Evidence map›Paper›PMID 26843451›Full record

ArticleJournal of medical entomology2016

Human C5a Protein Participates in the Mosquito Immune Response Against Dengue Virus.

Berlin Londono-Renteria, Crystal Grippin, Jenny C Cardenas, Andrea Troupin, Tonya M Colpitts

Open access · bronzeAbstract read
In one paragraph

Article in Journal of medical entomology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Transcriptome of theInternational journal of molecular sciences · 2020
    Article
  4. Article
  5. Frontiers in cellular and infection microbiology · 2020
    Review
  6. Article
  7. 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

5 authors at 3 institutions in 2 countries.

Berlin Londono-RenteriaDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC, 29209 (berlinlondo@yahoo.com; Andrea.Troupin@uscmed.sc.edu), berlinlondo@yahoo.com.
Crystal GrippinDepartment of Tropical Medicine, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA, 70130 (cgrippin@tulane.edu), and.
Jenny C CardenasMicrobiology and Clinical Laboratory, Hospital San Juan de Dios, Los Patios - Norte de Santander, Colombia (carocardenasg@hotmail.com).
Andrea TroupinDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC, 29209 (berlinlondo@yahoo.com; Andrea.Troupin@uscmed.sc.edu).
Tonya M ColpittsDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC, 29209 (berlinlondo@yahoo.com; Andrea.Troupin@uscmed.sc.edu).
Laboratoire Physiologie Cellulaire & Végétale · FRTulane University · USUniversity of South Carolina · US

Funding

The antiviral role of mosquito ubiquitin Ub3881 during dengue infectionK22AI103067 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI COLPITTS, TONYA MICHELLE · 2013 to 2014
$270k
NIAID NIH HHS K22 AI103067
6 · The paper itself

Abstract

Dengue virus (DENV) is transmitted by Aedes spp mosquitoes during a bloodmeal uptake. The bloodmeal consists of host cells, immune factors, and possibly blood-borne pathogens, such as arboviruses. Human cells and immune-related factors, like the complement system, can remain active in the bloodmeal and may be able to interact with pathogens in the mosquito. Previous studies have shown that active complement proteins impact Plasmodium parasite viability in the Anopheles midgut. Thus, we investigated the effects of the human complement on DENV infection in the midgut of Aedes aegypti. Our findings indicate that mosquitoes receiving DENV mixed with normal non-inactivated human serum showed significantly lower viremia than those fed with heat-inactivated serum. This implies that human complement may act to limit DENV infection in the mosquito midgut. In addition, we found that human complement C5a protein was able to directly communicate with mosquito cells, affecting the cell antiviral response against DENV. Our results also show that human C5a protein is able to interact with several membrane-bound mosquito proteins. Together these results suggest an important role of human complement protein in DENV transmission.

Indexed as

AedesAnimalsComplement C5aDengueDengue VirusHumansInsect VectorsComplement C5aAedesdenguehuman complementmosquito

Identifiers

PMID26843451
PMCPMC4892811
OpenAlexW2312130471

What OpenQuestion holds

Textmetadata
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.