TY - JOUR
T1 - Genomic Epidemiology Reconstructs the Introduction and Spread of Zika Virus in Central America and Mexico
AU - Thézé, Julien
AU - Li, Tony
AU - du Plessis, Louis
AU - Bouquet, Jerome
AU - Kraemer, Moritz U.G.
AU - Somasekar, Sneha
AU - Yu, Guixia
AU - de Cesare, Mariateresa
AU - Balmaseda, Angel
AU - Kuan, Guillermina
AU - Harris, Eva
AU - Wu, Chieh hsi
AU - Ansari, M. Azim
AU - Bowden, Rory
AU - Faria, Nuno R.
AU - Yagi, Shigeo
AU - Messenger, Sharon
AU - Brooks, Trevor
AU - Stone, Mars
AU - Bloch, Evan M.
AU - Busch, Michael
AU - Muñoz-Medina, José E.
AU - González-Bonilla, Cesar R.
AU - Wolinsky, Steven
AU - López, Susana
AU - Arias, Carlos F.
AU - Bonsall, David
AU - Chiu, Charles Y.
AU - Pybus, Oliver G.
N1 - Publisher Copyright:
© 2018 The Authors
PY - 2018/6/13
Y1 - 2018/6/13
N2 - The Zika virus (ZIKV) epidemic in the Americas established ZIKV as a major public health threat and uncovered its association with severe diseases, including microcephaly. However, genetic epidemiology in some at-risk regions, particularly Central America and Mexico, remains limited. We report 61 ZIKV genomes from this region, generated using metagenomic sequencing with ZIKV-specific enrichment, and combine phylogenetic, epidemiological, and environmental data to reconstruct ZIKV transmission. These analyses revealed multiple independent ZIKV introductions to Central America and Mexico. One introduction, likely from Brazil via Honduras, led to most infections and the undetected spread of ZIKV through the region from late 2014. Multiple lines of evidence indicate biannual peaks of ZIKV transmission in the region, likely driven by varying local environmental conditions for mosquito vectors and herd immunity. The spatial and temporal heterogeneity of ZIKV transmission in Central America and Mexico challenges arbovirus surveillance and disease control measures. Thézé et al. examine the genomic epidemiology of Zika virus in Central America and Mexico. Following its likely introduction to Honduras in 2014, the virus spread undetected in the region. Genetic and epidemiological data indicate that biannual transmission peaks occurred, and could potentially be explained by local variation in mosquito abundance.
AB - The Zika virus (ZIKV) epidemic in the Americas established ZIKV as a major public health threat and uncovered its association with severe diseases, including microcephaly. However, genetic epidemiology in some at-risk regions, particularly Central America and Mexico, remains limited. We report 61 ZIKV genomes from this region, generated using metagenomic sequencing with ZIKV-specific enrichment, and combine phylogenetic, epidemiological, and environmental data to reconstruct ZIKV transmission. These analyses revealed multiple independent ZIKV introductions to Central America and Mexico. One introduction, likely from Brazil via Honduras, led to most infections and the undetected spread of ZIKV through the region from late 2014. Multiple lines of evidence indicate biannual peaks of ZIKV transmission in the region, likely driven by varying local environmental conditions for mosquito vectors and herd immunity. The spatial and temporal heterogeneity of ZIKV transmission in Central America and Mexico challenges arbovirus surveillance and disease control measures. Thézé et al. examine the genomic epidemiology of Zika virus in Central America and Mexico. Following its likely introduction to Honduras in 2014, the virus spread undetected in the region. Genetic and epidemiological data indicate that biannual transmission peaks occurred, and could potentially be explained by local variation in mosquito abundance.
KW - Central America
KW - Mexico
KW - Zika virus
KW - bait capture enrichment
KW - effective reproductive number
KW - genomics
KW - metagenomic sequencing
KW - phylodynamics
KW - transmission
KW - “spiked” primer enrichment
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UR - http://www.scopus.com/inward/citedby.url?scp=85047227840&partnerID=8YFLogxK
U2 - 10.1016/j.chom.2018.04.017
DO - 10.1016/j.chom.2018.04.017
M3 - Article
C2 - 29805095
AN - SCOPUS:85047227840
SN - 1931-3128
VL - 23
SP - 855-864.e7
JO - Cell Host and Microbe
JF - Cell Host and Microbe
IS - 6
ER -