2011
DOI: 10.1128/aem.05709-11
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Comparison of Surface Sampling Methods for Virus Recovery from Fomites

Abstract: The role of fomites in infectious disease transmission relative to other exposure routes is difficult to discern due, in part, to the lack of information on the level and distribution of virus contamination on surfaces. Comparisons of studies intending to fill this gap are difficult because multiple different sampling methods are employed and authors rarely report their method's lower limit of detection. In the present study, we compare a subset of sampling methods identified from a literature review to demons… Show more

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Cited by 61 publications
(56 citation statements)
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References 81 publications
(97 reference statements)
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“…Notably, the vast majority of these studies have utilized B. anthracis spores (13,20,23,27,28,48) or spores of a surrogate organism (4,5,8,9,18,58). Comparatively little effort has been applied in recent years toward improved surface sampling of viruses (31) and vegetative bacterial cells that represent likely biothreat (BT) agents (or surrogates thereof) (7,29,39,60).…”
mentioning
confidence: 99%
“…Notably, the vast majority of these studies have utilized B. anthracis spores (13,20,23,27,28,48) or spores of a surrogate organism (4,5,8,9,18,58). Comparatively little effort has been applied in recent years toward improved surface sampling of viruses (31) and vegetative bacterial cells that represent likely biothreat (BT) agents (or surrogates thereof) (7,29,39,60).…”
mentioning
confidence: 99%
“…In previous studies, different elution media and swab materials for the recovery of rotavirus, MS2, feline calicivirus (FCV), and bacteriophage P22 were evaluated (19)(20)(21)(22). However, extrapolation of the results from these studies to a validated protocol for human norovirus is difficult, since many test variables, including the surrogate virus used for assessment of the recovery of infectious virus, the type of swab material, and the area of the swabbed surface, have not been evaluated and tested under field conditions.…”
mentioning
confidence: 99%
“…These results suggests that short MS2 indicator gene sequences, of less than 100 bp, commonly used to quantify MS2 abundance7891012, may lead to false abundance estimates. A combination of culture based plaque assay and possibly targeting of larger indicator sequences in qRT PCR would therefore be recommended for an accurate quantitation of virions in environmental samples.…”
Section: Discussionmentioning
confidence: 99%