Evidence map›Paper›PMID 41790810›Full record

ArticlePLoS neglected tropical diseases2026

Comparative susceptibility of Old World and New World bat cell lines to Zika virus: Insights into viral replication and inflammatory responses.

Alexander J Brown, Anna C Fagre, Julianna Gilson, Jennifer Horton, J Nick Allen, Ricardo Rivero, Mahsan Karimi, Emily Speranza, Michael Letko, Stephanie N Seifert

Abstract readComparative Study
In one paragraph

Article in PLoS neglected tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Alexander J BrownPaul G. Allen School for Global Health; Washington State University, Pullman, Washington, United States of America.
Anna C FagreDepartment of Microbiology, Immunology, and Pathology; Colorado State University, Fort Collins, Colorado, United States of America.
Julianna GilsonPaul G. Allen School for Global Health; Washington State University, Pullman, Washington, United States of America.
Jennifer HortonPaul G. Allen School for Global Health; Washington State University, Pullman, Washington, United States of America.
J Nick AllenPaul G. Allen School for Global Health; Washington State University, Pullman, Washington, United States of America.
Ricardo RiveroPaul G. Allen School for Global Health; Washington State University, Pullman, Washington, United States of America.
Mahsan KarimiPaul G. Allen School for Global Health; Washington State University, Pullman, Washington, United States of America.
Emily SperanzaFlorida Research and Innovation Center; Cleveland Clinic Lerner Research Institute, Port St. Lucie, Florida, United States of America.
Michael LetkoPaul G. Allen School for Global Health; Washington State University, Pullman, Washington, United States of America.
Stephanie N SeifertPaul G. Allen School for Global Health; Washington State University, Pullman, Washington, United States of America.ORCID https://orcid.org/0000-0002-4397-6156

Funding

Training in Biotechnology: Emphasis in Protein ChemistryT32GM152310 · NIGMS · WASHINGTON STATE UNIVERSITY · PI Bernd Markus Lange · 2024 to 2026
$1.6M
NIGMS NIH HHS T32 GM152310
6 · The paper itself

Abstract

backgroundThe emergence of flaviviruses and other arboviruses in novel geographic locations, arthropod vectors, and vertebrate amplification hosts complicates control and eradication efforts. Many flaviviruses continue to impact global health, including Zika virus (ZIKV) which has expanded to a global health threat, yet many questions remain surrounding its ecology and inter-epidemic maintenance. While bats are known to harbor several medically important viruses without clinical disease, their role in the sylvatic transmission cycle of arboviruses remains unresolved. Reports describing the susceptibility of different bat species to infection with ZIKV are inconsistent, and the immunological mechanisms underpinning this variability have not been well-characterized. METHODOLOGY/PRINCIPAL

findingsWe compared the permissiveness and immune responses of cell lines derived from two frugivorous bat species: the Egyptian fruit bat (Rousettus aegyptiacus) and Jamaican fruit bat (Artibeus jamaicensis). Using multi-step growth curves, we compared infection dynamics of two genetically distinct ZIKV strains, African lineage (ZIKV/MR766) and Asian-American lineage (ZIKV/PRVABC59) and compared transcriptomic responses to both lineages in susceptible bat-derived cell lines. CONCLUSIONS/SIGNIFICANCE: Our results highlight species-specific differences in ZIKV susceptibility across bat-derived cell lines, with both ZIKV strains replicating to high titers on R. aegyptiacus cells but not on A. jamaicensis cells. We detected pro-inflammatory transcriptomic signatures in R. aegyptiacus cells infected with both ZIKV lineages. Notably, both the Asian-American and African ZIKV lineages demonstrated some capacity for immune evasion and productive replication in the R. aegyptiacus cell line.

Indexed as

ChiropteraVirus ReplicationZika VirusZika Virus InfectionAnimalsCell LineInflammation

Identifiers

PMID41790810
PMCPMC12981558

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.