Evidence map›Paper›PMID 35458395›Full record

ArticleViruses2022

Sasha R Azar, Rafael K Campos, Ruimei Yun, Taylor Strange, Shannan L Rossi, Kathryn A Hanley, Nikos Vasilakis, Scott C Weaver

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. CD8Npj viruses · 2024
    Article
  3. Article
  4. 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

8 authors at 2 institutions in 1 country.

Sasha R AzarDepartment of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.ORCID 0000-0002-9182-216X
Rafael K CamposDepartment of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.ORCID 0000-0002-4852-0449
Ruimei YunDepartment of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, TX 77555-0610, USA.
Taylor StrangeDepartment of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Shannan L RossiDepartment of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.
Kathryn A HanleyDepartment of Biology, New Mexico State University, Las Cruces, NM 88003, USA.
Nikos VasilakisDepartment of Pathology, The University of Texas Medical Branch, Galveston, TX 77555-0609, USA.ORCID 0000-0002-0708-3289
Scott C WeaverDepartment of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, TX 77555-0610, USA.ORCID 0000-0001-8016-8556
The University of Texas Medical Branch at Galveston · USNew Mexico State University · US

Funding

Trajectory of Vector-adaptive Chikungunya Virus EvolutionR01AI121452 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI WEAVER, SCOTT C · 2016 to 2020
$2.3M
NIAID NIH HHS R01 AI121452NIH HHS 5R01AI121452-05
6 · The paper itself

Abstract

Chronic conditions like type II diabetes (T2DM) have long been known to exacerbate many infectious diseases. For many arboviruses, including Zika virus (ZIKV), severe outcomes, morbidity and mortality usually only occur in patients with such pre-existing conditions. However, the effects of T2DM and other pre-existing conditions on human blood (e.g., hypo/hyperinsulinemia, hyperglycemia and hyperlipidemia) that may impact infectivity of arboviruses for vectors is largely unexplored. We investigated whether the susceptibility of Aedes aegypti mosquitoes was affected when the mosquitoes fed on "diabetic" bloodmeals, such as bloodmeals composed of artificially glycosylated erythrocytes or those from viremic, diabetic mice (LEPRDB/DB). Increasing glycosylation of erythrocytes from hemoglobin A1c (HgbA1c) values of 5.5-5.9 to 6.2 increased the infection rate of a Galveston, Texas strain of Ae. aegypti to ZIKV strain PRVABC59 at a bloodmeal titer of 4.14 log10 FFU/mL from 0.0 to 40.9 and 42.9%, respectively. ZIKV was present in the blood of viremic LEPRDB/DB mice at similar levels as isogenic control C57BL/6J mice (3.3 log10 FFU/mL and 3.6 log10 FFU/mL, respectively. When mice sustained a higher ZIKV viremia of 4.6 log10 FFU/mL, LEPRDB/DB mice infected 36.3% of mosquitoes while control C57BL/6J mice with a viremia of 4.2 log10 FFU/mL infected only 4.1%. Additionally, when highly susceptible Ae. aegypti Rockefeller mosquitoes fed on homozygous LEPRDB/DB, heterozygous LEPRWT/DB, and control C57BL/6J mice with viremias of ≈ 4 log10 FFU/mL, 54%, 15%, and 33% were infected, respectively. In total, these data suggest that the prevalence of T2DM in a population may have a significant impact on ZIKV transmission and indicates the need for further investigation of the impacts of pre-existing metabolic conditions on arbovirus transmission.

Indexed as

AedesArbovirusesDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Zika VirusZika Virus InfectionAnimalsHumansMiceMice, Inbred C57BLMosquito VectorsViremiaAedes aegyptiimmunological cross-talkTGF-βtype II diabeteszika virus

Identifiers

PMID35458395
PMCPMC9024453
OpenAlexW4221036301

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.