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Ovine rotavirus strain LLR-85-based bovine rotavirus candidate vaccines: Construction, characterization and immunogenicity evaluation

机译:基于绵羊轮状病毒株LLR-85的牛轮状病毒候选疫苗:构建,表征和免疫原性评估

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Group A bovine rotaviruses (BRVs) are the most important cause of diarrheal diseases in neonatal calves and cause significant morbidity and mortality in the young animals, and epidemiologic surveillance of bovine rotavirus G genotypes conducted in various cattle populations throughout the world has shown that approximately 90% of the bovine rotavirus isolates belong to G6 and G10. Based on the modified Jennerian approach to immunization, we constructed and characterized a reassortant rotavirus stain, which bears a single bovine rotavirus VP7 gene encoding G genotype 6 specificity while the remaining 10 genes are derived from the ovine attenuated rotavirus LLR-85. The reassortant rotavirus strain, named as R191, and its parental virus strain LLR-85 were combined as bivalent vaccine candidates to inoculate the colostrums-deprived neonatal calves for evaluation of the immunogenicity. The calves were orally inoculated with the reassortant R191 (group 1), the parental rotavirus LLR-85 (group 2), or combined the R191 and LLR-85 (group 3), and serum specimens were detected to determine the immune response of IgG and IgA antibodies. Results showed that seroconversion to positivity for IgG and IgA antibodies occurred at postinoculation day (PID) 10 in all of the inoculated calves, and the highest titers of the serum IgG (range 1:800 to 1:6400) and IgA (range 1:800 to 1:3200) antibodies were obtained at PID 21 for all calves. Meanwhile, virus shedding was detected after inoculation, showing that the inoculated virus was positive in 2 of 77 fecal specimens (2.6%) collected from the inoculated calves during the first 7 days of oral inoculation with the rotavirus vaccine candidates. The results suggested that the rotavirus strains R191 and LLR-85 are promising bivalent vaccine candidates for the prevention of bovine G6 and G10 rotavirus infection
机译:A组牛轮状病毒(BRV)是新生犊牛腹泻病的最重要原因,并在幼小动物中引起大量发病和死亡,全世界对各种牛群进行的牛轮状病毒G基因型的流行病学监测显示,牛轮状病毒分离株的%属于G6和G10。基于改良的Jennerian免疫方法,我们构建并鉴定了重配轮状病毒染色剂,该染色剂带有编码G基因型6特异性的单个牛轮状病毒VP7基因,而其余10个基因则来自绵羊减毒轮状病毒LLR-85。将重配的轮状病毒株命名为R191,并将其亲本病毒株LLR-85结合为二价疫苗候选物,接种初乳剥夺的新生牛犊,以评估其免疫原性。将小牛口服重组R191(第1组),亲代轮状病毒LLR-85(第2组)或R191和LLR-85联合(第3组),并检测血清标本以确定IgG的免疫应答和IgA抗体。结果显示,所有接种牛犊在接种后第10天(PID)都发生了IgG和IgA抗体的血清转化为阳性,血清IgG(1:800至1:6400)和IgA(范围1:在PID 21下为所有犊牛获得了800至1:3200的抗体。同时,在接种轮状病毒疫苗后头7天内,从接种小牛收集的77份粪便样本中,有2份(2.6%)的阳性病毒在接种后被检测到呈病毒脱落。结果表明,轮状病毒株R191和LLR-85是有望预防牛G6和G10轮状病毒感染的二价疫苗候选物

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