<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bird IM</submitter><funding>Pennsylvania State University</funding><funding>University of Pittsburgh</funding><pagination>1840</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11433722</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(9)</volume><pubmed_abstract>Zika virus (ZIKV), a mosquito-borne flavivirus, is a significant global health concern due to its association with neurodevelopmental disorders such as congenital Zika syndrome (CZS). This study aimed to compare the replication kinetics, viral persistence, cytopathogenic effects, and immune gene expression in human microglia cells (CHME-3) infected with an Asian lineage ZIKV (PRVABC59, referred to as ZIKV-PRV) and an African lineage ZIKV (IBH30656, referred to as ZIKV-IBH). We found that ZIKV-PRV replicated more efficiently and persisted longer while inducing lower levels of cell death and inflammatory gene activation compared with ZIKV-IBH. These findings suggest that the enhanced replication and persistence of ZIKV-PRV, along with its ability to evade innate immune responses, may underli</pubmed_abstract><journal>Microorganisms</journal><pubmed_title>Distinct Replication Kinetics, Cytopathogenicity, and Immune Gene Regulation in Human Microglia Cells Infected with Asian and African Lineages of Zika Virus.</pubmed_title><pmcid>PMC11433722</pmcid><funding_grant_id>Huck Chair funds</funding_grant_id><funding_grant_id>Chair funds</funding_grant_id><pubmed_authors>Chothe SK</pubmed_authors><pubmed_authors>Jacob J</pubmed_authors><pubmed_authors>Cavener V</pubmed_authors><pubmed_authors>Surendran Nair M</pubmed_authors><pubmed_authors>Nissly RH</pubmed_authors><pubmed_authors>Bird IM</pubmed_authors><pubmed_authors>Kuchipudi SV</pubmed_authors></additional><is_claimable>false</is_claimable><name>Distinct Replication Kinetics, Cytopathogenicity, and Immune Gene Regulation in Human Microglia Cells Infected with Asian and African Lineages of Zika Virus.</name><description>Zika virus (ZIKV), a mosquito-borne flavivirus, is a significant global health concern due to its association with neurodevelopmental disorders such as congenital Zika syndrome (CZS). This study aimed to compare the replication kinetics, viral persistence, cytopathogenic effects, and immune gene expression in human microglia cells (CHME-3) infected with an Asian lineage ZIKV (PRVABC59, referred to as ZIKV-PRV) and an African lineage ZIKV (IBH30656, referred to as ZIKV-IBH). We found that ZIKV-PRV replicated more efficiently and persisted longer while inducing lower levels of cell death and inflammatory gene activation compared with ZIKV-IBH. These findings suggest that the enhanced replication and persistence of ZIKV-PRV, along with its ability to evade innate immune responses, may underli</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-04-08T18:52:24.083Z</modification><creation>2025-04-06T16:09:15.209Z</creation></dates><accession>S-EPMC11433722</accession><cross_references><pubmed>39338514</pubmed><doi>10.3390/microorganisms12091840</doi></cross_references></HashMap>