Ryan Jonathan T, Rose Timothy M
Center for Childhood Infections and Prematurity Research, Seattle Children's Research Institute, Seattle, WA, USA.
Clin Vaccine Immunol. 2013 Mar;20(3):409-19. doi: 10.1128/CVI.00673-12. Epub 2013 Jan 23.
Kaposi's sarcoma-associated herpesvirus (KSHV)/human herpesvirus 8 is a tumorigenic rhadinovirus that is associated with all forms of Kaposi's sarcoma. Current serological detection of KSHV is based on enzyme-linked immunosorbent or immunofluorescence assays that suffer from a variety of problems, including the lack of defined standards for test comparison. While KSHV is the only known human rhadinovirus, two lineages of KSHV-like rhadinoviruses are found in Old World primates: the RV1 lineage includes KSHV and retroperitoneal fibromatosis herpesvirus (RFHV) in macaques, and the RV2 lineage includes RRV and MneRV2 from different macaque species. To develop animal models of KSHV-associated diseases, we developed quantitative multiplex bead-based serological assays to detect antibodies against rhadinovirus antigens. Proteins from KSHV (RV1) and MneRV2 (RV2) virions were coupled to spectrally distinct fluorescent beads and used in Luminex flow cytometry-based assays to detect immune responses in macaques. Both assays showed large dynamic ranges with high levels of seroreactivity to both KSHV and MneRV2 proteins. A large set of macaque serum samples from the Washington National Primate Research Center was screened, and most of the samples (82%) were positive in both assays, consistent with the high level of RV1-RV2 coinfection detected by PCR. The macaque sera showed broad, variable, and unique serological responses to the different viral antigens, allowing an initial seroprevalence to be determined for the macaque viruses. The Luminex assays offer a novel multiplexed approach to assess rhadinovirus infection patterns in both humans and nonhuman primates. This will help advance our understanding of rhadinovirus biology and associated host immunological responses.
卡波西肉瘤相关疱疹病毒(KSHV)/人类疱疹病毒8型是一种致瘤性γ疱疹病毒,与各种形式的卡波西肉瘤相关。目前对KSHV的血清学检测基于酶联免疫吸附或免疫荧光测定法,这些方法存在各种问题,包括缺乏用于检测比较的明确标准。虽然KSHV是唯一已知的人类γ疱疹病毒,但在旧世界灵长类动物中发现了两种KSHV样γ疱疹病毒谱系:RV1谱系包括猕猴中的KSHV和腹膜后纤维瘤病疱疹病毒(RFHV),RV2谱系包括来自不同猕猴物种的RRV和MneRV2。为了开发KSHV相关疾病的动物模型,我们开发了基于定量多重微珠的血清学检测方法,以检测针对γ疱疹病毒抗原的抗体。将来自KSHV(RV1)和MneRV2(RV2)病毒体的蛋白质偶联到光谱不同的荧光微珠上,并用于基于Luminex流式细胞术的检测中,以检测猕猴的免疫反应。两种检测方法都显示出较大的动态范围,对KSHV和MneRV2蛋白都有高水平的血清反应性。对来自华盛顿国家灵长类动物研究中心的大量猕猴血清样本进行了筛查,大多数样本(82%)在两种检测中均为阳性,这与通过PCR检测到的高水平RV1-RV2共感染一致。猕猴血清对不同病毒抗原表现出广泛、可变且独特的血清学反应,从而可以确定猕猴病毒的初始血清流行率。Luminex检测方法提供了一种新颖的多重方法,用于评估人类和非人类灵长类动物中的γ疱疹病毒感染模式。这将有助于推进我们对γ疱疹病毒生物学及相关宿主免疫反应的理解。