Evidence map›Paper›PMID 41303542›Full record

ArticleInternational journal of molecular sciences2025

Genetic Diversity of Selected High-Risk HPV Types Prevalent in Africa and Not Covered by Current Vaccines: A Pooled Sequence Data Analysis.

Babalwa Nyide, Miranda Thomas, Lawrence Banks, Pamela P Mkhize, Nontokozo D Matume

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Babalwa NyideDiscipline of Biochemistry, School of Agriculture and Science, University of KwaZulu-Natal, Pietermaritzburg 3209, South Africa.
Miranda ThomasTumour Virology, International Centre for Genetic Engineering and Biotechnology (I.C.G.E.B.), 34149 Trieste, Italy.
Lawrence BanksTumour Virology, International Centre for Genetic Engineering and Biotechnology (I.C.G.E.B.), 34149 Trieste, Italy.
Pamela P MkhizeDiscipline of Biochemistry, School of Agriculture and Science, University of KwaZulu-Natal, Pietermaritzburg 3209, South Africa.ORCID 0000-0003-2176-9807
Nontokozo D MatumeDiscipline of Genetics, School of Agriculture and Science, University of KwaZulu-Natal, Pietermaritzburg 3209, South Africa.

Funding

National Research Foundation (NRF), Thuthuka TTK230430100291Poliomyelitis Research Foundation (PRF 24/64Poliomyelitis Research Foundation (PRF) 24/81
6 · The paper itself

Abstract

High-risk human papillomavirus (HR-HPV) types exhibit an uneven global distribution, with types 35, 51, 56, and 59 being more prevalent in Africa yet not covered by current L1-based vaccines. The genetic diversity of HR-HPV oncoproteins in Africa remains poorly characterized, despite their potential as alternative vaccine targets. This study investigates the genetic diversity of HR-HPV types 16, 18, 35, 51, 56, and 59 to inform vaccine development. We analyzed 14,332 sequences from the NCBI Virus database and 222 HPV reference sequences from the Papillomavirus Episteme (PaVE) database using phylogenetic analysis and variant identification. HPV16 and HPV35 exhibited close evolutionary relatedness, which may indicate shared traits relevant to vaccine design, although functional implications remain to be experimentally validated. A key finding of the study was the discovery of novel non-synonymous mutations, including E148K in HPV35 E6, S63C in HPV16 E7 and S495F in HPV18 L1, as well as known oncogenic variants such as L83V (E6) and N29S (E7) in HPV16. These findings highlight significant intra- and inter-type diversity among African HR-HPVs. This study provides new insights into the genetic diversity and evolutionary relationships of underrepresented HR-HPV types. The findings underscore the need for continued genomic surveillance and support efforts to develop region-specific vaccines that include HPV35, 51, 56, and 59 to address gaps in current vaccine coverage and help reduce the burden of HPV-related cancers in Africa.

Indexed as

AlphapapillomavirusHuman Papillomavirus VirusesPapillomavirus VaccinesUterine Cervical NeoplasmsVaccine EfficacyAfricaFemaleGenetic VariationHumansPrevalencePapillomavirus VaccinesAfricagenetic diversityhigh-risk human papillomavirus (HR-HPV)oncoproteinsphylogeneticsvaccines

Identifiers

PMID41303542
PMCPMC12652174

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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.