Evidence map›Paper›PMID 24348465›Full record

ArticleFrontiers in microbiology2013

Vibrio cholerae O1 epidemic variants in Angola: a retrospective study between 1992 and 2006.

Romy Valia, Elisa Taviani, Matteo Spagnoletti, Daniela Ceccarelli, Piero Cappuccinelli, Mauro M Colombo

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Article in Frontiers in microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Vibrio ecology, pathogenesis, and evolution.Frontiers in microbiology · 2014
    Article
  8. 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

6 authors.

Romy ValiaDipartimento di Biologia e Biotecnologie C. Darwin, Università di Roma Sapienza Rome, Italy.
Elisa TavianiDipartimento di Biologia e Biotecnologie C. Darwin, Università di Roma Sapienza Rome, Italy ; Centro de Biotecnologia, Universidade E. Mondlane Maputo Mozambique.
Matteo SpagnolettiDepartment of Genetics, University College London Genetics Institute, Evolution and Environment, University College London London, UK.
Daniela CeccarelliDepartment of Cell Biology and Molecular Genetics, Maryland Pathogen Research Institute, University of Maryland College Park, MD, USA.
Piero CappuccinelliDipartimento di Scienze Biomediche, Università di Sassari Sassari, Italy.
Mauro M ColomboDipartimento di Biologia e Biotecnologie C. Darwin, Università di Roma Sapienza Rome, Italy ; Centro de Biotecnologia, Universidade E. Mondlane Maputo Mozambique.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholera is still a major public health concern in many African countries. In Angola, after a decade of absence, cholera reemerged in 1987, spreading throughout the country until 1996, with outbreaks recurring in a seasonal pattern. In 2006 Angola was hit by one of the most severe outbreaks of the last decade, with ca. 240,000 cases reported. We analyzed 21 clinical strains isolated between 1992 and 2006 from several provinces throughout the country: Benguela, Bengo, Luanda, Cuando Cubango, and Cabinda. We used two multiplex PCR assays to investigate discriminatory mobile genetic elements (MGE) [Integrative Conjugative Elements (ICEs), VSP-II, GI12, GI14, GI15, K, and TLC phages] and we compared the profiles obtained with those of different reference V. cholerae O1 variants (prototypical, altered, and hybrid), responsible for the ongoing 7th pandemic. We also tested the strains for the presence of specific VSP-II variants and for the presence of a genomic island (GI) (WASA-1), correlated with the transmission of seventh pandemic cholera from Africa to South America. Based on the presence/absence of the analyzed genetic elements, five novel profiles were detected in the epidemic strains circulating in the 1990s. The most frequent profiles, F and G, were characterized by the absence of ICEs and the three GIs tested, and the presence of GI WASA-1 and the WASA variant of the VSP-II island. Our results identified unexpected variability within the 1990s epidemic, showing different rearrangements in a dynamic part of the genome not present in the prototypical V. cholerae O1 N16961. Moreover the 2006 strains differed from the current pandemic V. cholerae O1 strain. Taken together, our results highlight the role of horizontal gene transfer (HGT) in diversifying the genetic background of V. cholerae within a single epidemic.

Indexed as

Angolaepidemic variantsgenomic islandsmobilomeV. cholerae O1

Identifiers

PMID24348465
PMCPMC3842873

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