Evidence map›Paper›PMID 27837253›Full record

ArticleMicrobial ecology2017

Characterization of Nosema ceranae Genetic Variants from Different Geographic Origins.

B Branchiccela, D Arredondo, M Higes, C Invernizzi, R Martín-Hernández, I Tomasco, P Zunino, K Antúnez

Abstract read
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In one paragraph

Article in Microbial ecology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. The FungusMicroorganisms · 2023
    Article
  3. Review
  4. The Role ofVeterinary sciences · 2022
    Review
  5. First report ofParasitology · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Prevalence of the MicrosporidianVeterinary sciences · 2020
    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.

B BranchiccelaDepartamento de Microbiología, Instituto de Investigaciones Biológicas Clemente Estable, Avda. Italia 3318, CP 11600, Montevideo, Uruguay.
D ArredondoDepartamento de Microbiología, Instituto de Investigaciones Biológicas Clemente Estable, Avda. Italia 3318, CP 11600, Montevideo, Uruguay.
M HigesBee Pathology Laboratory, Regional Apicultural Center, Guadalajara, Spain.
C InvernizziSección Etología, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
R Martín-HernándezBee Pathology Laboratory, Regional Apicultural Center, Guadalajara, Spain.
I TomascoDepartamento de Ecología y Evolución, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay.
P ZuninoDepartamento de Microbiología, Instituto de Investigaciones Biológicas Clemente Estable, Avda. Italia 3318, CP 11600, Montevideo, Uruguay.
K AntúnezDepartamento de Microbiología, Instituto de Investigaciones Biológicas Clemente Estable, Avda. Italia 3318, CP 11600, Montevideo, Uruguay. kantunez03@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, large-scale colony losses of honey bees (Apis mellifera) have been reported and the infection with the microsporidia Nosema ceranae has been involved. However, the effect of N. ceranae at the colony level and its role in colony losses vary in different geographic areas. This difference may be related to the presence of multiple N. ceranae genetic variants resulting in different biological consequences. In this study, we analyzed the genetic diversity of 75 N. ceranae samples obtained from 13 countries and Hawaii through inter-sequence single repetition (ISSR) and evaluated if two of these genetic variants triggered different immune responses when infecting Apis mellifera iberiensis. The genetic diversity analysis showed that 41% of the samples had the same DNA amplification pattern, including samples from most European countries except Spain, while the remaining samples showed high variability. Infection assays were performed to analyze the infection levels and the immune response of bees infected with N. ceranae from Spain and Uruguay. The infected bees presented similar infection levels, and both isolates downregulated the expression of abaecin, confirming the ability of the microsporidia to depress the immune response. Only N. ceranae from Uruguay downregulated the expression level of imd compared to control bees. On the other hand, both genetic variants triggered different expression levels of lysozyme. As imd and lysozyme play important roles in the response to pathogens, these results could reflect differences in the biological consequences of N. ceranae variants in A. mellifera infection.

Indexed as

Genetic VariationAnimal DiseasesAnimalsAntimicrobial Cationic PeptidesBeesDNA, FungalDown-RegulationGene Expression RegulationGenes, FungalGeographyInsect ProteinsMicrosporidiosisMuramidaseNosemaReal-Time Polymerase Chain ReactionRNA, Fungalabaecin protein, Apis melliferaAntimicrobial Cationic PeptidesDNA, FungalInsect ProteinsMuramidaseRNA, FungalColony lossesGenetic diversityImmune responseNosema ceranae

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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.