Evidence map›Paper›PMID 32052727›Full record

ArticleParasitology2020

The mitochondrial genome of

Hayley Valentyne, David M Spratt, Mahdis Aghazadeh, Malcolm K Jones, Jan Šlapeta

Open access · greenAbstract read
In one paragraph

Article in Parasitology, 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
3.0field-weighted citation impact, top 10% 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, 21 citations in OpenAlex.

  1. Article
  2. Insights into the genetic diversity ofFood and waterborne parasitology · 2024
    Review
  3. The ZoonoticPathogens (Basel, Switzerland) · 2024
    Article
  4. Article
  5. Older urban rats are infected with the zoonotic nematodeCurrent research in parasitology & vector-borne diseases · 2024
    Article
  6. Article
  7. Article
  8. In the Dawn of an Early Invasion: No Genetic Diversity ofPathogens (Basel, Switzerland) · 2023
    Article
  9. Article
  10. Article
  11. AcanR3990 qPCR: A Novel, Highly Sensitive, Bioinformatically-Informed Assay to Detect Angiostrongylus cantonensis Infections.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Article
  12. Co-occurrence ofFood and waterborne parasitology · 2021
    Article
  13. Article
  14. Using cerebrospinal fluid to confirmCurrent research in parasitology & vector-borne diseases · 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

5 authors at 3 institutions in 1 country.

Hayley ValentyneSydney School of Veterinary Science, Faculty of Science, University of Sydney, 2006, New South Wales, Australia.
David M SprattAustralian National Wildlife Collection, National Research Collections Australia, CSIRO, GPO Box 1700, Canberra, 2601, Australia Capital Territory, Australia.
Mahdis AghazadehSydney School of Veterinary Science, Faculty of Science, University of Sydney, 2006, New South Wales, Australia.
Malcolm K JonesSchool of Veterinary Science, The University of Queensland, 4343, Queensland, Australia.
Jan ŠlapetaSydney School of Veterinary Science, Faculty of Science, University of Sydney, 2006, New South Wales, Australia.ORCID 0000-0003-1459-9117
The University of Sydney · AUAustralian National Wildlife Collection · AUThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The native rat lungworm (Angiostrongylus mackerrasae) and the invasive rat lungworm (Angiostrongylus cantonensis) occur in eastern Australia. The species identity of A. mackerrasae remained unquestioned until relatively recently, when compilation of mtDNA data indicated that A. mackerrasae sensu Aghazadeh et al. (2015b) clusters within A. cantonensis based on their mitochondrial genomes (mtDNA). To re-evaluate the species identity of A. mackerrasae, we sought material that would be morphologically conspecific with A. mackerrasae. We combined morphological and molecular approaches to confirm or refute the specific status of A. mackerrasae. Nematodes conspecific with A. mackerrasae from Rattus fuscipes and Rattus rattus were collected in Queensland, Australia. Morphologically identified A. mackerrasae voucher specimens were characterized using amplification of cox1 followed by the generation of reference complete mtDNA. The morphologically distinct A. cantonensis, A. mackerrasae and A. malaysiensis are genetically distinguishable forming a monophyletic mtDNA lineage. We conclude that A. mackerrasae sensu Aghazadeh et al. (2015b) is a misidentified specimen of A. cantonensis. The availability of the mtDNA genome of A. mackerrasae enables its unequivocal genetic identification and differentiation from other Angiostrongylus species.

Indexed as

Genome, HelminthGenome, MitochondrialAngiostrongylusAnimalsDNA, HelminthDNA, MitochondrialElectron Transport Complex IVHelminth ProteinsQueenslandRatsDNA, HelminthDNA, MitochondrialElectron Transport Complex IVHelminth ProteinsAustraliaidentitymtDNAphylogenyspeciestaxonomy

Identifiers

PMID32052727
PMCPMC10317689
OpenAlexW3006214379

What OpenQuestion holds

Textmetadata
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.