Evidence map›Paper›PMID 29722096›Full record

ArticleThe Journal of eukaryotic microbiology2018

The 14th International Workshops on Opportunistic Protists (IWOP 14).

Melanie T Cushion, Andrew H Limper, Aleksey Porollo, Vivian E Saper, Anthony P Sinai, Louis M Weiss

Abstract read
In one paragraph

Article in The Journal of eukaryotic microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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 6 institutions in 1 country.

Melanie T CushionDepartment of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, Ohio, 45267.ORCID 0000-0001-6621-2784
Andrew H LimperThoracic Diseases Research Unit, Department of Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota, 55905.
Aleksey PorolloCenter for Autoimmune Genomics and Etiology, and Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, 45229.
Vivian E SaperDepartment of Pediatrics, Stanford University of Medicine, Stanford, California, 94305.
Anthony P SinaiDepartment of Microbiology Immunology and Molecular Genetics, University of Kentucky College of Medicine, Lexington, Kentucky, 40536.
Louis M WeissDepartments of Medicine and Pathology, Albert Einstein College of Medicine, Bronx, New York, 10461.
Albert Einstein College of Medicine · USCincinnati Children's Hospital Medical Center · USCincinnati VA Medical Center · USMayo Clinic · USStanford Medicine · USUniversity of Kentucky · US

Funding

LCenter for Clinical and Translational Science and TrainingUL1TR001425 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E., KISSELA, BRETT M · 2015 to 2024
$37.5M
International Workshop on Opportunistic Protists (IWOP-14)R13AI134000 · NIAID · UNIVERSITY OF CINCINNATI · PI CUSHION, MELANIE T · 2017 to 2017
$5k
BLRD VA IK6 BX005232NCATS NIH HHS UL1 TR001425NIAID NIH HHS R13 AI134000
6 · The paper itself

Abstract

The 14th International Workshops on Opportunistic Protists (IWOP-14) was held August 10-12, 2017 in Cincinnati, OH, USA. The IWOP meetings focus on opportunistic protists (OIs); for example, free-living amoebae, Pneumocystis spp., Cryptosporidium spp., Toxoplasma, the Microsporidia, and kinetoplastid flagellates. The highlights of Pneumocystis spp. research included the reports of primary homothallism for mating; a potential requirement for sexual replication in its life cycle; a new antigen on the surface of small asci; roles for CLRs, Dectin-1, and Mincle in host responses; and identification of MSG families and mechanisms used for surface variation. Studies of Cryptosporidia spp. included comparative genomics, a new cryopreservation method; the role of mucin in attachment and invasion, and epidemiological surveys illustrating species diversity in animals. One of the five identified proteins in the polar tube of Microsporidia, PTP4, was shown to play a role in host infection. Zebrafish were used as a low cost vertebrate animal model for an evaluation of potential anti-toxoplasma drugs. Folk medicine compounds with anti-toxoplasma activity were presented, and reports on the chronic toxoplasma infection provided evidence for increased tractability for the study of this difficult life cycle stage. Escape from the parasitophorus vacuole and cell cycle regulation were the topics of the study in the acute phase.

Indexed as

EukaryotaAnimalsAntigens, ProtozoanCongresses as TopicCryptosporidiumDectin-1Disease Models, AnimalHumansKinetoplastidaLectins, C-TypeLife Cycle StagesMicrosporidiaMucinsOhioOpportunistic InfectionsPneumocystisAntigens, ProtozoanDectin-1Lectins, C-TypeMucinsCryptosporidiumHIVMicrosporidiaNaegleriaopportunistic infectionsPCPPneumocystispneumoniaToxoplasma gondii

Identifiers

PMID29722096
PMCPMC6215512
OpenAlexW2800177999

What OpenQuestion holds

Textmetadata
LicenceTDM
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.