Evidence map›Paper›PMID 31138276›Full record

ArticleParasites & vectors2019

Identification of proteins expressed by Babesia bigemina kinetes.

Gamila A R Bohaliga, Wendell C Johnson, Naomi S Taus, Hala E Hussein, Reginaldo G Bastos, Carlos E Suarez, Glen A Scoles, Massaro W Ueti

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  6. A TransfectedPathogens (Basel, Switzerland) · 2022
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  7. Comparison of high throughput RNA sequences betweenFrontiers in cellular and infection microbiology · 2022
    Article
  8. Article
  9. Review
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 at 1 institution in 2 countries.

Gamila A R BohaligaProgram in Vector-borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, 99164, USA.
Wendell C JohnsonAnimal Disease Research Unit, USDA-ARS, Pullman, WA, 99164-6630, USA.
Naomi S TausProgram in Vector-borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, 99164, USA.
Hala E HusseinProgram in Vector-borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, 99164, USA.
Reginaldo G BastosProgram in Vector-borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, 99164, USA.
Carlos E SuarezProgram in Vector-borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, 99164, USA.
Glen A ScolesProgram in Vector-borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, 99164, USA.
Massaro W UetiProgram in Vector-borne Diseases, Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, WA, 99164, USA. massaro_ueti@wsu.edu.
Washington State University · US

Funding

USDA-ARS CRIS project number 2090-32000-039-00D
6 · The paper itself

Abstract

backgroundBabesia bigemina is an apicomplexan parasite transovarially transmitted via Rhipicephalus ticks that infect red blood cells and causes bovine babesiosis, a poorly controlled severe acute disease in cattle. New methods of control are urgently needed, including the development of transmission blocking vaccines (TBV). Babesia bigemina reproduces sexually in the gut of adult female R. microplus upon acquisition following a blood meal. Sexual reproduction results in zygotes that infect gut epithelial cells to transform into kinete stage parasites, which invade tick ovaries and infects the egg mass. The subsequent tick generation transmits B. bigemina upon feeding on bovine hosts. An important limitation for developing novel TBV is that the pattern of protein expression in B. bigemina tick stages, such as the kinete stage, remain essentially uncharacterized.

resultsWe determined the protein expression profile of three B. bigemina putative tick stage candidates BbiKSP (BBBOND_0206730), CCp2 and CCp3. We found that BbiKSP expression was restricted to B. bigemina kinetes. CCp2 and CCp3, previously shown to be expressed by induced sexual stages, were also expressed by kinetes. Importantly, none of these proteins were expressed by B. bigemina blood stages.

conclusionsBabesia bigemina kinetes express BbiKSP, CCp2 and CCp3 proteins, therefore, these proteins may play important roles during B. bigemina development within tick hemolymph and may serve as potential candidate targets for the development of TBV.

Indexed as

ProteomicsAnimalsBabesiaBabesiosisCattleCattle DiseasesFemaleFluorescent Antibody TechniqueLife Cycle StagesOvaryProtozoan ProteinsReproductionRhipicephalusProtozoan ProteinsBabesia bigeminain vitro induced sexual stagesKineteKinete stage-specific proteinRhipicephalus microplus

Identifiers

PMID31138276
PMCPMC6537212
OpenAlexW2947270222

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.