Comparative Pathogenesis of Asian and African-Lineage Zika Virus in Indian Rhesus Macaque's and Development of a Non-Human Primate Model Suitable for the Evaluation of New Drugs and Vaccines

被引:28
作者
Rayner, Jonathan O. [1 ,2 ]
Kalkeri, Raj [3 ]
Goebel, Scott [3 ]
Cai, Zhaohui [3 ]
Green, Brian [3 ]
Lin, Shuling [3 ]
Snyder, Beth [3 ]
Hagelin, Kimberly [3 ]
Walters, Kevin B. [3 ]
Koide, Fusataka [3 ]
机构
[1] Southern Res Inst, Dept Infect Dis Res, Birmingham, AL 35205 USA
[2] Univ S Alabama, Dept Microbiol & Immunol, Mobile, AL 36688 USA
[3] Southern Res Inst, Dept Infect Dis Res, Frederick, MD 21701 USA
来源
VIRUSES-BASEL | 2018年 / 10卷 / 05期
基金
美国国家卫生研究院;
关键词
Zika virus; ZIKV; rhesus macaques; Non-human primates; NHP; infection; natural history; Asian-lineage; African-lineage; INFECTION; INOCULATION; OUTBREAK; BRAZIL;
D O I
10.3390/v10050229
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The establishment of a well characterized non-human primate model of Zika virus (ZIKV) infection is critical for the development of medical interventions. In this study, challenging Indian rhesus macaques (IRMs) with ZIKV strains of the Asian lineage resulted in dose-dependent peak viral loads between days 2 and 5 post infection and a robust immune response which protected the animals from homologous and heterologous re-challenge. In contrast, viremia in IRMs challenged with an African lineage strain was below the assay's lower limit of quantitation, and the immune response was insufficient to protect from re-challenge. These results corroborate previous observations but are contrary to reports using other African strains, obviating the need for additional studies to elucidate the variables contributing to the disparities. Nonetheless, the utility of an Asian lineage ZIKV IRM model for countermeasure development was verified by vaccinating animals with a formalin inactivated reference vaccine and demonstrating sterilizing immunity against a subsequent subcutaneous challenge.
引用
收藏
页数:16
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