Nishiura Hiroshi, Kinoshita Ryo, Mizumoto Kenji, Yasuda Yohei, Nah Kyeongah
Graduate School of Medicine, Hokkaido University, Kita 15 Jo Nishi 7 Chome, Kita-ku, Sapporo-shi, Hokkaido 060-8638, Japan; CREST, Japan Science and Technology Agency, Kawaguchi, Saitama, Japan; Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, 1130033, Japan.
Graduate School of Medicine, Hokkaido University, Kita 15 Jo Nishi 7 Chome, Kita-ku, Sapporo-shi, Hokkaido 060-8638, Japan; CREST, Japan Science and Technology Agency, Kawaguchi, Saitama, Japan; Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Tokyo, 1130033, Japan.
Int J Infect Dis. 2016 Apr;45:95-7. doi: 10.1016/j.ijid.2016.02.017. Epub 2016 Feb 26.
Zika virus has spread internationally through countries in the South Pacific and Americas. The present study aimed to estimate the basic reproduction number, R0, of Zika virus infection as a measurement of the transmission potential, reanalyzing past epidemic data from the South Pacific.
Incidence data from two epidemics, one on Yap Island, Federal State of Micronesia in 2007 and the other in French Polynesia in 2013-2014, were reanalyzed. R0 of Zika virus infection was estimated from the early exponential growth rate of these two epidemics.
The maximum likelihood estimate (MLE) of R0 for the Yap Island epidemic was in the order of 4.3-5.8 with broad uncertainty bounds due to the small sample size of confirmed and probable cases. The MLE of R0 for French Polynesia based on syndromic data ranged from 1.8 to 2.0 with narrow uncertainty bounds.
The transmissibility of Zika virus infection appears to be comparable to those of dengue and chikungunya viruses. Considering that Aedes species are a shared vector, this finding indicates that Zika virus replication within the vector is perhaps comparable to dengue and chikungunya.
寨卡病毒已在国际上传播至南太平洋和美洲的多个国家。本研究旨在估算寨卡病毒感染的基本再生数R0,以此衡量传播潜力,并重新分析南太平洋过去的疫情数据。
重新分析了两次疫情的发病率数据,一次是2007年在密克罗尼西亚联邦雅浦岛,另一次是2013 - 2014年在法属波利尼西亚。根据这两次疫情的早期指数增长率估算寨卡病毒感染的R0。
由于确诊和疑似病例样本量较小,雅浦岛疫情R0的最大似然估计(MLE)约为4.3 - 5.8,不确定性区间较宽。基于症状数据的法属波利尼西亚R0的MLE在1.8至2.0之间,不确定性区间较窄。
寨卡病毒感染的传播能力似乎与登革热病毒和基孔肯雅病毒相当。鉴于伊蚊是共同的传播媒介,这一发现表明寨卡病毒在媒介体内的复制情况可能与登革热病毒和基孔肯雅病毒类似。