Evidence map›Paper›PMID 32546252›Full record

ArticleParasites & vectors2020

Catalogue of stage-specific transcripts in Ixodes ricinus and their potential functions during the tick life-cycle.

Pavlina Vechtova, Zoltan Fussy, Radim Cegan, Jan Sterba, Jan Erhart, Vladimir Benes, Libor Grubhoffer

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.3field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

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  12. Mialostatin, a Novel Midgut Cystatin fromInternational journal of molecular sciences · 2021
    Article
  13. Article
  14. Iripin-3, a New Salivary Protein Isolated FromFrontiers in immunology · 2021
    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

7 authors at 4 institutions in 2 countries.

Pavlina VechtovaFaculty of Science, University of South Bohemia, České Budějovice, Czech Republic. vechtova@prf.jcu.cz.ORCID http://orcid.org/0000-0003-3947-2964
Zoltan FussyFaculty of Science, University of South Bohemia, České Budějovice, Czech Republic.
Radim CeganDepartment of Plant Developmental Genetics, Institute of Biophysics of the Czech Academy of Sciences, Brno, Czech Republic.
Jan SterbaFaculty of Science, University of South Bohemia, České Budějovice, Czech Republic.
Jan ErhartBiology Centre CAS, Institute of Parasitology, České Budějovice, Czech Republic.
Vladimir BenesGeneCore, EMBL, Heidelberg, Germany.
Libor GrubhofferFaculty of Science, University of South Bohemia, České Budějovice, Czech Republic.
University of South Bohemia in České Budějovice · CZCharles University · CZCzech Academy of Sciences, Institute of Biophysics · CZInstitute of Parasitology · CZ

Funding

Ministerstvo Školství, Mládeže a Tělovýchovy 18-27204SMinisterstvo Školství, Mládeže a Tělovýchovy EE2.3.30.0032Ministerstvo Školství, Mládeže a Tělovýchovy EF16_019/0000759Ministerstvo Školství, Mládeže a Tělovýchovy LM2015055Ministerstvo Školství, Mládeže a Tělovýchovy LTARF18021Ministerstvo Školství, Mládeže a Tělovýchovy LTAUSA18040
6 · The paper itself

Abstract

backgroundThe castor bean tick Ixodes ricinus is an important vector of several clinically important diseases, whose prevalence increases with accelerating global climate changes. Characterization of a tick life-cycle is thus of great importance. However, researchers mainly focus on specific organs of fed life stages, while early development of this tick species is largely neglected.

methodsIn an attempt to better understand the life-cycle of this widespread arthropod parasite, we sequenced the transcriptomes of four life stages (egg, larva, nymph and adult female), including unfed and partially blood-fed individuals. To enable a more reliable identification of transcripts and their comparison in all five transcriptome libraries, we validated an improved-fit set of five I. ricinus-specific reference genes for internal standard normalization of our transcriptomes. Then, we mapped biological functions to transcripts identified in different life stages (clusters) to elucidate life stage-specific processes. Finally, we drew conclusions from the functional enrichment of these clusters specifically assigned to each transcriptome, also in the context of recently published transcriptomic studies in ticks.

resultsWe found that reproduction-related transcripts are present in both fed nymphs and fed females, underlining the poorly documented importance of ovaries as moulting regulators in ticks. Additionally, we identified transposase transcripts in tick eggs suggesting elevated transposition during embryogenesis, co-activated with factors driving developmental regulation of gene expression. Our findings also highlight the importance of the regulation of energetic metabolism in tick eggs during embryonic development and glutamate metabolism in nymphs.

conclusionsOur study presents novel insights into stage-specific transcriptomes of I. ricinus and extends the current knowledge of this medically important pathogen, especially in the early phases of its development.

Indexed as

Gene Expression ProfilingAnimalsFeeding BehaviorFemaleIxodesLife Cycle StagesNymphReproductionIxodes ricinusLife stageReference gene validationTick developmentTranscriptome assembly

Identifiers

PMID32546252
PMCPMC7296661
OpenAlexW3034622970

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.