Suppr超能文献

尿路上皮AM9腮腺炎疫苗病毒基因变体的生物学特性

Biological characteristics of genetic variants of Urabe AM9 mumps vaccine virus.

作者信息

Wright K E, Dimock K, Brown E G

机构信息

Department of Biochemistry, Microbiology and Immunology, Faculty of Medicine, University of Ottawa, 451 Smyth Road, Ottawa, Canada.

出版信息

Virus Res. 2000 Mar;67(1):49-57. doi: 10.1016/s0168-1702(00)00129-5.

Abstract

The Urabe AM9 mumps vaccine is composed of a mixture of variants distinguishable by a difference at nucleotide (nt) 1081 of the hemagglutinin-neuraminidase (HN) gene (Brown, E.G., Dimock, K., Wright, K.E., 1996. The Urabe AM9 mumps vaccine is a mixture of viruses differing at amino acid (aa) 335 of the hemagglutinin-neuraminidase gene with one form associated with disease. J. Infect. Dis. 174, 619-622.). Further genetic and biological variation was detected in plaque purified viruses from the Urabe AM9 vaccine by examining the HN gene sequence, plaque morphology, cytopathic effects and growth in Vero cells, and temperature sensitivity (ts). Infection of Vero cells with plaque purified viruses with a G at nt 1081 of the HN gene produced large, clear plaques, caused significant CPE early after infection but yielded lower titres of virus than other purified viruses. None of these viruses were ts. In contrast, half of the plaque purified viruses with an A at nt 1081 were sensitive to a temperature of 39.5 degrees C. These viruses produced small plaques, caused significant CPE and grew to low titres. Two ts viruses possessed a unique aa substitution at aa 468 of HN. The remaining A(1081) viruses were not ts, produced large plaques but little CPE, and grew to titres 10-fold higher than the G(1081) viruses. Isolates of Urabe AM9 associated with post-vaccination illness were similar to these non-ts A(1081) viruses, but could be further sub-divided into two groups on the basis of a difference at aa 464 of HN. The post-vaccination isolates may represent insufficiently attenuated components of the vaccine, while the G(1081) and ts subset of A(1081) viruses may be more fully attenuated.

摘要

Urabe AM9腮腺炎疫苗由血凝素神经氨酸酶(HN)基因核苷酸(nt)1081处存在差异的多种变体混合物组成(Brown, E.G., Dimock, K., Wright, K.E., 1996年。Urabe AM9腮腺炎疫苗是血凝素神经氨酸酶基因氨基酸(aa)335处存在差异的病毒混合物,其中一种形式与疾病相关。《传染病杂志》174, 619 - 622页)。通过检查HN基因序列、噬斑形态、细胞病变效应、在Vero细胞中的生长情况以及温度敏感性(ts),在Urabe AM9疫苗的噬斑纯化病毒中检测到了进一步的遗传和生物学变异。用HN基因nt 1081处为G的噬斑纯化病毒感染Vero细胞,产生大而清晰的噬斑,感染后早期引起显著的细胞病变效应,但产生的病毒滴度低于其他纯化病毒。这些病毒均无温度敏感性。相比之下,nt 1081处为A的噬斑纯化病毒中有一半对39.5摄氏度敏感。这些病毒产生小噬斑,引起显著的细胞病变效应,且生长至低滴度。两种温度敏感病毒在HN的aa 468处具有独特的氨基酸取代。其余A(1081)病毒无温度敏感性,产生大噬斑但细胞病变效应轻微,生长至滴度比G(1081)病毒高10倍。与接种后疾病相关的Urabe AM9分离株与这些无温度敏感性的A(1081)病毒相似,但可根据HN的aa 464处的差异进一步分为两组。接种后分离株可能代表疫苗中减毒不足的成分,而G(1081)和A(1081)病毒的温度敏感亚群可能减毒更充分。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验