<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lemos D</submitter><funding>HHS | National Institutes of Health</funding><funding>Governo Brasil</funding><funding>NCATS NIH HHS</funding><funding>ACL HHS</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>HHS | Centers for Disease Control and Prevention</funding><funding>NIH HHS</funding><funding>NCEZID CDC HHS</funding><pagination>e01605-20</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7925200</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>94(24)</volume><pubmed_abstract>Although fetal death is now understood to be a severe outcome of congenital Zika syndrome, the role of viral genetics is still unclear. We sequenced Zika virus (ZIKV) from a rhesus macaque fetus that died after inoculation and identified a single intrahost substitution, M1404I, in the ZIKV polyprotein, located in nonstructural protein 2B (NS2B). Targeted sequencing flanking position 1404 in 9 additional macaque mothers and their fetuses identified M1404I at a subconsensus frequency in the majority (5 of 9, 56%) of animals and some of their fetuses. Despite its repeated presence in pregnant macaques, M1404I has occurred rarely in humans since 2015. Since the primary ZIKV transmission cycle is human-mosquito-human, mutations in one host must be retained in the alternate host to be perpetuate</pubmed_abstract><journal>Journal of virology</journal><pubmed_title>Two Sides of a Coin: a Zika Virus Mutation Selected in Pregnant Rhesus Macaques Promotes Fetal Infection in Mice but at a Cost of Reduced Fitness in Nonpregnant Macaques and Diminished Transmissibility by Vectors.</pubmed_title><pmcid>PMC7925200</pmcid><funding_grant_id>1R01HL105704</funding_grant_id><funding_grant_id>U01 CK000516</funding_grant_id><funding_grant_id>1U01CK000516</funding_grant_id><funding_grant_id>UC Davis School of Veterinary Medicine Graduate Student Support Program</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>Science without Borders</funding_grant_id><funding_grant_id>R21 AI129479</funding_grant_id><funding_grant_id>1R33AI129077</funding_grant_id><funding_grant_id>1R21AI129479-S</funding_grant_id><funding_grant_id>P51OD011107</funding_grant_id><funding_grant_id>R01 HL105704</funding_grant_id><funding_grant_id>Division of Intramural Research Program</funding_grant_id><funding_grant_id>R43 AI129077</funding_grant_id><funding_grant_id>U01CK000516</funding_grant_id><funding_grant_id>UC Davis</funding_grant_id><funding_grant_id>P51 OD011107</funding_grant_id><pubmed_authors>Louie W</pubmed_authors><pubmed_authors>Saraf S</pubmed_authors><pubmed_authors>Pletnev AG</pubmed_authors><pubmed_authors>Borucki M</pubmed_authors><pubmed_authors>Singapuri A</pubmed_authors><pubmed_authors>Tsetsarkin KA</pubmed_authors><pubmed_authors>Van Rompay KKA</pubmed_authors><pubmed_authors>Usachenko J</pubmed_authors><pubmed_authors>Keesler RI</pubmed_authors><pubmed_authors>Grubaugh ND</pubmed_authors><pubmed_authors>Andersen KG</pubmed_authors><pubmed_authors>Chiu CY</pubmed_authors><pubmed_authors>Sanchez-San Martin C</pubmed_authors><pubmed_authors>Martyn C</pubmed_authors><pubmed_authors>Watanabe J</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Allen J</pubmed_authors><pubmed_authors>Thissen J</pubmed_authors><pubmed_authors>Stuart JB</pubmed_authors><pubmed_authors>Lemos D</pubmed_authors><pubmed_authors>Coffey LL</pubmed_authors><pubmed_authors>Ramirez AL</pubmed_authors><pubmed_authors>Oliveira G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Two Sides of a Coin: a Zika Virus Mutation Selected in Pregnant Rhesus Macaques Promotes Fetal Infection in Mice but at a Cost of Reduced Fitness in Nonpregnant Macaques and Diminished Transmissibility by Vectors.</name><description>Although fetal death is now understood to be a severe outcome of congenital Zika syndrome, the role of viral genetics is still unclear. We sequenced Zika virus (ZIKV) from a rhesus macaque fetus that died after inoculation and identified a single intrahost substitution, M1404I, in the ZIKV polyprotein, located in nonstructural protein 2B (NS2B). Targeted sequencing flanking position 1404 in 9 additional macaque mothers and their fetuses identified M1404I at a subconsensus frequency in the majority (5 of 9, 56%) of animals and some of their fetuses. Despite its repeated presence in pregnant macaques, M1404I has occurred rarely in humans since 2015. Since the primary ZIKV transmission cycle is human-mosquito-human, mutations in one host must be retained in the alternate host to be perpetuate</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2026-05-03T08:42:02.614Z</modification><creation>2021-03-13T08:17:01Z</creation></dates><accession>S-EPMC7925200</accession><cross_references><pubmed>32999034</pubmed><doi>10.1128/JVI.01605-20</doi></cross_references></HashMap>