Metsky Hayden C, Matranga Christian B, Wohl Shirlee, Schaffner Stephen F, Freije Catherine A, Winnicki Sarah M, West Kendra, Qu James, Baniecki Mary Lynn, Gladden-Young Adrianne, Lin Aaron E, Tomkins-Tinch Christopher H, Ye Simon H, Park Daniel J, Luo Cynthia Y, Barnes Kayla G, Shah Rickey R, Chak Bridget, Barbosa-Lima Giselle, Delatorre Edson, Vieira Yasmine R, Paul Lauren M, Tan Amanda L, Barcellona Carolyn M, Porcelli Mario C, Vasquez Chalmers, Cannons Andrew C, Cone Marshall R, Hogan Kelly N, Kopp Edgar W, Anzinger Joshua J, Garcia Kimberly F, Parham Leda A, Ramírez Rosa M Gélvez, Montoya Maria C Miranda, Rojas Diana P, Brown Catherine M, Hennigan Scott, Sabina Brandon, Scotland Sarah, Gangavarapu Karthik, Grubaugh Nathan D, Oliveira Glenn, Robles-Sikisaka Refugio, Rambaut Andrew, Gehrke Lee, Smole Sandra, Halloran M Elizabeth, Villar Luis, Mattar Salim, Lorenzana Ivette, Cerbino-Neto Jose, Valim Clarissa, Degrave Wim, Bozza Patricia T, Gnirke Andreas, Andersen Kristian G, Isern Sharon, Michael Scott F, Bozza Fernando A, Souza Thiago M L, Bosch Irene, Yozwiak Nathan L, MacInnis Bronwyn L, Sabeti Pardis C
Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Nature. 2017 Jun 15;546(7658):411-415. doi: 10.1038/nature22402. Epub 2017 May 24.
Although the recent Zika virus (ZIKV) epidemic in the Americas and its link to birth defects have attracted a great deal of attention, much remains unknown about ZIKV disease epidemiology and ZIKV evolution, in part owing to a lack of genomic data. Here we address this gap in knowledge by using multiple sequencing approaches to generate 110 ZIKV genomes from clinical and mosquito samples from 10 countries and territories, greatly expanding the observed viral genetic diversity from this outbreak. We analysed the timing and patterns of introductions into distinct geographic regions; our phylogenetic evidence suggests rapid expansion of the outbreak in Brazil and multiple introductions of outbreak strains into Puerto Rico, Honduras, Colombia, other Caribbean islands, and the continental United States. We find that ZIKV circulated undetected in multiple regions for many months before the first locally transmitted cases were confirmed, highlighting the importance of surveillance of viral infections. We identify mutations with possible functional implications for ZIKV biology and pathogenesis, as well as those that might be relevant to the effectiveness of diagnostic tests.
尽管近期美洲地区的寨卡病毒(ZIKV)疫情及其与出生缺陷的关联引起了广泛关注,但由于缺乏基因组数据,寨卡病毒病的流行病学和病毒进化仍有许多未知之处。在此,我们通过多种测序方法,从10个国家和地区的临床及蚊虫样本中生成了110个寨卡病毒基因组,填补了这一知识空白,极大地扩展了此次疫情中观察到的病毒遗传多样性。我们分析了病毒传入不同地理区域的时间和模式;系统发育证据表明,该病毒在巴西迅速传播,且有多个疫情毒株传入波多黎各、洪都拉斯、哥伦比亚、其他加勒比岛屿以及美国大陆。我们发现,在首例本地传播病例确诊前的数月里,寨卡病毒已在多个地区悄然传播,这凸显了病毒感染监测的重要性。我们鉴定出了可能对寨卡病毒生物学特性和发病机制具有功能影响的突变,以及那些可能与诊断检测有效性相关的突变。