VIDO-InterVac., 120 Veterinary Road, University of Saskatchewan, Saskatoon, SK S7N 5E3, Canada.
Vaccinology & Immunotherapeutics Program, School of Public Health, University of Saskatchewan, Saskatoon, SK S7N 5E3, Canada.
Viruses. 2020 Dec 12;12(12):1431. doi: 10.3390/v12121431.
A number of characteristics including lack of virulence and the ability to grow to high titers, have made bovine adenovirus-3 (BAdV-3) a vector of choice for further development as a vaccine-delivery vehicle for cattle. Despite the importance of blood leukocytes, including dendritic cells (DC), in the induction of protective immune responses, little is known about the interaction between BAdV-3 and bovine blood leukocytes. Here, we demonstrate that compared to other leukocytes, bovine blood monocytes and neutrophils are significantly transduced by BAdV404a (BAdV-3, expressing enhanced yellow green fluorescent protein [EYFP]) at a MOI of 1-5 without a significant difference in the mean fluorescence of EYFP expression. Moreover, though expression of some BAdV-3-specific proteins was observed, no progeny virions were detected in the transduced monocytes or neutrophils. Interestingly, addition of the "RGD" motif at the C-terminus of BAdV-3 minor capsid protein pIX (BAV888) enhanced the ability of the virus to enter the monocytes without altering the tropism of BAdV-3. The increased uptake of BAV888 by monocytes was associated with a significant increase in viral genome copies and the abundance of EYFP and BAdV-3 19K transcripts compared to BAdV404a-transduced monocytes. Our results suggest that BAdV-3 efficiently transduces monocytes and neutrophils in the absence of viral replication. Moreover, RGD-modified capsid significantly increases vector uptake without affecting the initial interaction with monocytes.
牛腺病毒-3(BAdV-3)缺乏毒力且能够高滴度生长,因此成为进一步开发牛用疫苗载体的首选载体。尽管血液白细胞,包括树突状细胞(DC),在诱导保护性免疫应答方面非常重要,但人们对 BAdV-3 与牛血液白细胞之间的相互作用知之甚少。在这里,我们证明与其他白细胞相比,牛血液单核细胞和中性粒细胞在 MOI 为 1-5 时,通过 BAdV404a(表达增强型黄色荧光蛋白 [EYFP] 的 BAdV-3)显著转导,而 EYFP 表达的平均荧光强度没有显著差异。此外,尽管观察到一些 BAdV-3 特异性蛋白的表达,但在转导的单核细胞或中性粒细胞中未检测到后代病毒粒子。有趣的是,在 BAdV-3 次要衣壳蛋白 pIX(BAV888)的 C 末端添加“RGD”基序增强了病毒进入单核细胞的能力,而不改变 BAdV-3 的嗜性。与 BAdV404a 转导的单核细胞相比,单核细胞摄取 BAV888 的增加与病毒基因组拷贝数的显著增加以及 EYFP 和 BAdV-3 19K 转录物的丰度增加相关。我们的研究结果表明,在没有病毒复制的情况下,BAdV-3 能够有效地转导单核细胞和中性粒细胞。此外,RGD 修饰的衣壳显著增加了载体摄取量,而不影响与单核细胞的初始相互作用。