Evidence map›Paper›PMID 26069964›Full record

ArticlePLoS neglected tropical diseases2015

Diverse Genotypes of Yersinia pestis Caused Plague in Madagascar in 2007.

Julia M Riehm, Michaela Projahn, Amy J Vogler, Minoaerisoa Rajerison, Genevieve Andersen, Carina M Hall, Thomas Zimmermann, Rahelinirina Soanandrasana, Voahangy Andrianaivoarimanana, Reinhard K Straubinger and 4 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2015. 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.

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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

14 authors.

Julia M RiehmCentral Institute of the Bundeswehr Medical Service, Munich, Germany.
Michaela ProjahnBundeswehr Institute of Microbiology & German Center for Infectious Diseases, Munich, Germany.
Amy J VoglerCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, United States of America.
Minoaerisoa RajerisonInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Genevieve AndersenCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, United States of America.
Carina M HallCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, United States of America.
Thomas ZimmermannCentral Institute of the Bundeswehr Medical Service, Munich, Germany.
Rahelinirina SoanandrasanaInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Voahangy AndrianaivoarimananaInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Reinhard K StraubingerInstitute for Infectious Medicine and Zoonoses, Munich, Germany.
Roxanne NottinghamCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, United States of America.
Paul KeimCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, United States of America; Translational Genomics Research Institute North, Flagstaff, Arizona, United States of America.
David M WagnerCenter for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, United States of America.
Holger C ScholzBundeswehr Institute of Microbiology & German Center for Infectious Diseases, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundYersinia pestis is the causative agent of human plague and is endemic in various African, Asian and American countries. In Madagascar, the disease represents a significant public health problem with hundreds of human cases a year. Unfortunately, poor infrastructure makes outbreak investigations challenging. METHODOLOGY/PRINCIPAL

findingsDNA was extracted directly from 93 clinical samples from patients with a clinical diagnosis of plague in Madagascar in 2007. The extracted DNAs were then genotyped using three molecular genotyping methods, including, single nucleotide polymorphism (SNP) typing, multi-locus variable-number tandem repeat analysis (MLVA), and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) analysis. These methods provided increasing resolution, respectively. The results of these analyses revealed that, in 2007, ten molecular groups, two newly described here and eight previously identified, were responsible for causing human plague in geographically distinct areas of Madagascar. CONCLUSIONS/SIGNIFICANCE: Plague in Madagascar is caused by numerous distinct types of Y. pestis. Genotyping method choice should be based upon the discriminatory power needed, expense, and available data for any desired comparisons. We conclude that genotyping should be a standard tool used in epidemiological investigations of plague outbreaks.

Indexed as

GenotypeClustered Regularly Interspaced Short Palindromic RepeatsHumansMadagascarMultilocus Sequence TypingPhylogenyPlaguePolymorphism, Single NucleotideYersinia pestis

Identifiers

PMID26069964
PMCPMC4466568

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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.