ArticlePLoS neglected tropical diseases2015
Diverse Genotypes of Yersinia pestis Caused Plague in Madagascar in 2007.
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.
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Who cites it
8 citing papers in PubMed.
- Review of genotyping methods for Yersinia pestis in Madagascar.PLoS neglected tropical diseases · 2024Review
- Yersinia pestis and plague: an updated view on evolution, virulence determinants, immune subversion, vaccination, and diagnostics.Genes and immunity · 2019Review
- Genetic diversity and spatial-temporal distribution of Yersinia pestis in Qinghai Plateau, China.PLoS neglected tropical diseases · 2018Article
- Reemergence of human plague in Yunnan, China in 2016.PloS one · 2018Article
- Article
- Low cost, low tech SNP genotyping tools for resource-limited areas: Plague in Madagascar as a model.PLoS neglected tropical diseases · 2017Article
- Temporal phylogeography of Yersinia pestis in Madagascar: Insights into the long-term maintenance of plague.PLoS neglected tropical diseases · 2017Article
- Whole genome multilocus sequence typing as an epidemiologic tool for Yersinia pestis.Diagnostic microbiology and infectious disease · 2016Article
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Authors and funding
14 authors.
Funding
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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.
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