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- Volume 21, Issue 49, 08/Dec/2016
Eurosurveillance - Volume 21, Issue 49, 08 December 2016
Volume 21, Issue 49, 2016
- Rapid communication
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Highly pathogenic avian influenza A(H5N8) outbreaks: protection and management of exposed people in Europe, 2014/15 and 2016
Cornelia Adlhoch , Ian H. Brown , Svetla G. Angelova , Ádám Bálint , Ruth Bouwstra , Silke Buda , Maria R. Castrucci , Gavin Dabrera , Ádám Dán , Christian Grund , Timm Harder , Wim van der Hoek , Katalin Krisztalovics , Frances Parry-Ford , Rodica Popescu , Anders Wallensten , Anna Zdravkova , Siamak Zohari , Svetla Tsolova and Pasi PenttinenIntroduction of highly pathogenic avian influenza (HPAI) virus A(H5N8) into Europe prompted animal and human health experts to implement protective measures to prevent transmission to humans. We describe the situation in 2016 and list public health measures and recommendations in place. We summarise critical interfaces identified during the A(H5N1) and A(H5N8) outbreaks in 2014/15. Rapid exchange of information between the animal and human health sectors is critical for a timely, effective and efficient response.
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- Research article
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Comparison of Leishmania typing results obtained from 16 European clinical laboratories in 2014
Gert Van der Auwera , Aldert Bart , Carmen Chicharro , Sofia Cortes , Leigh Davidsson , Trentina Di Muccio , Jean-Claude Dujardin , Ingrid Felger , Maria Grazia Paglia , Felix Grimm , Gundel Harms , Charles L. Jaffe , Monika Manser , Christophe Ravel , Florence Robert-Gangneux , Jeroen Roelfsema , Seray Töz , Jaco J. Verweij and Peter L. ChiodiniLeishmaniasis is endemic in southern Europe, and in other European countries cases are diagnosed in travellers who have visited affected areas both within the continent and beyond. Prompt and accurate diagnosis poses a challenge in clinical practice in Europe. Different methods exist for identification of the infecting Leishmania species. Sixteen clinical laboratories in 10 European countries, plus Israel and Turkey, conducted a study to assess their genotyping performance. DNA from 21 promastigote cultures of 13 species was analysed blindly by the routinely used typing method. Five different molecular targets were used, which were analysed with PCR-based methods. Different levels of identification were achieved, and either the Leishmania subgenus, species complex, or actual species were reported. The overall error rate of strains placed in the wrong complex or species was 8.5%. Various reasons for incorrect typing were identified. The study shows there is considerable room for improvement and standardisation of Leishmania typing. The use of well validated standard operating procedures is recommended, covering testing, interpretation, and reporting guidelines. Application of the internal transcribed spacer 1 of the rDNA array should be restricted to Old World samples, while the heat-shock protein 70 gene and the mini-exon can be applied globally.
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Volumes & issues
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Volume 29 (2024)
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Volume 28 (2023)
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Volume 27 (2022)
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Volume 26 (2021)
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Volume 25 (2020)
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Volume 24 (2019)
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Volume 23 (2018)
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Volume 22 (2017)
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Volume 21 (2016)
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Volume 20 (2015)
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Volume 19 (2014)
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Volume 18 (2013)
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Volume 17 (2012)
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Volume 16 (2011)
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Volume 15 (2010)
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Volume 14 (2009)
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Volume 13 (2008)
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Volume 12 (2007)
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Volume 11 (2006)
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Volume 10 (2005)
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Volume 9 (2004)
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Volume 8 (2003)
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Volume 7 (2002)
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Volume 6 (2001)
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Volume 5 (2000)
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Volume 4 (1999)
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Volume 3 (1998)
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Volume 2 (1997)
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Volume 1 (1996)
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Volume 0 (1995)
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