Pedersen Janice C
Avian Viruses Section, Diagnostic Virology Laboratory, National Veterinary Services Laboratories, US Department of Agriculture, Ames, IA, USA.
Methods Mol Biol. 2008;436:67-75. doi: 10.1007/978-1-59745-279-3_9.
The neuraminidase-inhibition (NI) assay is a laboratory procedure for the identification of the neuraminidase (NA) glycoprotein subtype in influenza viruses or the NA subtype specificity of antibodies to influenza virus. A serological procedure for subtyping the NA glycoprotein is critical for the identification and classification of avian influenza (AI) viruses. The macro-procedure was first described in 1961 by D. Aminoff et al. [2] and was later modified to a microtiter plate procedure (micro-NI) by Van Deusen et al. [4]. The micro-NI procedure reduces the quantity of reagents required, permits the antigenic classification of many isolates simultaneously, and eliminates the spectrophotometric interpretation of results. Although the macro-NI has been shown to be more sensitive than the micro-NI, the micro-NI test is very suitable for testing sera for the presence of NA antibodies and has proven to be a practical and rapid method for virus classification. This chapter will provide an overview of the USDA-validated micro-NI procedure for the identification of subtype-specific NA in AIV and antibodies.
神经氨酸酶抑制(NI)试验是一种实验室方法,用于鉴定流感病毒中的神经氨酸酶(NA)糖蛋白亚型或流感病毒抗体的NA亚型特异性。对NA糖蛋白进行亚型分类的血清学方法对于禽流感(AI)病毒的鉴定和分类至关重要。宏观方法最早由D. Aminoff等人于1961年描述[2],后来Van Deusen等人将其改进为微量滴定板方法(微量NI)[4]。微量NI方法减少了所需试剂的量,允许同时对许多分离株进行抗原分类,并消除了结果的分光光度法解释。尽管宏观NI已被证明比微量NI更敏感,但微量NI试验非常适合检测血清中NA抗体的存在,并且已被证明是一种实用且快速的病毒分类方法。本章将概述经美国农业部验证的用于鉴定禽流感病毒中亚型特异性NA和抗体的微量NI方法。