Publications by authors named "S Blome"

African swine fever (ASF) emerged in Germany in 2020. A few weeks after the initial occurrence, infected wild boar were detected in Saxony. In this study, data from wild boar surveillance in Saxony were analyzed.

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African swine fever (ASF) has become a major focus of research after spreading to four continents besides Africa. In its natural African ecosystem, the causative ASF virus (ASFV) is maintained by indigenous Suidae as natural reservoirs and hard tick vectors. However, in Sus scrofa domesticated breeds and wild boar, ASFV causes devastating disease, with mortalities reaching over 90%.

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Background: Long-term pain is a common health problem that results in disability for patients of all ages, leading to an enormous economic burden. Over 20% of the population suffer from long-term pain. Unfortunately, there are no clinical tests that predicts who will develop long-term pain.

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Obtaining a complete good-quality sequence and annotation for the long double-stranded DNA genome of the African swine fever virus (ASFV) from next-generation sequencing (NGS) technology has proven difficult, despite the increasing availability of reference genome sequences and the increasing affordability of NGS. A gap analysis conducted by the global African swine fever research alliance (GARA) partners identified that a standardized, automatic pipeline for NGS analysis was urgently needed, particularly for new outbreak strains. Whilst there are several diagnostic and research labs worldwide that collect isolates of the ASFV from outbreaks, many do not have the capability to analyze, annotate, and format NGS data from outbreaks for submission to NCBI, and some publicly available ASFV genomes have missing or incorrect annotations.

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Article Synopsis
  • African swine fever virus (ASFV) poses a significant threat to domestic pigs and wild boar, necessitating better understanding and detection methods for disease control.
  • Researchers demonstrated that ASFV can be transmitted through artificial insemination from infected boars to healthy gilts, emphasizing the need for monitoring boar semen before use.
  • The study evaluated different nucleic acid extraction kits and qPCR protocols, ultimately establishing an effective workflow for detecting ASFV in boar semen just 2 days after infection, especially focusing on low-level virus detection.
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