2015
DOI: 10.1128/jcm.03686-14
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Detection of Enterovirus D68 in Canadian Laboratories

Abstract: The recent emergence of a severe respiratory disease caused by enterovirus D68 prompted investigation into whether Canadian hospital and provincial laboratories can detect this virus using commercial and laboratory-developed assays. This study demonstrated analytical sensitivity differences between commercial and laboratory-developed assays for the detection of enterovirus D68.

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Cited by 15 publications
(14 citation statements)
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“…Other EV types from species A, B and C were also detected at different rates. EV-A and B are occasionally detected in respiratory samples and their involvement in the respiratory pathology is not as clear as in the case of EV-D68 and EV-C104, EV-C105 or EV-C109 [2,[5][6][7][8][9][10][11][12][13][14][15][16]31,32]. This is in agreement with the fact that in our study, in most cases, EV-D68 was the single infectious agent.…”
Section: Discussionsupporting
confidence: 82%
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“…Other EV types from species A, B and C were also detected at different rates. EV-A and B are occasionally detected in respiratory samples and their involvement in the respiratory pathology is not as clear as in the case of EV-D68 and EV-C104, EV-C105 or EV-C109 [2,[5][6][7][8][9][10][11][12][13][14][15][16]31,32]. This is in agreement with the fact that in our study, in most cases, EV-D68 was the single infectious agent.…”
Section: Discussionsupporting
confidence: 82%
“…Since 2014, an increasing number of EV-D68 outbreaks associated with severe respiratory diseases, mainly in children, have been occurring in different countries, first in the US and Canada, followed by Europe and Asia. Concurrently, clusters of cases with neurological complications such as myelitis or acute flaccid paralysis were reported in the same geographical areas [9][10][11][12][13][14][15][16][17][18][19][20][21].…”
Section: Discussionmentioning
confidence: 88%
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“…(b) Commercially available molecular test panels may not fulfill all testing needs. A major drawback of multiplexed panels is the inability to differentiate closely related viruses or to detect all targets with equivalent sensitivity, and some targets on commercial multiplex panels continue to be detected more efficiently by singleplex assays (278) (also see comments on emerging pathogens below). In one study, detection of RSVA and FLUA had decreased sensitivity in panel tests compared to that with singleplex NAAT (279).…”
Section: Molecular Panel Testing For Respiratory Viruses (I) Defininmentioning
confidence: 99%
“…Another limitation in some available assays is the inability to distinguish EVs from RVs. This can lead to secondary laboratory differentiation algorithms to characterize infection (282), and this is compounded by the limited ability to detect emerging EV strains (278). For example, enterovirus D68 may require altered patient management compared to seasonal EV strains, as it is associated with extrapulmonary syndromes such as acute flaccid paralysis (282).…”
Section: Molecular Panel Testing For Respiratory Viruses (I) Defininmentioning
confidence: 99%