Evidence map›Paper›PMID 27619014›Full record

ArticleParasites & vectors2016

Conservation and diversification of the transcriptomes of adult Paragonimus westermani and P. skrjabini.

Ben-Wen Li, Samantha N McNulty, Bruce A Rosa, Rahul Tyagi, Qing Ren Zeng, Kong-Zhen Gu, Gary J Weil, Makedonka Mitreva

Abstract read
In one paragraph

Article in Parasites & vectors, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Paragonimiasis.Advances in experimental medicine and biology · 2024
    Review
  4. Lung flukes of the genusParasitology · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. 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.

Ben-Wen LiInfectious Diseases Division, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Samantha N McNultyThe McDonnell Genome Institute at Washington University, St. Louis, MO, USA.
Bruce A RosaThe McDonnell Genome Institute at Washington University, St. Louis, MO, USA.
Rahul TyagiThe McDonnell Genome Institute at Washington University, St. Louis, MO, USA.
Qing Ren ZengDepartment of Parasitology, Xiang-Ya School of Medicine, Central South University, Changsha, Hunan Province, People's Republic of China.
Kong-Zhen GuDepartment of Parasitology, Xiang-Ya School of Medicine, Central South University, Changsha, Hunan Province, People's Republic of China.
Gary J WeilInfectious Diseases Division, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Makedonka MitrevaInfectious Diseases Division, Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO, USA. mmitreva@wustl.edu.

Funding

COMPARATIVE GENOMICS OF PARASITIC NEMATODESR01AI081803 · NIAID · WASHINGTON UNIVERSITY · PI MITREVA, MAKEDONKA · 2009 to 2018
$3.1M
NIAID NIH HHS R01 AI081803
6 · The paper itself

Abstract

backgroundParagonimiasis is an important and widespread neglected tropical disease. Fifteen Paragonimus species are human pathogens, but two of these, Paragonimus westermani and P. skrjabini, are responsible for the bulk of human disease. Despite their medical and economic significance, there is limited information on the gene content and expression of Paragonimus lung flukes.

resultsThe transcriptomes of adult P. westermani and P. skrjabini were studied with deep sequencing technology. Approximately 30 million reads per species were assembled into 21,586 and 25,825 unigenes for P. westermani and P. skrjabini, respectively. Many unigenes showed homology with sequences from other food-borne trematodes, but 1,217 high-confidence Paragonimus-specific unigenes were identified. Analyses indicated that both species have the potential for aerobic and anaerobic metabolism but not de novo fatty acid biosynthesis and that they may interact with host signaling pathways. Some 12,432 P. westermani and P. skrjabini unigenes showed a clear correspondence in bi-directional sequence similarity matches. The expression of shared unigenes was mostly well correlated, but differentially expressed unigenes were identified and shown to be enriched for functions related to proteolysis for P. westermani and microtubule based motility for P. skrjabini.

conclusionsThe assembled transcriptomes of P. westermani and P. skrjabini, inferred proteins, and extensive functional annotations generated for this project (including identified primary sequence similarities to various species, protein domains, biological pathways, predicted proteases, molecular mimics and secreted proteins, etc.) represent a valuable resource for hypothesis driven research on these medically and economically important species.

Indexed as

Genetic VariationAnimalsBiological EvolutionBrachyuraGene Expression RegulationHelminth ProteinsHost-Parasite InteractionsMetacercariaeParagonimusRNA, HelminthTranscriptomeHelminth ProteinsRNA, HelminthAdult stageComparative transcriptomicsLung flukeParagonimusParagonimus skrjabiniParagonimus westermaniRNA-Seq

Identifiers

PMID27619014
PMCPMC5020434

What Socratic 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 Socratic graph.