Evidence map›Paper›PMID 27080723›Full record

ArticleInternational journal for parasitology2016

Limited genetic and antigenic diversity within parasite isolates used in a live vaccine against Theileria parva.

Johanneke D Hemmink, William Weir, Niall D MacHugh, Simon P Graham, Ekta Patel, Edith Paxton, Brian Shiels, Philip G Toye, W Ivan Morrison, Roger Pelle

Open access · hybridAbstract read
In one paragraph

Article in International journal for parasitology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 11% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Antigenic and genotypic relatedness of buffalo-derivedInternational journal for parasitology. Parasites and wildlife · 2026
    Article
  3. Discovery immunology · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. ExploringGenes · 2020
    Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Population Genetic Analysis of theFrontiers in microbiology · 2020
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 4 institutions in 2 countries.

Johanneke D HemminkThe Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Roslin, Midlothian EH25 9RG, UK.
William WeirCollege of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Henry Wellcome Building, Garscube Campus, Bearsden Road, Glasgow G61 1QH, UK.
Niall D MacHughThe Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Roslin, Midlothian EH25 9RG, UK.
Simon P GrahamThe International Livestock Research Institute, PO Box 30709, Nairobi, Kenya.
Ekta PatelThe International Livestock Research Institute, PO Box 30709, Nairobi, Kenya.
Edith PaxtonThe Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Roslin, Midlothian EH25 9RG, UK.
Brian ShielsCollege of Medical, Veterinary and Life Sciences, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Henry Wellcome Building, Garscube Campus, Bearsden Road, Glasgow G61 1QH, UK.
Philip G ToyeThe International Livestock Research Institute, PO Box 30709, Nairobi, Kenya.
W Ivan MorrisonThe Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Roslin, Midlothian EH25 9RG, UK. Electronic address: ivan.morrison@roslin.ed.ac.uk.
Roger PelleThe International Livestock Research Institute, PO Box 30709, Nairobi, Kenya.
International Livestock Research Institute · KEUniversity of Edinburgh · GBUniversity of Glasgow · GBRoslin Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BB/H009515/1Biotechnology and Biological Sciences Research Council BB/J004227/1Biotechnology and Biological Sciences Research Council BBS/E/D/05201234Biotechnology and Biological Sciences Research Council BBS/E/D/05201236
6 · The paper itself

Abstract

An infection and treatment protocol is used to vaccinate cattle against Theileria parva infection. Due to incomplete cross-protection between different parasite isolates, a mixture of three isolates, termed the Muguga cocktail, is used for vaccination. While vaccination of cattle in some regions provides high levels of protection, some animals are not protected against challenge with buffalo-derived T. parva. Knowledge of the genetic composition of the Muguga cocktail vaccine is required to understand how vaccination is able to protect against field challenge and to identify the potential limitations of the vaccine. The aim of the current study was to determine the extent of genetic and antigenic diversity within the parasite isolates that constitute the Muguga cocktail. High throughput multi-locus sequencing of antigen-encoding loci was performed in parallel with typing using a panel of micro- and mini-satellite loci. The former focused on genes encoding CD8(+) T cell antigens, believed to be relevant to protective immunity. The results demonstrate that each of the three component stocks of the cocktail contains limited parasite genotypic diversity, with single alleles detected at many gene/satellite loci and, moreover, that two of the components show a very high level of similarity. Thus, the vaccine incorporates very little of the genetic and antigenic diversity observed in field populations of T. parva. The presence of alleles at low frequency (<10%) within vaccine component populations also points to the possibility of variability in the content of vaccine doses and the potential for loss of allelic diversity during tick passage. The results demonstrate that there is scope to modify the content of the vaccine in order to enhance its diversity and thus its potential for providing broad protection. The ability to accurately quantify genetic diversity in vaccine component stocks will facilitate improved quality control procedures designed to ensure the long-term efficacy of the vaccine.

Indexed as

Antigenic VariationGenetic VariationAllelesAmino Acid SubstitutionAnimalsArachnid VectorsBuffaloesCattleCD8 AntigensCD8-Positive T-LymphocytesDNA, ProtozoanHigh-Throughput Nucleotide SequencingMicrosatellite RepeatsMinisatellite RepeatsProtozoan VaccinesRhipicephalusCD8 AntigensDNA, ProtozoanProtozoan VaccinesAntigenic diversityCattleGene sequencingSatellite DNATheileria parvaVaccination

Identifiers

PMID27080723
PMCPMC4935670
OpenAlexW2324458328

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.