Evidence map›Paper›PMID 26837273›Full record

ArticleHeredity2016

The genome of an Encephalitozoon cuniculi type III strain reveals insights into the genetic diversity and mode of reproduction of a ubiquitous vertebrate pathogen.

A Pelin, H Moteshareie, B Sak, M Selman, A Naor, M-È Eyahpaise, L Farinelli, A Golshani, M Kvac, N Corradi

Open access · bronzeAbstract read
In one paragraph

Article in Heredity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-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

16 citing papers in PubMed, 20 citations in OpenAlex.

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  6. Comparative Genomics of Microsporidia.Experientia supplementum (2012) · 2022
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  7. Genome and Evolutionary Analysis ofFrontiers in microbiology · 2021
    Article
  8. Article
  9. Article
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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 at 4 institutions in 3 countries.

A PelinDepartment of Biology, Canadian Institute for Advanced Research, University of Ottawa, Ottawa, ON, Canada.
H MoteshareieDepartment of Biology, Carleton University, Ottawa, Ontario, Canada.
B SakInstitute of Parasitology, Biology Centre of the Academy of Sciences of the Czech Republic, České Budějovice, Czech Republic.
M SelmanDepartment of Biology, Canadian Institute for Advanced Research, University of Ottawa, Ottawa, ON, Canada.
A NaorDepartment of Biology, Canadian Institute for Advanced Research, University of Ottawa, Ottawa, ON, Canada.
M-È EyahpaiseDepartment of Biology, Canadian Institute for Advanced Research, University of Ottawa, Ottawa, ON, Canada.
L FarinelliFASTERIS S.A., Ch. du Pont-du-Centenaire 109, Plan-les-Ouates, Switzerland.
A GolshaniDepartment of Biology, Carleton University, Ottawa, Ontario, Canada.
M KvacInstitute of Parasitology, Biology Centre of the Academy of Sciences of the Czech Republic, České Budějovice, Czech Republic.
N CorradiDepartment of Biology, Canadian Institute for Advanced Research, University of Ottawa, Ottawa, ON, Canada.
Canadian Institute for Advanced Research · CACarleton University · CAInstitute of Parasitology · CZL.A.C. (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Encephalitozoon cuniculi is a model microsporidian species with a mononucleate nucleus and a genome that has been extensively studied. To date, analyses of genome diversity have revealed the existence of four genotypes in E. cuniculi (EcI, II, III and IV). Genome sequences are available for EcI, II and III, and are all very divergent, possibly diploid and genetically homogeneous. The mechanisms that cause low genetic diversity in E. cuniculi (for example, selfing, inbreeding or a combination of both), as well as the degree of genetic variation in their natural populations, have been hard to assess because genome data have been so far gathered from laboratory-propagated strains. In this study, we aim to tackle this issue by analyzing the complete genome sequence of a natural strain of E. cuniculi isolated in 2013 from a steppe lemming. The strain belongs to the EcIII genotype and has been designated EcIII-L. The EcIII-L genome sequence harbors genomic features intermediate to known genomes of II and III lab strains, and we provide primers that differentiate the three E. cuniculi genotypes using a single PCR. Surprisingly, the EcIII-L genome is also highly homogeneous, harbors signatures of heterozygosity and also one strain-specific single-nucleotide polymorphism (SNP) that introduces a stop codon in a key meiosis gene, Spo11. Functional analyses using a heterologous system demonstrate that this SNP leads to a deficient meiosis in a model fungus. This indicates that EcIII-L meiotic machinery may be presently broken. Overall, our findings reveal previously unsuspected genome diversity in E. cuniculi, some of which appears to affect genes of primary importance for the biology of this pathogen.

Indexed as

Genetic VariationGenome, FungalAnimalsArvicolinaeChromosome MappingDNA, FungalEncephalitozoon cuniculiGenotypeHeterozygoteMeiosisPolymorphism, Single NucleotideSequence Analysis, DNADNA, Fungal

Identifiers

PMID26837273
PMCPMC4834387
OpenAlexW2270974174

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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.