Evidence map›Paper›PMID 33370303›Full record

ArticlePLoS neglected tropical diseases2020

Molecular signatures of sexual communication in the phlebotomine sand flies.

Paul V Hickner, Nataliya Timoshevskaya, Ronald J Nowling, Frédéric Labbé, Andrew D Nguyen, Mary Ann McDowell, Carolina N Spiegel, Zainulabeuddin Syed

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2020. 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
1.6field-weighted citation impact, top 15% 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, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. An oviposition pheromone, hexadecanoic acid, found on the eggs ofbioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. 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

8 authors at 4 institutions in 2 countries.

Paul V HicknerDepartment of Entomology, University of Kentucky, Lexington, Kentucky, United States of America.
Nataliya TimoshevskayaDepartment of Biology, University of Kentucky, Lexington, Kentucky, United States of America.ORCID 0000-0002-9775-5877
Ronald J NowlingElectrical Engineering and Computer Science, Milwaukee School of Engineering, Milwaukee, Wisconsin, United States of America.ORCID 0000-0002-2757-9986
Frédéric LabbéDepartment of Biological Sciences, Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America.ORCID 0000-0002-4064-2361
Andrew D NguyenDepartment of Biological Sciences, Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America.
Mary Ann McDowellDepartment of Biological Sciences, Eck Institute for Global Health, University of Notre Dame, Notre Dame, Indiana, United States of America.ORCID 0000-0003-4115-8464
Carolina N SpiegelDepartment of Molecular and Cell Biology, Institute of Biology, Fluminense Federal University, Niterói, Rio de Janeiro, Brazil.ORCID 0000-0003-3291-9903
Zainulabeuddin SyedDepartment of Entomology, University of Kentucky, Lexington, Kentucky, United States of America.ORCID 0000-0002-6235-7115
University of Kentucky · USUniversity of Notre Dame · USMilwaukee School of Engineering · USUniversidade Federal Fluminense · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phlebotomine sand flies employ an elaborate system of pheromone communication wherein males produce pheromones that attract other males to leks (thus acting as an aggregation pheromone) and females to the lekking males (sex pheromone). In addition, the type of pheromone produced varies among populations. Despite the numerous studies on sand fly chemical communication, little is known of their chemosensory genome. Chemoreceptors interact with chemicals in an organism's environment to elicit essential behaviors such as the identification of suitable mates and food sources. Thus, they play important roles during adaptation and speciation. Major chemoreceptor gene families, odorant receptors (ORs), gustatory receptors (GRs) and ionotropic receptors (IRs) together detect and discriminate the chemical landscape. Here, we annotated the chemoreceptor repertoire in the genomes of Lutzomyia longipalpis and Phlebotomus papatasi, major phlebotomine vectors in the New World and Old World, respectively. Comparison with other sequenced Diptera revealed a large and unique expansion where over 80% of the ~140 ORs belong to a single, taxonomically restricted clade. We next conducted a comprehensive analysis of the chemoreceptors in 63 L. longipalpis individuals from four different locations in Brazil representing allopatric and sympatric populations and three sex-aggregation pheromone types (chemotypes). Population structure based on single nucleotide polymorphisms (SNPs) and gene copy number in the chemoreceptors corresponded with their putative chemotypes, and corroborate previous studies that identified multiple populations. Our work provides genomic insights into the underlying behavioral evolution of sexual communication in the L. longipalpis species complex in Brazil, and highlights the importance of accounting for the ongoing speciation in central and South American Lutzomyia that could have important implications for vectorial capacity.

Indexed as

AnimalsBrazilChemoreceptor CellsFemaleInsect ProteinsInsect VectorsLeishmaniaLeishmaniasisMalePhlebotomusPolymorphism, Single NucleotideSex AttractantsInsect ProteinsSex Attractants

Identifiers

PMID33370303
PMCPMC7793272
OpenAlexW3117150273

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.