Evidence map›Paper›PMID 26817786›Full record

ArticleScientific reports2016

Ligand selectivity in tachykinin and natalisin neuropeptidergic systems of the honey bee parasitic mite Varroa destructor.

Hongbo Jiang, Donghun Kim, Sharon Dobesh, Jay D Evans, Ronald J Nachman, Krzysztof Kaczmarek, Janusz Zabrocki, Yoonseong Park

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Enlisting thePathogens (Basel, Switzerland) · 2021
    Article
  6. Article
  7. Review
  8. Article
  9. 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.

Hongbo JiangDepartment of Entomology, Kansas State University, Manhattan, Kansas 66506, United States.
Donghun KimDepartment of Entomology, Kansas State University, Manhattan, Kansas 66506, United States.
Sharon DobeshDepartment of Entomology, Kansas State University, Manhattan, Kansas 66506, United States.
Jay D EvansBee Research Laboratory, BARC-E, USDA-Agricultural Research Service, Beltsville, MD 20705, USA.
Ronald J NachmanInsect Control and Cotton Disease Research Unit, Southern Plains Agricultural Research Center, USDA, 2881 F/B Road, College Station, TX 77845, United States.
Krzysztof KaczmarekInsect Control and Cotton Disease Research Unit, Southern Plains Agricultural Research Center, USDA, 2881 F/B Road, College Station, TX 77845, United States.
Janusz ZabrockiInsect Control and Cotton Disease Research Unit, Southern Plains Agricultural Research Center, USDA, 2881 F/B Road, College Station, TX 77845, United States.
Yoonseong ParkDepartment of Entomology, Kansas State University, Manhattan, Kansas 66506, United States.

Funding

Signaling pathways for tick salivary secretionR01AI090062 · NIAID · KANSAS STATE UNIVERSITY · PI PARK, YOONSEONG · 2010 to 2014
$1.5M
NIAID NIH HHS R01 AI090062NIAID NIH HHS R01AI090062
6 · The paper itself

Abstract

The varroa mite, Varroa destructor, is a devastating ectoparasite of the honey bees Apis mellifera and A. cerana. Control of these mites in beehives is a challenge in part due to the lack of toxic agents that are specific to mites and not to the host honey bee. In searching for a specific toxic target of varroa mites, we investigated two closely related neuropeptidergic systems, tachykinin-related peptide (TRP) and natalisin (NTL), and their respective receptors. Honey bees lack both NTL and the NTL receptor in their genome sequences, providing the rationale for investigating these receptors to understand their specificities to various ligands. We characterized the receptors for NTL and TRP of V. destructor (VdNTL-R and VdTRP-R, respectively) and for TRP of A. mellifera (AmTRP-R) in a heterologous reporter assay system to determine the activities of various ligands including TRP/NTL peptides and peptidomimetics. Although we found that AmTRP-R is highly promiscuous, activated by various ligands including two VdNTL peptides when a total of 36 ligands were tested, we serendipitously found that peptides carrying the C-terminal motif -FWxxRamide are highly specific to VdTRP-R. This motif can serve as a seed sequence for designing a VdTRP-R-specific agonist.

Indexed as

Amino Acid MotifsAnimalsArthropod ProteinsLigandsTachykininsVarroidaeArthropod ProteinsLigandsTachykinins

Identifiers

PMID26817786
PMCPMC4730192

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.