaccination of mice with TsCRT+TsSP1.1, TsCRT and TsSP1.1 DNA vaccines elicited a gut local mucosal sIgA response and systemic Th1/Th2 mixed response. Oral vaccination with TsCRT+TsSP1.1 induced obviously higher level of serum specific antibodies, mucosal sIgA and cellular immune response than either of single TsCRT or TsSP1.1 DNA vaccination. Oral vaccination of mice with TsCRT+TsSP1.1 exhibited a 53.4% reduction of enteral adult worms and a 46.05% reduction of muscle larvae, conferred a higher immune protection than either of individual TsCRT (44.28 and 42.46%) or TsSP1.1 DNA vaccine (35.43 and 29.29%) alone. Oral vaccination with TsCRT+TsSP1.1, TsCRT and TsSP1.1 also obviously ameliorated inflammation of intestinal mucosa and skeletal muscles of vaccinated mice after challenge.
TsCRT and TsSP1.1 might be regarded the novel potential targets for anti-Trichinella vaccines. Attenuated Salmonella-delivered DNA vaccine provided a prospective approach to control T. spiralis infection in food animals.
旋毛虫是一种食源性寄生线虫,对肉类安全构成严重威胁。需要开发抗旋毛虫疫苗来控制食品动物中的旋毛虫感染。在本研究中,将两种新型旋毛虫基因(钙网蛋白和丝氨酸蛋白酶 1.1)联合构建口服 DNA 疫苗,并在小鼠模型中评估其诱导的保护免疫。
方法/主要发现:将 TsCRT+TsSP1.1、TsCRT 和 TsSP1.1 DNA 转化为减毒鼠伤寒沙门氏菌 ΔcyaSL1344。用 TsCRT+TsSP1.1、TsCRT 和 TsSP1.1 DNA 疫苗口服免疫小鼠可引起肠道局部黏膜 sIgA 反应和全身 Th1/Th2 混合反应。口服 TsCRT+TsSP1.1 疫苗可诱导明显高于单一 TsCRT 或 TsSP1.1 DNA 疫苗的血清特异性抗体、黏膜 sIgA 和细胞免疫反应。与单独 TsCRT(44.28%和 42.46%)或 TsSP1.1 DNA 疫苗(35.43%和 29.29%)相比,TsCRT+TsSP1.1 疫苗口服免疫可使肠道成虫减少 53.4%,肌肉幼虫减少 46.05%,提供了更高的免疫保护。口服 TsCRT+TsSP1.1、TsCRT 和 TsSP1.1 疫苗还明显改善了疫苗接种小鼠在挑战后肠道黏膜和骨骼肌的炎症。
TsCRT 和 TsSP1.1 可能被视为抗旋毛虫疫苗的新型潜在靶标。减毒沙门氏菌递送的 DNA 疫苗为控制食品动物旋毛虫感染提供了一种有前景的方法。