Daum L T, Canas L C, Klimov A I, Shaw M W, Gibbons R V, Shrestha S K, Myint K S, Acharya R P, Rimal N, Reese F, Niemeyer D M, Arulanandam B P, Chambers J P
Air Force Institute for Operational Health, Brooks City Base, TX 78235, USA.
Arch Virol. 2006 Sep;151(9):1863-74. doi: 10.1007/s00705-006-0777-0. Epub 2006 May 31.
Currently circulating influenza B viruses can be divided into two antigenically and genetically distinct lineages referred to by their respective prototype strains, B/Yamagata/16/88 and B/Victoria/2/87, based on amino acid differences in the hemagglutinin surface glycoprotein. During May and July 2005, clinical specimens from two early season influenza B outbreaks in Arizona and southeastern Nepal were subjected to antigenic (hemagglutinin inhibition) and nucleotide sequence analysis of hemagglutinin (HA1), neuraminidase (NA), and NB genes. All isolates exhibited little reactivity with the B/Shanghai/361/2002 (B/Yamagata-like) vaccine strain and significantly reduced reactivity with the previous 2003/04 B/Hong Kong/330/2001 (B/Victoria-like) vaccine strain. The majority of isolates were antigenically similar to B/Hawaii/33/2004, a B/Victoria-like reference strain. Sequence analysis indicated that 33 of 34 isolates contained B/Victoria-like HA and B/Yamagata-like NA and NB proteins. Thus, these outbreak isolates are both antigenically and genetically distinct from the current Northern Hemisphere vaccine virus strain as well as the previous 2003-04 B/Hong Kong/330/2001 (B/Victoria lineage) vaccine virus strain but are genetically similar to B/Malaysia/2506/2004, the vaccine strain proposed for the coming seasons in the Northern and Southern Hemispheres. Since these influenza B outbreaks occurred in two very distant geographical locations, these viruses may continue to circulate during the 2006 season, underscoring the importance of rapid molecular monitoring of HA, NA and NB for drift and reassortment.
目前流行的乙型流感病毒可根据血凝素表面糖蛋白的氨基酸差异,分为两个抗原性和基因上不同的谱系,分别以其各自的原型毒株B/山形/16/88和B/维多利亚/2/87来指代。在2005年5月和7月期间,对来自亚利桑那州和尼泊尔东南部两个早季乙型流感暴发的临床标本进行了抗原性(血凝素抑制)分析以及血凝素(HA1)、神经氨酸酶(NA)和NB基因的核苷酸序列分析。所有分离株与B/上海/361/2002(B/山形系)疫苗株几乎没有反应性,与之前的2003/04 B/香港/330/2001(B/维多利亚系)疫苗株的反应性显著降低。大多数分离株在抗原性上与B/夏威夷/33/2004(一种B/维多利亚系参考毒株)相似。序列分析表明,34个分离株中的33个含有B/维多利亚系的HA以及B/山形系的NA和NB蛋白。因此,这些暴发分离株在抗原性和基因上均与当前北半球疫苗病毒株以及之前的2003 - 04 B/香港/330/2001(B/维多利亚谱系)疫苗病毒株不同,但在基因上与B/马来西亚/2506/2004相似,后者是拟用于北半球和南半球未来季节的疫苗株。由于这些乙型流感暴发发生在两个非常遥远的地理位置,这些病毒可能在2006年季节继续传播,这突出了对HA、NA和NB进行快速分子监测以检测其漂移和重配的重要性。