It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Background
Norovirus is the most common cause of acute gastroenteritis in the United States and a major challenge for infection control efforts. The high burden of norovirus in most communities and health care systems makes it difficult to discern viral transmission patterns using traditional epidemiological approaches alone.
Methods
We performed real-time metagenomic sequencing of norovirus isolates from an outbreak among inpatients at Seattle Children’s Hospital (SCH). We also sequenced isolates from norovirus cases within the larger University of Washington (UW) Medical System that occurred during and after the outbreak.
Results
Our data showed that the month-long outbreak at SCH was actually characterized by 3 distinct concurrent transmission clusters contained within 3 different hospital units. We were able to report this information to the infection control team at SCH while the outbreak was still in progress. The virus responsible for one of these 3 clusters was genetically stable over a period of 4.5 weeks suggesting serial transmissions from a contaminated fomite, rather than patient to patient transmission. After cases meeting the epidemiological definition for hospital-acquired had ceased, we demonstrated that the virus from one of the 3 outbreak clusters continued to be transmitted to other patients within the SCH medical system. Finally, we showed that one of the patients who acquired norovirus during the outbreak developed a chronic infection with viral shedding documented up until the time of the patient’s death, 8 months after the outbreak.
Conclusion
These results demonstrate the value of using metagenomics as an adjunct to traditional epidemiologic techniques in the setting of a hospital-associated norovirus outbreak. Real-time metagenomic sequencing elucidated viral transmission patterns within the outbreak while it was still in progress and follow-up sequencing revealed further infections due to an outbreak-associated viral strain even after the outbreak was thought to be over. Given this potential, metagenomic analyses represent an invaluable, largely untapped resource for improving our understanding of and reducing adverse effects from viral outbreaks.
Disclosures
All authors: No reported disclosures.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
1 Department of Medicine, University of Washington, Seattle, Washington
2 Seattle Children’s Research Institute, Seattle, Washington
3 Department of Laboratory Medicine, University of Washington, Seattle, Washington
4 Laboratory Medicine, University of Washington, Seattle, Washington
5 Seattle Children’s Hospital, Seattle, Washington
6 Pediatrics, University of Washington, Seattle, Washington
7 University of Washington, Seattle, Washington