Evidence map›Paper›PMID 11724837›Full record

ArticleJournal of clinical microbiology2001

Molecular characterization of new clinical isolates of Candida albicans and C. dubliniensis in Japan: analysis reveals a new genotype of C. albicans with group I intron.

M Tamura, K Watanabe, Y Mikami, K Yazawa, K Nishimura

Abstract read
In one paragraph

Article in Journal of clinical microbiology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

31 citing papers in PubMed.

  1. Article
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  3. Mating type and genotyping ofIranian journal of microbiology · 2026
    Article
  4. Phenotypic and genotypic characterization ofJournal of oral microbiology · 2025
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  5. Microorganisms · 2024
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  6. Genotyping ofCurrent medical mycology · 2022
    Article
  7. Candida dubliniensis fungemia in a patient with severe COVID-19: A case report.Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy · 2022
    Article
  8. Co-Infection of OralMedicina (Kaunas, Lithuania) · 2022
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  9. Infection and drug resistance · 2022
    Article
  10. Article
  11. Article
  12. Genotype Analysis of ClinicalInfection and drug resistance · 2019
    Article
  13. Article
  14. Enterogenous infection ofWorld journal of emergency medicine · 2016
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

M TamuraResearch Center for Pathogenic Fungi and Microbial Toxicoses, Chiba University, Japan.
K Watanabe
Y Mikami
K Yazawa
K Nishimura

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The genetic diversity of recent clinical isolates of Candida albicans in Japan was studied on the basis of amplified DNA band lengths determined with a specific PCR primer reported to have been designed to span a transposable intron region in the 25S rRNA gene. Our analyses of 301 clinical isolates of C. albicans showed that they could be classified into five genotypes: genotype A (172 isolates), genotype B (66 isolates), genotype C (56 isolates), genotype D (C. dubliniensis; 5 isolates), and a new genotype (designated genotype E; 2 isolates). The new genotype E was characterized to have a group I intron-like sequence, which is longer than hitherto reported ones and which has a nucleotide sequence length of 962 bp. Our analysis of the 962-bp sequence indicated that it is composed of an intron similar to that of C. dubliniensis of 621 bp with a 341-bp insertion. Analysis of the sequence of the internal transcribed spacer (ITS) region of the genotype E strain showed that its sequence is identical to those of strains of other genotypes, with only a few base substitution differences. Throughout the study, the possible horizontal transfer of the group I intron between C. dubliniensis and C. albicans was suggested. A high degree of correlation between the presence of a group I intron in C. albicans genotype E and susceptibility to the antifungal agent flucytosine was observed. The five isolates of C. dubliniensis examined in the present study showed genetic diversity when they were compared by randomly amplified polymorphic DNA fingerprinting pattern analysis, and this diversity was also confirmed by the analysis of ITS region sequences.

Indexed as

Antifungal AgentsBase SequenceCandidaCandida albicansCandidiasisDNA, FungalDNA, Ribosomal SpacerGenotypeHumansIntronsJapanMicrobial Sensitivity TestsMolecular Sequence DataMycological Typing TechniquesPhenotypeRandom Amplified Polymorphic DNA TechniqueAntifungal AgentsDNA, FungalDNA, Ribosomal Spacer

Identifiers

PMID11724837
PMCPMC88541

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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.