The Impact of the Staphylococcus aureus Virulome on Infection in a Developing Country: A Cohort Study

We performed a cohort study to analyze the virulome of from the Democratic Republic of the Congo using whole genome sequencing and to assess its impact on the course of infections. Community-associated from nasal colonization ( = 100) and infection ( = 86) were prospectively collected. Phenotypic su...

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Published inFrontiers in microbiology Vol. 8; p. 1662
Main Authors Lebughe, Marthe, Phaku, Patrick, Niemann, Silke, Mumba, Dieudonné, Peters, Georg, Muyembe-Tamfum, Jean-Jacques, Mellmann, Alexander, Strauß, Lena, Schaumburg, Frieder
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 29.08.2017
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Summary:We performed a cohort study to analyze the virulome of from the Democratic Republic of the Congo using whole genome sequencing and to assess its impact on the course of infections. Community-associated from nasal colonization ( = 100) and infection ( = 86) were prospectively collected. Phenotypic susceptibility testing and WGS was done for each isolate. WGS data were used to screen for 79 different virulence factors and for genotyping purposes ( typing, multilocus sequence typing). The majority of the 79 virulence factors were equally distributed among isolates from colonization and infection. Panton-Valentine leukocidin (PVL) and the non-truncated hemolysin β were associated with skin and soft tissue infection (SSTI) and recurrence of disease but did not influence the course of infection (i.e., mortality, surgical intervention). For the first time, we show that not only PVL but also hemolysin β could contribute to the development of SSTI in PVL-endemic areas such as Africa.
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Edited by: Paul D. Brown, University of the West Indies, Jamaica
This article was submitted to Infectious Diseases, a section of the journal Frontiers in Microbiology
Reviewed by: Haider Abdul-Lateef Mousa, University of Basrah, Iraq; Rustam Aminov, University of Aberdeen, United Kingdom
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2017.01662