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Sökning: WFRF:(Shah Shiraz A)

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1.
  • Haahr, Thor, et al. (författare)
  • Vaginal dysbiosis in pregnancy associates with risk of emergency caesarean section: a prospective cohort study
  • 2022
  • Ingår i: Clinical Microbiology and Infection. - Oxford, United Kingdom : Elsevier. - 1198-743X .- 1469-0691. ; 28:4, s. 588-595
  • Tidskriftsartikel (refereegranskat)abstract
    • Objectives: To investigate changes in vaginal microbiota during pregnancy, and the association between vaginal dysbiosis and reproductive outcomes.Methods: A total of 730 (week 24) and 666 (week 36) vaginal samples from 738 unselected pregnant women were studied by microscopy (Nugent score) and characterized by 16S rRNA gene sequencing. A novel continuous vaginal dysbiosis score was developed based on these methods using a supervised partial least squares model.Results: Among women with bacterial vaginosis in week 24 (n = 53), 47% (n = 25) also had bacterial vaginosis in week 36. In contrast, among women without bacterial vaginosis in week 24, only 3% (n = 18) developed bacterial vaginosis in week 36. Vaginal samples dominated by Lactobacillus crispatus (OR 0.35, 95% CI 0.20–0.60) and Lactobacillus iners (OR 0.40, 95% CI 0.23–0.68) in week 24 were significantly more stable by week 36 when compared with other vaginal community state types. Vaginal dysbiosis score at week 24 was associated with a significant increased risk of emergency, but not elective, caesarean section (OR 1.37, 955 CI 1.15–1.64, p < 0.001), suggesting a 37% increased risk per standard deviation increase in vaginal dysbiosis score.Conclusions: Changes in vaginal microbiota from week 24 to week 36 of pregnancy correlated with bacterial vaginosis status and vaginal community state type. A novel vaginal dysbiosis score was associated with a significantly increased risk of emergency, but not elective, caesarean section. This was not found for bacterial vaginosis or any vaginal community state type and could point to the importance of investigating vaginal dysbiosis as a nuanced continuum instead of crude clusters. 
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2.
  • Hedman, Fredrik, et al. (författare)
  • Benchmarking of Integrated OGSA-BES with the Grid Middleware
  • 2009
  • Ingår i: EURO-PAR 2008 WORKSHOPS - PARALLEL PROCESSING. - Berlin : Springer Berlin/Heidelberg. - 9783642009549 ; , s. 113-122
  • Konferensbidrag (refereegranskat)abstract
    • This paper evaluates the performance of the emerging OGF standard OGSA - Basic Execution Service (BES) on three fundamentally different Grid middleware platforms: UNICORE 5/6, Globus Toolkit 4 and gLite. The particular focus within this paper is on the OGSA-BES implementation of UNICORE 6. A comparison is made with baseline measurements, for UNICORE 6 and Globus Toolkit 4, using the legacy job submission interfaces. Our results show that the BES components are comparable in performance to existing legacy interfaces. We also have a strong indication that other factors, attributable to the supporting infrastructure, have a bigger impact on performance than BES components.
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3.
  • Makarova, Kira S, et al. (författare)
  • An updated evolutionary classification of CRISPR-Cas systems
  • 2015
  • Ingår i: Nature Reviews Microbiology. - : Springer Science and Business Media LLC. - 1740-1526 .- 1740-1534. ; 13:11, s. 722-736
  • Tidskriftsartikel (refereegranskat)abstract
    • The evolution of CRISPR-cas loci, which encode adaptive immune systems in archaea and bacteria, involves rapid changes, in particular numerous rearrangements of the locus architecture and horizontal transfer of complete loci or individual modules. These dynamics complicate straightforward phylogenetic classification, but here we present an approach combining the analysis of signature protein families and features of the architecture of cas loci that unambiguously partitions most CRISPR-cas loci into distinct classes, types and subtypes. The new classification retains the overall structure of the previous version but is expanded to now encompass two classes, five types and 16 subtypes. The relative stability of the classification suggests that the most prevalent variants of CRISPR-Cas systems are already known. However, the existence of rare, currently unclassifiable variants implies that additional types and subtypes remain to be characterized.
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