Nguyen Diep T, Jang Yunho, Nguyen Tho D, Jones Joyce, Shepard Samuel S, Yang Hua, Gerloff Nancy, Fabrizio Thomas, Nguyen Long V, Inui Ken, Yang Genyan, Creanga Adrian, Wang Li, Mai Duong T, Thor Sharmi, Stevens James, To Thanh L, Wentworth David E, Nguyen Tung, Pham Dong V, Bryant Juliet E, Davis C Todd
National Center for Veterinary Diagnostics, Department of Animal Health, Hanoi, Vietnam
Department of Animal Health, Ministry of Agriculture and Rural Development of Vietnam, Hanoi, Vietnam.
J Virol. 2017 Feb 14;91(5). doi: 10.1128/JVI.01708-16. Print 2017 Mar 1.
Whole-genome sequences of representative highly pathogenic avian influenza A(H5) viruses from Vietnam were generated, comprising samples from poultry outbreaks and active market surveillance collected from January 2012 to August 2015. Six hemagglutinin gene clades were characterized. Clade 1.1.2 was predominant in southern Mekong provinces throughout 2012 and 2013 but gradually disappeared and was not detected after April 2014. Clade 2.3.2.1c viruses spread rapidly during 2012 and were detected in the south and center of the country. A number of clade 1.1.2 and 2.3.2.1c interclade reassortant viruses were detected with different combinations of internal genes derived from 2.3.2.1a and 2.3.2.1b viruses, indicating extensive cocirculation. Although reassortment generated genetic diversity at the genotype level, there was relatively little genetic drift within the individual gene segments, suggesting genetic stasis over recent years. Antigenically, clade 1.1.2, 2.3.2.1a, 2.3.2.1b, and 2.3.2.1c viruses remained related to earlier viruses and WHO-recommended prepandemic vaccine strains representing these clades. Clade 7.2 viruses, although detected in only low numbers, were the exception, as indicated by introduction of a genetically and antigenically diverse strain in 2013. Clade 2.3.4.4 viruses (H5N1 and H5N6) were likely introduced in April 2014 and appeared to gain dominance across northern and central regions. Antigenic analyses of clade 2.3.4.4 viruses compared to existing clade 2.3.4 candidate vaccine viruses (CVV) indicated the need for an updated vaccine virus. A/Sichuan/26221/2014 (H5N6) virus was developed, and ferret antisera generated against this virus were demonstrated to inhibit some but not all clade 2.3.4.4 viruses, suggesting consideration of alternative clade 2.3.4.4 CVVs. Highly pathogenic avian influenza (HPAI) A(H5) viruses have circulated continuously in Vietnam since 2003, resulting in hundreds of poultry outbreaks and sporadic human infections. Despite a significant reduction in the number of human infections in recent years, poultry outbreaks continue to occur and the virus continues to diversify. Vaccination of poultry has been used as a means to control the spread and impact of the virus, but due to the diversity and changing distribution of antigenically distinct viruses, the utility of vaccines in the face of mismatched circulating strains remains questionable. This study assessed the putative amino acid changes in viruses leading to antigenic variability, underscoring the complexity of vaccine selection for both veterinary and public health purposes. Given the overlapping geographic distributions of multiple, antigenically distinct clades of HPAI A(H5) viruses in Vietnam, the vaccine efficacy of bivalent poultry vaccine formulations should be tested in the future.
对越南具有代表性的高致病性甲型禽流感(H5)病毒进行了全基因组测序,样本包括2012年1月至2015年8月期间家禽疫情暴发点以及活跃市场监测所采集的样本。鉴定出了6个血凝素基因分支。1.1.2分支在2012年全年及2013年在湄公河三角洲南部省份占主导地位,但逐渐消失,2014年4月后未再检测到。2.3.2.1c分支病毒在2012年迅速传播,在该国南部和中部被检测到。检测到一些1.1.2和2.3.2.1c分支间的重配病毒,其内部基因具有来自2.3.2.1a和2.3.2.1b病毒的不同组合,表明存在广泛的共同流行。尽管重排在基因型水平上产生了遗传多样性,但各个基因片段内的遗传漂变相对较少,表明近年来遗传处于停滞状态。在抗原性方面,1.1.2、2.3.2.1a、2.3.2.1b和2.3.2.1c分支病毒仍与早期病毒以及代表这些分支的世界卫生组织推荐的大流行前疫苗株相关。7.2分支病毒尽管检测数量较少,但却是个例外,2013年引入了一种遗传和抗原性均不同的毒株就表明了这一点。2.3.4.4分支病毒(H5N1和H5N6)可能于2014年4月传入,并且似乎在北部和中部地区占据了主导地位。与现有的2.3.4候选疫苗病毒(CVV)相比,对2.3.4.4分支病毒进行的抗原分析表明需要更新疫苗病毒。研制出了A/四川/26221/2014(H5N6)病毒,针对该病毒产生的雪貂抗血清被证明可抑制部分但并非所有的2.3.4.4分支病毒,这表明需要考虑选用其他2.3.4.4分支CVV。自2003年以来,高致病性甲型禽流感(HPAI)A(H5)病毒在越南持续传播,导致数百起家禽疫情暴发和零星的人类感染。尽管近年来人类感染数量大幅减少,但家禽疫情仍持续发生,且病毒仍在不断变异。家禽接种疫苗一直被用作控制病毒传播和影响的手段,但由于抗原性不同的病毒具有多样性且分布不断变化,面对不匹配的流行毒株时疫苗的效用仍存在疑问。本研究评估了导致病毒抗原变异的假定氨基酸变化,强调了出于兽医和公共卫生目的进行疫苗选择的复杂性。鉴于越南多种抗原性不同的HPAI A(H5)病毒分支在地理分布上重叠,未来应测试二价家禽疫苗配方的疫苗效力。