Evidence map›Paper›PMID 40244593›Full record

ArticleHLA2025

Fully Phased Population-Prevalent East African Cattle BoLA-I Alleles Determined Using PacBio HiFi Long-Read Sequencing Represent Five Novel Specificities With Distinctive Peptide Binding Potential.

Isaiah Obara, Andreotti Sandro, Khawla Elati, Timothy Conneley, Morten Nielsen, Naftaly Githaka, Anne Nanteza, Richard Bishop, Ard Nijhof

Abstract read
In one paragraph

Article in HLA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

9 authors.

Isaiah ObaraFreie Universität Berlin, Institute for Parasitology and Tropical Veterinary Medicine, Department of Veterinary Medicine, Berlin, Germany.ORCID 0000-0003-0507-1476
Andreotti SandroFreie Universität Berlin, Institute of Computer Science, Department of Mathematics and Computer Science, Berlin, Germany.
Khawla ElatiFreie Universität Berlin, Institute for Parasitology and Tropical Veterinary Medicine, Department of Veterinary Medicine, Berlin, Germany.
Timothy ConneleyThe Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, UK.
Morten NielsenDepartment of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Naftaly GithakaThe International Livestock Research Institute, Nairobi, Kenya.
Anne NantezaDepartment of Biotechnical and Diagnostic Sciences, College of Veterinary Medicine, Animal Resources and Biosecurity (COVAB), Makerere University, Kampala, Uganda.
Richard BishopDepartment of Veterinary Microbiology and Pathology, Washington State University, Pullman, Washington, USA.
Ard NijhofFreie Universität Berlin, Institute for Parasitology and Tropical Veterinary Medicine, Department of Veterinary Medicine, Berlin, Germany.

Funding

Deutsche Forschungsgemeinschaft OB 490/2-1
6 · The paper itself

Abstract

Due to factors such as lower biosecurity, greater wildlife/farm animal interfaces, and environmental challenges, cattle in sub-Saharan Africa are exposed to more diverse and intensive bacterial, viral and protozoan pathogen challenges than cattle in Europe and other high-income regions of the world. Classical class I genes of the major histocompatibility complex (MHC) contribute to protection from diseases caused by these pathogens by refining a huge pool of potential pathogen-derived peptide ligands into a smaller ensemble for presentation to CD8+ T cells. Knowledge of population-prevalent MHC alleles is therefore critical for evidence-based approaches to vaccine design and improved understanding of pathogen resistance. Whereas variation in MHC molecules is understood in most detail for European Bos taurus, the alleles expressed by Africa's cattle remain poorly defined. We have leveraged recent improvements in the accuracy of PacBio high-fidelity (HiFi) circular consensus sequencing (CCS) and adapted stringent sequence filtering algorithms to identify hundreds of as yet uncharacterised fully phased BoLA-I alleles from multiple populations of African taurine (Ankole) and indicine (Zebu) cattle in East Africa. The analysis highlights a convergence of population-prevalent class I MHC allelic repertoires in taurine and indicine cattle, likely due to the similar pathogen-driven selective pressures. Our analysis of the anchor residue accommodating pockets of these prevalent alleles revealed extremely high levels of polymorphism, which contrast with Holstein alleles that exhibit a more limited repertoire of MHC specificity-determining pocket residues, potentially constraining the breadth of peptide presentation. However, in the context of considerable sequence and physicochemical variation in the pocket-forming residues, it was possible to discern overlaps in the predicted peptide binding spectrum. Interrogation of potential differences in peptide binding specificities with European B. taurus alleles revealed that the fully phased African cattle class I MHC alleles represent five novel specificities. We envisage that this novel finding will find broad application in assessing potentially achievable vaccination coverages of future pathogen-encoded vaccine candidates against important intracellular pathogens. One aim of future research should be to leverage recent improvements in the sensitivity of mass spectrometry combined with immunoprecipitation of peptides bound to African cattle MHC to search directly for T-cell epitopes in the context of the inferred 'supertype' diversity.

Indexed as

AllelesHistocompatibility Antigens Class IPeptidesAfrica, EasternAnimalsCattleCD8-Positive T-LymphocytesHigh-Throughput Nucleotide SequencingHistocompatibility Antigens Class IIProtein BindingSequence Analysis, DNABoLA-DRB3 antigenHistocompatibility Antigens Class IHistocompatibility Antigens Class IIPeptidescattlehigh‐throughput sequencingMHC

Identifiers

PMID40244593
PMCPMC12005355

What OpenQuestion holds

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Registered trials

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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.