Evidence map›Paper›PMID 27626437›Full record

ArticleViruses2016

Analysis of the Langat Virus Genome in Persistent Infection of an Ixodes scapularis Cell Line.

Luwanika Mlera, Wessam Melik, Danielle K Offerdahl, Eric Dahlstrom, Stephen F Porcella, Marshall E Bloom

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 22% of its field
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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Langat Virus Biology and Infection.Reviews in medical virology · 2026
    Review
  2. Article
  3. A Peroxiredoxin From theFrontiers in cellular and infection microbiology · 2020
    Article
  4. Article
  5. Article
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

6 authors at 1 institution in 1 country.

Luwanika MleraBiology of Vector-Borne Viruses Section, Laboratory of Virology, National Institutes of Health, Hamilton, MT 59840, USA. Luwanika.Mlera@nih.gov.
Wessam MelikBiology of Vector-Borne Viruses Section, Laboratory of Virology, National Institutes of Health, Hamilton, MT 59840, USA. Wessam.Melik@oru.se.
Danielle K OfferdahlBiology of Vector-Borne Viruses Section, Laboratory of Virology, National Institutes of Health, Hamilton, MT 59840, USA. offerdahld@niaid.nih.gov.
Eric DahlstromGenomics Unit, Research Technologies Branch, Hamilton, MT 59840, USA. eric.dahlstrom@nih.gov.
Stephen F PorcellaGenomics Unit, Research Technologies Branch, Hamilton, MT 59840, USA. SPORCELLA@niaid.nih.gov.
Marshall E BloomBiology of Vector-Borne Viruses Section, Laboratory of Virology, National Institutes of Health, Hamilton, MT 59840, USA. mbloom@niaid.nih.gov.
National Institutes of Health · US

Funding

Pathogenesis of Tick-Borne Flavivirus InfectionsZIAAI000940 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BLOOM, MARSHALL ELLIOTT · 2009 to 2025
$19.6M
6 · The paper itself

Abstract

Tick-borne flaviviruses (TBFVs) cause a broad spectrum of disease manifestations ranging from asymptomatic to mild febrile illness and life threatening encephalitis. These single-stranded positive-sense (ss(+)) RNA viruses are naturally maintained in a persistent infection of ixodid ticks and small-medium sized mammals. The development of cell lines from the ixodid ticks has provided a valuable surrogate system for studying the biology of TBFVs in vitro. When we infected ISE6 cells, an Ixodes scapularis embryonic cell line, with Langat virus (LGTV) we observed that the infection proceeded directly into persistence without any cytopathic effect. Analysis of the viral genome at selected time points showed that no defective genomes were generated during LGTV persistence by 10 weeks of cell passage. This was in contrast to LGTV persistence in 293T cells in which defective viral genomes are detectable by five weeks of serial cell passage. We identified two synonymous nucleotide changes i.e., 1893A→C (29% of 5978 reads at 12 h post infection (hpi)) and 2284T→A (34% of 4191 reads at 12 hpi) in the region encoding for the viral protein E. These results suggested that the mechanisms supporting LGTV persistence are different between tick and mammalian cells.

Indexed as

Genome, ViralAnimalsCell LineDefective VirusesEncephalitis Viruses, Tick-BorneIxodesMammalsPoint MutationSerial PassageTicksdeep-sequencingISE6 cellsIxodes scapularisLangat virus genomepersistent infectiontick-borne flavivirus

Identifiers

PMID27626437
PMCPMC5035966
OpenAlexW2520061901

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.