Evidence map›Paper›PMID 30401619›Full record

ArticleInternational journal for parasitology. Drugs and drug resistance2018

Investigating the function and possible biological role of an acetylcholine-gated chloride channel subunit (ACC-1) from the parasitic nematode Haemonchus contortus.

Micah K Callanan, Sarah A Habibi, Wen Jing Law, Kristen Nazareth, Richard L Komuniecki, Sean G Forrester

Open access · goldAbstract read
In one paragraph

Article in International journal for parasitology. Drugs and drug resistance, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Anthelmintics - From Discovery to Resistance III (Indian Rocks Beach, FL, 2018).International journal for parasitology. Drugs and drug resistance · 2018
    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

6 authors at 2 institutions in 2 countries.

Micah K CallananFaculty of Science, University of Ontario Institute of Technology, 2000, Simcoe Street North, Oshawa, ON, L1H 7K4, Canada.
Sarah A HabibiFaculty of Science, University of Ontario Institute of Technology, 2000, Simcoe Street North, Oshawa, ON, L1H 7K4, Canada.
Wen Jing LawDepartment of Biological Sciences, University of Toledo, Toledo, OH, 43606, USA.
Kristen NazarethFaculty of Science, University of Ontario Institute of Technology, 2000, Simcoe Street North, Oshawa, ON, L1H 7K4, Canada.
Richard L KomunieckiDepartment of Biological Sciences, University of Toledo, Toledo, OH, 43606, USA.
Sean G ForresterFaculty of Science, University of Ontario Institute of Technology, 2000, Simcoe Street North, Oshawa, ON, L1H 7K4, Canada. Electronic address: sean.forrester@uoit.ca.
Ontario Tech University · CAUniversity of Toledo · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cys-loop superfamily of ligand-gated ion channels are well recognized as important drug targets for many invertebrate specific compounds. With the rise in resistance seen worldwide to existing anthelmintics, novel drug targets must be identified so new treatments can be developed. The acetylcholine-gated chloride channel (ACC) family is a unique family of cholinergic receptors that have been shown, using Caenorhabditis elegans as a model, to have potential as anti-parasitic drug targets. However, there is little known about the function of these receptors in parasitic nematodes. Here, we have identified an acc gene (hco-acc-1) from the sheep parasitic nematode Haemonchus contortus. While similar in sequence to the previously characterized C. elegans ACC-1 receptor, Hco-ACC-1 does not form a functional homomeric channel in Xenopus oocytes. Instead, co-expression of Hco-ACC-1 with a previously characterized subunit Hco-ACC-2 produced a functional heteromeric channel which was 3x more sensitive to acetylcholine compared to the Hco-ACC-2 homomeric channel. We have also found that Hco-ACC-1 can be functionally expressed in C. elegans. Overexpression of both cel-acc-1 and hco-acc-1 in both C. elegans N2 and acc-1 null mutants decreased the time for worms to initiate reversal avoidance to octanol. Moreover, antibodies were generated against the Hco-ACC-1 protein for use in immunolocalization studies. Hco-ACC-1 consistently localized to the anterior half of the pharynx, specifically in pharyngeal muscle tissue in H. contortus. On the other hand, expression of Hco-ACC-1 in C. elegans was restricted to neuronal tissue. Overall, this research has provided new insight into the potential role of ACC receptors in parasitic nematodes.

Indexed as

AcetylcholineAnimalsAnthelminticsCaenorhabditis elegansChloride ChannelsCysteine Loop Ligand-Gated Ion Channel ReceptorsHaemonchusHelminth ProteinsLigand-Gated Ion ChannelsOctanolsOocytesPharyngeal MusclesReceptors, CholinergicXenopus laevisAcetylcholineAnthelminticsChloride ChannelsCysteine Loop Ligand-Gated Ion Channel ReceptorsHelminth ProteinsLigand-Gated Ion ChannelsOctanolsReceptors, CholinergicCholinergic receptorCys-loopHaemonchus contortusLigand-gated chloride channelPharynx

Identifiers

PMID30401619
PMCPMC6287539
OpenAlexW2898461026

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.