Evidence map›Paper›PMID 25226276›Full record

ArticlePloS one2014

Identification and characterization of the RouenBd1987 Babesia divergens Rhopty-Associated Protein 1.

Marilis Rodriguez, Andy Alhassan, Rosalynn L Ord, Jeny R Cursino-Santos, Manpreet Singh, Jeremy Gray, Cheryl A Lobo

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. 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
1.5field-weighted citation impact, top 22% 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. Article
  3. Article
  4. Advances inPathogens (Basel, Switzerland) · 2023
    Review
  5. Article
  6. The New HumanPathogens (Basel, Switzerland) · 2021
    Article
  7. Pathogens (Basel, Switzerland) · 2021
    Article
  8. Article
  9. Pathogens (Basel, Switzerland) · 2019
    Review
  10. Variable and Variant Protein Multigene Families inPathogens (Basel, Switzerland) · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. Human Babesiosis: Pathogens, Prevalence, Diagnosis and Treatment.Current clinical microbiology reports · 2015
    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

7 authors at 2 institutions in 2 countries.

Marilis RodriguezDepartment of Blood-Borne Parasites, New York Blood Center, New York, New York, United States of America.
Andy AlhassanDepartment of Blood-Borne Parasites, New York Blood Center, New York, New York, United States of America.
Rosalynn L OrdDepartment of Blood-Borne Parasites, New York Blood Center, New York, New York, United States of America.
Jeny R Cursino-SantosDepartment of Blood-Borne Parasites, New York Blood Center, New York, New York, United States of America.
Manpreet SinghDepartment of Blood-Borne Parasites, New York Blood Center, New York, New York, United States of America.
Jeremy GrayUniversity College Dublin School of Biology and Environmental Science, Dublin, Republic of Ireland.
Cheryl A LoboDepartment of Blood-Borne Parasites, New York Blood Center, New York, New York, United States of America.
New York Blood Center · USUniversity College Dublin · IE

Funding

Babesiosis: An Emerging Infectious Threat to Transfusion MedicineR01HL105694 · NHLBI · NEW YORK BLOOD CENTER · PI LOBO, CHERYL ANN · 2011 to 2015
$2.0M
NHLBI NIH HHS R01 HL105694NHLBI NIH HHS R01-HL105694
6 · The paper itself

Abstract

Human babesiosis is caused by one of several babesial species transmitted by ixodid ticks that have distinct geographical distributions based on the presence of competent animal hosts. The pathology of babesiosis, like malaria, is a consequence of the parasitaemia which develops through the cyclical replication of Babesia parasites in a patient's red blood cells, though symptoms typically are nonspecific. We have identified the gene encoding Rhoptry-Associated Protein -1 (RAP-1) from a human isolate of B. divergens, Rouen1987 and characterized its protein product at the molecular and cellular level. Consistent with other Babesia RAP-1 homologues, BdRAP-1 is expressed as a 46 kDa protein in the parasite rhoptries, suggesting a possible role in red cell invasion. Native BdRAP-1 binds to an unidentified red cell receptor(s) that appears to be non-sialylated and non-proteinacious in nature, but we do not find significant reduction in growth with anti-rRAP1 antibodies in vitro, highlighting the possibility the B. divergens is able to use alternative pathways for invasion, or there is an alternative, complementary, role for BdRAP-1 during the invasion process. As it is the parasite's ability to recognize and then invade host cells which is central to clinical disease, characterising and understanding the role of Babesia-derived proteins involved in these steps are of great interest for the development of an effective prophylaxis.

Indexed as

Amino Acid SequenceAnimalsBabesiaBabesiosisCattleCloning, MolecularErythrocytesGene ExpressionImmunodominant EpitopesMolecular Sequence DataMolecular WeightProtein BindingProtozoan ProteinsReceptors, Cell SurfaceRecombinant Fusion ProteinsSequence AlignmentImmunodominant EpitopesProtozoan ProteinsReceptors, Cell SurfaceRecombinant Fusion Proteinsrhoptry-associated protein-1, Babesia

Identifiers

PMID25226276
PMCPMC4166668
OpenAlexW1994735154

What OpenQuestion 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 OpenQuestion graph.