Evidence map›Paper›PMID 29435771›Full record

ArticleExperimental & applied acarology2018

Identification of spider-mite species and their endosymbionts using multiplex PCR.

Flore Zélé, Mylène Weill, Sara Magalhães

Abstract read
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In one paragraph

Article in Experimental & applied acarology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. mSystems · 2025
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
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  9. Article
  10. A rapid identification method for common astigmatid species based on multiplex polymerase chain reaction.Veterinary research forum : an international quarterly journal · 2022
    Article
  11. Article
  12. Article
  13. Population-specific effect ofEcology and evolution · 2020
    Article
  14. Article
  15. 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

3 authors.

Flore ZéléCentre for Ecology, Evolution and Environmental Changes (cE3c), Faculdade de Ciências da Universidade de Lisboa, Edificio C2, Piso-3 Campo Grande, 1749016, Lisbon, Portugal. fezele@fc.ul.pt.ORCID http://orcid.org/0000-0003-2954-5488
Mylène WeillInstitut des Sciences de l'Evolution, CNRS-Université de Montpellier-IRD-EPHE, 34095, Montpellier, Cedex 5, France.ORCID http://orcid.org/0000-0002-4043-1601
Sara MagalhãesCentre for Ecology, Evolution and Environmental Changes (cE3c), Faculdade de Ciências da Universidade de Lisboa, Edificio C2, Piso-3 Campo Grande, 1749016, Lisbon, Portugal.ORCID http://orcid.org/0000-0002-8609-7768

Funding

Faculdade de Ciências e Tecnologia (FCT), Universidade de Lisboa (PT) FCT-ANR//BIA-EVF/0013/2012Faculdade de Ciências e Tecnologia (FCT), Universidade de Lisboa (PT) FCT-TUBITAK/0001/2014Faculdade de Ciências e Tecnologia (FCT), Universidade de Lisboa (PT) SFRH/BPD/125020/2016
6 · The paper itself

Abstract

Spider mites of the genus Tetranychidae are severe crop pests. In the Mediterranean a few species coexist, but they are difficult to identify based on morphological characters. Additionally, spider mites often harbour several species of endosymbiotic bacteria, which may affect the biology of their hosts. Here, we propose novel, cost-effective, multiplex diagnostic methods allowing a quick identification of spider-mite species as well as of the endosymbionts they carry. First, we developed, and successfully multiplexed in a single PCR, primers to identify Tetranychus urticae, T. evansi and T. ludeni, some of the most common tetranychids found in southwest Europe. Moreover, we demonstrated that this method allows detecting multiple species in a single pool, even at low frequencies (up to 1/100), and can be used on entire mites without DNA extraction. Second, we developed another set of primers to detect spider-mite endosymbionts, namely Wolbachia, Cardinium and Rickettsia in a multiplex PCR, along with a generalist spider-mite primer to control for potential failure of DNA amplification in each PCR. Overall, our method represents a simple, cost-effective and reliable method to identify spider-mite species and their symbionts in natural field populations, as well as to detect contaminations in laboratory rearings. This method may easily be extended to other species.

Indexed as

MicrobiotaSymbiosisAnimalsBacteriaBacterial Physiological PhenomenaFemaleMaleMultiplex Polymerase Chain ReactionPortugalSpainTetranychidaeCardiniumMultiplex diagnosis toolRickettsiaSpecies identificationTetranychidaeWolbachia

Identifiers

What OpenQuestion holds

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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.