Evidence map›Paper›PMID 9256458›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

Typing of urinary JC virus DNA offers a novel means of tracing human migrations.

C Sugimoto, T Kitamura, J Guo, M N Al-Ahdal, S N Shchelkunov, B Otova, P Ondrejka, J Y Chollet, S El-Safi, M Ettayebi and 9 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

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

34 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Observational
  8. Molecular epidemiology of JC polyomavirus in HIV-infected patients and healthy individuals from Iran.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2020
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Phylogenetic analysis of beak and feather disease virus across a host ring-species complex.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Distinguishing human ethnic groups by means of sequences from Helicobacter pylori: lessons from Ladakh.Proceedings of the National Academy of Sciences of the United States of America · 2004
    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

19 authors.

C SugimotoDepartment of Viral Infection, the Institute of Medical Science, the University of Tokyo, Tokyo, Japan.
T Kitamura
J Guo
M N Al-Ahdal
S N Shchelkunov
B Otova
P Ondrejka
J Y Chollet
S El-Safi
M Ettayebi
G Grésenguet
T Kocagöz
S Chaiyarasamee
K Z Thant
S Thein
K Moe
N Kobayashi
F Taguchi
Y Yogo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although polyomavirus JC (JCV) is the proven pathogen of progressive multifocal leukoencephalopathy, the fatal demyelinating disease, this virus is ubiquitous as a usually harmless symbiote among human beings. JCV propagates in the adult kidney and excretes its progeny in urine, from which JCV DNA can readily be recovered. The main mode of transmission of JCV is from parents to children through long cohabitation. In this study, we collected a substantial number of urine samples from native inhabitants of 34 countries in Europe, Africa, and Asia. A 610-bp segment of JCV DNA was amplified from each urine sample, and its DNA sequence was determined. A worldwide phylogenetic tree subsequently constructed revealed the presence of nine subtypes including minor ones. Five subtypes (EU, Af2, B1, SC, and CY) occupied rather large territories that overlapped with each other at their boundaries. The entire Europe, northern Africa, and western Asia were the domain of EU, whereas the domain of Af2 included nearly all of Africa and southwestern Asia all the way to the northeastern edge of India. Partially overlapping domains in Asia were occupied by subtypes B1, SC, and CY. Of particular interest was the recovery of JCV subtypes in a pocket or pockets that were separated by great geographic distances from the main domains of those subtypes. Certain of these pockets can readily be explained by recent migrations of human populations carrying these subtypes. Overall, it appears that JCV genotyping promises to reveal previously unknown human migration routes: ancient as well as recent.

Indexed as

Biological EvolutionGenetics, PopulationJC VirusAdultBiomarkersDNA, ViralEmigration and ImmigrationHumansMolecular Sequence DataBiomarkersDNA, Viral

Identifiers

PMID9256458
PMCPMC23108

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.