Olagoke Olusola, Quigley Bonnie L, Hemmatzadeh Farhid, Tzipori Galit, Timms Peter
Genecology Research Center, Faculty of Science, Health, Education and Engineering, University of the Sunshine Coast, 90 Sippy Downs Drive, Sippy Downs, QLD 4556 Australia.
School of Animal and Veterinary Sciences, The University of Adelaide, Roseworthy, SA 5371 Australia.
NPJ Vaccines. 2020 Jul 16;5:60. doi: 10.1038/s41541-020-0210-9. eCollection 2020.
The long-term survival of the koala is under serious threat from multiple factors, including infectious disease agents such as and koala retrovirus (KoRV). KoRV is present in both exogenous and endogenous forms, depending on the geographical location of the population. In the northern half of Australia, it is present as an endogenous infection in all koalas, making a case for an urgent need to develop a therapeutic vaccine that might prevent KoRV-associated pathologies in these koalas. To this end, we determined the therapeutic effects of vaccinating koalas harbouring endogenous KoRV with a recombinant KoRV Env protein combined with a Tri-adjuvant. We found that vaccination led to a significant increase in circulating anti-KoRV IgG levels, as well as increase in neutralising antibodies. Our study also showed that post-vaccination antibodies were able to recognize epitopes on the Env protein that were unrecognised pre-vaccination, as well as resulting in an increase in the recognition of the previously recognised epitopes. The vaccine also induced antibodies that were cross-reactive against multiple KoRV-subtypes. Finally, we found a complete clearance of KoRV-A in plasma from koalas that had detectable levels of KoRV-A pre-vaccination. Similarly, there was a significant reduction in the expression of KoRV-B viral RNA levels post-vaccination. Collectively, this study showed that koalas harbouring endogenous KoRV can benefit from prophylactic vaccination against KoRV using a recombinant KoRV-A Env protein and that the mechanism of this protection might be through the boosting of natural anti-KoRV antibodies and expanding the breadth of the recognised epitopes.
考拉的长期生存受到多种因素的严重威胁,这些因素包括传染病病原体,如[此处原文缺失某种病原体名称]和考拉逆转录病毒(KoRV)。根据考拉种群的地理位置,KoRV以外部感染和内部感染两种形式存在。在澳大利亚的北半部,所有考拉都存在KoRV内部感染,这表明迫切需要开发一种治疗性疫苗,以预防这些考拉出现与KoRV相关的病变。为此,我们确定了用重组KoRV Env蛋白与三联佐剂联合接种携带内源性KoRV的考拉的治疗效果。我们发现接种疫苗导致循环抗KoRV IgG水平显著升高,同时中和抗体也有所增加。我们的研究还表明,接种疫苗后的抗体能够识别接种前未被识别的Env蛋白表位,同时也导致对先前已识别表位的识别增加。该疫苗还诱导产生了对多种KoRV亚型具有交叉反应性的抗体。最后,我们发现接种前血浆中可检测到KoRV-A的考拉血浆中的KoRV-A被完全清除。同样,接种疫苗后KoRV-B病毒RNA水平的表达也显著降低。总体而言,这项研究表明,携带内源性KoRV的考拉可以通过使用重组KoRV-A Env蛋白进行预防性接种来预防KoRV,这种保护机制可能是通过增强天然抗KoRV抗体和扩大已识别表位的广度来实现的。