Evidence map›Paper›PMID 39039817›Full record

ArticleInsect molecular biology2025

The salivary gland transcriptome of Varroa destructor reveals suitable targets for RNAi-based mite control.

Andrea Becchimanzi, Alfonso Cacace, Martina Parziale, Giovanna De Leva, Sergio Iacopino, Giovanni Jesu, Ilaria Di Lelio, Virgilio Stillittano, Emilio Caprio, Francesco Pennacchio

Abstract read
In one paragraph

Article in Insect molecular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Evaluating the new product Norroa™ againstFrontiers in insect science · 2026
    Article
  4. Article
  5. Article
  6. 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

10 authors.

Andrea BecchimanziDepartment of Agricultural Sciences, University of Naples 'Federico II', Naples, Italy.ORCID https://orcid.org/0000-0001-5117-0235
Alfonso CacaceDepartment of Agricultural Sciences, University of Naples 'Federico II', Naples, Italy.
Martina ParzialeDepartment of Agricultural Sciences, University of Naples 'Federico II', Naples, Italy.
Giovanna De LevaDepartment of Agricultural Sciences, University of Naples 'Federico II', Naples, Italy.
Sergio IacopinoArterra Bioscience, Naples, Italy.
Giovanni JesuDepartment of Agricultural Sciences, University of Naples 'Federico II', Naples, Italy.ORCID https://orcid.org/0000-0001-5006-1619
Ilaria Di LelioDepartment of Agricultural Sciences, University of Naples 'Federico II', Naples, Italy.
Virgilio StillittanoIstituto Zooprofilattico Sperimentale del Lazio e della Toscana, Rome, Italy.
Emilio CaprioDepartment of Agricultural Sciences, University of Naples 'Federico II', Naples, Italy.ORCID https://orcid.org/0000-0002-9763-0097
Francesco PennacchioDepartment of Agricultural Sciences, University of Naples 'Federico II', Naples, Italy.

Funding

European Union Next-Generation EU CN00000022
6 · The paper itself

Abstract

The mite Varroa destructor Anderson and Trueman (Mesostigmata: Varroidae) has a dramatic impact on beekeeping and is one of the main causes of honey bee colony losses. This ectoparasite feeds on honey bees' liquid tissues, through a wound created on the host integument, determining weight loss and a reduction of lifespan, as well as the transmission of viral pathogens. However, despite its importance, the mite feeding strategy and the host regulation role by the salivary secretions have been poorly explored. Here, we contribute to fill this gap by identifying the salivary components of V. destructor, to study their functional importance for mite feeding and survival. The differential expression analysis identified 30 salivary gland genes encoding putatively secreted proteins, among which only 15 were found to be functionally annotated. These latter include proteins with putative anti-bacterial, anti-fungal, cytolytic, digestive and immunosuppressive function. The three most highly transcribed genes, coding for a chitin-binding domain protein, a Kazal domain serine protease inhibitor and a papain-like cysteine protease were selected to study their functional importance by reverse genetics. Knockdown (90%-99%) by RNA interference (RNAi) of the transcript of a chitin-binding domain protein, likely interfering with the immune reaction to facilitate mite feeding, was associated with a 40%-50% decrease of mite survival. This work expands our knowledge of the host regulation and nutritional exploitation strategies adopted by ectoparasites of arthropods and allows the identification of potential targets for RNAi, paving the way towards the development of new strategies for Varroa mite control.

Indexed as

Arthropod ProteinsTranscriptomeVarroidaeAnimalsBeesRNA InterferenceSalivary GlandsArthropod Proteinsarthropod salivachitin‐bindinggene silencinghoney beeRNA sequencing

Identifiers

PMID39039817
PMCPMC12236051

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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.