7 research outputs found
Characterization of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection clusters based on integrated genomic surveillance, outbreak analysis and contact tracing in an urban setting
BACKGROUND: Tracing of SARS-CoV-2 transmission chains is still a major challenge for public health authorities, when incidental contacts are not recalled or are not perceived as potential risk contacts. Viral sequencing can address key questions about SARS-CoV-2 evolution and may support reconstruction of viral transmission networks by integration of molecular epidemiology into classical contact tracing.
METHODS: In collaboration with local public health authorities, we set up an integrated system of genomic surveillance in an urban setting, combining a) viral surveillance sequencing, b) genetically based identification of infection clusters in the population, c) integration of public health authority contact tracing data, and d) a user-friendly dashboard application as a central data analysis platform. RESULTS: Application of the integrated system from August to December 2020 enabled a characterization of viral population structure, analysis of four outbreaks at a maximum care hospital, and genetically based identification of five putative population infection clusters, all of which were confirmed by contact tracing. The system contributed to the development of improved hospital infection control and prevention measures and enabled the identification of previously unrecognized transmission chains, involving a martial arts gym and establishing a link between the hospital to the local population. CONCLUSIONS: Integrated systems of genomic surveillance could contribute to the monitoring and, potentially, improved management of SARS-CoV-2 transmission in the population
Integrated genomic surveillance enables tracing of person-to-person SARS-CoV-2 transmission chains during community transmission and reveals extensive onward transmission of travel-imported infections, Germany, June to July 2021
BackgroundTracking person-to-person SARS-CoV-2 transmission in the population is important to understand the epidemiology of community transmission and may contribute to the containment of SARS-CoV-2. Neither contact tracing nor genomic surveillance alone, however, are typically sufficient to achieve this objective.AimWe demonstrate the successful application of the integrated genomic surveillance (IGS) system of the German city of Düsseldorf for tracing SARS-CoV-2 transmission chains in the population as well as detecting and investigating travel-associated SARS-CoV-2 infection clusters.MethodsGenomic surveillance, phylogenetic analysis, and structured case interviews were integrated to elucidate two genetically defined clusters of SARS-CoV-2 isolates detected by IGS in Düsseldorf in July 2021.ResultsCluster 1 (n = 67 Düsseldorf cases) and Cluster 2 (n = 36) were detected in a surveillance dataset of 518 high-quality SARS-CoV-2 genomes from Düsseldorf (53% of total cases, sampled mid-June to July 2021). Cluster 1 could be traced back to a complex pattern of transmission in nightlife venues following a putative importation by a SARS-CoV-2-infected return traveller (IP) in late June; 28 SARS-CoV-2 cases could be epidemiologically directly linked to IP. Supported by viral genome data from Spain, Cluster 2 was shown to represent multiple independent introduction events of a viral strain circulating in Catalonia and other European countries, followed by diffuse community transmission in Düsseldorf.ConclusionIGS enabled high-resolution tracing of SARS-CoV-2 transmission in an internationally connected city during community transmission and provided infection chain-level evidence of the downstream propagation of travel-imported SARS-CoV-2 cases
Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020
We show the distribution of SARS-CoV-2 genetic clades over time and between countries and outline potential genomic surveillance objectives. We applied three available genomic nomenclature systems for SARS-CoV-2 to all sequence data from the WHO European Region available during the COVID-19 pandemic until 10 July 2020. We highlight the importance of real-time sequencing and data dissemination in a pandemic situation. We provide a comparison of the nomenclatures and lay a foundation for future European genomic surveillance of SARS-CoV-2.Peer reviewe
Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020
We show the distribution of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) genetic clades over time and between countries and outline potential genomic surveillance objectives. We applied three genomic nomenclature systems to all sequence data from the World Health Organization European Region available until 10 July 2020. We highlight the importance of real-time sequencing and data dissemination in a pandemic situation, compare the nomenclatures and lay a foundation for future European genomic surveillance of SARS-CoV-2
Experimental Characterization of the Properties of Double-Lap Needled and Hybrid Joints of Carbon/Epoxy Composites
The effect of through-thickness reinforcement by thin 1 mm steel needles (z-pins) on the static tensile strength of double-lap joints of a carbon/epoxy composite was investigated. Two types of joints—z-pinned and hybrid (including glued ones)—were considered. The joints were reinforced in the overlap region with 9, 25, or 36 z-pins. Comparing mechanical properties of the double-lap joints with the corresponding characteristics of their unpinned counterparts, the z-pins were found to be highly effective: the strength and stiffness of the pinned joints increased up to 300% and 280%, respectively. These improvements were due to a transition in the failure mechanism from debonding of the joint in the absence of z-pins to pullout or shear rupture of z-pins or to the tensile failure of laminate adherends, depending on the volume content of the pins
Comparative Analysis of Pyrosequencing and a Phylogenetic Microarray for Exploring Microbial Community Structures in the Human Distal Intestine
Background: Variations in the composition of the human intestinal microbiota are linked to diverse health conditions. Highthroughput
molecular technologies have recently elucidated microbial community structure at much higher resolution than
was previously possible. Here we compare two such methods, pyrosequencing and a phylogenetic array, and evaluate
classifications based on two variable 16S rRNA gene regions.
Methods and Findings: Over 1.75 million amplicon sequences were generated from the V4 and V6 regions of 16S rRNA
genes in bacterial DNA extracted from four fecal samples of elderly individuals. The phylotype richness, for individual
samples, was 1,400–1,800 for V4 reads and 12,500 for V6 reads, and 5,200 unique phylotypes when combining V4 reads
from all samples. The RDP-classifier was more efficient for the V4 than for the far less conserved and shorter V6 region, but
differences in community structure also affected efficiency. Even when analyzing only 20% of the reads, the majority of the
microbial diversity was captured in two samples tested. DNA from the four samples was hybridized against the Human
Intestinal Tract (HIT) Chip, a phylogenetic microarray for community profiling. Comparison of clustering of genus counts
from pyrosequencing and HITChip data revealed highly similar profiles. Furthermore, correlations of sequence abundance
and hybridization signal intensities were very high for lower-order ranks, but lower at family-level, which was probably due
to ambiguous taxonomic groupings.
Conclusions: The RDP-classifier consistently assigned most V4 sequences from human intestinal samples down to genuslevel
with good accuracy and speed. This is the deepest sequencing of single gastrointestinal samples reported to date, but
microbial richness levels have still not leveled out. A majority of these diversities can also be captured with five times lower
sampling-depth. HITChip hybridizations and resulting community profiles correlate well with pyrosequencing-based
compositions, especially for lower-order ranks, indicating high robustness of both approaches. However, incompatible
grouping schemes make exact comparison difficult.MJC, OOS, RPR and PWOT are members of the ELDERMET consortium (http://eldermet.ucc.ie), whose work is supported in part by the (Govt. of Ireland)
Dept. Agriculture Fisheries and Food/Health Research Board FHRI award to the ELDERMET project, as well as the Alimentary Pharmabiotic Centre. JN and WMdV
are supported by the Finnish Funding Agency for Technology and Innovation (TEKES grant 40274/06) and was performed in the Centre of Excellence on Microbial
Food Safety of the Academy of Finlan